A. Geurts van Kessel

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Variation of CNV distribution in five different ethnic populations

L. Vissers, H. Brunner, J. D. den Dunnen, 2007, Cytogenetic and Genome Research.

Cytogenetic classification of renal cell cancer.

E. van den Berg, S. Störkel, T. Dijkhuizen, 1997, Cancer genetics and cytogenetics.

Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma

G. Merkx, M. Weterman, M. Wilbrink, 2001, Cytogenetic and Genome Research.

EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients

R. Kuiper, M. Ligtenberg, N. Hoogerbrugge, 2012, Familial Cancer.

Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization.

R. Sinke, A. Sandberg, R. Suijkerbuijk, 1993, Cancer genetics and cytogenetics.

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are risk factors for colorectal cancer.

L. Vreede, R. Kuiper, C. V. van Ravenswaaij-Arts, 2013, Gastroenterology.

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2.

A. Monaco, R. Sinke, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization.

J. Cassiman, J. Cassiman, C. Buys, 1991, American journal of human genetics.

Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.

E. van den Berg, S. Fisher, I. Janssen, 1996, Cytogenetics and cell genetics.

Isochromosome 12p-positive pineal germ cell tumor.

T. D. de Bruin, R. Suijkerbuijk, J. Oosterhuis, 1994, Cancer research.

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.

W. Foulkes, G. Capellá, I. Tomlinson, 2019, Cancer cell.

Chromosome 12q heterozygosity is retained in i(12p)-positive testicular germ cell tumor cells.

A. Langeveld, E. van Drunen, J. Oosterhuis, 1989, Cancer genetics and cytogenetics.

Isolation and characterization of glioblastoma‐associated homozygously deleted DNA fragments from chromosomal region 9p21 suggests involvement of multiple tumour suppressor genes

A. Simons, J. Jeuken, R. Boerman, 1999, The Journal of pathology.

The Mitotic Arrest Deficient Protein MAD2B Interacts with the Small GTPase RAN throughout the Cell Cycle

L. Hetterschijt, L. Vreede, A. Geurts van Kessel, 2009, PloS one.

Multiplex Ligation‐dependent Probe Amplification (MLPA) as a stand‐alone test for rapid aneuploidy detection in amniotic fluid cells

A. Smits, A. Kooper, B. Faas, 2008, Prenatal diagnosis.

Disruption of a novel gene, DIRC3, and expression of DIRC3‐HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21)

M. Schepens, E. Schoenmakers, A. Geurts van Kessel, 2003, Genes, chromosomes & cancer.

Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenita.

R. Pfundt, J. Hehir-Kwa, E. Bongers, 2012, American journal of human genetics.

Germline copy number variation and cancer risk.

R. Kuiper, M. Ligtenberg, N. Hoogerbrugge, 2010, Current opinion in genetics & development.

Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells

I. Janssen, J. de Ligt, B. Faas, 2012, Expert opinion on biological therapy.

Translocation (12;22)(p13;q12) as sole karyotypic abnormality in a patient with nonlymphocytic leukemia.

A. Geurts van Kessel, J. van Gaal, W. van de Klundert, 1994, Cancer genetics and cytogenetics.

Chromosome 3 translocations and the risk to develop renal cell cancer: a Dutch intergroup study.

N. Hoogerbrugge, C. V. van Ravenswaaij, A. Geurts van Kessel, 2003, Genetic counseling.

Derivative (y)t(Y;1)(q12;q12),+9 in a patient with polycythemia vera during transition into myelodysplasia.

R. Raymakers, A. Geurts van Kessel, F. Stellink, 1996, Cancer genetics and cytogenetics.

Molecular cytogenetics of human germ cell tumours: i(12p) and related chromosomal anomalies.

R. Sinke, L. Looijenga, R. Suijkerbuijk, 1993, European urology.

Ring chromosomes in a malignant mesenchymoma.

