about
Genome-wide association scan of dental caries in the permanent dentition.Characterization of large structural genetic mosaicism in human autosomeDetectable clonal mosaicism from birth to old age and its relationship to cancerGenome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino AmericansEpigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosisPolymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.GATA2 is associated with familial early-onset coronary artery disease.Genetic and functional association of FAM5C with myocardial infarctionNeuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosisAging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulationGWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies.Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of LatinosHow Metaphors About the Genome Constrain CRISPR Metaphors: Separating the "Text" From Its "Editor"Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.Imputation-based genomic coverage assessments of current human genotyping arraysGenetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)."Bridge to the Literature"? Third-Party Genetic Interpretation Tools and the Views of Tool Developers.Is 'forward' the same as 'plus'?…and other adventures in SNP allele nomenclature.Use of metaphors about exome and whole genome sequencing.Discovery of common and rare genetic risk variants for colorectal cancerA content analysis of the views of genetics professionals on race, ancestry, and geneticsGenetic analyses of diverse populations improves discovery for complex traits
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P50
description
hulumtuese
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onderzoeker
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researcher
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հետազոտող
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name
Sarah C Nelson
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Sarah C Nelson
@en
Sarah C Nelson
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Sarah C Nelson
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Sarah C Nelson
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type
label
Sarah C Nelson
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Sarah C Nelson
@en
Sarah C Nelson
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Sarah C Nelson
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Sarah C Nelson
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prefLabel
Sarah C Nelson
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Sarah C Nelson
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Sarah C Nelson
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Sarah C Nelson
@nl
Sarah C Nelson
@sl
P106
P21
P31
P3835
sarah-nelson3
P496
0000-0002-2109-6465