July 02, 2015 article Open access LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants Bioinformatics DOI: 10.1093/bioinformatics/btv402 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 39 stored of 2,278 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Lipocalin 2 – mutation screen and serum levels in patients with anorexia nervosa or obesity and in lean individuals 2023 Frontiers in Endocrinology article Neuroscience Regulation of Appetite and Obesity Open access 6 citations The APOE locus is linked to decline in general cognitive function: 20-years follow-up in the Doetinchem Cohort Study 2022 Translational Psychiatry article Medicine Dementia and Cognitive Impairment Research Open access 5 citations A genome-wide association analysis of 2,622,830 individuals reveals new pathogenic pathways in gout 2022 medRxiv preprint Medicine Gout, Hyperuricemia, Uric Acid Open access 9 citations Variants in the GPR146 Gene Are Associated With a Favorable Cardiometabolic Risk Profile 2022 Arteriosclerosis Thrombosis and Vascular Biology article Medicine Lipid metabolism and disorders Open access 12 citations PTBP2 – a gene with relevance for both Anorexia nervosa and body weight regulation 2022 Translational Psychiatry article Psychology Eating Disorders and Behaviors Open access 14 citations Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations 2022 Journal of Thrombosis and Haemostasis article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access 31 citations Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients 2022 British Journal of Clinical Pharmacology article Medicine Cancer Treatment and Pharmacology Open access 9 citations Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries 2021 Circulation Research article Biochemistry, Genetics and Molecular Biology Congenital heart defects research Open access 40 citations The power of genetic diversity in genome-wide association studies of lipids 2021 Nature article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access cited by 1 patent 1,104 citations Mutations and variants of ONECUT1 in diabetes 2021 Nature Medicine article Medicine Pancreatic function and diabetes Open access 59 citations Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function 2021 Scientific Reports article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access 5 citations Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations 2021 Circulation Genomic and Precision Medicine article Biochemistry, Genetics and Molecular Biology Nutrition, Genetics, and Disease Open access 12 citations CONQUER: an interactive toolbox to understand functional consequences of GWAS hits 2020 NAR Genomics and Bioinformatics article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access 3 citations Variants of FOXO3 and RPA3 genes affecting IGF-1 levels alter the risk of development of primary osteoarthritis 2020 European Journal of Endocrinology article Medicine Osteoarthritis Treatment and Mechanisms 11 citations Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma 2020 PLoS ONE article Medicine Sarcoma Diagnosis and Treatment Open access 10 citations Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation 2020 Circulation Genomic and Precision Medicine article Medicine Cardiac electrophysiology and arrhythmias Open access 31 citations Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in SULT1E1, CYP2B6 and CYP4F8 and Methotrexate Levels and Toxicities 2020 Frontiers in Pharmacology article Pharmacology, Toxicology and Pharmaceutics Pharmacogenetics and Drug Metabolism Open access 14 citations Understanding functional consequences of type 2 diabetes risk loci using the universal data integration and visualization R package CONQUER 2020 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access 1 citations A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease 2020 Scientific Reports article Medicine Systemic Sclerosis and Related Diseases Open access 25 citations 21–39 of 39 ← Previous Page 2 / 2 References 0