| 1 | Comorbid Bronchial Asthma, Atopic Dermatitis and Hashimoto's Thyroiditis Are Risk Factors for Early‐Onset, Severe and Prolonged Alopecia Areata | 6.7 | 5 | Citations (PDF) |
| 2 | Männlicher Haarausfall – was uns unsere Gene verraten | 0.1 | 0 | Citations (PDF) |
| 3 | Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study | 5.2 | 20 | Citations (PDF) |
| 4 | Genetic associations of cardiovascular risk genes in European patients with coronary artery spasm | 2.8 | 6 | Citations (PDF) |
| 5 | The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression | 7.8 | 3 | Citations (PDF) |
| 6 | Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall study | 2.3 | 3 | Citations (PDF) |
| 7 | Cohort profile: BioMD-Y (biopsychosocial factors of major depression in youth) – a biobank study on the molecular genetics and environmental factors of depression in children and adolescents in Munich | 1.9 | 2 | Citations (PDF) |
| 8 | Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample | 5.2 | 3 | Citations (PDF) |
| 9 | Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings | 25.2 | 41 | Citations (PDF) |
| 10 | Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance | 5.5 | 2 | Citations (PDF) |
| 11 | Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure | 5.2 | 2 | Citations (PDF) |
| 12 | Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries | 25.2 | 20 | Citations (PDF) |
| 13 | Socioeconomic position interacts with the genetic effect of a CRP gene common variant to influence C-reactive protein values | 3.4 | 2 | Citations (PDF) |
| 14 | Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents | 2.3 | 0 | Citations (PDF) |
| 15 | Elucidation of the genetic causes of bicuspid aortic valve disease | 5.5 | 44 | Citations (PDF) |
| 16 | Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder | 7.8 | 19 | Citations (PDF) |
| 17 | Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology | 0.2 | 9 | Citations (PDF) |
| 18 | Association between urinary iodine excretion, genetic disposition and fluid intelligence in children, adolescents and young adults: the DONALD study | 3.4 | 1 | Citations (PDF) |
| 19 | IFN-γ secretion of PBMC from non-drug-allergic control persons: Considerations for the validity of a positive lymphocyte transformation test | 1.4 | 4 | Citations (PDF) |
| 20 | Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder | 7.8 | 38 | Citations (PDF) |
| 21 | Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment | 12.5 | 15 | Citations (PDF) |
| 22 | Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss | 13.7 | 12 | Citations (PDF) |
| 23 | European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation | 13.7 | 119 | Citations (PDF) |
| 24 | Deeplasia: deep learning for bone age assessment validated on skeletal dysplasias | 1.8 | 38 | Citations (PDF) |
| 25 | Nachruf Prof. Dr. rer. nat. Jeanette Erdmann | 0.2 | 0 | Citations (PDF) |
| 26 | Evidence for a shared genetic contribution to loneliness and borderline personality disorder | 5.2 | 6 | Citations (PDF) |
| 27 | Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders | 5.4 | 129 | Citations (PDF) |
| 28 | Cis-epistasis at the LPA locus and risk of cardiovascular diseases | 5.5 | 27 | Citations (PDF) |
| 29 | Ventral Striatal–Hippocampus Coupling During Reward Processing as a Stratification Biomarker for Psychotic Disorders | 5.4 | 17 | Citations (PDF) |
| 30 | Genetic risk for psychiatric illness is associated with the number of hospitalizations of bipolar disorder patients | 4.5 | 13 | Citations (PDF) |
| 31 | Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors | 5.4 | 236 | Citations (PDF) |
| 32 | Genome-wide interaction study with major depression identifies novel variants associated with cognitive function | 7.8 | 45 | Citations (PDF) |
| 33 | Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history | 4.2 | 38 | Citations (PDF) |
| 34 | Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease | 4.4 | 36 | Citations (PDF) |
| 35 | Effects of DRD2/ANKK1 and COMT Val158Met polymorphisms on stabilization against and adaptation to unexpected events | 2.8 | 0 | Citations (PDF) |
| 36 | Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia | 2.7 | 37 | Citations (PDF) |
| 37 | Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanisms | 0.7 | 9 | Citations (PDF) |
| 38 | A genetic risk score of alleles related to MGUS interacts with socioeconomic position in a population-based cohort | 3.4 | 0 | Citations (PDF) |
| 39 | Genetic variants associated with longitudinal changes in brain structure across the lifespan | 17.1 | 205 | Citations (PDF) |
| 40 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia | 37.9 | 2,593 | Citations (PDF) |
| 41 | ExomeChip-based rare variant association study in restless legs syndrome | 1.6 | 1 | Citations (PDF) |
| 42 | Epigenetic Signatures of Smoking in Five Brain Regions | 2.4 | 12 | Citations (PDF) |
| 43 | New insights into the genetic etiology of Alzheimer’s disease and related dementias | 25.2 | 2,243 | Citations (PDF) |
| 44 | Wie wichtig ist die Kenntnis des genetischen Populationshintergrundes in der Medizin? Ein humangenetischer Beitrag vor dem Hintergrund der aktuellen Diskussion um die Verwendung des Begriffs „Rasse“ | 0.2 | 0 | Citations (PDF) |
| 45 | Borderline personality disorder and the big five: molecular genetic analyses indicate shared genetic architecture with neuroticism and openness | 5.2 | 20 | Citations (PDF) |
| 46 | Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6 | 5.5 | 3 | Citations (PDF) |
| 47 | Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum | 5.2 | 34 | Citations (PDF) |
| 48 | Chemokine receptor 4 expression on blood T lymphocytes predicts severity of major depressive disorder | 4.5 | 10 | Citations (PDF) |
| 49 | GWAS of thyroid dysgenesis identifies a risk locus at 2q33.3 linked to regulation of Wnt signaling | 2.9 | 7 | Citations (PDF) |
| 50 | A novel longitudinal clustering approach to psychopathology across diagnostic entities in the hospital-based PsyCourse study | 2.3 | 14 | Citations (PDF) |
| 51 | eQTL Set–Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma | 1.1 | 7 | Citations (PDF) |
| 52 | Hepatic Expression of the Na+-Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation | 4.4 | 13 | Citations (PDF) |
| 53 | Staffelübergabe in der Redaktionsleitung | 0.2 | 0 | Citations (PDF) |
| 54 | Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people | 7.5 | 111 | Citations (PDF) |
| 55 | Analysis of associations between dietary patterns, genetic disposition, and cognitive function in data from UK Biobank | 3.4 | 9 | Citations (PDF) |
| 56 | Genetic and functional analyses implicate microRNA 499A in bipolar disorder development | 5.2 | 12 | Citations (PDF) |
| 57 | A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy | 4.4 | 11 | Citations (PDF) |
| 58 | A common variation in HCN1 is associated with heart rate variability in schizophrenia | 2.3 | 19 | Citations (PDF) |
| 59 | Generative network models of altered structural brain connectivity in schizophrenia | 4.4 | 39 | Citations (PDF) |
| 60 | Germline variation in the insulin-like growth factor pathway and risk of Barrett’s esophagus and esophageal adenocarcinoma | 2.8 | 13 | Citations (PDF) |
| 61 | Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease | 4.6 | 21 | Citations (PDF) |
| 62 | Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder | 5.2 | 28 | Citations (PDF) |
| 63 | Prediction of lithium response using genomic data | 3.4 | 20 | Citations (PDF) |
| 64 | Interaction of developmental factors and ordinary stressful life events on brain structure in adults | 3.3 | 9 | Citations (PDF) |
| 65 | Hyper-Coordinated DNA Methylation is Altered in Schizophrenia and Associated with Brain Function | 1.4 | 5 | Citations (PDF) |
| 66 | Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes | 3.4 | 22 | Citations (PDF) |
| 67 | Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families | 5.2 | 42 | Citations (PDF) |
| 68 | “The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment | 1.5 | 9 | Citations (PDF) |
| 69 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology | 25.2 | 1,471 | Citations (PDF) |
| 70 | Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2 | 0.6 | 1 | Citations (PDF) |
| 71 | Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors —results of the Heinz Nixdorf Recall Study | 2.6 | 6 | Citations (PDF) |
| 72 | Apolipoprotein E homozygous ε4 allele status: Effects on cortical structure and white matter integrity in a young to mid-age sample | 1.0 | 9 | Citations (PDF) |
| 73 | Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores | 13.7 | 293 | Citations (PDF) |
| 74 | Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning | 5.4 | 56 | Citations (PDF) |
