| 1 | The influence of affective temperaments on sleep quality in a general population sample. Data report from the CHRIS study | 3.2 | 6 | Citations (PDF) |
| 2 | Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2 | 4.8 | 4 | Citations (PDF) |
| 3 | Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number | 2.7 | 17 | Citations (PDF) |
| 4 | Hypoxia Sensing and Responses in Parkinson’s Disease | 3.2 | 17 | Citations (PDF) |
| 5 | Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits | 14.1 | 212 | Citations (PDF) |
| 6 | How to communicate and what to disclose to participants in a recall-by-genotype research approach: a multistep empirical study | 0.9 | 1 | Citations (PDF) |
| 7 | Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study | 2.1 | 4 | Citations (PDF) |
| 8 | Role of Ceramides and Sphingolipids in Parkinson's Disease | 3.0 | 39 | Citations (PDF) |
| 9 | The small GTPase Rit2 modulates LRRK2 kinase activity, is required for lysosomal function and protects against alpha-synuclein neuropathology | 4.5 | 24 | Citations (PDF) |
| 10 | Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers | 4.5 | 19 | Citations (PDF) |
| 11 | Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels | 4.3 | 5 | Citations (PDF) |
| 12 | Genetic insights into resting heart rate and its role in cardiovascular disease | 11.0 | 36 | Citations (PDF) |
| 13 | Prospective epidemiological, molecular, and genetic characterization of a novel coronavirus disease in the Val Venosta/Vinschgau: the CHRIS COVID-19 study protocol | 2.0 | 5 | Citations (PDF) |
| 14 | A multi-omics study of circulating phospholipid markers of blood pressure | 2.7 | 22 | Citations (PDF) |
| 15 | Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family | 0.3 | 1 | Citations (PDF) |
| 16 | Dihydroceramide- and ceramide-profiling provides insights into human cardiometabolic disease etiology | 11.0 | 59 | Citations (PDF) |
| 17 | Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways | 2.1 | 11 | Citations (PDF) |
| 18 | Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson’s disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method | 0.3 | 1 | Citations (PDF) |
| 19 | Functional Screening of Parkinson’s Disease Susceptibility Genes to Identify Novel Modulators of α-Synuclein Neurotoxicity in Caenorhabditis elegans | 2.7 | 18 | Citations (PDF) |
| 20 | A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson’s disease by highlighting the use of cybrid models | 3.5 | 8 | Citations (PDF) |
| 21 | Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals | 3.1 | 35 | Citations (PDF) |
| 22 | Pain sensitivity is modulated by affective temperament: Results from the population-based CHRIS Affective Disorder (CHRIS-AD) study | 3.2 | 6 | Citations (PDF) |
| 23 | Induced Pluripotent Stem Cell (iPSC) Lines from a Family with Resistant Epileptic Encephalopathy Caused by Compound Heterozygous Mutations in SZT2 Gene | 3.2 | 3 | Citations (PDF) |
| 24 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability | 11.0 | 143 | Citations (PDF) |
| 25 | Association of mitochondrial DNA copy number with metabolic syndrome and type 2 diabetes in 14 176 individuals | 3.5 | 100 | Citations (PDF) |
| 26 | Genetic variants in levodopa-induced dyskinesia (LID): A systematic review and meta-analysis | 2.0 | 18 | Citations (PDF) |
| 27 | Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls | 2.0 | 10 | Citations (PDF) |
| 28 | Balancing scientific interests and the rights of participants in designing a recall by genotype study | 2.1 | 9 | Citations (PDF) |
| 29 | The trans-ancestral genomic architecture of glycemic traits | 14.1 | 713 | Citations (PDF) |
| 30 | Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort | 1.6 | 35 | Citations (PDF) |
| 31 | Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture | 2.8 | 23 | Citations (PDF) |
| 32 | Exome-wide association study of levodopa-induced dyskinesia in Parkinson’s disease | 2.7 | 5 | Citations (PDF) |
| 33 | The SZT2 Interactome Unravels New Functions of the KICSTOR Complex | 3.4 | 9 | Citations (PDF) |
| 34 | Interaction of Alpha-Synuclein With Lipids: Mitochondrial Cardiolipin as a Critical Player in the Pathogenesis of Parkinson’s Disease | 2.0 | 54 | Citations (PDF) |
| 35 | Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes | 2.0 | 156 | Citations (PDF) |
| 36 | Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction | 11.0 | 115 | Citations (PDF) |
