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marcel mannens
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24
Wilde, Arthur
23
Alders, Marielle
21
Bliek, Jet
18
Westerveld, Andries
16
Hoovers, Jan
12
Bhuiyan, Zahurul
11
Bezzina, Connie
8
Steenman, MJ
7
van Langen, Irene
7
Leschot, Nico
5
Koopmann, Tamara
5
Maas, Saskia
5
Postma, Alex
5
Bleeker-Wagemakers, EM
5
Heyting, Christa
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All Publications
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2009: Bliek Jet; Verde Gaetano; Callaway Jonathan; Maas Saskia M; De Crescenzo Agostina; Sparago Angela; Cerrato Flavia; Russo Silvia; Ferraiuolo Serena; Rinaldi Maria Michela; Fischetto Rita; Lalatta Faustina; Giordano Lucio; Ferrari Paola; Cubellis Maria Vittoria; Larizza Lidia; Temple I Karen; Mannens Marcel M A M; Mackay Deborah J G; Riccio Andrea
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.
European journal of human genetics : EJHG 2009;17(5):611-9.
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2009: Alders Marielle; Koopmann Tamara T; Christiaans Imke; Postema Pieter G; Beekman Leander; Tanck Michael W T; Zeppenfeld Katja; Loh Peter; Koch Karel T; Demolombe Sophie; Mannens Marcel M A M; Bezzina Connie R; Wilde Arthur A M
Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.
American journal of human genetics 2009;84(4):468-76.
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2009: Alders Marielle; Bliek Jet; vd Lip Karin; vd Bogaard Ruud; Mannens Marcel
Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis.
European journal of human genetics : EJHG 2009;17(4):467-73.
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2008: Gijsbers Antoinet C J; D'haene Barbara; Hilhorst-Hofstee Yvonne; Mannens Marcel; Albrecht Beate; Seidel Joerg; Witt David R; Maisenbacher Melissa K; Loeys Bart; van Essen Ton; Bakker Egbert; Hennekam Raoul; Breuning Martijn H; De Baere Elfride; Ruivenkamp Claudia A L
Identification of copy number variants associated with BPES-like phenotypes.
Human genetics 2008;124(5):489-98.
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2008: Bhuiyan Zahurul A; Momenah Tarek S; Amin Ahmad S; Al-Khadra Ayman S; Alders Marielle; Wilde Arthur A M; Mannens Marcel M A M
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.
Progress in biophysics and molecular biology 2008;98(2-3):319-27.
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2008: Bliek Jet; Maas Saskia; Alders Mariel; Merks Johannes H M; Mannens Marcel
Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.
The Journal of pediatrics 2008;153(1):95-100.
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2008: Bhuiyan Zahurul A; Momenah Tarek S; Gong Qiuming; Amin Ahmad S; Ghamdi Saleh Al; Carvalho Julene S; Homfray Tessa; Mannens Marcel M A M; Zhou Zhengfeng; Wilde Arthur A M
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.
Heart rhythm : the official journal of the Heart Rhythm Society 2008;5(4):553-61.
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2008: Redeker Egbert J W; de Visser Annette S H; Bergen Arthur A B; Mannens Marcel M A M
Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders.
Molecular vision 2008;14():836-40.
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2007: Bhuiyan Zahurul A; van den Berg Maarten P; van Tintelen J Peter; Bink-Boelkens Margreet T E; Wiesfeld Ans C P; Alders Marielle; Postma Alex V; van Langen Irene; Mannens Marcel M A M; Wilde Arthur A M
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.
Circulation 2007;116(14):1569-76.
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2007: Bhuiyan Zahurul A; Hamdan Mohamed A; Shamsi Eman T A; Postma Alex V; Mannens Marcel M A M; Wilde Arthur A M; Al-Gazali Lihadh
A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22.
Journal of cardiovascular electrophysiology 2007;18(10):1060-6.
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2007: Koopmann Tamara T; Beekman Leander; Alders Marielle; Meregalli Paola G; Mannens Marcel M A M; Moorman Antoon F M; Wilde Arthur A M; Bezzina Connie R
Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort.
