Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and MAFB[original query] |
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Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.
Molecular medicine (Cambridge, Mass.) 0 14 (9-10): 575-81. Liu Chunyu, Batliwalla Franak, Li Wentian, Lee Annette, Roubenoff Ronenn, Beckman Evan, Khalili Houman, Damle Aarti, Kern Marlena, Furie Richard, Dupuis Josée, Plenge Robert M, Coenen Marieke J H, Behrens Timothy W, Carulli John P, Gregersen Peter |
| Common variants at 30 loci contribute to polygenic dyslipidemia.
Nature genetics 2009 Jan 41 (1): 56-65. Kathiresan Sekar, Willer Cristen J, Peloso Gina M, Demissie Serkalem, Musunuru Kiran, Schadt Eric E, Kaplan Lee, Bennett Derrick, Li Yun, Tanaka Toshiko, Voight Benjamin F, Bonnycastle Lori L, Jackson Anne U, Crawford Gabriel, Surti Aarti, Guiducci Candace, Burtt Noel P, Parish Sarah, Clarke Robert, Zelenika Diana, Kubalanza Kari A, Morken Mario A, Scott Laura J, Stringham Heather M, Galan Pilar, Swift Amy J, Kuusisto Johanna, Bergman Richard N, Sundvall Jouko, Laakso Markku, Ferrucci Luigi, Scheet Paul, Sanna Serena, Uda Manuela, Yang Qiong, Lunetta Kathryn L, Dupuis Josée, de Bakker Paul I W, O'Donnell Christopher J, Chambers John C, Kooner Jaspal S, Hercberg Serge, Meneton Pierre, Lakatta Edward G, Scuteri Angelo, Schlessinger David, Tuomilehto Jaakko, Collins Francis S, Groop Leif, Altshuler David, Collins Rory, Lathrop G Mark, Melander Olle, Salomaa Veikko, Peltonen Leena, Orho-Melander Marju, Ordovas Jose M, Boehnke Michael, Abecasis Gonçalo R, Mohlke Karen L, Cupples L Adrien |
| Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis. Journal of human genetics 2012 Jun 57 (6): 363-7. Mahasirimongkol Surakameth, Yanai Hideki, Mushiroda Taisei, Promphittayarat Watoo, Wattanapokayakit Sukanya, Phromjai Jurairat, Yuliwulandari Rika, Wichukchinda Nuanjun, Yowang Amara, Yamada Norio, Kantipong Patcharee, Takahashi Atsushi, Kubo Michiaki, Sawanpanyalert Pathom, Kamatani Naoyuki, Nakamura Yusuke, Tokunaga Katsus |
| Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study. Lipids in health and disease 2015 14 (1): 79. Yang Qian, Yin Rui-Xing, Zhou Yi-Jiang, Cao Xiao-Li, Guo Tao, Chen Wu-Xi |
| Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
| Association of genetic polymorphisms of VAX1, MAFB, and NTN1 with nonsyndromic cleft lip with or without cleft palate in Chinese population. Molecular genetics and genomics : MGG 2022 Feb . Peng Li, Niu Zhenmin, Chen Jiapei, Wan Teng, Wu Dandan, Yang Yusheng, Wang Guomin, Yang Lin, Huang Wei, Chen Zhen |
| Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease. Diabetologia 2024 8 . Jani K Haukka, Anni A Antikainen, Erkka Valo, Anna Syreeni, Emma H Dahlström, Bridget M Lin, Nora Franceschini, Andrzej S Krolewski, Valma Harjutsalo, Per-Henrik Groop, Niina Sandholm, |
| Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis. Genes 2024 4 15 (4): . Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda, Júlia Lôndero Heleno, Josep Jorente, On Behalf Of The Rare Genomes Project Consortium, Társis Paiva Vieira, Carlos Eduardo Stein |
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