| 1 | Functional host-specific adaptation of the intestinal microbiome in hominids | 13.9 | 22 | Citations (PDF) |
| 2 | Metabolic model predictions enable targeted microbiome manipulation through precision prebiotics | 3.7 | 13 | Citations (PDF) |
| 3 | Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction | 26.1 | 40 | Citations (PDF) |
| 4 | The microRNA Expression in Crypt-Top and Crypt-Bottom Colonic Epithelial Cell Populations Demonstrates Cell-Type Specificity and Correlates with Endoscopic Activity in Ulcerative Colitis | 1.3 | 1 | Citations (PDF) |
| 5 | A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodiesBrain, 2023, 146, 977-990 | 8.5 | 32 | Citations (PDF) |
| 6 | Protective and aggressive bacterial subsets and metabolites modify hepatobiliary inflammation and fibrosis in a murine model of PSC | 21.2 | 83 | Citations (PDF) |
| 7 | Long‐Term Dietary Effects on Human Gut Microbiota Composition Employing Shotgun Metagenomics Data Analysis | 4.1 | 12 | Citations (PDF) |
| 8 | Genetic variation in<i>TERT</i>modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study | 21.2 | 39 | Citations (PDF) |
| 9 | Activated regulatory T-cells promote duodenal bacterial translocation into necrotic areas in severe acute pancreatitis | 21.2 | 81 | Citations (PDF) |
| 10 | Resistance to thyroid hormone induced tachycardia in RTHα syndrome | 13.9 | 18 | Citations (PDF) |
| 11 | Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy | 26.1 | 143 | Citations (PDF) |
| 12 | Mechanisms by which the cystic fibrosis transmembrane conductance regulator may influence <scp>SARS‐CoV</scp>‐2 infection and <scp>COVID</scp>‐19 disease severity | 0.7 | 5 | Citations (PDF) |
| 13 | A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross‐disease analyses | 2.7 | 17 | Citations (PDF) |
| 14 | Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide | 1.6 | 37 | Citations (PDF) |
| 15 | Occasional paternal inheritance of the germline-restricted chromosome in songbirds | 7.6 | 21 | Citations (PDF) |
| 16 | Detailed Transcriptional Landscape of Peripheral Blood Points to Increased Neutrophil Activation in Treatment-Naïve Inflammatory Bowel Disease | 1.3 | 23 | Citations (PDF) |
| 17 | Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease | 4.4 | 34 | Citations (PDF) |
| 18 | Linkage analysis identifies novel genetic modifiers of microbiome traits in families with inflammatory bowel disease | 10.4 | 13 | Citations (PDF) |
| 19 | Circulating microbiome in patients with portal hypertension | 10.4 | 58 | Citations (PDF) |
| 20 | miRNome Profiling and Functional Analysis Reveal Involvement of hsa-miR-1246 in Colon Adenoma-Carcinoma Transition by Targeting AXIN2 and CFTR | 4.5 | 8 | Citations (PDF) |
| 21 | Detection of Cancer Mutations by Urine Liquid Biopsy as a Potential Tool in the Clinical Management of Bladder Cancer Patients | 4.0 | 7 | Citations (PDF) |
| 22 | A novel unconventional T cell population enriched in Crohn’s disease | 21.2 | 63 | Citations (PDF) |
| 23 | SARS-CoV-2 Nsp13 encodes for an HLA-E-stabilizing peptide that abrogates inhibition of NKG2A-expressing NK cells | 6.4 | 61 | Citations (PDF) |
| 24 | B-cell-depletion reverses dysbiosis of the microbiome in multiple sclerosis patients | 3.5 | 36 | Citations (PDF) |
| 25 | NMR Metabolomics Reveal Urine Markers of Microbiome Diversity and Identify Benzoate Metabolism as a Mediator between High Microbial Alpha Diversity and Metabolic Health | 3.5 | 17 | Citations (PDF) |
| 26 | Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction | 3.5 | 20 | Citations (PDF) |
| 27 | Genome-Wide Association Study of Alzheimer’s Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer’s Disease Multimodal Biomarker Discovery Dataset | 4.1 | 40 | Citations (PDF) |
| 28 | Heart Failure Severity Closely Correlates with Intestinal Dysbiosis and Subsequent Metabolomic Alterations | 3.5 | 22 | Citations (PDF) |
| 29 | A
<i>dietary carbohydrate – gut Parasutterella – human fatty acid biosynthesis</i>
metabolic axis in obesity and type 2 diabetes | 10.4 | 134 | Citations (PDF) |
| 30 | Genetic Associations and Differential mRNA Expression Levels of Host Genes Suggest a Viral Trigger for Endemic Pemphigus Foliaceus | 3.3 | 4 | Citations (PDF) |
| 31 | Dysbiosis in the Gut Microbiota in Patients with Inflammatory Bowel Disease during Remission | 3.7 | 102 | Citations (PDF) |
| 32 | Differential Effects of Obesity, Hyperlipidaemia, Dietary Intake and Physical Inactivity on Type I versus Type IV Allergies | 4.7 | 5 | Citations (PDF) |
| 33 | Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies | 5.0 | 46 | Citations (PDF) |
| 34 | Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals | 4.4 | 31 | Citations (PDF) |
| 35 | High-throughput method for the hybridisation-based targeted enrichment of long genomic fragments for PacBio third-generation sequencing | 2.2 | 17 | Citations (PDF) |
| 36 | Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota | 13.9 | 79 | Citations (PDF) |
| 37 | DNA methyltransferase 3A controls intestinal epithelial barrier function and regeneration in the colon | 13.9 | 36 | Citations (PDF) |
| 38 | SETDB1 is required for intestinal epithelial differentiation and the prevention of
intestinal inflammation | 21.2 | 72 | Citations (PDF) |
| 39 | Long-term instability of the intestinal microbiome is associated with metabolic
liver disease, low microbiota diversity, diabetes mellitus and impaired exocrine
pancreatic function | 21.2 | 152 | Citations (PDF) |
| 40 | Circulating sDPP-4 is Increased in Obesity and Insulin Resistance but Is Not Related to Systemic Metabolic Inflammation | 4.2 | 22 | Citations (PDF) |
| 41 | Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease | 4.6 | 21 | Citations (PDF) |
| 42 | Population connectivity of fan-shaped sponge holobionts in the deep Cantabrian Sea | 1.7 | 19 | Citations (PDF) |
| 43 | Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline | 5.0 | 86 | Citations (PDF) |
| 44 | Genetic variability of immune‐related lncRNAs: polymorphisms in <i>LINC‐PINT</i> and <i>LY86‐AS1</i> are associated with pemphigus foliaceus susceptibility | 2.8 | 15 | Citations (PDF) |
| 45 | Genome-wide study of a Neolithic Wartberg grave community reveals distinct HLA variation and hunter-gatherer ancestry | 4.4 | 31 | Citations (PDF) |
| 46 | Exome-Wide Association Study Identifies <i>FN3KRP</i> and <i>PGP</i> as New Candidate Longevity Genes | 3.5 | 19 | Citations (PDF) |
| 47 | Current Developments of Clinical Sequencing and the Clinical Utility of Polygenic Risk Scores in Inflammatory Diseases | 5.1 | 5 | Citations (PDF) |
| 48 | Large-scale association analyses identify host factors influencing human gut microbiome composition | 26.1 | 1,507 | Citations (PDF) |
| 49 | Clinical correlates of anti-SARS-CoV-2 antibody profiles in Spanish COVID-19 patients from a high incidence region | 3.5 | 10 | Citations (PDF) |
| 50 | Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism | 4.2 | 18 | Citations (PDF) |
| 51 | Human β-Defensin 2 Mutations Are Associated With Asthma and Atopy in Children and Its Application Prevents Atopic Asthma in a Mouse Model | 5.1 | 21 | Citations (PDF) |
| 52 | A heterozygous germline CD100 mutation in a family with primary sclerosing cholangitis | 12.7 | 16 | Citations (PDF) |
| 53 | Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations | 3.0 | 39 | Citations (PDF) |
| 54 | Carrying asymptomatic gallstones is not associated with changes in intestinal microbiota composition and diversity but cholecystectomy with significant dysbiosis | 3.5 | 40 | Citations (PDF) |
| 55 | Intestinal protozoan infections shape fecal bacterial microbiota in children from Guinea-Bissau | 3.1 | 22 | Citations (PDF) |
| 56 | Altered Gut Microbial Metabolism of Essential Nutrients in Primary Sclerosing Cholangitis | 1.0 | 114 | Citations (PDF) |
| 57 | Primate phageomes are structured by superhost phylogeny and environment | 7.6 | 23 | Citations (PDF) |
