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

Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia

基于全基因组序列的非裔美国人双相情感障碍和精神分裂症关联分析

Li, Runjia; Gagliano Taliun, Sarah A; Liao, Kevin; Flickinger, Matthew; Sobell, Janet L; Genovese, Giulio; Locke, Adam E; Chiu, Rebeca Rothwell; LeFaive, Jonathon; Wang, Jiongming; Martins, Taylor; Chapman, Sinéad; Neumann, Anna; Handsaker, Robert E; Arnett, Donna K; Barnes, Kathleen C; Boerwinkle, Eric; Braff, David; Cade, Brian E; Fornage, Myriam; Gibbs, Richard A; Hoth, Karin F; Hou, Lifang; Kooperberg, Charles; Loos, Ruth J F; Metcalf, Ginger A; Montgomery, Courtney G; Morrison, Alanna C; Qin, Zhaohui S; Redline, Susan; Reiner, Alexander P; Rich, Stephen S; Rotter, Jerome I; Taylor, Kent D; Viaud-Martinez, Karine A; Bigdeli, Tim B; Gabriel, Stacey; Zollner, Sebastian; Smith, Albert V; Abecasis, Goncalo; McCarroll, Steve A; Pato, Michele T; Pato, Carlos N; Boehnke, Michael; Knowles, James; Kang, Hyun Min; Ophoff, Roel A; Ernst, Jason; Scott, Laura J

MethylModes: computationally efficient detection of multimodal distributions in DNA methylation data

MethylModes:一种计算高效的DNA甲基化数据多峰分布检测方法

Luo, T Sophia; LeFaive, Jonathon; Dou, John; Bakulski, Kelly M; Ware, Erin B; Zawistowski, Matthew

Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia

基于全基因组序列的非裔美国人双相情感障碍和精神分裂症关联分析

Li, Runjia; Taliun, Sarah A Gagliano; Liao, Kevin; Flickinger, Matthew; Sobell, Janet L; Genovese, Giulio; Locke, Adam E; Chiu, Rebeca Rothwell; LeFaive, Jonathon; Wang, Jiongming; Martins, Taylor; Chapman, Sinéad; Neumann, Anna; Handsaker, Robert E; Arnett, Donna K; Barnes, Kathleen C; Boerwinkle, Eric; Braff, David; Cade, Brian E; Fornage, Myriam; Gibbs, Richard A; Hoth, Karin F; Hou, Lifang; Kooperberg, Charles; Loos, Ruth J F; Metcalf, Ginger A; Montgomery, Courtney G; Morrison, Alanna C; Qin, Zhaohui S; Redline, Susan; Reiner, Alexander P; Rich, Stephen S; Rotter, Jerome I; Taylor, Kent D; Viaud-Martinez, Karine A; Bigdeli, Tim B; Gabriel, Stacey; Zollner, Sebastian; Smith, Albert V; Abecasis, Goncalo; McCarroll, Steve; Pato, Michele T; Pato, Carlos N; Boehnke, Michael; Knowles, James; Kang, Hyun Min; Ophoff, Roel A; Ernst, Jason; Scott, Laura J

Imputation Server PGS: an automated approach to calculate polygenic risk scores on imputation servers

Imputation Server PGS:一种在插补服务器上自动计算多基因风险评分的方法

Forer, Lukas; Taliun, Daniel; LeFaive, Jonathon; Smith, Albert V; Boughton, Andrew P; Coassin, Stefan; Lamina, Claudia; Kronenberg, Florian; Fuchsberger, Christian; Schönherr, Sebastian

Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease

教程:利用统计遗传学方法识别驱动复杂疾病的HLA等位基因

Sakaue, Saori; Gurajala, Saisriram; Curtis, Michelle; Luo, Yang; Choi, Wanson; Ishigaki, Kazuyoshi; Kang, Joyce B; Rumker, Laurie; Deutsch, Aaron J; Schönherr, Sebastian; Forer, Lukas; LeFaive, Jonathon; Fuchsberger, Christian; Han, Buhm; Lenz, Tobias L; de Bakker, Paul I W; Okada, Yukinori; Smith, Albert V; Raychaudhuri, Soumya

FixItFelix: improving genomic analysis by fixing reference errors

FixItFelix:通过修复参考错误来改进基因组分析

Behera, Sairam; LeFaive, Jonathon; Orchard, Peter; Mahmoud, Medhat; Paulin, Luis F; Farek, Jesse; Soto, Daniela C; Parker, Stephen C J; Smith, Albert V; Dennis, Megan Y; Zook, Justin M; Sedlazeck, Fritz J