| 75 | DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations | 2.3 | 12 | Citations (PDF) |
| 76 | LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding | 29.8 | 74 | Citations (PDF) |
| 77 | Search for AL amyloidosis risk factors using Mendelian randomization | 5.0 | 11 | Citations (PDF) |
| 78 | TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19 | 4.3 | 55 | Citations (PDF) |
| 79 | Identification of pleiotropy at the gene level between psychiatric disorders and related traits | 5.2 | 16 | Citations (PDF) |
| 80 | Untersuchung genetischer Einflüsse auf Riechstörungen bei Patienten mit hereditärem Angioödem Typ 1 und 2 | 0.6 | 0 | Citations (PDF) |
| 81 | Interaction of Alzheimer’s Disease-Associated Genetic Risk with Indicators of Socioeconomic Position on Mild Cognitive Impairment in the Heinz Nixdorf Recall Study | 2.6 | 10 | Citations (PDF) |
| 82 | A genetic sum score of effect alleles associated with serum lipid concentrations interacts with educational attainment | 3.4 | 2 | Citations (PDF) |
| 83 | HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders | 3.4 | 23 | Citations (PDF) |
| 84 | Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness | 2.3 | 11 | Citations (PDF) |
| 85 | Systematic Investigation of a Potential Epidemiological and Genetic Association Between Male Androgenetic Alopecia and COVID-19 | 1.2 | 3 | Citations (PDF) |
| 86 | Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients | 1.7 | 23 | Citations (PDF) |
| 87 | Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 | 13.7 | 37 | Citations (PDF) |
| 88 | Epigenome-wide association study of alcohol use disorder in five brain regions | 5.4 | 35 | Citations (PDF) |
| 89 | Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients | 5.2 | 56 | Citations (PDF) |
| 90 | Polygenic risk scores across the extended psychosis spectrum | 5.2 | 26 | Citations (PDF) |
| 91 | Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology | 25.2 | 515 | Citations (PDF) |
| 92 | Pathway-Specific Genetic Risk for Alzheimer’s Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults | 2.8 | 13 | Citations (PDF) |
| 93 | Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression | 6.1 | 40 | Citations (PDF) |
| 94 | Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1 | 1.5 | 12 | Citations (PDF) |
| 95 | Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD | 4.5 | 25 | Citations (PDF) |
| 96 | Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia | 7.8 | 104 | Citations (PDF) |
| 97 | A large-scale genome-wide association study meta-analysis of cannabis use disorder | 17.3 | 356 | Citations (PDF) |
| 98 | Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany | 13.7 | 260 | Citations (PDF) |
| 99 | Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles | 2.5 | 6 | Citations (PDF) |
| 100 | Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study | 1.8 | 15 | Citations (PDF) |
| 101 | Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification—Results of the Heinz Nixdorf Recall study | 2.3 | 11 | Citations (PDF) |
| 102 | Shared Genetic Etiology of Obesity-Related Traits and Barrett's Esophagus/Adenocarcinoma: Insights from Genome-Wide Association Studies | 1.1 | 7 | Citations (PDF) |
| 103 | Replication of a hippocampus specific effect of the tescalcin regulating variant rs7294919 on gray matter structure | 1.0 | 2 | Citations (PDF) |
| 104 | Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies | 2.7 | 56 | Citations (PDF) |
| 105 | The genetic architecture of the human cerebral cortex | 36.3 | 758 | Citations (PDF) |
| 106 | Association of polygenic score for major depression with response to lithium in patients with bipolar disorder | 7.8 | 76 | Citations (PDF) |
| 107 | Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families | 5.2 | 38 | Citations (PDF) |
| 108 | Association of a Reproducible Epigenetic Risk Profile for Schizophrenia With Brain Methylation and Function | 12.4 | 66 | Citations (PDF) |
| 109 | Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank | 7.8 | 192 | Citations (PDF) |
| 110 | Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification | 1.8 | 34 | Citations (PDF) |
| 111 | Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition | 5.4 | 26 | Citations (PDF) |
| 112 | An Investigation of Psychosis Subgroups With Prognostic Validation and Exploration of Genetic Underpinnings | 12.4 | 59 | Citations (PDF) |
| 113 | A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q | 0.7 | 7 | Citations (PDF) |
| 114 | The role of environmental stress and DNA methylation in the longitudinal course of bipolar disorder | 2.1 | 21 | Citations (PDF) |
| 115 | Insights into the genomics of affective disorders | 0.2 | 4 | Citations (PDF) |
| 116 | Out of the lab and into the clinic: steps to a pragmatic new era in psychiatric genetics | 0.2 | 0 | Citations (PDF) |
| 117 | Polygenic scores for psychiatric disease: from research tool to clinical application | 0.2 | 21 | Citations (PDF) |
| 118 | Combating the SARS-CoV-2 pandemic: How can the field of Human Genetics contribute? | 0.2 | 0 | Citations (PDF) |
| 119 | Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study | 2.1 | 30 | Citations (PDF) |
| 120 | Molekulargenetische Erkenntnisse erweitern das Verständnis psychiatrischer Störungen | 0.8 | 0 | Citations (PDF) |
| 121 | Effects of a neurodevelopmental genes based polygenic risk score for schizophrenia and single gene variants on brain structure in non-clinical subjects: A preliminary report | 2.3 | 7 | Citations (PDF) |
| 122 | Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression | 7.8 | 140 | Citations (PDF) |
| 123 | HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype | 25.2 | 143 | Citations (PDF) |
| 124 | Die Rolle seltener Varianten bei häufigen Krankheiten | 0.2 | 1 | Citations (PDF) |
| 125 | Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes | 3.4 | 17 | Citations (PDF) |
| 126 | A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study | 2.3 | 16 | Citations (PDF) |
| 127 | Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population | 5.2 | 7 | Citations (PDF) |
| 128 | Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder | 5.2 | 48 | Citations (PDF) |
| 129 | PEDIA: prioritization of exome data by image analysis | 4.2 | 77 | Citations (PDF) |
| 130 | Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure | 2.3 | 13 | Citations (PDF) |
| 131 | Associations of schizophrenia risk genes ZNF804A and CACNA1C with schizotypy and modulation of attention in healthy subjects | 2.3 | 26 | Citations (PDF) |
| 132 | Genome-wide association study identifies 30 loci associated with bipolar disorder | 25.2 | 1,514 | Citations (PDF) |
| 133 | Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies | 8.8 | 430 | Citations (PDF) |
| 134 | Transcriptome-wide analysis of filarial extract-primed human monocytes reveal changes in LPS-induced PTX3 expression levels | 3.4 | 4 | Citations (PDF) |
| 135 | Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma | 4.4 | 16 | Citations (PDF) |
| 136 | No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study | 6.0 | 19 | Citations (PDF) |
| 137 | First genotype‐phenotype study reveals HLA‐DQβ1 insertion heterogeneity in high‐resolution manometry achalasia subtypes | 4.8 | 12 | Citations (PDF) |
| 138 | Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma | 7.7 | 17 | Citations (PDF) |
| 139 | Durchbrüche im Verständnis der molekularen Ursachen psychiatrischer Störungen | 0.8 | 15 | Citations (PDF) |
| 140 | Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia | 5.2 | 104 | Citations (PDF) |
| 141 | Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing | 25.2 | 2,920 | Citations (PDF) |
| 142 | Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study | 2.3 | 10 | Citations (PDF) |
| 143 | Identification of loci of functional relevance to Barrett’s esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data | 2.3 | 9 | Citations (PDF) |
| 144 | Genetic architecture of subcortical brain structures in 38,851 individuals | 25.2 | 272 | Citations (PDF) |
| 145 | Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric DisordersCell, 2019, 179, 1469-1482.e11 | 33.6 | 1,377 | Citations (PDF) |
| 146 | The influence of religious activity and polygenic schizophrenia risk on religious delusions in schizophrenia | 2.3 | 14 | Citations (PDF) |
| 147 | Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data | 2.3 | 16 | Citations (PDF) |
| 148 | Genetic variation associated with chromosomal aberration frequency: A genome‐wide association study | 2.0 | 11 | Citations (PDF) |
| 149 | Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder | 1.0 | 9 | Citations (PDF) |
| 150 | Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance | 7.7 | 16 | Citations (PDF) |
