Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and MAGI2[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 |
| MAGI2 genetic variation and inflammatory bowel disease. Inflammatory bowel diseases 2009 Jan 15 (1): 75-83. McGovern Dermot P B, Taylor Kent D, Landers Carol, Derkowski Carrie, Dutridge Deb, Dubinsky Marla, Ippoliti Andy, Vasiliauskas Eric, Mei Ling, Mengesha Emebet, King Lily, Pressman Sheila, Targan Stephan R, Rotter Jerome |
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.
PloS one 2009 4 (8): e6501. Potkin Steven G, Guffanti Guia, Lakatos Anita, Turner Jessica A, Kruggel Frithjof, Fallon James H, Saykin Andrew J, Orro Alessandro, Lupoli Sara, Salvi Erika, Weiner Michael, Macciardi Fabio, |
| 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 |
| [Genome-wide association study of allergic diseases in Russians of Western Siberia]. Molekuliarnaia biologiia 0 45 (3): 464-72. Fre?din M B, Bragina E Iu, Fedorova O S, Deev I A, Kulikov E S, Ogorodova L M, Puzyrev V |
| 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 |
| MAGI1 copy number variation in bipolar affective disorder and schizophrenia. Biological psychiatry 2012 May 71 (10): 922-30. Karlsson Robert, Graae Lisette, Lekman Magnus, Wang Dai, Favis Reyna, Axelsson Tomas, Galter Dagmar, Belin Andrea Carmine, Paddock Silv |
| Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. Brain imaging and behavior 2014 Jun 8 (2): 183-207. Shen Li, Thompson Paul M, Potkin Steven G, Bertram Lars, Farrer Lindsay A, Foroud Tatiana M, Green Robert C, Hu Xiaolan, Huentelman Matthew J, Kim Sungeun, Kauwe John S K, Li Qingqin, Liu Enchi, Macciardi Fabio, Moore Jason H, Munsie Leanne, Nho Kwangsik, Ramanan Vijay K, Risacher Shannon L, Stone David J, Swaminathan Shanker, Toga Arthur W, Weiner Michael W, Saykin Andrew J, |
| Novel genes for airway wall thickness identified with combined genome-wide association and expression analyses.
American journal of respiratory and critical care medicine 2015 Mar 191 (5): 547-56. Dijkstra Akkelies E, Postma Dirkje S, van Ginneken Bram, Wielpütz Mark O, Schmidt Michael, Becker Nikolaus, Owsijewitsch Michael, Kauczor Hans-Ulrich, de Koning Harry J, Lammers Jan W, Oudkerk Matthijs, Brandsma Corry-Anke, Bossé Yohan, Nickle David C, Sin Don D, Hiemstra Pieter S, Wijmenga Ciska, Smolonska Joanna, Zanen Pieter, Vonk Judith M, van den Berge Maarten, Boezen H Marike, Groen Harry J |
| 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, |
| 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 |
| The MAGI2 gene polymorphism rs2160322 is associated with Graves' disease but not with Hashimoto's thyroiditis. Journal of endocrinological investigation 2019 Jul 42 (7): 843-850. Jia X, Zhai T, Wang B, Zhang J, Zhang |
| Neuroblastoma in Adolescents and Children Older than 10 Years: Unusual Clinicopathologic and Biologic Features. Journal of pediatric hematology/oncology 2019 4 41 (8): 586-595. McCarthy Laura C, Chastain Katherine, Flatt Terrie G, Taboada Eugenio, Garola Robert, Herriges John, Cooley Linda D, Ahmed Atif |
| Polymorphism in the MAGI2 Gene Modifies the Effect of Amyloid ? on Neurodegeneration. Alzheimer disease and associated disorders 2020 Dec . Kim Hang-Rai, Lee Taeyeop, Choi Jung K, Jeong Yong, |
| MAGI2 Gene Region and Celiac Disease. Frontiers in nutrition 2019 6 187. Jauregi-Miguel Amaia, Santin Izortze, Garcia-Etxebarria Koldo, Olazagoitia-Garmendia Ane, Romero-Garmendia Irati, Sebastian-delaCruz Maialen, Irastorza Iñaki, , Castellanos-Rubio Ainara, Bilbao Jose Ram |
| Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study. Journal of biomedical science 2021 May 28 (1): 37. Williams Camilla J, Li Zhixiu, Harvey Nicholas, Lea Rodney A, Gurd Brendon J, Bonafiglia Jacob T, Papadimitriou Ioannis, Jacques Macsue, Croci Ilaria, Stensvold Dorthe, Wisloff Ulrik, Taylor Jenna L, Gajanand Trishan, Cox Emily R, Ramos Joyce S, Fassett Robert G, Little Jonathan P, Francois Monique E, Hearon Christopher M, Sarma Satyam, Janssen Sylvan L J E, Van Craenenbroeck Emeline M, Beckers Paul, Cornelissen Véronique A, Howden Erin J, Keating Shelley E, Yan Xu, Bishop David J, Bye Anja, Haupt Larisa M, Griffiths Lyn R, Ashton Kevin J, Brown Matthew A, Torquati Luciana, Eynon Nir, Coombes Jeff |
| Influence of Genetic Polymorphisms on Clinical Outcomes of Glatiramer Acetate in Multiple Sclerosis Patients. Journal of personalized medicine 2021 Oct 11 (10): . Zarzuelo-Romero María José, Pérez-Ramírez Cristina, Cura Yasmín, Carrasco-Campos María Isabel, Marangoni-Iglecias Luciana María, Ramírez-Tortosa María Carmen, Jiménez-Morales Alber |
| Implications of genetic variations, differential gene expression, and allele-specific expression on metformin response in drug-naïve type 2 diabetes. Journal of endocrinological investigation 2022 12 . Vohra M, Sharma A R, Mallya S, Prabhu N B, Jayaram P, Nagri S K, Umakanth S, Rai P |
| Bayesian mixed model analysis uncovered 21 risk loci for chronic kidney disease in boxer dogs. PLoS genetics 2023 1 19 (1): e1010599. Lingaas Frode, Tengvall Katarina, Jansen Johan Høgset, Pelander Lena, Hurst Maria H, Meuwissen Theo, Karlsson Åsa, Meadows Jennifer R S, Sundström Elisabeth, Thoresen Stein Istre, Arnet Ellen Frøysadal, Guttersrud Ole Albert, Kierczak Marcin, Hytönen Marjo K, Lohi Hannes, Hedhammar Åke, Lindblad-Toh Kerstin, Wang Ch |
| GWAS of depression in 4,520 individuals from the Russian population highlights the role of MAGI2 (S-SCAM) in the gut-brain axis.
Frontiers in genetics 2023 1 13 972196. Pinakhina Daria, Yermakovich Danat, Vergasova Ekaterina, Kasyanov Evgeny, Rukavishnikov Grigory, Rezapova Valeriia, Kolosov Nikita, Sergushichev Alexey, Popov Iaroslav, Kovalenko Elena, Ilinskaya Anna, Kim Anna, Plotnikov Nikolay, Ilinsky Valery, Neznanov Nikholay, Mazo Galina, Kibitov Alexander, Rakitko Alexander, Artomov Myky |
| Identification of biomarker associated with Trop2 in breast cancer: implication for targeted therapy. Discover oncology 2024 9 15 (1): 413. Jianguo Lai, Shuxuan Deng, Jiyuan Cao, Yongqi Ren, Zanmei Xu, Xiaofang Qi, Mian Xu, Ning Li |
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