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Quinten Waisfisz

Research Profile

Disorders

Chemicals & Drugs

Physiology

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Genetic Complementation Test

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Publications

TOP 3
Sietske H Kevelam; Nienke L Postma; Chitra Prasad; Gajja S Salomons; Quinten Waisfisz; Nicole I Wolf; Truus E M Abbink; Ingrid M C Bakker; Ivo Baric; Susan Blaser; Marianna Bugiani; Annette Feigenbaum; Johannes Häberle; Peter Heutink; Warsha A Kanhai; Marjo S van der Knaap
Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy.
Muriel A Adank; Annegien Broeks; Maartje J Hooning; Marianne A Jonker; John Martens; Rogier A Oldenburg; Matti A Rookus; Marjanka K Schmidt; Senno Verhoef; Quinten Waisfisz; Birgit I Witte; Hanne Meijers-Heijboer
Excess breast cancer risk in first degree relatives of CHEK2∗1100delC positive familial breast cancer cases.
Janine L Bakker; Kathleen Claes; Gerry Crossan; Kim De Leeneer; Johan P de Winter; Hans Gille; Hanne Meijers-Heijboer; Bruce Poppe; Nelly Sabbaghian; Marc Tischkowitz; Saskia E van Mil; Hendrik Verheul; Muriel Adank; Quinten Waisfisz
Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.

