Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 41 Records) |
| Query Trace: Disease and CLEC16A[original query] |
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| Genetic risk for myocardial infarction in Japanese individuals with or without chronic kidney disease. International journal of molecular medicine 2010 May 25 (5): 743-9. Fujimaki Tetsuo, Kato Kimihiko, Yokoi Kiyoshi, Yoshida Tetsuro, Oguri Mitsutoshi, Watanabe Sachiro, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Nozawa Yoshinori, Yamada Yoshi |
| Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients. PloS one 2010 5 (4): e10003. Jensen Cathy J, Stankovich Jim, Van der Walt Anneke, Bahlo Melanie, Taylor Bruce V, van der Mei Ingrid A F, Foote Simon J, Kilpatrick Trevor J, Johnson Laura J, Wilkins Ella, Field Judith, Danoy Patrick, Brown Matthew A, , Rubio Justin P, Butzkueven Helm |
| Genetic analysis of adult-onset autoimmune diabetes. Diabetes 2011 Oct 60 (10): 2645-53. Howson Joanna M M, Rosinger Silke, Smyth Deborah J, Boehm Bernhard O, , Todd John |
| No influence on disease progression of non-HLA susceptibility genes in MS. Journal of neuroimmunology 2011 Aug 237 (1-2): 98-100. Lundström Wangko, Greiner Eva, Lundmark Frida, Westerlind Helga, Smestad Cathrine, Lorentzen Aslaug R, Kockum Ingrid, Link Jenny, Brynedal Boel, Celius Elisabeth G, Harbo Hanne F, Masterman Thomas, Hillert J |
| Analysis of the HLA and non-HLA susceptibility loci in Japanese type 1 diabetes. Diabetes/metabolism research and reviews 2011 Nov 27 (8): 844-8. Yamashita Hisakuni, Awata Takuya, Kawasaki Eiji, Ikegami Hiroshi, Tanaka Shoichiro, Maruyama Taro, Shimada Akira, Nakanishi Koji, Takahashi Kazuma, Kobayashi Tetsuro, Kawabata Yumiko, Miyashita Yumi, Kurihara Susumu, Morita-Ohkubo Tomoko, Katayama Shigehiro, |
| Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus. Genes and immunity 2012 Nov . Leikfoss IS, Mero IL, Dahle MK, Lie BA, Harbo HF, Spurkland A, Berge T |
| Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes. Genes and immunity 2012 Dec 13 (8): 632-40. Gyllenberg A, Asad S, Piehl F, Swanberg M, Padyukov L, Van Yserloo B, Rutledge E A, McNeney B, Graham J, Orho-Melander M, Lindholm E, Graff C, Forsell C, Akesson K, Landin-Olsson M, Carlsson A, Forsander G, Ivarsson S A, Larsson H, Lindblad B, Ludvigsson J, Marcus C, Lernmark A, Alfredsson L, Akesson K, Olsson T, Kockum I, , , |
| Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. Diabetes 2014 Dec 63 (12): 4360-8. Tomlinson M Joseph, Pitsillides Achilleas, Pickin Rebecca, Mika Matthew, Keene Keith L, Hou Xuanlin, Mychaleckyj Josyf, Chen Wei-Min, Concannon Patrick, Onengut-Gumuscu Su |
| Polymorphisms of CLEC16A region and autoimmune thyroid diseases. G3 (Bethesda, Md.) 2014 Jun 4 (6): 973-7. Muhali Fatuma-Said, Cai Tian-Tian, Zhu Jiao-Li, Qin Qiu, Xu Jian, He Shuang-Tao, Shi Xiao-Hong, Jiang Wen-Juan, Xiao Ling, Li Dan-Feng, Zhang Jin- |
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.
