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American Journal of Medical Genetics. Part A|March 16, 2012
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial cleftsMin Shi, Jeffrey C Murray, Mary L Marazita, et al.Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, 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.Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.Nature Genetics|May 4, 2010
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4Terri H Beaty, Jeffrey C Murray, Mary L Marazita, et al.Environmental Health Perspectives|July 10, 2026
Prenatal Smoking Exposures and Epigenome-Wide Methylation in Newborn BloodThanh T Hoang, Marta Cosin-Tomas, Yunsung Lee, et al.Environmental Health Perspectives|June 6, 2025
Prenatal Smoking Exposures and Epigenome-wide Methylation in Newborn BloodThanh T Hoang, Marta Cosin-Tomas, Yunsung Lee, et al.Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.American Journal of Human Genetics|March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.Human Molecular Genetics|April 2, 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 19q13Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.Pageof 11