J. Herbergs

1.1k total citations
26 papers, 644 citations indexed

About

J. Herbergs is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, J. Herbergs has authored 26 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Plant Science. Recurrent topics in J. Herbergs's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (5 papers). J. Herbergs is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (5 papers). J. Herbergs collaborates with scholars based in Netherlands, Belgium and United States. J. Herbergs's co-authors include Jos Weusten, Ute Moog, Eric Smeets, Hubert J.M. Smeets, J.L.H. Evers, John C.M. Dumoulin, Anton H. N. Hopman, C. T. R. M. Schrander‐Stumpel, Sam Schoenmakers and Connie Schrander‐Stumpel and has published in prestigious journals such as International Journal of Cancer, Human Reproduction and Journal of Histochemistry & Cytochemistry.

In The Last Decade

J. Herbergs

25 papers receiving 618 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Herbergs Netherlands	15	405	321	127	113	68	26	644
Miroslav Mayer Croatia	18	654 1.6×	471 1.5×	135 1.1×	109 1.0×	142 2.1×	61	1.1k
Anna Marozzi Italy	21	672 1.7×	778 2.4×	133 1.0×	168 1.5×	130 1.9×	50	1.5k
Chansonette Harvard Canada	17	417 1.0×	294 0.9×	94 0.7×	185 1.6×	85 1.3×	19	681
R. Curtis Rogers United States	18	531 1.3×	519 1.6×	53 0.4×	108 1.0×	44 0.6×	37	1.2k
Isabel Filges Switzerland	18	435 1.1×	338 1.1×	35 0.3×	278 2.5×	44 0.6×	44	773
Maria Luisa Giovannucci Uzielli Italy	13	316 0.8×	287 0.9×	51 0.4×	49 0.4×	60 0.9×	26	546
Zoe Docherty United Kingdom	18	787 1.9×	378 1.2×	71 0.6×	540 4.8×	192 2.8×	36	1.1k
Brian P. Perry United States	12	233 0.6×	137 0.4×	79 0.6×	79 0.7×	64 0.9×	27	509
J. Britt Ravnan United States	12	811 2.0×	408 1.3×	83 0.7×	494 4.4×	160 2.4×	19	1.1k
Dunja Niedrist Switzerland	8	279 0.7×	263 0.8×	35 0.3×	119 1.1×	37 0.5×	11	571

Countries citing papers authored by J. Herbergs

Since Specialization

Citations

This map shows the geographic impact of J. Herbergs'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 J. Herbergs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Herbergs more than expected).

Fields of papers citing papers by J. Herbergs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. Herbergs. 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 J. Herbergs. The network helps show where J. Herbergs may publish in the future.

Co-authorship network of co-authors of J. Herbergs

This figure shows the co-authorship network connecting the top 25 collaborators of J. Herbergs. A scholar is included among the top collaborators of J. Herbergs 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 J. Herbergs. J. Herbergs is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Dukers–Muijrers, Nicole H. T. M., Petra Wolffs, Hannelore M Götz, et al.. (2016). Design of the FemCure study: prospective multicentre study on the transmission of genital and extra-genital Chlamydia trachomatis infections in women receiving routine care. BMC Infectious Diseases. 16(1). 381–381. 14 indexed citations

Weusten, Jos & J. Herbergs. (2011). A stochastic model of the processes in PCR based amplification of STR DNA in forensic applications. Forensic Science International Genetics. 6(1). 17–25. 42 indexed citations

Roessler, Erich, Felicitas Lacbawan, Aimée Paulussen, et al.. (2009). The full spectrum of holoprosencephaly-associated mutations within theZIC2gene in humans predicts loss-of-function as the predominant disease mechanism. Human Mutation. 30(4). E541–E554. 49 indexed citations

Stevens, Servi J.C., et al.. (2009). Identical cryptic partial monosomy 20pter and trisomy 20qter in three adult siblings due to a large maternal pericentric inversion: Detection by MLPA and breakpoint mapping by SNP array analysis. American Journal of Medical Genetics Part A. 149A(10). 2226–2230. 15 indexed citations

Dreesen, J., Marion Drüsedau, Hubert J.M. Smeets, et al.. (2008). Validation of preimplantation genetic diagnosis by PCR analysis: genotype comparison of the blastomere and corresponding embryo, implications for clinical practice. Molecular Human Reproduction. 14(10). 573–579. 17 indexed citations

