Charity Nofziger
Publications by Year
Research Areas
Pharmacogenetics and Drug Metabolism, Hearing, Cochlea, Tinnitus, Genetics, Asthma and respiratory diseases, Ion channel regulation and function, Ion Transport and Channel Regulation
Most-Cited Works
- → PharmVar GeneFocus: CYP2D6(2019)236 cited
- → Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA(2008)112 cited
- → Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome(2009)101 cited
- → Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation(2010)90 cited
- → Targeting SREBPs for treatment of the metabolic syndrome(2015)88 cited
- → Pharmacogenetics in the evaluation of new drugs: a multiregional regulatory perspective(2013)72 cited
- → Molecular and Functional Characterization of Human Pendrin and its Allelic Variants(2011)61 cited
- → STAT6 Links IL-4/IL-13 Stimulation With Pendrin Expression in Asthma and Chronic Obstructive Pulmonary Disease(2011)55 cited
- → PPARγ agonists do not directly enhance basal or insulin-stimulated Na+ transport via the epithelial Na+ channel(2005)54 cited
- → Identification of Allelic Variants of Pendrin (SLC26A4) with Loss and Gain of Function(2011)50 cited