Heart rhythm : the official journal of the Heart Rhythm Society 2007;4(6):752-5.
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2007: Vrouwe Mischa G; Elghalbzouri-Maghrani Elhaam; Meijers Matty; Schouten Peter; Godthelp Barbara C; Bhuiyan Zahurul A; Redeker Egbert J; Mannens Marcel M; Mullenders Leon H F; Pastink Albert; Darroudi Firouz
Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair.
Human molecular genetics 2007;16(12):1478-87.
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2007: Bhuiyan Zahurul A; Stewart Helen; Redeker Egbert J; Mannens Marcel M A M; Hennekam Raoul C M
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome.
European journal of human genetics : EJHG 2007;15(4):505-8.
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2007: Hofman Nynke; Wilde Arthur A M; Kääb Stefan; van Langen Irene M; Tanck Michael W T; Mannens Marcel M A M; Hinterseer Martin; Beckmann Britt-Maria; Tan Hanno L
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?
European heart journal 2007;28(5):575-80.
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2007: Vedder A C; Linthorst G E; van Breemen M J; Groener J E M; Bemelman F J; Strijland A; Mannens M M A M; Aerts J M F G; Hollak C E M
The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels.
Journal of inherited metabolic disease 2007;30(1):68-78.
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2006: Florijn Ralph J; Loves Willem; Maillette de Buy Wenniger-Prick Liesbeth J J M; Mannens Marcel M A M; Tijmes Nel; Brooks Simon P; Hardcastle Alison J; Bergen Arthur A B
New mutations in the NHS gene in Nance-Horan Syndrome families from the Netherlands.
European journal of human genetics : EJHG 2006;14(9):986-90.
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2006: Kannankeril Prince J; Bhuiyan Zahurul A; Darbar Dawood; Mannens Marcel M A M; Wilde Arthur A M; Roden Dan M
Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.
Heart rhythm : the official journal of the Heart Rhythm Society 2006;3(8):939-44.
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2006: Bhuiyan Z A; Klein M; Hammond P; van Haeringen A; Mannens M M A M; Van Berckelaer-Onnes I; Hennekam R C M
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience.
Journal of medical genetics 2006;43(7):568-75.
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2006: van Tintelen J Peter; Entius Mark M; Bhuiyan Zahurul A; Jongbloed Roselie; Wiesfeld Ans C P; Wilde Arthur A M; van der Smagt Jasper; Boven Ludolf G; Mannens Marcel M A M; van Langen Irene M; Hofstra Robert M W; Otterspoor Luuk C; Doevendans Pieter A F M; Rodriguez Luz-Maria; van Gelder Isabelle C; Hauer Richard N W
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Circulation 2006;113(13):1650-8.
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2006: Bliek Jet; Terhal Paulien; van den Bogaard Marie-José; Maas Saskia; Hamel Ben; Salieb-Beugelaar Georgette; Simon Marleen; Letteboer Tom; van der Smagt Jasper; Kroes Hester; Mannens Marcel
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype.
American journal of human genetics 2006;78(4):604-14.
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2006: Koopmann Tamara T; Alders Marielle; Jongbloed Roselie J; Guerrero Silvia; Mannens Marcel M A M; Wilde Arthur A M; Bezzina Connie R
Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.
Heart rhythm : the official journal of the Heart Rhythm Society 2006;3(1):52-5.
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2006: Lombardi M P; Redeker E J W; van Gent D H M; Smeele K L; Weerdesteijn R; Mannens M M A M
Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rate.
Genetic testing 2006;10(2):77-84.
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2005: Verkerk Arie O; Wilders Ronald; Schulze-Bahr Eric; Beekman Leander; Bhuiyan Zahurul A; Bertrand Jessica; Eckardt Lars; Lin Dongxin; Borggrefe Martin; Breithardt Günter; Mannens Marcel M A M; Tan Hanno L; Wilde Arthur A M; Bezzina Connie R
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome.
