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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 missense variant in CREBRF is associated with taller stature in Samoans

scientific article published on 19 March 2020

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

Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18

artículo científico publicado en 2020

Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Effects of enamel matrix genes on dental caries are moderated by fluoride exposures

artículo científico publicado en 2014

Exploring Subclinical Phenotypic Features in Twin Pairs Discordant for Cleft Lip and Palate

scientific article published on 16 February 2016

Exploring the Paradoxical Relationship of a Creb 3 Regulatory Factor Missense Variant With Body Mass Index and Diabetes Among Samoans: Protocol for the Soifua Manuia (Good Health) Observational Cohort Study

scientific article published on 23 July 2020

Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.

artículo científico publicado en 2018

Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels

artículo científico publicado en 2020

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Genome-wide mapping of global-to-local genetic effects on human facial shape.

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting.

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

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing

artículo científico publicado en 2017

Validation of the Vectra H1 portable three-dimensional photogrammetry system for facial imaging.

artículo científico publicado en 2017

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