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

All of Us Research Program year in review: 2024

“我们所有人”研究计划年度回顾:2024

Dutka, Tara; Faust, Erika J; Gallagher, C Scott; Hyams, Travis; Kozlowski, Elyse; Landis, Erica; Lee, Minnkyong; Liou, Grace F; Litwin, Tamara R; Lunt, Christopher; Mian, Sana H; Musick, Anjene; Park, Nguyen; Patten, Theresa; Sanchez, Janeth; Schully, Sheri D; Shyr, Cathy; Ginsburg, Geoffrey S

Population-scale Long-read Sequencing in the All of Us Research Program

“我们所有人”研究计划中的群体规模长读长测序

Garimella, Kiran V; Li, Qiuhui; Wertz, Julie; Lee, Samuel K; Cunial, Fabio; Huang, Yongqing; Mostovoy, Yulia; Lorig-Roach, Ryan; English, Adam; Su, Hang; Levy, Shawn; Muzny, Donna M; Berngruber, Chelsea; Danzi, Matt C; Harvey, William T; LaPlante, Emily L; Patterson, Karynne; Rozanski, Allison N; Schwartz, Sophie; Shifaw, Beri; Wang, Yuanyuan; Wong, Isaac; Xu, Isaac R L; Zaheri, Shadi; Zuchner, Stephan; Zheng, Xinchang; Dugan-Perez, Shannon; Izydorczyk, Michal; Mehta, Heer; Gibbs, Richard A; Lichtenstein, Lee; Gupta, Namrata; Lennon, Niall; Gabriel, Stacey; Timp, Winston; Doheny, Kimberly F; Dutka, Tara; Musick, Anjene; Wei, Chia-Lin; Sedlazeck, Fritz J; Schatz, Michael C; Talkowski, Michael E; Eichler, Evan E

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

针对美国不同人群,筛选、优化和验证十种慢性病多基因风险评分,以用于临床应用

Lennon, Niall J; Kottyan, Leah C; Kachulis, Christopher; Abul-Husn, Noura S; Arias, Josh; Belbin, Gillian; Below, Jennifer E; Berndt, Sonja I; Chung, Wendy K; Cimino, James J; Clayton, Ellen Wright; Connolly, John J; Crosslin, David R; Dikilitas, Ozan; Velez Edwards, Digna R; Feng, QiPing; Fisher, Marissa; Freimuth, Robert R; Ge, Tian; Glessner, Joseph T; Gordon, Adam S; Patterson, Candace; Hakonarson, Hakon; Harden, Maegan; Harr, Margaret; Hirschhorn, Joel N; Hoggart, Clive; Hsu, Li; Irvin, Marguerite R; Jarvik, Gail P; Karlson, Elizabeth W; Khan, Atlas; Khera, Amit; Kiryluk, Krzysztof; Kullo, Iftikhar; Larkin, Katie; Limdi, Nita; Linder, Jodell E; Loos, Ruth J F; Luo, Yuan; Malolepsza, Edyta; Manolio, Teri A; Martin, Lisa J; McCarthy, Li; McNally, Elizabeth M; Meigs, James B; Mersha, Tesfaye B; Mosley, Jonathan D; Musick, Anjene; Namjou, Bahram; Pai, Nihal; Pesce, Lorenzo L; Peters, Ulrike; Peterson, Josh F; Prows, Cynthia A; Puckelwartz, Megan J; Rehm, Heidi L; Roden, Dan M; Rosenthal, Elisabeth A; Rowley, Robb; Sawicki, Konrad Teodor; Schaid, Daniel J; Smit, Roelof A J; Smith, Johanna L; Smoller, Jordan W; Thomas, Minta; Tiwari, Hemant; Toledo, Diana M; Vaitinadin, Nataraja Sarma; Veenstra, David; Walunas, Theresa L; Wang, Zhe; Wei, Wei-Qi; Weng, Chunhua; Wiesner, Georgia L; Yin, Xianyong; Kenny, Eimear E

