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

Germline genetic variation impacts clonal hematopoiesis landscape and progression to malignancy

种系遗传变异影响克隆性造血格局和恶性肿瘤的进展

Liu, Jie; Tran, Duc; Xue, Liying; Wiley, Brian J; Vlasschaert, Caitlyn; Watson, Caroline J; MacGregor, Hamish A J; Zong, Xiaoyu; Chan, Irenaeus C C; Das, Indraniel; Uddin, Md Mesbah; Niroula, Abhishek; Griffin, Gabriel; Ebert, Benjamin L; Mack, Taralynn; Pershad, Yash; Sharber, Brian; Berger, Michael; Zehir, Ahmet; Ptashkin, Ryan; Levine, Ross L; Papaemmanuil, Elli; Joseph, Vijai; Gao, Teng; Kemel, Yelena; Mandelker, Diana; Stopsack, Konrad H; Pharoah, Paul D P; Mukherjee, Semanti; Ding, Li; Cao, Yin; Walter, Matthew J; Blundell, Jamie R; Chatterjee, Nilanjan; Offit, Kenneth; Godley, Lucy A; Link, Daniel C; Stadler, Zsofia K; Bick, Alexander G; Natarajan, Pradeep; Bolton, Kelly L

Genealogy based trait association with LOCATER boosts power at loci with allelic heterogeneity

利用LOCATER进行基于谱系的性状关联分析,可以提高具有等位基因异质性的位点的统计效力。

Wang, Xinxin; Christ, Ryan; Young, Erica; Kang, Chul Joo; Das, Indraniel; Belter, Edward A; Laakso, Markku; Aslett, Louis J M; Steinsaltz, David; Stitziel, Nathan O; Hall, Ira M

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

芬兰男性代谢物的全基因组关联研究发现了与疾病相关的基因位点

Yin, Xianyong; Chan, Lap Sum; Bose, Debraj; Jackson, Anne U; VandeHaar, Peter; Locke, Adam E; Fuchsberger, Christian; Stringham, Heather M; Welch, Ryan; Yu, Ketian; Fernandes Silva, Lilian; Service, Susan K; Zhang, Daiwei; Hector, Emily C; Young, Erica; Ganel, Liron; Das, Indraniel; Abel, Haley; Erdos, Michael R; Bonnycastle, Lori L; Kuusisto, Johanna; Stitziel, Nathan O; Hall, Ira M; Wagner, Gregory R; Kang, Jian; Morrison, Jean; Burant, Charles F; Collins, Francis S; Ripatti, Samuli; Palotie, Aarno; Freimer, Nelson B; Mohlke, Karen L; Scott, Laura J; Wen, Xiaoquan; Fauman, Eric B; Laakso, Markku; Boehnke, Michael

Association of structural variation with cardiometabolic traits in Finns

芬兰人结构变异与心血管代谢特征的关联

Chen, Lei; Abel, Haley J; Das, Indraniel; Larson, David E; Ganel, Liron; Kanchi, Krishna L; Regier, Allison A; Young, Erica P; Kang, Chul Joo; Scott, Alexandra J; Chiang, Colby; Wang, Xinxin; Lu, Shuangjia; Christ, Ryan; Service, Susan K; Chiang, Charleston W K; Havulinna, Aki S; Kuusisto, Johanna; Boehnke, Michael; Laakso, Markku; Palotie, Aarno; Ripatti, Samuli; Freimer, Nelson B; Locke, Adam E; Stitziel, Nathan O; Hall, Ira M

Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

通过DNA测序测量的人类血液中线粒体基因组拷贝数与代谢特征密切相关,这种关联是通过细胞类型组成差异实现的。

Ganel, Liron; Chen, Lei; Christ, Ryan; Vangipurapu, Jagadish; Young, Erica; Das, Indraniel; Kanchi, Krishna; Larson, David; Regier, Allison; Abel, Haley; Kang, Chul Joo; Scott, Alexandra; Havulinna, Aki; Chiang, Charleston W K; Service, Susan; Freimer, Nelson; Palotie, Aarno; Ripatti, Samuli; Kuusisto, Johanna; Boehnke, Michael; Laakso, Markku; Locke, Adam; Stitziel, Nathan O; Hall, Ira M