| 151 | Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders | 7.8 | 47 | Citations (PDF) |
| 152 | Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder | 12.4 | 120 | Citations (PDF) |
| 153 | Polygenic risk for schizophrenia affects working memory and its neural correlates in healthy subjects | 2.3 | 12 | Citations (PDF) |
| 154 | Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia | 13.7 | 73 | Citations (PDF) |
| 155 | Arzneimittelassoziierte Angioödeme | 1.0 | 10 | Citations (PDF) |
| 156 | Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation | 3.3 | 51 | Citations (PDF) |
| 157 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression | 25.2 | 2,987 | Citations (PDF) |
| 158 | El estudio Andalusian Bipolar Family (ABiF): protocolo y descripción de la muestra | 1.8 | 8 | Citations (PDF) |
| 159 | The influence of MIR137 on white matter fractional anisotropy and cortical surface area in individuals with familial risk for psychosis | 2.3 | 7 | Citations (PDF) |
| 160 | Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata | 2.3 | 27 | Citations (PDF) |
| 161 | Investigation of dominant and recessive inheritance models in genome‐wide association studies data of nonsyndromic cleft lip with or without cleft palate | 1.6 | 8 | Citations (PDF) |
| 162 | Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder | 4.5 | 16 | Citations (PDF) |
| 163 | Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders | 17.1 | 668 | Citations (PDF) |
| 164 | Exploring Genetic Associations of Alzheimer’s Disease Loci With Mild Cognitive Impairment Neurocognitive Endophenotypes | 3.9 | 12 | Citations (PDF) |
| 165 | Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder | 5.2 | 26 | Citations (PDF) |
| 166 | Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma | 13.7 | 109 | Citations (PDF) |
| 167 | Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphomaBlood, 2018, 132, 2040-2052 | 4.8 | 23 | Citations (PDF) |
| 168 | Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study | 5.6 | 13 | Citations (PDF) |
| 169 | Evidence for PTGER4,PSCA, and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level | 2.6 | 26 | Citations (PDF) |
| 170 | Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder | 2.4 | 31 | Citations (PDF) |
| 171 | Analysis of shared heritability in common disorders of the brain | 36.3 | 1,393 | Citations (PDF) |
| 172 | Evaluation of food allergy candidate loci in the Genetics of Food Allergy study | 6.1 | 2 | Citations (PDF) |
| 173 | Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology | 5.5 | 42 | Citations (PDF) |
| 174 | Effects of BDNF Val66Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans | 5.4 | 23 | Citations (PDF) |
| 175 | Neurobiology of the major psychoses: a translational perspective on brain structure and function—the FOR2107 consortium | 2.7 | 161 | Citations (PDF) |
| 176 | Cortical surface area alterations shaped by genetic load for neuroticism | 7.8 | 26 | Citations (PDF) |
| 177 | Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2 | 2.7 | 27 | Citations (PDF) |
| 178 | Novel genetic loci associated with hippocampal volume | 13.7 | 297 | Citations (PDF) |
| 179 | Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics | 4.1 | 53 | Citations (PDF) |
| 180 | Influence of age and cognitive performance on resting-state brain networks of older adults in a population-based cohort | 2.9 | 68 | Citations (PDF) |
| 181 | Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAs | 2.5 | 35 | Citations (PDF) |
| 182 | Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness | 13.7 | 93 | Citations (PDF) |
| 183 | Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifestyle) | 3.8 | 16 | Citations (PDF) |
| 184 | Genetische Grundlagen der bipolaren Störung | 0.8 | 18 | Citations (PDF) |
| 185 | Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach | 5.5 | 13 | Citations (PDF) |
| 186 | Polygenic risk for depression and the neural correlates of working memory in healthy subjects | 3.8 | 44 | Citations (PDF) |
| 187 | Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia | 5.2 | 188 | Citations (PDF) |
| 188 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans | 4.2 | 733 | Citations (PDF) |
| 189 | Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors | 25.2 | 339 | Citations (PDF) |
| 190 | Genomewide association study on monoclonal gammopathy of unknown significance (MGUS) | 1.8 | 20 | Citations (PDF) |
| 191 | Genetic effects influencing risk for major depressive disorder in China and Europe | 5.2 | 74 | Citations (PDF) |
| 192 | An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype | 5.4 | 96 | Citations (PDF) |
| 193 | Associations between SNPs and immune-related circulating proteins in schizophrenia | 3.4 | 25 | Citations (PDF) |
| 194 | Pharmacogenetic association of blood-lipid related genetic variants with 5-year progression of coronary artery calcification following the treatment with statin in the Heinz Nixdorf Recall study | 1.5 | 0 | Citations (PDF) |
| 195 | Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy | 13.7 | 103 | Citations (PDF) |
| 196 | Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations | 13.7 | 196 | Citations (PDF) |
| 197 | Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease | 25.2 | 998 | Citations (PDF) |
| 198 | Clinical Utility Gene Card for hereditary angioedema with normal C1 inhibitor (HAEnC1) | 3.0 | 10 | Citations (PDF) |
| 199 | Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing | 5.5 | 36 | Citations (PDF) |
| 200 | Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders | 5.2 | 11 | Citations (PDF) |
| 201 | Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility | 13.7 | 45 | Citations (PDF) |
| 202 | Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus | 13.7 | 79 | Citations (PDF) |
| 203 | Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes | 3.4 | 65 | Citations (PDF) |
| 204 | Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response | 4.1 | 81 | Citations (PDF) |
| 205 | Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data | 5.2 | 6 | Citations (PDF) |
| 206 | Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling | 2.9 | 50 | Citations (PDF) |
| 207 | Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis | 2.5 | 13 | Citations (PDF) |
| 208 | Identification of shared risk loci and pathways for bipolar disorder and schizophrenia | 2.3 | 87 | Citations (PDF) |
| 209 | Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function | 3.2 | 24 | Citations (PDF) |
| 210 | Syndromale und nichtsyndromale orofaziale Spalten | 0.2 | 4 | Citations (PDF) |
| 211 | The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders | 7.8 | 78 | Citations (PDF) |
| 212 | Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS | 3.2 | 37 | Citations (PDF) |
| 213 | The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine | 1.0 | 14 | Citations (PDF) |
| 214 | Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia | 1.3 | 0 | Citations (PDF) |
| 215 | Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families | 0.5 | 16 | Citations (PDF) |
| 216 | Analysis of Rare Variants in the Alcohol Dependence Candidate Gene
GATA
4 | 2.5 | 1 | Citations (PDF) |
| 217 | Perceived stress and hair cortisol: Differences in bipolar disorder and schizophrenia | 2.7 | 57 | Citations (PDF) |
| 218 | Differential Expression between Human Dermal Papilla Cells from Balding and Non-Balding Scalps Reveals New Candidate Genes for Androgenetic Alopecia | 2.3 | 92 | Citations (PDF) |
| 219 | Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data | 2.1 | 22 | Citations (PDF) |
| 220 | Novel genetic loci underlying human intracranial volume identified through genome-wide association | 17.1 | 240 | Citations (PDF) |
| 221 | Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis | 6.5 | 236 | Citations (PDF) |
| 222 | Immunochip analysis identifies association of the
RAD
50/
IL
13
region with human longevity | 6.8 | 24 | Citations (PDF) |
| 223 | Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio‐oedema | 6.7 | 14 | Citations (PDF) |
| 224 | Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us? | 2.7 | 60 | Citations (PDF) |
| 225 | Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis | 27.4 | 168 | Citations (PDF) |
| 226 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis | 25.2 | 593 | Citations (PDF) |
| 227 | Genome-wide association study identifies multiple susceptibility loci for multiple myeloma | 13.7 | 175 | Citations (PDF) |
| 228 | Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation | 10.9 | 167 | Citations (PDF) |
| 229 | Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population | 1.9 | 11 | Citations (PDF) |
| 230 | Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder | 2.9 | 218 | Citations (PDF) |
