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

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders

9619例抽动障碍患者的全基因组关联研究荟萃分析

Strom, Nora I; Halvorsen, Matthew W; Grove, Jakob; Ásbjörnsdóttir, Bergrún; Luðvígsson, Pétur; Thorarensen, Ólafur; de Schipper, Elles; Bäckmann, Julia; Andrén, Per; Tian, Chao; Als, Thomas Damm; Nissen, Judith Becker; Meier, Sandra M; Bybjerg-Grauholm, Jonas; Hougaard, David M; Werge, Thomas; Børglum, Anders D; Hinds, David A; Rück, Christian; Mataix-Cols, David; Stefánsson, Hreinn; Stefansson, Kari; Crowley, James J; Mattheisen, Manuel

Genetic Modifiers of Parkinson's Disease: A Case-Control Study

帕金森病遗传修饰因子:一项病例对照研究

Kmiecik, Matthew J; Holmes, Michael V; Fontanillas, Pierre; Riboldi, Giulietta M; Schneider, Ruth B; Shi, Jingchunzi; Guan, Anna; Tat, Susana; Micheletti, Steven; Stagaman, Keaton; Gottesman, Josh; Hinds, David A; Tung, Joyce Y; Aslibekyan, Stella; Norcliffe-Kaufmann, Lucy

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

对不宁腿综合征进行全基因组荟萃分析,可以深入了解其遗传结构、疾病生物学和风险预测。

Schormair, Barbara; Zhao, Chen; Bell, Steven; Didriksen, Maria; Nawaz, Muhammad S; Schandra, Nathalie; Stefani, Ambra; Högl, Birgit; Dauvilliers, Yves; Bachmann, Cornelius G; Kemlink, David; Sonka, Karel; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H; Hornyak, Magdolna; Teder-Laving, Maris; Metspalu, Andres; Hadjigeorgiou, Georgios M; Polo, Olli; Fietze, Ingo; Ross, Owen A; Wszolek, Zbigniew K; Ibrahim, Abubaker; Bergmann, Melanie; Kittke, Volker; Harrer, Philip; Dowsett, Joseph; Chenini, Sofiene; Ostrowski, Sisse Rye; Sørensen, Erik; Erikstrup, Christian; Pedersen, Ole B; Topholm Bruun, Mie; Nielsen, Kaspar R; Butterworth, Adam S; Soranzo, Nicole; Ouwehand, Willem H; Roberts, David J; Danesh, John; Burchell, Brendan; Furlotte, Nicholas A; Nandakumar, Priyanka; Earley, Christopher J; Ondo, William G; Xiong, Lan; Desautels, Alex; Perola, Markus; Vodicka, Pavel; Dina, Christian; Stoll, Monika; Franke, Andre; Lieb, Wolfgang; Stewart, Alexandre F R; Shah, Svati H; Gieger, Christian; Peters, Annette; Rye, David B; Rouleau, Guy A; Berger, Klaus; Stefansson, Hreinn; Ullum, Henrik; Stefansson, Kari; Hinds, David A; Di Angelantonio, Emanuele; Oexle, Konrad; Winkelmann, Juliane

Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant

LRRK2 G2019S 变异引起的帕金森病的遗传分析和自然史

Kmiecik, Matthew J; Micheletti, Steven; Coker, Daniella; Heilbron, Karl; Shi, Jingchunzi; Stagaman, Keaton; Filshtein Sonmez, Teresa; Fontanillas, Pierre; Shringarpure, Suyash; Wetzel, Madeleine; Rowbotham, Helen M; Cannon, Paul; Shelton, Janie F; Hinds, David A; Tung, Joyce Y; Holmes, Michael V; Aslibekyan, Stella; Norcliffe-Kaufmann, Lucy