Mapping and characterization of structural variation in 17,795 human genomes

对17795个人类基因组的结构变异进行定位和表征

Abel, Haley J; Larson, David E; Regier, Allison A; Chiang, Colby; Das, Indraniel; Kanchi, Krishna L; Layer, Ryan M; Neale, Benjamin M; Salerno, William J; Reeves, Catherine; Buyske, Steven; Matise, Tara C; Muzny, Donna M; Zody, Michael C; Lander, Eric S; Dutcher, Susan K; Stitziel, Nathan O; Hall, Ira M

svtools: population-scale analysis of structural variation

svtools:群体尺度结构变异分析

Larson, David E; Abel, Haley J; Chiang, Colby; Badve, Abhijit; Das, Indraniel; Eldred, James M; Layer, Ryan M; Hall, Ira M

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

量化罕见和超罕见编码变异对表型谱的影响

Ganna, Andrea; Satterstrom, F Kyle; Zekavat, Seyedeh M; Das, Indraniel; Kurki, Mitja I; Churchhouse, Claire; Alfoldi, Jessica; Martin, Alicia R; Havulinna, Aki S; Byrnes, Andrea; Thompson, Wesley K; Nielsen, Philip R; Karczewski, Konrad J; Saarentaus, Elmo; Rivas, Manuel A; Gupta, Namrata; Pietiläinen, Olli; Emdin, Connor A; Lescai, Francesco; Bybjerg-Grauholm, Jonas; Flannick, Jason; Mercader, Josep M; Udler, Miriam; Laakso, Markku; Salomaa, Veikko; Hultman, Christina; Ripatti, Samuli; Hämäläinen, Eija; Moilanen, Jukka S; Körkkö, Jarmo; Kuismin, Outi; Nordentoft, Merete; Hougaard, David M; Mors, Ole; Werge, Thomas; Mortensen, Preben Bo; MacArthur, Daniel; Daly, Mark J; Sullivan, Patrick F; Locke, Adam E; Palotie, Aarno; Børglum, Anders D; Kathiresan, Sekar; Neale, Benjamin M

Genome Modeling System: A Knowledge Management Platform for Genomics

基因组建模系统:基因组学知识管理平台

Griffith, Malachi; Griffith, Obi L; Smith, Scott M; Ramu, Avinash; Callaway, Matthew B; Brummett, Anthony M; Kiwala, Michael J; Coffman, Adam C; Regier, Allison A; Oberkfell, Ben J; Sanderson, Gabriel E; Mooney, Thomas P; Nutter, Nathaniel G; Belter, Edward A; Du, Feiyu; Long, Robert L; Abbott, Travis E; Ferguson, Ian T; Morton, David L; Burnett, Mark M; Weible, James V; Peck, Joshua B; Dukes, Adam; McMichael, Joshua F; Lolofie, Justin T; Derickson, Brian R; Hundal, Jasreet; Skidmore, Zachary L; Ainscough, Benjamin J; Dees, Nathan D; Schierding, William S; Kandoth, Cyriac; Kim, Kyung H; Lu, Charles; Harris, Christopher C; Maher, Nicole; Maher, Christopher A; Magrini, Vincent J; Abbott, Benjamin S; Chen, Ken; Clark, Eric; Das, Indraniel; Fan, Xian; Hawkins, Amy E; Hepler, Todd G; Wylie, Todd N; Leonard, Shawn M; Schroeder, William E; Shi, Xiaoqi; Carmichael, Lynn K; Weil, Matthew R; Wohlstadter, Richard W; Stiehr, Gary; McLellan, Michael D; Pohl, Craig S; Miller, Christopher A; Koboldt, Daniel C; Walker, Jason R; Eldred, James M; Larson, David E; Dooling, David J; Ding, Li; Mardis, Elaine R; Wilson, Richard K

DGIdb: mining the druggable genome

DGIdb:挖掘可成药基因组

Griffith, Malachi; Griffith, Obi L; Coffman, Adam C; Weible, James V; McMichael, Josh F; Spies, Nicholas C; Koval, James; Das, Indraniel; Callaway, Matthew B; Eldred, James M; Miller, Christopher A; Subramanian, Janakiraman; Govindan, Ramaswamy; Kumar, Runjun D; Bose, Ron; Ding, Li; Walker, Jason R; Larson, David E; Dooling, David J; Smith, Scott M; Ley, Timothy J; Mardis, Elaine R; Wilson, Richard K