| 37 | Silencing of CCR4-NOT complex subunits affects heart structure and function | 1.3 | 25 | Citations (PDF) |
| 38 | Kinase inhibition of G2019S-LRRK2 enhances autolysosome formation and function to reduce endogenous alpha-synuclein intracellular inclusions | 5.6 | 46 | Citations (PDF) |
| 39 | Genome-wide association study identifies 48 common genetic variants associated with handedness | 7.2 | 136 | Citations (PDF) |
| 40 | Evaluation of the role of STAP1 in Familial Hypercholesterolemia | 2.7 | 19 | Citations (PDF) |
| 41 | Lipidomics, Atrial Conduction, and Body Mass Index | 2.0 | 10 | Citations (PDF) |
| 42 | Mitochondrial DNA copy number is associated with mortality and infections in a large cohort of patients with chronic kidney disease | 4.6 | 73 | Citations (PDF) |
| 43 | Application of CRISPR/Cas9 editing and digital droplet PCR in human iPSCs to generate novel knock-in reporter lines to visualize dopaminergic neurons | 0.3 | 19 | Citations (PDF) |
| 44 | Associations of autozygosity with a broad range of human phenotypes | 11.0 | 122 | Citations (PDF) |
| 45 | Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | 11.0 | 223 | Citations (PDF) |
| 46 | Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels | 14.1 | 395 | Citations (PDF) |
| 47 | A catalog of genetic loci associated with kidney function from analyses of a million individuals | 14.1 | 863 | Citations (PDF) |
| 48 | Modeling Parkinson’s disease in midbrain-like organoids | 4.5 | 321 | Citations (PDF) |
| 49 | Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells | 3.2 | 15 | Citations (PDF) |
| 50 | Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene | 0.3 | 5 | Citations (PDF) |
| 51 | Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly | 1.5 | 16 | Citations (PDF) |
| 52 | The PPARGC1A locus and CNS-specific PGC-1α isoforms are associated with Parkinson's Disease | 3.6 | 34 | Citations (PDF) |
| 53 | Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation | 11.0 | 272 | Citations (PDF) |
| 54 | Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders | 4.5 | 433 | Citations (PDF) |
| 55 | Plasmid-normalized quantification of relative mitochondrial DNA copy number | 2.7 | 79 | Citations (PDF) |
| 56 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits | 14.1 | 1,378 | Citations (PDF) |
| 57 | Influence of collection tubes during quantitative targeted metabolomics studies in human blood samples | 0.7 | 60 | Citations (PDF) |
| 58 | Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance | 0.3 | 16 | Citations (PDF) |
| 59 | A new hypothesis for Parkinson’s disease pathogenesis: GTPase-p38 MAPK signaling and autophagy as convergence points of etiology and genomics | 9.7 | 95 | Citations (PDF) |
| 60 | PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity | 11.0 | 91 | Citations (PDF) |
| 61 | Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk | 14.1 | 586 | Citations (PDF) |
| 62 | Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease | 3.1 | 113 | Citations (PDF) |
| 63 | NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality | 0.3 | 29 | Citations (PDF) |
| 64 | SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons andDrosophila | 2.1 | 68 | Citations (PDF) |
| 65 | 32-channel time-correlated-single-photon-counting system for high-throughput lifetime imaging | 1.1 | 11 | Citations (PDF) |
| 66 | Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney | 4.7 | 147 | Citations (PDF) |
| 67 | Pre-analytic evaluation of volumetric absorptive microsampling and integration in a mass spectrometry-based metabolomics workflow | 2.7 | 59 | Citations (PDF) |
| 68 | CADPS2 gene expression is oppositely regulated by LRRK2 and alpha-synuclein | 1.5 | 26 | Citations (PDF) |
| 69 | Plasma and White Blood Cells Show Different miRNA Expression Profiles in Parkinson’s Disease | 1.4 | 53 | Citations (PDF) |
| 70 | Elevated levels of alpha-synuclein blunt cellular signal transduction downstream of Gq protein-coupled receptors | 2.8 | 9 | Citations (PDF) |
| 71 | The Impact of CRISPR/Cas9 Technology on Cardiac Research: From Disease Modelling to Therapeutic Approaches | 1.9 | 49 | Citations (PDF) |
| 72 | Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function | 6.8 | 135 | Citations (PDF) |
| 73 | SLP-2: a potential new target for improving mitochondrial function in Parkinson's disease | 3.4 | 8 | Citations (PDF) |
