J.M.N. Hoovers

2.8k citations

59 papers · 2.1k · h-index 24

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- Sexual Differentiation and Disorders

Papers in

Molecular Biology 34
- Renal and related cancers 7
- Epigenetics and DNA Methylation 7
Genetics 33
- Genomic variations and chromosomal abnormalities 19
- Genetic Syndromes and Imprinting 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5

Co-authors: Raoul C. M. Hennekam (13 shared papers)N. J. Leschot (15 shared papers)J. Wiegant (5 shared papers)Marja E. Jakobs (7 shared papers)Ronald J. A. Wanders (2 shared papers)Jet Bliek (8 shared papers)Jan W. A. de Vries (2 shared papers)Lodewijk IJlst (1 shared paper)
Journals: Genomics (11 papers)Prenatal Diagnosis (7 papers)Clinical Genetics (6 papers)Cytogenetic and Genome Research (5 papers)European Journal of Human Genetics (3 papers)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

J.M.N. Hoovers

59 papers receiving 2.0k citations

Peers

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-authors

The 25 scholars most cited alongside J.M.N. Hoovers, 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 J.M.N. Hoovers Line = papers co-authored together J.M.N. Hoovers links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Four DAZ Genes in Two Clusters Found in the AZFc Region of the Human Y Chromosome Genomics ·Richa Saxena, Jan W. A. de Vries, Sjoerd Repping, R. Alagappan, Helen Skaletsky, Laura Brown, Peter Ma, Ellson Chen, J.M.N. Hoovers, David C. Page	2000	181
2	Progression from colorectal adenoma to carcinoma is associated with non-random chromosomal gains as detected by comparative genomic hybridisation. Journal of Clinical Pathology ·Gerrit A. Meijer, Mario A. Hermsen, Jan P. A. Baak, P. J. van Diest, S. G. M. Meuwissen, Jeroen A.M. Beliën, J.M.N. Hoovers, Hans Joenje, Peter J.F. Snijders, Jan M.M. Walboomers	1998	153
3	Expression cloning and chromosomal mapping of the leukocyte activation antigen CD97, a new seven-span transmembrane molecule of the secretion receptor superfamily with an unusual extracellular domain The Journal of Immunology ·Jörg Hamann, Wd. Eichler, Dörte Hamann, Harold M.J. Kerstens, Pino J. Poddighe, J.M.N. Hoovers, Enno Hartmann, Mike Strauss, René A. W. van Lier	1995	137
4	High-resolution in situ hybridization using DNA halo preparations Human Molecular Genetics ·J. Wiegant, Wouter Kalle, L.H.F. Mullenders, Sharon Brookes, J.M.N. Hoovers, Johannes G. Dauwerse, G.J.B. van Ommen, Anton K. Raap	1992	135
5	Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene. Journal of Clinical Investigation ·Lodewijk IJlst, Jos P.N. Ruiter, J.M.N. Hoovers, Marja E. Jakobs, Ronald J. A. Wanders	1996	129
6	High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered Genomics ·J.M.N. Hoovers, M. Mannens, Rosalind M. John, Jet Bliek, Veronica van Heyningen, David J. Porteous, N. J. Leschot, A. Westerveld, Peter Little	1992	114
7	Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proceedings of the National Academy of Sciences ·J.M.N. Hoovers, Linda M. Kalikin, Laura A. Johnson, Mariëlle Alders, B. Redeker, David Law, Jet Bliek, Marja Steenman, Mark Q. Benedict, J. Wiegant	1995	94
8	Replication pattern of the X chromosomes in three X/autosomal translocations Cytogenetic and Genome Research ·A. Hagemeijer, J.M.N. Hoovers, E.M.E. Smit, D. Bootsma	1977	86
9	Etiology of Mental Retardation in Children Referred to a Tertiary Care Center: A Prospective Study American Journal on Mental Retardation ·Clara van Karnebeek, Frederike Y. Scheper, N. G. G. M. Abeling, Mariëlle Alders, P. G. Barth, J.M.N. Hoovers, Cindy Koevoets, Ronald J. A. Wanders, Raoul C. M. Hennekam	2005	74
10	Multiple and sensitive fluorescence in situ hybridization with rhodamine-, fluorescein-, and coumarin-labeled DNAs Cytogenetic and Genome Research ·J. Wiegant, C. Wiesmeijer, J.M.N. Hoovers, Ed Schuuring, Alessandra d’Azzo, J. Vrolijk, Hans J. Tanke, Anton K. Raap	1993	68
