Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and CTNNA3[original query] |
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| Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. Journal of medical genetics 2005 Oct 42 (10): 787-92. Martin E R, Bronson P G, Li Y-J, Wall N, Chung R-H, Schmechel D E, Small G, Xu P-T, Bartlett J, Schnetz-Boutaud N, Haines J L, Gilbert J R, Pericak-Vance M |
| Genetic association of CTNNA3 with late-onset Alzheimer's disease in females. Human molecular genetics 2007 Dec 16 (23): 2854-69. Miyashita Akinori, Arai Hiroyuki, Asada Takashi, Imagawa Masaki, Matsubara Etsuro, Shoji Mikio, Higuchi Susumu, Urakami Katsuya, Kakita Akiyoshi, Takahashi Hitoshi, Toyabe Shinichi, Akazawa Kohei, Kanazawa Ichiro, Ihara Yasuo, Kuwano Ryozo, |
| Is alpha-T catenin (VR22) an Alzheimer's disease risk gene? Journal of medical genetics 2007 Jan 44 (1): e63. Bertram Lars, Mullin Kristina, Parkinson Michele, Hsiao Monica, Moscarillo Thomas J, Wagner Steven L, Becker K David, Velicelebi Gonul, Blacker Deborah, Tanzi Rudolph |
| An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Jul 150B (5): 721-35. Edwards Todd L, Pericak-Vance Margaret, Gilbert Johnny R, Haines Jonathan L, Martin Eden R, Ritchie Marylyn |
| Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Sep 147B (6): 727-31. Morgan A R, Hamilton G, Turic D, Jehu L, Harold D, Abraham R, Hollingworth P, Moskvina V, Brayne C, Rubinsztein D C, Lynch A, Lawlor B, Gill M, O'Donovan M, Powell J, Lovestone S, Williams J, Owen M |
| An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings. BMC genetics 2010 11 (1): 49. Goldstein Benjamin A, Hubbard Alan E, Cutler Adele, Barcellos Lisa |
| Screening of three novel candidate genes in arrhythmogenic right ventricular cardiomyopathy. Genetic testing and molecular biomarkers 2011 1 15 (4): 267-71. Christensen Alex Hørby, Benn Marianne, Tybjærg-Hansen Anne, Haunso Stig, Svendsen Jesper Hastr |
| CTNNA3 (a-catenin) gene variants are associated with diisocyanate asthma: a replication study in a Caucasian worker population. Toxicological sciences : an official journal of the Society of Toxicology 2013 Jan 131 (1): 242-6. Bernstein David I, Kashon Michael, Lummus Zana L, Johnson Victor J, Fluharty Kara, Gautrin Denyse, Malo Jean-Luc, Cartier André, Boulet Louis-Philippe, Sastre Joaquin, Quirce Santiago, Germolec Dori, Tarlo Susan M, Cruz Maria-Jesus, Munoz Xavier, Luster Michael I, Yucesoy Berr |
| Mutations in the area composita protein aT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy. European heart journal 2013 Jan 34 (3): 201-10. van Hengel Jolanda, Calore Martina, Bauce Barbara, Dazzo Emanuela, Mazzotti Elisa, De Bortoli Marzia, Lorenzon Alessandra, Li Mura Ilena E A, Beffagna Giorgia, Rigato Ilaria, Vleeschouwers Mara, Tyberghein Koen, Hulpiau Paco, van Hamme Evelien, Zaglia Tania, Corrado Domenico, Basso Cristina, Thiene Gaetano, Daliento Luciano, Nava Andrea, van Roy Frans, Rampazzo Alessand |
| Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity. JAMA neurology 2013 Oct 70 (10): 1261-7. Ghani Mahdi, Sato Christine, Lee Joseph H, Reitz Christiane, Moreno Danielle, Mayeux Richard, St George-Hyslop Peter, Rogaeva Ekateri |
| LRRTM3 interacts with APP and BACE1 and has variants associating with late-onset Alzheimer's disease (LOAD). PloS one 2013 8 (6): 6. Lincoln S, Allen M, Cox CL, Walker LP, Malphrus K, Qiu Y, Nguyen T, Rowley C, Kouri N, Crook J, Pankratz VS, Younkin S, Younkin L, Carrasquillo M, Zou F, Abdul-Hay SO, Springer W, Sando SB, Aasly JO, Barcikowska M, Wszolek ZK, Lewis JM, Dickson D, Graff-Radford NR, Petersen RC, Eckman E, Younkin SG, Ertekin-Taner N |
BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.