| 58 | Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease | 21.2 | 35 | Citations (PDF) |
| 59 | Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans | 3.2 | 21 | Citations (PDF) |
| 60 | Mass burial genomics reveals outbreak of enteric paratyphoid fever in the Late Medieval trade city Lübeck | 3.6 | 17 | Citations (PDF) |
| 61 | Effect of various weight loss interventions on serum NT-proBNP concentration in severe obese subjects without clinical manifest heart failure | 3.5 | 16 | Citations (PDF) |
| 62 | TMEM106B and CPOX are genetic determinants of cerebrospinal fluid Alzheimer's disease biomarker levels | 0.4 | 36 | Citations (PDF) |
| 63 | Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism | 13.9 | 58 | Citations (PDF) |
| 64 | Unsuspected Associations of Variants within the Genes NOTCH4 and STEAP2-AS1 Uncovered by a GWAS in Endemic Pemphigus Foliaceus | 2.3 | 4 | Citations (PDF) |
| 65 | Short-term physical exercise impacts on the human holobiont obtained by a randomised intervention study | 3.9 | 37 | Citations (PDF) |
| 66 | Large-Scale Imputation of KIR Copy Number and HLA Alleles in North American and European Psoriasis Case-Control Cohorts Reveals Association of Inhibitory KIR2DL2 With Psoriasis | 5.1 | 11 | Citations (PDF) |
| 67 | Association Between Collagenous and Lymphocytic Colitis and Risk of Severe Coronavirus Disease 2019 | 1.0 | 5 | Citations (PDF) |
| 68 | The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome | 4.1 | 5 | Citations (PDF) |
| 69 | MRI‐Based Iron Phenotyping and Patient Selection for Next‐Generation Sequencing of Non–Homeostatic Iron Regulator Hemochromatosis Genes | 10.6 | 12 | Citations (PDF) |
| 70 | Single-cell atlas of hepatic T cells reveals expansion of liver-resident naive-like CD4+ T cells in primary sclerosing cholangitis | 3.6 | 104 | Citations (PDF) |
| 71 | Sex‐specific genetic factors affect the risk of early‐onset periodontitis in <scp>Europeans</scp> | 6.6 | 22 | Citations (PDF) |
| 72 | Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis | 6.9 | 26 | Citations (PDF) |
| 73 | Genetic association and differential expression of HLA Complex Group lncRNAs in pemphigus | 6.7 | 12 | Citations (PDF) |
| 74 | Rare genetic coding variants associated with human longevity and protection against age-related diseases | 16.0 | 41 | Citations (PDF) |
| 75 | Analysis of SARS-CoV-2 reverse transcription-quantitative polymerase chain reaction cycle threshold values vis-à-vis anti-SARS-CoV-2 antibodies from a high incidence region | 2.2 | 6 | Citations (PDF) |
| 76 | Microbial Diversity and Abundance of
<i>Parabacteroides</i>
Mediate the Associations Between Higher Intake of Flavonoid-Rich Foods and Lower Blood Pressure | 6.9 | 25 | Citations (PDF) |
| 77 | Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality | 10.7 | 103 | Citations (PDF) |
| 78 | Anti‐glycoprotein 2 (anti‐GP2) IgA and anti‐neutrophil cytoplasmic antibodies to serine proteinase 3 (PR3‐ANCA): antibodies to predict severe disease, poor survival and cholangiocarcinoma in primary sclerosing cholangitis | 3.9 | 36 | Citations (PDF) |
| 79 | Liquid Biopsy in Gastric Cancer: Analysis of Somatic Cancer Tissue Mutations in Plasma Cell-Free DNA for Predicting Disease State and Patient Survival | 2.9 | 14 | Citations (PDF) |
| 80 | BMI, Alcohol Consumption and Gut Microbiome Species Richness Are Related to Structural and Functional Neurological Abnormalities | 4.7 | 6 | Citations (PDF) |
| 81 | Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia | 2.6 | 4 | Citations (PDF) |
| 82 | Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases | 9.7 | 121 | Citations (PDF) |
| 83 | Ecology impacts the decrease of Spirochaetes and Prevotella in the fecal gut microbiota of urban humans | 3.9 | 27 | Citations (PDF) |
| 84 | Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders | 26.1 | 226 | Citations (PDF) |
| 85 | Epigenetic adaptations of the masticatory mucosa to periodontal inflammation | 4.0 | 12 | Citations (PDF) |
| 86 | Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation | 13.5 | 24 | Citations (PDF) |
| 87 | Using common genetic variants to find drugs for common epilepsies | 3.6 | 16 | Citations (PDF) |
| 88 | A Multi-Factorial Observational Study on Sequential Fecal Microbiota Transplant in Patients with Medically Refractory Clostridioides difficile Infection | 4.8 | 22 | Citations (PDF) |
| 89 | Methotrexate Treatment of Newly Diagnosed RA Patients Is Associated With DNA Methylation Differences at Genes Relevant for Disease Pathogenesis and Pharmacological Action | 5.1 | 16 | Citations (PDF) |
| 90 | Validity and Prognostic Value of a Polygenic Risk Score for Parkinson’s Disease | 2.6 | 32 | Citations (PDF) |
| 91 | Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 | 13.9 | 36 | Citations (PDF) |
| 92 | MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity | 2.6 | 11 | Citations (PDF) |
| 93 | Reporting guidelines for human microbiome research: the STORMS checklist | 39.5 | 375 | Citations (PDF) |
| 94 | Targeting the cytoplasmic polyadenylation element-binding protein CPEB4 protects against diet-induced obesity and microbiome dysbiosis | 6.0 | 16 | Citations (PDF) |
| 95 | The power of genetic diversity in genome-wide association studies of lipids | 38.7 | 845 | Citations (PDF) |
| 96 | Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology | 26.1 | 472 | Citations (PDF) |
| 97 | Interplay between Genome, Metabolome and Microbiome in Colorectal Cancer | 4.0 | 23 | Citations (PDF) |
| 98 | GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome | 6.9 | 30 | Citations (PDF) |
| 99 | Genetic background of high blood pressure is associated with reduced mortality in premature neonates | 3.1 | 8 | Citations (PDF) |
| 100 | Genetic Variation in HSD17B13 Reduces the Risk of Developing Cirrhosis and Hepatocellular Carcinoma in Alcohol Misusers | 10.6 | 91 | Citations (PDF) |
| 101 | Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression | 6.2 | 39 | Citations (PDF) |
| 102 | Identification of Disease-associated Traits and Clonotypes in the T Cell Receptor Repertoire of Monozygotic Twins Affected by Inflammatory Bowel Diseases | 1.3 | 23 | Citations (PDF) |
| 103 | Genomic Characterization of Cholangiocarcinoma in Primary Sclerosing Cholangitis Reveals Therapeutic Opportunities | 10.6 | 60 | Citations (PDF) |
| 104 | Rapid response of stage IV colorectal cancer with APC/TP53/KRAS mutations to FOLFIRI and Bevacizumab combination chemotherapy: a case report of use of liquid biopsy | 2.0 | 6 | Citations (PDF) |
| 105 | The role of the gut microbiome in the association between habitual anthocyanin intake and visceral abdominal fat in population-level analysis | 4.9 | 26 | Citations (PDF) |
| 106 | Chloroflexi Dominate the Deep-Sea Golf Ball Sponges Craniella zetlandica and Craniella infrequens Throughout Different Life Stages | 2.5 | 18 | Citations (PDF) |
| 107 | Elucidating the Influence of Chromosomal Architecture on Transcriptional Regulation in Prokaryotes – Observing Strong Local Effects of Nucleoid Structure on Gene Regulation | 3.9 | 5 | Citations (PDF) |
| 108 | Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan | 2.9 | 53 | Citations (PDF) |
| 109 | Comparative Studies of the Gut Microbiota in the Offspring of Mothers With and Without Gestational Diabetes | 4.3 | 43 | Citations (PDF) |
| 110 | Genome-wide association study of Alzheimer’s disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset | 5.5 | 58 | Citations (PDF) |
| 111 | Longitudinal Multi-omics Analyses Identify Responses of Megakaryocytes, Erythroid Cells, and Plasmablasts as Hallmarks of Severe COVID-19 | 23.3 | 355 | Citations (PDF) |
| 112 | Low-Avidity CD4+ T Cell Responses to SARS-CoV-2 in Unexposed Individuals and Humans with Severe COVID-19 | 23.3 | 317 | Citations (PDF) |
| 113 | Dense sampling of bird diversity increases power of comparative genomics | 38.7 | 385 | Citations (PDF) |
