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Eric Schoenmakers

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Maruja E Lira; Keunchil Park; Eric F P M Schoenmakers; Jong-Mu Sun; Jin Seok Ahn; Myung-Ju Ahn; Yoon-La Choi; Doo Hyun Chung; Shibing Deng; Heounjeong Go; Donghui Huang; Bogun Jang; Dong-Wan Kim; Tae Min Kim; Woo Ho Kim; Youngil Koh; Se-Hoon Lee; Mao Mao
Multiplexed gene expression and fusion transcript analysis to detect ALK fusions in lung cancer.
Eric F P M Schoenmakers; Jens Bunt; Maria Debiec-Rychter; Lianne Hermers; Erik H L P G Huys; Bert Janssen; Monique Kersten; Gerard F M Merkx; Patrick Pauwels; Marga Schepens; Ad Geurts van Kessel
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.
Arijit Mukhopadhyay; Jamie M Kramer; Gerard F M Merkx; Dorien Lugtenberg; Dominique Smeets; Merel A W Oortveld; Ellen A W Blokland; Jyoti Agrawal; Annette Schenck; Hans van Bokhoven; Erik Huys; Eric F P M Schoenmakers; Ad Geurts van Kessel; C Erik van Nouhuys; Frans P M Cremers
CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation.

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All Publications

2013: Maruja E Lira; Keunchil Park; Eric F P M Schoenmakers; Jong-Mu Sun; Jin Seok Ahn; Myung-Ju Ahn; Yoon-La Choi; Doo Hyun Chung; Shibing Deng; Heounjeong Go; Donghui Huang; Bogun Jang; Dong-Wan Kim; Tae Min Kim; Woo Ho Kim; Youngil Koh; Se-Hoon Lee; Mao Mao
Multiplexed gene expression and fusion transcript analysis to detect ALK fusions in lung cancer.
The Journal of molecular diagnostics : JMD 2013;15(1):51-61.
2013: Eric F P M Schoenmakers; Jens Bunt; Maria Debiec-Rychter; Lianne Hermers; Erik H L P G Huys; Bert Janssen; Monique Kersten; Gerard F M Merkx; Patrick Pauwels; Marga Schepens; Ad Geurts van Kessel
Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.
Genes, chromosomes & cancer 2013;52(1):11-23.
2010: Arijit Mukhopadhyay; Jamie M Kramer; Gerard F M Merkx; Dorien Lugtenberg; Dominique Smeets; Merel A W Oortveld; Ellen A W Blokland; Jyoti Agrawal; Annette Schenck; Hans van Bokhoven; Erik Huys; Eric F P M Schoenmakers; Ad Geurts van Kessel; C Erik van Nouhuys; Frans P M Cremers
CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation.
Human genetics 2010;128(3):281-91.
2010: Ludovica Volpi; Gaia Roversi; Elisa Adele Colombo; Nico Leijsten; Daniela Concolino; Andrea Calabria; Maria Antonietta Mencarelli; Michele Fimiani; Fabio Macciardi; Rolph Pfundt; Eric F P M Schoenmakers; Lidia Larizza
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene.
American journal of human genetics 2010;86(1):72-6.
2009: Roland P Kuiper; Lilian A Vreede; Ramprasath Venkatachalam; Chris Ricketts; Eveline Kamping; Eugene Verwiel; Lutgarde Govaerts; Maria Debiec-Rychter; Evelyne Lerut; Femke van Erp; Nicoline Hoogerbrugge; Léon C L van Kempen; Eric F P M Schoenmakers; Anita Bonne; Eamonn R Maher; Ad Geurts van Kessel
The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer.
Cancer genetics and cytogenetics 2009;195(2):105-11.
2009: Anke van Rijk; Marcel Sweers; Erik Huys; Monique Kersten; Gerard F M Merkx; Ad Geurts van Kessel; Maria Debiec-Rychter; Eric F P M Schoenmakers
Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma.
Cancer genetics and cytogenetics 2009;193(1):54-62.
2009: Gwendolyn H Woldringh; Irene M Janssen; Jayne Hehir-Kwa; Christa van den Elzen; Jan A M Kremer; Peter De Boer; Eric F P M Schoenmakers
Constitutional DNA copy number changes in ICSI children.
Human reproduction (Oxford, England) 2009;24(1):233-40.
