Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: HOXA1[original query] |
---|
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network. American journal of medical genetics 2002 Aug 114 (6): 667-72. Devlin Bernie, Bennett Pamela, Cook Edwin H, Dawson Geraldine, Gonen David, Grigorenko Elena L, McMahon William, Pauls David, Smith Moyra, Spence M Anne, Schellenberg Gerard D, |
The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project. Journal of autism and developmental disorders 2003 Jun 33 (3): 343-8. Collins Julianne S, Schroer Richard J, Bird Jeffrey, Michaelis Ron |
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism. Biological psychiatry 2004 Feb 55 (4): 413-9. Conciatori Monica, Stodgell Christopher J, Hyman Susan L, O'Bara Melanie, Militerni Roberto, Bravaccio Carmela, Trillo Simona, Montecchi Francesco, Schneider Cindy, Melmed Raun, Elia Maurizio, Crawford Lori, Spence Sarah J, Muscarella Lucianna, Guarnieri Vito, D'Agruma Leonardo, Quattrone Alessandro, Zelante Leopoldo, Rabinowitz Daniel, Pascucci Tiziana, Puglisi-Allegra Stefano, Reichelt Karl-Ludvig, Rodier Patricia M, Persico Antonio |
HOXA1 gene variants influence head growth rates in humans. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Apr 144B (3): 388-90. Muscarella Lucia Anna, Guarnieri Vito, Sacco Roberto, Militerni Roberto, Bravaccio Carmela, Trillo Simona, Schneider Cindy, Melmed Raun, Elia Maurizio, Mascia Maria Lucia, Rucci Emanuela, Piemontese Maria Rosaria, D'Agruma Leonardo, Persico Antonio |
HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans. Journal of neuroimaging : official journal of the American Society of Neuroimaging 2009 Oct 19 (4): 353-8. Canu Elisa, Boccardi Marina, Ghidoni Roberta, Benussi Luisa, Duchesne Simon, Testa Cristina, Binetti Giuliano, Frisoni Giovanni |
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders. Psychiatric genetics 2008 Dec 18 (6): 295-301. Laroche Fabrice, Ramoz Nicolas, Leroy Sophie, Fortin Célia, Rousselot-Paillet Bérangère, Philippe Anne, Colleaux Laurence, Bresson Jean-Louis, Mogenet Agnès, Golse Bernard, Mouren-Simeoni Marie-Christine, Gorwood Philip, Galli Thierry, Simonneau Michel, Krebs Marie-Odile, Robel Lauren |
Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome. Autism research : official journal of the International Society for Autism Research 2009 Jun 2 (3): 157-77. Chakrabarti B, Dudbridge F, Kent L, Wheelwright S, Hill-Cawthorne G, Allison C, Banerjee-Basu S, Baron-Cohen |
Candidate gene study of HOXB1 in autism spectrum disorder. Molecular autism 2010 1 (1): 9. Muscarella Lucia A, Guarnieri Vito, Sacco Roberto, Curatolo Paolo, Manzi Barbara, Alessandrelli Riccardo, Giana Grazia, Militerni Roberto, Bravaccio Carmela, Lenti Carlo, Saccani Monica, Schneider Cindy, Melmed Raun, D'Agruma Leonardo, Persico Antonio |
An integrated meta-analysis of two variants in HOXA1/HOXB1 and their effect on the risk of autism spectrum disorders. PloS one 2011 6 (9): e25603. Song Ran-Ran, Zou Li, Zhong Rong, Zheng Xia-Wen, Zhu Bei-Bei, Chen Wei, Liu Li, Miao Xiao-Pi |
HOXA1 gene is not potentially related to ventricular septal defect in Chinese children. Pediatric cardiology 2012 Jul . Liu J, Wang B, Chen X, Li H, Wang J, Cheng L, Ma X, Gao B |
Allelic variation within the putative autism spectrum disorder risk gene homeobox A1 and cerebellar maturation in typically developing children and adolescents. Autism research : official journal of the International Society for Autism Research 2012 Apr 5 (2): 93-100. Raznahan Armin, Lee Yohan, Vaituzis Catherine, Tran Lan, Mackie Susan, Tiemeier Henning, Clasen Liv, Lalonde Francois, Greenstein Dede, Pierson Ron, Giedd Jay |
The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death. Medical science monitor : international medical journal of experimental and clinical research 2014 20 1531-8. Lozi? Bernarda, Krželj Vjekoslav, Kuzmi?-Prusac Ivana, Kuzmani?-Šamija Radenka, ?apkun Vesna, Lasan Ružica, Zemunik Tatija |
The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia. Nature genetics 2017 Jul . Liu Yu, Easton John, Shao Ying, Maciaszek Jamie, Wang Zhaoming, Wilkinson Mark R, McCastlain Kelly, Edmonson Michael, Pounds Stanley B, Shi Lei, Zhou Xin, Ma Xiaotu, Sioson Edgar, Li Yongjin, Rusch Michael, Gupta Pankaj, Pei Deqing, Cheng Cheng, Smith Malcolm A, Auvil Jaime Guidry, Gerhard Daniela S, Relling Mary V, Winick Naomi J, Carroll Andrew J, Heerema Nyla A, Raetz Elizabeth, Devidas Meenakshi, Willman Cheryl L, Harvey Richard C, Carroll William L, Dunsmore Kimberly P, Winter Stuart S, Wood Brent L, Sorrentino Brian P, Downing James R, Loh Mignon L, Hunger Stephen P, Zhang Jinghui, Mullighan Charles |
A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles. BMC research notes 2017 Nov 10 (1): 562. Abu-Amero Khaled K, Kondkar Altaf A, Khan Arif |
Characteristics of genetic alterations of peripheral T-cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG). British journal of haematology 2021 7 194 (4): 718-729. Ohki Kentaro, Kiyokawa Nobutaka, Watanabe Satoru, Iwafuchi Hideto, Nakazawa Astuko, Ishiwata Keisuke, Ogata-Kawata Hiroko, Nakabayashi Kazuhiko, Okamura Kohji, Tanaka Fumiko, Fukano Reiji, Hata Kenichiro, Mori Tetsuya, Moriya Saito Akiko, Hayashi Yasuhide, Taga Takashi, Sekimizu Masahiro, Kobayashi Ryoji, |
Genetic analysis of a malignant meningioma and associated metastases. Acta neurochirurgica 2022 1 164 (5): 1401-1405. Huntoon Kristin, Yilmaz Ayse Selen, Pietrzak Maciej, Chen Xi, Yan Pearlly, Toland Amanda Ewart, Elder J Bradl |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: