Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Ron Hochstenbach | Researchclopedia

Back to researchers

Ron Hochstenbach

University Medical Center Utrecht ORCID

64

Works

3,869

Citations

30

h-index

52

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Prenatal Screening and Diagnostics Chromosomal and Genetic Variations

Affiliations

Radboud University Nijmegen1990–1996

Utrecht University2002–2015

Heidelberg University2008–2008

University Hospital Heidelberg2008–2008

University Medical Center Utrecht2000–2019

Top Works

Recombinant Vitronectin Is a Functionally Defined Substrate That Supports Human Embryonic Stem Cell Self-Renewal via αVβ5 Integrin

Stefan Braam,Laura Zeinstra,et al.

2008431 citations

Genomics and Rare Diseases

Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin,Harrison Brand,et al.

2016350 citations

Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

Ron Hochstenbach,Ellen van Binsbergen,et al.

2009283 citations

TGF-β1 induces efficient differentiation of human cardiomyocyte progenitor cells into functional cardiomyocytes in vitro

Marie‐José Goumans,Teun P. de Boer,et al.

2008229 citations

Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms

Wigard P. Kloosterman,Masoumeh Tavakoli‐Yaraki,et al.

2012194 citations

Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism

Bert van der Zwaag,Lude Franke,et al.

2009143 citations

Selective chromosome analysis in couples with two or more miscarriages: case-control study

Maureen Franssen,Johanna C. Korevaar,et al.

2005142 citations

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

Deniz Kanber,Jacques C. Giltay,et al.

2008135 citations

Diploid/triploid mosaicism in dysmorphic patients

Ingrid M.B.H. van de Laar,Gwenda M. Rabelink,et al.

2002132 citations