| 114 | Concentration and chemical form of dietary zinc shape the porcine colon microbiome, its functional capacity and antibiotic resistance gene repertoire | 9.1 | 53 | Citations (PDF) |
| 115 | The Impact of Oral Sodium Chloride Supplementation on Thrive and the Intestinal Microbiome in Neonates With Small Bowel Ostomies: A Prospective Cohort Study | 5.1 | 20 | Citations (PDF) |
| 116 | Dickkopf-1 Overexpression in vitro Nominates Candidate Blood Biomarkers Relating to Alzheimer’s Disease Pathology | 2.6 | 7 | Citations (PDF) |
| 117 | Genetic risk factors predict disease progression in Crohn’s disease patients of the Swiss inflammatory bowel disease cohort | 3.5 | 16 | Citations (PDF) |
| 118 | Targeted analysis of polymorphic loci from low-coverage shotgun sequence data allows accurate genotyping of HLA genes in historical human populations | 3.5 | 13 | Citations (PDF) |
| 119 | Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage | 3.5 | 21 | Citations (PDF) |
| 120 | RE: Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study | 4.7 | 5 | Citations (PDF) |
| 121 | A disease‐specific decline of the relative abundance of <i>Bifidobacterium</i> in patients with autoimmune hepatitis | 3.9 | 74 | Citations (PDF) |
| 122 | The mutational constraint spectrum quantified from variation in 141,456 humans | 38.7 | 8,804 | Citations (PDF) |
| 123 | Amino acid encoding for deep learning applications | 3.0 | 90 | Citations (PDF) |
| 124 | Genomewide Association Study of Severe Covid-19 with Respiratory Failure | 43.7 | 1,799 | Citations (PDF) |
| 125 | IL-22 Paucity in APECED Is Associated With Mucosal and Microbial Alterations in Oral Cavity | 5.1 | 21 | Citations (PDF) |
| 126 | Translation of mouse model to human gives insights into periodontitis etiology | 3.5 | 15 | Citations (PDF) |
| 127 | Sugar-Induced Obesity and Insulin Resistance Are Uncoupled from Shortened Survival in Drosophila | 26.2 | 126 | Citations (PDF) |
| 128 | DNA methylation QTL analysis identifies new regulators of human longevity | 3.0 | 16 | Citations (PDF) |
| 129 | Arrhythmic Gut Microbiome Signatures Predict Risk of Type 2 Diabetes | 15.3 | 248 | Citations (PDF) |
| 130 | Rheumatoid Arthritis Patients, Both Newly Diagnosed and Methotrexate Treated, Show More DNA Methylation Differences in CD4+ Memory Than in CD4+ Naïve T Cells | 5.1 | 25 | Citations (PDF) |
| 131 | Quantitative comparison of within-sample heterogeneity scores for DNA methylation data | 15.7 | 66 | Citations (PDF) |
| 132 | A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease | 3.5 | 21 | Citations (PDF) |
| 133 | In Silico Guided Discovery of Novel Class I and II <i>Trypanosoma cruzi</i> Epitopes Recognized by T Cells from Chagas’ Disease Patients | 0.6 | 15 | Citations (PDF) |
| 134 | Depletion of erythropoietic miR-486-5p and miR-451a improves detectability of rare microRNAs in peripheral blood-derived small RNA sequencing libraries | 2.2 | 15 | Citations (PDF) |
| 135 | Stage IV Colorectal Cancer Patients with High Risk Mutation Profiles Survived 16 Months Longer with Individualized Therapies | 4.0 | 3 | Citations (PDF) |
| 136 | Monocytes as Potential Mediators of Pathogen‐Induced T‐Helper 17 Differentiation in Patients With Primary Sclerosing Cholangitis (PSC) | 10.6 | 83 | Citations (PDF) |
| 137 | A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples | 3.5 | 13 | Citations (PDF) |
| 138 | A fungal pathogen induces systemic susceptibility and systemic shifts in wheat metabolome and microbiome composition | 13.9 | 145 | Citations (PDF) |
| 139 | Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study | 2.0 | 11 | Citations (PDF) |
| 140 | The Gut Microbiome in Patients With Chronic Pancreatitis Is Characterized by Significant Dysbiosis and Overgrowth by Opportunistic Pathogens | 2.9 | 78 | Citations (PDF) |
| 141 | On giant shoulders: how a seamount affects the microbial community composition of seawater and sponges | 3.1 | 27 | Citations (PDF) |
| 142 | Molecular Subtypes with Distinct Clinical Phenotypes and Actionable Targets in Adult B Cell Precursor ALL Treatment According to GMALL Protocols | 4.2 | 2 | Citations (PDF) |
| 143 | Obese Individuals with and without Type 2 Diabetes Show Different Gut Microbial Functional Capacity and Composition | 15.3 | 398 | Citations (PDF) |
| 144 | A structured weight loss program increases gut microbiota phylogenetic diversity and reduces levels of Collinsella in obese type 2 diabetics: A pilot study | 2.4 | 108 | Citations (PDF) |
| 145 | Consistent alterations in faecal microbiomes of patients with primary sclerosing cholangitis independent of associated colitis | 3.9 | 93 | Citations (PDF) |
| 146 | A combined epigenome- and transcriptome-wide association study of the oral masticatory mucosa assigns CYP1B1 a central role for epithelial health in smokers | 4.0 | 28 | Citations (PDF) |
| 147 | Pseudomonas aeruginosa populations in the cystic fibrosis lung lose susceptibility to newly applied β-lactams within 3 days | 3.2 | 25 | Citations (PDF) |
| 148 | Differential genetic and functional background in inflammatory bowel disease phenotypes of a Greek population: a systems bioinformatics approach | 4.0 | 15 | Citations (PDF) |
| 149 | GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways | 13.9 | 164 | Citations (PDF) |
| 150 | Associations of autozygosity with a broad range of human phenotypes | 13.9 | 117 | Citations (PDF) |
| 151 | Host-Microbe-Drug-Nutrient Screen Identifies Bacterial Effectors of Metformin TherapyCell, 2019, 178, 1299-1312.e29 | 34.1 | 253 | Citations (PDF) |
| 152 | Automated real-time monitoring of human pluripotent stem cell aggregation in stirred tank reactors | 3.5 | 40 | Citations (PDF) |
| 153 | Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | 13.9 | 207 | Citations (PDF) |
| 154 | Comparative analysis of amplicon and metagenomic sequencing methods reveals key features in the evolution of animal metaorganisms | 11.5 | 201 | Citations (PDF) |
| 155 | Identifying Crohn’s disease signal from variome analysis | 9.7 | 28 | Citations (PDF) |
| 156 | Metabolic Functions of Gut Microbes Associate With Efficacy of Tumor Necrosis Factor Antagonists in Patients With Inflammatory Bowel Diseases | 1.0 | 254 | Citations (PDF) |
| 157 | Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms | 21.2 | 114 | Citations (PDF) |
| 158 | Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry | 3.5 | 50 | Citations (PDF) |
| 159 | Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery – a sub-analysis of the RIPHeart-Study | 2.2 | 29 | Citations (PDF) |
| 160 | Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2 | 1.5 | 14 | Citations (PDF) |
| 161 | Liver infiltrating T cells regulate bile acid metabolism in experimental cholangitis | 3.6 | 37 | Citations (PDF) |
| 162 | A catalog of genetic loci associated with kidney function from analyses of a million individuals | 26.1 | 796 | Citations (PDF) |
| 163 | Linking pre-existing biorepositories for medical research: the PopGen 2.0 Network | 1.1 | 13 | Citations (PDF) |
| 164 | Genetic mechanism underlying sexual plasticity and its association with colour patterning in zebrafish (Danio rerio) | 3.3 | 20 | Citations (PDF) |
| 165 | VarWatch—A stand-alone software tool for variant matching | 2.4 | 1 | Citations (PDF) |
| 166 | Integrating Culture-Based Antibiotic Resistance Profiles with Whole-Genome Sequencing Data for 11,087 Clinical Isolates | 6.2 | 11 | Citations (PDF) |
| 167 | Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy | 4.6 | 40 | Citations (PDF) |
| 168 | No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors | 13.4 | 13 | Citations (PDF) |
| 169 | Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping | 2.6 | 12 | Citations (PDF) |
| 170 | Atopic Dermatitis Is an IL-13–Dominant Disease with Greater Molecular Heterogeneity Compared to Psoriasis | 2.3 | 413 | Citations (PDF) |
| 171 | <i>ZNF133</i> is associated with infliximab responsiveness in patients with inflammatory bowel diseases | 2.7 | 13 | Citations (PDF) |
