Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Kevin T Booth, Ph.D.

Concepts

This page shows the publications Kevin Booth has written about Consanguinity.
Connection Strength

0.389
  1. Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment. J Med Genet. 2018 08; 55(8):555-560.
    View in: PubMed
    Score: 0.161
  2. Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review. Arch Iran Med. 2016 Oct 01; 19(10):720-728.
    View in: PubMed
    Score: 0.145
  3. A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. Hum Genet. 2021 Jun; 140(6):915-931.
    View in: PubMed
    Score: 0.049
  4. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. J Med Genet. 2015 Dec; 52(12):823-9.
    View in: PubMed
    Score: 0.034
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.

Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.