Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: CTNNA3[original query] |
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A CTNNA3 compound heterozygous deletion implicates a role for aT-catenin in susceptibility to autism spectrum disorder. Journal of neurodevelopmental disorders 2014 6 (1): 17. Bacchelli Elena, Ceroni Fabiola, Pinto Dalila, Lomartire Silvia, Giannandrea Maila, D'Adamo Patrizia, Bonora Elena, Parchi Piero, Tancredi Raffaella, Battaglia Agatino, Maestrini Ele |
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 |
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy. Journal of immunology (Baltimore, Md. : 1950) 2015 Aug 195 (4): 1599-607. Li Jin, Fung Irene, Glessner Joseph T, Pandey Rahul, Wei Zhi, Bakay Marina, Mentch Frank D, Pellegrino Renata, Wang Tiancheng, Kim Cecilia, Hou Cuiping, Wang Fengxiang, Chiavacci Rosetta M, Thomas Kelly A, Spergel Jonathan M, Hakonarson Hakon, Sleiman Patrick M |
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 |
Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation.
PloS one 2015 10 (3): e0116696. Avramopoulos Dimitrios, Pearce Brad D, McGrath John, Wolyniec Paula, Wang Ruihua, Eckart Nicole, Hatzimanolis Alexandros, Goes Fernando S, Nestadt Gerald, Mulle Jennifer, Coneely Karen, Hopkins Myfanwy, Ruczinski Ingo, Yolken Robert, Pulver Ann |
GWAS, cytomegalovirus infection, and schizophrenia. Current behavioral neuroscience reports 2014 Dec 1 (4): 215-223. Grove Jakob, Børglum Anders D, Pearce Brad |
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 |
High Prevalence of Smoking in the Roma Population Seems to Have No Genetic Background. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2016 12 18 (12): 2260-2267. Fiatal Szilvia, Tóth Réka, Moravcsik-Kornyicki Ágota, Kósa Zsigmond, Sándor János, McKee Martin, Ádány Ró |
Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway. BMC psychiatry 2016 16 (1): 106. Cocchi Enrico, Fabbri Chiara, Han Changsu, Lee Soo-Jung, Patkar Ashwin A, Masand Prakash S, Pae Chi-Un, Serretti Alessand |
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 |
A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration.
Scientific reports 2017 Aug 7 (1): 7173. Kawashima-Kumagai Kyoko, Yamashiro Kenji, Yoshikawa Munemitsu, Miyake Masahiro, Ming Gemmy Cheung Chui, Fan Qiao, Koh Jia Yu, Saito Masaaki, Sugahara-Kuroda Masako, Oishi Maho, Akagi-Kurashige Yumiko, Nakata Isao, Nakanishi Hideo, Gotoh Norimoto, Oishi Akio, Tamura Hiroshi, Ooto Sotaro, Tsujikawa Akitaka, Kurimoto Yasuo, Sekiryu Tetsuju, Matsuda Fumihiko, Khor Chiea-Chuen, Cheng Ching-Yu, Wong Tien Yin, Yoshimura Nagahi |
Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population. Scientific reports 2017 08 7 (1): 7981. Zhang Yuan, Zhao Yuwen, Zhou Xiaoting, Li Kai, Yi Minhan, Guo Jifeng, Yan Xinxiang, Tang Beisha, Sun Qiyi |
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 |
Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage.
Biomedical reports 2018 Jul 9 (1): 8-20. Yamada Yoshiji, Kato Kimihiko, Oguri Mitsutoshi, Horibe Hideki, Fujimaki Tetsuo, Yasukochi Yoshiki, Takeuchi Ichiro, Sakuma J |
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 |
No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor. Neurology. Genetics 2018 12 3 (5): e195. Houle Gabrielle, Ambalavanan Amirthagowri, Schmouth Jean-François, Leblond Claire S, Spiegelman Dan, Laurent Sandra B, Bourassa Cynthia V, Grayson Celene, Panisset Michel, Chouinard Sylvain, Dupré Nicolas, Vilariño-Güell Carles, Rajput Alex, Girard Simon L, Dion Patrick A, Rouleau Guy |
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.
