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Genetic Epidemiology|October 3, 2018
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial cleftsJenna C Carlson, Nichole L Nidey, Azeez Butali, et al.
Plos Genetics|September 30, 2025
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft riskJenna C Carlson, Xinyi Zhang, Zeynep Erdogan-Yildirim, et al.
Molecular Genetics & Genomic Medicine|June 18, 2014
Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan AfricaAzeez Butali, Peter A Mossey, Wasiu L Adeyemo, et al.
European Journal of Oral Sciences|March 16, 2013
X-linked markers in the Duchenne muscular dystrophy gene associated with oral cleftsPoorav J Patel, Terri H Beaty, Ingo Ruczinski, et al.
Genetic Epidemiology|April 18, 2012
Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and EuropeansTanda Murray, Margaret A Taub, Ingo Ruczinski, et al.
Molecular Genetics & Genomic Medicine|April 1, 2017
The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub-Saharan AfricaLord Jephthah Joojo Gowans, Tamara D Busch, Peter A Mossey, et al.
Pediatric Research|August 21, 2012
No observed association for mitochondrial SNPs with preterm delivery and related outcomesBrandon W Alleman, Solveig Myking, Kelli K Ryckman, et al.
Plos Genetics|September 21, 2011
Genome-wide association study identifies four loci associated with eruption of permanent teethFrank Geller, Bjarke Feenstra, Hao Zhang, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
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