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All Publications

2013: Sietske H Kevelam; Nienke L Postma; Chitra Prasad; Gajja S Salomons; Quinten Waisfisz; Nicole I Wolf; Truus E M Abbink; Ingrid M C Bakker; Ivo Baric; Susan Blaser; Marianna Bugiani; Annette Feigenbaum; Johannes Häberle; Peter Heutink; Warsha A Kanhai; Marjo S van der Knaap
Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy.
Brain : a journal of neurology 2013;136(Pt 5):1534-43.
2013: Muriel A Adank; Annegien Broeks; Maartje J Hooning; Marianne A Jonker; John Martens; Rogier A Oldenburg; Matti A Rookus; Marjanka K Schmidt; Senno Verhoef; Quinten Waisfisz; Birgit I Witte; Hanne Meijers-Heijboer
Excess breast cancer risk in first degree relatives of CHEK2∗1100delC positive familial breast cancer cases.
European journal of cancer (Oxford, England : 1990) 2013;49(8):1993-9.
2013: Janine L Bakker; Kathleen Claes; Gerry Crossan; Kim De Leeneer; Johan P de Winter; Hans Gille; Hanne Meijers-Heijboer; Bruce Poppe; Nelly Sabbaghian; Marc Tischkowitz; Saskia E van Mil; Hendrik Verheul; Muriel Adank; Quinten Waisfisz
Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.
Human mutation 2013;34(1):70-3.
2012: Marc Warmoes; Epie Boven; Janneke E Jaspers; Jos Jonkers; Maarten P G Massink; Gideon Oudgenoeg; Thang V Pham; Sander R Piersma; Sven Rottenberg; Quinten Waisfisz; Connie R Jimenez
Proteomics of mouse BRCA1-deficient mammary tumors identifies DNA repair proteins with potential diagnostic and prognostic value in human breast cancer.
Molecular & cellular proteomics : MCP 2012;11(7):M111.013334.
2012: Femme Harinck; Irma Kluijt; Ernst J Kuipers; Maran Olderode-Berends; Jan-Werner Poley; Rolf Sijmons; Saskia E van Mil; Theo A M van Os; Anja Wagner; Quinten Waisfisz; Cora M Aalfs; Paul Fockens; Marco J Bruno
Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated.
European journal of human genetics : EJHG 2012;20(5):577-9.
2012: Theo M Starink; Martijn B A van Doorn; R Jeroen A Van Moorselaar; Jan Hein van Waesberghe; Quinten Waisfisz; Johan J P Gille; Arjan C Houweling; Elisabeth H Jaspars; Paul C Johannesma; Marieke T Kramer; Edward M Leter; Martijn H Ploeger; Piet E Postmus; Fred H Menko
Familial multiple discoid fibromas: a look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus.
Journal of the American Academy of Dermatology 2012;66(2):259.e1-9.
2011: Muriel A Adank; Johan J P Gille; Frans B L Hogervorst; Marianne A Jonker; Irma Kluijt; Hanne Meijers-Heijboer; Wolter J Mooi; Rogier A Oldenburg; Marjanka K Schmidt; Ans M W van den Ouweland; Aad W van der Vaart; Saskia E van Mil; Quinten Waisfisz
CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women.
Journal of medical genetics 2011;48(12):860-3.
2011: M A Adank; Saskia E van Mil; J J P Gille; Quinten Waisfisz; H Meijers-Heijboer
PALB2 analysis in BRCA2-like families.
Breast cancer research and treatment 2011;127(2):357-62.
2011: Raphael Ceccaldi; Delphine Briot; Jérôme Larghero; Nadia Vasquez; Catherine Dubois d'Enghien; Delphine Chamousset; Maria-Elena Noguera; Quinten Waisfisz; Olivier Hermine; Corinne Pondarre; Thierry Leblanc; Eliane Gluckman; Hans Joenje; Dominique Stoppa-Lyonnet; Gérard Socié; Jean Soulier
Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients.
The Journal of clinical investigation 2011;121(1):184-94.
2010: Muriel A Adank; Heidi Segers; Saskia E van Mil; Yvette M van Helsdingen; Najim Ameziane; Ans M W van den Ouweland; Anja Wagner; Hanne Meijers-Heijboer; Marcel Kool; Jan de Kraker; Quinten Waisfisz; Marry M van den Heuvel-Eibrink
Fanconi anemia gene mutations are not involved in sporadic Wilms tumor.
Pediatric blood & cancer 2010;55(4):742-4.
2009: Najim Ameziane; Ans M W van den Ouweland; Muriel A Adank; Raymon Vijzelaar; a Errami; Josephine C Dorsman; Hans Joenje; Hanne Meijers-Heijboer; Quinten Waisfisz
Lack of large genomic deletions in BRIP1, PALB2, and FANCD2 genes in BRCA1/2 negative familial breast cancer.