2008: Margit Schraders; Pedro Jares; Silvia Bea; Eric F P M Schoenmakers; J H J M van Krieken; Elias Campo; Patricia J T A Groenen
Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene-dosage regulated candidate genes.
British journal of haematology 2008;143(2):210-21.
2008: Kazutoyo Osoegawa; Gery M Vessere; K H Utami; M Adela Mansilla; M K Johnson; Bridget M Riley; J L'Heureux; Rolph Pfundt; Johan Staaf; Walter A Van Der Vliet; Andrew C Lidral; Eric F P M Schoenmakers; Ake Borg; Brian C Schutte; Edward J Lammer; Jeffrey C Murray; P J de Jong
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
Journal of medical genetics 2008;45(2):81-6.
2007: Anita Bonne; Lilian A Vreede; Roland P Kuiper; Daniëlle Bodmer; Corine Jansen; Marc J Eleveld; Femke van Erp; Ger Arkesteijn; Nicoline Hoogerbrugge; Conny van Ravenswaaij-Arts; Eric F P M Schoenmakers; Ad Geurts van Kessel
Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.
Cancer genetics and cytogenetics 2007;179(1):11-8.
2007: Roland P Kuiper; Eric F P M Schoenmakers; Simon van Reijmersdal; Jayne Hehir-Kwa; Ad Geurts van Kessel; Frank N Van Leeuwen; Peter M Hoogerbrugge
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression.
Leukemia 2007;21(6):1258-66.
2007: K Medendorp; Jan J M van Groningen; Marga Schepens; Lilian A Vreede; José Thijssen; Eric F P M Schoenmakers; Wilhelmina H van den Hurk; Ad Geurts van Kessel; Roland P Kuiper
Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas.
Cytogenetic and genome research 2007;118(2-4):157-65.
2006: Piergiorgio Modena; Elena Lualdi; Federica Facchinetti; Joris Veltman; James F Reid; Simone Minardi; Irene Janssen; Felice Giangaspero; Marco Forni; Gaetano Finocchiaro; Lorenzo Genitori; Flavio Giordano; Riccardo Riccardi; Eric F P M Schoenmakers; maura massimino; Gabriella Sozzi
Identification of tumor-specific molecular signatures in intracranial ependymoma and association with clinical characteristics.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2006;24(33):5223-33.
2006: Merryn V E Macville; Wim H Loneus; Dominique Marcus-Soekarman; Erik H L P G Huys; Eric F P M Schoenmakers; April Schrank-Hacker; Beverly S Emanuel; J J M Engelen
XX male with sex reversal and a de novo 11;22 translocation.
American journal of medical genetics. Part A 2006;140(18):1973-7.
2006: M-J P L Stevens-Kroef; Eric F P M Schoenmakers; M van Kraaij; Erik H L P G Huys; S Vermeulen; B van der Reijden; Ad Geurts van Kessel
Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML.
Leukemia 2006;20(6):1187-9.
2006: Gaia Roversi; Rolph Pfundt; Ramona Frida Moroni; Ivana Magnani; Simon van Reijmersdal; Bianca Pollo; huub straatman; Lidia Larizza; Eric F P M Schoenmakers
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines.
Oncogene 2006;25(10):1571-83.
2006: Lambertus A L M Kiemeney; Roland P Kuiper; Rolph Pfundt; Simon van Reijmersdal; Mark P Schoenberg; Katja K H Aben; Martinus F Niermeijer; J Alfred Witjes; Eric F P M Schoenmakers
No evidence for large-scale germline genomic aberrations in hereditary bladder cancer patients with high-resolution array-based comparative genomic hybridization.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006;15(1):180-3.
2006: Leendert H J Looijenga; Remko Hersmus; Ad J M Gillis; Rolph Pfundt; hans stoop; Ruud van Gurp; Joris Veltman; Berna Beverloo; Ellen van Drunen; Ad Geurts van Kessel; Renee Reijo Pera; Dominik Schneider; Brenda Summersgill; Janet Shipley; Alan McIntyre; Peter van der Spek; Eric F P M Schoenmakers; J Wolter Oosterhuis
Genomic and expression profiling of human spermatocytic seminomas: primary spermatocyte as tumorigenic precursor and DMRT1 as candidate chromosome 9 gene.
Cancer research 2006;66(1):290-302.