I. Janssen, A. Simons, A. Forus, 1999, Cancer genetics and cytogenetics.

Comparative genomic hybridization of germ cell tumors of the adult testis: confirmation of karyotypic findings and identification of a 12p-amplicon.

L. Looijenga, R. Suijkerbuijk, J. Oosterhuis, 1996, Cancer genetics and cytogenetics.

Fluorescence in situ hybridization-based approaches for detection of 12p overrepresentation, in particular i(12p), in cell lines of human testicular germ cell tumors of adults.

D. Weghuis, L. Looijenga, J. Oosterhuis, 1996, Cancer genetics and cytogenetics.

Generation of a panel of somatic cell hybrids containing fragments of human chromosome 12P by X-ray irradiation and cell fusion.

R. Sinke, J. Herbergs, J. Cassiman, 1992, Genomics.

Cytogenetics of the progression of adult testicular germ cell tumors.

L. Looijenga, A. G. Kessel, J. Oosterhuis, 1997, Cancer genetics and cytogenetics.

Amplification of chromosome subregion 12p11.2-p12.1 in a metastasis of an i(12p)-negative seminoma: relationship to tumor progression?

D. Weghuis, R. Sinke, J. Soares, 1994, Cancer genetics and cytogenetics.

Verification of isochromosome 12p and identification of other chromosome 12 aberrations in gonadal and extragonadal human germ cell tumors by bicolor double fluorescence in situ hybridization.

L. Looijenga, J. Cassiman, R. Suijkerbuijk, 1992, Cancer genetics and cytogenetics.

A 46,XY female with mixed gonadal dysgenesis and a 48,XY, +7, +i(12p) chromosome pattern in a primary gonadal tumor.

F. Bosman, R. Suijkerbuijk, J. Oosterhuis, 1991, Cancer genetics and cytogenetics.

Novel candidate tumour suppressor gene loci on chromosomes 11q23–24 and 22q13 involved in human insulinoma tumourigenesis

T. Feuth, A. Geurts van Kessel, J. Veltman, 2006, The Journal of pathology.

Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.

D. Weghuis, T. Feuth, A. Simons, 2009, Cancer genetics and cytogenetics.

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

Bba, L. Vissers, B. D. de Vries, 2005, Journal of Medical Genetics.

Recurrent CNVs disrupt three candidate genes in schizophrenia patients.

J. Buizer-Voskamp, C. Sabatti, R. Ophoff, 2008, American journal of human genetics.

Molecular analysis of isochromosome 12p in testicular germ cell tumors.

R. Suijkerbuijk, J. Oosterhuis, A. Geurts van Kessel, 1991, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

The cancer genome: from structure to function

A. Geurts van Kessel, 2014, Cellular Oncology.

New insights and clinical advancements in cellular oncology

A. Geurts van Kessel, 2012, Cellular oncology.

Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling

Annet Simons, Rolph Pfundt, R. Pfundt, 2014, Molecular Cytogenetics.

NTHL1 and MUTYH polyposis syndromes: two sides of the same coin?

R. Kuiper, M. Ligtenberg, N. Hoogerbrugge, 2018, The Journal of pathology.

Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.

R. Kuiper, M. Ligtenberg, P. Jin, 2015, World journal of gastroenterology.

A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer

J. Shendure, A. Hoischen, J. Hehir-Kwa, 2015, Nature Genetics.

Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas

L. Vreede, R. Kuiper, M. Schepens, 2007, Cytogenetic and Genome Research.

Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomas.

A. G. Kessel, M. Weterman, M. Wilbrink, 1996, Proceedings of the National Academy of Sciences of the United States of America.

SNP Array Analysis in Constitutional and Cancer Genome Diagnostics – Copy Number Variants, Genotyping and Quality Control

N. de Leeuw, J. Hehir-Kwa, D. Smeets, 2011, Cytogenetic and Genome Research.

The epigenetics of (hereditary) colorectal cancer.