The phenotype-genotype reference map: Improving biobank data science through replication

表型-基因型参考图谱:通过可重复性改进生物样本库数据科学

Bastarache, Lisa; Delozier, Sarah; Pandit, Anita; He, Jing; Lewis, Adam; Annis, Aubrey C; LeFaive, Jonathon; Denny, Joshua C; Carroll, Robert J; Altman, Russ B; Hughey, Jacob J; Zawistowski, Matthew; Peterson, Josh F

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

一项大规模全基因组测序研究揭示了收缩压、舒张压和高血压的奥秘

Kelly, Tanika N; Sun, Xiao; He, Karen Y; Brown, Michael R; Taliun, Sarah A Gagliano; Hellwege, Jacklyn N; Irvin, Marguerite R; Mi, Xuenan; Brody, Jennifer A; Franceschini, Nora; Guo, Xiuqing; Hwang, Shih-Jen; de Vries, Paul S; Gao, Yan; Moscati, Arden; Nadkarni, Girish N; Yanek, Lisa R; Elfassy, Tali; Smith, Jennifer A; Chung, Ren-Hua; Beitelshees, Amber L; Patki, Amit; Aslibekyan, Stella; Blobner, Brandon M; Peralta, Juan M; Assimes, Themistocles L; Palmas, Walter R; Liu, Chunyu; Bress, Adam P; Huang, Zhijie; Becker, Lewis C; Hwa, Chii-Min; O'Connell, Jeffrey R; Carlson, Jenna C; Warren, Helen R; Das, Sayantan; Giri, Ayush; Martin, Lisa W; Craig Johnson, W; Fox, Ervin R; Bottinger, Erwin P; Razavi, Alexander C; Vaidya, Dhananjay; Chuang, Lee-Ming; Chang, Yen-Pei C; Naseri, Take; Jain, Deepti; Kang, Hyun Min; Hung, Adriana M; Srinivasasainagendra, Vinodh; Snively, Beverly M; Gu, Dongfeng; Montasser, May E; Reupena, Muagututi'a Sefuiva; Heavner, Benjamin D; LeFaive, Jonathon; Hixson, James E; Rice, Kenneth M; Wang, Fei Fei; Nielsen, Jonas B; Huang, Jianfeng; Khan, Alyna T; Zhou, Wei; Nierenberg, Jovia L; Laurie, Cathy C; Armstrong, Nicole D; Shi, Mengyao; Pan, Yang; Stilp, Adrienne M; Emery, Leslie; Wong, Quenna; Hawley, Nicola L; Minster, Ryan L; Curran, Joanne E; Munroe, Patricia B; Weeks, Daniel E; North, Kari E; Tracy, Russell P; Kenny, Eimear E; Shimbo, Daichi; Chakravarti, Aravinda; Rich, Stephen S; Reiner, Alex P; Blangero, John; Redline, Susan; Mitchell, Braxton D; Rao, Dabeeru C; Ida Chen, Yii-Der; Kardia, Sharon L R; Kaplan, Robert C; Mathias, Rasika A; He, Jiang; Psaty, Bruce M; Fornage, Myriam; Loos, Ruth J F; Correa, Adolfo; Boerwinkle, Eric; Rotter, Jerome I; Kooperberg, Charles; Edwards, Todd L; Abecasis, Gonçalo R; Zhu, Xiaofeng; Levy, Daniel; Arnett, Donna K; Morrison, Alanna C

Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels

元插补:一种将插补后的基因型数据与多个参考面板数据相结合的有效方法

Yu, Ketian; Das, Sayantan; LeFaive, Jonathon; Kwong, Alan; Pleiness, Jacob; Forer, Lukas; Schönherr, Sebastian; Fuchsberger, Christian; Smith, Albert Vernon; Abecasis, Gonçalo Rocha

Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing

利用大型参考面板进行芯片基因分型和插补的近似程度与深度全基因组测序的近似程度

Hanks, Sarah C; Forer, Lukas; Schönherr, Sebastian; LeFaive, Jonathon; Martins, Taylor; Welch, Ryan; Gagliano Taliun, Sarah A; Braff, David; Johnsen, Jill M; Kenny, Eimear E; Konkle, Barbara A; Laakso, Markku; Loos, Ruth F J; McCarroll, Steven; Pato, Carlos; Pato, Michele T; Smith, Albert V; Boehnke, Michael; Scott, Laura J; Fuchsberger, Christian