Breast cancer research and treatment 2009;118(3):651-3.
2009: Petra van der Lelij; Barbara C Godthelp; Wouter van Zon; Djoke van Gosliga; Anneke B Oostra; Jûrgen Steltenpool; Jan de Groot; Rik J Scheper; Rob M Wolthuis; Quinten Waisfisz; Firouz Darroudi; Hans Joenje; Johan P de Winter
The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2.
PloS one 2009;4(9):e6936.
2009: Corine J Hess; Nicole Feller; Fedor Denkers; Angèle Kelder; Pauline A Merle; Michael C Heinrich; Amy Harlow; Johannes Berkhof; Gert Ossenkoppele; Quinten Waisfisz; Gerrit J Schuurhuis
Correlation of minimal residual disease cell frequency with molecular genotype in patients with acute myeloid leukemia.
Haematologica 2009;94(1):46-53.
2008: Corine J Hess; a Errami; Johannes Berkhof; Fedor Denkers; Gert Ossenkoppele; Anders O H Nygren; Gerrit J Schuurhuis; Quinten Waisfisz
Concurrent methylation of promoters from tumor associated genes predicts outcome in acute myeloid leukemia.
Leukemia & lymphoma 2008;49(6):1132-41.
2008: Ilse Houtenbos; Saskia Santegoets; Theresia M Westers; Quinten Waisfisz; Sergey Kipriyanov; Fedor Denkers; Rik J Scheper; Tanja D de Gruijl; Gert Ossenkoppele; Arjan A van de Loosdrecht
The novel bispecific diabody alphaCD40/alphaCD28 strengthens leukaemic dendritic cell-induced T-cell reactivity.
British journal of haematology 2008;142(2):273-83.
2008: Corine J Hess; Najim Ameziane; Gerrit J Schuurhuis; a Errami; Fedor Denkers; G J L Kaspers; Jacqueline Cloos; Hans Joenje; Dirk Reinhardt; Gert Ossenkoppele; Christian M Zwaan; Quinten Waisfisz
Hypermethylation of the FANCC and FANCL promoter regions in sporadic acute leukaemia.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2008;30(4):299-306.
2007: Corine J Hess; Johannes Berkhof; Fedor Denkers; Gert Ossenkoppele; Jan P Schouten; Joost Oudejans; Quinten Waisfisz; Gerrit J Schuurhuis
Activated intrinsic apoptosis pathway is a key related prognostic parameter in acute myeloid leukemia.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2007;25(10):1209-15.
2007: Josephine C Dorsman; Marieke Levitus; Davy A P Rockx; Martin A Rooimans; Anneke B Oostra; Anneke Haitjema; Sietske T Bakker; Jûrgen Steltenpool; Dezsö Schuler; Sheila Mohan; Detlev Schindler; Fré Arwert; Gerard Pals; Christopher G Mathew; Quinten Waisfisz; Johan P de Winter; Hans Joenje
Identification of the Fanconi anemia complementation group I gene, FANCI.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2007;29(3):211-8.
2006: Ilse Houtenbos; Theresia M Westers; Corine J Hess; Quinten Waisfisz; Gert Ossenkoppele; Arjan A van de Loosdrecht
Flt-3 internal tandem duplication hampers differentiation of AML blasts towards leukemic dendritic cells.
Leukemia 2006;20(10):1892-5.
2006: Jacqueline Cloos; Bianca Goemans; Corine J Hess; Johan W van Oostveen; Quinten Waisfisz; S Corthals; Desiree de Lange; N Boeckx; Karel Hählen; Dirk Reinhardt; Ursula Creutzig; Gerrit J Schuurhuis; Ch M Zwaan; G J L Kaspers
Stability and prognostic influence of FLT3 mutations in paired initial and relapsed AML samples.
Leukemia 2006;20(7):1217-20.
2006: Barbara C Godthelp; Wouter W Wiegant; Quinten Waisfisz; Annette L Medhurst; Fré Arwert; Hans Joenje; Malgorzata Z Zdzienicka
Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.
Mutation research 2006;594(1-2):39-48.
2005: Anna van Rhenen; Nicole Feller; Angèle Kelder; August H Westra; Elwin Rombouts; Sonja Zweegman; Marjolein A van der Pol; Quinten Waisfisz; Gert Ossenkoppele; Gerrit J Schuurhuis
High stem cell frequency in acute myeloid leukemia at diagnosis predicts high minimal residual disease and poor survival.
Clinical cancer research : an official journal of the American Association for Cancer Research 2005;11(18):6520-7.
2005: Marieke Levitus; Quinten Waisfisz; Barbara C Godthelp; Yne de Vries; Shobbir Hussain; Wouter W Wiegant; Elhaam Elghalbzouri-Maghrani; Jûrgen Steltenpool; Martin A Rooimans; Gerard Pals; Fré Arwert; Christopher G Mathew; Malgorzata Z Zdzienicka; Kevin Hiom; Johan P de Winter; Hans Joenje
