G. Schmidt

发表

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

S. Cichon, M. Nöthen, T. Wienker, 2010, Nature Genetics.

Mutation screening in the IRF6‐gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal‐dominant inheritance

Markus Martini, A. Hemprich, H. Reutter, 2008, American journal of medical genetics. Part A.

IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.

M. Nöthen, T. Wienker, P. Hoffmann, 2009, European journal of oral sciences.

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 descent.

M. Nöthen, P. Hoffmann, M. Knapp, 2009, International journal of pediatric otorhinolaryngology.

Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.

M. Nöthen, M. Knapp, S. Herms, 2009, European journal of oral sciences.

Cleft Lip and/or Palate with Monogenic Autosomal Recessive Transmission in Pyrenees Shepherd Dogs

H. Thiele, C. Kemp, R. Lauster, 2009, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing

A. Hoischen, M. Nöthen, C. Gilissen, 2017, Journal of dental research.

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

Bernhard Horsthemke, Jan Freudenberg, Elisabeth Mangold, 2009, Nature Genetics.

Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.

M. Nöthen, M. Knapp, P. Stanier, 2016, American journal of human genetics.

Genome‐wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin

T. Wienker, M. Krimmel, M. Mattheisen, 2009, American journal of medical genetics. Part A.

TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate

M. Nöthen, M. Knapp, Markus Martini, 2008, Journal of Human Genetics.

Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.

M. Knapp, F. Degenhardt, A. Zink, 2016, Birth defects research. Part A, Clinical and molecular teratology.

Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.

M. Nöthen, C. Lange, P. Hoffmann, 2014, Birth defects research. Part A, Clinical and molecular teratology.