Britt I. Drögemöller
0000-0002-3348-5855
Publication & Citation Trends
Publications
0 total
Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults from the CLSA
Cited by 0
Semantic Scholar
A computational model for quantifying instability of tandem repeats across the genome
Cited by 0
Semantic Scholar
Unbiased human genomic characterization of polyglutamine disorder genes to guide biological understanding and therapeutic strategies
Cited by 0
Semantic Scholar
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.
Cited by 2
Semantic Scholar
Navigating the Genetic Risk of Chemotherapy‐Induced Hearing Loss in the Stria Vascularis
Cited by 1
Semantic Scholar
Large-scale audiometric phenotyping identifies distinct genes and pathways involved in hearing loss subtypes
Cited by 1
Semantic Scholar
Genetic Variations in Bitter Taste Receptors and COVID-19 in the Canadian Longitudinal Study on Aging
Cited by 3
Semantic Scholar
Research Topics
Genomics and Rare Diseases
(23)
Pharmacogenetics and Drug Metabolism
(19)
Genetic Associations and Epidemiology
(17)
Hearing, Cochlea, Tinnitus, Genetics
(10)
Metabolism and Genetic Disorders
(9)
Affiliations
Northwell Health
University of British Columbia
University of Alberta
University of Cape Town
Stellenbosch University