| 231 | CNV analysis in 169 patients with bladder exstrophy-epispadias complex | 1.8 | 18 | Citations (PDF) |
| 232 | Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis | 1.4 | 49 | Citations (PDF) |
| 233 | Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study | 62.1 | 369 | Citations (PDF) |
| 234 | Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases | 3.8 | 63 | Citations (PDF) |
| 235 | Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project | 4.7 | 68 | Citations (PDF) |
| 236 | Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes | 6.1 | 196 | Citations (PDF) |
| 237 | Genetic variants of lipase activity in chronic pancreatitis | 16.8 | 11 | Citations (PDF) |
| 238 | Genome-wide significant risk factors for Alzheimer’s disease: role in progression to dementia due to Alzheimer's disease among subjects with mild cognitive impairment | 7.8 | 119 | Citations (PDF) |
| 239 | Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma | 7.7 | 38 | Citations (PDF) |
| 240 | Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 | 3.7 | 12 | Citations (PDF) |
| 241 | A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1 | 7.7 | 80 | Citations (PDF) |
| 242 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects | 25.2 | 1,063 | Citations (PDF) |
| 243 | Supportive evidence for FOXP1,BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma | 2.6 | 29 | Citations (PDF) |
| 244 | Quantifying the heritability of glioma using genome-wide complex trait analysis | 3.4 | 41 | Citations (PDF) |
| 245 | The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A | 3.4 | 34 | Citations (PDF) |
| 246 | A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder | 1.0 | 15 | Citations (PDF) |
| 247 | Pluripotent stem cell-derived radial glia-like cells as stable intermediate for efficient generation of human oligodendrocytesGlia, 2015, 63, 2152-2167 | 5.0 | 61 | Citations (PDF) |
| 248 | A novelKRT86mutation in a Turkish family with monilethrix, and identification of maternal mosaicism | 1.1 | 10 | Citations (PDF) |
| 249 | DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations | 3.9 | 72 | Citations (PDF) |
| 250 | Investigation of the role of TCF4 rare sequence variants in schizophrenia | 1.5 | 17 | Citations (PDF) |
| 251 | First report of a FXII
gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor | 1.7 | 6 | Citations (PDF) |
| 252 | Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array | 3.1 | 16 | Citations (PDF) |
| 253 | Meta-analysis identifies seven susceptibility loci involved in the atopic march | 13.7 | 170 | Citations (PDF) |
| 254 | Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms | 6.5 | 189 | Citations (PDF) |
| 255 | Identification and functional characterization of rare SHANK2 variants in schizophrenia | 7.8 | 88 | Citations (PDF) |
| 256 | Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci | 13.7 | 284 | Citations (PDF) |
| 257 | Common genetic variants influence human subcortical brain structures | 37.9 | 895 | Citations (PDF) |
| 258 | A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome | 25.2 | 116 | Citations (PDF) |
| 259 | Recurrent null mutation in SPG20 leads to Troyer syndrome | 2.6 | 17 | Citations (PDF) |
| 260 | Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy | 3.2 | 54 | Citations (PDF) |
| 261 | Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells | 13.7 | 69 | Citations (PDF) |
| 262 | Systematic Integration of Brain eQTL and GWAS IdentifiesZNF323as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function | 3.9 | 55 | Citations (PDF) |
| 263 | Genome-wide association study identifies multiple susceptibility loci for glioma | 13.7 | 126 | Citations (PDF) |
| 264 | NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression | 5.4 | 62 | Citations (PDF) |
| 265 | Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases | 25.2 | 193 | Citations (PDF) |
| 266 | A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis | 25.2 | 542 | Citations (PDF) |
| 267 | Rare SHANK2 variants in schizophrenia | 7.8 | 21 | Citations (PDF) |
| 268 | Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture | 6.5 | 303 | Citations (PDF) |
| 269 | Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder | 5.2 | 73 | Citations (PDF) |
| 270 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci | 25.2 | 413 | Citations (PDF) |
| 271 | Immunochip-Based Analysis: High-Density Genotyping of Immune-Related Loci Sheds Further Light on the Autoimmune Genetic Architecture of Alopecia Areata | 2.3 | 8 | Citations (PDF) |
| 272 | Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium | 5.4 | 74 | Citations (PDF) |
| 273 | Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis | 3.0 | 9 | Citations (PDF) |
| 274 | Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis | 3.7 | 26 | Citations (PDF) |
| 275 | Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts | 1.3 | 108 | Citations (PDF) |
| 276 | High loading of polygenic risk in cases with chronic schizophrenia | 7.8 | 75 | Citations (PDF) |
| 277 | GWAS for executive function and processing speed suggests involvement of the CADM2 gene | 7.8 | 145 | Citations (PDF) |
| 278 | A novel Alzheimer disease locus located near the gene encoding tau protein | 7.8 | 313 | Citations (PDF) |
| 279 | Using Network Methodology to Infer Population Substructure | 2.3 | 0 | Citations (PDF) |
| 280 | Molecular Characterization of F8 Secreting CellBlood, 2015, 126, 4671-4671 | 4.8 | 0 | Citations (PDF) |
| 281 | Genetik bipolar affektiver Störungen Gegenwärtiger Stand der Arbeiten zur Identifikation von Dispositionsgenen | 0.8 | 0 | Citations (PDF) |
| 282 | Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS | 3.9 | 127 | Citations (PDF) |
| 283 | Genetic markers associated with abstinence length in alcohol-dependent subjects treated with acamprosate | 5.2 | 60 | Citations (PDF) |
| 284 | Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myeloma | 7.7 | 13 | Citations (PDF) |
| 285 | MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD | 5.2 | 88 | Citations (PDF) |
| 286 | Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia | 3.2 | 53 | Citations (PDF) |
| 287 | Striatal Response to Reward Anticipation | 12.4 | 107 | Citations (PDF) |
| 288 | Genetic variation in the
lymphotoxin-α
(
LTA
)/
tumour necrosis factor-α
(
TNFα
) locus as a risk factor for idiopathic achalasia | 16.8 | 24 | Citations (PDF) |
| 289 | Smoking behaviour | 1.3 | 3 | Citations (PDF) |
| 290 | Common variant at 16p11.2 conferring risk of psychosis | 7.8 | 97 | Citations (PDF) |
| 291 | A genome-wide supported variant in CACNA1C influences hippocampal activation during episodic memory encoding and retrieval | 2.7 | 34 | Citations (PDF) |
| 292 | Genome-wide association study reveals two new risk loci for bipolar disorder | 13.7 | 326 | Citations (PDF) |
| 293 | FARVAT: a family-based rare variant association test | 4.7 | 34 | Citations (PDF) |
| 294 | Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes | 13.7 | 72 | Citations (PDF) |
| 295 | Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder | 2.9 | 21 | Citations (PDF) |
| 296 | Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association | 5.3 | 123 | Citations (PDF) |
| 297 | Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status | 3.1 | 1 | Citations (PDF) |
| 298 | Defining the role of common variation in the genomic and biological architecture of adult human height | 25.2 | 1,982 | Citations (PDF) |
| 299 | Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia | 25.2 | 116 | Citations (PDF) |
| 300 | Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | 25.2 | 325 | Citations (PDF) |
| 301 | Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder | 5.2 | 39 | Citations (PDF) |
| 302 | Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects | 4.4 | 35 | Citations (PDF) |
| 303 | Hippocampal and Frontolimbic Function as Intermediate Phenotype for Psychosis: Evidence from Healthy Relatives and a Common Risk Variant in CACNA1C | 5.4 | 60 | Citations (PDF) |
| 304 | Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients | 7.8 | 117 | Citations (PDF) |
| 305 | XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans | 5.4 | 14 | Citations (PDF) |
| 306 | Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease | 2.3 | 165 | Citations (PDF) |
| 307 | Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability | 2.3 | 35 | Citations (PDF) |
| 308 | Longer telomere length in patients with schizophrenia | 2.3 | 59 | Citations (PDF) |
| 309 | Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study | 1.8 | 38 | Citations (PDF) |
| 310 | Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk | 25.2 | 157 | Citations (PDF) |
| 311 | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma | 25.2 | 106 | Citations (PDF) |
