Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: ADAMTS3[original query] |
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Genetic association analysis of the IGFBP7, ADAMTS3, and IL8 genes as the potential osteoarthritis susceptibility that maps to chromosome 4q. Annals of the rheumatic diseases 2005 Mar 64 (3): 474-6. Kawahara C, Forster T, Chapman K, Carr A, Loughlin |
Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival. Molecular carcinogenesis 2017 Aug . Xu Yinghui, Wang Yanru, Liu Hongliang, Shi Qiong, Zhu Dakai, Amos Christopher I, Fang Shenying, Lee Jeffrey E, Hyslop Terry, Li Xin, Han Jiali, Wei Qing |
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
PLoS genetics 2017 Oct 13 (10): e1007079. Davis James P, Huyghe Jeroen R, Locke Adam E, Jackson Anne U, Sim Xueling, Stringham Heather M, Teslovich Tanya M, Welch Ryan P, Fuchsberger Christian, Narisu Narisu, Chines Peter S, Kangas Antti J, Soininen Pasi, Ala-Korpela Mika, Kuusisto Johanna, Collins Francis S, Laakso Markku, Boehnke Michael, Mohlke Karen |
Explorative results from multistep screening for potential genetic risk loci of Alzheimer's disease in the longitudinal VITA study cohort. Journal of neural transmission (Vienna, Austria : 1996) 2018 01 125 (1): 77-87. Scholz Claus-Jürgen, Weber Heike, Jungwirth Susanne, Danielczyk Walter, Reif Andreas, Tragl Karl-Heinz, Fischer Peter, Riederer Peter, Deckert Jürgen, Grünblatt Ed |
An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. PLoS genetics 2019 5 15 (5): e1008102. Marchant Thomas W, Dietschi Elisabeth, Rytz Ulrich, Schawalder Peter, Jagannathan Vidhya, Hadji Rasouliha Sheida, Gurtner Corinne, Waldvogel Andreas S, Harrington Ronan S, Drögemüller Michaela, Kidd Jeffrey, Ostrander Elaine A, Warr Amanda, Watson Mick, Argyle David, Ter Haar Gert, Clements Dylan N, Leeb Tosso, Schoenebeck Jeffrey |
Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American journal of medical genetics. Part A 2019 10 182 (1): 189-194. Boone Philip M, Paterson Scott, Mohajeri Kiana, Zhu Wenmiao, Genetti Casie A, Tai Derek J C, Nori Neeharika, Agrawal Pankaj B, Bacino Carlos A, Bi Weimin, Talkowski Michael E, Hogan Benjamin M, Rodan Lance |
CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations. Frontiers in psychiatry 2021 1 11 606372. Gregoric Kumperscak Hojka, Krgovic Danijela, Drobnic Radobuljac Maja, Senica Nina, Zagorac Andreja, Kokalj Vokac Nad |
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