Steensel, Maurice A. M. Van, Maaike Vreeburg, Jan Engelen, et al.. (2008). Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy–Walker malformation. American Journal of Medical Genetics Part A. 146A(22). 2944–2949. 21 indexed citations

Koolen, David A., J. Herbergs, Joris A. Veltman, et al.. (2006). Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1. Journal of Human Genetics. 51(8). 721–726. 9 indexed citations

Casaer, Paul, A.A.W. Peters, Alina T. Midro, et al.. (2004). Rett syndrome in females with CTS hot spot deletions: A disorder profile. American Journal of Medical Genetics Part A. 132A(2). 117–120. 57 indexed citations

Hamers, Guus, J.G. Nijhuis, J. Herbergs, et al.. (2003). Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes. American Journal of Medical Genetics Part A. 124A(3). 288–291. 11 indexed citations

10.

Smeets, Eric, Els Schollen, Ute Moog, et al.. (2003). Rett syndrome in adolescent and adult females: Clinical and molecular genetic findings. American Journal of Medical Genetics Part A. 122A(3). 227–233. 44 indexed citations

11.

Dreesen, Jos, L.J.A.M. Jacobs, M. Bras, et al.. (2000). Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis*. Molecular Human Reproduction. 6(5). 391–396. 69 indexed citations

12.

Engelen, Jan, et al.. (2000). Mosaic telomeric (2;14) association in a child with motor delay. American Journal of Medical Genetics. 92(5). 318–321. 6 indexed citations

13.

Herbergs, J., Maria Siwek, R.P.M.A. Crooijmans, J.J. van der Poel, & Martien A. M. Groenen. (1999). Multicolour fluorescent detection and mapping of AFLP markers in chicken (Gallus domesticus). Animal Genetics. 30(4). 274–285. 35 indexed citations

14.

Ruyter‐Spira, Carolien, J. Herbergs, Erik Limpens, et al.. (1998). Nucleotide sequence of the chicken HMGI-C cDNA and expression of the HMGI-C and IGF1 genes in autosomal dwarf chicken embryos. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1399(1). 83–87. 11 indexed citations

15.

Herbergs, J., Anton H. N. Hopman, Adriaan P. de Bruı̈ne, Frans C. S. Ramaekers, & Jan‐Willem Arends. (1996). IN SITU HYBRIDIZATION AND FLOW CYTOMETRIC ANALYSIS OF COLORECTAL TUMOURS SUGGESTS TWO ROUTES OF TUMOURIGENESIS CHARACTERIZED BY GAIN OF CHROMOSOME 7 OR LOSS OF CHROMOSOMES 17 AND 18. The Journal of Pathology. 179(3). 243–247. 20 indexed citations

16.

Herbergs, J., et al.. (1996). Combination of lamin immunocytochemistry and in situ hybridization for the analysis of chromosome copy numbers in tumor cell areas with high nuclear density. Cytometry. 23(1). 1–7. 7 indexed citations

17.

Speel, Ernst‐Jan M., et al.. (1994). Combined immunocytochemistry and fluorescence in situ hybridization for simultaneous tricolor detection of cell cycle, genomic, and phenotypic parameters of tumor cells.. Journal of Histochemistry & Cytochemistry. 42(7). 961–966. 34 indexed citations

18.

Herbergs, J., Adriaan P. de Bruı̈ne, Patrick Marx, et al.. (1994). Chromosome aberrations in adenomas of the colon. Proof of trisomy 7 in tumor cells by combined interphase cytogenetics and immunocytochemistry. International Journal of Cancer. 57(6). 781–785. 27 indexed citations

19.

Sinke, Richard J., Ron F. Suijkerbuijk, J. Herbergs, et al.. (1992). Generation of a panel of somatic cell hybrids containing fragments of human chromosome 12p by X-ray irradiation and cell fusion. Genomics. 12(2). 206–213. 30 indexed citations

20.

Suijkerbuijk, Ron F., Demetrios P. Matthopoulos, Robert E. Kearney, et al.. (1992). Fluorescent in situ identification of human marker chromosomes using flow sorting and Alu element-mediated PCR. Genomics. 13(2). 355–362. 37 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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