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

Clonal Hematopoiesis and Cardiovascular Disease Risk After Cancer Therapy in Patients With Solid Tumors

实体瘤患者癌症治疗后克隆性造血与心血管疾病风险

Shyr, Derek; Pershad, Yash; Zhao, Kun; Kishtagari, Ashwin; Corty, Robert W; Shinohara, Eric; Park, Ben Ho; Heimlich, J Brett; Luo, Leo; Bick, Alexander G

Detection of clonal hematopoiesis of indeterminate potential via genome or exome sequencing underestimates disease associations

通过基因组或外显子组测序检测未定潜能的克隆性造血会低估疾病关联性。

Corty, Robert; Pershad, Yash; Heimlich, J Brett; Vlasschaert, Caitlyn; Luo, Leo; Mack, Taralynn; Amancherla, Kaushik; Robinson-Cohen, Cassianne; Savona, Michael; Bick, Alexander G

Mutation-specific impairment of TET2 and DNMT3A enzymatic activity predicts clonal hematopoiesis disease risk

TET2 和 DNMT3A 酶活性的突变特异性损害可预测克隆性造血疾病风险。

Pershad, Yash; Zhao, Kun; Van Amburg, Joseph C; Corty, Robert W; Parker, Alyssa C; Silver, Alexander J; Almadani, Yara; Kishtagari, Ashwin; Hodges, Emily; Savona, Michael R; Heimlich, J Brett; Bick, Alexander G

A coding single nucleotide polymorphism in the interleukin-6 receptor enhances IL-6 signalling in CD4 T cells and predicts treatment response to tocilizumab in giant cell arteritis

白细胞介素-6受体编码单核苷酸多态性增强CD4 T细胞中IL-6信号传导,并可预测巨细胞动脉炎患者对托珠单抗的治疗反应。

Zorc, Robert; Redmond, Christopher; Sylvester, McKella; Maclean, Mary; Yamamoto de Almeida, Luciana; Quinn, Kaitlin A; Tomelleri, Alessandro; Campochiaro, Corrado; Dagna, Lorenzo; Gutierrez-Rodrigues, Fernanda; Wells, Kristina V; Rankin, Cameron; Hait, Sabrina Helmold; Palmer, Chloe; Corty, Robert; Bick, Alexander; Lambert, Kathi; Buckner, Jane H; O'Shea, John J; Park, Jin Kyun; Gadina, Massimo; Grayson, Peter C

Incident cytopenia and risk of subsequent myeloid neoplasm in age-related clonal hematopoiesis: a multi-biobank case-control study

年龄相关性克隆性造血中新发血细胞减少症与后续髓系肿瘤风险:一项多生物样本库病例对照研究

Brogan, James; Kishtagari, Ashwin; Corty, Robert W; Pershad, Yash; Vlasschaert, Caitlyn; Sharber, Brian; Heimlich, J Brett; Luo, Leo; Ferrell, P Brent; Savona, Michael R; Xu, Yaomin; Bick, Alexander G

Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcare

对35024名主要具有非洲血统的人进行基因组测序,填补了基因组学和医疗保健领域的空白。

Avery, Cecile; Babanejad, Mojgan; Baker, James; Bledsoe, Xavier; Blostein, Freida; Corty, Robert W; Ellis, Kimberlyn; Hung, Adriana M; Lake, Allison; Shelley, John; Sheng, Quanhu; Aldrich, Melinda; Basford, Melissa; Bastarache, Lisa; Below, Jennifer; Bick, Alexander G; Embi, Peter; Feng, QiPing; Gamazon, Eric; Han, Lide; Hirbo, Jibril; Marginean, Kayla; Mosley, Jonathan; Pulley, Jill; Roden, Dan M; Ruderfer, Douglas M; Shuey, Megan; Shyr, Yu; Stein, C Michael; Walsh, Colin; Wilkins, Consuelo

Genetic drivers and clinical consequences of mosaic chromosomal alterations in 1 million individuals

一百万个体中嵌合染色体改变的遗传驱动因素和临床后果

Zhao, Kun; Pershad, Yash; Poisner, Hannah M; Ma, Xiaolong; Quade, Kali; Vlasschaert, Caitlyn; Mack, Taralynn; Khankari, Nikhil K; von Beck, Kelly; Brogan, James; Kishtagari, Ashwin; Corty, Robert W; Li, Yajing; Xu, Yaomin; Reiner, Alexander P; Scheet, Paul; Auer, Paul L; Bick, Alexander G

A clinical algorithm to identify people with the glucose-6-phosphate dehydrogenase p.Val68Met variant at risk for diabetes undertreatment

一种用于识别携带葡萄糖-6-磷酸脱氢酶 p.Val68Met 变异且糖尿病治疗不足风险人群的临床算法

Pershad, Yash; Breeyear, Joseph H; Corty, Robert W; Mosley, Jonathan D; Phillips, Lawrence S; Giri, Ayush; Roden, Dan M; Edwards, Todd L; Bick, Alexander G

VEXAS-Defining UBA1 Somatic Variants in 245,368 Diverse Individuals in the NIH All Of Us Cohort

NIH All Of Us队列中245,368名不同个体的VEXAS定义UBA1体细胞变异

Corty, Robert W; Brogan, James; Byram, Kevin; Springer, Jason; Grayson, Peter C; Bick, Alexander G

Identification of DAGLA as an autoantibody target in cerebellar ataxia

确定 DAGLA 为小脑性共济失调的自身抗体靶点

Ramona Miske, Madeleine Scharf, Kathrin Borowski, Ina Specht, Merle Corty, Monika-Johanna Loritz, Frederik Rombach, Guy Laureys, Nadine Rochow, Christiane Radzimski, Linda Schnitter, Dominica Ratuszny, Thomas Skripuletz, Mike P Wattjes, Stefanie Hahn, Yvonne Denno, Khadija Guerti, Matthijs Oyaert, F