2005: Bert B A de Vries; Rolph Pfundt; Martijn A R Leisink; David A Koolen; Lisenka E L M Vissers; Irene M Janssen; Simon van Reijmersdal; Willy M Nillesen; Erik H L P G Huys; Nicole de Leeuw; Dominique Smeets; Erik A Sistermans; Ton Feuth; Conny van Ravenswaaij-Arts; Ad Geurts van Kessel; Eric F P M Schoenmakers; Han G Brunner; Joris Veltman
Diagnostic genome profiling in mental retardation.
American journal of human genetics 2005;77(4):606-16.
2005: Ivana Magnani; Ramona Frida Moroni; Ramona Frida Ramona; Gaia Roversi; Alessandro Beghini; Rolph Pfundt; Eric F P M Schoenmakers; Lidia Larizza
Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses.
Cancer genetics and cytogenetics 2005;161(2):140-5.
2005: Imke M Veltman; Lilian A Vreede; Jinke Cheng; Leendert H J Looijenga; Bert Janssen; Eric F P M Schoenmakers; Edward T H Yeh; Ad Geurts van Kessel
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).
Human molecular genetics 2005;14(14):1955-63.
2005: Markus Heidenblad; David Lindgren; Joris Veltman; Tord Jonson; Eija H Mahlamäki; Ludmila Gorunova; Ad Geurts van Kessel; Eric F P M Schoenmakers; Mattias Höglund
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications.
Oncogene 2005;24(10):1794-801.
2005: Margit Schraders; Rolph Pfundt; huub straatman; Irene M Janssen; Ad Geurts van Kessel; Eric F P M Schoenmakers; J H J M van Krieken; Patricia J T A Groenen
Novel chromosomal imbalances in mantle cell lymphoma detected by genome-wide array-based comparative genomic hybridization.
Blood 2005;105(4):1686-93.
2004: Anita C M Bonné; Daniëlle Bodmer; Eric F P M Schoenmakers; Conny van Ravenswaaij-Arts; Nicoline Hoogerbrugge; Ad Geurts van Kessel
Chromosome 3 translocations and familial renal cell cancer.
Current molecular medicine 2004;4(8):849-54.
2004: Lisenka E L M Vissers; Conny van Ravenswaaij-Arts; Ronald J C Admiraal; Jane A Hurst; Bert B A de Vries; Irene M Janssen; Walter A Van Der Vliet; Erik H L P G Huys; Pieter J de Jong; Ben C J Hamel; Eric F P M Schoenmakers; Han G Brunner; Joris Veltman; Ad Geurts van Kessel
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Nature genetics 2004;36(9):955-7.
2004: Joris Veltman; Helger G Yntema; Dorien Lugtenberg; H Arts; Sylvain Briault; Erik H L P G Huys; Kazutoyo Osoegawa; Pieter de Jong; Han G Brunner; Ad Geurts van Kessel; Hans van Bokhoven; Eric F P M Schoenmakers
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation.
Journal of medical genetics 2004;41(6):425-32.
2004: Markus Heidenblad; Eric F P M Schoenmakers; Tord Jonson; Ludmila Gorunova; Joris Veltman; Ad Geurts van Kessel; Mattias Höglund
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
Cancer research 2004;64(9):3052-9.
2004: M Belén González; Norma C Gutiérrez; Juan L García; Eric F P M Schoenmakers; Francesc Solé; María J Calasanz; Jesús F San Miguel; Jesús M Hernández
Heterogeneity of structural abnormalities in the 7q31.3 approximately q34 region in myeloid malignancies.
Cancer genetics and cytogenetics 2004;150(2):136-43.
2004: Martin I Krzywinski; Ian Bosdet; Duane E Smailus; Readman Chiu; Carrie Mathewson; Natasja Wye; Sarah Barber; Mabel Brown-John; Susanna Chan; Steve Chand; Alison Cloutier; Noreen Girn; Darlene Lee; Amara Masson; Michael Mayo; Teika Olson; Pawan Pandoh; Anna-Liisa Prabhu; Eric F P M Schoenmakers; Miranda Tsai; Donna G Albertson; Wan Lam; Chik On Choy; Kazutoyo Osoegawa; Shaying Zhao; Pieter J de Jong; Jacqueline E Schein; Steven J M Jones; Marco A Marra
A set of BAC clones spanning the human genome.
Nucleic acids research 2004;32(12):3651-60.
2004: Roland P Kuiper; Marga Schepens; José Thijssen; Eric F P M Schoenmakers; Ad Geurts van Kessel
Regulation of the MiTF/TFE bHLH-LZ transcription factors through restricted spatial expression and alternative splicing of functional domains.