| 312 | Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease | 25.2 | 4,413 | Citations (PDF) |
| 313 | Dysfunctional nitric oxide signalling increases risk of myocardial infarction | 37.9 | 263 | Citations (PDF) |
| 314 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs | 25.2 | 2,286 | Citations (PDF) |
| 315 | Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology | 2.3 | 114 | Citations (PDF) |
| 316 | High-density genotyping study identifies four new susceptibility loci for atopic dermatitis | 25.2 | 195 | Citations (PDF) |
| 317 | The Effect of Neurogranin on Neural Correlates of Episodic Memory Encoding and Retrieval | 3.9 | 34 | Citations (PDF) |
| 318 | Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma | 13.7 | 71 | Citations (PDF) |
| 319 | Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets | 5.2 | 14 | Citations (PDF) |
| 320 | A One-Degree-of-Freedom Test for Supra-Multiplicativity of SNP Effects | 2.3 | 2 | Citations (PDF) |
| 321 | A Genetic Deconstruction of Neurocognitive Traits in Schizophrenia and Bipolar Disorder | 2.3 | 21 | Citations (PDF) |
| 322 | MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review | 3.4 | 58 | Citations (PDF) |
| 323 | Further Evidence for the Impact of a Genome-Wide-Supported Psychosis Risk Variant in ZNF804A on the Theory of Mind Network | 5.4 | 44 | Citations (PDF) |
| 324 | Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort | 3.0 | 62 | Citations (PDF) |
| 325 | Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene | 7.8 | 60 | Citations (PDF) |
| 326 | Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility | 7.8 | 64 | Citations (PDF) |
| 327 | Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases | 3.2 | 120 | Citations (PDF) |
| 328 | Identification of common variants associated with human hippocampal and intracranial volumes | 25.2 | 648 | Citations (PDF) |
| 329 | Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci | 25.2 | 346 | Citations (PDF) |
| 330 | Common Genetic Variants and Gene-Expression Changes Associated with Bipolar Disorder Are Over-Represented in Brain Signaling Pathway Genes | 5.4 | 57 | Citations (PDF) |
| 331 | Familial occurrence of the VATER/VACTERL association | 1.3 | 43 | Citations (PDF) |
| 332 | Etiopathological aspects of achalasia: lessons learned with Hirschsprung's disease | 0.5 | 9 | Citations (PDF) |
| 333 | Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder | 7.8 | 86 | Citations (PDF) |
| 334 | Reduced Anxiety and Depression-Like Behaviours in the Circadian Period Mutant Mouse Afterhours | 2.3 | 59 | Citations (PDF) |
| 335 | De novo microduplication at 22q11.21 in a patient with VACTERL association | 1.6 | 58 | Citations (PDF) |
| 336 | The genetics of panic disorder | 3.8 | 50 | Citations (PDF) |
| 337 | Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report | 1.8 | 16 | Citations (PDF) |
| 338 | Breakthroughs in the genetics of orofacial clefting | 7.4 | 130 | Citations (PDF) |
| 339 | Morbus Galli-Galli | 1.0 | 26 | Citations (PDF) |
| 340 | Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample | 1.3 | 6 | Citations (PDF) |
| 341 | Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay | 1.7 | 3 | Citations (PDF) |
| 342 | Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness | 1.7 | 64 | Citations (PDF) |
| 343 | A systematic eQTL study of cis–trans epistasis in 210 HapMap individuals | 3.0 | 28 | Citations (PDF) |
| 344 | Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk | 25.2 | 150 | Citations (PDF) |
| 345 | A systematic association mapping on chromosome 6q in bipolar affective disorder—evidence for the melanin‐concentrating‐hormone‐receptor‐2 gene as a risk factor for bipolar affective disorder | 1.5 | 7 | Citations (PDF) |
| 346 | The impact of dystrobrevin‐binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval | 3.5 | 18 | Citations (PDF) |
| 347 | Impact of schizophrenia‐risk gene dysbindin 1 on brain activation in bilateral middle frontal gyrus during a working memory task in healthy individuals | 3.5 | 40 | Citations (PDF) |
| 348 | Association study of 20 genetic variants at the D-amino acid oxidase gene in schizophrenia | 1.3 | 2 | Citations (PDF) |
| 349 | VEGF Gene Haplotypes Are Associated With SarcoidosisChest, 2010, 137, 156-163 | 1.0 | 40 | Citations (PDF) |
| 350 | Susceptibility locus for non‐syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients | 1.7 | 22 | Citations (PDF) |
| 351 | Achalasia: will genetic studies provide insights? | 2.9 | 93 | Citations (PDF) |
| 352 | Variation in GRIN2B contributes to weak performance in verbal short‐term memory in children with dyslexia | 1.5 | 38 | Citations (PDF) |
| 353 | A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3 | 1.5 | 17 | Citations (PDF) |
| 354 | Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias | 1.9 | 7 | Citations (PDF) |
| 355 | The
TRAF1/C5
locus confers risk for familial and severe alopecia areata | 1.7 | 20 | Citations (PDF) |
| 356 | Systematic mutation screening of KRT5
supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease | 1.7 | 61 | Citations (PDF) |
| 357 | Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1 | 25.2 | 166 | Citations (PDF) |
| 358 | Common variants in KCNN3 are associated with lone atrial fibrillation | 25.2 | 468 | Citations (PDF) |
| 359 | New genetic findings in schizophrenia: is there still room for the dopamine hypothesis of schizophrenia? | 2.4 | 24 | Citations (PDF) |
| 360 | A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia | 2.9 | 52 | Citations (PDF) |
| 361 | A genome-wide association study of alcohol dependence | 7.5 | 424 | Citations (PDF) |
| 362 | Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups | 3.2 | 301 | Citations (PDF) |
| 363 | A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case–control and family-based sample of German ancestry | 2.3 | 17 | Citations (PDF) |
| 364 | The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample | 2.3 | 21 | Citations (PDF) |
| 365 | Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder | 1.9 | 42 | Citations (PDF) |
| 366 | Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy | 1.6 | 119 | Citations (PDF) |
| 367 | Volition diminishes genetically mediated amygdala hyperreactivity | 4.4 | 104 | Citations (PDF) |
| 368 | Disruption of the neurexin 1 gene is associated with schizophrenia | 2.9 | 446 | Citations (PDF) |
| 369 | Genome-wide Association Study of Alcohol Dependence | 12.7 | 363 | Citations (PDF) |
| 370 | The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations | 2.9 | 82 | Citations (PDF) |
| 371 | Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients | 1.5 | 37 | Citations (PDF) |
| 372 | Genome‐wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin | 1.5 | 39 | Citations (PDF) |
| 373 | Association of major depression with rare functional variants in norepinephrine transporter and serotonin1Areceptor genes | 1.5 | 45 | Citations (PDF) |
| 374 | Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples | 1.5 | 55 | Citations (PDF) |
| 375 | Genetic variation in the schizophrenia‐risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals | 3.5 | 53 | Citations (PDF) |
| 376 | Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness | 2.9 | 39 | Citations (PDF) |
| 377 | Genetik der androgenetischen Alopezie | 0.2 | 0 | Citations (PDF) |
| 378 | Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects | 3.1 | 10 | Citations (PDF) |
| 379 | In Vitro Analysis of LIPH Mutations Causing Hypotrichosis Simplex: Evidence Confirming the Role of Lipase H and Lysophosphatidic Acid in Hair Growth | 2.3 | 32 | Citations (PDF) |
| 380 | Supporting evidence for LRRTM1 imprinting effects in schizophrenia | 7.8 | 61 | Citations (PDF) |
| 381 | Common variants conferring risk of schizophrenia | 37.9 | 1,662 | Citations (PDF) |
| 382 | Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis | 25.2 | 209 | Citations (PDF) |
| 383 | Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 | 25.2 | 444 | Citations (PDF) |
| 384 | Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease | 25.2 | 2,930 | Citations (PDF) |
| 385 | Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis | 25.2 | 388 | Citations (PDF) |
| 386 | Microduplications of 16p11.2 are associated with schizophrenia | 25.2 | 698 | Citations (PDF) |
| 387 | Further evidence for the involvement ofMYH9in the etiology of non‐syndromic cleft lip with or without cleft palate | 1.7 | 25 | Citations (PDF) |
| 388 | IRF6 gene variants in Central European patients with non‐syndromic cleft lip with or without cleft palate | 1.7 | 50 | Citations (PDF) |
| 389 | Mood‐incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome‐wide suggestive linkage at 1q32.3, 7p13 and 20q13.31 | 2.1 | 24 | Citations (PDF) |
