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

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

作者更正:发现了与阅读障碍相关的42个全基因组显著位点

Doust, Catherine; Fontanillas, Pierre; Eising, Else; Gordon, Scott D; Wang, Zhengjun; Alagöz, Gökberk; Molz, Barbara; Pourcain, Beate St; Francks, Clyde; Marioni, Riccardo E; Zhao, Jingjing; Paracchini, Silvia; Talcott, Joel B; Monaco, Anthony P; Stein, John F; Gruen, Jeffrey R; Olson, Richard K; Willcutt, Erik G; DeFries, John C; Pennington, Bruce F; Smith, Shelley D; Wright, Margaret J; Martin, Nicholas G; Auton, Adam; Bates, Timothy C; Fisher, Simon E; Luciano, Michelle

Discovery of 42 genome-wide significant loci associated with dyslexia

发现与阅读障碍相关的42个全基因组显著位点

Doust, Catherine; Fontanillas, Pierre; Eising, Else; Gordon, Scott D; Wang, Zhengjun; Alagöz, Gökberk; Molz, Barbara; Pourcain, Beate St; Francks, Clyde; Marioni, Riccardo E; Zhao, Jingjing; Paracchini, Silvia; Talcott, Joel B; Monaco, Anthony P; Stein, John F; Gruen, Jeffrey R; Olson, Richard K; Willcutt, Erik G; DeFries, John C; Pennington, Bruce F; Smith, Shelley D; Wright, Margaret J; Martin, Nicholas G; Auton, Adam; Bates, Timothy C; Fisher, Simon E; Luciano, Michelle