Cardiovascular research 2005;68(3):441-53.
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2005: Postma A V; Denjoy I; Kamblock J; Alders M; Lupoglazoff J-M; Vaksmann G; Dubosq-Bidot L; Sebillon P; Mannens M M A M; Guicheney P; Wilde A A M
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
Journal of medical genetics 2005;42(11):863-70.
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2005: Wilde A A M; van Langen I M; Mannens M M A M; Waalewijn R A; Maes A
[Sudden death at young age and the importance of molecular-pathologic investigation]
Nederlands tijdschrift voor geneeskunde 2005;149(29):1601-4.
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2005: Smits Jeroen P P; Koopmann Tamara T; Wilders Ronald; Veldkamp Marieke W; Opthof Tobias; Bhuiyan Zahir A; Mannens Marcel M A M; Balser Jeffrey R; Tan Hanno L; Bezzina Connie R; Wilde Arthur A M
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.
Journal of molecular and cellular cardiology 2005;38(6):969-81.
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2005: van der Velde E T; Vriend J W J; Mannens M M A M; Uiterwaal C S P M; Brand R; Mulder Barbara J M
CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: rationale, design, and first results.
European journal of epidemiology 2005;20(6):549-57.
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2004: Bliek Jet; Gicquel Christine; Maas Saskia; Gaston Véronique; Le Bouc Yves; Mannens Marcel
Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS).
The Journal of pediatrics 2004;145(6):796-9.
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2004: Leschot N J; Mannens M M A M
[The disquieting consequences of granting patents on human genes for healthcare and scientific research in The Netherlands]
Nederlands tijdschrift voor geneeskunde 2004;148(35):1712-5.
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2004: Bellocq Chloé; van Ginneken Antoni C G; Bezzina Connie R; Alders Mariel; Escande Denis; Mannens Marcel M A M; Baró Isabelle; Wilde Arthur A M
Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.
Circulation 2004;109(20):2394-7.
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2004: Hu Xiaofeng; Plomp Astrid; Gorgels Theo; Brink Jacoline Ten; Loves Willem; Mannens Marcel; de Jong Paulus T V M; Bergen Arthur A B
Efficient molecular diagnostic strategy for ABCC6 in pseudoxanthoma elasticum.
Genetic testing 2004;8(3):292-300.
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2003: Alders Marielle; Jongbloed Roselie; Deelen Wout; van den Wijngaard Arthur; Doevendans Pieter; Ten Cate Folkert; Regitz-Zagrosek Vera; Vosberg Hans Peter; van Langen Irene; Wilde Arthur; Dooijes Dennis; Mannens Marcel
The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands.
European heart journal 2003;24(20):1848-53.
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2003: Gianotten Judith; van der Veen Fulco; Alders Mariëlle; Leschot Nico J; Tanck Michael W T; Land Jolande A; Kremer Jan A M; Hoefsloot Lies H; Mannens Marcel M; Lombardi M Paola; Hoffer Mariëtte J V
Chromosomal region 11p15 is associated with male factor subfertility.
Molecular human reproduction 2003;9(10):587-92.
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2003: Bezzina Connie R; Verkerk Arie O; Busjahn Andreas; Jeron Andreas; Erdmann Jeanette; Koopmann Tamara T; Bhuiyan Zahurul A; Wilders Ronald; Mannens Marcel M A M; Tan Hanno L; Luft Friedrich C; Schunkert Heribert; Wilde Arthur A M
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.
Cardiovascular research 2003;59(1):27-36.
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2003: Groenewegen W Antoinette; Bezzina Connie R; van Tintelen J Peter; Hoorntje Theo M; Mannens Marcel M A M; Wilde Arthur A M; Jongsma Habo J; Rook Martin B
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.
Cardiovascular research 2003;57(4):1072-8.
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2003: Bezzina Connie R; Rook Martin B; Groenewegen W Antoinette; Herfst Lucas J; van der Wal Allard C; Lam Jan; Jongsma Habo J; Wilde Arthur A M; Mannens Marcel M A M
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.
