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

Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多族裔全基因组分析鉴定出与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Arehart, Christopher H; Evans, Luke M; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; Edris, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta R; Brumpton, Ben M; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan A; Sanders, Alan R; Whiteman, David C; MacGregor, Stuart; Medland, Sarah E; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlinger, Gregory; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle L; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin G; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zöllner, Sebastian; Verma, Anurag; Preuss, Michael H; Kenny, Eimear; Hendricks, Audrey E; Fishbein, Lauren; Kraft, Peter; Daly, Mark J; Neale, Benjamin M; Martin, Alicia R; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Improved polygenic risk prediction models for breast cancer subtypes in women of African ancestry

改进的针对非洲裔女性乳腺癌亚型的多基因风险预测模型

Li, James L; Zhang, Haoyu; Wang, Xiaoyu; Jia, Guochong; McClellan, Julian C; Guo, Wenji; Sun, Yijia; Fiorica, Peter N; Ambs, Stefan; Barnard, Mollie E; Chen, Yu; Garcia-Closas, Montserrat; Gu, Jian; Hu, Jennifer J; John, Esther M; Nathanson, Katherine L; Nemesure, Barbara; Pal, Tuya; Shu, Xiao-Ou; Press, Michael F; Sanderson, Maureen; Sandler, Dale P; Troester, Melissa A; Yao, Song; Long, Jirong; Ahearn, Thomas U; Brewster, Abenaa M; Falusi, Adeyinka; Kraft, Peter; Hennis, Anselm J M; Makumbi, Timothy; Mapoko, Berthe S E; O'Brien, Katie M; Ojengbede, Oladosu; Olshan, Andrew F; Reid, Sonya; Zirpoli, Gary; Cai, Qiuyin; Butler, Eboneé N; Huang, Maosheng; Obafunwa, John; Weinberg, Clarice R; Ambrosone, Christine; Ping, Jie; Tao, Ran; Li, Bingshan; Guo, Xingyi; Gao, Guimin; Conti, David V; Chatterjee, Nilanjan; Palmer, Julie R; Olopade, Olufunmilayo I; Zheng, Wei; Haiman, Christopher A; Huo, Dezheng

Phenome-derived polygenic scores and social determinants jointly shape context-dependent disease risk

表型组衍生的多基因评分和社会决定因素共同塑造了与环境相关的疾病风险。

Wang, Ying; Truong, Buu; Lu, Wenhan; Fadil, Chaimaa; He, Yixuan; Luo, Weijun; Koyama, Satoshi; Tsuo, Kristin; Paruchuri, Kaavya; Yu, Zhi; Hull, Leland E; Zheng, Zhili; Carey, Caitlin E; Walters, Raymond K; Neale, Benjamin M; Robinson, Elise B; Kraft, Peter; Natarajan, Pradeep; Martin, Alicia R

Interplay of genetic predisposition, plasma metabolome and Mediterranean diet in dementia risk and cognitive function

遗传易感性、血浆代谢组和地中海饮食在痴呆风险和认知功能中的相互作用

Liu, Yuxi; Gu, Xiao; Li, Yanping; Wang, Fenglei; Vyas, Chirag M; Peng, Cheng; Dong, Danyue; Li, Yuhan; Zhang, Yu; Zhang, Yin; Zeleznik, Oana A; Kang, Jae H; Wang, Molin; Hu, Frank B; Willett, Walter C; Okereke, Olivia I; Eliassen, A Heather; Kraft, Peter; Stampfer, Meir J; Wang, Dong D

Author Correction: Interplay of genetic predisposition, plasma metabolome and Mediterranean diet in dementia risk and cognitive function

作者更正:遗传易感性、血浆代谢组和地中海饮食在痴呆风险和认知功能中的相互作用

Liu, Yuxi; Gu, Xiao; Li, Yanping; Wang, Fenglei; Vyas, Chirag M; Peng, Cheng; Dong, Danyue; Li, Yuhan; Zhang, Yu; Zhang, Yin; Zeleznik, Oana A; Kang, Jae H; Wang, Molin; Hu, Frank B; Willett, Walter C; Okereke, Olivia I; Eliassen, A Heather; Kraft, Peter; Stampfer, Meir J; Wang, Dong D