Nucleic acids research 2004;32(8):2315-22.
2003: Lisenka E L M Vissers; Bert B A de Vries; Kazutoyo Osoegawa; Irene M Janssen; Ton Feuth; Chik On Choy; huub straatman; Walter A Van Der Vliet; Erik H L P G Huys; Anke van Rijk; Dominique Smeets; Conny van Ravenswaaij-Arts; Nine V A M Knoers; Ineke van der Burgt; Pieter J de Jong; Han G Brunner; Ad Geurts van Kessel; Eric F P M Schoenmakers; Joris Veltman
Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.
American journal of human genetics 2003;73(6):1261-70.
2003: Thierry Voet; Eric F P M Schoenmakers; Sebastien Carpentier; Charlotte Labaere; Peter Marynen
Controlled transgene dosage and PAC-mediated transgenesis in mice using a chromosomal vector.
Genomics 2003;82(6):596-605.
2003: Imke M Veltman; Joris Veltman; Ger Arkesteijn; Irene M Janssen; Lisenka E L M Vissers; Pieter J de Jong; Ad Geurts van Kessel; Eric F P M Schoenmakers
Chromosomal breakpoint mapping by arrayCGH using flow-sorted chromosomes.
BioTechniques 2003;35(5):1066-70.
2003: Gaetano Zafarana; Beata Grygalewicz; Ad J M Gillis; Lisenka E L M Vissers; Walter van de Vliet; Ruud van Gurp; hans stoop; Maria Debiec-Rychter; J Wolter Oosterhuis; Ad Geurts van Kessel; Eric F P M Schoenmakers; Leendert H J Looijenga; Joris Veltman
12p-amplicon structure analysis in testicular germ cell tumors of adolescents and adults by array CGH.
Oncogene 2003;22(48):7695-701.
2003: Karin Leunen; Frederic Amant; Maria Debiec-Rychter; Romaric Croes; Anne Hagemeijer; Eric F P M Schoenmakers; Ignace Vergote
Endometrial stromal sarcoma presenting as postpartum haemorrhage: report of a case with a sole t(10;17)(q22;p13) translocation.
Gynecologic oncology 2003;91(1):265-71.
2003: Maren Meiboom; Gazanfer Belge; Silvia Bol; Chiraz El-Aouni; Eric F P M Schoenmakers; Jörn Bullerdiek
Does conventional cytogenetics detect the real frequency of 19q13 aberrations in benign thyroid lesions? A survey of 38 cases.
Cancer genetics and cytogenetics 2003;146(1):70-2.
2003: Daniëlle Bodmer; Marga Schepens; Marc J Eleveld; Eric F P M Schoenmakers; Ad Geurts van Kessel
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).
Genes, chromosomes & cancer 2003;38(2):107-16.
2003: Roland P Kuiper; Marga Schepens; José Thijssen; Martien van Asseldonk; Eva van den Berg; Julia Bridge; Ed Schuuring; Eric F P M Schoenmakers; Ad Geurts van Kessel
Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitution.
Human molecular genetics 2003;12(14):1661-9.
2003: Joris Veltman; Yvonne Jonkers; Inge Nuijten; Irene M Janssen; Walter A Van Der Vliet; Erik H L P G Huys; Joris R Vermeesch; Griet Van Buggenhout; Jean-Pierre Fryns; Ronald J C Admiraal; Paulien Terhal; Didier Lacombe; Ad Geurts van Kessel; Dominique Smeets; Eric F P M Schoenmakers; Conny van Ravenswaaij-Arts
Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH.
American journal of human genetics 2003;72(6):1578-84.
2003: Frederic Amant; Erik H L P G Huys; Anneke Geurts-Moespot; B G P Lindeque; Ignace Vergote; Fred Sweep; Eric F P M Schoenmakers
Ethnic variations in uterine leiomyoma biology are not caused by differences in myometrial estrogen receptor alpha levels.
Journal of the Society for Gynecologic Investigation 2003;10(2):105-9.
2003: Leendert H J Looijenga; Gaetano Zafarana; Beata Grygalewicz; Brenda Summersgill; Maria Debiec-Rychter; Joris Veltman; Eric F P M Schoenmakers; Sandrine Rodriguez; Osman Jafer; Jeremy Clark; Ad Geurts van Kessel; Janet Shipley; Ruud van Gurp; Ad J M Gillis; J Wolter Oosterhuis
Role of gain of 12p in germ cell tumour development.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2003;111(1):161-71; discussion 172-3.
