Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: SLC12A2[original query] |
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A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.
Schizophrenia bulletin 2009 Jan 35 (1): 96-108. Potkin Steven G, Turner Jessica A, Guffanti Guia, Lakatos Anita, Fallon James H, Nguyen Dana D, Mathalon Daniel, Ford Judith, Lauriello John, Macciardi Fabio, |
Expression of GABA signaling molecules KCC2, NKCC1, and GAD1 in cortical development and schizophrenia. The Journal of neuroscience : the official journal of the Society for Neuroscience 2011 Jul 31 (30): 11088-95. Hyde Thomas M, Lipska Barbara K, Ali Towhid, Mathew Shiny V, Law Amanda J, Metitiri Ochuko E, Straub Richard E, Ye Tianzhang, Colantuoni Carlo, Herman Mary M, Bigelow Llewellyn B, Weinberger Daniel R, Kleinman Joel |
Association of CTXN3-SLC12A2 polymorphisms and schizophrenia in a Thai population. Behavioral and brain functions : BBF 2012 8 (1): 27. Panichareon Benjaporn, Nakayama Kazuhiro, Iwamoto Sadahiko, Thurakitwannakarn Wanpen, Sukhumsirichart Wasa |
Analysis of inner ear potassium recycling genes as potential factors associated with tinnitus. International journal of occupational medicine and environmental health 2012 Sep 25 (4): 356-64. Pawe?czyk Ma?gorzata, Rajkowska El?bieta, Koty?o Piotr, Dudarewicz Adam, Van Camp Guy, ?liwi?ska-Kowalska Mario |
DISC1 and SLC12A2 interaction affects human hippocampal function and connectivity. The Journal of clinical investigation 2013 Jul 123 (7): 2961-4. Callicott Joseph H, Feighery Emer L, Mattay Venkata S, White Michael G, Chen Qiang, Baranger David A A, Berman Karen F, Lu Bai, Song Hongjun, Ming Guo-li, Weinberger Daniel |
Characteristics of the cation cotransporter NKCC1 in human brain: alternate transcripts, expression in development, and potential relationships to brain function and schizophrenia. The Journal of neuroscience : the official journal of the Society for Neuroscience 2014 Apr 34 (14): 4929-40. Morita Yukitaka, Callicott Joseph H, Testa Lauren R, Mighdoll Michelle I, Dickinson Dwight, Chen Qiang, Tao Ran, Lipska Barbara K, Kolachana Bhaskar, Law Amanda J, Ye Tianzhang, Straub Richard E, Weinberger Daniel R, Kleinman Joel E, Hyde Thomas |
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
PLoS genetics 2017 Apr 13 (4): e1006760. Hodonsky Chani J, Jain Deepti, Schick Ursula M, Morrison Jean V, Brown Lisa, McHugh Caitlin P, Schurmann Claudia, Chen Diane D, Liu Yong Mei, Auer Paul L, Laurie Cecilia A, Taylor Kent D, Browning Brian L, Li Yun, Papanicolaou George, Rotter Jerome I, Kurita Ryo, Nakamura Yukio, Browning Sharon R, Loos Ruth J F, North Kari E, Laurie Cathy C, Thornton Timothy A, Pankratz Nathan, Bauer Daniel E, Sofer Tamar, Reiner Alex |
Novel caries loci in children and adults implicated by genome-wide analysis of families. BMC oral health 2018 6 18 (1): 98. Govil Manika, Mukhopadhyay Nandita, Weeks Daniel E, Feingold Eleanor, Shaffer John R, Levy Steven M, Vieira Alexandre R, Slayton Rebecca L, McNeil Daniel W, Weyant Robert J, Crout Richard J, Marazita Mary |
GWAS Identifies LINC01184/SLC12A2 as a Risk Locus for Skin and Soft Tissue Infections.
The Journal of investigative dermatology 2021 . Rogne Tormod, Liyanarachi Kristin V, Rasheed Humaira, Thomas Laurent F, Flatby Helene M, Stenvik Jørgen, Løset Mari, Gill Dipender, Burgess Stephen, Willer Cristen J, Hveem Kristian, Åsvold Bjørn O, Brumpton Ben M, DeWan Andrew T, Solligård Erik, Damås Jan |
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India. Annals of human genetics 2021 Aug . Vanniya S Paridhy, Chandru Jayasankaran, Jeffrey Justin Margret, Rabinowitz Tom, Brownstein Zippora, Krishnamoorthy Mathuravalli, Avraham Karen B, Cheng Le, Shomron Noam, Srisailapathy C R Srikuma |
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes. Orphanet journal of rare diseases 2022 3 17 (1): 114. Mutai Hideki, Momozawa Yukihide, Kamatani Yoichiro, Nakano Atsuko, Sakamoto Hirokazu, Takiguchi Tetsuya, Nara Kiyomitsu, Kubo Michiaki, Matsunaga Tats |
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