| 172 | Genome‐wide association study of psoriasis in an Egyptian population | 2.8 | 16 | Citations (PDF) |
| 173 | Analysis of long non-coding RNA and mRNA expression in bovine macrophages brings up novel aspects of Mycobacterium avium subspecies paratuberculosis infections | 3.5 | 37 | Citations (PDF) |
| 174 | Impaired Exocrine Pancreatic Function Associates With Changes in Intestinal Microbiota Composition and Diversity | 1.0 | 100 | Citations (PDF) |
| 175 | Normal gut microbiome in NMDA receptor encephalitis | 6.9 | 13 | Citations (PDF) |
| 176 | Complement Receptor 1 (CR1, CD35) Polymorphisms and Soluble CR1: A Proposed Anti-inflammatory Role to Quench the Fire of “Fogo Selvagem” Pemphigus Foliaceus | 5.1 | 16 | Citations (PDF) |
| 177 | Helicobacter pylori infection associates with fecal microbiota composition and diversity | 3.5 | 71 | Citations (PDF) |
| 178 | Minor compositional alterations in faecal microbiota after five weeks and five months storage at room temperature on filter papers | 3.5 | 7 | Citations (PDF) |
| 179 | Leptin induces TNFα-dependent inflammation in acquired generalized lipodystrophy and combined Crohn’s disease | 13.9 | 34 | Citations (PDF) |
| 180 | IL-17A is functionally relevant and a potential therapeutic target in bullous pemphigoid | 6.7 | 108 | Citations (PDF) |
| 181 | Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis | 24.2 | 186 | Citations (PDF) |
| 182 | Genetic markers associated with long-term cardiovascular outcome in kidney transplant recipients | 4.6 | 8 | Citations (PDF) |
| 183 | Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles | 3.0 | 60 | Citations (PDF) |
| 184 | Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease | 6.2 | 146 | Citations (PDF) |
| 185 | Vedolizumab is associated with changes in innate rather than adaptive immunity in patients with inflammatory bowel disease | 21.2 | 193 | Citations (PDF) |
| 186 | Copy number variants in lipid metabolism genes are associated with gallstones disease in men | 3.2 | 6 | Citations (PDF) |
| 187 | Comparing genome versus proteome-based identification of clinical bacterial isolates | 6.7 | 7 | Citations (PDF) |
| 188 | Increased Prevalence of Rare Sucrase-isomaltase Pathogenic Variants in Irritable Bowel Syndrome Patients | 6.2 | 88 | Citations (PDF) |
| 189 | Epidermal lipid composition, barrier integrity, and eczematous inflammation are associated with skin microbiome configuration | 6.2 | 178 | Citations (PDF) |
| 190 | Whither systems medicine? | 11.6 | 57 | Citations (PDF) |
| 191 | Small ncRNA-Seq Results of Human Tissues: Variations Depending on Sample Integrity | 1.1 | 6 | Citations (PDF) |
| 192 | NGS-Based Methylation Profiling Differentiates TCF3-HLF and TCF3-PBX1 Positive B-cell Acute Lymphoblastic Leukemia | 2.3 | 13 | Citations (PDF) |
| 193 | A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis | 3.0 | 19 | Citations (PDF) |
| 194 | A high-resolution map of the human small non-coding transcriptome | 4.8 | 27 | Citations (PDF) |
| 195 | Functional sequencing read annotation for high precision microbiome analysis | 15.7 | 49 | Citations (PDF) |
| 196 | Formula Feeding Predisposes Neonatal Piglets to Clostridium difficile Gut Infection | 3.8 | 23 | Citations (PDF) |
| 197 | Exposure to the gut microbiota drives distinct methylome and transcriptome changes in intestinal epithelial cells during postnatal development | 9.7 | 146 | Citations (PDF) |
| 198 | The antibiotic resistome and microbiota landscape of refugees from Syria, Iraq and Afghanistan in Germany | 11.5 | 27 | Citations (PDF) |
| 199 | Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans | 13.9 | 87 | Citations (PDF) |
| 200 | Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome | 1.0 | 72 | Citations (PDF) |
| 201 | Genetic predisposition in anti‐LGI1 and anti‐NMDA receptor encephalitis | 6.3 | 147 | Citations (PDF) |
| 202 | Targeted Microbiome Intervention by Microencapsulated Delayed-Release Niacin Beneficially Affects Insulin Sensitivity in Humans | 6.5 | 99 | Citations (PDF) |
| 203 | Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis | 21.2 | 49 | Citations (PDF) |
| 204 | Impact of red and processed meat and fibre intake on treatment outcomes among patients with chronic inflammatory diseases: protocol for a prospective cohort study of prognostic factors and personalised medicine | 2.0 | 23 | Citations (PDF) |
| 205 | Evolutionary Distance Predicts Recurrence After Liver Transplantation in Multifocal Hepatocellular Carcinoma | 1.2 | 7 | Citations (PDF) |
| 206 | Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel disease | 1.4 | 15 | Citations (PDF) |
| 207 | Identification of long intergenic non-coding RNAs (lincRNAs) deregulated in gastrointestinal stromal tumors (GISTs) | 2.4 | 31 | Citations (PDF) |
| 208 | Rhinovirus infections change DNA methylation and mRNA expression in children with asthma | 2.4 | 54 | Citations (PDF) |
| 209 | Mucosal Autoimmunity to Cell-Bound GP2 Isoforms Is a Sensitive Marker in PSC and Associated With the Clinical Phenotype | 5.1 | 18 | Citations (PDF) |
| 210 | Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients | 13.9 | 137 | Citations (PDF) |
| 211 | Genetic and transcriptional analysis of inflammatory bowel disease-associated pathways in patients with <i>GUCY2C</i>-linked familial diarrhea | 1.8 | 12 | Citations (PDF) |
| 212 | Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data | 1.5 | 207 | Citations (PDF) |
| 213 | RNA based individualized drug selection in breast cancer patients without patient-matched normal tissue | 1.7 | 1 | Citations (PDF) |
| 214 | Role of wnt5a in Metabolic Inflammation in Humans | 4.2 | 32 | Citations (PDF) |
| 215 | Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus | 3.5 | 47 | Citations (PDF) |
| 216 | Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects | 6.2 | 430 | Citations (PDF) |
| 217 | The Changing Landscape of Naive T Cell Receptor Repertoire With Human Aging | 5.1 | 107 | Citations (PDF) |
| 218 | Whole-exome sequencing identifies rare genetic variations in German families with pulmonary sarcoidosis | 3.0 | 21 | Citations (PDF) |
| 219 | Gestational diabetes is associated with change in the gut microbiota composition in third trimester of pregnancy and postpartum | 11.5 | 401 | Citations (PDF) |
| 220 | Genetik des Morbus Crohn und der Colitis ulcerosa | 0.1 | 1 | Citations (PDF) |
| 221 | Serum anti-glycan-antibodies in relatives of patients with inflammatory bowel disease | 2.4 | 6 | Citations (PDF) |
| 222 | Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population | 3.3 | 85 | Citations (PDF) |
| 223 | Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies | 8.5 | 132 | Citations (PDF) |
| 224 | DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis | 13.9 | 196 | Citations (PDF) |
| 225 | Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci | 3.2 | 75 | Citations (PDF) |
| 226 | miRNAs in ancient tissue specimens of the Tyrolean Iceman | 4.7 | 17 | Citations (PDF) |
| 227 | Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis | 21.2 | 57 | Citations (PDF) |
| 228 | Uncoupling of mucosal gene regulation, mRNA splicing and adherent microbiota signatures in inflammatory bowel disease | 21.2 | 93 | Citations (PDF) |
| 229 | Inflammatory bowel disease and oral health: systematic review and a meta‐analysis | 6.6 | 150 | Citations (PDF) |
| 230 | Association mapping of morphological traits in wild and captive zebra finches: reliable within, but not between populations | 3.7 | 19 | Citations (PDF) |
| 231 | Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases | 14.6 | 464 | Citations (PDF) |
| 232 | Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolismBlood, 2017, 129, 783-790 | 4.2 | 23 | Citations (PDF) |
| 233 | Opportunities and challenges of whole-genome and -exome sequencing | 2.9 | 199 | Citations (PDF) |
| 234 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease | 2.4 | 243 | Citations (PDF) |
