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Matthew P. Conomos

university of washington
H指数:42
被引数:1.0万

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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
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
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
2024-05-240
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
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
2023-10-304
OAAI
Principles and methods for transferring polygenic risk scores across global populations

在全球人群中转移多基因风险评分的原则和方法

2023-08-2451
OA
Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts
2023-08-013
PRE
Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing
2023-04-040
PRE
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

静脉血栓栓塞的全基因组分析: 精准医学的跨组学计划

2023-04-016
OA
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

全基因组测序确定了NHLBI TOPMed程序中有助于血液学性状的结构变异

2022-12-084
OAAI
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

检测大规模全基因组测序研究的非编码罕见变异关联的框架

2022-10-2739
OA
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
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

Top-ld: 一种利用TOPMed全基因组序列数据探索连锁不平衡的工具

2022-06-0128
OAAI
Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program
2022-05-023
OAAI
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus (vol 13, 1222, 2022)

阐明原血管疾病位点遗传交叉疾病关联的机制 (第13卷,1222,2022)

2022-04-060
OAAI
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
2022-01-0130
OAAI