| 390 | Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent | 1.2 | 3 | Citations (PDF) |
| 391 | Premorbid adjustment: A phenotype highlighting a distinction rather than an overlap between schizophrenia and bipolar disorder | 2.3 | 24 | Citations (PDF) |
| 392 | Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter | 2.3 | 73 | Citations (PDF) |
| 393 | A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe | 4.4 | 37 | Citations (PDF) |
| 394 | Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals | 4.4 | 35 | Citations (PDF) |
| 395 | No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample | 1.3 | 5 | Citations (PDF) |
| 396 | No association between the D-aspartate oxidase locus and schizophrenia | 1.3 | 1 | Citations (PDF) |
| 397 | Further evidence for DYX1C1 as a susceptibility factor for dyslexia | 1.3 | 65 | Citations (PDF) |
| 398 | Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate | 25.2 | 415 | Citations (PDF) |
| 399 | An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia | 0.0 | 0 | Citations (PDF) |
| 400 | The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata | 1.7 | 45 | Citations (PDF) |
| 401 | TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate | 2.0 | 35 | Citations (PDF) |
| 402 | Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample | 3.4 | 42 | Citations (PDF) |
| 403 | Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type? | 1.5 | 6 | Citations (PDF) |
| 404 | Large recurrent microdeletions associated with schizophrenia | 37.9 | 1,674 | Citations (PDF) |
| 405 | Identification of loci associated with schizophrenia by genome-wide association and follow-up | 25.2 | 1,024 | Citations (PDF) |
| 406 | Susceptibility variants for male-pattern baldness on chromosome 20p11 | 25.2 | 130 | Citations (PDF) |
| 407 | G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth | 25.2 | 399 | Citations (PDF) |
| 408 | The Opioid Peptides Enkephalin and β-Endorphin in Alcohol Dependence | 5.4 | 66 | Citations (PDF) |
| 409 | Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with differences in frontal brain activation in a working memory task in healthy individuals | 4.4 | 47 | Citations (PDF) |
| 410 | G72 and Its Association With Major Depression and Neuroticism in Large Population-Based Groups From Germany | 8.8 | 50 | Citations (PDF) |
| 411 | TCF7L2Polymorphismrs7903146and Predisposition for Type 2 Diabetes Mellitus in Obese Children | 1.8 | 8 | Citations (PDF) |
| 412 | Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15–q21 | 1.3 | 15 | Citations (PDF) |
| 413 | Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder | 1.3 | 13 | Citations (PDF) |
| 414 | Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population | 1.3 | 25 | Citations (PDF) |
| 415 | A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families | 1.6 | 20 | Citations (PDF) |
| 416 | Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects? | 7.8 | 99 | Citations (PDF) |
| 417 | Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo | 7.8 | 366 | Citations (PDF) |
| 418 | Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder | 7.8 | 181 | Citations (PDF) |
| 419 | Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 | 7.8 | 69 | Citations (PDF) |
| 420 | Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples | 7.8 | 74 | Citations (PDF) |
| 421 | Genetics of dyslexia: the evolving landscape | 3.8 | 114 | Citations (PDF) |
| 422 | Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder | 2.9 | 115 | Citations (PDF) |
| 423 | A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia | 2.9 | 103 | Citations (PDF) |
| 424 | No association between the serine racemase gene (SRR) and bipolar disorder in a German case–control sample | 1.3 | 0 | Citations (PDF) |
| 425 | No association between the serine racemase gene (SRR) and schizophrenia in a German case–control sample | 1.3 | 9 | Citations (PDF) |
| 426 | The First Genomewide Interaction and Locus-Heterogeneity Linkage Scan in Bipolar Affective Disorder: Strong Evidence of Epistatic Effects between Loci on Chromosomes 2q and 6q | 6.5 | 49 | Citations (PDF) |
| 427 | Premorbid adjustment in schizophrenia — An important aspect of phenotype definition | 2.3 | 48 | Citations (PDF) |
| 428 | Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene | 6.1 | 65 | Citations (PDF) |
| 429 | High incidence of the CFTR mutations 3272-26A→G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A→G, E588V, and 1671insTATCA) | 0.8 | 5 | Citations (PDF) |
| 430 | Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease | 2.3 | 102 | Citations (PDF) |
| 431 | HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study | 7.8 | 34 | Citations (PDF) |
| 432 | Interrelationship and Familiality of Dyslexia Related Quantitative Measures | 1.1 | 36 | Citations (PDF) |
| 433 | Identification of a keratin-associated protein with a putative role in vesicle transport | 3.9 | 44 | Citations (PDF) |
| 434 | Genetics and Neuroscience in Dyslexia: Perspectives for Education and Remediation | 1.8 | 26 | Citations (PDF) |
| 435 | The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function | 3.0 | 38 | Citations (PDF) |
| 436 | Identification of mutations in the human hairless gene in two new families with congenital atrichia | 1.6 | 17 | Citations (PDF) |
| 437 | Genetik der Alopecia areata | 0.2 | 1 | Citations (PDF) |
| 438 | A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder | 7.8 | 651 | Citations (PDF) |
| 439 | Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder | 7.8 | 41 | Citations (PDF) |
| 440 | Genes and Schizophrenia: The G72/G30 Gene Locus in Psychiatric Disorders: A Challenge to Diagnostic Boundaries? | 3.9 | 46 | Citations (PDF) |
| 441 | Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia | 6.5 | 216 | Citations (PDF) |
| 442 | Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations | 6.1 | 596 | Citations (PDF) |
| 443 | No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample | 1.3 | 7 | Citations (PDF) |
| 444 | The Impact of Genetics on Psychiatric Nosology | 8.8 | 1 | Citations (PDF) |
| 445 | No evidence for association between NOTCH4 and schizophrenia in a large family-based and case–control association analysis | 1.3 | 6 | Citations (PDF) |
| 446 | No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample | 1.3 | 8 | Citations (PDF) |
| 447 | Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata | 0.6 | 28 | Citations (PDF) |
| 448 | A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci | 3.0 | 12 | Citations (PDF) |
| 449 | Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata | 1.2 | 4 | Citations (PDF) |
| 450 | Family-based association study of theMTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex | 1.5 | 6 | Citations (PDF) |
| 451 | Association study of a functional promoter polymorphism in theXBP1 gene and schizophrenia | 1.5 | 13 | Citations (PDF) |
| 452 | Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder | 1.5 | 11 | Citations (PDF) |
| 453 | No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder | 1.3 | 8 | Citations (PDF) |
| 454 | A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp | 1.7 | 29 | Citations (PDF) |
| 455 | A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder | 7.8 | 37 | Citations (PDF) |
| 456 | Systematic investigation of genetic variability in 111 human genes—implications for studying variable drug response | 2.6 | 15 | Citations (PDF) |
| 457 | An interstitial deletion of chromosome 7 at band q21: A case report and review 2005, 134A, 12-23 | | 24 | Citations (PDF) |
| 458 | Family history influences age of onset in bipolar I disorder in females but not in males 2005, 133B, 6-11 | | 10 | Citations (PDF) |
| 459 | Genotype-Phenotype Studies in Bipolar Disorder Showing Association Between the DAOA/G30 Locus and Persecutory Delusions: A First Step Toward a Molecular Genetic Classification of Psychiatric Phenotypes | 8.8 | 124 | Citations (PDF) |
| 460 | Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q | 6.5 | 221 | Citations (PDF) |
| 461 | Norepinephrine transporter (NET) promoter and 5′-UTR polymorphisms: association analysis in panic disorder | 1.9 | 35 | Citations (PDF) |
| 462 | The power of sample size and homogenous sampling: Association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder | 5.4 | 136 | Citations (PDF) |
| 463 | Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression | 5.4 | 292 | Citations (PDF) |
| 464 | Linkage analyses of chromosomal region 18p11-q12 in dyslexia | 3.4 | 20 | Citations (PDF) |
| 465 | Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin | 25.2 | 57 | Citations (PDF) |
| 466 | Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study | 3.0 | 80 | Citations (PDF) |
