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J. Hoovers · SciRah

Researcher profile · Semantic Scholar

J. Hoovers

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J. Hoovers — researcher profile on SciRah

h-index: 28
Works: 80
Citations: 2,897

Most-cited papers

Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome.
Richa Saxena, J. D. de Vries, S. Repping, R. Alagappan +6 more
2000Genomics241 citations
Semantic Scholar
Progression from colorectal adenoma to carcinoma is associated with non-random chromosomal gains as detected by comparative genomic hybridisation.
G. Meijer, M. Hermsen, J. Baak, P. V. van Diest +6 more
1998Journal of Clinical Pathology200 citations Open access
Semantic Scholar
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.
J. Hamann, W. Eichler, D. Hamann, H. M. Kerstens +5 more
1995Journal of Immunology182 citations
Semantic Scholar
High-resolution in situ hybridization using DNA halo preparations.
J. Wiegant, Wouter Kalle, Leon H. F. Mullenders, S. Brookes +4 more
1992Human Molecular Genetics179 citations
Semantic Scholar
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.
L. Ijlst, J. P. N. Ruiter, J. Hoovers, M. Jakobs +1 more
1996Journal of Clinical Investigation161 citations Open access
Semantic Scholar
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.
J. Hoovers, M. Mannens, Rosalind M. John, J. Bliek +5 more
1992Genomics141 citations
Semantic Scholar
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.
J. Hoovers, L. Kalikin, L. Johnson, M. Alders +16 more
1995Proceedings of the National Academy of Sciences of the United States of America119 citations Open access
Semantic Scholar
Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia
M. Mannens, J. Hoovers, E. Redeker, M. Verjaal +20 more
1994European Journal of Human Genetics111 citations
Semantic Scholar
Etiology of mental retardation in children referred to a tertiary care center: a prospective study.
C. van Karnebeek, F. Scheper, N. Abeling, M. Alders +5 more
2005American journal of mental retardation : AJMR108 citations
Semantic Scholar
Further delineation of the chromosome 14q terminal deletion syndrome.
C. van Karnebeek, Safira Quik, S. Sluijter, M. Hulsbeek +2 more
2002American journal of medical genetics90 citations
Semantic Scholar
Multiple and sensitive fluorescence in situ hybridization with rhodamine-, fluorescein-, and coumarin-labeled DNAs.
J. Wiegant, C. Wiesmeijer, J. Hoovers, E. Schuuring +4 more
1993Cytogenetics and Cell Genetics88 citations
Semantic Scholar
Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience
C. van Karnebeek, C. Koevoets, S. Sluijter, E. Bijlsma +4 more
2002Journal of Medical Genetics86 citations Open access
Semantic Scholar
Genetic Alterations in Childhood Medulloblastoma Analyzed by Comparative Genomic Hybridization
E. Michiels, M. Weiss, J. Hoovers, J. Baak +3 more
2002Journal of pediatric hematology/oncology79 citations
Semantic Scholar
Celsr1, a neural-specific gene encoding an unusual seven-pass transmembrane receptor, maps to mouse chromosome 15 and human chromosome 22qter.
A. Hadjantonakis, W. Sheward, A. J. Harmar, L. de Galan +2 more
1997Genomics74 citations Open access
Semantic Scholar
Two novel human members of an emerging mammalian gene family related to mono-ADP-ribosylating bacterial toxins.
F. Koch-Nolte, Friedrich Haag, Rickmer Braren, Maren Kühl +4 more
1997Genomics66 citations Open access
Semantic Scholar
A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.
J. Fantes, Kathy Oghene, Shelagh Boyle, Sarah Danes +19 more
1995Genomics61 citations
Semantic Scholar
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)
A. V. van Kuilenburg, J. Meijer, A. Mul, R. Hennekam +16 more
2009Human Genetics58 citations Open access
Semantic Scholar
Reduced copy number of DAZ genes in subfertile and infertile men.
J. D. de Vries, M. Hoffer, S. Repping, J. Hoovers +2 more
2002Fertility and Sterility58 citations Open access
Semantic Scholar
Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype
E. Bijlsma, Cora M. Aalfs, S. Sluijter, M. M. OudeLuttikhuis +3 more
1999Journal of Medical Genetics44 citations Open access
Semantic Scholar
Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?
Cora M. Aalfs, Judy Fantes, L. Wenniger-Prick, S. Sluijter +3 more
1997American journal of medical genetics43 citations
Semantic Scholar
Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion
V. van Heyningen, J. Hoovers, J. de Kraker, J. Crolla
2007Journal of Medical Genetics38 citations Open access
Semantic Scholar
Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system
I. D. de Graaf, M. Jakobs, N. Leschot, I. Ravkin +2 more
1999Prenatal Diagnosis37 citations Open access
Semantic Scholar
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.
J. Hoovers, E. J. Redeker, F. Speleman, J. Höppener +6 more
1993Genomics36 citations
Semantic Scholar
An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.
