Michael Lingen

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?

Moneef Shoukier, Nina Klein, Bernd Auber et al. · Clinical Genetics · 2012 · 67 citations · Full text

Array Cgh, Genetics, Genetic Epidemiology +17

Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life

Michael Lingen, Lucia Albers, Matthew Borchers et al. · Clinical Genetics · 2015 · 61 citations

Genetic Testing, Disability, Genetic Epidemiology +16

Microduplication of 3p26.3 in Nonsyndromic Intellectual Disability Indicates an Important Role of CHL1 for Normal Cognitive Function

Moneef Shoukier, Sigrid Fuchs, Eva Maria Christina Schwaibold et al. · Neuropediatrics · 2013 · 47 citations

Cyclosporin a resistance of Herpes simplex virus-induced “fusion from within” as a phenotypical marker of mutations in the syn 3 locus of the glycoprotein B gene

Iwan Walev, Michael Lingen, Mathias Lazzaro et al. · Virus Genes · 1994 · 29 citations

Phenotypical Marker, Molecular Virology, Pathogenesis +9

Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study

Sarah Wente, Simone Schröder, Johannes Buckard et al. · Orphanet Journal of Rare Diseases · 2016 · 25 citations · Full text