Ron Hochstenbach

3.9k citations

49 papers · 2.1k · h-index 25

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics

Papers in

Genetics 41
- Genomic variations and chromosomal abnormalities 29
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 6
Molecular Biology 19
- Congenital heart defects research 6

Co-authors: Martin Poot (17 shared papers)Christine L. Mummery (3 shared papers)Robert Passier (2 shared papers)Stefan Braam (2 shared papers)Stieneke van den Brink (2 shared papers)Ruben van ‘t Slot (7 shared papers)Johannes H. P. Hackstein (4 shared papers)Ellen van Binsbergen (5 shared papers)
Journals: European Journal of Medical Genetics (5 papers)European Journal of Human Genetics (3 papers)Journal of Intellectual Disability Research (2 papers)Prenatal Diagnosis (2 papers)Genome Medicine (2 papers)
Partner nations: Netherlands Germany United States

In The Last Decade

Ron Hochstenbach

49 papers receiving 2.0k citations

Peers

Countries citing papers authored by Ron Hochstenbach

Since Specialization

Citations

This map shows the geographic impact of Ron Hochstenbach's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ron Hochstenbach with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ron Hochstenbach more than expected).

Fields of papers citing papers by Ron Hochstenbach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ron Hochstenbach. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ron Hochstenbach. The network helps show where Ron Hochstenbach may publish in the future.