Circulation research 2003;92(2):159-68.
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2002: Postma Alex V; Denjoy Isabelle; Hoorntje Theo M; Lupoglazoff Jean-Marc; Da Costa Antoine; Sebillon Pascale; Mannens Marcel M A M; Wilde Arthur A M; Guicheney Pascale
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia.
Circulation research 2002;91(8):e21-6.
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2002: Breugem Corstiaan C; Alders Marielle; Salieb-Beugelaar Georgette B; Mannens Marcel M A M; Van der Horst Chantal M; Hennekam Raoul C M
A locus for hereditary capillary malformations mapped on chromosome 5q.
Human genetics 2002;110(4):343-7.
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2001: Bliek J; Maas S M; Ruijter J M; Hennekam R C; Alders M; Westerveld A; Mannens M M
Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.
Human molecular genetics 2001;10(5):467-76.
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2000: van den Bogaard R; Fijen C A; Schipper M G; de Galan L; Kuijper E J; Mannens M M
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
European journal of human genetics : EJHG 2000;8(7):513-8.
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2000: Postma A V; Bezzina C R; de Vries J F; Wilde A A; Moorman A F; Mannens M M
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.
Human genetics 2000;106(6):614-9.
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2000: Leschot N J; Mannens M M
[Decoding of the human genome: a milestone, but not the end of the road]
Nederlands tijdschrift voor geneeskunde 2000;144(23):1093-6.
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2000: Alders M; Ryan A; Hodges M; Bliek J; Feinberg A P; Privitera O; Westerveld A; Little P F; Mannens M
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.
American journal of human genetics 2000;66(5):1473-84.
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2000: Steenman M; Westerveld A; Mannens M
Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.
Genes, chromosomes & cancer 2000;28(1):1-13.
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2000: Lombardi M P; Redeker E J; Defesche J C; Kamerling S W; Trip M D; Mannens M M; Havekes L M; Kastelein J J
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands.
Clinical genetics 2000;57(2):116-24.
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2000: Aalfs C M; Salieb-Beugelaar G B; Wanders R J; Mannens M M; Wijburg F A
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis.
Human mutation 2000;16(1):18-22.
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2000: Steenman M J; Zijlstra N; Kruitbosch D L; Wiesmeijer C; Larizza L; Voûte P A; Westerveld A; Mannens M M
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors.
Cytogenetics and cell genetics 2000;88(3-4):289-95.
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1999: Rook M B; Bezzina Alshinawi C; Groenewegen W A; van Gelder I C; van Ginneken A C; Jongsma H J; Mannens M M; Wilde A A
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
Cardiovascular research 1999;44(3):507-17.
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1999: Bezzina C; Veldkamp M W; van Den Berg M P; Postma A V; Rook M B; Viersma J W; van Langen I M; Tan-Sindhunata G; Bink-Boelkens M T; van Der Hout A H; Mannens M M; Wilde A A
A single Na(+) channel mutation causing both long-QT and Brugada syndromes.
Circulation research 1999;85(12):1206-13.
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1999: Fijen C A; van den Bogaard R; Schipper M; Mannens M; Schlesinger M; Nordin F G; Dankert J; Daha M R; Sjöholm A G; Truedsson L; Kuijper E J
Properdin deficiency: molecular basis and disease association.
Molecular immunology 1999;36(13-14):863-7.
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1999: Hoorntje T; Alders M; van Tintelen P; van der Lip K; Sreeram N; van der Wal A; Mannens M; Wilde A
Homozygous premature truncation of the HERG protein : the human HERG knockout.
Circulation 1999;100(12):1264-7.
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1999: Schott J J; Alshinawi C; Kyndt F; Probst V; Hoorntje T M; Hulsbeek M; Wilde A A; Escande D; Mannens M M; Le Marec H
Cardiac conduction defects associate with mutations in SCN5A.
Nature genetics 1999;23(1):20-1.
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1999: Mannens M; Alders M
Genomic imprinting: concept and clinical consequences.