| 74 | Genetic variants in RBFOX3 are associated with sleep latency | 2.1 | 36 | Citations (PDF) |
| 75 | PLA2G6 mutations and Parkinsonism: Long‐term follow‐up of clinical features and neuropathology | 3.2 | 21 | Citations (PDF) |
| 76 | Genomewide meta‐analysis identifies loci associated with
IGF
‐I and
IGFBP
‐3 levels with impact on age‐related traits | 4.8 | 89 | Citations (PDF) |
| 77 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape | 11.0 | 92 | Citations (PDF) |
| 78 | 52 Genetic Loci Influencing Myocardial Mass | 0.7 | 134 | Citations (PDF) |
| 79 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals | 14.1 | 422 | Citations (PDF) |
| 80 | Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease | 26.5 | 525 | Citations (PDF) |
| 81 | Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels | 11.0 | 177 | Citations (PDF) |
| 82 | Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci | 2.2 | 392 | Citations (PDF) |
| 83 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study | 2.2 | 412 | Citations (PDF) |
| 84 | New genetic loci link adipose and insulin biology to body fat distribution | 31.3 | 1,606 | Citations (PDF) |
| 85 | Genetic studies of body mass index yield new insights for obesity biology | 31.3 | 4,579 | Citations (PDF) |
| 86 | Generation of Induced Pluripotent Stem Cells from Frozen Buffy Coats using Non-integrating Episomal Plasmids | 0.2 | 18 | Citations (PDF) |
| 87 | Directional dominance on stature and cognition in diverse human populations | 31.3 | 201 | Citations (PDF) |
| 88 | Overexpression of blood microRNAs 103a, 30b, and 29a in
l
-dopa–treated patients with PD | 0.7 | 118 | Citations (PDF) |
| 89 | Large-scale assessment of polyglutamine repeat expansions in Parkinson disease | 0.7 | 30 | Citations (PDF) |
| 90 | Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans | 1.5 | 73 | Citations (PDF) |
| 91 | Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson’s disease blood samples | 0.9 | 35 | Citations (PDF) |
| 92 | Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium | 2.1 | 96 | Citations (PDF) |
| 93 | The Arachidonic Acid Metabolome Serves as a Conserved Regulator of Cholesterol Metabolism | 20.9 | 116 | Citations (PDF) |
| 94 | Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis | 11.0 | 252 | Citations (PDF) |
| 95 | Defining the role of common variation in the genomic and biological architecture of adult human height | 14.1 | 1,994 | Citations (PDF) |
| 96 | Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | 14.1 | 328 | Citations (PDF) |
| 97 | Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels | 2.1 | 15 | Citations (PDF) |
| 98 | Discovery and refinement of loci associated with lipid levels | 14.1 | 3,061 | Citations (PDF) |
| 99 | Common variants associated with plasma triglycerides and risk for coronary artery disease | 14.1 | 856 | Citations (PDF) |
| 100 | SNP Prioritization Using a Bayesian Probability of Association | 2.5 | 13 | Citations (PDF) |
| 101 | Importance of Different Types of Prior Knowledge in Selecting Genome‐Wide Findings for Follow‐Up | 2.5 | 14 | Citations (PDF) |
| 102 | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture | 14.1 | 660 | Citations (PDF) |
| 103 | Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders | 14.1 | 311 | Citations (PDF) |
| 104 | Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits | 2.2 | 425 | Citations (PDF) |
| 105 | A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function | 2.2 | 219 | Citations (PDF) |
| 106 | Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study | 4.2 | 126 | Citations (PDF) |
| 107 | Profiling of Parkin-Binding Partners Using Tandem Affinity Purification | 1.5 | 44 | Citations (PDF) |
| 108 | Evidence of Inbreeding Depression on Human Height | 2.2 | 98 | Citations (PDF) |
| 109 | Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations | 2.2 | 203 | Citations (PDF) |
| 110 | Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals | 2.2 | 458 | Citations (PDF) |
| 111 | Genome-wide analysis of epistasis in body mass index using multiple human populations | 2.1 | 34 | Citations (PDF) |
| 112 | Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways | 14.1 | 812 | Citations (PDF) |
| 113 | A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants | 2.2 | 101 | Citations (PDF) |
| 114 | Seventy-five genetic loci influencing the human red blood cell | 31.3 | 346 | Citations (PDF) |
