Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Osteoporosis and COL1A2[original query] |
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Bone mineral density and five prominent candidate genes in Chinese men: associations, interaction effects and their implications. Maturitas 2005 Jun 51 (2): 199-206. Lei Shu-Feng, Zhang Yuan-Yuan, Deng Fei-Yan, Liu Man-Yuan, Liu Xiang-Hua, Zhou Xiao-Gang, Deng Hong-W |
Heterozygosity for a coding SNP in COL1A2 confers a lower BMD and an increased stroke risk. Biochemical and biophysical research communications 2009 Jul 384 (4): 501-5. Lindahl Katarina, Rubin Carl-Johan, Brändström Helena, Karlsson Magnus K, Holmberg Anna, Ohlsson Claes, Mellström Dan, Orwoll Eric, Mallmin Hans, Kindmark Andreas, Ljunggren Ost |
Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016 Jan 31 (1): 173-9. Styrkarsdottir Unnur, Thorleifsson Gudmar, Eiriksdottir Berglind, Gudjonsson Sigurjon A, Ingvarsson Thorvaldur, Center Jacqueline R, Nguyen Tuan V, Eisman John A, Christiansen Claus, Thorsteinsdottir Unnur, Sigurdsson Gunnar, Stefansson Ka |
Identification of a p.Arg708Gln variant in COL1A2 in atypical femoral fractures. Joint bone spine 2016 Dec . Funck-Brentano Thomas, Ostertag Agnes, Debiais Francoise, Fardellone Patrice, Collet Corinne, Mornet Etienne, Cohen-Solal Marti |
An insertion/deletion polymorphism within the 3'-untranslated region of COL1A2 confers susceptibility to osteoporosis. Molecular medicine reports 2016 Sep . Jiang Zhen-Song, Hao Zhen-H |
The importance of polymorphic variants of collagen 1A2 gene (COL1A2) in the development of osteopenia and osteoporosis in postmenopausal women. Ginekologia polska 2017 88 (8): 414-420. Majchrzycki Marian, Bartkowiak-Wieczorek Joanna, Bogacz Anna, Szyfter-Harris Joanna, Wolski Hubert, Klejewski Andrzej, Goch Maciej, Drews Krzysztof, Barlik Magdalena, O?arowski Marcin, Kami?ski Adam, Gryszczy?ska Agnieszka, Seremak-Mrozikiewicz Agniesz |
Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility. Frontiers in endocrinology 2018 9 380. Costantini Alice, Skarp Sini, Kämpe Anders, Mäkitie Riikka E, Pettersson Maria, Männikkö Minna, Jiao Hong, Taylan Fulya, Lindstrand Anna, Mäkitie Ou |
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal Genes. JBMR plus 2018 Jan 2 (1): 12-21. Collet Corinne, Ostertag Agnès, Ricquebourg Manon, Delecourt Marine, Tueur Giulia, Isidor Bertrand, Guillot Pascale, Schaefer Elise, Javier Rose-Marie, Funck-Brentano Thomas, Orcel Philippe, Laplanche Jean-Louis, Cohen-Solal Marti |
Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosis. Bone 2021 11 154 116253. Cohen Adi, Hostyk Joseph, Baugh Evan H, Buchovecky Christie M, Aggarwal Vimla S, Recker Robert R, Lappe Joan M, Dempster David W, Zhou Hua, Kamanda-Kosseh Mafo, Bucovsky Mariana, Stubby Julie, Goldstein David B, Shane Elizabe |
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
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- Page last updated:Mar 25, 2024
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