Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and HLA-DQA2[original query] |
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Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.
The Journal of allergy and clinical immunology 2010 Feb 125 (2): 328-335.e11. Li Xingnan, Howard Timothy D, Zheng Siqun L, Haselkorn Tmirah, Peters Stephen P, Meyers Deborah A, Bleecker Eugene |
| Psoriasis regression analysis of MHC loci identifies shared genetic variants with vitiligo. PloS one 2011 6 (11): e23089. Zhu Kun-Ju, Lv Yong-Mei, Yin Xian-Yong, Wang Zai-Xing, Sun Liang-Dan, He Su-Min, Cheng Hui, Hu Da-Yan, Zhang Zheng, Li Yang, Zuo Xian-Bo, Zhou You-Wen, Yang Sen, Fan Xing, Zhang Xue-Jun, Zhang Feng- |
| HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2012 Dec 42 (12): 12. Lasky-Su J, Himes BE, Raby BA, Klanderman BJ, Sylvia JS, Lange C, Melen E, Martinez FD, Israel E, Gauderman J, Gilliland F, Sleiman P, Hakonarson H, Celedón JC, Soto-Quiros M, Avila L, Lima JJ, Irvin CG, Peters SP, Boushey H, Chinchilli VM, Mauger D, Tantisira K, Weiss ST |
| A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese.
PloS one 2014 9 (6): e99724. Chang Su-Wei, Fann Cathy Shen-Jang, Su Wen-Hui, Wang Yu Chen, Weng Chia Chan, Yu Chia-Jung, Hsu Chia-Lin, Hsieh Ai-Ru, Chien Rong-Nan, Chu Chia-Ming, Tai Dar- |
| Deep resequencing of 131 Crohn's disease associated genes in pooled DNA confirmed three reported variants and identified eight novel variants. Gut 2015 Mar . Hong Sung Noh, Park Changho, Park Soo Jung, Lee Chang Kyun, Ye Byong Duk, Kim You Sun, Lee Seungbok, Chae Jeesoo, Kim Jong-Il, Kim Young-Ho, |
| Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
The Lancet. Respiratory medicine 2015 Oct 3 (10): 769-81. Wain Louise V, Shrine Nick, Miller Suzanne, Jackson Victoria E, Ntalla Ioanna, Soler Artigas María, Billington Charlotte K, Kheirallah Abdul Kader, Allen Richard, Cook James P, Probert Kelly, Obeidat Ma'en, Bossé Yohan, Hao Ke, Postma Dirkje S, Paré Peter D, Ramasamy Adaikalavan, , Mägi Reedik, Mihailov Evelin, Reinmaa Eva, Melén Erik, O'Connell Jared, Frangou Eleni, Delaneau Olivier, , Freeman Colin, Petkova Desislava, McCarthy Mark, Sayers Ian, Deloukas Panos, Hubbard Richard, Pavord Ian, Hansell Anna L, Thomson Neil C, Zeggini Eleftheria, Morris Andrew P, Marchini Jonathan, Strachan David P, Tobin Martin D, Hall Ian |
| Cross-phenotype analysis of Immunochip data identifies KDM4C as a relevant locus for the development of systemic vasculitis.
Annals of the rheumatic diseases 2018 1 77 (4): 589-595. Ortiz-Fernández Lourdes, Carmona Francisco David, López-Mejías Raquel, González-Escribano Maria Francisca, Lyons Paul A, Morgan Ann W, Sawalha Amr H, Merkel Peter A, Smith Kenneth G C, González-Gay Miguel A, Martín Javier, |
| Pneumonia: host susceptibility and shared genetics with pulmonary function and other traits. Clinical and experimental immunology 2019 Sep . Khadzhieva M B, Kuzovlev A N, Salnikova L |
| Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta neuropathologica 2019 Feb . Pottier Cyril, Ren Yingxue, Perkerson Ralph B, Baker Matt, Jenkins Gregory D, van Blitterswijk Marka, DeJesus-Hernandez Mariely, van Rooij Jeroen G J, Murray Melissa E, Christopher Elizabeth, McDonnell Shannon K, Fogarty Zachary, Batzler Anthony, Tian Shulan, Vicente Cristina T, Matchett Billie, Karydas Anna M, Hsiung Ging-Yuek Robin, Seelaar Harro, Mol Merel O, Finger Elizabeth C, Graff Caroline, Öijerstedt Linn, Neumann Manuela, Heutink Peter, Synofzik Matthis, Wilke Carlo, Prudlo Johannes, Rizzu Patrizia, Simon-Sanchez Javier, Edbauer Dieter, Roeber Sigrun, Diehl-Schmid Janine, Evers Bret M, King Andrew, Mesulam M Marsel, Weintraub Sandra, Geula Changiz, Bieniek Kevin F, Petrucelli Leonard, Ahern Geoffrey L, Reiman Eric M, Woodruff Bryan K, Caselli Richard J, Huey Edward D, Farlow Martin R, Grafman Jordan, Mead Simon, Grinberg Lea T, Spina Salvatore, Grossman Murray, Irwin David J, Lee Edward B, Suh EunRan, Snowden Julie, Mann David, Ertekin-Taner Nilufer, Uitti Ryan J, Wszolek Zbigniew K, Josephs Keith A, Parisi Joseph E, Knopman David S, Petersen Ronald C, Hodges John R, Piguet