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ArmstrongNicola|Albert V. Smith

university of michigan
H指数:154
被引数:11.7万
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Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed

TOPMed中表达和剪接数量性状位点的跨队列分析

Science
IF45.8
2026-07-160
PRE
Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk

同时发生的克隆造血具有很强的选择性和高的白血病风险

2026-05-210
OAAI
Whole Genome Sequence Analysis of Weight Loss in 16 972 Participants With COPD Reveals Novel Risk Loci in DRAIC and RFX3

16972名COPD患者体重减轻的全基因组序列分析揭示了 <i>DRAIC</i> 和 <i>RFX3</i>中的新型风险位点

2026-04-230
OA
An integrated germline and somatic genomic model for coronary artery disease

冠心病整合了生殖细胞和体细胞基因组模型

2026-03-260
OAAI
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations

非白血病源性体细胞点突变的遗传决定因素及其基因组后果

2025-10-160
OAAI
Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program

与胰岛素抵抗相关的遗传评分与 ancestry 多样化队列中神经病学结局的关联:来自精准医学跨组学计划 (TOPMed) 的数据

2025-09-240
OAAI
Genetic architecture and analysis practices of circulating metabolites in the NHLBI Trans-Omics for Precision Medicine Program

循环代谢物的遗传结构与分析实践:美国国立心肺血液研究所精准医学跨组学计划

2025-09-180
PRE
Protective mechanisms against Alzheimer's disease in APOE3-Christchurch homozygous astrocytes

APOE3-Christchurch纯合子星形胶质细胞中对抗阿尔茨海默病的保护机制

2025-09-180
OAAI
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia

基于全基因组序列的关联分析:非裔美国人个体中双相障碍与精神分裂症的研究

2025-08-300
OAAI
Genome-wide gene by sleepiness interaction analysis for sleep apnea

全基因组范围基因与嗜睡相互作用分析,用于睡眠呼吸暂停研究

SLEEP
IF4.9
2025-08-010
OAAI
Serum microRNA expression quantitative trait loci in children with asthma colocalize with asthma-related GWAS results

哮喘患儿血清microRNA表达数量性状位点的共定位与哮喘相关全基因组关联研究结果的共定位

2025-07-170
OAAI
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

血液中嵌合体Y染色体缺失的基因组与表型相关性

2025-02-010
OAAI
Understanding the genetic complexity of puberty timing across the allele frequency spectrum

了解等位基因频谱中青春期时间的遗传复杂性

2024-07-013
OAAI
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

表观遗传和蛋白质组学特征与克隆造血扩增率相关

2024-06-040
PRE
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
Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers
2024-05-062
OAAI
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
2023-10-012
OAAI
Association of Genetic Variants with Postsurgical Pain: A Systematic Review and Meta-analyses

遗传变异与术后疼痛的关系: 系统回顾和荟萃分析

2023-09-2912
OA
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

多血统全基因组研究确定冠状动脉钙化的效应基因和药物途径

2023-09-2822
OA
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (vol 55, pg 410, 2023)

多血统全基因组关联分析可改善影响肺功能和慢性阻塞性肺疾病风险的基因和通路的分辨率 (第55卷,410页,2023)

2023-09-251
OAAI