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Nature genetics 2005;37(9):934-5.
2005: J J W M Janssen; S M Klaver; Quinten Waisfisz; G Pasterkamp; Dominique P V de Kleijn; Gerrit J Schuurhuis; Gert Ossenkoppele
Identification of genes potentially involved in disease transformation of CML.
Leukemia 2005;19(6):998-1004.
2005: P K Ilja Boor; Koen de Groot; Quinten Waisfisz; Wouter Kamphorst; Cees B M Oudejans; James M Powers; Jan C Pronk; Gert C Scheper; Marjo S van der Knaap
MLC1: a novel protein in distal astroglial processes.
Journal of neuropathology and experimental neurology 2005;64(5):412-9.
2005: Hugo Vega; Quinten Waisfisz; Miriam Gordillo; Norio Sakai; Itaru Yanagihara; Minoru Yamada; Djoke van Gosliga; Hulya Kayserili; Chengzhe Xu; Keiichi Ozono; Ethylin Jabs; Koji Inui; Hans Joenje
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.
Nature genetics 2005;37(5):468-70.
2005: Stefan Meyer; William Fergusson; Anneke B Oostra; Annette L Medhurst; Quinten Waisfisz; Johan P de Winter; Fei Chen; Trevor F Carr; Jill Clayton-Smith; Tara Clancy; Mike Green; Lisa Barber; Osborn B Eden; Andrew M Will; Hans Joenje; G Malcolm Taylor
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.
Genes, chromosomes & cancer 2005;42(4):404-15.
2005: Anders O H Nygren; Najim Ameziane; Helena M B Duarte; Raymon Vijzelaar; Quinten Waisfisz; Corine J Hess; Jan P Schouten; a Errami
Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences.
Nucleic acids research 2005;33(14):e128.
2004: Corine J Hess; Fedor Denkers; Gert Ossenkoppele; Quinten Waisfisz; Cathal J McElgunn; Eric Eldering; Jan P Schouten; Gerrit J Schuurhuis
Gene expression profiling of minimal residual disease in acute myeloid leukaemia by novel multiplex-PCR-based method.
Leukemia 2004;18(12):1981-8.
2004: F Chen; Annette L Medhurst; Johan P de Winter; Quinten Waisfisz; Martin A Rooimans; Anneke B Oostra; Stefan Meyer; K J Zhang; Bing Xia; Gerard Pals; Fré Arwert; C M Zwaan; Hans Joenje
Apparent absence of BRCA2 protein in a proportion of acute myeloid leukemia cell lines.
Leukemia 2004;18(11):1918-20.
2004: France Léveillé; Eric Blom; Annette L Medhurst; Patrick Bier; El Houari Laghmani; Mark Johnson; Martin A Rooimans; Alexandra Sobeck; Quinten Waisfisz; Fré Arwert; Ketan J Patel; Maureen Hoatlin; Hans Joenje; Johan P de Winter
The Fanconi anemia gene product FANCF is a flexible adaptor protein.
The Journal of biological chemistry 2004;279(38):39421-30.
2004: J J W M Janssen; A Hochhaus; Johan W van Oostveen; Quinten Waisfisz; Gerrit J Schuurhuis; Gert Ossenkoppele
Secondary imatinib resistance associated with an aberrant bcr-abl fusion gene.
Leukemia 2004;18(5):1020-1.
2004: Marieke Levitus; Martin A Rooimans; Jûrgen Steltenpool; Nicolle F C Cool; Anneke B Oostra; Christopher G Mathew; Maureen Hoatlin; Quinten Waisfisz; Fré Arwert; Johan P de Winter; Hans Joenje
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.
Blood 2004;103(7):2498-503.
2003: Marc Tischkowitz; Najim Ameziane; Quinten Waisfisz; Johan P de Winter; Richard Harris; Toshiyasu Taniguchi; Alan D D'Andrea; Shirley V Hodgson; Christopher G Mathew; Hans Joenje
Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia.
British journal of haematology 2003;123(3):469-71.
2003: Tanja Reuter; Annette L Medhurst; Quinten Waisfisz; Yu Zhi; Sabine Herterich; Holger Hoehn; Hans J Gross; Hans Joenje; Maureen Hoatlin; Christopher G Mathew; Pia A J Huber
Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport.
Experimental cell research 2003;289(2):211-21.
2003: Amom Ruhikanta Meetei; Johan P de Winter; Annette L Medhurst; Michael Wallisch; Quinten Waisfisz; Henri J van de Vrugt; Anneke B Oostra; Zhijiang Yan; Chen Ling; Jack alvarez; Maureen Hoatlin; Hans Joenje; Weidong Wang
A novel ubiquitin ligase is deficient in Fanconi anemia.
Nature genetics 2003;35(2):165-70.
