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Birth Defects Research. Part A, Clinical and Molecular Teratology|June 22, 2010
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25Augusto Rojas-Martinez, Heiko Reutter, Oscar Chacon-Camacho, et al.
American Journal of Medical Genetics. Part A|February 18, 2020
Nine newly identified individuals refine the phenotype associated with MYT1L mutationsIsabelle C Windheuser, Jessica Becker, Kirsten Cremer, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex familiesEmily R Holzinger, Qing Li, Margaret M Parker, et al.
Plos Genetics|March 12, 2016
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative GeneKerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European originElisabeth Mangold, Heiko Reutter, Stefanie Birnbaum, et al.
Genes|December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility GeneIris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
European Journal of Human Genetics : EJHG|June 23, 2011
Genetic determination of human facial morphology: links between cleft-lips and normal variationStefan Boehringer, Fedde van der Lijn, Fan Liu, et al.
Cancer Letters|July 16, 2008
Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German familiesBernd Frank, Barbara Burwinkel, Justo Lorenzo Bermejo, et al.
Human Mutation|May 18, 2021
Extending the allelic spectrum at noncoding risk loci of orofacial cleftingFrederic Thieme, Leonie Henschel, Nigel L Hammond, et al.
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