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

Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

出版商更正:性别二态性遗传效应和空腹血糖和胰岛素变异性的新位点

Lagou, Vasiliki; Mägi, Reedik; Hottenga, Jouke- Jan; Grallert, Harald; Perry, John R B; Bouatia-Naji, Nabila; Marullo, Letizia; Rybin, Denis; Jansen, Rick; Min, Josine L; Dimas, Antigone S; Ulrich, Anna; Zudina, Liudmila; Gådin, Jesper R; Jiang, Longda; Faggian, Alessia; Bonnefond, Amélie; Fadista, Joao; Stathopoulou, Maria G; Isaacs, Aaron; Willems, Sara M; Navarro, Pau; Tanaka, Toshiko; Jackson, Anne U; Montasser, May E; O'Connell, Jeff R; Bielak, Lawrence F; Webster, Rebecca J; Saxena, Richa; Stafford, Jeanette M; Pourcain, Beate St; Timpson, Nicholas J; Salo, Perttu; Shin, So-Youn; Amin, Najaf; Smith, Albert V; Li, Guo; Verweij, Niek; Goel, Anuj; Ford, Ian; Johnson, Paul C D; Johnson, Toby; Kapur, Karen; Thorleifsson, Gudmar; Strawbridge, Rona J; Rasmussen-Torvik, Laura J; Esko, Tõnu; Mihailov, Evelin; Fall, Tove; Fraser, Ross M; Mahajan, Anubha; Kanoni, Stavroula; Giedraitis, Vilmantas; Kleber, Marcus E; Silbernagel, Günther; Meyer, Julia; Müller-Nurasyid, Martina; Ganna, Andrea; Sarin, Antti-Pekka; Yengo, Loic; Shungin, Dmitry; Luan, Jian'an; Horikoshi, Momoko; An, Ping; Sanna, Serena; Boettcher, Yvonne; Rayner, N William; Nolte, Ilja M; Zemunik, Tatijana; Iperen, Erik van; Kovacs, Peter; Hastie, Nicholas D; Wild, Sarah H; McLachlan, Stela; Campbell, Susan; Polasek, Ozren; Carlson, Olga; Egan, Josephine; Kiess, Wieland; Willemsen, Gonneke; Kuusisto, Johanna; Laakso, Markku; Dimitriou, Maria; Hicks, Andrew A; Rauramaa, Rainer; Bandinelli, Stefania; Thorand, Barbara; Liu, Yongmei; Miljkovic, Iva; Lind, Lars; Doney, Alex; Perola, Markus; Hingorani, Aroon; Kivimaki, Mika; Kumari, Meena; Bennett, Amanda J; Groves, Christopher J; Herder, Christian; Koistinen, Heikki A; Kinnunen, Leena; Faire, Ulf de; Bakker, Stephan J L; Uusitupa, Matti; Palmer, Colin N A; Jukema, J Wouter; Sattar, Naveed; Pouta, Anneli; Snieder, Harold; Boerwinkle, Eric; Pankow, James S; Magnusson, Patrik K; Krus, Ulrika; Scapoli, Chiara; de Geus, Eco J C N; Blüher, Matthias; Wolffenbuttel, Bruce H R; Province, Michael A; Abecasis, Goncalo R; Meigs, James B; Hovingh, G Kees; Lindström, Jaana; Wilson, James F; Wright, Alan F; Dedoussis, George V; Bornstein, Stefan R; Schwarz, Peter E H; Tönjes, Anke; Winkelmann, Bernhard R; Boehm, Bernhard O; März, Winfried; Metspalu, Andres; Price, Jackie F; Deloukas, Panos; Körner, Antje; Lakka, Timo A; Keinanen-Kiukaanniemi, Sirkka M; Saaristo, Timo E; Bergman, Richard N; Tuomilehto, Jaakko; Wareham, Nicholas J; Langenberg, Claudia; Männistö, Satu; Franks, Paul W; Hayward, Caroline; Vitart, Veronique; Kaprio, Jaakko; Visvikis-Siest, Sophie; Balkau, Beverley; Altshuler, David; Rudan, Igor; Stumvoll, Michael; Campbell, Harry; van Duijn, Cornelia M; Gieger, Christian; Illig, Thomas; Ferrucci, Luigi; Pedersen, Nancy L; Pramstaller, Peter P; Boehnke, Michael; Frayling, Timothy M; Shuldiner, Alan R; Peyser, Patricia A; Kardia, Sharon L R; Palmer, Lyle J; Penninx, Brenda W; Meneton, Pierre; Harris, Tamara B; Navis, Gerjan; Harst, Pim van der; Smith, George Davey; Forouhi, Nita G; Loos, Ruth J F; Salomaa, Veikko; Soranzo, Nicole; Boomsma, Dorret I; Groop, Leif; Tuomi, Tiinamaija; Hofman, Albert; Munroe, Patricia B; Gudnason, Vilmundur; Siscovick, David S; Watkins, Hugh; Lecoeur, Cecile; Vollenweider, Peter; Franco-Cereceda, Anders; Eriksson, Per; Jarvelin, Marjo-Riitta; Stefansson, Kari; Hamsten, Anders; Nicholson, George; Karpe, Fredrik; Dermitzakis, Emmanouil T; Lindgren, Cecilia M; McCarthy, Mark I; Froguel, Philippe; Kaakinen, Marika A; Lyssenko, Valeriya; Watanabe, Richard M; Ingelsson, Erik; Florez, Jose C; Dupuis, Josée; Barroso, Inês; Morris, Andrew P; Prokopenko, Inga

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

全基因组关联研究揭示了发育性阅读障碍的遗传性和遗传相关性的新见解

Gialluisi, Alessandro; Andlauer, Till F M; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U; Czamara, Darina; Pourcain, Beate St; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; Huguet, Guillaume; Chaix, Yves; Iannuzzi, Stephanie; Demonet, Jean-Francois; Morris, Andrew P; Hulslander, Jacqueline; Willcutt, Erik G; DeFries, John C; Olson, Richard K; Smith, Shelley D; Pennington, Bruce F; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppänen, Paavo H T; Brandeis, Daniel; Bonte, Milene; Stein, John F; Talcott, Joel B; Fauchereau, Fabien; Wilcke, Arndt; Kirsten, Holger; Müller, Bent; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S; Paracchini, Silvia; Fisher, Simon E; Schumacher, Johannes; Nöthen, Markus M; Müller-Myhsok, Bertram; Schulte-Körne, Gerd

