Cargando…
Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk
Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting approximately 1 in 700 births. NSCL/P has complex etiology including several known genes and environmental factors; however, known genetic risk variants only account for a small fraction of the heritabi...
Autores principales: | Carlson, Jenna C., Shaffer, John R., Deleyiannis, Fred, Hecht, Jacqueline T., Wehby, George L., Christensen, Kaare, Feingold, Eleanor, Weinberg, Seth M., Marazita, Mary L., Leslie, Elizabeth J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866867/ https://www.ncbi.nlm.nih.gov/pubmed/35223824 http://dx.doi.org/10.3389/fcell.2022.621261 |
Ejemplares similares
-
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions
por: Mukhopadhyay, Nandita, et al.
Publicado: (2021) -
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial Variation
por: Indencleef, Karlijne, et al.
Publicado: (2021) -
Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft
por: Zhang, Wanying, et al.
Publicado: (2021) -
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21
por: Mukhopadhyay, Nandita, et al.
Publicado: (2019) -
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
por: Perez, Kimberly K. Diaz, et al.
Publicado: (2023)