World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
60
Citations
9838
World Ranking
3180
National Ranking
111

Overview

Andries Westerveld is affiliated with the University of Amsterdam in the Netherlands. Their academic career is connected to this institution, which is known for its research activities across various disciplines.

Currently, there is no public information available regarding their recent papers, co-authors, or frequent publication venues. Additionally, there are no documented contributions in book publications, main fields of study, subfields, or specific research topics associated with their name in the accessible data.

No award recognitions or honors are recorded at this time for Andries Westerveld. Furthermore, they are not listed as deceased, indicating ongoing professional activity or current affiliation status.

Given the limited publicly available data, a detailed outline of their research focus, academic impact, or collaborative networks cannot be provided at this moment.

Best Publications

  • Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).

    A.I. den Hollander;J.B. ten Brink;Y.J.M. de Kok;S. van Soest

  • Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma.

    H.N. Caron;P. van Sluis;J. de Kraker;J.P.M. Bökkerink

  • Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10.

    Marcel van Duin;Jan de Wit;Hanny Odijk;Andries Westerveld

  • Retinitis pigmentosa: defined from a molecular point of view.

    S. van Soest;A. Westerveld;P.T.V.M. de Jong;E.M. Bleeker-Wagemakers

  • Molecular cloning of a human dna repair gene

    A. Westerveld;J. H. J. Hoeijmakers;M. van Duin;J. de Wit

  • Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

    Jet Bliek;Saskia M. Maas;Jan M. Ruijter;Raoul C.M. Hennekam

  • Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.

    S. Brul;A. Westerveld;A. Strijland;R. J. A. Wanders

  • Loss of human genetic markers in man--Chinese hamster somatic cell hybrids.

    A. Westerveld;R. P. L. S. Visser;P. Meera Khan;D. Bootsma

  • High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered

    J.M.N. Hoovers;M. Mannens;R. John;J. Bliek

  • Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.

    H Caron;P van Sluis;M van Hoeve;J de Kraker

  • Human antigen and enzyme markers in man-Chinese hamster somatic cell hybrids: evidence for synteny between the HL-A, PGM3, ME1, and IPO-B loci.

    H. Van Someren;A. Westerveld;A. Hagemeijer;J. R. Mees

  • Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

    Huib Caron;Martine Peter;Peter van Sluis;Frank Speleman

  • Molecular cloning and biological characterization of the human excision repair gene ERCC-3.

    G. Weeda;R. C. A. Van Ham;R. Masurel;A. Westerveld

  • Molecular cloning of the human DNA excision repair gene ERCC-6.

    C. Troelstra;H. Odijk;J. De Wit;A. Westerveld

  • Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

    Jan M.N. Hoovers;Linda M. Kalikin;Linda M. Kalikin;Laura A. Johnson;Marielle Alders

  • Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids. Assignment of PGM3 to chromosome C6 and regional mapping of the PGD, PGM1 and pep-C genes on chromosome A1.

    Ans Jongsma;Harry van Someren;Andries Westerveld;Ann Hagemeijer

  • Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies

    Barneveld Ra;Keijzer W;Tegelaers Fp;Ginns Ei

  • 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.

    N C Cheng;N Van Roy;A Chan;M Beitsma

  • Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma.

    Mario A. J. A. Hermsen;Hans Joenje;Fré Arwert;Marij J. P. Welters

  • Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population

    S. Van Soest;L. I. Van Den Born;A. Gal;G. J. Farrar

Frequent Co-Authors

Dirk Bootsma
Dirk Bootsma Erasmus University Rotterdam
P. Meera Khan
P. Meera Khan Leiden University
Marcel M.A.M. Mannens
Marcel M.A.M. Mannens University of Amsterdam
Thomas B. Shows
Thomas B. Shows Roswell Park Cancer Institute
Rogier Versteeg
Rogier Versteeg University of Amsterdam
Stephen J. O'Brien
Stephen J. O'Brien Nova Southeastern University
Malcolm A. Ferguson-Smith
Malcolm A. Ferguson-Smith University of Cambridge
Frank H. Ruddle
Frank H. Ruddle Yale University
Peter L. Pearson
Peter L. Pearson Universidade de São Paulo
Newton E. Morton
Newton E. Morton University of Southampton

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Best Scientists Citing Andries Westerveld