Harvard Catalyst Profiles

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Kevin T Booth, Ph.D.

Concepts

This page shows the publications Kevin Booth has written about Genetic Association Studies.
Connection Strength

0.458
  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: 0.350
  2. A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Hum Genet. 2020 Oct; 139(10):1315-1323.
    View in: PubMed
    Score: 0.025
  3. When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS). J Hum Genet. 2020 Jul; 65(7):609-617.
    View in: PubMed
    Score: 0.025
  4. CDC14A phosphatase is essential for hearing and male fertility in mouse and human. Hum Mol Genet. 2018 03 01; 27(5):780-798.
    View in: PubMed
    Score: 0.022
  5. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. J Med Genet. 2015 Dec; 52(12):823-9.
    View in: PubMed
    Score: 0.018
  6. Mutations in LOXHD1 gene cause various types and severities of hearing loss. Ann Otol Rhinol Laryngol. 2015 May; 124 Suppl 1:135S-41S.
    View in: PubMed
    Score: 0.018
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.