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Sarah C. Nelson

University of Washington
H指数:47
被引数:1.2万

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Recommendations for responsible use of population descriptors in polygenic risk score development

关于在多基因风险评分开发中负责任使用人群描述符的建议

2025-11-240
PRE
A data model for population descriptors in genomic research

基因组研究中人口描述符的数据模型

2025-06-120
PRE
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

在超过50,000例样本中的测序研究确定了与心房颤动风险相关的编码和结构变异

2025-03-063
PRE
The PRIMED Consortium: Reducing disparities in polygenic risk assessment

PRIMED联盟: 减少多基因风险评估中的差异

2024-12-011
OAAI
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

全基因组测序揭示了冠状动脉钙化的两个基因座,并将ARSE鉴定为血管钙化的调节剂

2023-12-044
OA
Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Health of Latinos
2023-01-014
OAAI
Perspective Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program
2022-08-0146
OAAI
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes

35个基因的罕见编码变异与循环脂质水平相关 -- 170,000外显子组的多祖先分析

2022-01-0123
OAAI
CONSENT FOR USE OF GENETIC DATA AMONG US HISPANICS/LATINOS: RESULTS FROM THE HISPANIC COMMUNITY HEALTH STUDY/ STUDY OF LATINOS

同意在美国西班牙裔/拉丁裔中使用遗传数据: 来自西班牙裔社区健康研究/拉丁裔研究的结果

2021-10-219
OA
The trans-ancestral genomic architecture of glycemic traits

血糖性状的跨祖先基因组结构

2021-05-31361
OAAI
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

多个计算机功能注释的动态整合使大规模全基因组测序研究的罕见变异关联分析成为可能

2020-08-24138
OAAI