2002: Daniëlle Bodmer; Irene M Janssen; Yvonne Jonkers; Eva van den Berg; Trijnie Dijkhuizen; Maria Debiec-Rychter; Eric F P M Schoenmakers; Ad Geurts van Kessel
Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13 approximately q22 breakpoints.
Cancer genetics and cytogenetics 2002;136(2):95-100.
2002: Joris Veltman; Eric F P M Schoenmakers; Bert H J Eussen; Irene M Janssen; Gerard F M Merkx; Brigitte van Cleef; Conny van Ravenswaaij-Arts; Han G Brunner; Dominique Smeets; Ad Geurts van Kessel
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.
American journal of human genetics 2002;70(5):1269-76.
2002: Daniëlle Bodmer; Marc J Eleveld; Ellen Kater-Baats; Irene M Janssen; Bert Janssen; Marian A J Weterman; Eric F P M Schoenmakers; Michael L Nickerson; Marston Linehan; Berton Zbar; Ad Geurts van Kessel
Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).
Human molecular genetics 2002;11(6):641-9.
2002: Philippe Debeer; Eric F P M Schoenmakers; Waleed O Twal; Scott Argraves; L De Smet; Jean-Pierre Fryns; Wim J M Van De Ven
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly.
Journal of medical genetics 2002;39(2):98-104.
2002: Guy Verrijdt; Annemie Haelens; Eric F P M Schoenmakers; Wilfried Rombauts; Frank Claessens
Comparative analysis of the influence of the high-mobility group box 1 protein on DNA binding and transcriptional activation by the androgen, glucocorticoid, progesterone and mineralocorticoid receptors.
The Biochemical journal 2002;361(Pt 1):97-103.
2001: Frederic Amant; Maria Debiec-Rychter; Eric F P M Schoenmakers; A Hagemeijer-Hausman; Ignace Vergote
Cumulative dosage effect of a RAD51L1/HMGA2 fusion and RAD51L1 loss in a case of pseudo-Meigs' syndrome.
Genes, chromosomes & cancer 2001;32(4):324-9.
2001: Maria Debiec-Rychter; Raf Sciot; Patrick Pauwels; Eric F P M Schoenmakers; Paola Dal Cin; Anne Hagemeijer
Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors.
Genes, chromosomes & cancer 2001;32(1):26-32.
2001: C Blank; Eric F P M Schoenmakers; Piere Rogalla; Erik H L P G Huys; A A van Rijk; Norbert Drieschner; Jörn Bullerdiek
Intragenic breakpoint within RAD51L1 in a t(6;14)(p21.3;q24) of a pulmonary chondroid hamartoma.
Cytogenetics and cell genetics 2001;95(1-2):17-9.
2001: Frank Claessens; Guy Verrijdt; Eric F P M Schoenmakers; Annemie Haelens; Ben Peeters; Guido Verhoeven; Wilfried Rombauts
Selective DNA binding by the androgen receptor as a mechanism for hormone-specific gene regulation.
The Journal of steroid biochemistry and molecular biology 2001;76(1-5):23-30.
2000: Philippe Debeer; Eric F P M Schoenmakers; Reinhilde Thoelen; Maureen Holvoet; T Kuittinen; Guy Fabry; Jean-Pierre Fryns; Frances R Goodman; Wim J M Van De Ven
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint.
European journal of human genetics : EJHG 2000;8(8):561-70.
2000: Guy Verrijdt; Eric F P M Schoenmakers; Annemie Haelens; Ben Peeters; Guido Verhoeven; Wilfried Rombauts; Frank Claessens
Change of specificity mutations in androgen-selective enhancers. Evidence for a role of differential DNA binding by the androgen receptor.
The Journal of biological chemistry 2000;275(16):12298-305.
2000: Eric F P M Schoenmakers; Guy Verrijdt; Ben Peeters; Guido Verhoeven; Wilfried Rombauts; Frank Claessens
Differences in DNA binding characteristics of the androgen and glucocorticoid receptors can determine hormone-specific responses.
The Journal of biological chemistry 2000;275(16):12290-7.
1999: Roberta Vanni; Eric F P M Schoenmakers; M Andria
Deletion 7q in uterine leiomyoma: fluorescence in situ hybridization characterization on primary cytogenetic preparations.
