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A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

artículo científico publicado en 2016

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

artículo científico publicado en 2019

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

artículo científico publicado en 2017

Ear Infection in Isolated Cleft Lip: Etiological Implications.

artículo científico publicado en 2015

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

artículo científico publicado en 2016

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

artículo científico publicado en 2018

Hypertelorism and Orofacial Clefting Revisited: An Anthropometric Investigation

scientific article published on 09 August 2016

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

artículo científico publicado en 2017

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci

artículo científico publicado en 2015

The Effects of ACA Medicaid Expansions on Health After 5 Years

artículo científico publicado en 2020

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