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American Journal of Human Genetics|February 24, 2015
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS lociElizabeth J Leslie, Margaret A Taub, Huan Liu, et al.
American Journal of Human Genetics|May 29, 2018
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft PalateLiza L Cox, Timothy C Cox, Lina M Moreno Uribe, et al.
Genetic Epidemiology|May 28, 2011
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palateTerri H Beaty, Ingo Ruczinski, Jeffrey C Murray, et al.
Pediatric Research|January 3, 2025
Building a growing genomic repository for maternal and fetal health through the PING ConsortiumClara M Abdelmalek, Shriya Singh, Blain Fasil, et al.
Medrxiv : the Preprint Server for Health Sciences|June 3, 2024
Building a growing genomic data repository for maternal and fetal health through the PING ConsortiumClara M Abdelmalek, Shriya Singh, Blain Fasil, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 17, 2022
Damaging Mutations in Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft PalateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Scientific Reports|July 11, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Lancet (London, England)|May 21, 2013
Moving beyond essential interventions for reduction of maternal mortality (the WHO Multicountry Survey on Maternal and Newborn Health): a cross-sectional studyJoão Paulo Souza, Ahmet Metin Gülmezoglu, Joshua Vogel, et al.
Molecular Genetics & Genomic Medicine|June 20, 2020
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndromeAzeez A Alade, Carmen J Buxo-Martinez, Peter A Mossey, et al.
Human Molecular Genetics|September 8, 2012
Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weightJessica Tyrrell, Ville Huikari, Jennifer T Christie, et al.
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