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European Journal of Oral Sciences|September 19, 2012
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palateElisabeth Mangold, Heiko Reutter, Rafael B R León-Cachón, et al.
Human Molecular Genetics|January 15, 2017
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate onlyKerstin U Ludwig, Anne C Böhmer, John Bowes, et al.
Clinical Epigenetics|January 16, 2024
Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylationLaura K Godfrey, Jan Forster, Sven-Thorsten Liffers, et al.
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.
Psychiatric Genetics|September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, 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.
Annals of Clinical and Translational Neurology|August 5, 2025
The rs10191329 Risk Allele Is Associated With Pronounced Retinal Layer Atrophy in Multiple SclerosisGabriel Bsteh, Ruchi Tanavade, Nik Krajnc, 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.
Biomolecules|July 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease FormationRicarda Köllges, Jil Stegmann, Sophia Schneider, 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.
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