| 235 | Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci | 3.5 | 61 | Citations (PDF) |
| 236 | Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice | 1.0 | 84 | Citations (PDF) |
| 237 | A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis | 3.0 | 109 | Citations (PDF) |
| 238 | Metastatic triple-negative breast cancer patient with <i>TP53</i> tumor mutation experienced 11 months progression-free survival on bortezomib monotherapy without adverse events after ending standard treatments with grade 3 adverse events | 1.5 | 15 | Citations (PDF) |
| 239 | Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases | 15.1 | 316 | Citations (PDF) |
| 240 | Hypothalamic Inflammation in Human Obesity Is Mediated by Environmental and Genetic Factors | 4.4 | 145 | Citations (PDF) |
| 241 | Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants | 13.9 | 333 | Citations (PDF) |
| 242 | A haplotype block downstream of plasminogen is associated with chronic and aggressive periodontitis | 6.6 | 23 | Citations (PDF) |
| 243 | Cold-induced conversion of cholesterol to bile acids in mice shapes the gut microbiome and promotes adaptive thermogenesis | 39.5 | 277 | Citations (PDF) |
| 244 | miR-146b Probably Assists miRNA-146a in the Suppression of Keratinocyte Proliferation and Inflammatory Responses in Psoriasis | 2.3 | 86 | Citations (PDF) |
| 245 | Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis | 18.4 | 237 | Citations (PDF) |
| 246 | A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis | 6.5 | 89 | Citations (PDF) |
| 247 | Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea | 3.0 | 36 | Citations (PDF) |
| 248 | Microbiomarkers in inflammatory bowel diseases: caveats come with caviar | 21.2 | 58 | Citations (PDF) |
| 249 | Heart failure is associated with depletion of core intestinal microbiota | 3.3 | 274 | Citations (PDF) |
| 250 | A sex-chromosome inversion causes strong overdominance for sperm traits that affect siring success | 10.3 | 79 | Citations (PDF) |
| 251 | Iterative Sequencing and Variant Screening (ISVS) as a novel pathogenic mutations search strategy - application for TMPRSS3 mutations screen | 3.5 | 11 | Citations (PDF) |
| 252 | A comprehensive, cell specific microRNA catalogue of human peripheral blood | 15.7 | 181 | Citations (PDF) |
| 253 | Web-based NGS data analysis using miRMaster: a large-scale meta-analysis of human miRNAs | 15.7 | 68 | Citations (PDF) |
| 254 | Identification and characterization of two functional variants in the human longevity gene FOXO3 | 13.9 | 86 | Citations (PDF) |
| 255 | c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia | 2.9 | 12 | Citations (PDF) |
| 256 | Anti-Tnf Therapy Systematically Influences Intestinal Microbial Community Structure in Chronic Inflammatory Diseases | 1.0 | 0 | Citations (PDF) |
| 257 | Fine-mapping inflammatory bowel disease loci to single-variant resolution | 38.7 | 583 | Citations (PDF) |
| 258 | CD4+ T cells from patients with primary sclerosing cholangitis exhibit reduced apoptosis and down-regulation of proapoptotic Bim in peripheral blood | 3.0 | 24 | Citations (PDF) |
| 259 | Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling | 3.0 | 47 | Citations (PDF) |
| 260 | MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing | 1.7 | 39 | Citations (PDF) |
| 261 | A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine | 4.7 | 27 | Citations (PDF) |
| 262 | Transcriptomic Analysis of Intestinal Tissues from Two 90-Day Feeding Studies in Rats Using Genetically Modified MON810 Maize Varieties | 2.4 | 6 | Citations (PDF) |
| 263 | Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency | 5.1 | 24 | Citations (PDF) |
| 264 | Overview of methodologies for T-cell receptor repertoire analysis | 2.9 | 312 | Citations (PDF) |
| 265 | Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity | 26.1 | 387 | Citations (PDF) |
| 266 | Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome | 3.1 | 42 | Citations (PDF) |
| 267 | A post-GWAS analysis of predicted regulatory variants and tuberculosis susceptibility | 2.4 | 29 | Citations (PDF) |
| 268 | Fitness consequences of polymorphic inversions in the zebra finch genome | 8.2 | 68 | Citations (PDF) |
| 269 | Meta-Analysis of Genome-Wide Association Studies and Network Analysis-Based Integration with Gene Expression Data Identify New Suggestive Loci and Unravel a Wnt-Centric Network Associated with Dupuytren’s Disease | 2.4 | 33 | Citations (PDF) |
| 270 | Microrna Response of Primary Human Macrophages to Arcobacter Butzleri Infection | 5.6 | 12 | Citations (PDF) |
| 271 | Serologic Anti-GP2 Antibodies Are Associated with Genetic Polymorphisms, Fibrostenosis, and Need for Surgical Resection in Crohnʼs Disease | 3.0 | 28 | Citations (PDF) |
| 272 | Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study | 2.4 | 21 | Citations (PDF) |
| 273 | 1053 Bloom of Fecal Megamonas After a 4 Week High Oral Fructose Challenge Disturbs Energy and Lipid Metabolism: Linking Diet to Microbiota, Bile Acid and Host Metabolism Alterations | 1.0 | 6 | Citations (PDF) |
| 274 | Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages | 6.2 | 24 | Citations (PDF) |
| 275 | Coding Variation in<i>ANGPTL4,</i><i>LPL,</i>and<i>SVEP1</i>and the Risk of Coronary Disease | 43.7 | 481 | Citations (PDF) |
| 276 | Association Between Genetic Traits for Immune-Mediated Diseases and Alzheimer Disease | 15.1 | 177 | Citations (PDF) |
| 277 | HLA Associations Distinguish Collagenous From Lymphocytic Colitis | 0.7 | 29 | Citations (PDF) |
| 278 | Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota | 26.1 | 608 | Citations (PDF) |
| 279 | Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis Risk | 2.3 | 33 | Citations (PDF) |
| 280 | Immunochip analysis identifies association of the
<i>
<scp>RAD</scp>
50/
<scp>IL</scp>
13
</i>
region with human longevity | 7.0 | 24 | Citations (PDF) |
| 281 | Rare phenotypes in the understanding of autoimmunity | 2.7 | 2 | Citations (PDF) |
| 282 | A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis | 13.9 | 56 | Citations (PDF) |
| 283 | Genetic Factors of the Disease Course After Sepsis: Rare Deleterious Variants Are Predictive | 9.9 | 39 | Citations (PDF) |
| 284 | Neuromuscular endplate pathology in recessive desminopathies | 1.0 | 31 | Citations (PDF) |
| 285 | Paternal chronic colitis causes epigenetic inheritance of susceptibility to colitis | 3.5 | 18 | Citations (PDF) |
| 286 | Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation | 11.0 | 160 | Citations (PDF) |
| 287 | Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci | 2.0 | 14 | Citations (PDF) |
| 288 | Interdisciplinary approach towards a systems medicine toolbox using the example of inflammatory diseases | 6.7 | 13 | Citations (PDF) |
| 289 | Congenital secretory diarrhoea caused by activating germline mutations in<i>GUCY2C</i> | 21.2 | 88 | Citations (PDF) |
| 290 | High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences | 12.2 | 83 | Citations (PDF) |
| 291 | Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci | 4.8 | 3 | Citations (PDF) |
| 292 | Deep characterization of blood cell miRNomes by NGS | 5.6 | 15 | Citations (PDF) |
| 293 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | 13.9 | 493 | Citations (PDF) |
| 294 | Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci | 26.1 | 728 | Citations (PDF) |
| 295 | Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes | 6.2 | 195 | Citations (PDF) |
| 296 | New technologies for DNA analysis – a review of the READNA Project | 4.7 | 10 | Citations (PDF) |
| 297 | Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study | 52.8 | 719 | Citations (PDF) |
| 298 | Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2 | 2.4 | 31 | Citations (PDF) |
| 299 | Paired proteomics, transcriptomics and miRNomics in non-small cell lung cancers: known and novel signaling cascades | 1.7 | 10 | Citations (PDF) |
