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

COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstruction

COMPADRE:结合谱系信息的远亲关系估计方法,用于改进谱系重建

Evans, Grahame F; Baker, James T; Petty, Lauren E; Petty, Alexander S; Polikowsky, Hannah G; Bohlender, Ryan J; Chen, Hung-Hsin; Chou, Che-Yu; Viljoen, Kathryn Z; Beilby, Janet M; Kraft, Shelly Jo; Zhu, Wanying; Landman, Joshua M; Morrow, Autumn R; Bian, Dayi; Scartozzi, Alyssa C; Huff, Chad D; Below, Jennifer E

Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

通过多种族基因组分析发现187个新的风险变异,从而表征前列腺癌风险

Wang, Anqi; Shen, Jiayi; Rodriguez, Alex A; Saunders, Edward J; Chen, Fei; Janivara, Rohini; Darst, Burcu F; Sheng, Xin; Xu, Yili; Chou, Alisha J; Benlloch, Sara; Dadaev, Tokhir; Brook, Mark N; Plym, Anna; Sahimi, Ali; Hoffman, Thomas J; Takahashi, Atushi; Matsuda, Koichi; Momozawa, Yukihide; Fujita, Masashi; Laisk, Triin; Figuerêdo, Jéssica; Muir, Kenneth; Ito, Shuji; Liu, Xiaoxi; Uchio, Yuji; Kubo, Michiaki; Kamatani, Yoichiro; Lophatananon, Artitaya; Wan, Peggy; Andrews, Caroline; Lori, Adriana; Choudhury, Parichoy P; Schleutker, Johanna; Tammela, Teuvo L J; Sipeky, Csilla; Auvinen, Anssi; Giles, Graham G; Southey, Melissa C; MacInnis, Robert J; Cybulski, Cezary; Wokolorczyk, Dominika; Lubinski, Jan; Rentsch, Christopher T; Cho, Kelly; Mcmahon, Benjamin H; Neal, David E; Donovan, Jenny L; Hamdy, Freddie C; Martin, Richard M; Nordestgaard, Borge G; Nielsen, Sune F; Weischer, Maren; Bojesen, Stig E; Røder, Andreas; Stroomberg, Hein V; Batra, Jyotsna; Chambers, Suzanne; Horvath, Lisa; Clements, Judith A; Tilly, Wayne; Risbridger, Gail P; Gronberg, Henrik; Aly, Markus; Szulkin, Robert; Eklund, Martin; Nordstrom, Tobias; Pashayan, Nora; Dunning, Alison M; Ghoussaini, Maya; Travis, Ruth C; Key, Tim J; Riboli, Elio; Park, Jong Y; Sellers, Thomas A; Lin, Hui-Yi; Albanes, Demetrius; Weinstein, Stephanie; Cook, Michael B; Mucci, Lorelei A; Giovannucci, Edward; Lindstrom, Sara; Kraft, Peter; Hunter, David J; Penney, Kathryn L; Turman, Constance; Tangen, Catherine M; Goodman, Phyllis J; Thompson, Ian M Jr; Hamilton, Robert J; Fleshner, Neil E; Finelli, Antonio; Parent, Marie-Élise; Stanford, Janet L; Ostrander, Elaine A; Koutros, Stella; Beane Freeman, Laura E; Stampfer, Meir; Wolk, Alicja; Håkansson, Niclas; Andriole, Gerald L; Hoover, Robert N; Machiela, Mitchell J; Sørensen, Karina Dalsgaard; Borre, Michael; Blot, William J; Zheng, Wei; Yeboah, Edward D; Mensah, James E; Lu, Yong-Jie; Zhang, Hong-Wei; Feng, Ninghan; Mao, Xueying; Wu, Yudong; Zhao, Shan-Chao; Sun, Zan; Thibodeau, Stephen N; McDonnell, Shannon K; Schaid, Daniel J; West, Catharine M L; Barnett, Gill; Maier, Christiane; Schnoeller, Thomas; Luedeke, Manuel; Kibel, Adam S; Drake, Bettina F; Cussenot, Olivier; Cancel-Tassin, Geraldine; Menegaux, Florence; Truong, Thérèse; Koudou, Yves