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Asian oral-facial cleft birth prevalence.
Cooper ME, Ratay JS, Marazita ML. Cooper ME, et al. Among authors: ratay js. Cleft Palate Craniofac J. 2006 Sep;43(5):580-9. doi: 10.1597/05-167. Cleft Palate Craniofac J. 2006. PMID: 16986997 Review.
A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct.
Chattaraj P, Munjal T, Honda K, Rendtorff ND, Ratay JS, Muskett JA, Risso DS, Roux I, Gertz EM, Schäffer AA, Friedman TB, Morell RJ, Tranebjærg L, Griffith AJ. Chattaraj P, et al. Among authors: ratay js. J Med Genet. 2017 Oct;54(10):665-673. doi: 10.1136/jmedgenet-2017-104721. Epub 2017 Aug 5. J Med Genet. 2017. PMID: 28780564 Free PMC article.
NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy.
Nakanishi H, Kawashima Y, Kurima K, Chae JJ, Ross AM, Pinto-Patarroyo G, Patel SK, Muskett JA, Ratay JS, Chattaraj P, Park YH, Grevich S, Brewer CC, Hoa M, Kim HJ, Butman JA, Broderick L, Hoffman HM, Aksentijevich I, Kastner DL, Goldbach-Mansky R, Griffith AJ. Nakanishi H, et al. Among authors: ratay js. Proc Natl Acad Sci U S A. 2017 Sep 12;114(37):E7766-E7775. doi: 10.1073/pnas.1702946114. Epub 2017 Aug 28. Proc Natl Acad Sci U S A. 2017. PMID: 28847925 Free PMC article.