Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: DLGAP2[original query] |
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Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010 Jul 466 (7304): 368-72. Pinto Dalila, Pagnamenta Alistair T, Klei Lambertus, Anney Richard, Merico Daniele, Regan Regina, Conroy Judith, Magalhaes Tiago R, Correia Catarina, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bader Gary D, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bölte Sven, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Brian Jessica, Bryson Susan E, Carson Andrew R, Casallo Guillermo, Casey Jillian, Chung Brian H Y, Cochrane Lynne, Corsello Christina, Crawford Emily L, Crossett Andrew, Cytrynbaum Cheryl, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Drmic Irene, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Goldberg Jeremy, Green Andrew, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Heron Elizabeth A, Hill Matthew, Holt Richard, Howe Jennifer L, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Korvatska Olena, Kustanovich Vlad, Lajonchere Clara M, Lamb Janine A, Laskawiec Magdalena, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lionel Anath C, Liu Xiao-Qing, Lord Catherine, Lotspeich Linda, Lund Sabata C, Maestrini Elena, Mahoney William, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Migita Ohsuke, Minshew Nancy J, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Noakes Carolyn, Noor Abdul, Nygren Gudrun, Oliveira Guiomar, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Paton Tara, Pickles Andrew, Pilorge Marion, Piven Joseph, Ponting Chris P, Posey David J, Poustka Annemarie, Poustka Fritz, Prasad Aparna, Ragoussis Jiannis, Renshaw Katy, Rickaby Jessica, Roberts Wendy, Roeder Kathryn, Roge Bernadette, Rutter Michael L, Bierut Laura J, Rice John P, Salt Jeff, Sansom Katherine, Sato Daisuke, Segurado Ricardo, Sequeira Ana F, Senman Lili, Shah Naisha, Sheffield Val C, Soorya Latha, Sousa Inês, Stein Olaf, Sykes Nuala, Stoppioni Vera, Strawbridge Christina, Tancredi Raffaella, Tansey Katherine, Thiruvahindrapduram Bhooma, Thompson Ann P, Thomson Susanne, Tryfon Ana, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Wallace Simon, Wang Kai, Wang Zhouzhi, Wassink Thomas H, Webber Caleb, Weksberg Rosanna, Wing Kirsty, Wittemeyer Kerstin, Wood Shawn, Wu Jing, Yaspan Brian L, Zurawiecki Danielle, Zwaigenbaum Lonnie, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Devlin Bernie, Ennis Sean, Gallagher Louise, Geschwind Daniel H, Gill Michael, Haines Jonathan L, Hallmayer Joachim, Miller Judith, Monaco Anthony P, Nurnberger John I, Paterson Andrew D, Pericak-Vance Margaret A, Schellenberg Gerard D, Szatmari Peter, Vicente Astrid M, Vieland Veronica J, Wijsman Ellen M, Scherer Stephen W, Sutcliffe James S, Betancur Catali |
Glutamate system genes and brain volume alterations in pediatric obsessive-compulsive disorder: a preliminary study. Psychiatry research 2012 Nov . Wu K, Hanna GL, Easter P, Kennedy JL, Rosenberg DR, Arnold PD |
Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease. Journal of Alzheimer's disease : JAD 2015 Jan 44 (3): 989-94. Chaudhry Mamoonah, Wang Xingbin, Bamne Mikhil N, Hasnain Shahida, Demirci F Yesim, Lopez Oscar L, Kamboh M Ily |
Role of the DLGAP2 gene encoding the SAP90/PSD-95-associated protein 2 in schizophrenia. PloS one 2014 9 (1): e85373. Li Jun-Ming, Lu Chao-Lin, Cheng Min-Chih, Luu Sy-Ueng, Hsu Shih-Hsin, Hu Tsung-Ming, Tsai Hsin-Yao, Chen Chia-Hsia |
Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders. Scientific reports 2016 Jun 6 27491. Xing Jingrui, Kimura Hiroki, Wang Chenyao, Ishizuka Kanako, Kushima Itaru, Arioka Yuko, Yoshimi Akira, Nakamura Yukako, Shiino Tomoko, Oya-Ito Tomoko, Takasaki Yuto, Uno Yota, Okada Takashi, Iidaka Tetsuya, Aleksic Branko, Mori Daisuke, Ozaki Nor |
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. Journal of neurodevelopmental disorders 2016 8 36. Gazzellone Matthew J, Zarrei Mehdi, Burton Christie L, Walker Susan, Uddin Mohammed, Shaheen S M, Coste Julie, Rajendram Rageen, Schachter Reva J, Colasanto Marlena, Hanna Gregory L, Rosenberg David R, Soreni Noam, Fitzgerald Kate D, Marshall Christian R, Buchanan Janet A, Merico Daniele, Arnold Paul D, Scherer Stephen |
Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing. Neurobiology of disease 2021 12 162 105578. Raposo Mafalda, Bettencourt Conceição, Melo Ana Rosa Vieira, Ferreira Ana F, Alonso Isabel, Silva Paulo, Vasconcelos João, Kay Teresa, Saraiva-Pereira Maria Luiza, Costa Marta D, Vilasboas-Campos Daniela, Bettencourt Bruno Filipe, Bruges-Armas Jácome, Houlden Henry, Heutink Peter, Jardim Laura Bannach, Sequeiros Jorge, Maciel Patrícia, Lima Manue |
Whole Exome Sequencing Revealed Variants That Predict Pulmonary Artery Involvement in Patients with Takayasu Arteritis.
Journal of inflammation research 2022 15 4817-4831. Liu Lingyu, Chen Jing, Li Jing, Yang Yunjiao, Zeng Xiaofeng, Tian Xinpi |
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