J.M.N. Hoovers

2.8k total citations
59 papers, 2.1k citations indexed

About

J.M.N. Hoovers is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J.M.N. Hoovers has authored 59 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 33 papers in Genetics and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J.M.N. Hoovers's work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (19 papers) and Chromosomal and Genetic Variations (10 papers). J.M.N. Hoovers is often cited by papers focused on Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (19 papers) and Chromosomal and Genetic Variations (10 papers). J.M.N. Hoovers collaborates with scholars based in Netherlands, United Kingdom and United States. J.M.N. Hoovers's co-authors include Raoul C. M. Hennekam, N. J. Leschot, J. Wiegant, Marja E. Jakobs, Ronald J. A. Wanders, Jet Bliek, M. Mannens, Jan W. A. de Vries, Anton K. Raap and Lodewijk IJlst and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Immunology.

In The Last Decade

J.M.N. Hoovers

59 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
J.M.N. Hoovers Netherlands 24 1.3k 1.0k 342 342 183 59 2.1k
Jay W. Ellison United States 23 1.2k 0.9× 1.2k 1.2× 438 1.3× 210 0.6× 144 0.8× 52 2.6k
Lingqian Wu China 24 1.2k 0.9× 865 0.8× 619 1.8× 93 0.3× 124 0.7× 186 2.4k
Svetlana A. Yatsenko United States 26 1.5k 1.2× 1.8k 1.7× 628 1.8× 366 1.1× 98 0.5× 110 3.0k
M Prieur France 26 1.4k 1.1× 1.5k 1.5× 449 1.3× 445 1.3× 77 0.4× 75 2.6k
H F Willard United States 22 1.2k 0.9× 804 0.8× 124 0.4× 545 1.6× 112 0.6× 28 1.8k
Eric Engel United States 27 1.1k 0.9× 1.8k 1.7× 922 2.7× 258 0.8× 87 0.5× 99 2.6k
Tatsuro Ikeuchi Japan 28 1.4k 1.1× 869 0.8× 271 0.8× 370 1.1× 451 2.5× 106 2.6k
L.-C. Tsui Canada 20 1.5k 1.2× 692 0.7× 120 0.4× 177 0.5× 95 0.5× 33 2.4k
S Malcolm United Kingdom 29 1.7k 1.3× 1.8k 1.7× 394 1.2× 164 0.5× 116 0.6× 51 3.0k
Aslıhan Tolun Türkiye 24 1.4k 1.0× 936 0.9× 72 0.2× 87 0.3× 178 1.0× 81 2.3k

Countries citing papers authored by J.M.N. Hoovers

Since Specialization
Citations

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

Fields of papers citing papers by J.M.N. Hoovers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.M.N. Hoovers

This figure shows the co-authorship network connecting the top 25 collaborators of J.M.N. Hoovers. A scholar is included among the top collaborators of J.M.N. Hoovers 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.M.N. Hoovers. J.M.N. Hoovers 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.
Mathijssen, Inge B., et al.. (2005). Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: A recognizable syndrome. American Journal of Medical Genetics Part A. 136A(1). 76–80. 11 indexed citations
2.
Engels, Hartmut, Susanne Zahn, Kristin Bosse, et al.. (2003). Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation. European Journal of Human Genetics. 11(9). 643–651. 13 indexed citations
3.
Vries, Jan W. A. de, Mariëtte J.V. Hoffer, Sjoerd Repping, et al.. (2002). Reduced copy number of DAZ genes in subfertile and infertile men. Fertility and Sterility. 77(1). 68–75. 45 indexed citations
4.
Schuring‐Blom, G. Heleen, J.M.N. Hoovers, J. M. M. van Lith, Alida C. Knegt, & N. J. Leschot. (2001). FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy. Prenatal Diagnosis. 21(10). 864–867. 3 indexed citations
5.
6.
Grierson, Andrew J., Marjon van Groenigen, Kerstin Lindblad, et al.. (1999). An integrated map of chromosome 18 CAG trinucleotide repeat loci. European Journal of Human Genetics. 7(1). 12–19. 5 indexed citations
7.
Hoovers, J.M.N., et al.. (1998). Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6. American Journal of Medical Genetics. 80(5). 448–453. 11 indexed citations
8.
Aalfs, Cora M., et al.. (1997). Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: Dose effect of the PAX6 gene product?. American Journal of Medical Genetics. 73(3). 267–271. 33 indexed citations
9.
Hadjantonakis, Anna‐Katerina, et al.. (1997). Celsr1, a Neural-Specific Gene Encoding an Unusual Seven-Pass Transmembrane Receptor, Maps to Mouse Chromosome 15 and Human Chromosome 22qter. Genomics. 45(1). 97–104. 56 indexed citations
10.
Aalfs, Cora M., et al.. (1996). Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay. Clinical Genetics. 49(1). 42–45. 13 indexed citations
11.
Redeker, E., Mariëlle Alders, J.M.N. Hoovers, et al.. (1995). Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3. Cytogenetic and Genome Research. 68(3-4). 222–225. 18 indexed citations
12.
Engelen, J.J.M., et al.. (1994). Partial trisomy and monosomy 8p due to inversion duplication. Clinical Genetics. 45(4). 203–207. 16 indexed citations
13.
Redeker, E., J.M.N. Hoovers, Mariëlle Alders, et al.. (1994). An Integrated Physical Map of 210 Markers Assigned to the Short Arm of Human Chromosome 11. Genomics. 21(3). 538–550. 23 indexed citations
14.
Henry, Isabelle, J.M.N. Hoovers, F. Barichard, et al.. (1993). Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family. Genes Chromosomes and Cancer. 7(1). 57–62. 10 indexed citations
15.
Hoovers, J.M.N., M. Mannens, Rosalind M. John, et al.. (1992). High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered. Genomics. 12(2). 254–263. 114 indexed citations
16.
Mannens, M., J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, et al.. (1991). The distal region of 11p13 and associated genetic diseases. Genomics. 11(2). 284–293. 19 indexed citations
17.
Bout, A., J.M.N. Hoovers, E.H. Bakker, et al.. (1989). Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22→p23. Cytogenetic and Genome Research. 52(3-4). 147–150. 9 indexed citations
18.
Mannens, M., E. M. Bleeker‐Wagemakers, Jet Bliek, et al.. (1989). Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenetic and Genome Research. 52(1-2). 32–36. 27 indexed citations
19.
Hoovers, J.M.N., J. W. E. Oorthuys, & M. Visser. (1989). Mosaic 47,XY, + 8/48,XXYY in a mentally non‐retarded man with phenotypical and neurological abnormalities. Clinical Genetics. 35(6). 446–449. 7 indexed citations
20.
Ronde, Anthony de, Marcel M. A. M. Mannens, Rosalyn Slater, et al.. (1988). Morphological Transformation by Early Region Human Polyomavirus BK DNA of Human Fibroblasts with Deletions in the Short Arm of One Chromosome 11. Journal of General Virology. 69(2). 467–471. 9 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Jay W. Ellison Breakdown of academic impact, for papers by Lingqian Wu Breakdown of academic impact, for papers by Svetlana A. Yatsenko Breakdown of academic impact, for papers by M Prieur Breakdown of academic impact, for papers by H F Willard Breakdown of academic impact, for papers by Eric Engel Breakdown of academic impact, for papers by Tatsuro Ikeuchi Breakdown of academic impact, for papers by L.-C. Tsui Breakdown of academic impact, for papers by S Malcolm Breakdown of academic impact, for papers by Aslıhan Tolun
Rankless by CCL
2026