| 300 | Integrated quantitative proteomic and transcriptomic analysis of lung tumor and control tissue: a lung cancer showcase | 1.7 | 20 | Citations (PDF) |
| 301 | Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer | 3.5 | 25 | Citations (PDF) |
| 302 | Genome‐wide association study identifies new susceptibility loci for cutaneous lupus erythematosus | 2.8 | 76 | Citations (PDF) |
| 303 | Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array | 3.1 | 16 | Citations (PDF) |
| 304 | The Influence of the Autoimmunity-Associated Ancestral HLA Haplotype AH8.1 on the Human Gut Microbiota: A Cross-Sectional Study | 2.4 | 36 | Citations (PDF) |
| 305 | Development of a high-resolution NGS-based HLA-typing and analysis pipeline | 15.7 | 87 | Citations (PDF) |
| 306 | Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility | 13.9 | 179 | Citations (PDF) |
| 307 | Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci | 13.9 | 174 | Citations (PDF) |
| 308 | Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk | 12.2 | 118 | Citations (PDF) |
| 309 | Less functional variants of TLR-1/-6/-10 genes are associated with age | 5.1 | 7 | Citations (PDF) |
| 310 | Meta-analysis identifies seven susceptibility loci involved in the atopic march | 13.9 | 167 | Citations (PDF) |
| 311 | Impaired hepcidin expression in alpha-1-antitrypsin deficiency associated with iron overload and progressive liver disease | 3.0 | 34 | Citations (PDF) |
| 312 | The genetics of Crohn’s disease and ulcerative colitis –<i>status quo</i>and beyond | 1.8 | 82 | Citations (PDF) |
| 313 | Childhood acute lymphoblastic leukemia-associated risk-loci<i>IKZF1, ARID5B</i>and<i>CEBPE</i>and risk of pediatric non-Hodgkin lymphoma: a report from the Berlin–Frankfurt–Münster Study Group | 1.5 | 9 | Citations (PDF) |
| 314 | Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms | 6.5 | 184 | Citations (PDF) |
| 315 | Psoriasis and Cardiometabolic Traits: Modest Association but Distinct Genetic Architectures | 2.3 | 62 | Citations (PDF) |
| 316 | Is there a male-specific effect on hypertension? | 3.0 | 0 | Citations (PDF) |
| 317 | Genomics and drug profiling of fatal TCF3-HLF−positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options | 26.1 | 227 | Citations (PDF) |
| 318 | Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations | 26.1 | 2,490 | Citations (PDF) |
| 319 | Exome Sequencing Analysis Reveals Variants in Primary Immunodeficiency Genes in Patients With Very Early Onset Inflammatory Bowel Disease | 1.0 | 112 | Citations (PDF) |
| 320 | Vy-PER: eliminating false positive detection of virus integration events in next generation sequencing data | 3.5 | 44 | Citations (PDF) |
| 321 | Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies | 3.3 | 98 | Citations (PDF) |
| 322 | Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells | 13.9 | 69 | Citations (PDF) |
| 323 | A Large-Scale Genetic Analysis Reveals a Strong Contribution of the HLA Class II Region to Giant Cell Arteritis Susceptibility | 6.5 | 167 | Citations (PDF) |
| 324 | Analysis of intestinal microbiota in hybrid house mice reveals evolutionary divergence in a vertebrate hologenome | 13.9 | 122 | Citations (PDF) |
| 325 | Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation | 26.1 | 335 | Citations (PDF) |
| 326 | Imputation of KIR Types from SNP Variation Data | 6.5 | 80 | Citations (PDF) |
| 327 | Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea | 3.0 | 129 | Citations (PDF) |
| 328 | A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis | 6.2 | 54 | Citations (PDF) |
| 329 | Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture | 6.5 | 293 | Citations (PDF) |
| 330 | Genome-wide association study of kidney function decline in individuals of European descent | 5.0 | 123 | Citations (PDF) |
| 331 | XIAP variants in male Crohn's disease | 21.2 | 145 | Citations (PDF) |
| 332 | Early-onset Crohn’s disease and autoimmunity associated with a variant in CTLA-4 | 21.2 | 126 | Citations (PDF) |
| 333 | No significant impact of IFN-γ pathway gene variants on tuberculosis susceptibility in a West African population | 3.2 | 11 | Citations (PDF) |
| 334 | Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms | 2.4 | 43 | Citations (PDF) |
| 335 | Sparse Modeling Reveals miRNA Signatures for Diagnostics of Inflammatory Bowel Disease | 2.4 | 40 | Citations (PDF) |
| 336 | New insights into the genetics of glioblastoma multiforme by familial exome sequencing | 1.7 | 33 | Citations (PDF) |
| 337 | Investigation of Complement Component C4 Copy Number Variation in Human Longevity | 2.4 | 11 | Citations (PDF) |
| 338 | Refinement of the MHC Risk Map in a Scandinavian Primary Sclerosing Cholangitis Population | 2.4 | 28 | Citations (PDF) |
| 339 | Clinical and laboratory characteristics of paediatric and adolescent index cases with venous thromboembolism and antithrombin deficiency | 4.2 | 27 | Citations (PDF) |
| 340 | 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy | 3.0 | 64 | Citations (PDF) |
| 341 | miRNAs can be generally associated with human pathologies as exemplified for miR-144* | 7.5 | 80 | Citations (PDF) |
| 342 | Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia | 3.0 | 16 | Citations (PDF) |
| 343 | Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis | 3.3 | 24 | Citations (PDF) |
| 344 | Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies | 1.8 | 24 | Citations (PDF) |
| 345 | Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis | 3.0 | 53 | Citations (PDF) |
| 346 | Comprehensive analysis of microRNA profiles in multiple sclerosis including next-generation sequencing | 4.1 | 124 | Citations (PDF) |
| 347 | Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations | 39.5 | 785 | Citations (PDF) |
| 348 | <i><scp>SLC</scp>23A1</i> polymorphism rs6596473 in the vitamin C transporter <scp>SVCT</scp>1 is associated with aggressive periodontitis | 6.6 | 28 | Citations (PDF) |
| 349 | Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12 | 1.0 | 93 | Citations (PDF) |
| 350 | Fine Mapping Major Histocompatibility Complex Associations in Psoriasis and Its Clinical Subtypes | 6.5 | 201 | Citations (PDF) |
| 351 | Whole genome and exome sequencing of monozygotic twins discordant for Crohn’s disease | 3.3 | 40 | Citations (PDF) |
| 352 | GrabBlur - a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files | 3.3 | 6 | Citations (PDF) |
| 353 | Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | 26.1 | 320 | Citations (PDF) |
| 354 | Genetic variation in TH17 pathway genes, childhood asthma, and total serum IgE levels | 6.2 | 10 | Citations (PDF) |
| 355 | HLA variants related to primary sclerosing cholangitis influence rejection after liver transplantation | 4.8 | 14 | Citations (PDF) |
| 356 | Mitochondrial DNA Variants in Obesity | 2.4 | 32 | Citations (PDF) |
| 357 | Analyses of a Pair of Concordant Twins with Infant ALL and Discordant Clinical Outcome Reveals Immunoescape As a Mechanism of Disease Persistence in MLL-Rearranged LeukemiaBlood, 2014, 124, 3791-3791 | 4.2 | 2 | Citations (PDF) |
| 358 | A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis | 6.2 | 106 | Citations (PDF) |
| 359 | Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma | 6.2 | 1 | Citations (PDF) |
| 360 | Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies | 1.0 | 160 | Citations (PDF) |
| 361 | Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project | 21.2 | 249 | Citations (PDF) |
| 362 | Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function | 0.4 | 35 | Citations (PDF) |
| 363 | Genome-wide association analysis in Primary sclerosing cholangitis and ulcerative colitis identifies risk loci at<i>GPR35</i>and<i>TCF4</i> | 10.6 | 178 | Citations (PDF) |
| 364 | Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls | 6.5 | 171 | Citations (PDF) |
| 365 | Paleoproteomic study of the Iceman’s brain tissue | 5.6 | 51 | Citations (PDF) |
| 366 | Association of a common TLR-6 polymorphism with coronary artery disease – implications for healthy ageing? | 5.1 | 26 | Citations (PDF) |