The Journal of allergy and clinical immunology 2014 Jun 133 (6): 1564-71. Ferreira Manuel A R, Matheson Melanie C, Tang Clara S, Granell Raquel, Ang Wei, Hui Jennie, Kiefer Amy K, Duffy David L, Baltic Svetlana, Danoy Patrick, Bui Minh, Price Loren, Sly Peter D, Eriksson Nicholas, Madden Pamela A, Abramson Michael J, Holt Patrick G, Heath Andrew C, Hunter Michael, Musk Bill, Robertson Colin F, Le Souëf Peter, Montgomery Grant W, Henderson A John, Tung Joyce Y, Dharmage Shyamali C, Brown Matthew A, James Alan, Thompson Philip J, Pennell Craig, Martin Nicholas G, Evans David M, Hinds David A, Hopper John L, |
| Variability in the CIITA gene interacts with HLA in multiple sclerosis. Genes and immunity 0 15 (3): 162-7. Gyllenberg A, Piehl F, Alfredsson L, Hillert J, Bomfim I L, Padyukov L, Orho-Melander M, Lindholm E, Landin-Olsson M, Lernmark Å, , , Olsson T, Kockum |
| Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.
Circulation. Cardiovascular genetics 2015 Aug 8 (4): 628-36. Proust Carole, Empana Jean-Philippe, Boutouyrie Pierre, Alivon Maureen, Challande Pascal, Danchin Nicolas, Escriou Guillaume, Esslinger Ulrike, Laurent Stéphane, Li Zhenlin, Pannier Bruno, Regnault Veronique, Thomas Frederique, Jouven Xavier, Cambien François, Lacolley Patri |
| Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability. Neurogenetics 2015 Jul 16 (3): 161-8. Akkad Denis A, Bellenberg Barbara, Esser Sarika, Weiler Florian, Epplen Jörg T, Gold Ralf, Lukas Carsten, Haghikia Aid |
| A variant of CLEC16A gene confers protection for Vogt-Koyanagi-Harada syndrome but not for Behcet's disease in a Chinese Han population. Experimental eye research 2015 Mar 132 225-30. Li Ke, Hou Shengping, Qi Jian, Kijlstra Aize, Yang Peize |
| Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis.
Genes and immunity 2018 Jun . Kottyan Leah C, Maddox Avery, Braxton Julian R, Stucke Emily M, Mukkada Vince, Putnam Philip E, Abonia J Pablo, Chehade Mirna, Wood Robert A, Pesek Robbie D, Vickery Brian P, Furuta Glenn T, Dawson Peter, Sampson Hugh A, Martin Lisa J, Kelly Jennifer A, Kimberly Robert P, Sivils Kathy, Gaffney Patrick M, Kaufman Kenneth, Harley John B, Rothenberg Marc |
| Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.
PloS one 2018 13 (1): e0189498. Gorlova Olga Y, Li Yafang, Gorlov Ivan, Ying Jun, Chen Wei V, Assassi Shervin, Reveille John D, Arnett Frank C, Zhou Xiaodong, Bossini-Castillo Lara, Lopez-Isac Elena, Acosta-Herrera Marialbert, Gregersen Peter K, Lee Annette T, Steen Virginia D, Fessler Barri J, Khanna Dinesh, Schiopu Elena, Silver Richard M, Molitor Jerry A, Furst Daniel E, Kafaja Suzanne, Simms Robert W, Lafyatis Robert A, Carreira Patricia, Simeon Carmen Pilar, Castellvi Ivan, Beltran Emma, Ortego Norberto, Amos Christopher I, Martin Javier, Mayes Maureen |
| Post-mortem multiple sclerosis lesion pathology is influenced by single nucleotide polymorphisms. Brain pathology (Zurich, Switzerland) 2019 6 30 (1): 106-119. Fransen Nina L, Crusius Jakob B A, Smolders Joost, Mizee Mark R, van Eden Corbert G, Luchetti Sabina, Remmerswaal Ester B M, Hamann Jörg, Mason Matthew R J, Huitinga In |
| [The analysis of association between multiple sclerosis and genetic markers identified in genome-wide association studies]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2020 8 120 (7. Vyp. 2): 54-60. Timasheva Y R, Nasibullin T R, Tuktarova I A, Erdman V V, Galiullin T R, Zaplakhova O V, Bakhtiiarova K Z, Mustafina O |
| Mitonuclear interactions influence multiple sclerosis risk. Gene 2020 Jul 144962. Kozin Maxim, Kulakova Olga, Kiselev Ivan, Baulina Natalia, Boyko Alexey, Favorova Ol |
| Replication study of susceptibility variants associated with allergic rhinitis and allergy in Han Chinese. Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2020 16 13. Gao Yunbo, Li Jingyun, Zhang Yuan, Zhang L |
| Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.