Genome-wide association study identifies new loci associated with OCD

全基因组关联研究发现了与强迫症相关的新基因位点

Strom, Nora I; Halvorsen, Matthew W; Tian, Chao; Rück, Christian; Kvale, Gerd; Hansen, Bjarne; Bybjerg-Grauholm, Jonas; Grove, Jakob; Boberg, Julia; Nissen, Judith Becker; Damm Als, Thomas; Werge, Thomas; de Schipper, Elles; Fundin, Bengt; Hultman, Christina; Höffler, Kira D; Pedersen, Nancy; Sandin, Sven; Bulik, Cynthia; Landén, Mikael; Karlsson, Elinor; Hagen, Kristen; Lindblad-Toh, Kerstin; Hougaard, David M; Meier, Sandra M; Hellard, Stéphanie Le; Mors, Ole; Børglum, Anders D; Haavik, Jan; Hinds, David A; Mataix-Cols, David; Crowley, James J; Mattheisen, Manuel

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

利用对300万个体进行全基因组关联分析,对家庭内部和家庭之间的教育程度进行多基因预测

Okbay, Aysu; Wu, Yeda; Wang, Nancy; Jayashankar, Hariharan; Bennett, Michael; Nehzati, Seyed Moeen; Sidorenko, Julia; Kweon, Hyeokmoon; Goldman, Grant; Gjorgjieva, Tamara; Jiang, Yunxuan; Hicks, Barry; Tian, Chao; Hinds, David A; Ahlskog, Rafael; Magnusson, Patrik K E; Oskarsson, Sven; Hayward, Caroline; Campbell, Archie; Porteous, David J; Freese, Jeremy; Herd, Pamela; Watson, Chelsea; Jala, Jonathan; Conley, Dalton; Koellinger, Philipp D; Johannesson, Magnus; Laibson, David; Meyer, Michelle N; Lee, James J; Kong, Augustine; Yengo, Loic; Cesarini, David; Turley, Patrick; Visscher, Peter M; Beauchamp, Jonathan P; Benjamin, Daniel J; Young, Alexander I

Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis

多性状遗传关联分析发现了50个新的胃食管反流风险位点、7个新的巴雷特食管风险位点,并揭示了反流诊断中临床异质性的机制。

Ong, Jue-Sheng; An, Jiyuan; Han, Xikun; Law, Matthew H; Nandakumar, Priyanka; Schumacher, Johannes; Gockel, Ines; Bohmer, Anne; Jankowski, Janusz; Palles, Claire; Olsen, Catherine M; Neale, Rachel E; Fitzgerald, Rebecca; Thrift, Aaron P; Vaughan, Thomas L; Buas, Matthew F; Hinds, David A; Gharahkhani, Puya; Kendall, Bradley J; MacGregor, Stuart

Genome-wide association study of musical beat synchronization demonstrates high polygenicity

全基因组关联研究表明,音乐节拍同步具有高度多基因性。

Niarchou, Maria; Gustavson, Daniel E; Sathirapongsasuti, J Fah; Anglada-Tort, Manuel; Eising, Else; Bell, Eamonn; McArthur, Evonne; Straub, Peter; McAuley, J Devin; Capra, John A; Ullén, Fredrik; Creanza, Nicole; Mosing, Miriam A; Hinds, David A; Davis, Lea K; Jacoby, Nori; Gordon, Reyna L

Resource profile and user guide of the Polygenic Index Repository

多基因指数库的资源概况和用户指南

Becker, Joel; Burik, Casper A P; Goldman, Grant; Wang, Nancy; Jayashankar, Hariharan; Bennett, Michael; Belsky, Daniel W; Karlsson Linnér, Richard; Ahlskog, Rafael; Kleinman, Aaron; Hinds, David A; Caspi, Avshalom; Corcoran, David L; Moffitt, Terrie E; Poulton, Richie; Sugden, Karen; Williams, Benjamin S; Harris, Kathleen Mullan; Steptoe, Andrew; Ajnakina, Olesya; Milani, Lili; Esko, Tõnu; Iacono, William G; McGue, Matt; Magnusson, Patrik K E; Mallard, Travis T; Harden, K Paige; Tucker-Drob, Elliot M; Herd, Pamela; Freese, Jeremy; Young, Alexander; Beauchamp, Jonathan P; Koellinger, Philipp D; Oskarsson, Sven; Johannesson, Magnus; Visscher, Peter M; Meyer, Michelle N; Laibson, David; Cesarini, David; Benjamin, Daniel J; Turley, Patrick; Okbay, Aysu

