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

Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score.

比较用于跨种族结直肠癌多基因风险评分的祖源标准化方法

Rosenthal Elisabeth A, Hsu Li, Thomas Minta, Peters Ulrike, Kachulis Christopher, Patterson Karynne, Jarvik Gail P

Celeste: A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projects

Celeste:一个基于云的基因组学基础设施,配备适用于群体规模测序项目的变异检测流程。

Siddiqui, Noora; Lee, Breanna; Yi, Victoria; Farek, Jesse; Khan, Ziad; Kalla, Sara E; Wang, Qiaoyan; Walker, Kimberly; Meldrim, James; Kachulis, Christopher; Gatzen, Michael; Lennon, Niall J; Mehtalia, Shyamal; Catreux, Severine; Mehio, Rami; Gibbs, Richard A; Venner, Eric

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

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner

基因组和外显子组混合测序方法能够以无偏倚、高质量且经济高效的方式捕获遗传变异。

Boltz, Toni A; Chu, Benjamin B; Liao, Calwing; Sealock, Julia M; Ye, Robert; Majara, Lerato; Fu, Jack M; Service, Susan; Zhan, Lingyu; Medland, Sarah E; Chapman, Sinéad B; Rubinacci, Simone; DeFelice, Matthew; Grimsby, Jonna L; Abebe, Tamrat; Alemayehu, Melkam; Ashaba, Fred K; Atkinson, Elizabeth G; Bigdeli, Tim; Bradway, Amanda B; Brand, Harrison; Chibnik, Lori B; Fekadu, Abebaw; Gatzen, Michael; Gelaye, Bizu; Gichuru, Stella; Gildea, Marissa L; Hill, Toni C; Huang, Hailiang; Hubbard, Kalyn M; Injera, Wilfred E; James, Roxanne; Joloba, Moses; Kachulis, Christopher; Kalmbach, Phillip R; Kamulegeya, Rogers; Kigen, Gabriel; Kim, Soyeon; Koen, Nastassja; Kwobah, Edith K; Kyebuzibwa, Joseph; Lee, Seungmo; Lennon, Niall J; Lind, Penelope A; Lopera-Maya, Esteban A; Makale, Johnstone; Mangul, Serghei; McMahon, Justin; Mowlem, Pierre; Musinguzi, Henry; Mwema, Rehema M; Nakasujja, Noeline; Newman, Carter P; Nkambule, Lethukuthula L; O'Neil, Conor R; Olivares, Ana Maria; Olsen, Catherine M; Ongeri, Linnet; Parsa, Sophie J; Pretorius, Adele; Ramesar, Raj; Reagan, Faye L; Sabatti, Chiara; Schneider, Jacquelyn A; Shiferaw, Welelta; Stevenson, Anne; Stricker, Erik; Stroud, Rocky E 2nd; Tang, Jessie; Whiteman, David; Yohannes, Mary T; Yu, Mingrui; Yuan, Kai; Akena, Dickens; Atwoli, Lukoye; Kariuki, Symon M; Koenen, Karestan C; Newton, Charles R J C; Stein, Dan J; Teferra, Solomon; Zingela, Zukiswa; Pato, Carlos N; Pato, Michele T; Lopez-Jaramillo, Carlos; Freimer, Nelson; Ophoff, Roel A; Olde Loohuis, Loes M; Talkowski, Michael E; Neale, Benjamin M; Howrigan, Daniel P; Martin, Alicia R