Cancer genetics and cytogenetics 1999;113(2):183-7.
1999: Guy Verrijdt; Eric F P M Schoenmakers; Philippe Alen; Annemie Haelens; Ben Peeters; Wilfried Rombauts; Frank Claessens
Androgen specificity of a response unit upstream of the human secretory component gene is mediated by differential receptor binding to an essential androgen response element.
Molecular endocrinology (Baltimore, Md.) 1999;13(9):1558-70.
1999: Eric F P M Schoenmakers; Philippe Alen; Guy Verrijdt; Ben Peeters; Guido Verhoeven; Wilfried Rombauts; Frank Claessens
Differential DNA binding by the androgen and glucocorticoid receptors involves the second Zn-finger and a C-terminal extension of the DNA-binding domains.
The Biochemical journal 1999;341 ( Pt 3)():515-21.
1999: Annemie Haelens; Guy Verrijdt; Eric F P M Schoenmakers; Philippe Alen; Ben Peeters; Wilfried Rombauts; Frank Claessens
The first exon of the human sc gene contains an androgen responsive unit and an interferon regulatory factor element.
Molecular and cellular endocrinology 1999;153(1-2):91-102.
1999: Marleen MR Petit; Eric F P M Schoenmakers; Christel Huysmans; Jan Geurts; Nils Mandahl; Wim J M Van De Ven
LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes.
Genomics 1999;57(3):438-41.
1999: koenraad devriendt; Gert Matthijs; Maureen Holvoet; Eric F P M Schoenmakers; Jean-Pierre Fryns
Triplication of distal chromosome 10q.
Journal of medical genetics 1999;36(3):242-5.
1999: Eric F P M Schoenmakers; Christel Huysmans; Wim J M Van De Ven
Allelic knockout of novel splice variants of human recombination repair gene RAD51B in t(12;14) uterine leiomyomas.
Cancer research 1999;59(1):19-23.
1999: Philippe Alen; Frank Claessens; Eric F P M Schoenmakers; Johannes V Swinnen; Guido Verhoeven; Wilfried Rombauts; Ben Peeters
Interaction of the putative androgen receptor-specific coactivator ARA70/ELE1alpha with multiple steroid receptors and identification of an internally deleted ELE1beta isoform.
Molecular endocrinology (Baltimore, Md.) 1999;13(1):117-28.
1998: Philippe Debeer; Eric F P M Schoenmakers; L De Smet; Wim J M Van De Ven; J P Fryns
Co-segregation of an apparently balanced reciprocal t(12;22)(p11.2;q13.3) with a complex type of 3/3'/4 synpolydactyly associated with metacarpal, metatarsal and tarsal synostoses in three family members.
Clinical dysmorphology 1998;7(3):225-8.
1998: Jan Geurts; Eric F P M Schoenmakers; Eva Röijer; AK Aström; Göran Stenman; Wim J M Van De Ven
Identification of NFIB as recurrent translocation partner gene of HMGIC in pleomorphic adenomas.
Oncogene 1998;16(7):865-72.
1998: Philippe Debeer; Eric F P M Schoenmakers; Reinhilde Thoelen; Jean-Pierre Fryns; Wim J M Van De Ven
Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3'/4 synpolydactyly.
Cytogenetics and cell genetics 1998;81(3-4):229-34.
1998: Frank Claessens; H Vanaken; I Vercaeren; Guy Verrijdt; Annemie Haelens; Eric F P M Schoenmakers; Philippe Alen; Ann Devos; Ben Peeters; Guido Verhoeven; Wilfried Rombauts; Walter Heyns
Androgen-regulated transcription in the epithelium of the rat lacrimal gland.
Advances in experimental medicine and biology 1998;438():43-8.
1997: Jan Geurts; Eric F P M Schoenmakers; Wim J M Van De Ven
Molecular characterization of a complex chromosomal rearrangement in a pleomorphic salivary gland adenoma involving the 3'-UTR of HMGIC.
Cancer genetics and cytogenetics 1997;95(2):198-205.
1997: Eric F P M Schoenmakers; Wim J M Van De Ven
From chromosome aberrations to the high mobility group protein gene family: evidence for a common genetic denominator in benign solid tumor development.
Cancer genetics and cytogenetics 1997;95(1):51-8.
1997: Roberta Vanni; S Marras; Eric F P M Schoenmakers; P Dal Cin; B Kazmierczak; G Senger; J Bullerdiek; W J Van de Ven; H Van den Berghe
Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines.
