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American Journal of Medical Genetics. Part A|September 17, 2013
Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sampleAnne C Böhmer, Elisabeth Mangold, Peter Tessmann, et al.HGG Advances|January 20, 2022
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palateJulia Welzenbach, Nigel L Hammond, Miloš Nikolić, et al.HGG Advances|January 2, 2023
Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutationsHanna K Zieger, Leonie Weinhold, Axel Schmidt, et al.European Journal of Oral Sciences|March 27, 2009
Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Heiko Reutter, Meinhard Mende, et al.Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.International Journal of Pediatric Otorhinolaryngology|July 10, 2009
Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descentHeiko Reutter, Stefanie Birnbaum, Meinhard Mende, et al.International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 16, 2006
Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC ConsortiumTimm Goecke, Karsten Schulmann, Christoph Engel, et al.International Journal of Cancer|April 26, 2005
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancerElisabeth Mangold, Constanze Pagenstecher, Waltraut Friedl, et al.Pageof 14