| 115 | Large-scale replication and heterogeneity in Parkinson disease genetic loci | 0.7 | 129 | Citations (PDF) |
| 116 | FTO genotype is associated with phenotypic variability of body mass index | 31.3 | 433 | Citations (PDF) |
| 117 | A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans | 1.5 | 205 | Citations (PDF) |
| 118 | Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping | 1.5 | 123 | Citations (PDF) |
| 119 | A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance | 14.1 | 838 | Citations (PDF) |
| 120 | Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids | 4.5 | 256 | Citations (PDF) |
| 121 | Genome-wide association analyses identify 18 new loci associated with serum urate concentrations | 14.1 | 802 | Citations (PDF) |
| 122 | Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts | 1.5 | 3 | Citations (PDF) |
| 123 | Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels | 13.1 | 496 | Citations (PDF) |
| 124 | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | 31.3 | 2,017 | Citations (PDF) |
| 125 | New gene functions in megakaryopoiesis and platelet formation | 31.3 | 431 | Citations (PDF) |
| 126 | Copy Number Variation across European Populations | 1.5 | 26 | Citations (PDF) |
| 127 | Genetic architecture of circulating lipid levels | 2.1 | 23 | Citations (PDF) |
| 128 | Variants in STAT5B Associate with Serum TC and LDL-C Levels | 3.3 | 9 | Citations (PDF) |
| 129 | Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27 | 2.2 | 7 | Citations (PDF) |
| 130 | Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster | 2.1 | 51 | Citations (PDF) |
| 131 | Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels | 2.1 | 65 | Citations (PDF) |
| 132 | Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels | 2.1 | 70 | Citations (PDF) |
| 133 | Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits | 2.1 | 10 | Citations (PDF) |
| 134 | A KATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila | 5.3 | 145 | Citations (PDF) |
| 135 | Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates | 1.5 | 17 | Citations (PDF) |
| 136 | Parkin gene modifies the effect of RLS4 on the age at onset of restless legs syndrome (RLS) | 0.8 | 8 | Citations (PDF) |
| 137 | Copy number variation and association over T-cell receptor genes—influence of DNA source | 1.1 | 14 | Citations (PDF) |
| 138 | Biological, clinical and population relevance of 95 loci for blood lipids | 31.3 | 3,486 | Citations (PDF) |
| 139 | Hundreds of variants clustered in genomic loci and biological pathways affect human height | 31.3 | 1,893 | Citations (PDF) |
| 140 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution | 14.1 | 907 | Citations (PDF) |
| 141 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | 14.1 | 2,809 | Citations (PDF) |
| 142 | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction | 14.1 | 344 | Citations (PDF) |
| 143 | Update on the management of restless legs syndrome: existing and emerging treatment options | 3.5 | 4 | Citations (PDF) |
| 144 | Modeling of Environmental Effects in Genome-Wide Association Studies Identifies SLC2A2 and HP as Novel Loci Influencing Serum Cholesterol Levels | 2.2 | 56 | Citations (PDF) |
| 145 | Genome-wide association analysis identifies multiple loci related to resting heart rate | 2.1 | 144 | Citations (PDF) |
| 146 | A Global In Vivo Drosophila RNAi Screen Identifies NOT3 as a Conserved Regulator of Heart Function | 23.8 | 218 | Citations (PDF) |
| 147 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk | 14.1 | 2,127 | Citations (PDF) |
| 148 | Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals | 1.9 | 149 | Citations (PDF) |
| 149 | Linkage and Genome‐wide Association Analysis of Obesity‐related Phenotypes: Association of Weight With the MGAT1 Gene | 2.9 | 60 | Citations (PDF) |
| 150 | Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease | 1.4 | 45 | Citations (PDF) |
| 151 | Genome-Wide Association Study Identifies Multiple Genetic Loci for Activated Partial Thromboplastin Time and Prothrombin TimeBlood, 2010, 116, 4222-4222 | 3.6 | 0 | Citations (PDF) |
| 152 | Consenting in Population Genomics as an Open Communication Process | 0.2 | 12 | Citations (PDF) |
| 153 | Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations | 2.2 | 206 | Citations (PDF) |
| 154 | Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis | 2.1 | 91 | Citations (PDF) |