Genes, chromosomes & cancer 1997;18(3):155-61.
1997: J M Hernández; Eric F P M Schoenmakers; Paola Dal Cin; Lucienne Michaux; Wim J M Van De Ven; Herman Van Den Berghe
Molecular delineation of the commonly deleted segment in mature B-cell lymphoid neoplasias with deletion of 7q.
Genes, chromosomes & cancer 1997;18(2):147-50.
1997: Jan Geurts; Eric F P M Schoenmakers; Eva Röijer; Göran Stenman; Wim J M Van De Ven
Expression of reciprocal hybrid transcripts of HMGIC and FHIT in a pleomorphic adenoma of the parotid gland.
Cancer research 1997;57(1):13-7.
1996: Marleen MR Petit; R Mols; Eric F P M Schoenmakers; Nils Mandahl; Wim J M Van De Ven
LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family.
Genomics 1996;36(1):118-29.
1996: S Wanschura; Eric F P M Schoenmakers; Christel Huysmans; S Bartnitzke; Wim J M Van De Ven; Jörn Bullerdiek
Mapping of the gene encoding the human hepatoma-derived growth factor (HDGF) with homology to the high-mobility group (HMG)-1 protein to Xq25.
Genomics 1996;32(2):298-300.
1996: Anton J M Roebroek; Torik A Y Ayoubi; Hilde Van de Velde; Eric F P M Schoenmakers; Ilse Pauli; Wim J M Van De Ven
Genomic organization of the human NSP gene, prototype of a novel gene family encoding reticulons.
Genomics 1996;32(2):191-9.
1996: S Wanschura; Eric F P M Schoenmakers; Christel Huysmans; S Bartnitzke; Wim J M Van De Ven; J Bullrdiek
Mapping of the human HMG2 gene to 4q31.
Genomics 1996;31(2):264-5.
1996: Peter Groenen; E Garcia; R Thoelen; M Aly; Eric F P M Schoenmakers; koenraad devriendt; J P Fryns; Wim J M Van De Ven
Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasia.
Cytogenetics and cell genetics 1996;75(4):210-5.
1996: B Staats; Ulrich Bonk; S Wanschura; P Hanisch; Eric F P M Schoenmakers; Wim J M Van De Ven; S Bartnitzke; Jörn Bullerdiek
A fibroadenoma with a t(4;12) (q27;q15) affecting the HMGI-C gene, a member of the high mobility group protein gene family.
Breast cancer research and treatment 1996;38(3):299-303.
1996: S Wanschura; Gazanfer Belge; G Stenman; P Kools; Paola Dal Cin; Eric F P M Schoenmakers; Christel Huysmans; Herman Van Den Berghe; S Bartnitzke; Wim J M Van De Ven; Jörn Bullerdiek
Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12.
Cancer genetics and cytogenetics 1996;86(1):39-45.
1995: Koen Kas; Eric F P M Schoenmakers; Wim J M Van De Ven
Physical map location of the human carboxypeptidase M gene (CPM) distal to D12S375 and proximal to D12S8 at chromosome 12q15.
Genomics 1995;30(2):403-5.
1995: Eric F P M Schoenmakers; Jan Geurts; P F Kools; R Mols; Christel Huysmans; Jörn Bullerdiek; Herman Van Den Berghe; Wim J M Van De Ven
A 6-Mb yeast artificial chromosome contig and long-range physical map encompassing the region on chromosome 12q15 frequently rearranged in a variety of benign solid tumors.
Genomics 1995;29(3):665-78.
1995: C Rohen; Jörg Caselitz; C Stern; S Wanschura; Eric F P M Schoenmakers; Wim J M Van De Ven; S Bartnitzke; Jörn Bullerdiek
A hamartoma of the breast with an aberration of 12q mapped to the MAR region by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1995;84(1):82-4.
1995: S Wanschura; B Kazmierczak; Eric F P M Schoenmakers; E Meyen; S Bartnitzke; W Van de Ven; Jörn Bullerdiek; W Schloot
Regional fine mapping of the multiple-aberration region involved in uterine leiomyoma, lipoma, and pleomorphic adenoma of the salivary gland to 12q15.
Genes, chromosomes & cancer 1995;14(1):68-70.
1995: Eric F P M Schoenmakers; S Wanschura; R Mols; Jörn Bullerdiek; Herman Van Den Berghe; Wim J M Van De Ven
Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours.
