Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Otosclerosis and RELN[original query] |
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A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
American journal of human genetics 2009 Mar 84 (3): 328-38. Schrauwen Isabelle, Ealy Megan, Huentelman Matthew J, Thys Melissa, Homer Nils, Vanderstraeten Kathleen, Fransen Erik, Corneveaux Jason J, Craig David W, Claustres Mireille, Cremers Cor W R J, Dhooge Ingeborg, Van de Heyning Paul, Vincent Robert, Offeciers Erwin, Smith Richard J H, Van Camp G |
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations. Human genetics 2010 Feb 127 (2): 155-62. Schrauwen Isabelle, Ealy Megan, Fransen Erik, Vanderstraeten Kathleen, Thys Melissa, Meyer Nicole C, Cosgarea Marcel, Huber Alex, Mazzoli Manuela, Pfister Markus, Smith Richard J H, Van Camp G |
Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia. Annals of human genetics 2010 Sep 74 (5): 399-405. Khalfallah Ayda, Schrauwen Isabelle, Mnaja Malek, Fransen Erik, Lahmar Imed, Ealy Megan, Dhouib Leila, Ayadi Hammadi, Charfedine Ilhem, Driss Nabil, Ghorbel Abdelmonem, Smith Richard J H, Masmoudi Saber, Van Camp G |
Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India. Genetics and molecular research : GMR 2010 9 (3): 1914-20. Priyadarshi S, Panda K C, Panda A K, Ramchander P |
The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population. Acta otorhinolaryngologica Italica : organo ufficiale della Società italiana di otorinolaringologia e chirurgia cervico-facciale 2013 Oct 33 (5): 320-3. Iossa S, Corvino V, Giannini P, Salvato R, Cavaliere M, Panetti M, Panetti G, Piantedosi B, Marciano E, Franzè |
Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2014 Jul 35 (6): 1058-64. Sommen Manou, Van Camp Guy, Liktor Balázs, Csomor Péter, Fransen Erik, Sziklai István, Schrauwen Isabelle, Karosi Tam |
Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. Human genetics 2018 May . Mowat Andrew J, Crompton Michael, Ziff Joanna L, Aldren Christopher P, Lavy Jeremy A, Saeed Shakeel R, Dawson Sally |
Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis. BMC medical genetics 2020 6 21 (1): 122. Bouzid Amal, Tekari Adel, Jbeli Fida, Chakroun Amine, Hansdah Kirtal, Souissi Amal, Singh Neha, Mosrati Mohamed Ali, Achour Imen, Ghorbel Abdelmonem, Charfeddine Ilhem, Ramchander Puppala Venkat, Masmoudi Sab |
The risks of RELN polymorphisms and its expression in the development of otosclerosis. PloS one 2022 17 (6): e0269558. Priyadarshi Saurabh, Hansdah Kirtal, Singh Neha, Bouzid Amal, Ray Chinmay Sundar, Panda Khirod Chandra, Biswal Narayan Chandra, Desai Ashim, Choudhury Jyotish Chandra, Tekari Adel, Masmoudi Saber, Ramchander Puppala Venk |
Targeted Resequencing of Otosclerosis Patients from Different Populations Replicates Results from a Previous Genome-Wide Association Study. Journal of clinical medicine 2022 12 11 (23): . Tavernier Lisse J M, Vanpoucke Thomas, Schrauwen Isabelle, Van Camp Guy, Fransen Er |
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
Nature communications 2023 1 14 (1): 157. Rämö Joel T, Kiiskinen Tuomo, Seist Richard, Krebs Kristi, Kanai Masahiro, Karjalainen Juha, Kurki Mitja, Hämäläinen Eija, Häppölä Paavo, Havulinna Aki S, Hautakangas Heidi, , Mägi Reedik, Palta Priit, Esko Tõnu, Metspalu Andres, Pirinen Matti, Karczewski Konrad J, Ripatti Samuli, Milani Lili, Stankovic Konstantina M, Mäkitie Antti, Daly Mark J, Palotie Aar |
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