Genome-wide association study identifies 48 common genetic variants associated with handedness

全基因组关联研究发现了48个与惯用手相关的常见遗传变异

Cuellar-Partida, Gabriel; Tung, Joyce Y; Eriksson, Nicholas; Albrecht, Eva; Aliev, Fazil; Andreassen, Ole A; Barroso, Inês; Beckmann, Jacques S; Boks, Marco P; Boomsma, Dorret I; Boyd, Heather A; Breteler, Monique M B; Campbell, Harry; Chasman, Daniel I; Cherkas, Lynn F; Davies, Gail; de Geus, Eco J C; Deary, Ian J; Deloukas, Panos; Dick, Danielle M; Duffy, David L; Eriksson, Johan G; Esko, Tõnu; Feenstra, Bjarke; Geller, Frank; Gieger, Christian; Giegling, Ina; Gordon, Scott D; Han, Jiali; Hansen, Thomas F; Hartmann, Annette M; Hayward, Caroline; Heikkilä, Kauko; Hicks, Andrew A; Hirschhorn, Joel N; Hottenga, Jouke-Jan; Huffman, Jennifer E; Hwang, Liang-Dar; Ikram, M Arfan; Kaprio, Jaakko; Kemp, John P; Khaw, Kay-Tee; Klopp, Norman; Konte, Bettina; Kutalik, Zoltan; Lahti, Jari; Li, Xin; Loos, Ruth J F; Luciano, Michelle; Magnusson, Sigurdur H; Mangino, Massimo; Marques-Vidal, Pedro; Martin, Nicholas G; McArdle, Wendy L; McCarthy, Mark I; Medina-Gomez, Carolina; Melbye, Mads; Melville, Scott A; Metspalu, Andres; Milani, Lili; Mooser, Vincent; Nelis, Mari; Nyholt, Dale R; O'Connell, Kevin S; Ophoff, Roel A; Palmer, Cameron; Palotie, Aarno; Palviainen, Teemu; Pare, Guillaume; Paternoster, Lavinia; Peltonen, Leena; Penninx, Brenda W J H; Polasek, Ozren; Pramstaller, Peter P; Prokopenko, Inga; Raikkonen, Katri; Ripatti, Samuli; Rivadeneira, Fernando; Rudan, Igor; Rujescu, Dan; Smit, Johannes H; Smith, George Davey; Smoller, Jordan W; Soranzo, Nicole; Spector, Tim D; Pourcain, Beate St; Starr, John M; Stefánsson, Hreinn; Steinberg, Stacy; Teder-Laving, Maris; Thorleifsson, Gudmar; Stefánsson, Kári; Timpson, Nicholas J; Uitterlinden, André G; van Duijn, Cornelia M; van Rooij, Frank J A; Vink, Jaqueline M; Vollenweider, Peter; Vuoksimaa, Eero; Waeber, Gérard; Wareham, Nicholas J; Warrington, Nicole; Waterworth, Dawn; Werge, Thomas; Wichmann, H-Erich; Widen, Elisabeth; Willemsen, Gonneke; Wright, Alan F; Wright, Margaret J; Xu, Mousheng; Zhao, Jing Hua; Kraft, Peter; Hinds, David A; Lindgren, Cecilia M; Mägi, Reedik; Neale, Benjamin M; Evans, David M; Medland, Sarah E