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- 2024
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A genome-wide association study of social trust in 33,882 Danish blood donors
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- Contribution to journal › Article
- 2023
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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
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- Contribution to journal › Article
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A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
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- Contribution to journal › Article
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Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
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- Contribution to journal › Article
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Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans
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- Contribution to journal › Article
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Mendelian randomization suggests a potential causal effect of eosinophil count on influenza vaccination responsiveness
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- Contribution to journal › Article
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European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
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- Contribution to journal › Article
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A large meta-analysis identifies genes associated with anterior uveitis
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- Contribution to journal › Article
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How Well do Polygenic Risk Scores Identify Men at High Risk for Prostate Cancer? Systematic Review and Meta-Analysis
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- Contribution to journal › Article
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Genetic insights into resting heart rate and its role in cardiovascular disease
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- Contribution to journal › Article
- 2022
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Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk
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- Contribution to journal › Article
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Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium
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- Contribution to journal › Article
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
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- Contribution to journal › Article
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Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
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- Contribution to journal › Article
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Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization
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- Contribution to journal › Article
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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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- Contribution to journal › Article
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A saturated map of common genetic variants associated with human height
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- Contribution to journal › Article
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
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- Contribution to journal › Article
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Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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- Contribution to journal › Article
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Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells
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- Contribution to journal › Article
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Polygenic risk modeling for prediction of epithelial ovarian cancer risk
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- Contribution to journal › Article
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Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors
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- Contribution to journal › Article
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Identification of Putative Causal Relationships Between Type 2 Diabetes and Blood-Based Biomarkers in East Asians by Mendelian Randomization
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- Contribution to journal › Article
- 2021
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Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
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- Contribution to journal › Article
- 2020
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Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis
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- Contribution to journal › Article
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Divergent mutational processes distinguish hypoxic and normoxic tumours
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- Contribution to journal › Article
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Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig
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- Contribution to journal › Article
- 2019
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Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke
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- Contribution to journal › Article
- 2018
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ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies
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- Contribution to journal › Article
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Identification of FAM173B as a protein methyltransferase promoting chronic pain
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- Contribution to journal › Article
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Assessment of moderate coffee consumption and risk of epithelial ovarian cancer : a Mendelian randomization study
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- Contribution to journal › Article
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A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
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- Contribution to journal › Article
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Characterization of the enhancer and promoter landscape of inflammatory bowel disease from human colon biopsies
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- Contribution to journal › Article
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Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
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- Contribution to journal › Article
- 2017
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Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
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- Contribution to journal › Article
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Genetic determinants of growth hormone and GH-related phenotypes
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- Contribution to journal › Article
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Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
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- Contribution to journal › Article
- 2016
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Genetic variants in CETP increase risk of intracerebral hemorrhage
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- Contribution to journal › Article
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Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
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- Contribution to journal › Article
- 2015
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Identification of six new susceptibility loci for invasive epithelial ovarian cancer
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- Contribution to journal › Article
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The role of tau in the pathological process and clinical expression of Huntington's disease
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- Contribution to journal › Article
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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
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- Contribution to journal › Article
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Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
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- Contribution to journal › Article
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Early and exudative age-related macular degeneration is associated with increased plasma levels of soluble TNF receptor II
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- Contribution to journal › Article
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Genetic variation in caveolin-1 correlates with long-term pancreas transplant function
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- Contribution to journal › Article
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Endothelial nitric oxide synthase single nucleotide polymorphism and left ventricular function in early chronic kidney disease
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- Contribution to journal › Article
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Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis
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- Contribution to journal › Article
- 2014
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Inherited variation in the PARP1 gene and survival from melanoma
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- Contribution to journal › Article
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The chromosome 9p21 variant interacts with vegetable and wine intake to influence the risk of cardiovascular disease : a population based cohort study
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- Contribution to journal › Article
- 2013
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Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
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- Contribution to journal › Article
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Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry. : combined analysis of 111,421 individuals of European ancestry
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- Contribution to journal › Article
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The missing link of Jewish European ancestry : contrasting the Rhineland and the Khazarian hypotheses
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- Contribution to journal › Article
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Rare allelic forms of PRDM9 associated with childhood leukemogenesis
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- Contribution to journal › Article
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The association between plasma 25-hydroxyvitamin D and subgroups in age-related macular degeneration : a cross-sectional study
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- Contribution to journal › Article
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Age-related macular degeneration is associated with increased proportion of CD56(+) T cells in peripheral blood
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- Contribution to journal › Article
- 2012
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Large-scale replication and heterogeneity in Parkinson disease genetic loci
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- Contribution to journal › Article
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Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers
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- Contribution to journal › Article
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Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers
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- Contribution to journal › Article
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Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
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- Contribution to journal › Article
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Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk
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- Contribution to journal › Letter
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HapZipper : sharing HapMap populations just got easier
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- Contribution to journal › Article
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ANKRD55 and DHCR7 are novel multiple sclerosis risk loci
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- Contribution to journal › Article
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CRYAB-650 C>G (rs2234702) affects susceptibility to Type 1 diabetes and IAA-positivity in Swedish population
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- Contribution to journal › Article
- 2011
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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
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- Contribution to journal › Article
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Pathway-based analysis of a melanoma genome-wide association study : analysis of genes related to tumour-immunosuppression
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- Contribution to journal › Article
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Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
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- Contribution to journal › Article
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Single nucleotide polymorphism (SNP) analysis demonstrates a significant association of tumour necrosis factor-alpha (TNFA) with primary immune thrombocytopenia among Caucasian adults
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- Contribution to journal › Article
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Polymorphic variation in the androgen receptor gene : association with risk of testicular germ cell cancer and metastatic disease
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- Contribution to journal › Article
- 2010
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Mark
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers : implications for risk prediction
(
- Contribution to journal › Article
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Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood
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- Contribution to journal › Article
- 2008
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Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis
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- Contribution to journal › Article
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Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis : the GENOMOS study
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- Contribution to journal › Article
- 2007
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Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
2007) In Proceedings of the National Academy of Sciences of the United States of America 104(27). p.51-11346(
- Contribution to journal › Article
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Analysis of ocular hypopigmentation in Rab38cht/cht mice
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- Contribution to journal › Article
- 2005
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Polymorphisms of the CLCN7 gene are associated with BMD in women
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- Contribution to journal › Article
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Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22
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- Contribution to journal › Article
- 2004
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Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin
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- Contribution to journal › Article
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Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes
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- Contribution to journal › Article
- 2002
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Single nucleotide polymorphism detection : allelic discrimination using TaqMan
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- Contribution to journal › Article
- 2000
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Mark
Susceptibility to osteoporotic fracture is determined by allelic variation at the Sp1 site, rather than other polymorphic sites at the COL1A1 locus
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- Contribution to journal › Article
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Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation
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- Contribution to journal › Article