Nature genetics 1995;10(4):436-44.
1995: B Kazmierczak; S Wanschura; J Rosigkeit; K Meyer-Bolte; K Uschinsky; R Haupt; Eric F P M Schoenmakers; S Bartnitzke; Wim J M Van De Ven; Jörn Bullerdiek
Molecular characterization of 12q14-15 rearrangements in three pulmonary chondroid hamartomas.
Cancer research 1995;55(12):2497-9.
1995: Wim J M Van De Ven; Eric F P M Schoenmakers; S Wanschura; B Kazmierczak; P F Kools; Jan Geurts; S Bartnitzke; Herman Van Den Berghe; Jörn Bullerdiek
Molecular characterization of MAR, a multiple aberration region on human chromosome segment 12q13-q15 implicated in various solid tumors.
Genes, chromosomes & cancer 1995;12(4):296-303.
1995: P F Kools; S Wanschura; Eric F P M Schoenmakers; Jan Geurts; R Mols; B Kazmierczak; Jörn Bullerdiek; Herman Van Den Berghe; Wim J M Van De Ven
Identification of the chromosome 12 translocation breakpoint region of a pleomorphic salivary gland adenoma with t(1;12)(p22;q15) as the sole cytogenetic abnormality.
Cancer genetics and cytogenetics 1995;79(1):1-7.
1995: M Chaffanet; Mathijs Baens; Jeroen Aerssens; Eric F P M Schoenmakers; Jean-Jacques Cassiman; Peter Marynen
Mapping of an ordered set of 14 cosmids to human chromosome 12p by two-color in situ hybridization.
Cytogenetics and cell genetics 1995;69(1-2):27-32.
1995: S Wanschura; Y Hennig; U Deichert; Eric F P M Schoenmakers; Wim J M Van De Ven; S Bartnitzke; Jörn Bullerdiek
Molecular-cytogenetic refinement of the 12q14-->q15 breakpoint region affected in uterine leiomyomas.
Cytogenetics and cell genetics 1995;71(2):131-5.
1994: Eric F P M Schoenmakers; R Mols; S Wanschura; P F Kools; Jan Geurts; S Bartnitzke; Jörn Bullerdiek; Herman Van Den Berghe; Wim J M Van De Ven
Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas.
Genes, chromosomes & cancer 1994;11(2):106-18.
1994: Anne Forus; P F Kools; Eric F P M Schoenmakers; Wim J M Van De Ven; Ola Myklebost
A long range restriction map spanning the myxoid liposarcoma breakpoint in the q13-14 region of human chromosome 12.
Human genetics 1994;94(3):259-64.
1994: Klaas Kok; Anke Van den Berg; P M Veldhuis; Anneke Y van der Veen; M Franke; Eric F P M Schoenmakers; M M Hulsbeek; Annemarie H Van Der Hout; Lou de Leij; W van de Ven
A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes.
Cancer research 1994;54(15):4183-7.
1994: Eric F P M Schoenmakers; P F Kools; R Mols; B Kazmierczak; S Bartnitzke; Jörn Bullerdiek; Paola Dal Cin; P J De Jong; Herman Van Den Berghe; Wim J M Van De Ven
Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.
Genomics 1994;20(2):210-22.
1993: Iwona Wlodarska; Eric F P M Schoenmakers; Koen Kas; Joseph Merregaert; V Lemahieu; U Weier; Herman Van Den Berghe; Wim J M Van De Ven
Molecular mapping of the chromosome 11 breakpoint of t(11;17)(q13;q21) in a t(11;14)(q13;q32)-positive B non-Hodgkin's lymphoma.
Genes, chromosomes & cancer 1993;8(4):224-9.
1993: Koen Kas; Eric F P M Schoenmakers; W van de Ven; Günther Weber; M Nordenskjöld; L Michiels; Joseph Merregaert; C Larsson
Assignment of the human FAU gene to a subregion of chromosome 11q13.
Genomics 1993;17(2):387-92.
1992: Iwona Wlodarska; Cristina Mecucci; E Vandenberghe; Christiane De Wolf-Peeters; J Thomas; C Hilliker; Eric F P M Schoenmakers; Michel Stul; Peter Marynen; Jean-Jacques Cassiman
dup(12)(q13----qter) in two t(14;18)-negative follicular B-non-Hodgkin's lymphomas.
Genes, chromosomes & cancer 1992;4(4):302-8.