Genome-wide association study of circulating interleukin 6 levels identifies novel loci

全基因组关联研究发现循环白细胞介素 6 水平存在新的关联位点

Ahluwalia, Tarunveer S; Prins, Bram P; Abdollahi, Mohammadreza; Armstrong, Nicola J; Aslibekyan, Stella; Bain, Lisa; Jefferis, Barbara; Baumert, Jens; Beekman, Marian; Ben-Shlomo, Yoav; Bis, Joshua C; Mitchell, Braxton D; de Geus, Eco; Delgado, Graciela E; Marek, Diana; Eriksson, Joel; Kajantie, Eero; Kanoni, Stavroula; Kemp, John P; Lu, Chen; Marioni, Riccardo E; McLachlan, Stela; Milaneschi, Yuri; Nolte, Ilja M; Petrelis, Alexandros M; Porcu, Eleonora; Sabater-Lleal, Maria; Naderi, Elnaz; Seppälä, Ilkka; Shah, Tina; Singhal, Gaurav; Standl, Marie; Teumer, Alexander; Thalamuthu, Anbupalam; Thiering, Elisabeth; Trompet, Stella; Ballantyne, Christie M; Benjamin, Emelia J; Casas, Juan P; Toben, Catherine; Dedoussis, George; Deelen, Joris; Durda, Peter; Engmann, Jorgen; Feitosa, Mary F; Grallert, Harald; Hammarstedt, Ann; Harris, Sarah E; Homuth, Georg; Hottenga, Jouke-Jan; Jalkanen, Sirpa; Jamshidi, Yalda; Jawahar, Magdalene C; Jess, Tine; Kivimaki, Mika; Kleber, Marcus E; Lahti, Jari; Liu, Yongmei; Marques-Vidal, Pedro; Mellström, Dan; Mooijaart, Simon P; Müller-Nurasyid, Martina; Penninx, Brenda; Revez, Joana A; Rossing, Peter; Räikkönen, Katri; Sattar, Naveed; Scharnagl, Hubert; Sennblad, Bengt; Silveira, Angela; Pourcain, Beate St; Timpson, Nicholas J; Trollor, Julian; van Dongen, Jenny; Van Heemst, Diana; Visvikis-Siest, Sophie; Vollenweider, Peter; Völker, Uwe; Waldenberger, Melanie; Willemsen, Gonneke; Zabaneh, Delilah; Morris, Richard W; Arnett, Donna K; Baune, Bernhard T; Boomsma, Dorret I; Chang, Yen-Pei C; Deary, Ian J; Deloukas, Panos; Eriksson, Johan G; Evans, David M; Ferreira, Manuel A; Gaunt, Tom; Gudnason, Vilmundur; Hamsten, Anders; Heinrich, Joachim; Hingorani, Aroon; Humphries, Steve E; Jukema, J Wouter; Koenig, Wolfgang; Kumari, Meena; Kutalik, Zoltan; Lawlor, Deborah A; Lehtimäki, Terho; März, Winfried; Mather, Karen A; Naitza, Silvia; Nauck, Matthias; Ohlsson, Claes; Price, Jackie F; Raitakari, Olli; Rice, Ken; Sachdev, Perminder S; Slagboom, Eline; Sørensen, Thorkild I A; Spector, Tim; Stacey, David; Stathopoulou, Maria G; Tanaka, Toshiko; Wannamethee, S Goya; Whincup, Peter; Rotter, Jerome I; Dehghan, Abbas; Boerwinkle, Eric; Psaty, Bruce M; Snieder, Harold; Alizadeh, Behrooz Z