R. Kuiper, M. Ligtenberg, N. Hoogerbrugge, 2010, Cancer genetics and cytogenetics.

Upfront Treatment Influences the Composition of Genetic Alterations in Relapsed Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia

R. Pieters, R. Kuiper, E. Sonneveld, 2020, HemaSphere.

Molecular cytogenetics of bone and soft tissue tumors.

O. Myklebost, E. van den Berg, O. Fodstad, 1997, Cancer genetics and cytogenetics.

Renal oncocytoma with t(5;12;11), der(1)t(1;8) and add(19): “true” oncocytoma or chromophobe adenoma?

E. van den Berg, A. Veen, E. Berg, 1997, International journal of cancer.

Clonal dynamics in pediatric B‐cell precursor acute lymphoblastic leukemia with very early relapse

H. Cavé, C. Eckert, R. Kuiper, 2021, Pediatric blood & cancer.

The Origin and Nature of Tightly Clustered BTG1 Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution

R. Kuiper, B. Scheijen, E. Sonneveld, 2012, PLoS genetics.

Comparative genomic hybridization as a tool to define two distinct chromosome 12-derived amplification units in well-differentiated liposarcomas.

O. Myklebost, C. Turc‐Carel, F. Pedeutour, 1994, Genes, chromosomes & cancer.

Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.

L. Vreede, R. Kuiper, G. Arkesteijn, 2007, Cancer genetics and cytogenetics.

Predisposition to colorectal cancer: exploiting copy number variation to identify novel predisposing genes and mechanisms

M. Ligtenberg, N. Hoogerbrugge, R. Kuiper, 2009, Cytogenetic and Genome Research.

High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation

P. D. de Jong, K. Osoegawa, J. Veltman, 2004, Journal of Medical Genetics.

Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility

L. Vreede, C. Gilissen, R. Kuiper, 2016, PLoS genetics.

The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer.

C. Ricketts, L. Vreede, M. Debiec‐Rychter, 2009, Cancer genetics and cytogenetics.

Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21).

M. Ligtenberg, A. Smits, D. Smeets, 2002, Cancer genetics and cytogenetics.

An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation.

E. van den Berg, M. Ligtenberg, D. Smeets, 1998, American journal of human genetics.

A familial case of renal cell carcinoma and a t(2;3) chromosome translocation.

E. van den Berg, H. Brunner, A. Smits, 1998, Kidney international.

EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients

R. Kuiper, M. Ligtenberg, N. Hoogerbrugge, 2013, Familial Cancer.

Isolation and characterization of the Xenopus laevis orthologs of the human papillary renal cell carcinoma-associated genes PRCC and MAD2L2 (MAD2B)

G. Martens, A. Geurts van Kessel, W. H. van den Hurk, 2004, Cytogenetic and Genome Research.

Changing landscapes in cellular oncology

A. Geurts van Kessel, 2012, Cellular Oncology.

Molecular parameters associated with insulinoma progression: chromosomal instability versus p53 and CK19 status

B. Skogseid, A. Geurts van Kessel, J. Veltman, 2006, Cytogenetic and Genome Research.

Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development

L. Kiemeney, H. Clevers, I. Nagtegaal, 2015, The Journal of pathology.

Relationship of the human protooncogene CBL2 on 11q23 to the t(4;11), t(11;22), and t(11;14) breakpoints.

Y. Akao, H. Seuánez, W. Langdon, 1991, Cytogenetics and cell genetics.

Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24h after venipuncture.

K. Buysse, I. Janssen, C. Gilissen, 2013, Clinical biochemistry.

Genomic and expression profiling of human spermatocytic seminomas: primary spermatocyte as tumorigenic precursor and DMRT1 as candidate chromosome 9 gene.

R. Pfundt, L. Looijenga, H. Stoop, 2006, Cancer research.

Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

M. Ligtenberg, A. Smits, D. Smeets, 2001, Genes, chromosomes & cancer.

Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation

L. Kiemeney, A. V. van Kessel, R. Kuiper, 2011, European Journal of Human Genetics.