Translational genomics of osteoarthritis in 1,962,069 individuals

对 1,962,069 名个体进行骨关节炎转化基因组学研究

Hatzikotoulas, Konstantinos; Southam, Lorraine; Stefansdottir, Lilja; Boer, Cindy G; McDonald, Merry-Lynn; Pett, J Patrick; Park, Young-Chan; Tuerlings, Margo; Mulders, Rick; Barysenka, Andrei; Arruda, Ana Luiza; Tragante, Vinicius; Rocco, Alison; Bittner, Norbert; Chen, Shibo; Horn, Susanne; Srinivasasainagendra, Vinodh; To, Ken; Katsoula, Georgia; Kreitmaier, Peter; Tenghe, Amabel M M; Gilly, Arthur; Arbeeva, Liubov; Chen, Lane G; de Pins, Agathe M; Dochtermann, Daniel; Henkel, Cecilie; Höijer, Jonas; Ito, Shuji; Lind, Penelope A; Lukusa-Sawalena, Bitota; Minn, Aye Ko Ko; Mola-Caminal, Marina; Narita, Akira; Nguyen, Chelsea; Reimann, Ene; Silberstein, Micah D; Skogholt, Anne-Heidi; Tiwari, Hemant K; Yau, Michelle S; Yue, Ming; Zhao, Wei; Zhou, Jin J; Alexiadis, George; Banasik, Karina; Brunak, Søren; Campbell, Archie; Cheung, Jackson T S; Dowsett, Joseph; Faquih, Tariq; Faul, Jessica D; Fei, Lijiang; Fenstad, Anne Marie; Funayama, Takamitsu; Gabrielsen, Maiken E; Gocho, Chinatsu; Gromov, Kirill; Hansen, Thomas; Hudjashov, Georgi; Ingvarsson, Thorvaldur; Johnson, Jessica S; Jonsson, Helgi; Kakehi, Saori; Karjalainen, Juha; Kasbohm, Elisa; Lemmelä, Susanna; Lin, Kuang; Liu, Xiaoxi; Loef, Marieke; Mangino, Massimo; McCartney, Daniel; Millwood, Iona Y; Richman, Joshua; Roberts, Mary B; Ryan, Kathleen A; Samartzis, Dino; Shivakumar, Manu; Skou, Søren T; Sugimoto, Sachiyo; Suzuki, Ken; Takuwa, Hiroshi; Teder-Laving, Maris; Thomas, Laurent; Tomizuka, Kohei; Turman, Constance; Weiss, Stefan; Wu, Tian T; Zengini, Eleni; Zhang, Yanfei; Ferreira, Manuel Allen Revez; Babis, George; Baras, Aris; Barker, Tyler; Carey, David J; Cheah, Kathryn S E; Chen, Zhengming; Cheung, Jason Pui-Yin; Daly, Mark; de Mutsert, Renée; Eaton, Charles B; Erikstrup, Christian; Furnes, Ove Nord; Golightly, Yvonne M; Gudbjartsson, Daniel F; Hailer, Nils P; Hayward, Caroline; Hochberg, Marc C; Homuth, Georg; Huckins, Laura M; Hveem, Kristian; Ikegawa, Shiro; Ishijima, Muneaki; Isomura, Minoru; Jones, Marcus; Kang, Jae H; Kardia, Sharon L R; Kloppenburg, Margreet; Kraft, Peter; Kumahashi, Nobuyuki; Kuwata, Suguru; Lee, Ming Ta Michael; Lee, Phil H; Lerner, Robin; Li, Liming; Lietman, Steve A; Lotta, Luca; Lupton, Michelle K; Mägi, Reedik; Martin, Nicholas G; McAlindon, Timothy E; Medland, Sarah E; Michaëlsson, Karl; Mitchell, Braxton D; Mook-Kanamori, Dennis O; Morris, Andrew P; Nabika, Toru; Nagami, Fuji; Nelson, Amanda E; Ostrowski, Sisse Rye; Palotie, Aarno; Pedersen, Ole Birger; Rosendaal, Frits R; Sakurai-Yageta, Mika; Schmidt, Carsten Oliver; Sham, Pak Chung; Singh, Jasvinder A; Smelser, Diane T; Smith, Jennifer A; Song, You-Qiang; Sørensen, Erik; Tamiya, Gen; Tamura, Yoshifumi; Terao, Chikashi; Thorleifsson, Gudmar; Troelsen, Anders; Tsezou, Aspasia; Uchio, Yuji; Uitterlinden, A G; Ullum, Henrik; Valdes, Ana M; van Heel, David A; Walters, Robin G; Weir, David R; Wilkinson, J Mark; Winsvold, Bendik S; Yamamoto, Masayuki; Zwart, John-Anker; Stefansson, Kari; Meulenbelt, Ingrid; Teichmann, Sarah A; van Meurs, Joyce B J; Styrkarsdottir, Unnur; Zeggini, Eleftheria

Pathogenic Variants, Family History, and Cumulative Risk of Breast Cancer in US Women

