Carla Nishimura
University of Iowa(US)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connexins and lens biology, Complement system in diseases, Renal Diseases and Glomerulopathies, Vestibular and auditory disorders
Most-Cited Works
- → Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss(2016)578 cited
- → GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study(2005)551 cited
- → Genomic Landscape and Mutational Signatures of Deafness-Associated Genes(2018)314 cited
- → Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome(2010)306 cited
- → Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)(2005)215 cited
- → Copy number variants are a common cause of non-syndromic hearing loss(2014)194 cited
- → Causes of Alternative Pathway Dysregulation in Dense Deposit Disease(2012)181 cited
- → Genetic Association Studies of Cleft Lip and/or Palate With Hypodontia Outside the Cleft Region(2003)115 cited
- → Association of Specific Language Impairment (SLI) to the Region of 7q31(2003)114 cited
- → High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies(2015)113 cited