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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 7, 2024. (Total: 234175Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Autoimmune Diseases and DHCR7[original query]
Inherited variation in vitamin D genes is associated with predisposition to autoimmune disease type 1 diabetes.
Diabetes 2011 May 60 (5): 1624-31.
Cooper Jason D, Smyth Deborah J, Walker Neil M, Stevens Helen, Burren Oliver S, Wallace Chris, Greissl Christopher, Ramos-Lopez Elizabeth, Hyppönen Elina, Dunger David B, Spector Timothy D, Ouwehand Willem H, Wang Thomas J, Badenhoop Klaus, Todd John
Polymorphisms in genetics of vitamin D metabolism confer susceptibility to ocular Behçet disease in a Chinese Han population.
American journal of ophthalmology 2014 Feb 157 (2): 488-494.e6.
Fang Jing, Hou Shengping, Xiang Qin, Qi Jian, Yu Hongsong, Shi Yanyun, Zhou Yan, Kijlstra Aize, Yang Peize
Single nucleotide polymorphisms in the vitamin D pathway associating with circulating concentrations of vitamin D metabolites and non-skeletal health outcomes: Review of genetic association studies.
The Journal of steroid biochemistry and molecular biology 2015 Dec .
Jolliffe David A, Walton Robert T, Griffiths Christopher J, Martineau Adrian
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. GWAS Catalog
Nature communications 2018 Jan 9 (1): 260.
Jiang Xia, O'Reilly Paul F, Aschard Hugues, Hsu Yi-Hsiang, Richards J Brent, Dupuis Josée, Ingelsson Erik, Karasik David, Pilz Stefan, Berry Diane, Kestenbaum Bryan, Zheng Jusheng, Luan Jianan, Sofianopoulou Eleni, Streeten Elizabeth A, Albanes Demetrius, Lutsey Pamela L, Yao Lu, Tang Weihong, Econs Michael J, Wallaschofski Henri, Völzke Henry, Zhou Ang, Power Chris, McCarthy Mark I, Michos Erin D, Boerwinkle Eric, Weinstein Stephanie J, Freedman Neal D, Huang Wen-Yi, Van Schoor Natasja M, van der Velde Nathalie, Groot Lisette C P G M de, Enneman Anke, Cupples L Adrienne, Booth Sarah L, Vasan Ramachandran S, Liu Ching-Ti, Zhou Yanhua, Ripatti Samuli, Ohlsson Claes, Vandenput Liesbeth, Lorentzon Mattias, Eriksson Johan G, Shea M Kyla, Houston Denise K, Kritchevsky Stephen B, Liu Yongmei, Lohman Kurt K, Ferrucci Luigi, Peacock Munro, Gieger Christian, Beekman Marian, Slagboom Eline, Deelen Joris, Heemst Diana van, Kleber Marcus E, März Winfried, de Boer Ian H, Wood Alexis C, Rotter Jerome I, Rich Stephen S, Robinson-Cohen Cassianne, den Heijer Martin, Jarvelin Marjo-Riitta, Cavadino Alana, Joshi Peter K, Wilson James F, Hayward Caroline, Lind Lars, Michaëlsson Karl, Trompet Stella, Zillikens M Carola, Uitterlinden Andre G, Rivadeneira Fernando, Broer Linda, Zgaga Lina, Campbell Harry, Theodoratou Evropi, Farrington Susan M, Timofeeva Maria, Dunlop Malcolm G, Valdes Ana M, Tikkanen Emmi, Lehtimäki Terho, Lyytikäinen Leo-Pekka, Kähönen Mika, Raitakari Olli T, Mikkilä Vera, Ikram M Arfan, Sattar Naveed, Jukema J Wouter, Wareham Nicholas J, Langenberg Claudia, Forouhi Nita G, Gundersen Thomas E, Khaw Kay-Tee, Butterworth Adam S, Danesh John, Spector Timothy, Wang Thomas J, Hyppönen Elina, Kraft Peter, Kiel Douglas
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing.
Brain and behavior 2019 3 9 (4): e01272.
Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor
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