Eva‐Maria Gerlach

Partial deletion of GLRB and GRIA2 in a patient with intellectual disability

Karl Hackmann, Sarah Matko, Eva‐Maria Gerlach et al. · European Journal of Human Genetics · 2012 · 24 citations · Full text

Partial Deletion, Inherited Metabolic Disease, Neurology +2

Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3

Karl Hackmann, Anja Stadler, Jens Schallner et al. · American Journal of Medical Genetics Part A · 2013 · 22 citations

1.6 Mb deletion in chromosome band 3q29 associated with eye abnormalities

Nataliya Tyshchenko, Karl Hackmann, Eva‐Maria Gerlach et al. · European Journal of Medical Genetics · 2009 · 20 citations

Novel CIC Point Mutations and an Exon-Spanning, Homozygous Deletion Identified in Oligodendroglial Tumors by a Comprehensive Genomic Approach Including Transcriptome Sequencing

Sophie Eisenreich, Khalil Abou‐El‐Ardat, Karol Szafranski et al. · PLoS ONE · 2013 · 17 citations · Full text

Array Cgh, Homozygous Deletion Identified, Distinct Subgroup +17

Neuromuscular Contacts Induce Nitric Oxide Signals in Skeletal Myotubes in vitro

Britta Püttmann, Eva‐Maria Gerlach, Mark G. Kruger et al. · Neurosignals · 2005 · 11 citations