Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia-Reference-Cited by-同舟云学术

Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia

Published:2010-08-15 Issue:5 Volume:74 Page:399-405
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:

Author:

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 Guy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2010.00595.x/fullpdf

Reference31 articles.

1. The incidence of otosclerosis as related to race and sex;Altmann;Ann Otol Rhinol Laryngol,1967

2. A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9;Bel Hadj Ali;Hum Genet,2008

3. [Otosclerosis in populations living in northern Tunisia: epidemiology and etiology];Ben Arab;Ann Otolaryngol Chir Cervicofac,2001

4. Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus;Brownstein;Arch Otolaryngol Head Neck Surg,2006

5. Replicating genotype-phenotype associations;Chanock;Nature,2007

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1. Targeted Resequencing of Otosclerosis Patients from Different Populations Replicates Results from a Previous Genome-Wide Association Study;Journal of Clinical Medicine;2022-11-26

2. The risks of RELN polymorphisms and its expression in the development of otosclerosis;PLOS ONE;2022-06-03

3. Genetics of otosclerosis: finally catching up with other complex traits?;Human Genetics;2021-09-09

4. Analysis of major otosclerosis-associated variants in RELN and TGFB1 genes in Polish patients;Archives of Medical Science;2020-09-16

5. Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis;BMC Medical Genetics;2020-06-03