Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: PARD3[original query] |
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Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis. Gut 2008 Apr 57 (4): 463-7. Wapenaar M C, Monsuur A J, van Bodegraven A A, Weersma R K, Bevova M R, Linskens R K, Howdle P, Holmes G, Mulder C J, Dijkstra G, van Heel D A, Wijmenga |
Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability. Human immunology 2010 Apr 71 (4): 392-6. Wolters Victorien M, Alizadeh Behrooz Z, Weijerman Michel E, Zhernakova Alexandra, van Hoogstraten Ingrid M W, Mearin M Luisa, Wapenaar Martin C, Wijmenga Cisca, Schreurs Marco W |
Replication of genetic variation in the MYO9B gene in Crohn's disease. Human immunology 2011 Jul 72 (7): 592-7. Wolters Victorien M, Xu Wei, Zhao Xingqiu, Walters Thomas D, Griffiths Anne M, Silverberg Mark S, Muise Aleixo |
Association study between polymorphisms of the PARD3 gene and schizophrenia. Experimental and therapeutic medicine 2012 May 3 (5): 881-885. Kim Su Kang, Lee Jong Yoon, Park Hae Jeong, Kim Jong Woo, Chung Joo- |
Association study of PARD3 gene polymorphisms with neural tube defects in a Chinese Han population. Reproductive sciences (Thousand Oaks, Calif.) 2012 Jul 19 (7): 764-71. Gao Yonghui, Chen Xiaoli, Shangguan Shaofang, Bao Yihua, Lu Xiaoli, Zou Jizhen, Guo Jin, Dai Yaohua, Zhang Ti |
Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes. Psychophysiology 2014 Dec 51 (12): 1300-8. Vrieze Scott I, Malone Stephen M, Pankratz Nathan, Vaidyanathan Uma, Miller Michael B, Kang Hyun Min, McGue Matt, Abecasis Gonçalo, Iacono William |
Mutational landscape of aggressive cutaneous squamous cell carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2014 Dec 20 (24): 6582-92. Pickering Curtis R, Zhou Jane H, Lee J Jack, Drummond Jennifer A, Peng S Andrew, Saade Rami E, Tsai Kenneth Y, Curry Jonathan L, Tetzlaff Michael T, Lai Stephen Y, Yu Jun, Muzny Donna M, Doddapaneni Harshavardhan, Shinbrot Eve, Covington Kyle R, Zhang Jianhua, Seth Sahil, Caulin Carlos, Clayman Gary L, El-Naggar Adel K, Gibbs Richard A, Weber Randal S, Myers Jeffrey N, Wheeler David A, Frederick Mitchell |
Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis. PloS one 2013 8 (12): e85870. Nijmeijer Rian M, van Santvoort Hjalmar C, Zhernakova Alexandra, Teller Steffen, Scheiber Jonas A, de Kovel Carolien G, Besselink Marc G H, Visser Jeroen T J, Lutgendorff Femke, Bollen Thomas L, Boermeester Marja A, Rijkers Ger T, Weiss Frank U, Mayerle Julia, Lerch Markus M, Gooszen Hein G, Akkermans Louis M A, Wijmenga Cisca, |
Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. Human mutation 2016 Dec . Chen Xiaoli, An Yu, Gao Yonghui, Guo Liu, Rui Lei, Xie Hua, Sun Mei, Lam Hung Siv, Sheng Xiaoming, Zou Jizhen, Bao Yihua, Guan Hongyan, Niu Bo, Li Zandong, Finnell Richard H, Gusella James F, Wu Bai-Lin, Zhang Ti |
Genetic variation and expression levels of tight junction genes identifies association between MAGI3 and inflammatory bowel disease. BMC gastroenterology 2017 May 17 (1): 68. Norén Elisabeth, Almer Sven, Söderman J |
Genetic Variation and Gene Expression Levels of Tight Junction Genes Indicates Relationships Between PTEN as well as MAGI1 and Microscopic Colitis. Digestive diseases and sciences 2017 Dec . Norén Elisabeth, Mellander Marie-Rose, Almer Sven, Söderman J |
Germline mutation analyses of malignant ground glass opacity nodules in non-smoking lung adenocarcinoma patients. PeerJ 2021 9 e12048. Mao Wenjun, Chen Ruo, Lu Rongguo, Wang Shengfei, Song Huizhu, You Dan, Liu Feng, He Yijun, Zheng Mingfe |
A cross-tissue transcriptome-wide association study identifies novel susceptibility genes for lung cancer in Chinese populations. Human molecular genetics 2021 Apr . Zhu Meng, Fan Jingyi, Zhang Chang, Xu Jing, Yin Rong, Zhang Erbao, Wang Yuzhuo, Ji Mengmeng, Sun Qi, Dai Juncheng, Jin Guangfu, Chen Liang, Xu Lin, Hu Zhibin, Ma Hongxia, Shen Hongbi |
Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing. Neurobiology of disease 2021 12 162 105578. Raposo Mafalda, Bettencourt Conceição, Melo Ana Rosa Vieira, Ferreira Ana F, Alonso Isabel, Silva Paulo, Vasconcelos João, Kay Teresa, Saraiva-Pereira Maria Luiza, Costa Marta D, Vilasboas-Campos Daniela, Bettencourt Bruno Filipe, Bruges-Armas Jácome, Houlden Henry, Heutink Peter, Jardim Laura Bannach, Sequeiros Jorge, Maciel Patrícia, Lima Manue |
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels.
Communications biology 2022 4 5 (1): 336. Sarnowski Chloé, Ghanbari Mohsen, Bis Joshua C, Logue Mark, Fornage Myriam, Mishra Aniket, Ahmad Shahzad, Beiser Alexa S, Boerwinkle Eric, Bouteloup Vincent, Chouraki Vincent, Cupples L Adrienne, Damotte Vincent, DeCarli Charles S, DeStefano Anita L, Djoussé Luc, Fohner Alison E, Franz Carol E, Kautz Tiffany F, Lambert Jean-Charles, Lyons Michael J, Mosley Thomas H, Mukamal Kenneth J, Pase Matthew P, Portilla Fernandez Eliana C, Rissman Robert A, Satizabal Claudia L, Vasan Ramachandran S, Yaqub Amber, Debette Stephanie, Dufouil Carole, Launer Lenore J, Kremen William S, Longstreth William T, Ikram M Arfan, Seshadri Sud |
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. Human genetics 2024 2 . Ashraf Yahia, Danyang Li, Sanna Lejerkrans, Shyam Rajagopalan, Nelli Kalnak, Kristiina Tammimi |
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