All of Us Research Program year in review: 2023-2024

“我们所有人”研究项目年度回顾:2023-2024

Kozlowski, Elyse; Farrell, Margaret M; Faust, Erika J; Gallagher, C Scott; Jones, Grant; Landis, Erica; Litwin, Tamara R; Lunt, Chris; Mian, Sana H; Mockrin, Stephen C; Musick, Anjene; Patten, Theresa; Sanchez, Janeth; Schully, Sheri; Ginsburg, Geoffrey S

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

“我们所有人”队列中致病变异的频率揭示了祖先因素造成的差异

Venner, Eric; Patterson, Karynne; Kalra, Divya; Wheeler, Marsha M; Chen, Yi-Ju; Kalla, Sara E; Yuan, Bo; Karnes, Jason H; Walker, Kimberly; Smith, Joshua D; McGee, Sean; Radhakrishnan, Aparna; Haddad, Andrew; Empey, Philip E; Wang, Qiaoyan; Lichtenstein, Lee; Toledo, Diana; Jarvik, Gail; Musick, Anjene; Gibbs, Richard A

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

作者更正:All of Us队列中致病变异的频率揭示了祖先驱动的差异

Venner, Eric; Patterson, Karynne; Kalra, Divya; Wheeler, Marsha M; Chen, Yi-Ju; Kalla, Sara E; Yuan, Bo; Karnes, Jason H; Walker, Kimberly; Smith, Joshua D; McGee, Sean; Radhakrishnan, Aparna; Haddad, Andrew; Empey, Philip E; Wang, Qiaoyan; Lichtenstein, Lee; Toledo, Diana; Jarvik, Gail; Musick, Anjene; Gibbs, Richard A

Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

全基因组测序作为一种研究性手段,用于评估遗传疾病风险和药物基因组学结果,这是“我们所有人”研究计划的一部分。

Venner, Eric; Muzny, Donna; Smith, Joshua D; Walker, Kimberly; Neben, Cynthia L; Lockwood, Christina M; Empey, Phillip E; Metcalf, Ginger A; Kachulis, Chris; Mian, Sana; Musick, Anjene; Rehm, Heidi L; Harrison, Steven; Gabriel, Stacey; Gibbs, Richard A; Nickerson, Deborah; Zhou, Alicia Y; Doheny, Kimberly; Ozenberger, Bradley; Topper, Scott E; Lennon, Niall J

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

精神疾病的全基因组测序:WGSPD联盟

Sanders, Stephan J; Neale, Benjamin M; Huang, Hailiang; Werling, Donna M; An, Joon-Yong; Dong, Shan; Abecasis, Goncalo; Arguello, P Alexander; Blangero, John; Boehnke, Michael; Daly, Mark J; Eggan, Kevin; Geschwind, Daniel H; Glahn, David C; Goldstein, David B; Gur, Raquel E; Handsaker, Robert E; McCarroll, Steven A; Ophoff, Roel A; Palotie, Aarno; Pato, Carlos N; Sabatti, Chiara; State, Matthew W; Willsey, A Jeremy; Hyman, Steven E; Addington, Anjene M; Lehner, Thomas; Freimer, Nelson B

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

16p11.2 微缺失和微重复对整体转录谱的影响

Kusenda Mary, Vacic Vladimir, Malhotra Dheeraj, Rodgers Linda, Pavon Kevin, Meth Jennifer, Kumar Ravinesh A, Christian Susan L, Peeters Hilde, Cho Shawn S, Addington Anjene, Rapoport Judith L, Sebat Jonathan

Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls

儿茶酚-O-甲基转移酶 (COMT) val158met 多态性与儿童期起病精神分裂症患者、其非精神病性兄弟姐妹以及健康对照组的青少年皮质发育的关系

Raznahan, Armin; Greenstein, Deanna; Lee, Yohan; Long, Robert; Clasen, Liv; Gochman, Pete; Addington, Anjene; Giedd, Jay N; Rapoport, Judith L; Gogtay, Nitin