日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

APOE genotype differentially modulates prion pathology in a mouse model.

APOE 基因型对小鼠模型中的朊病毒病理有差异性调节作用。

Lizińczyk Anita M, Pankiewicz Joanna E, Cullina William L, Franco Leor A, Sullivan Patrick M, Sadowski Martin J

A spectral component approach leveraging identity-by-descent graphs to address recent population structure in genomic analysis

利用同源性图的谱成分方法解决基因组分析中近期群体结构问题

Shemirani, Ruhollah; Belbin, Gillian M; Cullina, Sinead; Caggiano, Christa; Gignoux, Christopher R; Zaitlen, Noah; Kenny, Eimear E

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences

“我们所有人”研究计划中的大规模混合分析提高了对跨群体表型差异的表征能力。

Mandla, Ravi; Shi, Zhuozheng; Hou, Kangcheng; Wang, Ying; Mies, Georgia; Aw, Alan J; Cullina, Sinead; Kenny, Eimear; Atkinson, Elizabeth; Martin, Alicia R; Pasaniuc, Bogdan

SPC: a SPectral Component approach leveraging Identity-by-Descent graphs to address recent population structure in genomic analysis

SPC:一种利用同源性图谱分析近期群体结构的光谱成分方法

Shemirani, Ruhollah; Belbin, Gillian M; Cullina, Sinead; Caggiano, Christa; Gignoux, Christopher; Zaitlen, Noah; Kenny, Eimear E

APOE Genotype Differentially Modulates Prion Pathology in a Mouse Model.

APOE基因型对小鼠模型中的朊病毒病理有差异性调节作用。

Lizińczyk Anita M, Pankiewicz Joanna E, Cullina William L, Franco Leor A, Sullivan Patrick M, Sadowski Martin J

Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35

对多米尼加人群外周动脉疾病的混合基因定位分析揭示了2q35上的潜在风险位点

Cullina, Sinead; Wojcik, Genevieve L; Shemirani, Ruhollah; Klarin, Derek; Gorman, Bryan R; Sorokin, Elena P; Gignoux, Christopher R; Belbin, Gillian M; Pyarajan, Saiju; Asgari, Samira; Tsao, Philip S; Damrauer, Scott M; Abul-Husn, Noura S; Kenny, Eimear E

TOPORS as a novel causal gene for Joubert syndrome

TOPORS 是 Joubert 综合征的一种新的致病基因。

Strong, Alanna; Qu, Hui-Qi; Cullina, Sinéad; McManus, Morgan L; Zackai, Elaine H; Glessner, Joseph; Kenny, Eimear E; Hakonarson, Hakon

CDH1 pathogenic variants and cancer risk in an unselected patient population

CDH1致病变异与未选择患者人群的癌症风险

Bar-Mashiah, Ariel; Soper, Emily R; Cullina, Sinead; Belbin, Gillian M; Kenny, Eimear E; Lucas, Aimee L; Abul-Husn, Noura S

Implementing genomic screening in diverse populations

在不同人群中实施基因组筛查

Abul-Husn, Noura S; Soper, Emily R; Braganza, Giovanna T; Rodriguez, Jessica E; Zeid, Natasha; Cullina, Sinead; Bobo, Dean; Moscati, Arden; Merkelson, Amanda; Loos, Ruth J F; Cho, Judy H; Belbin, Gillian M; Suckiel, Sabrina A; Kenny, Eimear E

Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans

利用卫生系统数据来描述波多黎各人患肝病风险中一个具有显著影响的变异基因的特征

Belbin, Gillian M; Rutledge, Stephanie; Dodatko, Tetyana; Cullina, Sinead; Turchin, Michael C; Kohli, Sumita; Torre, Denis; Yee, Muh-Ching; Gignoux, Christopher R; Abul-Husn, Noura S; Houten, Sander M; Kenny, Eimear E