Annals of medicine 1999;31(1):4-11.
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1999: Gaudray P; Carle G F; Gerhard D S; Gessler M; Mannens M M; Athanasiou M; Bliek J; Calender A; Debelenko L V; Devignes M; Evans G A; Favier R; Forbes S; Gaudray G; Gawin B; Gordon M; Grimmond S; Grossfeld P; Harris J; Hattori M; Hosoda F; Hummerich H; James M; Kalla J; Katsanis N
Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998.
Cytogenetics and cell genetics 1999;86(3-4):167-86.
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1999: Steenman M; Tomlinson G; Westerveld A; Mannens M
Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma.
Cytogenetics and cell genetics 1999;86(2):157-61.
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1998: Boot R G; Renkema G H; Verhoek M; Strijland A; Bliek J; de Meulemeester T M; Mannens M M; Aerts J M
The human chitotriosidase gene. Nature of inherited enzyme deficiency.
The Journal of biological chemistry 1998;273(40):25680-5.
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1998: Henderson H E; Bijvoet S M; Mannens M A; Bruin T; Erkelens D W; Hayden M R; Kastelein J J
Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo event.
American journal of medical genetics 1998;78(4):313-6.
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1998: Van Langen I M; Wilde A A; Mannens M A
[Sudden death in young men due to arrhythmogenic right ventricular dysplasia]
Nederlands tijdschrift voor geneeskunde 1998;142(13):739-40.
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1998: Speleman F; van den Berg E; Dhooge C; Oosterhuis W; Redeker B; De Potter C R; Tamminga R Y; Van Roy N; Mannens M
Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma.
Genes, chromosomes & cancer 1998;21(3):265-9.
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1998: Demolombe S; Baró I; Péréon Y; Bliek J; Mohammad-Panah R; Pollard H; Morid S; Mannens M; Wilde A; Barhanin J; Charpentier F; Escande D
A dominant negative isoform of the long QT syndrome 1 gene product.
The Journal of biological chemistry 1998;273(12):6837-43.
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1997: Oudejans C; Westerman B; van Elk E; Könst A; Mulders M; Alders M; van Vugt J; van Wijk I; Mannens M
Growth regulation of extraembryonic tissues. The effect of genomic imprinting on development of the placenta.
European journal of obstetrics, gynecology, and reproductive biology 1997;75(1):29-32.
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1997: Nesbit M A; Hodges M D; Campbell L; de Meulemeester T M; Alders M; Rodrigues N R; Talbot K; Theodosiou A M; Mannens M A; Nakamura Y; Little P F; Davies K E
Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2.
Genomics 1997;42(2):284-94.
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1997: Alders M; Hodges M; Hadjantonakis A K; Postmus J; van Wijk I; Bliek J; de Meulemeester M; Westerveld A; Guillemot F; Oudejans C; Little P; Mannens M
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.
Human molecular genetics 1997;6(6):859-67.
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1997: Wilde A A; Mannens M M
[Iatrogenic collapse; can this be prevented?]
Nederlands tijdschrift voor geneeskunde 1997;141(16):796-7.
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1997: Mannens M; Wilde A
KVLQT1, the rhythm of imprinting.
Nature genetics 1997;15(2):113-5.
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1997: Boot R G; Hollak C E; Verhoek M; Sloof P; Poorthuis B J; Kleijer W J; Wevers R A; van Oers M H; Mannens M M; Aerts J M; van Weely S
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value.
Human mutation 1997;10(5):348-58.
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1997: Steenman M; Redeker B; de Meulemeester M; Wiesmeijer K; Voûte P A; Westerveld A; Slater R; Mannens M
Comparative genomic hybridization analysis of Wilms tumors.
Cytogenetics and cell genetics 1997;77(3-4):296-303.
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1996: de Meulemeester M; Vink A; Jakobs M; Hermsen M; Steenman M; Slater R; Dietrich A; Mannens M
The application of microwave denaturation in comparative genomic hybridization.
Genetic analysis : biomolecular engineering 1996;13(5):129-33.
