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Comparison of family history and SNPs for predicting risk of complex diseaseSix novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesGenome-wide detection and characterization of positive selection in human populationsReplicability and robustness of genome-wide-association studies for behavioral traitsA common allele on chromosome 9 associated with coronary heart diseaseA genomewide association study of skin pigmentation in a South Asian populationA second generation human haplotype map of over 3.1 million SNPsThe biology of genomes: sequence gives way to functionGenetic variants associated with breast size also influence breast cancer riskA genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility lociGenome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotypeGerm line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasmsNovel associations for hypothyroidism include known autoimmune risk lociEfficient replication of over 180 genetic associations with self-reported medical dataWhole-genome patterns of common DNA variation in three human populationsGenetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosisWhole-genome sequencing identifies EN1 as a determinant of bone density and fracture.Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineGWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition lociTwo-stage genome-wide association study identifies a novel susceptibility locus associated with melanomaVariation in the FGFR2 gene and the effect of a low-fat dietary pattern on invasive breast cancer.Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus.Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants.Matching strategies for genetic association studies in structured populations.Genome-wide association study identifies 74 loci associated with educational attainment.Genome-wide definitive haplotypes determined using a collection of complete hydatidiform molesAssessment of clinical validity of a breast cancer risk model combining genetic and clinical information.minimac2: faster genotype imputation.Escape from crossover interference increases with maternal age.A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk.Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.Pooled versus individual genotyping in a breast cancer genome-wide association studyGenome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana.Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence.A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mappingGenetic variants in the MRPS30 region and postmenopausal breast cancer risk
P50
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P50
description
hulumtues
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A. Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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David A Hinds
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P106
P108
P21
P31
P496
0000-0002-4911-803X