The genetic architecture of the human cerebral cortex

人类大脑皮层的遗传结构

Katrina L Grasby #, Neda Jahanshad #, Jodie N Painter #, Lucía Colodro-Conde #, Janita Bralten #, Derrek P Hibar #, Penelope A Lind #, Fabrizio Pizzagalli #, Christopher R K Ching, Mary Agnes B McMahon, Natalia Shatokhina, Leo C P Zsembik, Sophia I Thomopoulos, Alyssa H Zhu, Lachlan T Strike, Ingrid Agartz, Saud Alhusaini, Marcio A A Almeida, Dag Alnæs, Inge K Amlien, Micael Andersson, Tyler Ard, Nicola J Armstrong, Allison Ashley-Koch, Joshua R Atkins, Manon Bernard, Rachel M Brouwer, Elizabeth E L Buimer, Robin Bülow, Christian Bürger, Dara M Cannon, Mallar Chakravarty, Qiang Chen, Joshua W Cheung, Baptiste Couvy-Duchesne, Anders M Dale, Shareefa Dalvie, Tânia K de Araujo, Greig I de Zubicaray, Sonja M C de Zwarte, Anouk den Braber, Nhat Trung Doan, Katharina Dohm, Stefan Ehrlich, Hannah-Ruth Engelbrecht, Susanne Erk, Chun Chieh Fan, Iryna O Fedko, Sonya F Foley, Judith M Ford, Masaki Fukunaga, Melanie E Garrett, Tian Ge, Sudheer Giddaluru, Aaron L Goldman, Melissa J Green, Nynke A Groenewold, Dominik Grotegerd, Tiril P Gurholt, Boris A Gutman, Narelle K Hansell, Mathew A Harris, Marc B Harrison, Courtney C Haswell, Michael Hauser, Stefan Herms, Dirk J Heslenfeld, New Fei Ho, David Hoehn, Per Hoffmann, Laurena Holleran, Martine Hoogman, Jouke-Jan Hottenga, Masashi Ikeda, Deborah Janowitz, Iris E Jansen, Tianye Jia, Christiane Jockwitz, Ryota Kanai, Sherif Karama, Dalia Kasperaviciute, Tobias Kaufmann, Sinead Kelly, Masataka Kikuchi, Marieke Klein, Michael Knapp, Annchen R Knodt, Bernd Krämer, Max Lam, Thomas M Lancaster, Phil H Lee, Tristram A Lett, Lindsay B Lewis, Iscia Lopes-Cendes, Michelle Luciano, Fabio Macciardi, Andre F Marquand, Samuel R Mathias, Tracy R Melzer, Yuri Milaneschi, Nazanin Mirza-Schreiber, Jose C V Moreira, Thomas W Mühleisen, Bertram Müller-Myhsok, Pablo Najt, Soichiro Nakahara, Kwangsik Nho, Loes M Olde Loohuis, Dimitri Papadopoulos Orfanos, John F Pearson, Toni L Pitcher, Benno Pütz, Yann Quidé, Anjanibhargavi Ragothaman, Faisal M Rashid, William R Reay, Ronny Redlich, Céline S Reinbold, Jonathan Repple, Geneviève Richard, Brandalyn C Riedel, Shannon L Risacher, Cristiane S Rocha, Nina Roth Mota, Lauren Salminen, Arvin Saremi, Andrew J Saykin, Fenja Schlag, Lianne Schmaal, Peter R Schofield, Rodrigo Secolin, Chin Yang Shapland, Li Shen, Jean Shin, Elena Shumskaya, Ida E Sønderby, Emma Sprooten, Katherine E Tansey, Alexander Teumer, Anbupalam Thalamuthu, Diana Tordesillas-Gutiérrez, Jessica A Turner, Anne Uhlmann, Costanza Ludovica Vallerga, Dennis van der Meer, Marjolein M J van Donkelaar, Liza van Eijk, Theo G M van Erp, Neeltje E M van Haren, Daan van Rooij, Marie-José van Tol, Jan H Veldink, Ellen Verhoef, Esther Walton, Mingyuan Wang, Yunpeng Wang, Joanna M Wardlaw, Wei Wen, Lars T Westlye, Christopher D Whelan, Stephanie H Witt, Katharina Wittfeld, Christiane Wolf, Thomas Wolfers, Jing Qin Wu, Clarissa L Yasuda, Dario Zaremba, Zuo Zhang, Marcel P Zwiers, Eric Artiges, Amelia A Assareh, Rosa Ayesa-Arriola, Aysenil Belger, Christine L Brandt, Gregory G Brown, Sven Cichon, Joanne E Curran, Gareth E Davies, Franziska Degenhardt, Michelle F Dennis, Bruno Dietsche, Srdjan Djurovic, Colin P Doherty, Ryan Espiritu, Daniel Garijo, Yolanda Gil, Penny A Gowland, Robert C Green, Alexander N Häusler, Walter Heindel, Beng-Choon Ho, Wolfgang U Hoffmann, Florian Holsboer, Georg Homuth, Norbert Hosten, Clifford R Jack Jr, MiHyun Jang, Andreas Jansen, Nathan A Kimbrel, Knut Kolskår, Sanne Koops, Axel Krug, Kelvin O Lim, Jurjen J Luykx, Daniel H Mathalon, Karen A Mather, Venkata S Mattay, Sarah Matthews, Jaqueline Mayoral Van Son, Sarah C McEwen, Ingrid Melle, Derek W Morris, Bryon A Mueller, Matthias Nauck, Jan E Nordvik, Markus M Nöthen, Daniel S O'Leary, Nils Opel, Marie-Laure Paillère Martinot, G Bruce Pike, Adrian Preda, Erin B Quinlan, Paul E Rasser, Varun Ratnakar, Simone Reppermund, Vidar M Steen, Paul A Tooney, Fábio R Torres, Dick J Veltman, James T Voyvodic, Robert Whelan, Tonya White, Hidenaga Yamamori, Hieab H H Adams, Joshua C Bis, Stephanie Debette, Charles Decarli, Myriam Fornage, Vilmundur Gudnason, Edith Hofer, M Arfan Ikram, Lenore Launer, W T Longstreth, Oscar L Lopez, Bernard Mazoyer, Thomas H Mosley, Gennady V Roshchupkin, Claudia L Satizabal, Reinhold Schmidt, Sudha Seshadri, Qiong Yang; Alzheimer’s Disease Neuroimaging Initiative; CHARGE Consortium; EPIGEN Consortium; IMAGEN Consortium; SYS Consortium; Parkinson’s Progression Markers Initiative; Marina K M Alvim, David Ames, Tim J Anderson, Ole A Andreassen, Alejandro Arias-Vasquez, Mark E Bastin, Bernhard T Baune, Jean C Beckham, John Blangero, Dorret I Boomsma, Henry Brodaty, Han G Brunner, Randy L Buckner, Jan K Buitelaar, Juan R Bustillo, Wiepke Cahn, Murray J Cairns, Vince Calhoun, Vaughan J Carr, Xavier Caseras, Svenja Caspers, Gianpiero L Cavalleri, Fernando Cendes, Aiden Corvin, Benedicto Crespo-Facorro, John C Dalrymple-Alford, Udo Dannlowski, Eco J C de Geus, Ian J Deary, Norman Delanty, Chantal Depondt, Sylvane Desrivières, Gary Donohoe, Thomas Espeseth, Guillén Fernández, Simon E Fisher, Herta Flor, Andreas J Forstner, Clyde Francks, Barbara Franke, David C Glahn, Randy L Gollub, Hans J Grabe, Oliver Gruber, Asta K Håberg, Ahmad R Hariri, Catharina A Hartman, Ryota Hashimoto, Andreas Heinz, Frans A Henskens, Manon H J Hillegers, Pieter J Hoekstra, Avram J Holmes, L Elliot Hong, William D Hopkins, Hilleke E Hulshoff Pol, Terry L Jernigan, Erik G Jönsson, René S Kahn, Martin A Kennedy, Tilo T J Kircher, Peter Kochunov, John B J Kwok, Stephanie Le Hellard, Carmel M Loughland, Nicholas G Martin, Jean-Luc Martinot, Colm McDonald, Katie L McMahon, Andreas Meyer-Lindenberg, Patricia T Michie, Rajendra A Morey, Bryan Mowry, Lars Nyberg, Jaap Oosterlaan, Roel A Ophoff, Christos Pantelis, Tomas Paus, Zdenka Pausova, Brenda W J H Penninx, Tinca J C Polderman, Danielle Posthuma, Marcella Rietschel, Joshua L Roffman, Laura M Rowland, Perminder S Sachdev, Philipp G Sämann, Ulrich Schall, Gunter Schumann, Rodney J Scott, Kang Sim, Sanjay M Sisodiya, Jordan W Smoller, Iris E Sommer, Beate St Pourcain, Dan J Stein, Arthur W Toga, Julian N Trollor, Nic J A Van der Wee, Dennis van 't Ent, Henry Völzke, Henrik Walter, Bernd Weber, Daniel R Weinberger, Margaret J Wright, Juan Zhou, Jason L Stein #, Paul M Thompson #, Sarah E Medland #; Enhancing NeuroImaging Genetics through Meta-Analysis Consortium (ENIGMA)—Genetics working group