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1996: Alders M; Bliek J; Redeker B; Ryan A; Feinberg A; Westerveld A; Little P; Mannens M
Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.
Medical and pediatric oncology 1996;27(5):495-7.
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1996: Mannens M; Alders M; Redeker B; Bliek J; Steenman M; Wiesmeyer C; de Meulemeester M; Ryan A; Kalikin L; Voûte T; De Kraker J; Hoovers J; Slater R; Feinberg A; Little P; Westerveld A
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
Medical and pediatric oncology 1996;27(5):490-4.
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1996: Fijen C A; van den Bogaard R; Daha M R; Dankert J; Mannens M; Kuijper E J
Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families.
European journal of clinical investigation 1996;26(10):902-6.
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1995: Aalfs C M; Hoovers J M; Nieste-Otter M A; Mannens M M; Hennekam R C; Leschot N J
Further delineation of the partial proximal trisomy 10q syndrome.
Journal of medical genetics 1995;32(12):968-71.
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1995: Hoovers J M; Kalikin L M; Johnson L A; Alders M; Redeker B; Law D J; Bliek J; Steenman M; Benedict M; Wiegant J; Lengauer C; Taillon-Miller P; Schlessinger D; Edwards M C; Elledge S J; Ivens A; Westerveld A; Little P; Mannens M; Feinberg A P
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(26):12456-60.
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1995: Austruy E; Candon S; Henry I; Gyapay G; Tournade M F; Mannens M; Callen D; Junien C; Jeanpierre C
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis.
Genes, chromosomes & cancer 1995;14(4):285-94.
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1995: Fijen C A; Derkx B H; Kuijper E J; Mannens M; Poort S R; Peters M; Daha M R; Dankert J
Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency.
Clinical and experimental immunology 1995;102(2):290-6.
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1995: Fantes J; Redeker B; Breen M; Boyle S; Brown J; Fletcher J; Jones S; Bickmore W; Fukushima Y; Mannens M
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.
Human molecular genetics 1995;4(3):415-22.
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1995: Redeker E; Alders M; Hoovers J M; Richard C W; Westerveld A; Mannens M
Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.
Cytogenetics and cell genetics 1995;68(3-4):222-5.
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1994: Mannens M; Hoovers J M; Redeker E; Verjaal M; Feinberg A P; Little P; Boavida M; Coad N; Steenman M; Bliek J
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
European journal of human genetics : EJHG 1994;2(1):3-23.
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1993: Mannens M; Hoovers J M; Bleeker-Wagemakers E M; Mäntyjärvi M; Tuppurainen K
The importance of DNA analysis in sporadic aniridia.
Acta ophthalmologica 1993;71(6):841-5.
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1993: Redeker E; Van Moorsel C J; Feinberg A; Mannens M
TaqI and RsaI polymorphisms in the H19 gene (D11S813E).
Human molecular genetics 1993;2(6):823.
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1993: Caron H; van Sluis P; van Hoeve M; de Kraker J; Bras J; Slater R; Mannens M; Voûte P A; Westerveld A; Versteeg R
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.
Nature genetics 1993;4(2):187-90.
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1993: Henry I; Hoovers J; Barichard F; Berthéas M F; Puech A; Prieur F; Gessler M; Bruns G; Mannens M; Junien C
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family.
Genes, chromosomes & cancer 1993;7(1):57-62.
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1993: Fukushima Y; Hoovers J; Mannens M; Wakui K; Ohashi H; Ohno T; Ueoka Y; Niikawa N
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.
Human genetics 1993;91(3):205-9.
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1993: Hoovers J M; Redeker E; Speleman F; Höppener J W; Bhola S; Bliek J; van Roy N; Leschot N J; Westerveld A; Mannens M
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.
Genomics 1993;15(3):525-9.
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1993: Little M H; Williamson K A; Mannens M; Kelsey A; Gosden C; Hastie N D; van Heyningen V
Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
Human molecular genetics 1993;2(3):259-64.
