Ron Hochstenbach

1.8k total citations
18 papers, 512 citations indexed

About

Ron Hochstenbach is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Ron Hochstenbach has authored 18 papers receiving a total of 512 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Ron Hochstenbach's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Rare Diseases (5 papers). Ron Hochstenbach is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Rare Diseases (5 papers). Ron Hochstenbach collaborates with scholars based in Netherlands, Germany and Aruba. Ron Hochstenbach's co-authors include Johannes H. P. Hackstein, Martin Poot, Wigard P. Kloosterman, P. Pearson, Edwin Cuppen, Karen Duran, Tom G.W. Letteboer, Victor Guryev, Ewart de Bruijn and Thomas Liehr and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Trends in Genetics.

In The Last Decade

Ron Hochstenbach

17 papers receiving 495 citations

Peers

Ron Hochstenbach

GENET

PPCH

Claude‐Lise Richer Canada

Maxine J. Sutcliffe United States

Andrew Fedoriw United States

C. Rasberry United Kingdom

Candice L. Wike United States

Sandra S. de Vries Netherlands

Aurélie Dipietromaria France

Marion Drüsedau Netherlands

Michiel J. Noordam Netherlands

Gregor Schlüter Germany

Claude‐Lise Richer Canada

Ron Hochstenbach

397 ×1.2

GENET

458 ×1.5

194 ×1.2

95 ×1.1

PPCH

68 ×1.1

Citations per year, relative to Ron Hochstenbach Ron Hochstenbach (= 1×) peers Claude‐Lise Richer

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

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18 of 18 papers shown

Poot, Martin & Ron Hochstenbach. (2021). Prevalence and Phenotypic Impact of Robertsonian Translocations. Molecular Syndromology. 12(1). 1–11. 23 indexed citations

Hochstenbach, Ron, et al.. (2020). Chromosomes in the genomic age. Preserving cytogenomic competence of diagnostic genome laboratories. European Journal of Human Genetics. 29(4). 541–552. 14 indexed citations

Hochstenbach, Ron, Ellen van Binsbergen, Heleen Schuring‐Blom, Arjan Buijs, & Hans Kristian Ploos van Amstel. (2018). A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing. European Journal of Medical Genetics. 62(9). 103543–103543. 13 indexed citations

Hochstenbach, Ron, Martin Poot, & Thomas Liehr. (2017). Mechanisms of Origin and Clinical Effects of Multiple Small Supernumerary Marker Chromosomes, Each Derived from a Different Chromosome. 1(1). 1–38. 4 indexed citations

Veken, Lars T. van der, et al.. (2016). De NovoTrisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies. SHILAP Revista de lepidopterología. 2016. 1–5.

Kloosterman, Wigard P. & Ron Hochstenbach. (2014). Deciphering the pathogenic consequences of chromosomal aberrations in human genetic disease. Molecular Cytogenetics. 7(1). 100–100. 25 indexed citations

Hochstenbach, Ron, Martin Poot, Isaäc J. Nijman, et al.. (2012). Discovery of variants unmasked by hemizygous deletions. European Journal of Human Genetics. 20(7). 748–753. 14 indexed citations

Kloosterman, Wigard P., Victor Guryev, Karen Duran, et al.. (2011). Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†. Human Molecular Genetics. 20(10). 1916–1924. 225 indexed citations

Kroes, Hester Y., Ron Hochstenbach, Rutger A. J. Nievelstein, et al.. (2011). Chromosomal abnormalities resembling Joubert syndrome. Clinical Dysmorphology. 20(3). 136–142. 2 indexed citations

10.

Smagt, Jasper J. van der, Martin Poot, Ron Hochstenbach, et al.. (2009). A duplication including GATA4 does not co‐segregate with congenital heart defects. American Journal of Medical Genetics Part A. 149A(5). 1062–1066. 12 indexed citations

11.

Boer, P. de, Maud Giele, M.T.W.T. Lock, et al.. (2004). Kinetics of meiosis in azoospermic males: a joint histological and cytological approach. Cytogenetic and Genome Research. 105(1). 36–46. 10 indexed citations

12.

Littooij, Annemieke S., Ron Hochstenbach, Richard J. Sinke, J. Peter van Tintelen, & Jacques C. Giltay. (2002). Two cases with partial trisomy 9p: Molecular cytogenetic characterization and clinical follow‐up. American Journal of Medical Genetics. 109(2). 125–132. 24 indexed citations

13.

Hackstein, Johannes H. P., Ron Hochstenbach, & P. Pearson. (2000). Towards an understanding of the genetics of human male infertility: lessons from flies. Trends in Genetics. 16(12). 565–572. 72 indexed citations

14.

Hochstenbach, Ron, Peter de Groot, John Jacobs, J. A. M. Schrauwen, & G. J. Wullems. (1996). The promoter of a gene that is expressed only in pollen interacts with ubiquitous transcription factors. Sexual Plant Reproduction. 9(4). 197–202. 2 indexed citations

15.

Hackstein, Johannes H. P. & Ron Hochstenbach. (1995). The elusive fertility genes of Drosophila: the ultimate haven for selfish genetic elements. Trends in Genetics. 11(5). 195–200. 36 indexed citations

16.

Hochstenbach, Ron, et al.. (1994). Transcription of repetitive DNA sequences in the lampbrush loop pair Nooses formed by sterile alleles of fertility gene Q on the Y chromosome of Drosophila hydei. Molecular and General Genetics MGG. 244(6). 653–660. 5 indexed citations

17.

Hackstein, J.H.P., et al.. (1992). Constructing balancer chromosomes for genetic screens in Drosophila hydei. Theoretical and Applied Genetics. 83-83(6-7). 821–826. 1 indexed citations

18.

Hulsebos, Theo J.M., B. Wieringa, Ron Hochstenbach, et al.. (1986). Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome. Cytogenetic and Genome Research. 43(1-2). 47–56. 30 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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