Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Disease and GABRG2[original query] |
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| A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions. Archives of neurology 2002 Jul 59 (7): 1137-41. Kananura Colette, Haug Karsten, Sander Thomas, Runge Uwe, Gu Wenli, Hallmann Kerstin, Rebstock Johannes, Heils Armin, Steinlein Ortrud |
| Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. American journal of human genetics 2005 Sep 77 (3): 377-88. Ma D Q, Whitehead P L, Menold M M, Martin E R, Ashley-Koch A E, Mei H, Ritchie M D, Delong G R, Abramson R K, Wright H H, Cuccaro M L, Hussman J P, Gilbert J R, Pericak-Vance M |
| Examining the role of common genetic variation in the gamma2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs. Epilepsy research 2006 Aug 70 (2-3): 229-38. Kinirons Peter, Cavalleri Gianpiero L, Shahwan Amre, Wood Nicholas W, Goldstein David B, Sisodiya Sanjay M, Delanty Norman, Doherty Colin |
| No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia. Psychiatric genetics 2007 Feb 17 (1): 43-5. Jamra Rami Abou, Becker Tim, Klopp Norman, Dahdouh Faten, Schulze Thomas G, Gross Magdalena, Deschner Monika, Schmäl Christine, Illig Thomas, Rietschel Marcella, Propping Peter, Cichon Sven, Nöthen Markus M, Schumacher Johann |
| Association analysis of gamma2 subunit of gamma-aminobutyric acid (GABA) type A receptor and voltage-gated sodium channel type II alpha-polypeptide gene mutation in southern Chinese children with febrile seizures. Journal of child neurology 2007 Jun 22 (6): 714-9. Xiumin Wang , Meichun Xu , Lizhong D |
| A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy. Neurobiology of disease 2008 Dec 32 (3): 349-54. Ohmori Iori, Ouchida Mamoru, Miki Takafumi, Mimaki Nobuyoshi, Kiyonaka Shigeki, Nishiki Teiichi, Tomizawa Kazuhito, Mori Yasuo, Matsui Hide |
| Polymorphism in cytochrome P450 2E1 and interaction with other genetic risk factors and susceptibility to alcoholic liver cirrhosis. Mutation research 2009 May 664 (1-2): 55-63. Khan Anwar Jamal, Ruwali Munindra, Choudhuri Gourdas, Mathur Neeraj, Husain Qayyum, Parmar Devend |
| Variants in SELL, MRPS36P2, TP63, DDB2, CACNA1H, ADAM19, GNAI1, CDH13 and GABRG2 interact to confer risk of acne in Chinese population. The Journal of dermatology 2015 Apr 42 (4): 378-81. Wang HongYan, Guo MeiHua, Shen SongKe, He Li, Zhang XueJun, Zuo XianBo, Yang S |
| Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2016 40 (3-4): 509-526. Wang Yang, Wang Jun, Zhou Ying, Wei Zhiyun, Xiao Yongtao, Zhou Kejun, Wen Jie, Yan Junkai, Cai W |
| Association of a novel GABRG2 splicing variation and a PTGS2/COX-2 single nucleotide polymorphism with Taiwanese febrile seizures. Epilepsy research 2016 Nov 129 1-7. Hung Kun-Long, Liang Jao-Shwann, Wang Jinn-Shyan, Chen Hui-Ju, Lin Li-Ju, Lu Jyh-Fe |
| Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. Journal of cellular and molecular medicine 2018 Apr . Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W |
| MAPT haplotype-stratified GWAS reveals differential association for AD risk variants. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 May . Strickland Samantha L, Reddy Joseph S, Allen Mariet, N'songo Aurelie, Burgess Jeremy D, Corda Morgane M, Ballard Travis, Wang Xue, Carrasquillo Minerva M, Biernacka Joanna M, Jenkins Gregory D, Mukherjee Shubhabrata, Boehme Kevin, Crane Paul, Kauwe John S, Ertekin-Taner Nilüfer, |
| Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
| Genetic Determinants of Sudden Unexpected Death in Pediatrics. Genetics in medicine : official journal of the American College of Medical Genetics 2022 1 24 (4): 839-850. Koh Hyun Yong, Haghighi Alireza, Keywan Christine, Alexandrescu Sanda, Plews-Ogan Erin, Haas Elisabeth A, Brownstein Catherine A, Vargas Sara O, Haynes Robin L, Berry Gerard T, Holm Ingrid A, Poduri Annapurna H, Goldstein Richard |
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes.
Brain : a journal of neurology 2022 1 145 (2): 555-568. Skotte Line, Fadista João, Bybjerg-Grauholm Jonas, Appadurai Vivek, Hildebrand Michael S, Hansen Thomas F, Banasik Karina, Grove Jakob, Albiñana Clara, Geller Frank, Bjurström Carmen F, Vilhjálmsson Bjarni J, Coleman Matthew, Damiano John A, Burgess Rosemary, Scheffer Ingrid E, Pedersen Ole Birger Vesterager, Erikstrup Christian, Westergaard David, Nielsen Kaspar René, Sørensen Erik, Bruun Mie Topholm, Liu Xueping, Hjalgrim Henrik, Pers Tune H, Mortensen Preben Bo, Mors Ole, Nordentoft Merete, Dreier Julie W, Børglum Anders D, Christensen Jakob, Hougaard David M, Buil Alfonso, Hviid Anders, Melbye Mads, Ullum Henrik, Berkovic Samuel F, Werge Thomas, Feenstra Bjar |
| Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' families. EBioMedicine 2024 10 109 105404. Karen L Oliver, Ingrid E Scheffer, Colin A Ellis, Bronwyn E Grinton, , Samuel F Berkovic, Melanie Bah |
- Page last reviewed:Feb 1, 2024
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