Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Communication[original query] |
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Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature 2009 May 459 (7246): 528-33. Wang Kai, Zhang Haitao, Ma Deqiong, Bucan Maja, Glessner Joseph T, Abrahams Brett S, Salyakina Daria, Imielinski Marcin, Bradfield Jonathan P, Sleiman Patrick M A, Kim Cecilia E, Hou Cuiping, Frackelton Edward, Chiavacci Rosetta, Takahashi Nagahide, Sakurai Takeshi, Rappaport Eric, Lajonchere Clara M, Munson Jeffrey, Estes Annette, Korvatska Olena, Piven Joseph, Sonnenblick Lisa I, Alvarez Retuerto Ana I, Herman Edward I, Dong Hongmei, Hutman Ted, Sigman Marian, Ozonoff Sally, Klin Ami, Owley Thomas, Sweeney John A, Brune Camille W, Cantor Rita M, Bernier Raphael, Gilbert John R, Cuccaro Michael L, McMahon William M, Miller Judith, State Matthew W, Wassink Thomas H, Coon Hilary, Levy Susan E, Schultz Robert T, Nurnberger John I, Haines Jonathan L, Sutcliffe James S, Cook Edwin H, Minshew Nancy J, Buxbaum Joseph D, Dawson Geraldine, Grant Struan F A, Geschwind Daniel H, Pericak-Vance Margaret A, Schellenberg Gerard D, Hakonarson Hak |
A large-scale, consortium-based genomewide association study of asthma.
The New England journal of medicine 2010 Sep 363 (13): 1211-21. Moffatt Miriam F, Gut Ivo G, Demenais Florence, Strachan David P, Bouzigon Emmanuelle, Heath Simon, von Mutius Erika, Farrall Martin, Lathrop Mark, Cookson William O C M, |
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.
Genome medicine 2011 3 (1): 3. Wang Joanne H, Pappas Derek, De Jager Philip L, Pelletier Daniel, de Bakker Paul Iw, Kappos Ludwig, Polman Chris H, , Chibnik Lori B, Hafler David A, Matthews Paul M, Hauser Stephen L, Baranzini Sergio E, Oksenberg Jorge |
Common variation contributes to the genetic architecture of social communication traits.
Molecular autism 2013 4 (1): 34. St Pourcain Beate, Whitehouse Andrew J O, Ang Wei Q, Warrington Nicole M, Glessner Joseph T, Wang Kai, Timpson Nicholas J, Evans David M, Kemp John P, Ring Susan M, McArdle Wendy L, Golding Jean, Hakonarson Hakon, Pennell Craig E, Smith George Dav |
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.
Molecular autism 2014 5 (1): 18. St Pourcain Beate, Skuse David H, Mandy William P, Wang Kai, Hakonarson Hakon, Timpson Nicholas J, Evans David M, Kemp John P, Ring Susan M, McArdle Wendy L, Golding Jean, Smith George Dav |
ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains.
Molecular psychiatry 2017 May . Cantor R M, Navarro L, Won H, Walker R L, Lowe J K, Geschwind D |
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Nature genetics 2018 07 50 (8): 1112-1121. Lee James J, Wedow Robbee, Okbay Aysu, Kong Edward, Maghzian Omeed, Zacher Meghan, Nguyen-Viet Tuan Anh, Bowers Peter, Sidorenko Julia, Karlsson Linnér Richard, Fontana Mark Alan, Kundu Tushar, Lee Chanwook, Li Hui, Li Ruoxi, Royer Rebecca, Timshel Pascal N, Walters Raymond K, Willoughby Emily A, Yengo Loïc, , , , Alver Maris, Bao Yanchun, Clark David W, Day Felix R, Furlotte Nicholas A, Joshi Peter K, Kemper Kathryn E, Kleinman Aaron, Langenberg Claudia, Mägi Reedik, Trampush Joey W, Verma Shefali Setia, Wu Yang, Lam Max, Zhao Jing Hua, Zheng Zhili, Boardman Jason D, Campbell Harry, Freese Jeremy, Harris Kathleen Mullan, Hayward Caroline, Herd Pamela, Kumari Meena, Lencz Todd, Luan Jian'an, Malhotra Anil K, Metspalu Andres, Milani Lili, Ong Ken K, Perry John R B, Porteous David J, Ritchie Marylyn D, Smart Melissa C, Smith Blair H, Tung Joyce Y, Wareham Nicholas J, Wilson James F, Beauchamp Jonathan P, Conley Dalton C, Esko Tõnu, Lehrer Steven F, Magnusson Patrik K E, Oskarsson Sven, Pers Tune H, Robinson Matthew R, Thom Kevin, Watson Chelsea, Chabris Christopher F, Meyer Michelle N, Laibson David I, Yang Jian, Johannesson Magnus, Koellinger Philipp D, Turley Patrick, Visscher Peter M, Benjamin Daniel J, Cesarini Dav |
Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery.
Journal of obesity 2018 2018 3253096. Cha Elliot D K, Veturi Yogasudha, Agarwal Chirag, Patel Aalpen, Arbabshirani Mohammad R, Pendergrass Sarah |
Social and non-social autism symptoms and trait domains are genetically dissociable.
Communications biology 2019 2 328. Warrier Varun, Toro Roberto, Won Hyejung, Leblond Claire S, Cliquet Freddy, Delorme Richard, De Witte Ward, Bralten Janita, Chakrabarti Bhismadev, Børglum Anders D, Grove Jakob, Poelmans Geert, Hinds David A, Bourgeron Thomas, Baron-Cohen Sim |
Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
Molecular biology reports 2020 Oct 47 (10): 7623-7632. Alsubaie Laila M, Alsuwat Hind Saleh, Almandil Noor B, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Translational psychiatry 2020 Jul 10 (1): 215. Yousaf Afsheen, Waltes Regina, Haslinger Denise, Klauck Sabine M, Duketis Eftichia, Sachse Michael, Voran Anette, Biscaldi Monica, Schulte-Rüther Martin, Cichon Sven, Nöthen Markus, Ackermann Jörg, Koch Ina, Freitag Christine M, Chiocchetti Andreas |
A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior.
Molecular psychiatry 2020 May . Meyers Jacquelyn L, Zhang Jian, Chorlian David B, Pandey Ashwini K, Kamarajan Chella, Wang Jen-Chyong, Wetherill Leah, Lai Dongbing, Chao Michael, Chan Grace, Kinreich Sivan, Kapoor Manav, Bertelsen Sarah, McClintick Jeanette, Bauer Lance, Hesselbrock Victor, Kuperman Samuel, Kramer John, Salvatore Jessica E, Dick Danielle M, Agrawal Arpana, Foroud Tatiana, Edenberg Howard J, Goate Alison, Porjesz Berni |
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.
Genes 2021 May 12 (5): . Al-Sarraj Yasser, Al-Dous Eman, Taha Rowaida Z, Ahram Dina, Alshaban Fouad, Tolfat Mohammed, El-Shanti Hatem, Albagha Omar M |
The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
Nature communications 2021 05 12 (1): 2909. Elvsåshagen Torbjørn, Shadrin Alexey, Frei Oleksandr, van der Meer Dennis, Bahrami Shahram, Kumar Vinod Jangir, Smeland Olav, Westlye Lars T, Andreassen Ole A, Kaufmann Tobi |
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