致病变异、家族史和美国女性乳腺癌的累积风险

O'Brien, Katie M; Keil, Alexander P; Taylor, Jack A; Weinberg, Clarice R; Polley, Eric C; Yadav, Siddhartha; Boddicker, Nicholas J; Hu, Chunling; Ambrosone, Christine B; Anton-Culver, Hoda; Auer, Paul L; Bodelon, Clara; Brantley, Kristen; Burnside, Elizabeth S; Chen, Fei; Domchek, Susan M; Eliassen, A Heather; Haiman, Christopher A; Hodge, James M; Kraft, Peter; Lacey, James V; Lindstroem, Sara; Martinez, Maria Elena; Nathanson, Katherine L; Neuhausen, Susan L; Olson, Janet E; Palmer, Julie R; Patel, Alpa V; Penney, Kathryn L; Ruddy, Kathryn J; Scott, Christopher G; Teras, Lauren R; Trentham-Dietz, Amy; Vachon, Celine M; Weitzel, Jeffrey N; Yao, Song; Zirpoli, Gary; Couch, Fergus J; Sandler, Dale P

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

对超过40万名女性的分析为BRCA1和BRCA2变异分类提供了病例对照证据。

Zanti, Maria; O'Mahony, Denise G; Parsons, Michael T; Dorling, Leila; Dennis, Joe; Boddicker, Nicholas J; Chen, Wenan; Hu, Chunling; Naven, Marc; Yiangou, Kristia; Ahearn, Thomas U; Ambrosone, Christine B; Andrulis, Irene L; Antoniou, Antonis C; Auer, Paul L; Baynes, Caroline; Bodelon, Clara; Bogdanova, Natalia V; Bojesen, Stig E; Bolla, Manjeet K; Brantley, Kristen D; Camp, Nicola J; Campbell, Archie; Castelao, Jose E; Cessna, Melissa H; Chang-Claude, Jenny; Chen, Fei; Chenevix-Trench, Georgia; Conroy, Don M; Czene, Kamila; De Nicolo, Arcangela; Domchek, Susan M; Dörk, Thilo; Dunning, Alison M; Eliassen, A Heather; Evans, D Gareth; Fasching, Peter A; Figueroa, Jonine D; Flyger, Henrik; Gago-Dominguez, Manuela; García-Closas, Montserrat; Glendon, Gord; González-Neira, Anna; Grassmann, Felix; Hadjisavvas, Andreas; Haiman, Christopher A; Hamann, Ute; Hart, Steven N; Hartman, Mikael B A; Ho, Weang-Kee; Hodge, James M; Hoppe, Reiner; Howell, Sacha J; Jakubowska, Anna; Khusnutdinova, Elza K; Ko, Yon-Dschun; Kraft, Peter; Kristensen, Vessela N; Lacey, James V; Li, Jingmei; Lim, Geok Hoon; Lindström, Sara; Lophatananon, Artitaya; Luccarini, Craig; Mannermaa, Arto; Martinez, Maria Elena; Mavroudis, Dimitrios; Milne, Roger L; Muir, Kenneth; Nathanson, Katherine L; Nuñez-Torres, Rocio; Obi, Nadia; Olson, Janet E; Palmer, Julie R; Panayiotidis, Mihalis I; Patel, Alpa V; Pharoah, Paul D P; Polley, Eric C; Rashid, Muhammad U; Ruddy, Kathryn J; Saloustros, Emmanouil; Sawyer, Elinor J; Schmidt, Marjanka K; Southey, Melissa C; Tan, Veronique Kiak-Mien; Teo, Soo Hwang; Teras, Lauren R; Torres, Diana; Trentham-Dietz, Amy; Truong, Thérèse; Vachon, Celine M; Wang, Qin; Weitzel, Jeffrey N; Yadav, Siddhartha; Yao, Song; Zirpoli, Gary R; Cline, Melissa S; Devilee, Peter; Tavtigian, Sean V; Goldgar, David E; Couch, Fergus J; Easton, Douglas F; Spurdle, Amanda B; Michailidou, Kyriaki

Genome-wide association studies in a large Korean cohort identify quantitative trait loci for 36 traits and illuminate their genetic architectures

一项针对韩国大型人群的全基因组关联研究,鉴定出36个性状的数量性状基因座,并阐明了它们的遗传结构。

Jee, Yon Ho; Wang, Ying; Jung, Keum Ji; Lee, Ji-Young; Kimm, Heejin; Duan, Rui; Price, Alkes L; Martin, Alicia R; Kraft, Peter

Identifying chronic obstructive pulmonary disease subtypes using multi-trait genetics

利用多性状遗传学识别慢性阻塞性肺疾病亚型

Ziyatdinov, Andrey; Hobbs, Brian D; Kanaan-Izquierdo, Samir; Moll, Matthew; Sakornsakolpat, Phuwanat; Shrine, Nick; Chen, Jing; Song, Kijoung; Bowler, Russell P; Castaldi, Peter J; Tobin, Martin D; Kraft, Peter; Silverman, Edwin K; Julienne, Hanna; Cho, Michael H; Aschard, Hugues