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1993: Henry I; van Heyningen V; Puech A; Scrable H; Augereau P; Boehm T; Rabbitts T; Mannens M; Rochefort H; Jones C
Reassessment of breakpoints in chromosome 11p15.
Cytogenetics and cell genetics 1993;62(1):52-3.
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1993: Henry I; Puech A; Riesewijk A; Ahnine L; Mannens M; Beldjord C; Bitoun P; Tournade M F; Landrieu P; Junien C
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event.
European journal of human genetics : EJHG 1993;1(1):19-29.
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1992: van den Ouweland A M; Verdijk M; Mannens M M; van Oost B A
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor.
Human genetics 1992;90(1-2):144-6.
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1992: Slater R M; Mannens M M
Cytogenetics and molecular genetics of Wilms' tumor of childhood.
Cancer genetics and cytogenetics 1992;61(2):111-21.
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1992: Heding I J; Ivens A C; Wilson J; Strivens M; Gregory S; Hoovers J M; Mannens M; Redeker B; Porteous D; van Heyningen V
The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.
Genomics 1992;13(1):89-94.
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1992: Hoovers J M; Dietrich A J; Mannens M M
Imprinting and Beckwith-Wiedemann syndrome.
Lancet 1992;339(8803):1228.
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1992: Junien C; van Heyningen V; Evans G; Little P; Mannens M
Report of the second chromosome 11 workshop.
Genomics 1992;12(3):620-5.
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1992: Hoovers J M; Mannens M; John R; Bliek J; van Heyningen V; Porteous D J; Leschot N J; Westerveld A; Little P F
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.
Genomics 1992;12(2):254-63.
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1991: Verbraak F D; Mannens M A; Redeker E J; Saunders G F; Bleeker-Wagemakers E M
DNA diagnosis in a family with autosomal dominant aniridia.
Ophthalmic paediatrics and genetics 1991;12(4):165-70.
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1991: Mannens M; Hoovers J M; Bleeker-Wagemakers E M; Redeker E; Bliek J; Overbeeke-Melkert M; Saunders G; Williams B; van Heyningen V; Junien C
The distal region of 11p13 and associated genetic diseases.
Genomics 1991;11(2):284-93.
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1991: Devilee P; van den Broek M; Mannens M; Slater R; Cornelisse C J; Westerveld A; Khan P M
Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood.
International journal of cancer. Journal international du cancer 1991;47(6):817-21.
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1991: Speleman F; Mannens M; Redeker B; Vercruyssen M; Van Oostveldt P; Leroy J; Slater R
Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization.
Cytogenetics and cell genetics 1991;56(3-4):129-31.
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1990: Mannens M; Devilee P; Bliek J; Mandjes I; de Kraker J; Heyting C; Slater R M; Westerveld A
Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.
Cancer research 1990;50(11):3279-83.
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1989: Bout A; Hoovers J M; Bakker E; Mannens M M; Geurts van Kessel A; Westerveld A; Tager J M; Benne R
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23.
Cytogenetics and cell genetics 1989;52(3-4):147-50.
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1989: Mannens M; Bleeker-Wagemakers E M; Bliek J; Hoovers J; Mandjes I; van Tol S; Frants R R; Heyting C; Westerveld A; Slater R M
Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.
Cytogenetics and cell genetics 1989;52(1-2):32-6.
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1988: Mannens M; Slater R M; Heyting C; Bliek J; de Kraker J; Coad N; de Pagter-Holthuizen P; Pearson P L
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.
Human genetics 1988;81(1):41-8.
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1988: de Ronde A; Mannens M; Slater R M; Hoovers J; Heyting C; Bleeker-Wagemakers E M; Leschot N J; van Strien A; Sol C J; ter Schegget J
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11.
The Journal of general virology 1988;69 ( Pt 2)():467-71.
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1987: Mannens M; Slater R M; Heyting C; Geurts van Kessel A; Goedde-Salz E; Frants R R; Van Ommen G J; Pearson P L
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions.
Human genetics 1987;75(2):180-7.
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