| 467 | Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder | 7.8 | 297 | Citations (PDF) |
| 468 | The FU gene and its possible protein isoforms | 3.3 | 13 | Citations (PDF) |
| 469 | Prenatal diagnosis of Pfeiffer syndrome type II | 2.3 | 29 | Citations (PDF) |
| 470 | Family-based association studies of α-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder 2004, 126B, 79-81 | | 5 | Citations (PDF) |
| 471 | Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene 2004, 127B, 97-103 | | 43 | Citations (PDF) |
| 472 | Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients | 1.5 | 54 | Citations (PDF) |
| 473 | Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease | 4.6 | 40 | Citations (PDF) |
| 474 | Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women | 2.7 | 147 | Citations (PDF) |
| 475 | DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population | 1.9 | 5 | Citations (PDF) |
| 476 | Association of a functional −1019C>G 5-HT1A receptor gene polymorphism with panic disorder with agoraphobia | 2.7 | 109 | Citations (PDF) |
| 477 | Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population | 1.3 | 4 | Citations (PDF) |
| 478 | Investigation of the DAOA/G30 locus in panic disorder | 7.8 | 28 | Citations (PDF) |
| 479 | Androgenetische Alopezie | 1.0 | 23 | Citations (PDF) |
| 480 | Human nuclear transcription factor geneCREM: Genomic organization, mutation screening, and association analysis in panic disorder 2003, 117B, 70-78 | | 23 | Citations (PDF) |
| 481 | Is there a phenotypic difference between probands in case-control versus family-based association studies? 2003, 118B, 25-26 | | 1 | Citations (PDF) |
| 482 | Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin | 25.2 | 171 | Citations (PDF) |
| 483 | Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment | 5.4 | 46 | Citations (PDF) |
| 484 | Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder | 6.5 | 407 | Citations (PDF) |
| 485 | Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population | 4.6 | 72 | Citations (PDF) |
| 486 | Genetik bipolar affektiver Störungen | 0.1 | 1 | Citations (PDF) |
| 487 | Can long-range microsatellite data be used to predict short-range linkage disequilibrium? | 2.9 | 22 | Citations (PDF) |
| 488 | Moclobemide Response in Depressed Patients: Association Study with a Functional Polymorphism in the Monoamine Oxidase A Promoter | 1.8 | 41 | Citations (PDF) |
| 489 | Title is missing! | 6.7 | 6 | Citations (PDF) |
| 490 | No association between dopamine D4 receptor gene variants and Novelty Seeking | 7.8 | 82 | Citations (PDF) |
| 491 | Norepinephrine transporter gene (NET) variants in patients with panic disorder | 1.9 | 28 | Citations (PDF) |
| 492 | Further evidence for age of onset being an indicator for severity in bipolar disorder | 4.5 | 44 | Citations (PDF) |
| 493 | Association between a polymorphism in the pseudoautosomal X-linked geneSYBL1and bipolar affective disorder | 0.5 | 26 | Citations (PDF) |
| 494 | Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder | 0.5 | 19 | Citations (PDF) |
| 495 | Estrogen receptor 1 gene (ESR1) variants in panic disorder | 0.5 | 10 | Citations (PDF) |
| 496 | Human metabotropic glutamate receptor 2 gene (GRM2): Chromosomal sublocalization (3p21.1-p21.2) and genomic organization | 0.5 | 10 | Citations (PDF) |
| 497 | Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population | 0.5 | 87 | Citations (PDF) |
| 498 | The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach | 1.7 | 17 | Citations (PDF) |
| 499 | Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study | 5.4 | 66 | Citations (PDF) |
| 500 | Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder | 5.4 | 164 | Citations (PDF) |
| 501 | Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia | 6.5 | 15 | Citations (PDF) |
| 502 | Title is missing! | 6.7 | 64 | Citations (PDF) |
| 503 | Association between the 5′ UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder | 6.7 | 125 | Citations (PDF) |
| 504 | No association between serotonin 2A receptor gene variants and personality traits | 1.3 | 17 | Citations (PDF) |
| 505 | Analysis of the TSC2 gene in human medulloblastoma | 9.1 | 7 | Citations (PDF) |
| 506 | Mutational analysis of TSC1
and TSC2
genes in gangliogliomas | 3.1 | 73 | Citations (PDF) |
| 507 | Nonreplication of association between ?-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence | 0.5 | 113 | Citations (PDF) |
| 508 | Different familial transmission patterns in bipolar I disorder with onset before and after age 25 | 0.5 | 76 | Citations (PDF) |
| 509 | Caught in the trio trap? Potential selection bias inherent to association studies usings parent‐offspring trios | 0.5 | 22 | Citations (PDF) |
| 510 | Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia | 0.5 | 57 | Citations (PDF) |
| 511 | No association between a promoter dopamine D4receptor gene variant and schizophrenia | 0.5 | 20 | Citations (PDF) |
| 512 | Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease | 25.2 | 216 | Citations (PDF) |
| 513 | A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26 | 7.8 | 50 | Citations (PDF) |
| 514 | A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q | 2.9 | 126 | Citations (PDF) |
| 515 | Familial occurrence of tardive dyskinesia | 4.1 | 32 | Citations (PDF) |
| 516 | Exonic variants of the GABAB receptor gene and panic disorder | 1.3 | 20 | Citations (PDF) |
| 517 | Search for association between suicide attempt and serotonergic polymorphisms | 1.3 | 88 | Citations (PDF) |
| 518 | Title is missing! | 6.7 | 43 | Citations (PDF) |
| 519 | Investigation of the human serotonin 6 (5-HT6) receptor gene in bipolar affective disorder and schizophrenia 2000, 96, 217-221 | | 64 | Citations (PDF) |
| 520 | Pharmacogenetics of schizophrenia 2000, 97, 98-106 | | 45 | Citations (PDF) |
| 521 | Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls | 0.5 | 17 | Citations (PDF) |
| 522 | Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder | 0.5 | 170 | Citations (PDF) |
| 523 | Reply | 2.3 | 2 | Citations (PDF) |
| 524 | A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family | 1.7 | 36 | Citations (PDF) |
| 525 | DRD4 exon III VNTR polymorphism—susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach | 7.8 | 43 | Citations (PDF) |
| 526 | Strauch et al reply | 7.8 | 4 | Citations (PDF) |
| 527 | Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1) | 7.8 | 112 | Citations (PDF) |
| 528 | Dopamine D3 receptor variant and tardive dyskinesia | 2.7 | 60 | Citations (PDF) |
| 529 | Novel 5′-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder | 2.7 | 32 | Citations (PDF) |
| 530 | Polymorphic MAO-A and 5-HT-Transporter Genes: Analysis of Interactions in Panic Disorder | 4.1 | 19 | Citations (PDF) |
| 531 | Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach | 7.8 | 75 | Citations (PDF) |
| 532 | Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia | 2.3 | 61 | Citations (PDF) |
| 533 | Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families | 7.8 | 124 | Citations (PDF) |
| 534 | Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers | 7.8 | 696 | Citations (PDF) |
| 535 | Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15 | 3.1 | 39 | Citations (PDF) |
| 536 | Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening 1999, 88, 158-163 | | 45 | Citations (PDF) |
| 537 | Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: Replication tests | 0.5 | 85 | Citations (PDF) |
| 538 | No association between serotonin transporter gene polymorphisms and personality traits | 0.5 | 71 | Citations (PDF) |
| 539 | Human ?-opioid receptor gene and susceptibility to heroin and alcohol dependence 1999, 88, 462-464 | | 59 | Citations (PDF) |
| 540 | Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia | 2.3 | 79 | Citations (PDF) |
| 541 | Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder | 2.9 | 576 | Citations (PDF) |
| 542 | Factor Analysis of Mania | 12.7 | 37 | Citations (PDF) |
| 543 | hSKCa3 | 1.3 | 15 | Citations (PDF) |
| 544 | Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease | 7.8 | 165 | Citations (PDF) |
| 545 | Genetic Variation in Human 5-HT Receptors: Potential Pathogenetic and Pharmacological Rolea | 4.0 | 37 | Citations (PDF) |
| 546 | Serotonin Subtype 2 Receptor Genes and Clinical Response to Clozapine in Schizophrenia Patients | 5.4 | 227 | Citations (PDF) |
| 547 | Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies 1998, 81, 18-23 | | 15 | Citations (PDF) |
| 548 | Patterns of parental transmission and familial aggregation models in bipolar affective disorder 1998, 81, 397-404 | | 22 | Citations (PDF) |
| 549 | Polymorphisms in the dopamine, serotonin, and norepinephrine transporter genes and their relationships to monoamine metabolite concentrations in CSF of healthy volunteers | 3.1 | 94 | Citations (PDF) |