Brain sciences 2020 Nov 10 (11): . Rebelo Miguel Ângelo, Gómez Carlos, Gomes Iva, Poza Jesús, Martins Sandra, Maturana-Candelas Aarón, Ruiz-Gómez Saúl J, Durães Luis, Sousa Patrícia, Figueruelo Manuel, Rodríguez María, Pita Carmen, Arenas Miguel, Álvarez Luis, Hornero Roberto, Pinto Nádia, Lopes Alexandra |
| Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.
Clinical rheumatology 2021 Jun . Nikopensius Tiit, Niibo Priit, Haller Toomas, Jagomägi Triin, Voog-Oras Ülle, Tõnisson Neeme, Metspalu Andres, Saag Mare, Pruunsild Chr |
| Type 1 Diabetes and Autoimmune Thyroid Disease-The Genetic Link. Frontiers in endocrinology 2021 3 12 618213. Frommer Lara, Kahaly George |
| 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 |
| Autoimmune Disease Associated CLEC16A Variants Convey Risk of Parkinson's Disease in Han Chinese. Frontiers in genetics 2022 4 13 856493. Fan Hui-Hui, Cui Lei, Jiang Xiao-Xia, Song Ya-Dan, Liu Shu-Shu, Wu Ke-Yun, Dong Hao-Jia, Mao Miao, Ovlyakulov Begench, Wu Hong-Mei, Zhu Jian-Hong, Zhang Xio |
| HLA signatures as pathophysiological discriminants of microscopic colitis subtypes. Journal of Crohn's & colitis 2023 9 . Tenghao Zheng, Giulia Roda, Yamile Zabana, Celia Escudero-Hernández, Xingrong Liu, Ye Chen, Leticia Camargo Tavares, Ferdinando Bonfiglio, Marie-Rose Mellander, Izabella Janczewska, Lina Vigren, Klas Sjöberg, Bodil Ohlsson, Sven Almer, Jonas Halfvarson, Stephan Miehlke, Ahmed Madisch, Wolfgang Lieb, Juozas Kup?inskas, Rinse K Weersma, Luis Bujanda, Antonio Julià, Sara Marsal, Maria Esteve, Danila Guagnozzi, Fernando Fernández-Bañares, Carmen Ferrer, , Inga Peter, Jonas F Ludvigsson, Darrell Pardi, Bas Verhaegh, Daisy Jonkers, Marieke Pierik, Andreas Münch, Andre Franke, Francesca Bresso, Hamed Khalili, Jean-Frederic Colombel, Mauro D'Ama |
| CTLA4, SH2B3 and CLEC16A diversely affect the progression of early islet autoimmunity in relatives of type 1 diabetes patients. Clinical and experimental immunology 2023 1 . Vandewalle Julie, Desouter Aster K, Van der Auwera Bart J, Tenoutasse Sylvie, Gillard Pieter, De Block Christophe, Keymeulen Bart, Gorus Frans K, Van de Casteele Mark, |
| CLEC16A variants conferred a decreased risk to allergic rhinitis in the Chinese population. Frontiers in genetics 2023 1 13 1053761. Niu Yongliang, Wang Haiying, Li Zhengqing, Shamsi Bilal Haider, Liu Mingxia, Liu Juan, Wang Qiang, Liu Yongl |
| Prevalence of Selected Polymorphisms of Il7R, CD226, CAPSL, and CLEC16A Genes in Children and Adolescents with Autoimmune Thyroid Diseases. International journal of molecular sciences 2024 4 25 (7): . Hanna Borysewicz-Sa?czyk, Natalia Wawrusiewicz-Kurylonek, Joanna Go?cik, Beata Sawicka, Filip Bossowski, Domenico Corica, Tommaso Aversa, Ma?gorzata Wa?niewska, Artur Bossows |
| Trio-based exome sequencing and high-resolution HLA typing in families of patients with autoimmune adrenal insufficiency and autoimmune polyglandular syndrome. PloS one 2024 10 19 (10): e0312335. Anastasiia Buianova, Marina Yukina, Valery Cheranev, Oleg Suchalko, Anna Shmitko, Alina Samitova, Nurana Nuralieva, Elena Kulagina, Elena Savvateeva, Ekaterina Troshina, Denis Rebrikov, Dmitry Gryadunov, Dmitriy Korost |
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