A. Westerveld

7.8k citations
153 papers · 5.7k · h-index 42

Impact in

  • Neurology top 1%
    • Neuroblastoma Research and Treatments
  • Molecular Biology top 1%
    • DNA Repair Mechanisms
    • CRISPR and Genetic Engineering
    • Retinal Development and Disorders
    • Genomics and Chromatin Dynamics
    • Epigenetics and DNA Methylation

Papers in

  • Molecular Biology 102
    • DNA Repair Mechanisms 29
    • CRISPR and Genetic Engineering 20
    • Biochemical and Molecular Research 13
    • Epigenetics and DNA Methylation 12
  • Genetics 49
    • Virus-based gene therapy research 13
    • Genetic Syndromes and Imprinting 11
Co-authors
D. Bootsma (34 shared papers)Jan H.J. Hoeijmakers (13 shared papers)Hanny Odijk (10 shared papers)Rosalyn Slater (17 shared papers)P. Meera Khan (14 shared papers)Rogier Versteeg (13 shared papers)Jan de Wit (10 shared papers)Arthur A. Bergen (5 shared papers)
Journals
Human Genetics (18 papers)Genes Chromosomes and Cancer (13 papers)Experimental Cell Research (9 papers)Genomics (8 papers)Nature (5 papers)
Partner nations
NetherlandsUnited KingdomUnited States

In The Last Decade

A. Westerveld

145 papers receiving 5.5k citations

Peers

A. Westerveld
Comparison fields: 5 of 127
  • Neurology 882
  • Molecular Biology 3.8k
  • Cancer Research 767
  • Genetics 1.2k
  • Genetics 264
Replace Jan P. Dumanski with:
Jan P. Dumanski Sweden
Ute Felbor Germany
J. David Brook United Kingdom
Eric Rappaport United States
Kei Tashiro Japan
John R.W. Yates United Kingdom
Camilynn I. Brannan United States
Thomas Maciag United States
G.J.B. van Ommen Netherlands
Marco Tartaglia Italy
A. Westerveld relative to Jan P. Dumanski Sweden Jan P. Dumanski's profile →
Citations per field
00.5×1.5×
Jan P. Dumanski · 1×
Citations per year