| 367 | Genetic variation in the Toll-like receptor signaling pathway is associated with childhood asthma | 6.2 | 13 | Citations (PDF) |
| 368 | Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis | 12.1 | 48 | Citations (PDF) |
| 369 | Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis | 3.3 | 205 | Citations (PDF) |
| 370 | Replication Study of Ulcerative Colitis Risk Loci in a Lithuanian–Latvian Case–Control Sample | 3.0 | 11 | Citations (PDF) |
| 371 | A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis | 3.0 | 223 | Citations (PDF) |
| 372 | From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software | 15.7 | 23 | Citations (PDF) |
| 373 | Deciphering the 8q24.21 association for glioma | 3.0 | 52 | Citations (PDF) |
| 374 | Rare exonic deletions of the <scp><i>RBFOX1</i></scp> gene increase risk of idiopathic generalized epilepsy | 4.6 | 67 | Citations (PDF) |
| 375 | Exon‐disrupting deletions of <scp><i>NRXN1</i></scp> in idiopathic generalized epilepsy | 4.6 | 66 | Citations (PDF) |
| 376 | Base-pair resolution DNA methylome of the EBV-positive Endemic Burkitt lymphoma cell line DAUDI determined by SOLiD bisulfite-sequencing | 10.4 | 31 | Citations (PDF) |
| 377 | Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the<i>ABCG5/8</i>lithogenic locus | 10.6 | 76 | Citations (PDF) |
| 378 | A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe | 2.4 | 38 | Citations (PDF) |
| 379 | Intestinal DMBT1 Expression Is Modulated by Crohn’s Disease-Associated IL23R Variants and by a DMBT1 Variant Which Influences Binding of the Transcription Factors CREB1 and ATF-2 | 2.4 | 25 | Citations (PDF) |
| 380 | B-SOLANA: an approach for the analysis of two-base encoding bisulfite sequencing data | 4.8 | 38 | Citations (PDF) |
| 381 | Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function | 3.3 | 182 | Citations (PDF) |
| 382 | Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants | 3.0 | 153 | Citations (PDF) |
| 383 | Fine mapping and replication of genetic risk loci in primary sclerosing cholangitis | 1.8 | 55 | Citations (PDF) |
| 384 | Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function | 3.0 | 65 | Citations (PDF) |
| 385 | A functional methylome map of ulcerative colitis | 4.6 | 126 | Citations (PDF) |
| 386 | Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis | 3.8 | 83 | Citations (PDF) |
| 387 | A Novel Sarcoidosis Risk Locus for Europeans on Chromosome 11q13.1 | 12.2 | 56 | Citations (PDF) |
| 388 | Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 | 3.0 | 144 | Citations (PDF) |
| 389 | DNA methylome analysis using short bisulfite sequencing data | 25.9 | 351 | Citations (PDF) |
| 390 | New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing | 13.9 | 402 | Citations (PDF) |
| 391 | Mapping of quantitative trait loci controlling lifespan in the short‐lived fish <i>Nothobranchius furzeri</i>– a new vertebrate model for age research | 7.0 | 79 | Citations (PDF) |
| 392 | Genome‐wide miRNA signatures of human longevity | 7.0 | 146 | Citations (PDF) |
| 393 | Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci | 3.6 | 220 | Citations (PDF) |
| 394 | Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases | 3.3 | 1 | Citations (PDF) |
| 395 | Accurate variant detection across non-amplified and whole genome amplified DNA using targeted next generation sequencing | 3.3 | 23 | Citations (PDF) |
| 396 | Mechanisms of IFN-γ–induced apoptosis of human skin keratinocytes in patients with atopic dermatitis | 6.2 | 153 | Citations (PDF) |
| 397 | The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma | 6.2 | 19 | Citations (PDF) |
| 398 | Genetics in primary sclerosing cholangitis | 1.9 | 20 | Citations (PDF) |
| 399 | Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing | 3.3 | 8 | Citations (PDF) |
| 400 | Limited Evidence for Parent-of-Origin Effects in Inflammatory Bowel Disease Associated Loci | 2.4 | 10 | Citations (PDF) |
| 401 | PTGER4 Expression-Modulating Polymorphisms in the 5p13.1 Region Predispose to Crohn's Disease and Affect NF-κB and XBP1 Binding Sites | 2.4 | 45 | Citations (PDF) |
| 402 | Leveraging Ethnic Group Incidence Variation to Investigate Genetic Susceptibility to Glioma: A Novel Candidate SNP Approach | 2.4 | 12 | Citations (PDF) |
| 403 | Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci | 6.5 | 332 | Citations (PDF) |
| 404 | Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL | 2.3 | 109 | Citations (PDF) |
| 405 | A case-only study of gene-environment interaction between genetic susceptibility variants in NOD2 and cigarette smoking in Crohn's disease aetiology | 2.0 | 26 | Citations (PDF) |
| 406 | Genome-wide investigation of gene–environment interactions in colorectal cancer | 3.0 | 40 | Citations (PDF) |
| 407 | PTPN2 is Associated with Crohn’s Disease and Its Expression Is Regulated by NKX2-3 | 1.8 | 13 | Citations (PDF) |
| 408 | Genetic Variation in the Epidermal Transglutaminase Genes Is Not Associated with Atopic Dermatitis | 2.4 | 10 | Citations (PDF) |
| 409 | Colonic mucosa-associated microbiota is influenced by an interaction of Crohn disease and
<i>FUT2</i>
(
<i>Secretor</i>
) genotype | 7.6 | 340 | Citations (PDF) |
| 410 | Three Genetic Susceptibility Loci Indicate a Role for IL2, REL and CARD9 in Primary Sclerosing Cholangitis | 1.0 | 0 | Citations (PDF) |
| 411 | A comprehensive analysis of the COL29A1 gene does not support a role in eczema | 6.2 | 16 | Citations (PDF) |
| 412 | Whole Genome Sequence of a Crohn Disease Trio – A Paradigm for Individualized Disease Etiology Discovery | 1.0 | 0 | Citations (PDF) |
| 413 | The Complete Individual Genome of a Female Crohn's Disease Patient – What Can You Learn? | 1.0 | 1 | Citations (PDF) |
| 414 | New gene functions in megakaryopoiesis and platelet formation | 38.7 | 426 | Citations (PDF) |
| 415 | Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease | 26.1 | 749 | Citations (PDF) |
| 416 | Early Alterations in Endogenous Hepatocyte Lipid Antigens in Hepatitis B Virus Infection Are Associated With CD1D-Restricted Natural Killer T Cell Activation and Viral Clearance | 1.0 | 0 | Citations (PDF) |
| 417 | Genetics in primary sclerosing cholangitis | 3.0 | 21 | Citations (PDF) |
| 418 | Chromosome 7p11.2 (EGFR) variation influences glioma risk | 3.0 | 164 | Citations (PDF) |
| 419 | Polymorphisms in the 3'-untranslated region of the CDH1 gene are a risk factor for primary gastric diffuse large B-cell lymphoma | 4.1 | 21 | Citations (PDF) |
| 420 | Genetic polymorphisms of matrix metalloproteinase 3 in primary sclerosing cholangitis | 4.1 | 21 | Citations (PDF) |
| 421 | Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach | 4.6 | 8 | Citations (PDF) |
| 422 | Distinct barrier integrity phenotypes in filaggrin-related atopic eczema following sequential tape stripping and lipid profiling | 2.8 | 111 | Citations (PDF) |
| 423 | A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals | 4.9 | 195 | Citations (PDF) |
| 424 | Toward the blood-borne miRNome of human diseases | 25.9 | 359 | Citations (PDF) |
| 425 | Assessment of heterogeneity between European Populations: a Baltic and Danish replication case-control study of SNPs from a recent European ulcerative colitis genome wide association study | 2.0 | 6 | Citations (PDF) |
| 426 | A tissue-specific landscape of sense/antisense transcription in the mouse intestine | 3.3 | 19 | Citations (PDF) |
| 427 | Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for
<i>IL2, REL</i>
, and
<i>CARD9</i> | 10.6 | 120 | Citations (PDF) |
| 428 | Differential analysis of Crohnʼs disease and ulcerative colitis by mass spectrometry | 3.0 | 7 | Citations (PDF) |
| 429 | Mutual Antagonism of T Cells Causing Psoriasis and Atopic Eczema | 43.7 | 215 | Citations (PDF) |
| 430 | 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 | 3.0 | 50 | Citations (PDF) |
