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

HLA and KIR Associations of Cervical Neoplasia

宫颈肿瘤的HLA和KIR相关性

Bao, Xiao; Hanson, Aimee L; Madeleine, Margaret M; Wang, Sophia S; Schwartz, Stephen M; Newell, Felicity; Pettersson-Kymmer, Ulrika; Hemminki, Kari; Tiews, Sven; Steinberg, Winfried; Rader, Janet S; Castro, Felipe; Safaeian, Mahboobeh; Franco, Eduardo L; Coutlée, François; Ohlsson, Claes; Cortes, Adrian; Marshall, Mhairi; Mukhopadhyay, Pamela; Cremin, Katie; Johnson, Lisa G; Garland, Suzanne M; Tabrizi, Sepehr N; Wentzensen, Nicolas; Sitas, Freddy; Trimble, Cornelia; Little, Julian; Cruickshank, Maggie; Frazer, Ian H; Hildesheim, Allan; Brown, Matthew A; Duncan, Emma L; Sun, Ying Pu; Leo, Paul J

Correction: Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study

更正:定义宫颈肿瘤的遗传易感性——一项全基因组关联研究

Leo, Paul J; Madeleine, Margaret M; Wang, Sophia; Schwartz, Stephen M; Newell, Felicity; Pettersson-Kymmer, Ulrika; Hemminki, Kari; Hallmans, Goran; Tiews, Sven; Steinberg, Winfried; Rader, Janet S; Castro, Felipe; Safaeian, Mahboobeh; Franco, Eduardo L; Coutlée, François; Ohlsson, Claes; Cortes, Adrian; Marshall, Mhairi; Mukhopadhyay, Pamela; Cremin, Katie; Johnson, Lisa G; Trimble, Cornelia L; Garland, Suzanne; Tabrizi, Sepehr N; Wentzensen, Nicolas; Sitas, Freddy; Little, Julian; Cruickshank, Maggie; Frazer, Ian H; Hildesheim, Allan; Brown, Matthew A

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese

肌萎缩侧索硬化症的全外显子组测序表明,NEK1是中国肌萎缩侧索硬化症患者的风险基因。

Gratten, Jacob; Zhao, Qiongyi; Benyamin, Beben; Garton, Fleur; He, Ji; Leo, Paul J; Mangelsdorf, Marie; Anderson, Lisa; Zhang, Zong-Hong; Chen, Lu; Chen, Xiang-Ding; Cremin, Katie; Deng, Hong-Weng; Edson, Janette; Han, Ying-Ying; Harris, Jessica; Henders, Anjali K; Jin, Zi-Bing; Li, Zhongshan; Lin, Yong; Liu, Xiaolu; Marshall, Mhairi; Mowry, Bryan J; Ran, Shu; Reutens, David C; Song, Sharon; Tan, Li-Jun; Tang, Lu; Wallace, Robyn H; Wheeler, Lawrie; Wu, Jinyu; Yang, Jian; Xu, Huji; Visscher, Peter M; Bartlett, Perry F; Brown, Matthew A; Wray, Naomi R; Fan, Dongsheng

Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study

确定宫颈肿瘤的遗传易感性——一项全基因组关联研究

Leo, Paul J; Madeleine, Margaret M; Wang, Sophia; Schwartz, Stephen M; Newell, Felicity; Pettersson-Kymmer, Ulrika; Hemminki, Kari; Hallmans, Goran; Tiews, Sven; Steinberg, Winfried; Rader, Janet S; Castro, Felipe; Safaeian, Mahboobeh; Franco, Eduardo L; Coutlée, François; Ohlsson, Claes; Cortes, Adrian; Marshall, Mhairi; Mukhopadhyay, Pamela; Cremin, Katie; Johnson, Lisa G; Trimble, Cornelia L; Garland, Suzanne; Tabrizi, Sepehr N; Wentzensen, Nicolas; Sitas, Freddy; Little, Julian; Cruickshank, Maggie; Frazer, Ian H; Hildesheim, Allan; Brown, Matthew A

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

一项针对强直性脊柱炎的全外显子组研究表明,该疾病与炎症性肠病具有额外的共同遗传背景。

Robinson, Philip C; Leo, Paul J; Pointon, Jennifer J; Harris, Jessica; Cremin, Katie; Bradbury, Linda A; Stebbings, Simon; Harrison, Andrew A; Duncan, Emma L; Evans, David M; Wordsworth, Paul B; Brown, Matthew A