2003: Hideyuki Ikeda; Maiko Matsushita; Quinten Waisfisz; Akitoshi Kinoshita; Anneke B Oostra; A W M Nieuwint; Johan P de Winter; Maureen Hoatlin; Yohko Kawai; Masao S Sasaki; Alan D D'Andrea; Yutaka Kawakami; Hans Joenje
Genetic reversion in an acute myelogenous leukemia cell line from a Fanconi anemia patient with biallelic mutations in BRCA2.
Cancer research 2003;63(10):2688-94.
2002: Niall G Howlett; Toshiyasu Taniguchi; Susan B Olson; Barbara Cox; Quinten Waisfisz; C E M de Die-Smulders; Nicole Persky; Markus Grompe; Hans Joenje; Gerard Pals; Hideyuki Ikeda; Edward A Fox; Alan D D'Andrea
Biallelic inactivation of BRCA2 in Fanconi anemia.
Science (New York, N.Y.) 2002;297(5581):606-9.
2001: Annette L Medhurst; Pia A J Huber; Quinten Waisfisz; Johan P de Winter; Christopher G Mathew
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway.
Human molecular genetics 2001;10(4):423-9.
2000: Y Xie; Johan P de Winter; Quinten Waisfisz; A W M Nieuwint; Rik J Scheper; Fré Arwert; Maureen Hoatlin; Gert Ossenkoppele; Gerrit J Schuurhuis; Hans Joenje
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cells.
British journal of haematology 2000;111(4):1057-64.
2000: Johan P de Winter; Laura van der Weel; Jan de Groot; Stacie Stone; Quinten Waisfisz; Fré Arwert; Rik J Scheper; Frank A E Kruyt; Maureen Hoatlin; Hans Joenje
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.
Human molecular genetics 2000;9(18):2665-74.
2000: Johan P de Winter; France Léveillé; Carola G M van Berkel; Martin A Rooimans; Laura van der Weel; Jûrgen Steltenpool; Ilja Demuth; Neil V Morgan; Noa Alon; Lucine Bosnoyan-Collins; J Lightfoot; P A J Leegwater; Quinten Waisfisz; K Komatsu; Fré Arwert; Jan C Pronk; Christopher G Mathew; Martin Digweed; Manuel Buchwald; Hans Joenje
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
American journal of human genetics 2000;67(5):1306-8.
2000: Hans Joenje; Marieke Levitus; Quinten Waisfisz; Alan D D'Andrea; Irene Garcia-Higuera; T Pearson; Carola G M van Berkel; Martin A Rooimans; N Morgan; Christopher G Mathew; Fré Arwert
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.
American journal of human genetics 2000;67(3):759-62.
2000: Johan P de Winter; Martin A Rooimans; Laura van der Weel; Carola G M van Berkel; Noa Alon; Lucine Bosnoyan-Collins; Jan de Groot; Yu Zhi; Quinten Waisfisz; Jan C Pronk; Fré Arwert; Christopher G Mathew; Rik J Scheper; Maureen Hoatlin; Manuel Buchwald; Hans Joenje
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.
Nature genetics 2000;24(1):15-6.
1999: Quinten Waisfisz; Johan P de Winter; Frank A E Kruyt; Jan de Groot; Laura van der Weel; LM Dijkmans; Yu Zhi; Fré Arwert; Rik J Scheper; Hagop Youssoufian; Maureen Hoatlin; Hans Joenje
A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(18):10320-5.
1999: Quinten Waisfisz; Neil V Morgan; Maria Savino; Johan P de Winter; Carola G M van Berkel; Maureen Hoatlin; L Ianzano; Robert Alan Gibson; Fré Arwert; Anna Savoia; Christopher G Mathew; Jan C Pronk; Hans Joenje
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
Nature genetics 1999;22(4):379-83.
1999: Quinten Waisfisz; Kathrin Saar; Neil V Morgan; Cigdem Altay; P A J Leegwater; Johan P de Winter; K Komatsu; G R Evans; Rolf-Dieter Wegner; A Reis; Hans Joenje; Fré Arwert; Christopher G Mathew; Jan C Pronk; Martin Digweed
The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.
American journal of human genetics 1999;64(5):1400-5.
1998: Johan P de Winter; Quinten Waisfisz; Martin A Rooimans; Carola G M van Berkel; Lucine Bosnoyan-Collins; Noa Alon; Madeleine Carreau; O Bender; Ilja Demuth; Detlev Schindler; Jan C Pronk; Fré Arwert; Holger Hoehn; Martin Digweed; Manuel Buchwald; Hans Joenje
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
Nature genetics 1998;20(3):281-3.
1997: Frank A E Kruyt; Quinten Waisfisz; LM Dijkmans; Mario A J A Hermsen; Hagop Youssoufian; Fré Arwert; Hans Joenje
Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cells.
Blood 1997;90(9):3288-95.