Janssen IM - Search Results

1

Isolation of osteosarcoma-associated amplified DNA sequences using representational difference analysis.

Simons A, Janssen IM, Suijkerbuijk RF, Veth RP, Pruszczynski M, Hulsbergen-van de Kaa CA, du Manoir S, Geurts van Kessel A. Simons A, et al. Among authors: janssen im. Genes Chromosomes Cancer. 1997 Oct;20(2):196-200. doi: 10.1002/(sici)1098-2264(199710)20:2<196::aid-gcc10>3.0.co;2-p. Genes Chromosomes Cancer. 1997. PMID: 9331570 Free article.

2

Masked t(X;18)(p11;q11) in a biphasic synovial sarcoma revealed by FISH and RT-PCR.

Geurts van Kessel A, de Bruijn D, Hermsen L, Janssen I, dos Santos NR, Willems R, Makkus L, Schreuder H, Veth R. Geurts van Kessel A, et al. Genes Chromosomes Cancer. 1998 Oct;23(2):198-201. doi: 10.1002/(sici)1098-2264(199810)23:2<198::aid-gcc15>3.3.co;2-h. Genes Chromosomes Cancer. 1998. PMID: 9739025

3

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

Weterman MA, Wilbrink M, Janssen I, Janssen HA, van den Berg E, Fisher SE, Craig I, Geurts van Kessel A. Weterman MA, et al. Cytogenet Cell Genet. 1996;75(1):2-6. doi: 10.1159/000134444. Cytogenet Cell Genet. 1996. PMID: 8995477

4

Ring chromosomes in a malignant mesenchymoma.

Geurts van Kessel A, Simons A, Comtesse PP, Siepman A, Janssen I, Suijkerbuijk RF, Forus A, Pruszczynski M, Veth RP. Geurts van Kessel A, et al. Cancer Genet Cytogenet. 1999 Mar;109(2):119-22. doi: 10.1016/s0165-4608(98)00170-8. Cancer Genet Cytogenet. 1999. PMID: 10087943

5

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

Veltman I, Veltman J, Janssen I, Hulsbergen-van de Kaa C, Oosterhuis W, Schneider D, Stoop H, Gillis A, Zahn S, Looijenga L, Göbel U, van Kessel AG. Veltman I, et al. Genes Chromosomes Cancer. 2005 Aug;43(4):367-76. doi: 10.1002/gcc.20208. Genes Chromosomes Cancer. 2005. PMID: 15880464

6

Detecting fetal subchromosomal aberrations by MPS: an unexpected discrepancy between amniocyte DNA and ccffDNA.

Buysse K, de Ligt J, Janssen IM, van Bon BW, Gomes I, Hehir-Kwa J, Eggink AJ, van Vugt JM, Vissers LE, Geurts van Kessel A, Faas BH. Buysse K, et al. Among authors: janssen im. Prenat Diagn. 2014 Apr;34(4):402-5. doi: 10.1002/pd.4312. Epub 2014 Feb 6. Prenat Diagn. 2014. PMID: 24391091 No abstract available.

7

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.

Faas BH, de Ligt J, Janssen I, Eggink AJ, Wijnberger LD, van Vugt JM, Vissers L, Geurts van Kessel A. Faas BH, et al. Expert Opin Biol Ther. 2012 Jun;12 Suppl 1:S19-26. doi: 10.1517/14712598.2012.670632. Epub 2012 Apr 16. Expert Opin Biol Ther. 2012. PMID: 22500971

8

Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13 approximately q22 breakpoints.

Bodmer D, Janssen I, Jonkers Y, van den Berg E, Dijkhuizen T, Debiec-Rychter M, Schoenmakers E, van Kessel AG. Bodmer D, et al. Cancer Genet Cytogenet. 2002 Jul 15;136(2):95-100. doi: 10.1016/s0165-4608(02)00517-4. Cancer Genet Cytogenet. 2002. PMID: 12237231

9

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

Buysse K, Beulen L, Gomes I, Gilissen C, Keesmaat C, Janssen IM, Derks-Willemen JJ, de Ligt J, Feenstra I, Bekker MN, van Vugt JM, Geurts van Kessel A, Vissers LE, Faas BH. Buysse K, et al. Among authors: janssen im. Clin Biochem. 2013 Dec;46(18):1783-6. doi: 10.1016/j.clinbiochem.2013.07.020. Epub 2013 Aug 8. Clin Biochem. 2013. PMID: 23933476

10

Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).

Bodmer D, Eleveld M, Kater-Baats E, Janssen I, Janssen B, Weterman M, Schoenmakers E, Nickerson M, Linehan M, Zbar B, van Kessel AG. Bodmer D, et al. Hum Mol Genet. 2002 Mar 15;11(6):641-9. doi: 10.1093/hmg/11.6.641. Hum Mol Genet. 2002. PMID: 11912179

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