Evelin Schröck

Multicolor Spectral Karyotyping of Human Chromosomes

Evelin Schröck, Stanislas du Manoir, Timothy Veldman et al. · Science · 1996 · 1.8K citations

Life Sciences, Genetics, Molecular Genetics +17

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Anita Rauch, Dagmar Wieczorek, Elisabeth Graf et al. · The Lancet · 2012 · 1.1K citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

Marta Chesi, Elena Nardini, Leslie A. Brents et al. · Nature Genetics · 1997 · 647 citations

Medicine, Molecular Genetics, Oncology +13

Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization

Stanislas du Manoir, Michael R. Speicher, Stefan Joos et al. · Human Genetics · 1993 · 558 citations

Life Sciences, Genetics, Molecular Genetics +11

Role of Chromosome Territories in the Functional Compartmentalization of the Cell Nucleus

Thomas Cremer, A. Kurz, R. M. Zirbel et al. · Cold Spring Harbor Symposia on Quantitative Biology · 1993 · 494 citations

Life Sciences, Botany, Cell Biology +17