M. Voigt

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3.

S. Mundlos, P. Krawitz, J. Hecht, 2014, Brain : a journal of neurology.

Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome

V. Trifonov, K. Mrasek, T. Liehr, 2015, Cytogenetic and Genome Research.

Small Supernumerary Marker Chromosomes and Uniparental Disomy Have a Story to Tell

T. Liehr, M. Voigt, A. Weise, 2011, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Clinical Impact of Proximal Autosomal Imbalances

T. Liehr, M. Voigt, A. Weise, 2012, Balkan journal of medical genetics : BJMG.

Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors.

K. Mrasek, T. Liehr, N. Corrales, 2012, Gene.

Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines

K. Mrasek, T. Liehr, M. Voigt, 2012, Applied & translational genomics.

How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set

K. Mrasek, T. Liehr, T. Karamysheva, 2012, Journal of Applied Genetics.

Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant

I. Katona, S. Heinemann, P. Gong, 2015, Nature Communications.

Hereditary Sensory Polyneuropathy, Pain Insensitivity and Global Developmental Delay due to Novel Mutation in PRDM12 Gene

I. Kurth, A. Saini, P. Singhi, 2017, The Indian Journal of Pediatrics.