I. Veltman

Most-cited papers

1. High‐throughput microRNAome analysis in human germ cell tumours

   A. Gillis, H. Stoop, R. Hersmus, J. Oosterhuis +9 more

   2007Journal of Pathology231 citations

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2. Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array‐based comparative genomic hybridization

   I. Veltman, J. Veltman, I. Janssen, C. Hulsbergen-van de Kaa +8 more

   2005Genes, Chromosomes and Cancer41 citations

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3. COMMENTS

   I. Veltman, M. Schepens, L. Looijenga, L. Strong +1 more

   2003Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS)37 citations

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4. Chromosomal breakpoint mapping by arrayCGH using flow-sorted chromosomes.

   I. Veltman, J. Veltman, G. Arkesteijn, I. Janssen +4 more

   2003BioTechniques36 citations Open access

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5. Fusion of the SUMO/Sentrin-specific protease 1 gene SENP1 and the embryonic polarity-related mesoderm development gene MESDC2 in a patient with an infantile teratoma and a constitutional t(12;15)(q13;q25).

   I. Veltman, L. Vreede, Jinke Cheng, L. Looijenga +4 more

   2005Human Molecular Genetics30 citations

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6. Comparative proteome, transcriptome, and genome analysis of a gonadal and an extragonadal germ cell tumor cell line.

   S. Glaesener, F. Honecker, I. Veltman, A. Gillis +7 more

   2008Journal of Proteome Research18 citations

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7. Gene expression profiling and gene copy‐number changes in malignant mesothelioma cell lines

   C. Zanazzi, R. Hersmus, I. Veltman, Ad J. M. Gillis +7 more

   2007Genes, Chromosomes and Cancer18 citations

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8. A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat.

   I. Veltman, M. van Asseldonk, M. Schepens, H. Stoop +5 more

   2002Cancer Genetics and Cytogenetics17 citations

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9. Mutation of a Single Conserved Residue in VH Complementarity-Determining Region 2 Results in a Severe Ig Secretion Defect1

   G. Wiens, A. Lekkerkerker, I. Veltman, M. Rittenberg

   2001Journal of Immunology15 citations Open access

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10. DYNC2H1 Mutations are commonly found in Jeune Asphyxating Thoracic Dysplasia (JATD) without extraskeletal features while IFT140 mutations cause JATD with renal involvement

    M. Schmidts, H. Arts, Z. Yap, Emhf Boengers +21 more

    20120 citations

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11. Genetic analysis of neonatal and infantile germ cell tumours.

    I. Veltman

    20060 citations

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12. P49: Identification of recurrent chromosomal aberrations in different types of human germ cell tumours using array CGH

    I. Veltman, A. Kersemaekers, J. Veltman, I. Janssen +9 more

    20050 citations

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13. Results in a Severe Ig Secretion Defect Complementarity-Determining Region 2 H Mutation of a Single Conserved Residue in V and

    M. Rittenberg, G. Wiens, A. Lekkerkerker, I. Veltman

    20010 citations

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