Returning integrated genomic risk and clinical recommendations: The eMERGE study

整合基因组风险和临床建议:eMERGE 研究

Linder, Jodell E; Allworth, Aimee; Bland, Harris T; Caraballo, Pedro J; Chisholm, Rex L; Clayton, Ellen Wright; Crosslin, David R; Dikilitas, Ozan; DiVietro, Alanna; Esplin, Edward D; Forman, Sophie; Freimuth, Robert R; Gordon, Adam S; Green, Richard; Harden, Maegan V; Holm, Ingrid A; Jarvik, Gail P; Karlson, Elizabeth W; Labrecque, Sofia; Lennon, Niall J; Limdi, Nita A; Mittendorf, Kathleen F; Murphy, Shawn N; Orlando, Lori; Prows, Cynthia A; Rasmussen, Luke V; Rasmussen-Torvik, Laura; Rowley, Robb; Sawicki, Konrad Teodor; Schmidlen, Tara; Terek, Shannon; Veenstra, David; Velez Edwards, Digna R; Absher, Devin; Abul-Husn, Noura S; Alsip, Jorge; Bangash, Hana; Beasley, Mark; Below, Jennifer E; Berner, Eta S; Booth, James; Chung, Wendy K; Cimino, James J; Connolly, John; Davis, Patrick; Devine, Beth; Fullerton, Stephanie M; Guiducci, Candace; Habrat, Melissa L; Hain, Heather; Hakonarson, Hakon; Harr, Margaret; Haverfield, Eden; Hernandez, Valentina; Hoell, Christin; Horike-Pyne, Martha; Hripcsak, George; Irvin, Marguerite R; Kachulis, Christopher; Karavite, Dean; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Korf, Bruce; Kottyan, Leah; Kullo, Iftikhar J; Larkin, Katie; Liu, Cong; Malolepsza, Edyta; Manolio, Teri A; May, Thomas; McNally, Elizabeth M; Mentch, Frank; Miller, Alexandra; Mooney, Sean D; Murali, Priyanka; Mutai, Brenda; Muthu, Naveen; Namjou, Bahram; Perez, Emma F; Puckelwartz, Megan J; Rakhra-Burris, Tejinder; Roden, Dan M; Rosenthal, Elisabeth A; Saadatagah, Seyedmohammad; Sabatello, Maya; Schaid, Dan J; Schultz, Baergen; Seabolt, Lynn; Shaibi, Gabriel Q; Sharp, Richard R; Shirts, Brian; Smith, Maureen E; Smoller, Jordan W; Sterling, Rene; Suckiel, Sabrina A; Thayer, Jeritt; Tiwari, Hemant K; Trinidad, Susan B; Walunas, Theresa; Wei, Wei-Qi; Wells, Quinn S; Weng, Chunhua; Wiesner, Georgia L; Wiley, Ken; Peterson, Josh F

Genome-wide polygenic score to predict chronic kidney disease across ancestries

利用全基因组多基因评分预测不同种族人群的慢性肾病

Khan, Atlas; Turchin, Michael C; Patki, Amit; Srinivasasainagendra, Vinodh; Shang, Ning; Nadukuru, Rajiv; Jones, Alana C; Malolepsza, Edyta; Dikilitas, Ozan; Kullo, Iftikhar J; Schaid, Daniel J; Karlson, Elizabeth; Ge, Tian; Meigs, James B; Smoller, Jordan W; Lange, Christoph; Crosslin, David R; Jarvik, Gail P; Bhatraju, Pavan K; Hellwege, Jacklyn N; Chandler, Paulette; Torvik, Laura Rasmussen; Fedotov, Alex; Liu, Cong; Kachulis, Christopher; Lennon, Niall; Abul-Husn, Noura S; Cho, Judy H; Ionita-Laza, Iuliana; Gharavi, Ali G; Chung, Wendy K; Hripcsak, George; Weng, Chunhua; Nadkarni, Girish; Irvin, Marguerite R; Tiwari, Hemant K; Kenny, Eimear E; Limdi, Nita A; Kiryluk, Krzysztof

Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

针对不同人群,开发和验证跨种族多基因2型糖尿病风险评分

Ge, Tian; Irvin, Marguerite R; Patki, Amit; Srinivasasainagendra, Vinodh; Lin, Yen-Feng; Tiwari, Hemant K; Armstrong, Nicole D; Benoit, Barbara; Chen, Chia-Yen; Choi, Karmel W; Cimino, James J; Davis, Brittney H; Dikilitas, Ozan; Etheridge, Bethany; Feng, Yen-Chen Anne; Gainer, Vivian; Huang, Hailiang; Jarvik, Gail P; Kachulis, Christopher; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Kottyan, Leah; Kullo, Iftikhar J; Lange, Christoph; Lennon, Niall; Leong, Aaron; Malolepsza, Edyta; Miles, Ayme D; Murphy, Shawn; Namjou, Bahram; Narayan, Renuka; O'Connor, Mark J; Pacheco, Jennifer A; Perez, Emma; Rasmussen-Torvik, Laura J; Rosenthal, Elisabeth A; Schaid, Daniel; Stamou, Maria; Udler, Miriam S; Wei, Wei-Qi; Weiss, Scott T; Ng, Maggie C Y; Smoller, Jordan W; Lebo, Matthew S; Meigs, James B; Limdi, Nita A; Karlson, Elizabeth W