# Richard J. Smith

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/richard-j-smith/

## Facts

| Field | Value |
| --- | --- |
| Citations | 52,853 |
| Field | Hearing, Cochlea, Tinnitus, Genetics |
| h-index | 114 |
| i10-index | 683 |
| Last Known Institution | University of Iowa |
| OpenAlex ID | https://openalex.org/A5014833790 |
| ORCID iD | 0000-0003-1201-6731 |
| Works | 1,416 |

## Researcher papers

Showing 12 of 19.

- [A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration](https://scholariq.org/papers/a-common-haplotype-in-the-complement-regulatory-gene-factor-h-i-hf1-cfh-i/)
- [Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference](https://scholariq.org/papers/atypical-hemolytic-uremic-syndrome-and-c3-glomerulopathy-conclusions-from-a/)
- [C3 glomerulopathy: consensus report](https://scholariq.org/papers/c3-glomerulopathy-consensus-report/)
- [Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss](https://scholariq.org/papers/comprehensive-genetic-testing-in-the-clinical-evaluation-of-1119-patients-with/)
- [GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study](https://scholariq.org/papers/gjb2-mutations-and-degree-of-hearing-loss-a-multicenter-study/)
- [Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23](https://scholariq.org/papers/usher-syndrome-1d-and-nonsyndromic-autosomal-recessive-deafness-dfnb12-are/)
- [A candidate prostate cancer susceptibility gene at chromosome 17p](https://scholariq.org/papers/a-candidate-prostate-cancer-susceptibility-gene-at-chromosome-17p/)
- [Congenital hearing loss](https://scholariq.org/papers/congenital-hearing-loss/)
- [Congenital Cytomegalovirus Infection](https://scholariq.org/papers/congenital-cytomegalovirus-infection/)
- [Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?](https://scholariq.org/papers/forty-six-genes-causing-nonsyndromic-hearing-impairment-which-ones-should-be/)
- [C3 glomerulopathy — understanding a rare complement-driven renal disease](https://scholariq.org/papers/c3-glomerulopathy-understanding-a-rare-complement-driven-renal-disease/)
- [Membranoproliferative Glomerulonephritis Type II (Dense Deposit Disease)](https://scholariq.org/papers/membranoproliferative-glomerulonephritis-type-ii-dense-deposit-disease/)

## Researcher topics

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)
- [Complement system in diseases](https://scholariq.org/topics/complement-system-in-diseases/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Vestibular and auditory disorders](https://scholariq.org/topics/vestibular-and-auditory-disorders/)
- [Hearing Loss and Rehabilitation](https://scholariq.org/topics/hearing-loss-and-rehabilitation/)

## Researcher university

- [University of Iowa](https://scholariq.org/institutions/university-of-iowa/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.