Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and TNFSF11[original query] |
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| Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms. Molecular genetics and metabolism 2011 Jul 103 (3): 287-92. Chung Pui Yan Jenny, Beyens Greet, de Freitas Fenna, Boonen Steven, Geusens Piet, Vanhoenacker Filip, Verbruggen Leon, Van Offel Jan, Goemaere Stefan, Zmierczak Hans-Georg, Westhovens René, Devogelaer Jean-Pierre, Van Hul W |
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.
Human molecular genetics 2012 Aug . Juran BD, Hirschfield GM, Invernizzi P, Atkinson EJ, Li Y, Xie G, Kosoy R, Ransom M, Sun Y, Bianchi I, Schlicht EM, Lleo A, Coltescu C, Bernuzzi F, Podda M, Lammert C, Shigeta R, Chan LL, Balschun T, Marconi M, Cusi D, Mason AL, Myers RP, Milkiewicz P, Odin JA, Luketic VA, Bacon BR, Bodenheimer HC, Liakina V, Vincent C, Levy C, Franke A, Gregersen PK, Bossa F, Gershwin ME, Deandrade M, Amos CI, Lazaridis KN, Seldin MF, Siminovitch KA |
| Are bone mineral density loci associated with hip osteoporotic fractures? A validation study on previously reported genome-wide association loci in a Chinese population. Genetics and molecular research : GMR 2012 11 (1): 202-10. Guo Y, Wang J-T, Liu H, Li M, Yang T-L, Zhang X-W, Liu Y-Z, Tian Q, Deng H |
| Association of osteoporosis susceptibility genes with bone mineral density and bone metabolism related markers in Koreans: the Chungju Metabolic Disease Cohort (CMC) study. Endocrine journal 2014 Nov 61 (11): 1069-78. Park Se Eun, Oh Ki Won, Lee Won Young, Baek Ki Hyun, Yoon Kun Ho, Son Ho Young, Lee Won Chul, Kang Moo |
| Periodontal Initial Radiological Findings of Genetically Predisposed Finnish Adolescents. Journal of clinical and diagnostic research : JCDR 2017 07 11 (7): ZC25-ZC28. Heikkinen Anna Maria, Pakbaznejad Esmaeili Elmira, Kovanen Leena, Ruokonen Hellevi, Kettunen Kaisa, Haukka Jari, Tervahartiala Taina, Sorsa Ti |
| Receptor activator of nuclear factor kappa-B ligand (RANKL) but not sclerostin or gene polymorphisms is related to joint destruction in early rheumatoid arthritis. Clinical rheumatology 2017 Feb . Boman Antonia, Kokkonen Heidi, Ärlestig Lisbeth, Berglin Ewa, Rantapää-Dahlqvist Solbri |
| VDR and TNFSF11 polymorphisms are associated with osteoporosis in Thai patients. Biomedical reports 2018 Oct 9 (4): 350-356. Techapatiphandee Mananya, Tammachote Nattapol, Tammachote Rachaneekorn, Wongkularb Anna, Yanatatsaneejit Pattamawad |
| The Influence of TLR4, CD14, OPG, and RANKL Polymorphisms in Periodontitis: A Case-Control Study. Mediators of inflammation 2019 7 2019 4029217. Zacarias Joana Maira Valentini, de Alencar Josiane Bazzo, Tsuneto Patrícia Yumeko, de Souza Victor Hugo, Silva Cléverson O, Visentainer Jeane Eliete Laguila, Sell Ana Mar |
| Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss. Frontiers in medicine 2022 5 9 870244. Bouzid Amal, Chelly Ameni, Tekari Adel, Singh Neha, Hansdah Kirtal, Achour Imen, Ben Ayed Ikhlas, Jbeli Fida, Charfeddine Ilhem, Ramchander Puppala Venkat, Hamoudi Rifat, Masmoudi Sab |
| Autoimmune hypothyroidism GWAS reveals independent autoimmune and thyroid-specific contributions and an inverse relation with cancer risk. Research square 2024 7 . Mary Reeve, Masahiro Kanai, Daniel Graham, Juha Karjalainen, Shuang Luo, Nikita Kolosov, Cameron Adams, Jarmo Ritari, Konrad Karczewski, Tuomo Kiiskinen, Zachary Fuller, Juha Mehtonen, Mitja Kurki, Zia Khan, Jukka Partanen, Mark McCarthy, Mykyta Artomov, Tiinamaija Tuomi, Matti Pirinen, Jukka Kero, Ramnik Xavier, Mark Daly, Samuli Ripatti, Finn G |
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