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

Multi-ancestry Genome-Wide Association Meta-Analysis Identifies Novel Loci in Atopic Dermatitis

多祖先全基因组关联荟萃分析确定了特应性皮炎的新位点

Meritxell Oliva, Mrinal K Sarkar, Michael E March, Amir Hossein Saeidian, Frank D Mentch, Chen-Lin Hsieh, Fanying Tang, Ranjitha Uppala, Matthew T Patrick, Qinmengge Li, Rachael Bogle, J Michelle Kahlenberg, Deborah Watson, Joseph T Glessner, Lam C Tsoi, Hakon Hakonarson, Johann E Gudjonsson, Kathle

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

定义病态人类基因组中的各种倒位、复杂结构变异和染色体碎裂

Ryan L Collins, Harrison Brand, Claire E Redin, Carrie Hanscom, Caroline Antolik, Matthew R Stone, Joseph T Glessner, Tamara Mason, Giulia Pregno, Naghmeh Dorrani, Giorgia Mandrile, Daniela Giachino, Danielle Perrin, Cole Walsh, Michelle Cipicchio, Maura Costello, Alexei Stortchevoi, Joon-Yong An, B

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications

人类基因组拷贝数变异的高分辨率映射和分析:用于临床和研究应用的数据资源

Tamim H Shaikh, Xiaowu Gai, Juan C Perin, Joseph T Glessner, Hongbo Xie, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K Conlin, Monica D'Arcy, Edward C Frackelton, Elizabeth A Geiger, Chad Haldeman-Englert, Marcin Imielinski, Cecilia E Kim, Livija Medne, Kiran Annaiah, Jonathan P Bradfield, El

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes

全基因组关联数据的后续分析确定了 1 型糖尿病的新基因位点

Struan F A Grant, Hui-Qi Qu, Jonathan P Bradfield, Luc Marchand, Cecilia E Kim, Joseph T Glessner, Rosemarie Grabs, Shayne P Taback, Edward C Frackelton, Andrew W Eckert, Kiran Annaiah, Margaret L Lawson, F George Otieno, Erin Santa, Julie L Shaner, Ryan M Smith, Robert Skraban, Marcin Imielinski, R

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry

BANK 1 R61H 变异与欧洲和非洲血统的美国人系统性红斑狼疮的关联

Struan Fa Grant, Michelle Petri, Jonathan P Bradfield, Cecilia E Kim, Erin Santa, Kiran Annaiah, Edward C Frackelton, Joseph T Glessner, F George Otieno, Julie L Shaner, Ryan M Smith, Andrew W Eckert, Rosetta M Chiavacci, Marcin Imielinski, Kathleen E Sullivan, Hakon Hakonarson

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

调查欧洲和非洲血统的美国人中 MC4R 附近基因位点与儿童肥胖的关系

Struan F A Grant, Jonathan P Bradfield, Haitao Zhang, Kai Wang, Cecilia E Kim, Kiran Annaiah, Erin Santa, Joseph T Glessner, Kelly Thomas, Maria Garris, Edward C Frackelton, F George Otieno, Julie L Shaner, Ryan M Smith, Marcin Imielinski, Rosetta M Chiavacci, Mingyao Li, Robert I Berkowitz, Hakon H

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

20q13 和 21q22 上的基因位点与儿童发病的炎症性肠病有关

Subra Kugathasan, Robert N Baldassano, Jonathan P Bradfield, Patrick M A Sleiman, Marcin Imielinski, Stephen L Guthery, Salvatore Cucchiara, Cecilia E Kim, Edward C Frackelton, Kiran Annaiah, Joseph T Glessner, Erin Santa, Tara Willson, Andrew W Eckert, Erin Bonkowski, Julie L Shaner, Ryan M Smith, 

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP

FTO 基因与白种人和非洲裔儿童肥胖的关联分析揭示了一个共同的标记 SNP

Struan F A Grant, Mingyao Li, Jonathan P Bradfield, Cecilia E Kim, Kiran Annaiah, Erin Santa, Joseph T Glessner, Tracy Casalunovo, Edward C Frackelton, F George Otieno, Julie L Shaner, Ryan M Smith, Marcin Imielinski, Andrew W Eckert, Rosetta M Chiavacci, Robert I Berkowitz, Hakon Hakonarson