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Richard J. Smith

Publications by Year

Research Areas

Hearing, Cochlea, Tinnitus, Genetics, Complement system in diseases, Renal Diseases and Glomerulopathies, Vestibular and auditory disorders, Ear Surgery and Otitis Media

Most-Cited Works

→ A common haplotype in the complement regulatory gene factor H ( HF1/CFH ) predisposes individuals to age-related macular degeneration(2005)1,958 cited
→ Sensorineural hearing loss in children(2005)828 cited
→ Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference(2016)680 cited
→ C3 glomerulopathy: consensus report(2013)627 cited
→ Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss(2016)578 cited
→ A candidate prostate cancer susceptibility gene at chromosome 17p(2001)555 cited

→ Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23(2001)

552 cited

→ GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study(2005)551 cited

→ Congenital hearing loss(2017)521 cited

→ Congenital Cytomegalovirus Infection(1977)491 cited