Ron Hochstenbach
University Medical Center Utrecht(NL)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Chromosomal and Genetic Variations, Genomics and Rare Diseases, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Most-Cited Works
- → Recombinant Vitronectin Is a Functionally Defined Substrate That Supports Human Embryonic Stem Cell Self-Renewal via αVβ5 Integrin(2008)431 cited
- → The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies(2016)350 cited
- → Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands(2009)283 cited
- → TGF-β1 induces efficient differentiation of human cardiomyocyte progenitor cells into functional cardiomyocytes in vitro(2008)229 cited
- → Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms(2012)194 cited
- → Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism(2009)143 cited
- → Selective chromosome analysis in couples with two or more miscarriages: case-control study(2005)142 cited
- → A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome(2008)135 cited
- → Diploid/triploid mosaicism in dysmorphic patients(2002)132 cited
- → Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring(2015)126 cited