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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
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Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
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- Contribution to journal › Article
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Association of Body Mass Index and Parkinson Disease A Bidirectional Mendelian Randomization Study
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- Contribution to journal › Article
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An intronic polymorphism associated with 2,3-bisphosphoglycerate levels in human red cells is linked to expression of RhCE blood groups
2024) In Proceedings of the National Academy of Sciences of the United States of America 121(36). p.1-2(
- Contribution to journal › Letter
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Understanding the genetic complexity of puberty timing across the allele frequency spectrum
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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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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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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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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
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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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A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
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- Contribution to journal › Article
- 2022
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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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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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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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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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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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A saturated map of common genetic variants associated with human height
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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
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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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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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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
- 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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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
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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
- 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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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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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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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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Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- Contribution to journal › Article
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Assessment of moderate coffee consumption and risk of epithelial ovarian cancer : a Mendelian randomization study
(
- 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
- 2017
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Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- 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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Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
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- Contribution to journal › Article
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Genetic variants in CETP increase risk of intracerebral hemorrhage
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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
(
- 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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Genetic variation in caveolin-1 correlates with long-term pancreas transplant function
(
- 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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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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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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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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Large-scale replication and heterogeneity in Parkinson disease genetic loci
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- Contribution to journal › Article
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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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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
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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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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
- 2010
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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
(
- Contribution to journal › Article
- 2007
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Analysis of ocular hypopigmentation in Rab38cht/cht mice
(
- Contribution to journal › Article
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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
- 2005
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Polymorphisms of the CLCN7 gene are associated with BMD in women
(
- 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
(
- 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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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
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Susceptibility to osteoporotic fracture is determined by allelic variation at the Sp1 site, rather than other polymorphic sites at the COL1A1 locus
(
- Contribution to journal › Article