Identification of common genetic risk variants for autism spectrum disorder

识别自闭症谱系障碍的常见遗传风险变异

Grove, Jakob; Ripke, Stephan; Als, Thomas D; Mattheisen, Manuel; Walters, Raymond K; Won, Hyejung; Pallesen, Jonatan; Agerbo, Esben; Andreassen, Ole A; Anney, Richard; Awashti, Swapnil; Belliveau, Rich; Bettella, Francesco; Buxbaum, Joseph D; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felecia; Chambert, Kimberly; Christensen, Jane H; Churchhouse, Claire; Dellenvall, Karin; Demontis, Ditte; De Rubeis, Silvia; Devlin, Bernie; Djurovic, Srdjan; Dumont, Ashley L; Goldstein, Jacqueline I; Hansen, Christine S; Hauberg, Mads Engel; Hollegaard, Mads V; Hope, Sigrun; Howrigan, Daniel P; Huang, Hailiang; Hultman, Christina M; Klei, Lambertus; Maller, Julian; Martin, Joanna; Martin, Alicia R; Moran, Jennifer L; Nyegaard, Mette; Nærland, Terje; Palmer, Duncan S; Palotie, Aarno; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; dPoterba, Timothy; Poulsen, Jesper Buchhave; Pourcain, Beate St; Qvist, Per; Rehnström, Karola; Reichenberg, Abraham; Reichert, Jennifer; Robinson, Elise B; Roeder, Kathryn; Roussos, Panos; Saemundsen, Evald; Sandin, Sven; Satterstrom, F Kyle; Davey Smith, George; Stefansson, Hreinn; Steinberg, Stacy; Stevens, Christine R; Sullivan, Patrick F; Turley, Patrick; Walters, G Bragi; Xu, Xinyi; Stefansson, Kari; Geschwind, Daniel H; Nordentoft, Merete; Hougaard, David M; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Neale, Benjamin M; Daly, Mark J; Børglum, Anders D

Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate

DNA甲基化介导非综合征型唇腭裂遗传易感性的证据

Howe, Laurence J; Richardson, Tom G; Arathimos, Ryan; Alvizi, Lucas; Passos-Bueno, Maria R; Stanier, Philip; Nohr, Ellen; Ludwig, Kerstin U; Mangold, Elisabeth; Knapp, Michael; Stergiakouli, Evie; Pourcain, Beate St; Smith, George Davey; Sandy, Jonathan; Relton, Caroline L; Lewis, Sarah J; Hemani, Gibran; Sharp, Gemma C

Genetic Overlap Between Schizophrenia and Developmental Psychopathology: Longitudinal and Multivariate Polygenic Risk Prediction of Common Psychiatric Traits During Development

精神分裂症与发育精神病理学之间的遗传重叠:发育过程中常见精神病特征的纵向和多变量多基因风险预测

Nivard, Michel G; Gage, Suzanne H; Hottenga, Jouke J; van Beijsterveldt, Catharina E M; Abdellaoui, Abdel; Bartels, Meike; Baselmans, Bart M L; Ligthart, Lannie; Pourcain, Beate St; Boomsma, Dorret I; Munafò, Marcus R; Middeldorp, Christel M