Olivier, Geier Ethan G, Yokoyama Jennifer S, Rissman Robert A, Rogaeva Ekaterina, Keith Julia, Zinman Lorne, Tartaglia Maria Carmela, Cairns Nigel J, Cruchaga Carlos, Ghetti Bernardino, Kofler Julia, Lopez Oscar L, Beach Thomas G, Arzberger Thomas, Herms Jochen, Honig Lawrence S, Vonsattel Jean Paul, Halliday Glenda M, Kwok John B, White Charles L, Gearing Marla, Glass Jonathan, Rollinson Sara, Pickering-Brown Stuart, Rohrer Jonathan D, Trojanowski John Q, Van Deerlin Vivianna, Bigio Eileen H, Troakes Claire, Al-Sarraj Safa, Asmann Yan, Miller Bruce L, Graff-Radford Neill R, Boeve Bradley F, Seeley William W, Mackenzie Ian R A, van Swieten John C, Dickson Dennis W, Biernacka Joanna M, Rademakers Ro |
| HLA-D and PLA2R1 risk alleles associate with recurrent primary membranous nephropathy in kidney transplant recipients. Kidney international 2020 Sep . Berchtold Lena, Letouzé Eric, Alexander Mariam Priya, Canaud Guillaume, Logt Anne-Els van de, Hamilton Patrick, Mousson Christiane, Vuiblet Vincent, Moyer Ann M, Guibert Sylvain, Mrázová Petra, Levi Charlène, Dubois Valérie, Cruzado Josep Maria, Torres Armando, Gandhi Manish J, Yousfi Nadhir, Tesar Vladimir, OndrejViklický , Hourmant Maryvonne, Moulin Bruno, Rieu Philippe, Choukroun Gabriel, Legendre Christophe, Wetzels Jack, Brenchley Paul, Ballarín Castan José Aurelio, Debiec Hanna, Ronco Pier |
| An Intergenic rs9275596 Polymorphism on Chr. 6p21 Is Associated with Multiple Sclerosis in Latvians. Medicina (Kaunas, Lithuania) 2020 Mar 56 (4): . Paramonova Natalia, Trapina Ilva, Dokane Kristine, Kalnina Jolanta, Sjakste Tatjana, Sjakste Nikola |
| Major histocompatibility complex class II polymorphic variants are associated with asthma predisposition in the Punjabi population of Lahore, Pakistan. The clinical respiratory journal 2020 Nov . Aslam Raheela, Shahid Mariam, Bano Iqbal, Ayoub Muhammad, Sabar Muhammad Farooq, Altaf Saba, Kousar Samra, Ghani Muhammad Usman, Husnain Tayyab, Shahid Ahmad A |
| Association of HLA-DQA2 and HLA-B With Moyamoya Disease in the Chinese Han Population. Neurology. Genetics 2021 Jun 7 (3): e592. Wan Jiang, Ling Wei, Zhengshan Zhang, Xianbo Zuo, Lian Duan, Kai Wa |
| Brain molecular mechanisms in Rasmussen encephalitis. Epilepsia 2022 11 64 (1): 218-230. Leitner Dominique F, Lin Ziyan, Sawaged Zacharia, Kanshin Evgeny, Friedman Daniel, Devore Sasha, Ueberheide Beatrix, Chang Julia W, Mathern Gary W, Anink Jasper J, Aronica Eleonora, Wisniewski Thomas, Devinsky Orr |
| Stratified Genetic Analysis Reveals Sex Differences In MPO-ANCA-associated Vasculitis. Rheumatology (Oxford, England) 2023 4 . Ekman Diana, Sennblad Bengt, Knight Ann, Karlsson Åsa, Rantapää-Dahlqvist Solbritt, Berglin Ewa, Stegmayr Bernd, Baslund Bo, Palm Øyvind, Haukeland Hilde, Gunnarsson Iva, Bruchfeld Annette, Segelmark Mårten, Ohlsson Sophie, Mohammad Aladdin J, Svärd Anna, Pullerits Rille, Herlitz Hans, Söderbergh Annika, Omdal Roald, Jonsson Roland, Rönnblom Lars, Eriksson Per, Lindblad-Toh Kerstin, Dahlqvist Johan |
| Proteome-wide Mendelian randomization highlights AIF1 and HLA-DQA2 as targets for primary sclerosing cholangitis. Hepatology international 2023 11 . Lanlan Chen, Yuexuan Zhao, Mingyue Li, Guoyue |
| Genome-wide identification of mA-associated single nucleotide polymorphisms in complex diseases of nervous system. Neuroscience letters 2023 10 817 137513. Fei Guo, Jingxuan Kang, Jing Xu, Siyu Wei, Junxian Tao, Yu Dong, Yingnan Ma, Hongsheng Tian, Xuying Guo, Shuo Bi, Chen Zhang, Hongchao Lv, Zhenwei Shang, Yongshuai Jiang, Mingming Zha |
| A genome-wide association study suggests new susceptibility loci for primary antiphospholipid syndrome. Arthritis & rheumatology (Hoboken, N.J.) 2024 7 . Desiré Casares-Marfil, Manuel Martínez-Bueno, Maria Orietta Borghi, Guillermo Pons-Estel, , Guillermo Reales, Yu Zuo, Gerard Espinosa, Timothy Radstake, Lucas L van den Hoogen, Chris Wallace, Joel Guthridge, Judith A James, Ricard Cervera, Pier Luigi Meroni, Javier Martin, Jason S Knight, Marta E Alarcón-Riquelme, Amr H Sawal |
- Page last reviewed:Feb 1, 2024
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