11	Further delineation of the chromosome 14q terminal deletion syndrome American Journal of Medical Genetics ·Clara van Karnebeek, Safira Quik, Sigrid Sluijter, Miriam Hulsbeek, J.M.N. Hoovers, Raoul C. M. Hennekam	2002	67
12	Genetic Alterations in Childhood Medulloblastoma Analyzed by Comparative Genomic Hybridization Journal of Pediatric Hematology/Oncology ·Erna Michiels, Marjan M. Weiss, J.M.N. Hoovers, Jan P. A. Baak, P. A. Voûte, Frank Baas, Mario Hermsen	2002	56
13	Celsr1, a Neural-Specific Gene Encoding an Unusual Seven-Pass Transmembrane Receptor, Maps to Mouse Chromosome 15 and Human Chromosome 22qter Genomics ·Anna‐Katerina Hadjantonakis, W. John Sheward, Anthony J. Harmar, Louis de Galan, J.M.N. Hoovers, Peter Little	1997	56
14	Two Novel Human Members of an Emerging Mammalian Gene Family Related to Mono-ADP-Ribosylating Bacterial Toxins Genomics ·Friedrich Koch‐Nolte, Friedrich Haag, Rickmer Braren, Maren Kühl, J.M.N. Hoovers, Sriram Balasubramanian, Fernando Bazán, Heinz‐Günter Thiele	1997	53
15	Reduced copy number of DAZ genes in subfertile and infertile men Fertility and Sterility ·Jan W. A. de Vries, Mariëtte J.V. Hoffer, Sjoerd Repping, J.M.N. Hoovers, N. J. Leschot, Fulco van der Veen	2002	45
16	Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3) Human Genetics ·André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Raoul C. M. Hennekam, J.M.N. Hoovers, Christine de Die‐Smulders, Christian Weber, Andrea Mori, Jörgen Bierau, Brian Fowler, Klaus Macke, Jörn Oliver Sass, Rutger Meinsma, Julia B. Hennermann, Peter Miny, Lida Zoetekouw, Raymon Vijzelaar, Joost Nicolai, Bauke Ylstra, M. Estela Rubio‐Gozalbo	2009	39
17	Human Synaptonemal Complex Protein 1 (SCP1): Isolation and Characterization of the cDNA and Chromosomal Localization of the Gene Genomics ·Ralph Meuwissen, I. Meerts, J.M.N. Hoovers, N. J. Leschot, Christa Heyting	1997	39
18	Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype Journal of Medical Genetics ·Emilia K. Bijlsma, Cora M. Aalfs, Sigrid Sluijter, M E Oude Luttikhuis, Richard C. Trembath, J.M.N. Hoovers, Raoul C. M. Hennekam	1999	34
19	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 ·Cora M. Aalfs, Judy Fantes, Liesbeth J.J.M. Wenniger-Prick, Sigrid Sluijter, Raoul C. M. Hennekam, Veronica van Heyningen, J.M.N. Hoovers	1997	33
20	Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system Prenatal Diagnosis ·Irene M. de Graaf, Marja E. Jakobs, N. J. Leschot, Ilya Ravkin, Simon Goldbard, J.M.N. Hoovers	1999	29

About J.M.N. Hoovers

J.M.N. Hoovers is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Infectious Diseases, having authored 59 papers that have together received 2.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (10 papers), Genetic Syndromes and Imprinting (8 papers), Renal and related cancers (7 papers), Epigenetics and DNA Methylation (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Parvovirus B19 Infection Studies (4 papers). The work is most often cited by research in Genetics (1.0k citations), Molecular Biology (1.3k citations), Clinical Biochemistry (124 citations), Pediatrics, Perinatology and Child Health (342 citations) and Reproductive Medicine (140 citations). J.M.N. Hoovers has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Raoul C. M. Hennekam, N. J. Leschot, J. Wiegant, Marja E. Jakobs, Ronald J. A. Wanders, Jet Bliek, Jan W. A. de Vries, Lodewijk IJlst, A. Westerveld and Anton K. Raap. Their work appears in journals such as Genomics, Prenatal Diagnosis, Clinical Genetics, Cytogenetic and Genome Research and European Journal of Human Genetics.

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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J.M.N. Hoovers

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