Countries citing papers authored by A. Westerveld

Since Specialization
Citations

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

Fields of papers citing papers by A. Westerveld

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 153 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
Nature Genetics ·Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok, S. van Soest, L. Ingeborgh van den Born, Marc A. van Driel, Dorien J.R. van de Pol, Annette Payne, Shomi S. Bhattacharya, Ulrich Kellner, Carel B. Hoyng, A. Westerveld, Han G. Brunner, Elisabeth M. Bleeker‐Wagemakers, August F. Deutman, John R. Heckenlively, Frans P.M. Cremers, Arthur A. Bergen
1999382
2
Allelic Loss of Chromosome 1p as a Predictor of Unfavorable Outcome in Patients with Neuroblastoma
New England Journal of Medicine ·Huib N. Caron, Peter van Sluis, Jan de Kraker, Jos P.M. Bökkerink, Maarten Egeler, Geneviève Laureys, Rosalyn Slater, A. Westerveld, P.A. Voûte, Rogier Versteeg
1996326
3
Molecular characterization of the human excision repair gene : cDNA cloning and amino acid homology with the yeast DNA repair gene
Cell ·M. Vanduin, (unknown), Hanny Odijk, A. Westerveld, Akira Yasui, Marcel Koken, Jan H.J. Hoeijmakers, D. Bootsma
1986282
4
Molecular cloning of a human DNA repair gene
Nature ·A. Westerveld, Jan H.J. Hoeijmakers, Marcel van Duin, Jan de Wit, Hanny Odijk, Albert Pastink, Richard D. Wood, D. Bootsma
1984259
5
Retinitis Pigmentosa
Survey of Ophthalmology ·S. van Soest, A. Westerveld, Paulus T. V. M. de Jong, Elisabeth M. Bleeker‐Wagemakers, Arthur A. Bergen
1999222
6
Loss of Human Genetic Markers in Man-Chinese Hamster Somatic Cell Hybrids
Nature New Biology ·A. Westerveld, Rianne Visser, P. Meera Khan, D. Bootsma
1971157
7
Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification
Human Molecular Genetics ·Huib N. Caron, Martine Peter, Peter van Sluis, Frank Speleman, Jan de Kraker, Geneviève Laureys, Jean Michon, Laurence Brugières, P.A. Voûte, A. Westerveld, Rosalyn Slater, Olivier Delattre, Rogier Versteeg
1995126
8
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
Journal of Clinical Investigation ·Stanley Brul, A. Westerveld, Anneke Strijland, Ronald J. A. Wanders, A. W. Schram, H. S. A. Heymans, R. B. H. Schutgens, H. van den Bosch, J. M. Tager
1988125
9
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
1992114
10
Molecular cloning of the human DNA excision repair gene ERCC-6.
Molecular and Cellular Biology ·Christine Troelstra, Hanny Odijk, Jan de Wit, A. Westerveld, L.H. Thompson, D. Bootsma, Jan H.J. Hoeijmakers
1990111
11
Human Antigen and Enzyme Markers in Man-Chinese Hamster Somatic Cell Hybrids: Evidence for Synteny Between the HL-A, PGM 3 , ME 1 , and IPO-B Loci
Proceedings of the National Academy of Sciences ·H. van Someren, A. Westerveld, A. Hagemeijer, J. R. Mees, P. Meera Khan, O.B. Zaalberg
1974109
12
Molecular cloning and biological characterization of the human excision repair gene ERCC-3.
Molecular and Cellular Biology ·Geert Weeda, R C van Ham, Remco Masurel, A. Westerveld, Hanny Odijk, Jan de Wit, D. Bootsma, A.J. van der Eb, J H Hoeijmakers
1990103
13
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.
PubMed ·N C Cheng, Nadine Van Roy, Alvin Chan, M. Beitsma, A. Westerveld, Frank Speleman, Rogier Versteeg
1995102
14
Maintenance of Vascular Endothelial Cell-Specific Properties after Immortalization with an Amphotrophic Replication-Deficient Retrovirus Containing Human Papilloma Virus 16 E6/E7 DNA
Experimental Cell Research ·Ruud D. Fontijn, Caroline Hop, Herm‐Jan Brinkman, Rosalyn Slater, A. Westerveld, Jan A. van Mourik, Hans Pannekoek
199597
15
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma
Genes Chromosomes and Cancer ·Mario Hermsen, Hans Joenje, Fré Arwert, Marij J.P. Welters, Boudewijn J.M. Braakhuis, Marjan Bagnay, A. Westerveld, Rosalyn Slater
199696
16
Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids
Human Genetics ·A.P.M. Jongsma, H. van Someren, A. Westerveld, A. Hagemeijer, P. Pearson
197396
17
Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
Human Genetics ·R. A. Barneveld, W. Keiizer, F. P. W. Tegelaers, Edward I. Ginns, Ad Geurts van Kessel, Roscoe O. Brady, J. A. Barranger, J. M. Tager, H. Galjaard, A. Westerveld, Arnold Reuser
198379
18
Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3
Nature Genetics ·Jan C. Pronk, Rachel A. Gibson, Anna Savoia, Mario Wijker, Neil V. Morgan, Salvatore Melchionda, Deborah Ford, Samia A. Temtamy, Juan Ortega, S Jansen, Charmaine Havenga, Richard J. Cohn, Thomy de Ravel, Irene Roberts, A. Westerveld, Douglas F. Easton, Hans Joenje, Christopher G. Mathew, Fré Arwert
199578
19
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
European Journal of Human Genetics ·Jet Bliek, Mariëlle Alders, Saskia M. Maas, Roelof‐Jan Oostra, Deborah Mackay, K. Lip, Johnatan L Callaway, Alice S. Brooks, Sandra van ‘t Padje, A. Westerveld, N. J. Leschot, Marcel M. A. M. Mannens
200974
20
Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.
PubMed ·Marcel M. A. M. Mannens, Peter Devilee, Jet Bliek, Ingrid A.M. Mandjes, Jan de Kraker, Christa Heyting, Rosalyn Slater, A. Westerveld
199071

About A. Westerveld

A. Westerveld is a scholar working on Molecular Biology, Genetics, Neurology, Cancer Research and Physiology, having authored 153 papers that have together received 5.7k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (29 papers), CRISPR and Genetic Engineering (20 papers), Virus-based gene therapy research (13 papers), Biochemical and Molecular Research (13 papers), Epigenetics and DNA Methylation (12 papers), Lysosomal Storage Disorders Research (11 papers), Genetic Syndromes and Imprinting (11 papers) and Neuroblastoma Research and Treatments (10 papers). The work is most often cited by research in Neurology (882 citations), Molecular Biology (3.8k citations), Cancer Research (767 citations), Genetics (1.2k citations) and Genetics (264 citations). A. Westerveld has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include D. Bootsma, Jan H.J. Hoeijmakers, Hanny Odijk, Rosalyn Slater, P. Meera Khan, Rogier Versteeg, Jan de Wit, Arthur A. Bergen, S. van Soest and Theo J.M. Hulsebos. Their work appears in journals such as Human Genetics, Genes Chromosomes and Cancer, Experimental Cell Research, Genomics and Nature.

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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