Ron Hochstenbach

3.9k total citations
49 papers, 2.1k citations indexed

About

Ron Hochstenbach is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ron Hochstenbach has authored 49 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 19 papers in Molecular Biology and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ron Hochstenbach's work include Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (19 papers) and Chromosomal and Genetic Variations (15 papers). Ron Hochstenbach is often cited by papers focused on Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (19 papers) and Chromosomal and Genetic Variations (15 papers). Ron Hochstenbach collaborates with scholars based in Netherlands, Germany and United States. Ron Hochstenbach's 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 Laura Zeinstra and has published in prestigious journals such as SHILAP Revista de lepidopterología, Nature Methods and Genetics.

In The Last Decade

Ron Hochstenbach

49 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ron Hochstenbach Netherlands 25 1.2k 1.1k 446 376 318 49 2.1k
Cédric Le Caignec France 29 1.7k 1.5× 1.5k 1.4× 770 1.7× 209 0.6× 298 0.9× 76 3.1k
Elisabeth Blennow Sweden 34 1.6k 1.3× 1.5k 1.4× 678 1.5× 242 0.6× 704 2.2× 87 3.0k
Gérard Tachdjian France 28 1.5k 1.3× 973 0.9× 893 2.0× 780 2.1× 262 0.8× 113 3.4k
Valeria Capra Italy 33 1.9k 1.7× 1.2k 1.1× 797 1.8× 690 1.8× 98 0.3× 146 3.7k
Claudia Spits Belgium 26 1.2k 1.1× 496 0.5× 566 1.3× 158 0.4× 125 0.4× 66 2.0k
Frances A. Brook United Kingdom 17 2.8k 2.4× 524 0.5× 248 0.6× 501 1.3× 53 0.2× 26 3.3k
Ruth M. Arkell Australia 27 2.2k 1.9× 773 0.7× 138 0.3× 175 0.5× 136 0.4× 57 2.7k
Albrecht Röpke Germany 24 1.2k 1.0× 660 0.6× 123 0.3× 206 0.5× 69 0.2× 52 2.1k
Shoukhrat Mitalipov United States 31 2.6k 2.2× 574 0.5× 267 0.6× 240 0.6× 37 0.1× 65 3.1k
Heinz‐Ulrich G. Weier United States 17 712 0.6× 507 0.5× 153 0.3× 86 0.2× 174 0.5× 47 1.3k

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-authorship network of co-authors of Ron Hochstenbach

This figure shows the co-authorship network connecting the top 25 collaborators of Ron Hochstenbach. A scholar is included among the top collaborators of Ron Hochstenbach based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ron Hochstenbach. Ron Hochstenbach is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hochstenbach, Ron, et al.. (2018). Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cf DNA by a demised trisomy‐14 cotwin. Clinical Case Reports. 6(5). 788–791. 8 indexed citations
2.
Middelkamp, Sjors, Sebastiaan van Heesch, A. Koen Braat, et al.. (2017). Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells. Genome Medicine. 9(1). 9–9. 25 indexed citations
3.
Pagter, Mirjam S. de, Markus J. van Roosmalen, Annette F. Baas, et al.. (2015). Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring. The American Journal of Human Genetics. 96(4). 651–656. 80 indexed citations
4.
Graaf, Gert de, Meindert Haveman, Ron Hochstenbach, et al.. (2011). Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in the Netherlands. Journal of Intellectual Disability Research. 55(5). 462–473. 35 indexed citations
5.
Hochstenbach, Ron, Jacobine E. Buizer‐Voskamp, J.A.S. Vorstman, & Roel A. Ophoff. (2011). 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. 135(3-4). 174–202. 80 indexed citations
6.
7.
Hannes, Femke, Jeroen Van Houdt, Oliver Quarrell, et al.. (2010). Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions. Human Mutation. 31(12). 1343–1351. 15 indexed citations
8.
Zwaag, Bert van der, Wouter Staal, Ron Hochstenbach, et al.. (2009). 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. 153B(4). 960–966. 80 indexed citations
9.
Poot, Martin, Marc J. Eleveld, Ruben van ‘t Slot, Hans Kristian Ploos van Amstel, & Ron Hochstenbach. (2009). Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex. European Journal of Human Genetics. 18(1). 39–46. 36 indexed citations
10.
Hochstenbach, Ron, Ellen van Binsbergen, J.J.M. Engelen, et al.. (2009). 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. 52(4). 161–169. 149 indexed citations
11.
Özgen, Mihriban Heval, Emma van Daalen, PF Bolton, et al.. (2009). Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders. Clinical Genetics. 76(4). 348–356. 31 indexed citations
12.
Braam, Stefan, Chris Denning, Stieneke van den Brink, et al.. (2008). Improved genetic manipulation of human embryonic stem cells. Nature Methods. 5(5). 389–392. 88 indexed citations
13.
Eussen, Bert H.J., Ingrid M.B.H. van de Laar, Hannie Douben, et al.. (2006). A familial inverted duplication 2q33–q34 identified and delineated by multiple cytogenetic techniques. European Journal of Medical Genetics. 50(2). 112–119. 8 indexed citations
14.
Klaassens, Merel, Daryl A. Scott, Marieke van Dooren, et al.. (2006). Congenital diaphragmatic hernia associated with duplication of 11q23‐qter. American Journal of Medical Genetics Part A. 140A(14). 1580–1586. 41 indexed citations
15.
Franssen, Maureen, Johanna C. Korevaar, N. J. Leschot, et al.. (2005). Selective chromosome analysis in couples with two or more miscarriages: case-control study. BMJ. 331(7509). 137–141. 94 indexed citations
16.
Lichtenbelt, Klaske D., et al.. (2004). Supernumerary ring chromosome 7 mosaicism: Case report, investigation of the gene content, and delineation of the phenotype. American Journal of Medical Genetics Part A. 132A(1). 93–100. 27 indexed citations
17.
Terhal, Pauline, Ralph J. B. Sakkers, Ron Hochstenbach, et al.. (2004). Cerebellar hypoplasia, zonular cataract, and peripheral neuropathy in trisomy 17 mosaicism. American Journal of Medical Genetics Part A. 130A(4). 410–414. 13 indexed citations
18.
Hochstenbach, Ron, et al.. (1994). Degenerating gypsy retrotransposons in a male fertility gene on the Y chromosome of Drosophila hydei. Journal of Molecular Evolution. 39(5). 452–65. 11 indexed citations
19.
Hochstenbach, Ron, et al.. (1994). Discrimination of related transcribed and non-transcribed repetitive DNA sequences from the Y chromosomes of Drosophila hydei and Drosophila eohydei. Molecular and General Genetics MGG. 243(1). 54–62. 7 indexed citations
20.
Hochstenbach, Ron, et al.. (1993). Partial reconstruction of the lampbrush loop pair Nooses on the Y chromosome of Drosophila hydei. Chromosoma. 102(8). 526–545. 14 indexed citations

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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