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Nature Genetics|October 7, 2008
Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lipFedik Rahimov, Mary L Marazita, Axel Visel, et al.
Human Genetics|January 6, 2017
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palateElizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Frontiers in Cell and Developmental Biology|April 26, 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel RegionsNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|April 18, 2024
Shared genetic risk between major orofacial cleft phenotypes in an African populationAzeez Alade, Tabitha Peter, Tamara Busch, et al.
Pediatrics|June 12, 2013
Individual and center-level factors affecting mortality among extremely low birth weight infantsBrandon W Alleman, Edward F Bell, Lei Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeRenata L L Ferreira de Lima, Sarah A Hoper, Michella Ghassibe, et al.
Genetic Epidemiology|February 22, 2022
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
Developmental Biology|April 5, 2011
The FaceBase Consortium: a comprehensive program to facilitate craniofacial researchHarry Hochheiser, Bruce J Aronow, Kristin Artinger, et al.
Genetics|May 6, 2014
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral cleftsAlexandre Bureau, Margaret M Parker, Ingo Ruczinski, et al.
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