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Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
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FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research
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Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios
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Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk
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FAT4 identified as a potential modifier of orofacial cleft laterality
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Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts
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Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18
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Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts
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Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21
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Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes
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Authors
Leslie, Elizabeth
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Feingold, Eleanor
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Christensen, Kaare
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Marazita, Mary L
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Weinberg, Seth M.
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Butali, Azeez
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Hecht, Jacqueline T.
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Marazita, Mary L.
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Murray, Jeffrey C.
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Padilla, Carmencita
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GENETIC EPIDEMIOLOGY
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A
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DEVELOPMENT
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ELIFE
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Environmental Research
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FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY
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Life Sciences & Biomedicine
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PALATE
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Science & Technology
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LIP
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Genetics & Heredity
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RISK
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GENOME-WIDE ASSOCIATION
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Mathematical & Computational Biology
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VARIANTS
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