Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Attention and ASTN2[original query] |
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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
Journal of neural transmission (Vienna, Austria : 1996) 2008 Nov 115 (11): 1573-85. Lesch Klaus-Peter, Timmesfeld Nina, Renner Tobias J, Halperin Rebecca, Röser Christoph, Nguyen T Trang, Craig David W, Romanos Jasmin, Heine Monika, Meyer Jobst, Freitag Christine, Warnke Andreas, Romanos Marcel, Schäfer Helmut, Walitza Susanne, Reif Andreas, Stephan Dietrich A, Jacob Christi |
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Schizophrenia research 2010 Dec 124 (1-3): 192-9. Wang Ke-Sheng, Liu Xue-Feng, Aragam Nage |
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Science translational medicine 2011 Aug 3 (95): 95ra75. Lionel Anath C, Crosbie Jennifer, Barbosa Nicole, Goodale Tara, Thiruvahindrapuram Bhooma, Rickaby Jessica, Gazzellone Matthew, Carson Andrew R, Howe Jennifer L, Wang Zhuozhi, Wei John, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Fiebig Andreas, Franke Andre, Schreiber Stefan, Zwaigenbaum Lonnie, Fernandez Bridget A, Roberts Wendy, Arnold Paul D, Szatmari Peter, Marshall Christian R, Schachar Russell, Scherer Stephen |
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Human molecular genetics 2014 May 23 (10): 2752-68. Lionel Anath C, Tammimies Kristiina, Vaags Andrea K, Rosenfeld Jill A, Ahn Joo Wook, Merico Daniele, Noor Abdul, Runke Cassandra K, Pillalamarri Vamsee K, Carter Melissa T, Gazzellone Matthew J, Thiruvahindrapuram Bhooma, Fagerberg Christina, Laulund Lone W, Pellecchia Giovanna, Lamoureux Sylvia, Deshpande Charu, Clayton-Smith Jill, White Ann C, Leather Susan, Trounce John, Melanie Bedford H, Hatchwell Eli, Eis Peggy S, Yuen Ryan K C, Walker Susan, Uddin Mohammed, Geraghty Michael T, Nikkel Sarah M, Tomiak Eva M, Fernandez Bridget A, Soreni Noam, Crosbie Jennifer, Arnold Paul D, Schachar Russell J, Roberts Wendy, Paterson Andrew D, So Joyce, Szatmari Peter, Chrysler Christina, Woodbury-Smith Marc, Brian Lowry R, Zwaigenbaum Lonnie, Mandyam Divya, Wei John, Macdonald Jeffrey R, Howe Jennifer L, Nalpathamkalam Thomas, Wang Zhuozhi, Tolson Daniel, Cobb David S, Wilks Timothy M, Sorensen Mark J, Bader Patricia I, An Yu, Wu Bai-Lin, Musumeci Sebastiano Antonino, Romano Corrado, Postorivo Diana, Nardone Anna M, Monica Matteo Della, Scarano Gioacchino, Zoccante Leonardo, Novara Francesca, Zuffardi Orsetta, Ciccone Roberto, Antona Vincenzo, Carella Massimo, Zelante Leopoldo, Cavalli Pietro, Poggiani Carlo, Cavallari Ugo, Argiropoulos Bob, Chernos Judy, Brasch-Andersen Charlotte, Speevak Marsha, Fichera Marco, Ogilvie Caroline Mackie, Shen Yiping, Hodge Jennelle C, Talkowski Michael E, Stavropoulos Dimitri J, Marshall Christian R, Scherer Stephen |
The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits. Journal of neural transmission (Vienna, Austria : 1996) 2016 Apr . Freitag Christine M, Lempp Thomas, Nguyen T Trang, Jacob Christian P, Weissflog Lena, Romanos Marcel, Renner Tobias J, Walitza Susanne, Warnke Andreas, Rujescu Dan, Lesch Klaus-Peter, Reif Andre |
The conserved ASTN2/BRINP1 locus at 9q33.1-33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain. Scientific reports 2021 Jul 11 (1): 14529. Pol-Fuster Josep, Cañellas Francesca, Ruiz-Guerra Laura, Medina-Dols Aina, Bisbal-Carrió Bàrbara, Ortega-Vila Bernat, Llinàs Jaume, Hernandez-Rodriguez Jessica, Lladó Jerònia, Olmos Gabriel, Strauch Konstantin, Heine-Suñer Damià, Vives-Bauzà Cristòfol, Flaquer Antòn |
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