| 431 | A genome-wide association study reveals evidence of association with sarcoidosis at<i>6p12.1</i> | 12.1 | 59 | Citations (PDF) |
| 432 | Association of inflammatory bowel disease risk loci with sarcoidosis, and its acute and chronic subphenotypes | 12.1 | 58 | Citations (PDF) |
| 433 | Pregnancy in primary sclerosing cholangitis | 21.2 | 69 | Citations (PDF) |
| 434 | Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD | 12.7 | 333 | Citations (PDF) |
| 435 | Targeted enrichment of genomic DNA regions for next-generation sequencing | 2.5 | 243 | Citations (PDF) |
| 436 | Wnt Signaling and Dupuytren's Disease | 43.7 | 225 | Citations (PDF) |
| 437 | Characterization of Changes in Serum Anti-Glycan Antibodies in Crohn's Disease – a Longitudinal Analysis | 2.4 | 29 | Citations (PDF) |
| 438 | Gene Expression in Skin and Lymphoblastoid Cells: Refined Statistical Method Reveals Extensive Overlap in cis-eQTL Signals | 6.5 | 179 | Citations (PDF) |
| 439 | Association to the Glypican-5 gene in multiple sclerosis | 2.4 | 22 | Citations (PDF) |
| 440 | Investigation of genetic susceptibility factors for human longevity – A targeted nonsynonymous SNP study | 1.8 | 17 | Citations (PDF) |
| 441 | The utility of genome-wide association studies in hepatology | 10.6 | 44 | Citations (PDF) |
| 442 | SNP discovery performance of two second-generation sequencing platforms in the NOD2 gene region | 3.9 | 15 | Citations (PDF) |
| 443 | Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits | 3.9 | 136 | Citations (PDF) |
| 444 | Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis | 1.8 | 22 | Citations (PDF) |
| 445 | A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level | 2.0 | 53 | Citations (PDF) |
| 446 | A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy | 4.6 | 12 | Citations (PDF) |
| 447 | Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL) | 26.1 | 188 | Citations (PDF) |
| 448 | New loci associated with kidney function and chronic kidney disease | 26.1 | 764 | Citations (PDF) |
| 449 | Mutational Characterization of the Bile Acid Receptor TGR5 in Primary Sclerosing Cholangitis | 2.4 | 118 | Citations (PDF) |
| 450 | Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies | 8.5 | 424 | Citations (PDF) |
| 451 | Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies | 3.3 | 429 | Citations (PDF) |
| 452 | CNVineta: a data mining tool for large case–control copy number variation datasets | 4.8 | 5 | Citations (PDF) |
| 453 | Disruption at the
<i>PTCHD1</i>
Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability | 12.7 | 189 | Citations (PDF) |
| 454 | A Functional Haplotype in the 3′Untranslated Region of<i>TNFRSF1B</i>Is Associated with Tuberculosis in Two African Populations | 12.2 | 27 | Citations (PDF) |
| 455 | Genetic Analysis in A Dutch Study Sample Identifies More Ulcerative Colitis Susceptibility Loci and Shows Their Additive Role in Disease Risk | 0.7 | 40 | Citations (PDF) |
| 456 | OCTN1 variant L503F is associated with familial and sporadic inflammatory bowel disease | 1.3 | 24 | Citations (PDF) |
| 457 | Genome-Wide Association Analysis in Primary Sclerosing Cholangitis | 1.0 | 346 | Citations (PDF) |
| 458 | Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition | 1.0 | 106 | Citations (PDF) |
| 459 | Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci | 26.1 | 237 | Citations (PDF) |
| 460 | C20orf94 deletion Is Strongly Associated with TEL/AML1 Rearrangement and Links Illegitimate V(D)J Recombination with Gender Bias In Childhood Acute Lymphoblastic LeukemiaBlood, 2010, 116, 1718-1718 | 4.2 | 1 | Citations (PDF) |
| 461 | <i>NOD2</i>,<i>IL23R</i>and<i>ATG16L1</i>polymorphisms in Lithuanian patients with inflammatory bowel disease | 4.8 | 25 | Citations (PDF) |
| 462 | Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance | 3.0 | 223 | Citations (PDF) |
| 463 | G Protein-Coupled Receptor 43 Is Essential for Neutrophil Recruitment during Intestinal Inflammation | 0.6 | 341 | Citations (PDF) |
| 464 | A functional EXO1 promoter variant is associated with prolonged life expectancy in centenarians | 4.9 | 50 | Citations (PDF) |
| 465 | Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case‐control sample | 4.5 | 44 | Citations (PDF) |
| 466 | DMBT1 functions as pattern‐recognition molecule for poly‐sulfated and poly‐phosphorylated ligands | 3.2 | 62 | Citations (PDF) |
| 467 | Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer | 2.4 | 44 | Citations (PDF) |
| 468 | Association of UCP2 −866 G/A polymorphism with chronic inflammatory diseases | 3.8 | 91 | Citations (PDF) |
| 469 | 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy | 26.1 | 529 | Citations (PDF) |
| 470 | Towards a molecular risk map—Recent advances on the etiology of inflammatory bowel disease | 6.8 | 74 | Citations (PDF) |
| 471 | Confirmation of Multiple Crohn's Disease Susceptibility Loci in a Large Dutch–Belgian Cohort | 0.7 | 115 | Citations (PDF) |
| 472 | A characterization in childhood inflammatory bowel disease, a new population-based inception cohort from South-Eastern Norway, 2005–07, showing increased incidence in Crohn's disease | 1.8 | 117 | Citations (PDF) |
| 473 | Genetic Risk Profiling and Prediction of Disease Course in Crohn's Disease Patients | 6.2 | 141 | Citations (PDF) |
| 474 | Current software for genotype imputation | 3.6 | 21 | Citations (PDF) |
| 475 | Genetic Association of Nonsynonymous Variants of the IL23R with Familial and Sporadic Inflammatory Bowel Disease in Women | 2.3 | 22 | Citations (PDF) |
| 476 | Genome-wide association studies - A summary for theclinical gastroenterologist | 4.8 | 15 | Citations (PDF) |
| 477 | Confirmation of Multiple Crohnʼs Disease Susceptibility Loci in a Large Dutch-Belgian Cohort | 0.7 | 23 | Citations (PDF) |
| 478 | Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis | 26.1 | 342 | Citations (PDF) |
| 479 | Genome-Wide Association Analysis in Sarcoidosis and Crohn's Disease Unravels a Common Susceptibility Locus on 10p12.2 | 1.0 | 86 | Citations (PDF) |
| 480 | XBP1 Links ER Stress to Intestinal Inflammation and Confers Genetic Risk for Human Inflammatory Bowel Disease | 34.1 | 1,330 | Citations (PDF) |
| 481 | A comprehensive evaluation of SNP genotype imputation | 3.0 | 147 | Citations (PDF) |
| 482 | Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci | 7.6 | 201 | Citations (PDF) |
| 483 | Efficacy assessment of SNP sets for genome-wide disease association studies | 15.7 | 17 | Citations (PDF) |
| 484 | A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5 | 1.0 | 279 | Citations (PDF) |
| 485 | Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene | 2.4 | 126 | Citations (PDF) |
| 486 | Genetic investigation of DNA-repair pathway genesPMS2,MLH1,MSH2,MSH6,MUTYH,OGG1 andMTH1 in sporadic colon cancer | 4.5 | 45 | Citations (PDF) |
| 487 | Investigation of the Lith6 candidate genes APOBEC1 and PPARG in human gallstone disease | 4.1 | 7 | Citations (PDF) |
| 488 | Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression | 3.3 | 31 | Citations (PDF) |
| 489 | Dickkopf related genes are components of the positional value gradient in Hydra | 1.9 | 88 | Citations (PDF) |
| 490 | Investigation of theLith1 candidate genesABCB11 andLXRA in human gallstone disease | 10.6 | 35 | Citations (PDF) |
| 491 | GENOMIZER: an integrated analysis system for genome-wide association data | 3.9 | 24 | Citations (PDF) |
| 492 | Sarcoidosis is associated with a truncating splice site mutation in BTNL2 | 26.1 | 465 | Citations (PDF) |
| 493 | Genome-wide association study of serum coenzyme Q<sub>10</sub>levels identifies susceptibility loci linked to neuronal diseases | 3.0 | 17 | Citations (PDF) |
| 494 | Longitudinal high-throughput TCR repertoire profiling reveals the dynamics of T-cell memory formation after mild COVID-19 infection | 1.6 | 137 | Citations (PDF) |
| 495 | Primary and secondary anti-viral response captured by the dynamics and phenotype of individual T cell clones | 1.6 | 63 | Citations (PDF) |