European journal of human genetics : EJHG 2019 03 27 (3): 442-454. Tasa Tõnis, Krebs Kristi, Kals Mart, Mägi Reedik, Lauschke Volker M, Haller Toomas, Puurand Tarmo, Remm Maido, Esko Tõnu, Metspalu Andres, Vilo Jaak, Milani Li |
Putative role of Brugada syndrome genes in familial atrial fibrillation. European review for medical and pharmacological sciences 2019 9 23 (17): 7582-7598. Maltese P E, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli |
Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
Expression of ovine CTNNA3 and CAP2 genes and their association with growth traits. Gene 2021 9 807 145949. Zhao Liming, Li Fadi, Yuan Lvfeng, Zhang Xiaoxue, Zhang Deyin, Li Xiaolong, Zhang Yukun, Zhao Yuan, Song Qizhi, Wang Jianghui, Zhou Bubo, Cheng Jiangbo, Xu Dan, Li Wenxin, Lin Changchun, Wang Weim |
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 |
Polymorphous Low-Grade Neuroepithelial Tumor of the Young (PLNTY): Molecular Profiling Confirms Frequent MAPK Pathway Activation. Journal of neuropathology and experimental neurology 2021 8 80 (9): 821-829. Ida Cristiane M, Johnson Derek R, Nair Asha A, Davila Jaime, Kollmeyer Thomas M, Minn Kay, Fadra Numrah M, Balcom Jessica R, Fung Kar-Ming A, Kim Dong Kun, Kaufmann Timothy J, Kipp Benjamin R, Halling Kevin C, Jenkins Robert B, Giannini Cateri |
Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction. Frontiers in cardiovascular medicine 2021 6 8 635141. Leone Maria Pia, Palumbo Pietro, Saenen Johan, Mastroianno Sandra, Castellana Stefano, Amico Cesare, Mazza Tommaso, Potenza Domenico Rosario, Petracca Antonio, Castori Marco, Carella Massimo, Di Stolfo Giusep |
Genomic Markers for Essential Tremor. Pharmaceuticals (Basel, Switzerland) 2021 6 14 (6): . Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, García-Martín Elena, Álvarez Ignacio, Pastor Pau, Agúndez José A |
Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients. PloS one 2021 16 (4): e0249997. Weng Saizheng, Wang Bo, Li Mo, Chao Shan, Lin Ruiqian, Zheng Rongyan, Yu Yinliang, Guo Shaonan, Lin Xianh |
CTNNA3 genetic polymorphism may be a new genetic signal of type 2 diabetes in the Chinese Han population: a case control study. BMC medical genomics 2021 Oct 14 (1): 257. Zhang Yunjun, Zhou Xiaoman, Dai Wanjuan, Sun Juan, Lin Mei, Zhang Yutian, Ding Yipe |
Novel Recurrent Altered Genes in Chinese Patients With Anaplastic Thyroid Cancer. The Journal of clinical endocrinology and metabolism 2021 Jan . Zhang Lingyun, Ren Zhixiang, Su Zhengzheng, Liu Yang, Yang Tian, Cao Minyuan, Jiang Yong, Tang Ying, Chen Haining, Zhang Weihan, Gong Rixiang, Wei Tao, Peng Yong, Liu Bo, Zhang Wei, Yang Li, Hu Yiguo, Li Zhihui, Zhu Jingqiang, Xu Heng, Shu Yang, Luo H |
Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank.
Translational psychiatry 2021 8 11 (1): 431. Cheng Shiqiang, Wen Yan, Liu Li, Cheng Bolun, Liang Chujun, Ye Jing, Chu Xiaomeng, Yao Yao, Jia Yumeng, Kafle Om Prakash, Zhang Fe |
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.
HGG advances 2022 2 3 (2): 100093. Gehlen Jan, Giel Ann-Sophie, Köllges Ricarda, Haas Stephan L, Zhang Rong, Trcka Jiri, Sungur Ayse Ö, Renziehausen Florian, Bornholdt Dorothea, Jung Daphne, Hoyer Paul D, Nordenskjöld Agneta, Tibboel Dick, Vlot John, Spaander Manon C W, Smigiel Robert, Patkowski Dariusz, Roeleveld Nel, van Rooij Iris Alm, de Blaauw Ivo, Hölscher Alice, Pauly Marcus, Leutner Andreas, Fuchs Joerg, Niethammer Joel, Melissari Maria-Theodora, Jenetzky Ekkehart, Zwink Nadine, Thiele Holger, Hilger Alina Christine, Hess Timo, Trautmann Jessica, Marks Matthias, Baumgarten Martin, Bläss Gaby, Landén Mikael, Fundin Bengt, Bulik Cynthia M, Pennimpede Tracie, Ludwig Michael, Ludwig Kerstin U, Mangold Elisabeth, Heilmann-Heimbach Stefanie, Moebus Susanne, Herrmann Bernhard G, Alsabeah Kristina, Burgos Carmen M, Lilja Helene E, Azodi Sahar, Stenström Pernilla, Arnbjörnsson Einar, Frybova Barbora, Lebensztejn Dariusz M, Debek Wojciech, Kolodziejczyk Elwira, Kozera Katarzyna, Kierkus Jaroslaw, Kalici?ski Piotr, Stefanowicz Marek, Socha-Banasiak Anna, Kolejwa Michal, Piaseczna-Piotrowska Anna, Czkwianianc Elzbieta, Nöthen Markus M, Grote Phillip, Rygl Michal, Reinshagen Konrad, Spychalski Nicole, Ludwikowski Barbara, Hubertus Jochen, Heydweiller Andreas, Ure Benno, Muensterer Oliver J, Aubert Ophelia, Gosemann Jan-Hendrik, Lacher Martin, Degenhardt Petra, Boemers Thomas M, Mokrowiecka Anna, Ma?ecka-Panas Ewa, Wöhr Markus, Knapp Michael, Seitz Guido, de Klein Annelies, Oracz Grzegorz, Brosens Erwin, Reutter Heiko, Schumacher Johann |
Germline Genetic Variants and Pediatric Rhabdomyosarcoma Outcomes: A Report from the Children's Oncology Group. Journal of the National Cancer Institute 2023 3 . Martin-Giacalone Bailey A, Richard Melissa A, Scheurer Michael E, Khan Javed, Sok Pagna, Shetty Priya B, Chanock Stephen J, Li Shengchao Alfred, Yeager Meredith, Marquez-Do Deborah A, Barkauskas Donald A, Hall David, McEvoy Matthew T, Brown Austin L, Sabo Aniko, Scheet Paul, Huff Chad D, Skapek Stephen X, Hawkins Douglas S, Venkatramani Rajkumar, Mirabello Lisa, Lupo Philip |
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- Page last updated:Apr 16, 2024
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