Co-authors

The 25 scholars most cited alongside Ron Hochstenbach, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ron Hochstenbach Line = papers co-authored together Ron Hochstenbach links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 49 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Recombinant Vitronectin Is a Functionally Defined Substrate That Supports Human Embryonic Stem Cell Self-Renewal via αVβ5 Integrin Stem Cells ·Stefan Braam, Laura Zeinstra, Sandy H.M. Litjens, Dorien Ward‐van Oostwaard, Stieneke van den Brink, Linda van Laake, Franck Lebrin, Peter Kats, Ron Hochstenbach, Robert Passier, Arnoud Sonnenberg, Christine L. Mummery	2008	325
2	TGF-β1 induces efficient differentiation of human cardiomyocyte progenitor cells into functional cardiomyocytes in vitro Stem Cell Research ·Marie‐José Goumans, Teun P. de Boer, Anke M. Smits, Linda W. van Laake, Patrick van Vliet, Corina H.G. Metz, Tom H. Korfage, K. Peter Kats, Ron Hochstenbach, Gerard Pasterkamp, Marianne C. Verhaar, Marcel A. G. van der Heyden, Dominique P.V. de Kleijn, Christine L. Mummery, Toon A.B. van Veen, Joost P. G. Sluijter, Pieter A. Doevendans	2008	188
3	Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands European Journal of Medical Genetics ·Ron Hochstenbach, Ellen van Binsbergen, J.J.M. Engelen, Aggie Nieuwint, Abeltje M. Polstra, Pino J. Poddighe, Claudia Ruivenkamp, Birgit Sikkema‐Raddatz, Dominique Smeets, Martin Poot	2009	149
4	A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome European Journal of Human Genetics ·Deniz Kanber, Jacques C. Giltay, Dagmar Wieczorek, Corinna Zogel, Ron Hochstenbach, Almuth Caliebe, Alma Kuechler, Bernhard Horsthemke, Karin Buiting	2008	102
5	Selective chromosome analysis in couples with two or more miscarriages: case-control study BMJ ·Maureen Franssen, Johanna C. Korevaar, N. J. Leschot, Patrick M. Bossuyt, Alida C. Knegt, Klasien B.J. Gerssen‐Schoorl, Carine Wouters, Kerstin Hansson, Ron Hochstenbach, K. Madan, Fulco van der Veen, Mariëtte Goddijn	2005	94
6	Improved genetic manipulation of human embryonic stem cells Nature Methods ·Stefan Braam, Chris Denning, Stieneke van den Brink, Peter Kats, Ron Hochstenbach, Robert Passier, Christine L. Mummery	2008	88
7	Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring The American Journal of Human Genetics ·Mirjam S. de Pagter, Markus J. van Roosmalen, Annette F. Baas, Ivo Renkens, Karen Duran, Ellen van Binsbergen, Masoumeh Tavakoli‐Yaraki, Ron Hochstenbach, Lars T. van der Veken, Edwin Cuppen, Wigard P. Kloosterman	2015	80
8	A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Bert van der Zwaag, Wouter Staal, Ron Hochstenbach, Martin Poot, Henk A. Spierenburg, Maretha Jonge, Nienke E. Verbeek, Ruben van ‘t Slot, Michael A. van Es, Frank J. T. Staal, Christine M. Freitag, Jacobine E. Buizer‐Voskamp, Marcel Nelen, Leonard H. van den Berg, Hans Kristian Ploos van Amstel, Hermán van Engeland, J. Peter H. Burbach	2009	80
9	Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research Cytogenetic and Genome Research ·Ron Hochstenbach, Jacobine E. Buizer‐Voskamp, J.A.S. Vorstman, Roel A. Ophoff	2011	80
10	Is the Y chromosome of Drosophila an evolved supernumerary chromosome? BioEssays ·Johannes H. P. Hackstein, Ron Hochstenbach, Elisabeth Hauschteck‐Jungen, Leo W. Beukeboom	1996	65
11	Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism Neurogenetics ·Emma van Daalen, Chantal Kemner, Nienke E. Verbeek, Bert van der Zwaag, Trijnie Dijkhuizen, Patrick Rump, Renske H. Houben, Ruben van ‘t Slot, Maretha Jonge, Wouter Staal, Frits A. Beemer, Jacob Vorstman, J. Peter H. Burbach, Hans Kristian Ploos van Amstel, Ron Hochstenbach, Eva H. Brilstra, Martin Poot	2011	62
12	Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene European Journal of Medical Genetics ·Almuth Caliebe, Hester Y. Kroes, Jasper J. van der Smagt, José I. Martı́n-Subero, Holger Tönnies, Ruben van ‘t Slot, Rutger A. J. Nievelstein, Hiltrud Muhle, Ulrich Stephani, Karsten Alfke, Irina Stefanova, Yorck Hellenbroich, Gabriele Gillessen‐Kaesbach, Ron Hochstenbach, Reiner Siebert, Martin Poot	2010	54
13	Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA) Prenatal Diagnosis ·Ron Hochstenbach, Judith Meijer, J. van de Brug, I. Vossebeld-Hoff, Renée S. Jansen, Rob B. van der Luijt, Richard J. Sinke, Godelieve C.M.L. Page‐Christiaens, Johannes Kristian Ploos van Amstel, Jennie M. Pater	2005	52
14	Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions European Journal of Human Genetics ·Hannelie M. Engbers, Jasper J. van der Smagt, Ruben van ‘t Slot, Joris Vermeesch, Ron Hochstenbach, Martin Poot	2008	45
15	Diploid/triploid mosaicism in dysmorphic patients Clinical Genetics ·Ingrid M.B.H. van de Laar, Gwenda M. Rabelink, Ron Hochstenbach, J.H.A.M. Tuerlings, Jeannette Hoogeboom, Jacques C. Giltay	2002	44
16	Congenital diaphragmatic hernia associated with duplication of 11q23‐qter American Journal of Medical Genetics Part A ·Merel Klaassens, Daryl A. Scott, Marieke van Dooren, Ron Hochstenbach, H. J. Eussen, Wei Cai, R. J. H. Galjaard, Carine Wouters, Martin Poot, J. A. M. Laudy, B. Lee, Dick Tibboel, Annelies de Klein	2006	41
17	Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2→qter European Journal of Medical Genetics ·Martin Poot, Marc J. Eleveld, Ruben van ‘t Slot, Maria M. van Genderen, A. A. Verrijn Stuart, Ron Hochstenbach, Frits A. Beemer	2007	38
18	Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex European Journal of Human Genetics ·Martin Poot, Marc J. Eleveld, Ruben van ‘t Slot, Hans Kristian Ploos van Amstel, Ron Hochstenbach	2009	36
19	Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in the Netherlands Journal of Intellectual Disability Research ·Gert de Graaf, Meindert Haveman, Ron Hochstenbach, J.J.M. Engelen, K.B.J. Gerssen-Schoorl, Pino J. Poddighe, Dominique Smeets, Geert Van Hove	2011	35
20	Y chromosomal fertility genes of Drosophila: a new type of eukaryotic genes Genome ·Wolfgang Hennig, Reindert C. Brand, Johannes H. P. Hackstein, Ron Hochstenbach, Hannie Kremer, Dirk‐Henner Lankenau, Susanne Lankenau, Koos Miedema, Andy J.G. Pötgens	1989	33

About Ron Hochstenbach

Ron Hochstenbach is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Cognitive Neuroscience, having authored 49 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (19 papers), Chromosomal and Genetic Variations (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (6 papers), Genomics and Rare Diseases (6 papers) and Autism Spectrum Disorder Research (4 papers). The work is most often cited by research in Genetics (1.1k citations), Pediatrics, Perinatology and Child Health (446 citations), Molecular Biology (1.2k citations), Plant Science (318 citations) and Surgery (376 citations). Ron Hochstenbach has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Martin Poot, Christine L. Mummery, Robert Passier, Stefan Braam, Stieneke van den Brink, Ruben van ‘t Slot, Johannes H. P. Hackstein, Ellen van Binsbergen, Jacques C. Giltay and Linda van Laake. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Journal of Intellectual Disability Research, Prenatal Diagnosis and Genome Medicine.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Ron Hochstenbach

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Ron Hochstenbach

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