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EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, 09/2019, Volume 27, Issue 9, pp. 1456 - 1465
Hearing impairment (HI) is characterized by extensive genetic heterogeneity. To determine the population-specific contribution of known autosomal recessive... 
GENE-MUTATIONS | ALLELES | MYO15A | CONNEXIN-26 | BIOCHEMISTRY & MOLECULAR BIOLOGY | FREQUENCY | GENETICS & HEREDITY | PHENOTYPE | POPULATIONS | DEAFNESS | SPECTRUM | GJB6 MUTATIONS | African Americans | Deafness | Population studies | Hearing impairment | Etiology | Hearing loss
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2012, Volume 44, Issue 8, pp. 916 - 921
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2013, Volume 93, Issue 1, pp. 132 - 140
Journal Article
Journal Article
Acta Medica Philippina, ISSN 0001-6071, 2013, Volume 47, Issue 4, pp. 52 - 57
Journal Article
Bioinformatics, ISSN 1367-4803, 08/2014, Volume 30, Issue 16, pp. 2377 - 2378
Motivation: Statistical methods have been developed to test for complex trait rare variant (RV) associations, in which variants are aggregated across a region,... 
RARE VARIANTS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENOME | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Genetic Variation | Data Interpretation, Statistical | Phenotype | Sample Size | Disease - genetics | Humans | Alleles | Genetic Association Studies - methods | Software | Sequence Analysis, DNA - methods | Applications Notes
Journal Article
Human Mutation, ISSN 1059-7794, 01/2019, Volume 40, Issue 1, pp. 53 - 72
Journal Article