| 155 | A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations | 3.7 | 67 | Citations (PDF) |
| 156 | 2q37 as a Susceptibility Locus for Idiopathic Basal Ganglia Calcification (IBGC) in a Large South Tyrolean Family | 1.4 | 52 | Citations (PDF) |
| 157 | Common variants at ten loci modulate the QT interval duration in the QTSCD Study | 14.1 | 379 | Citations (PDF) |
| 158 | Genome-wide linkage analysis of serum creatinine in three isolated European populations | 4.6 | 72 | Citations (PDF) |
| 159 | Restless legs syndrome: an update on genetics and future perspectives | 1.5 | 34 | Citations (PDF) |
| 160 | Assessing mitochondrial morphology and dynamics using fluorescence wide-field microscopy and 3D image processing | 2.0 | 53 | Citations (PDF) |
| 161 | Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts | 14.1 | 795 | Citations (PDF) |
| 162 | A Genetic Risk Factor for Periodic Limb Movements in Sleep | 19.4 | 612 | Citations (PDF) |
| 163 | PARK10 Candidate RNF11 Is Expressed by Vulnerable Neurons and Localizes to Lewy Bodies in Parkinson Disease Brain | 1.5 | 29 | Citations (PDF) |
| 164 | A common inversion under selection in Europeans | 14.1 | 810 | Citations (PDF) |
| 165 | A genome wide linkage disequilibrium screen in Parkinson’s disease | 2.7 | 7 | Citations (PDF) |
| 166 | A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction | 14.1 | 347 | Citations (PDF) |
| 167 | A susceptibility gene for late‐onset idiopathic Parkinson's disease | 4.7 | 247 | Citations (PDF) |
| 168 | Familial Aggregation of Parkinson's Disease in Iceland | 19.4 | 281 | Citations (PDF) |
| 169 | Increase in syntaxin 1B and glutamate release in mossy fibre terminals following induction of LTP in the dentate gyrus: a candidate molecular mechanism underlying transsynaptic plasticity | 1.6 | 32 | Citations (PDF) |
| 170 | Induction of Long‐Term Potentiation In Vivo Regulates Alternate Splicing to Alter Syntaxin 3 Isoform Expression in Rat Dentate Gyrus | 2.7 | 21 | Citations (PDF) |
| 171 | Increase in Syntaxin 1B mRNA in Hippocampal and Cortical Circuits During Spatial Learning Reflects a Mechanism of Trans-synaptic Plasticity Involved in Establishing a Memory Trace | 0.8 | 24 | Citations (PDF) |
| 172 | Synapsin I and syntaxin 1B: Key elements in the control of neurotransmitter release are regulated by neuronal activation and long-term potentiation in vivo | 1.8 | 66 | Citations (PDF) |
| 173 | Learning spatial working and reference memory tasks induces region-specific increases in the expression of the gene encoding syntaxin 1B | 1.7 | 0 | Citations (PDF) |
| 174 | Pre- and post-synaptic regulation of synapsin I and syntaxin 1B expression in neuronal networks: Differential effects of neuronal activity and long-term potentiation in vivo | 1.7 | 1 | Citations (PDF) |
| 175 | Brain Structure and Task-specific Increase in Expression of the Gene Encoding Syntaxin 1B During Learning in the Rat: A Potential Molecular Marker for Learning-induced Synaptic Plasticity in Neural Networks | 1.6 | 32 | Citations (PDF) |
| 176 | Further Evidence for Clustering of Human GABAA Receptor Subunit Genes: Localization of the α6-Subunit Gene (GABRA6) to Distal Chromosome 5q by Linkage Analysis | 2.0 | 55 | Citations (PDF) |
| 177 | GABAA receptor subunit genes as candidate genes for bipolar affective disorder—an association analysis | 0.6 | 20 | Citations (PDF) |
| 178 | Confirmation of the localization of the human GABAA receptor α1-subunit gene (GABRA1) to distal 5q by linkage analysis | 2.0 | 46 | Citations (PDF) |
| 179 | GABA-A receptor subunit genes. An association analysis | 1.6 | 1 | Citations (PDF) |
| 180 | The chicken GABAA receptor α1 subunit: cDNA sequence and localization of the corresponding mRNA | 2.5 | 45 | Citations (PDF) |
| 181 | Dinucleotide repeat polymorphism in the human X-linked GABAAreceptora3-subunit gene | 11.2 | 27 | Citations (PDF) |
| 182 | Distinct regional expression of nicotinic acetylcholine receptor genes in chick brain | 2.5 | 73 | Citations (PDF) |
| 183 | The ripple phase of phosphatidylcholines: effect of chain length and cholesterol | 1.5 | 51 | Citations (PDF) |
| 184 | Caenorhabditis elegans Parkin: Regulators of its abundance and role in autophagy-lysosomal dynamics | 0.0 | 3 | Citations (PDF) |
| 185 | Fluorescent reporter of Caenorhabditis elegans Parkin: Regulators of its abundance and role in autophagy-lysosomal dynamics | 0.0 | 1 | Citations (PDF) |
