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

Inherited genetic risk in stillbirth: A shared genomic segments analysis of high-risk pedigrees

死产的遗传风险:高风险家系共享基因组片段分析

Workalemahu, Tsegaselassie; Madsen, Michael J; Lopez, Sarah; Page, Jessica M; Blue, Nathan R; Avery, Cecile; Sargent, Rob; Yu, Zhe; Guinto, Emily; Branch, D Ware; Leisher, Susannah; Jorde, Lynn B; Quinlan, Aaron; Coon, Hilary; Varner, Michael W; Roberts, Claire T; Neklason, Deborah W; Camp, Nicola J; Silver, Robert M

The Platinum Pedigree: a long-read benchmark for genetic variants

白金谱系:基因变异的长读长基准

Kronenberg, Zev; Nolan, Cillian; Porubsky, David; Mokveld, Tom; Rowell, William J; Lee, Sangjin; Dolzhenko, Egor; Chang, Pi-Chuan; Holt, James M; Saunders, Christopher T; Olson, Nathan D; Steely, Cody J; McGee, Sean; Guarracino, Andrea; Koundinya, Nidhi; Harvey, William T; Watkins, W Scott; Munson, Katherine M; Hoekzema, Kendra; Chua, Khi Pin; Chen, Xiao; Fanslow, Cairbre; Lambert, Christine; Dashnow, Harriet; Garrison, Erik; Smith, Joshua D; Lansdorp, Peter M; Zook, Justin M; Carroll, Andrew; Jorde, Lynn B; Neklason, Deborah W; Quinlan, Aaron R; Eichler, Evan E; Eberle, Michael A

Mapping genetic susceptibility to spontaneous preterm birth: analysis of Utah pedigrees to find inherited genetic factors

绘制自发性早产的遗传易感性图谱:分析犹他州家系以寻找遗传因素

Workalemahu, Tsegaselassie; Clark, Erin A S; Madsen, Michael J; Yu, Zhe; Dalton, Susan E; Esplin, M Sean; Manuck, Tracy; Neklason, Deborah; Wu, Chen-Han Wilfred; Jorde, Lynn B; Camp, Nicola J; Silver, Robert M; Varner, Michael W

Familial Risk of Hashimoto's Thyroiditis in a Large Genealogical Database

大型家谱数据库中桥本甲状腺炎的家族风险

Bujnis, Melissa; DeSalvo, Kelsey; Neklason, Deborah W; Madsen, Michael J; Jorde, Lynn B

Genetic resonance: dissecting the heritability and genetic correlations of human hearing acuity

遗传共振:剖析人类听力敏锐度的遗传性和遗传相关性

Duran, Jerry A; Watkins, W Scott; Neklason, Deborah W; Jorde, Lynn B

Human acrocentric chromosome short arm de novo mutation and recombination

人类端着丝粒染色体短臂新生突变和重组

Lin, Jiadong; Mastrorosa, F Kumara; Noyes, Michelle D; Yoo, DongAhn; Rhie, Arang; Porubsky, David; Hoekzema, Kendra; Munson, Katherine M; Koundinya, Nidhi; Watkins, W Scott; Jorde, Lynn B; Quinlan, Aaron R; Neklason, Deborah W; Phillippy, Adam M; Eichler, Evan E

Shared genomic segments analysis identifies MHC class I and class III molecules as genetic risk factors for juvenile idiopathic arthritis

共享基因组片段分析确定MHC I类和III类分子是幼年特发性关节炎的遗传风险因素

Avery, Cecile N; Russell, Nicole D; Steely, Cody J; Hersh, Aimee O; Bohnsack, John F; Prahalad, Sampath; Jorde, Lynn B

Familial aggregation of stillbirth: A pedigree analysis of a matched case-control study

死产的家族聚集性:一项匹配病例对照研究的系谱分析

Workalemahu, Tsegaselassie; Page, Jessica M; Meeks, Huong; Yu, Zhe; Guinto, Emily; Fraser, Alison; Varner, Michael W; Theilen, Lauren H; Quinlan, Aaron; Coon, Hilary; Enquobahrie, Daniel A; Ananth, Cande V; Tekola-Ayele, Fasil; Jorde, Lynn B; Silver, Robert M

Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study

对复发性流产家族进行全基因组测序分析:一项初步研究

Workalemahu, Tsegaselassie; Avery, Cecile; Lopez, Sarah; Blue, Nathan R; Wallace, Amelia; Quinlan, Aaron R; Coon, Hilary; Warner, Derek; Varner, Michael W; Branch, D Ware; Jorde, Lynn B; Silver, Robert M

Characterizing genetic variation in the regulation of the ER stress response through computational and cis-eQTL analyses

通过计算和顺式eQTL分析表征内质网应激反应调控中的遗传变异

Russell, Nikki D; Jorde, Lynn B; Chow, Clement Y