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R

Ryan L. Minster

university of pittsburgh
H指数:41
被引数:1.0万

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The Soifua Manuia reference panel with 2,570 Samoan haplotypes improves genotype imputation quality among Samoans

包含2,570个萨摩亚人单倍型的Soifua Manuia参考面板提高了萨摩亚人群中的基因型推断质量

2026-09-170
OAAI
Variant Harmonization Critically Determines Polygenic Score Transferability for Lipid Traits in Samoan Populations

变异体调和对于萨摩亚人群中脂质性状的多基因评分转移性的决定性作用

2026-08-220
OAAI
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

cellSTAAR:整合基于单细胞测序的功能数据,以提升非编码区域稀有变异关联检验的功效

2025-12-310
PRE
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

333,100个体的全基因组测序揭示了罕见的非编码单一变异和与身高的聚集关联

2024-10-032
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
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
2023-10-012
OAAI
A Polynesian-specific missense CETP variant alters the lipid profile
2023-07-014
OAAI
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

多血统转录组全关联分析产生了对烟草使用生物学和药物再利用的见解

2023-01-2622
OAAI
A stop-gain variant in BTNL9 is associated with atherogenic lipid profiles
2023-01-011
OAAI
Rare Variants in Genes Encoding Subunits of the Epithelial Na+ Channel Are Associated With Blood Pressure and Kidney Function

编码上皮Na通道亚基的基因的罕见变异与血压和肾功能相关

2022-11-0114
OA
The protective effect of rs373863828 on type 2 diabetes does not operate through a body composition pathway in adult Samoans
OBESITY
IF4.7
2022-10-255
OA
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

来自收缩压,舒张压和高血压的大规模全基因组测序研究的见解

2022-08-0111
OA
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

来自NHLBI TOPMed计划的不同队列中空腹血糖和空腹胰岛素水平的全基因组序列关联分析

2022-07-288
OAAI
A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes
2022-04-2034
OAAI
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

孟德尔随机化支持端粒长度与不确定电位的克隆造血之间的双向因果关系

2022-04-0841
OAAI
CREBRF missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesian peoples living in Samoa and Aotearoa New Zealand
2022-02-106
OAAI
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
2022-01-0130
OAAI