| 550 | Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain | 2.6 | 100 | Citations (PDF) |
| 551 | A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22 | 6.5 | 62 | Citations (PDF) |
| 552 | Evidence for Linkage of Spelling Disability to Chromosome 15 | 6.5 | 155 | Citations (PDF) |
| 553 | Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis | 6.5 | 212 | Citations (PDF) |
| 554 | Assignment of the human serotonin 4 receptor gene (HTR4) to the long arm of chromosome 5 (5q31–q33) | 2.9 | 3 | Citations (PDF) |
| 555 | Cloning, Genomic Organization, Alternative Transcripts and Mutational Analysis of the Gene Responsible for Autosomal Recessive Universal Congenital Alopecia | 2.9 | 163 | Citations (PDF) |
| 556 | Familial occurrence of primary premature ejaculation | 1.3 | 166 | Citations (PDF) |
| 557 | Association study of schizophrenia and the histidase gene | 1.3 | 1 | Citations (PDF) |
| 558 | Lack of evidence for allelic association between personality traits and the dopamine D4 receptor gene polymorphisms | 8.8 | 127 | Citations (PDF) |
| 559 | Functional promoter polymorphism of the human serotonin transporter | 1.3 | 121 | Citations (PDF) |
| 560 | A Novel Splice Site Associated Polymorphism in the Tuberous Sclerosis 2 (TSC2) Gene May Predispose to the Development of Sporadic Gangliogliomas | 1.8 | 30 | Citations (PDF) |
| 561 | Efficacy and side-effects of clozapine not associated with variation in the 5-HT2C receptor | 1.5 | 113 | Citations (PDF) |
| 562 | Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1) | 2.9 | 5 | Citations (PDF) |
| 563 | Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia | 62.1 | 166 | Citations (PDF) |
| 564 | Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene | 2.3 | 0 | Citations (PDF) |
| 565 | Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region | 2.1 | 22 | Citations (PDF) |
| 566 | Nonreplication of Linkage Disequilibrium between the Dopamine D4 Receptor Locus and Tourette Syndrome | 6.5 | 37 | Citations (PDF) |
| 567 | 5-HT2A receptor and bipolar affective disorder: association studies in affected patients | 1.9 | 54 | Citations (PDF) |
| 568 | Mapping of the human adenosine A 2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region | 2.9 | 38 | Citations (PDF) |
| 569 | Neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) and panic disorder: An association study 1997, 74, 199-201 | | 37 | Citations (PDF) |
| 570 | Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases | 2.3 | 26 | Citations (PDF) |
| 571 | The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3 | 1.1 | 12 | Citations (PDF) |
| 572 | Localization of the Human Glucosidase I Gene to Chromosome 2p12–p13 by Fluorescencein SituHybridization and PCR Analysis of Somatic Cell Hybrids | 2.8 | 8 | Citations (PDF) |
| 573 | Trisomy of human chromosome 18: Molecular studies on parental origin and cell stage of nondisjunction | 2.9 | 55 | Citations (PDF) |
| 574 | Tetrasomy 18p de novo: Identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing | 2.9 | 17 | Citations (PDF) |
| 575 | Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia | 2.9 | 197 | Citations (PDF) |
| 576 | Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene | 62.1 | 243 | Citations (PDF) |
| 577 | Association study of a null mutation in the dopamine D4 receptor gene in Italian patients with obsessive-compulsive disorder, bipolar mood disorder and schizophrenia | 1.3 | 26 | Citations (PDF) |
| 578 | Apolipoprotein E genotype distribution in schizophrenia | 1.3 | 23 | Citations (PDF) |
| 579 | Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia | 3.4 | 46 | Citations (PDF) |
| 580 | Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees | 1.3 | 3 | Citations (PDF) |
| 581 | Efficacy and Side-Effects of Clozapine: Testing for Association with Allelic Variation in the Dopamine D4 Receptor Gene | 5.4 | 83 | Citations (PDF) |
| 582 | Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia 1996, 67, 225-228 | | 17 | Citations (PDF) |
| 583 | Lack of imprinting of the human dopamine D4 receptor (DRD4) gene 1996, 67, 229-231 | | 10 | Citations (PDF) |
| 584 | Systematic screening for mutations in the 5′-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder | 0.5 | 58 | Citations (PDF) |
| 585 | Systematic search for variation in the human norepinephrine transporter gene: Identification of five naturally occurring missense mutations and study of association with major psychiatric disorders | 0.5 | 113 | Citations (PDF) |
| 586 | CNTF and psychiatric disorders | 25.2 | 12 | Citations (PDF) |
| 587 | Schizophrenia: genetic tools for unraveling the nature of a complex disorder. | 7.5 | 25 | Citations (PDF) |
| 588 | Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1 | 0.5 | 107 | Citations (PDF) |
| 589 | Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene | 0.5 | 62 | Citations (PDF) |
| 590 | Human Adenosine A1 Receptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 1q31-32.1 Using a Silent Polymorphism in the Coding Region | 2.1 | 11 | Citations (PDF) |
| 591 | No association between length of the (CAG)n repeat of the huntington's disease gene and tourette's syndrome | 5.4 | 3 | Citations (PDF) |
| 592 | Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation | 2.6 | 23 | Citations (PDF) |
| 593 | Genetic variation of the 5-HT2A receptor and response to clozapine | 62.1 | 111 | Citations (PDF) |
| 594 | Dinucleotide repeat polymorphism at the human CD59 locus | 2.1 | 3 | Citations (PDF) |
| 595 | Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene | 1.3 | 42 | Citations (PDF) |
| 596 | Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity | 2.9 | 123 | Citations (PDF) |
| 597 | A common amino acid polymorphism in complement component C1R | 2.9 | 6 | Citations (PDF) |
| 598 | Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1) | 2.9 | 62 | Citations (PDF) |
| 599 | Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method | 0.5 | 53 | Citations (PDF) |
| 600 | No evidence of association between dopamine D4 receptor variants and bipolar affective disorder | 0.5 | 52 | Citations (PDF) |
| 601 | Identification of Genetic Variation in the Human Serotonin 1Dβ Receptor Gene | 2.1 | 65 | Citations (PDF) |
| 602 | Human complement component C8 | 2.7 | 7 | Citations (PDF) |
| 603 | Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls | 1.3 | 37 | Citations (PDF) |
| 604 | An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia | 1.3 | 21 | Citations (PDF) |
| 605 | Pemphigus chronicus benignus familiaris (Morbus Hailey-Hailey) und bipolare affektive Erkrankung bei drei Mitgliedern einer Familie | 1.0 | 13 | Citations (PDF) |
| 606 | Steinfeld syndrome: Report of a second family and further delineation of a rare autosomal dominant disorder | 0.5 | 34 | Citations (PDF) |
| 607 | Polymorphism of Human Complement Component C6: An Amino Acid Substitution (GLU/ALA) within the Second Thrombospondin Repeat Differentiates between the Two Common Allotypes C6A and C6B | 2.1 | 16 | Citations (PDF) |
| 608 | The presence of glutamic acid or alanene at position 98 in human complement component C6 differentiates between the two common allotypes C6 A and C6 B | 2.2 | 1 | Citations (PDF) |
| 609 | A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: No role in the genetic predisposition to bipolar affective disorder | 3.1 | 55 | Citations (PDF) |
| 610 | Distribution of a novel mutation in the first exon of the human dopamine D4 receptor gene in psychotic patients | 5.4 | 118 | Citations (PDF) |
| 611 | Association versus linkage studies in psychosis genetics. | 3.8 | 48 | Citations (PDF) |
| 612 | Dinucleotide repeat polymorphism at the D18S99 locus | 2.9 | 0 | Citations (PDF) |
| 613 | Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed. | 3.8 | 47 | Citations (PDF) |
| 614 | Dinucleotide repeat polymorphism at the D18S365 locus | 2.9 | 0 | Citations (PDF) |
| 615 | Identifying Genetic Factors in Common Diseases | 0.1 | 0 | Citations (PDF) |
| 616 | Genetisch informierte Therapie in der Psychiatrie: neue Dynamik durch APOE und Antikörpertherapie der Alzheimer-Krankheit | 0.8 | 0 | Citations (PDF) |
| 617 | Ein Geburtstagsgruß für Thomas Cremer zum 80. Geburtstag | 0.2 | 0 | Citations (PDF) |
| 618 | Personality and well-being are genetically associated: Extending previous twin and molecular genetic studies | 2.8 | 1 | Citations (PDF) |
| 619 | Genome and Transcriptome-Wide Analyses Identify Multiple Candidate Genes and a Significant Polygenic Contribution in Bicuspid Aortic Valve | 18.0 | 1 | Citations (PDF) |
| 620 | Do Alopecia Areata and Hair Colour Have a Shared Genetic Component? | 2.7 | 0 | Citations (PDF) |