E. J. Redeker, J. Hoovers, Marielle Alders, C. J. V. van Moorsel +12 more
1994Genomics34 citations
Semantic Scholar
Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization
I. M. Langen, Mariëlle A. Otter, Daniël C. Aronson, W. Overweg-Plandsoen +3 more
1996Clinical Genetics32 citations
Semantic Scholar
Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.
M. Mannens, E. Bleeker-wagemakers, J. Bliek, J. Hoovers +6 more
1989Cytogenetics and Cell Genetics32 citations
Semantic Scholar
Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization
G. Schuring-Blom, M. Keuzer, M. Jakobs, D. M. van den Brande +4 more
1993Prenatal Diagnosis31 citations
Semantic Scholar
A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2
Redeker, A. V. van Eeghen, J. Hoovers, R. Hennekam +5 more
200228 citations
Semantic Scholar
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
M. Mannens, Marielle Alders, B. Redeker, J. Bliek +12 more
1996Medical and Pediatric Oncology26 citations
Semantic Scholar
The distal region of 11p13 and associated genetic diseases.
M. Mannens, J. Hoovers, E. Bleeker-wagemakers, E. Redeker +12 more
1991Genomics25 citations
Semantic Scholar
A male infant with holoprosencephaly, associated with ring chromosome 21
Daniel C. Aronson, M. C. E. Jansweijer, J. Hoovers, P. Barth
1987Clinical Genetics25 citations
Semantic Scholar
An aetiological study of 25 mentally retarded adults with autism [research letter]
D. KarnebeekvanC., I. Gelderenvan, G. Nijhof, N. Abeling +5 more
200224 citations
Semantic Scholar
Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.
E. J. Redeker, M. Alders, J. Hoovers, C. W. Richard +2 more
1995Cytogenetics and Cell Genetics24 citations
Semantic Scholar
Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation
H. Engels, Antje Ehrbrecht, Susanne Zahn, K. Bosse +9 more
2003European Journal of Human Genetics23 citations
Semantic Scholar
Interstitial deletion of the long arm of chromosome 2: a clinically recognizable microdeletion syndrome?
S. Maas, J. Hoovers, Marleen E. van Seggelen, Daria M. Menzel +1 more
2000Clinical Dysmorphology23 citations
Semantic Scholar
Celsr 1 , a Neural-Specific Gene Encoding an Unusual Seven-Pass Transmembrane Receptor , Maps to Mouse Chromosome 15 and Human Chromosome 22 qter
A. Hadjantonakis, W. Sheward, A. J. Harmar, L. de Galan +2 more
199720 citations
Semantic Scholar
Human synaptonemal complex protein 1 (SCP1): isolation and characterization of the cDNA and chromosomal localization of the gene.
R. L. J. Meuwissen, I. Meerts, J. Hoovers, N. Leschot +1 more
1997Genomics17 citations Open access
Semantic Scholar
Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion
Trijn Israëls, J. Hoovers, Hanne M. Turpijn, F. Wijburg +1 more
1996Clinical Genetics16 citations
Semantic Scholar
Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: A recognizable syndrome
I. B. Mathijssen, J. Hoovers, A. Mul, H. Man +2 more
2005American Journal of Medical Genetics. Part A15 citations
Semantic Scholar
First‐trimester non‐invasive prenatal diagnosis of triploidy
I. D. de Graaf, Saskia M. C. A. van Bezouw, M. Jakobs, N. Leschot +3 more
1999Prenatal Diagnosis15 citations Open access
Semantic Scholar
Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6.
S. E. Groen, J. G. Drewes, Ellen G. de Boer, J. Hoovers +1 more
1998American journal of medical genetics15 citations
Semantic Scholar
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family
I. Henry, J. Hoovers, F. Barichard, M. Berthéas +6 more
1993Genes, Chromosomes and Cancer15 citations Open access
Semantic Scholar
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11.
A. de Ronde, M. Mannens, R. Slater, J. Hoovers +7 more
1988Journal of General Virology14 citations Open access
Semantic Scholar
Further delineation of the partial proximal trisomy 10q syndrome.
C. Aalfs, J. Hoovers, M. A. Nieste-Otter, M. Mannens +2 more
1995Journal of Medical Genetics13 citations Open access
Semantic Scholar
Imprinting and Beckwith-Wiedemann syndrome.
J. Hoovers, A. Dietrich, M. Mannens
1992The Lancet13 citations
Semantic Scholar
Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features
T. Kleefstra, G. van de Zande, G. Merkx, H. Mieloo +2 more
2000European Journal of Human Genetics12 citations
Semantic Scholar
Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay
Cora M. Aalfs, M. E. Jacobs, Marlëlle A. Nieste-Otter, R. Hennekam +1 more
1996Clinical Genetics12 citations
Semantic Scholar
The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.
Ian J. J. P. Heding, A. Ivens, Jeff Wilson, M. Strivens +7 more
1992Genomics11 citations
Semantic Scholar
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization
Y. Fukushima, J. Hoovers, M. Mannens, K. Wakui +4 more
1993Human Genetics9 citations
Semantic Scholar
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23.
A. Bout, J. Hoovers, E. Bakker, M. Mannens +4 more
1989Cytogenetics and Cell Genetics9 citations
Semantic Scholar

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