Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: TRIM32[original query] |
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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 |
Genomic profile in gestational and non-gestational choriocarcinomas. Placenta 2017 02 50 8-15. Mello Julia Bette Homem de, Ramos Cirilo Priscila Daniele, Michelin Odair Carlito, Custódio Domingues Maria Aparecida, Cunha Rudge Marilza Vieira, Rogatto Silvia Regina, Maestá Izildin |
Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population. Journal of neurology, neurosurgery, and psychiatry 2018 6 90 (4): 490-493. Johnson Katherine, De Ridder Willem, Töpf Ana, Bertoli Marta, Phillips Lauren, De Jonghe Peter, Baets Jonathan, Deconinck Tine, Rakocevic Stojanovic Vidosava, Peri? Stojan, Durmus Hacer, Jamal-Omidi Shirin, Nafissi Shahriar, Mongini Tiziana, ?usakowska Anna, Busby Mark, Miller James, Norwood Fiona, Hudson Judith, Barresi Rita, Lek Monkol, MacArthur Daniel G, Straub Volk |
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients. Clinical genetics 2019 3 96 (2): 126-133. Ten Dam Leroy, Frankhuizen Wendy S, Linssen Wim H J P, Straathof Chiara S, Niks Erik H, Faber Karin, Fock Annemarie, Kuks Jan B, Brusse Esther, de Coo René, Voermans Nicol, Verrips Aad, Hoogendijk Jessica E, van der Pol Ludo, Westra Dineke, de Visser Marianne, van der Kooi Anneke J, Ginjaar Ie |
Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity.
Genes 2020 Feb 11 (3): . Adewuyi Emmanuel O, Sapkota Yadav, International Endogene Consortium Iec , andMe Research Team , International Headache Genetics Consortium Ihgc , Auta Asa, Yoshihara Kosuke, Nyegaard Mette, Griffiths Lyn R, Montgomery Grant W, Chasman Daniel I, Nyholt Dale |
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 |
Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year's Journey. Journal of neuromuscular diseases 2021 1 8 (2): 261-272. Ten Dam L, de Visser M, Ginjaar Ieke B, van Duyvenvoorde Hermine A, van Koningsbruggen Silvana, van der Kooi Anneke |
Gene-Based Analysis Reveals Sex-Specific Genetic Risk Factors of COPD.
AMIA ... Annual Symposium proceedings. AMIA Symposium 2022 3 2021 601-610. Joo Jaehyun, Himes Blan |
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- Page last updated:Apr 22, 2024
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