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European Journal of Human Genetics : EJHG|December 20, 2024
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish modelsNina Ishorst, Selina Hölzel, Carola Greve, et al.Nature Communications|February 25, 2017
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneityYanqin Yu, Xianbo Zuo, Miao He, et al.American Journal of Human Genetics|February 8, 2011
FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafishMichella Ghassibe-Sabbagh, Laurence Desmyter, Tobias Langenberg, et al.Journal of Dental Research|February 25, 2014
Strong association of variants around FOXE1 and orofacial cleftingK U Ludwig, A C Böhmer, M Rubini, et al.Archives of General Psychiatry|July 8, 2009
Genome-wide association study of alcohol dependenceJens Treutlein, Sven Cichon, Monika Ridinger, et al.Journal of Dental Research|August 3, 2017
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome SequencingA K Hoebel, D Drichel, M van de Vorst, et al.European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.Frontiers in Genetics|August 4, 2022
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema GenesCarina M Mathey, Carlo Maj, Annika B Scheer, et al.Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.American Journal of Human Genetics|March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft PalateElisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.Pageof 24