Akoli; John, Esther M; Grindedal, Eli Marie; Maehle, Lovise; Khaw, Kay-Tee; Ingles, Sue A; Stern, Mariana C; Vega, Ana; Gómez-Caamaño, Antonio; Fachal, Laura; Rosenstein, Barry S; Kerns, Sarah L; Ostrer, Harry; Teixeira, Manuel R; Paulo, Paula; Brandão, Andreia; Watya, Stephen; Lubwama, Alexander; Bensen, Jeannette T; Butler, Ebonee N; Mohler, James L; Taylor, Jack A; Kogevinas, Manolis; Dierssen-Sotos, Trinidad; Castaño-Vinyals, Gemma; Cannon-Albright, Lisa; Teerlink, Craig C; Huff, Chad D; Pilie, Patrick; Yu, Yao; Bohlender, Ryan J; Gu, Jian; Strom, Sara S; Multigner, Luc; Blanchet, Pascal; Brureau, Laurent; Kaneva, Radka; Slavov, Chavdar; Mitev, Vanio; Leach, Robin J; Brenner, Hermann; Chen, Xuechen; Holleczek, Bernd; Schöttker, Ben; Klein, Eric A; Hsing, Ann W; Kittles, Rick A; Murphy, Adam B; Logothetis, Christopher J; Kim, Jeri; Neuhausen, Susan L; Steele, Linda; Ding, Yuan Chun; Isaacs, William B; Nemesure, Barbara; Hennis, Anselm J M; Carpten, John; Pandha, Hardev; Michael, Agnieszka; De Ruyck, Kim; De Meerleer, Gert; Ost, Piet; Xu, Jianfeng; Razack, Azad; Lim, Jasmine; Teo, Soo-Hwang; Newcomb, Lisa F; Lin, Daniel W; Fowke, Jay H; Neslund-Dudas, Christine M; Rybicki, Benjamin A; Gamulin, Marija; Lessel, Davor; Kulis, Tomislav; Usmani, Nawaid; Abraham, Aswin; Singhal, Sandeep; Parliament, Matthew; Claessens, Frank; Joniau, Steven; Van den Broeck, Thomas; Gago-Dominguez, Manuela; Castelao, Jose Esteban; Martinez, Maria Elena; Larkin, Samantha; Townsend, Paul A; Aukim-Hastie, Claire; Bush, William S; Aldrich, Melinda C; Crawford, Dana C; Srivastava, Shiv; Cullen, Jennifer; Petrovics, Gyorgy; Casey, Graham; Wang, Ying; Tettey, Yao; Lachance, Joseph; Tang, Wei; Biritwum, Richard B; Adjei, Andrew A; Tay, Evelyn; Truelove, Ann; Niwa, Shelley; Yamoah, Kosj; Govindasami, Koveela; Chokkalingam, Anand P; Keaton, Jacob M; Hellwege, Jacklyn N; Clark, Peter E; Jalloh, Mohamed; Gueye, Serigne M; Niang, Lamine; Ogunbiyi, Olufemi; Shittu, Olayiwola; Amodu, Olukemi; Adebiyi, Akindele O; Aisuodionoe-Shadrach, Oseremen I; Ajibola, Hafees O; Jamda, Mustapha A; Oluwole, Olabode P; Nwegbu, Maxwell; Adusei, Ben; Mante, Sunny; Darkwa-Abrahams, Afua; Diop, Halimatou; Gundell, Susan M; Roobol, Monique J; Jenster, Guido; van Schaik, Ron H N; Hu, Jennifer J; Sanderson, Maureen; Kachuri, Linda; Varma, Rohit; McKean-Cowdin, Roberta; Torres, Mina; Preuss, Michael H; Loos, Ruth J F; Zawistowski, Matthew; Zöllner, Sebastian; Lu, Zeyun; Van Den Eeden, Stephen K; Easton, Douglas F; Ambs, Stefan; Edwards, Todd L; Mägi, Reedik; Rebbeck, Timothy R; Fritsche, Lars; Chanock, Stephen J; Berndt, Sonja I; Wiklund, Fredrik; Nakagawa, Hidewaki; Witte, John S; Gaziano, J Michael; Justice, Amy C; Mancuso, Nick; Terao, Chikashi; Eeles, Rosalind A; Kote-Jarai, Zsofia; Madduri, Ravi K; Conti, David V; Haiman, Christopher A