PloS one 2013 8 (1): 1. Xu C, Aragam N, Li X, Villla EC, Wang L, Briones D, Petty L, Posada Y, Arana TB, Cruz G, Mao C, Camarillo C, Su BB, Escamilla MA, Wang K |
| Polymorphisms in recent GWA identified asthma genes CA10, SGK493, and CTNNA3 are associated with disease severity and treatment response in childhood asthma. Immunogenetics 2014 Mar 66 (3): 143-51. Perin Petra, Poto?nik Ur |
| A genome-wide association study of suicidal behavior.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct 168 (7): 557-63. Galfalvy Hanga, Haghighi Fatemeh, Hodgkinson Colin, Goldman David, Oquendo Maria A, Burke Ainsley, Huang Yung-Yu, Giegling Ina, Rujescu Dan, Bureau Alexandre, Turecki Gustavo, Mann J Jo |
| Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome. Molecular genetics and metabolism 2015 Oct . Tekola-Ayele Fasil, Doumatey Ayo P, Shriner Daniel, Bentley Amy R, Chen Guanjie, Zhou Jie, Fasanmade Olufemi, Johnson Thomas, Oli Johnnie, Okafor Godfrey, Eghan Benjami A, Agyenim-Boateng Kofi, Adebamowo Clement, Amoah Albert, Acheampong Joseph, Adeyemo Adebowale, Rotimi Charles |
| Genome-wide association study in essential tremor identifies three new loci.
Brain : a journal of neurology 2016 Dec 139 (Pt 12): 3163-3169. Müller Stefanie H, Girard Simon L, Hopfner Franziska, Merner Nancy D, Bourassa Cynthia V, Lorenz Delia, Clark Lorraine N, Tittmann Lukas, Soto-Ortolaza Alexandra I, Klebe Stephan, Hallett Mark, Schneider Susanne A, Hodgkinson Colin A, Lieb Wolfgang, Wszolek Zbigniew K, Pendziwiat Manuela, Lorenzo-Betancor Oswaldo, Poewe Werner, Ortega-Cubero Sara, Seppi Klaus, Rajput Alex, Hussl Anna, Rajput Ali H, Berg Daniela, Dion Patrick A, Wurster Isabel, Shulman Joshua M, Srulijes Karin, Haubenberger Dietrich, Pastor Pau, Vilariño-Güell Carles, Postuma Ronald B, Bernard Geneviève, Ladwig Karl-Heinz, Dupré Nicolas, Jankovic Joseph, Strauch Konstantin, Panisset Michel, Winkelmann Juliane, Testa Claudia M, Reischl Eva, Zeuner Kirsten E, Ross Owen A, Arzberger Thomas, Chouinard Sylvain, Deuschl Günther, Louis Elan D, Kuhlenbäumer Gregor, Rouleau Guy |
| Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.
The Journal of allergy and clinical immunology 2017 Oct . Asai Yuka, Eslami Aida, van Ginkel C Dorien, Akhabir Loubna, Wan Ming, Ellis George, Ben-Shoshan Moshe, Martino David, Ferreira Manuel A, Allen Katrina, Mazer Bruce, de Groot Hans, de Jong Nicolette W, Gerth van Wijk Roy N, Dubois Anthony E J, Chin Rick, Cheuk Stephen, Hoffman Joshua, Jorgensen Eric, Witte John S, Melles Ronald B, Hong Xiumei, Wang Xiaobin, Hui Jennie, Musk Arthur W Bill, Hunter Michael, James Alan L, Koppelman Gerard H, Sandford Andrew J, Clarke Ann E, Daley Deni |
| Analysis of Single Nucleotide Polymorphisms of STK32B, PPARGC1A and CTNNA3 Gene With Sporadic Parkinson's Disease Susceptibility in Chinese Han Population. Frontiers in neurology 2018 9 387. Shi Chang-He, Cheng Yuan, Tang Mi-Bo, Liu Yu-Tao, Yang Zhi-Hua, Li Fang, Fan Yu, Yang Jing, Xu Yu-Mi |
| Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.
PloS one 2021 9 16 (9): e0247287. Ashvetiya Tamara, Fan Sherry X, Chen Yi-Ju, Williams Charles H, O'Connell Jeffery R, Perry James A, Hong Charles |
| Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk. JAMA cardiology 2024 6 . Oliver B Vad, Laia M Monfort, Christian Paludan-Müller, Konstantin Kahnert, Søren Z Diederichsen, Laura Andreasen, Luca A Lotta, Jonas B Nielsen, Alicia Lundby, Jesper H Svendsen, Morten S Olesen, |
| Genome-wide scan of Flortaucipir PET levels finds JARID2 associated with cerebral tau deposition. medRxiv : the preprint server for health sciences 2024 10 . Tamil Iniyan Gunasekaran, Devendra Meena, Annie J Lee, Siwei Wu, Logan Dumitrescu, Reisa Sperling, Timothy J Hohman, , , Jingxian Huang, Abbas Dehghan, Ioanna Tzoulaki, Richard Mayeux, Badri Vardaraj |
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