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

全基因组测序发现EN1是骨密度和骨折的决定因素

Zheng, Hou-Feng; Forgetta, Vincenzo; Hsu, Yi-Hsiang; Estrada, Karol; Rosello-Diez, Alberto; Leo, Paul J; Dahia, Chitra L; Park-Min, Kyung Hyun; Tobias, Jonathan H; Kooperberg, Charles; Kleinman, Aaron; Styrkarsdottir, Unnur; Liu, Ching-Ti; Uggla, Charlotta; Evans, Daniel S; Nielson, Carrie M; Walter, Klaudia; Pettersson-Kymmer, Ulrika; McCarthy, Shane; Eriksson, Joel; Kwan, Tony; Jhamai, Mila; Trajanoska, Katerina; Memari, Yasin; Min, Josine; Huang, Jie; Danecek, Petr; Wilmot, Beth; Li, Rui; Chou, Wen-Chi; Mokry, Lauren E; Moayyeri, Alireza; Claussnitzer, Melina; Cheng, Chia-Ho; Cheung, Warren; Medina-Gómez, Carolina; Ge, Bing; Chen, Shu-Huang; Choi, Kwangbom; Oei, Ling; Fraser, James; Kraaij, Robert; Hibbs, Matthew A; Gregson, Celia L; Paquette, Denis; Hofman, Albert; Wibom, Carl; Tranah, Gregory J; Marshall, Mhairi; Gardiner, Brooke B; Cremin, Katie; Auer, Paul; Hsu, Li; Ring, Sue; Tung, Joyce Y; Thorleifsson, Gudmar; Enneman, Anke W; van Schoor, Natasja M; de Groot, Lisette C P G M; van der Velde, Nathalie; Melin, Beatrice; Kemp, John P; Christiansen, Claus; Sayers, Adrian; Zhou, Yanhua; Calderari, Sophie; van Rooij, Jeroen; Carlson, Chris; Peters, Ulrike; Berlivet, Soizik; Dostie, Josée; Uitterlinden, Andre G; Williams, Stephen R; Farber, Charles; Grinberg, Daniel; LaCroix, Andrea Z; Haessler, Jeff; Chasman, Daniel I; Giulianini, Franco; Rose, Lynda M; Ridker, Paul M; Eisman, John A; Nguyen, Tuan V; Center, Jacqueline R; Nogues, Xavier; Garcia-Giralt, Natalia; Launer, Lenore L; Gudnason, Vilmunder; Mellström, Dan; Vandenput, Liesbeth; Amin, Najaf; van Duijn, Cornelia M; Karlsson, Magnus K; Ljunggren, Östen; Svensson, Olle; Hallmans, Göran; Rousseau, François; Giroux, Sylvie; Bussière, Johanne; Arp, Pascal P; Koromani, Fjorda; Prince, Richard L; Lewis, Joshua R; Langdahl, Bente L; Hermann, A Pernille; Jensen, Jens-Erik B; Kaptoge, Stephen; Khaw, Kay-Tee; Reeve, Jonathan; Formosa, Melissa M; Xuereb-Anastasi, Angela; Åkesson, Kristina; McGuigan, Fiona E; Garg, Gaurav; Olmos, Jose M; Zarrabeitia, Maria T; Riancho, Jose A; Ralston, Stuart H; Alonso, Nerea; Jiang, Xi; Goltzman, David; Pastinen, Tomi; Grundberg, Elin; Gauguier, Dominique; Orwoll, Eric S; Karasik, David; Davey-Smith, George; Smith, Albert V; Siggeirsdottir, Kristin; Harris, Tamara B; Zillikens, M Carola; van Meurs, Joyce B J; Thorsteinsdottir, Unnur; Maurano, Matthew T; Timpson, Nicholas J; Soranzo, Nicole; Durbin, Richard; Wilson, Scott G; Ntzani, Evangelia E; Brown, Matthew A; Stefansson, Kari; Hinds, David A; Spector, Tim; Cupples, L Adrienne; Ohlsson, Claes; Greenwood, Celia M T; Jackson, Rebecca D; Rowe, David W; Loomis, Cynthia A; Evans, David M; Ackert-Bicknell, Cheryl L; Joyner, Alexandra L; Duncan, Emma L; Kiel, Douglas P; Rivadeneira, Fernando; Richards, J Brent

Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis

对急性前葡萄膜炎的基因分析揭示了其与强直性脊柱炎关联的异同

Robinson, Philip C; Claushuis, Theodora A M; Cortes, Adrian; Martin, Tammy M; Evans, David M; Leo, Paul; Mukhopadhyay, Pamela; Bradbury, Linda A; Cremin, Katie; Harris, Jessica; Maksymowych, Walter P; Inman, Robert D; Rahman, Proton; Haroon, Nigil; Gensler, Lianne; Powell, Joseph E; van der Horst-Bruinsma, Irene E; Hewitt, Alex W; Craig, Jamie E; Lim, Lyndell L; Wakefield, Denis; McCluskey, Peter; Voigt, Valentina; Fleming, Peter; Degli-Esposti, Mariapia; Pointon, Jennifer J; Weisman, Michael H; Wordsworth, B Paul; Reveille, John D; Rosenbaum, James T; Brown, Matthew A

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci.

通过对免疫相关基因位点进行高密度基因分型,鉴定强直性脊柱炎的多个风险变异

Cortes Adrian, Hadler Johanna, Pointon Jenny P, Robinson Philip C, Karaderi Tugce, Leo Paul, Cremin Katie, Pryce Karena, Harris Jessica, Lee Seunghun, Joo Kyung Bin, Shim Seung-Cheol, Weisman Michael, Ward Michael, Zhou Xiaodong, Garchon Henri-Jean, Chiocchia Gilles, Nossent Johannes, Lie Benedicte A, Førre Øystein, Tuomilehto Jaakko, Laiho Kari, Jiang Lei, Liu Yu, Wu Xin, Bradbury Linda A, Elewaut Dirk, Burgos-Vargas Ruben, Stebbings Simon, Appleton Louise, Farrah Claire, Lau Jonathan, Kenna Tony J, Haroon Nigil, Ferreira Manuel A, Yang Jian, Mulero Juan, Fernandez-Sueiro Jose Luis, Gonzalez-Gay Miguel A, Lopez-Larrea Carlos, Deloukas Panos, Donnelly Peter, Bowness Paul, Gafney Karl, Gaston Hill, Gladman Dafna D, Rahman Proton, Maksymowych Walter P, Xu Huji, Crusius J Bart A, van der Horst-Bruinsma Irene E, Chou Chung-Tei, Valle-Oñate Raphael, Romero-Sánchez Consuelo, Hansen Inger Myrnes, Pimentel-Santos Fernando M, Inman Robert D, Videm Vibeke, Martin Javier, Breban Maxime, Reveille John D, Evans David M, Kim Tae-Hwan, Wordsworth Bryan Paul, Brown Matthew A