RAB1A haploinsufficiency phenocopies the 2p14-p15 microdeletion and is associated with impaired neuronal differentiation

RAB1A单倍体不足的表型与2p14-p15微缺失相似,并且与神经元分化受损有关。

Rios, Jonathan J; Li, Yang; Paria, Nandina; Bohlender, Ryan J; Huff, Chad; Rosenfeld, Jill A; Liu, Pengfei; Bi, Weimin; Haga, Kentaro; Fukuda, Mitsunori; Vashisth, Shayal; Kaur, Kiran; Chahrour, Maria H; Bober, Michael B; Duker, Angela L; Ladha, Farah A; Hanchard, Neil A; Atala, Kristhen; Khanshour, Anas M; Smith, Linsley; Wise, Carol A; Delgado, Mauricio R

A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk

一项全外显子组病例对照关联研究,旨在阐明罕见编码变异对胰腺癌风险的贡献。

Yu, Yao; Chang, Kyle; Chen, Jiun-Sheng; Bohlender, Ryan J; Fowler, Jerry; Zhang, Di; Huang, Maosheng; Chang, Ping; Li, Yanan; Wong, Justin; Wang, Huamin; Gu, Jian; Wu, Xifeng; Schildkraut, Joellen; Cannon-Albright, Lisa; Ye, Yuanqing; Zhao, Hua; Hildebrandt, Michelle A T; Permuth, Jennifer B; Li, Donghui; Scheet, Paul; Huff, Chad D

Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate.

多基因风险影响 PDGFRA 突变在非综合征性唇腭裂中的外显率

Yu Yao, Alvarado Rolando, Petty Lauren E, Bohlender Ryan J, Shaw Douglas M, Below Jennifer E, Bejar Nada, Ruiz Oscar E, Tandon Bhavna, Eisenhoffer George T, Kiss Daniel L, Huff Chad D, Letra Ariadne, Hecht Jacqueline T

Host genetic effects in pneumonia

肺炎中的宿主遗传效应

Chen, Hung-Hsin; Shaw, Douglas M; Petty, Lauren E; Graff, Misa; Bohlender, Ryan J; Polikowsky, Hannah G; Zhong, Xue; Kim, Daeeun; Buchanan, Victoria L; Preuss, Michael H; Shuey, Megan M; Loos, Ruth J F; Huff, Chad D; Cox, Nancy J; Bastarache, Julie A; Bastarache, Lisa; North, Kari E; Below, Jennifer E

XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets

XPAT:用于对异质测序数据集进行跨平台关联研究的工具包

Yu, Yao; Hu, Hao; Bohlender, Ryan J; Hu, Fulan; Chen, Jiun-Sheng; Holt, Carson; Fowler, Jerry; Guthery, Stephen L; Scheet, Paul; Hildebrandt, Michelle A T; Yandell, Mark; Huff, Chad D

Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeon

调控等位基因的渗入和错义编码突变驱动了岩鸽羽毛图案的多样性

Vickrey, Anna I; Bruders, Rebecca; Kronenberg, Zev; Mackey, Emma; Bohlender, Ryan J; Maclary, Emily T; Maynez, Raquel; Osborne, Edward J; Johnson, Kevin P; Huff, Chad D; Yandell, Mark; Shapiro, Michael D

Early history of Neanderthals and Denisovans

尼安德特人和丹尼索瓦人的早期历史

Rogers, Alan R; Bohlender, Ryan J; Huff, Chad D