FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

marcel mannens

Research Profile

Anatomy

Chromosomes, Human, Pair 11

Disorders

Concepts & Ideas

Physiology

Procedures

Geographic Areas

Netherlands

Living Beings

Heterozygote

Chemicals & Drugs

Co-author Network

Publications

TOP 3
Sylvia A Huisman; Saskia M Maas; marcel mannens; Egbert J Redeker; Raoul C M Hennekam
High rate of mosaicism in individuals with Cornelia de Lange syndrome.
Judith B A van de Meerakker; Klaartje van Engelen; Arthur A M Wilde; Marieke J H Baars; Jan Lam; Ronald H Lekanne dit Deprez; marcel mannens; Inge B Mathijssen; Antoon F M Moorman; Barbara J M Mulder; Alex V Postma
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q.
Imke Christiaans; Erwin Birnie; Gouke J Bonsel; marcel mannens; Michelle Michels; Daniëlle Majoor-Krakauer; Dennis Dooijes; J Peter van Tintelen; Maarten P van den Berg; Paul G A Volders; Yvonne H Arens; Arthur van den Wijngaard; Douwe E Atsma; Apollonia T J M Helderman-van den Enden; Arjan C Houweling; Karin de Boer; Jasper J van der Smagt; Richard N W Hauer; Carlo L M Marcelis; Janneke Timmermans; Irene M van Langen; Arthur A M Wilde
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of marcel mannens (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Sylvia A Huisman; Saskia M Maas; marcel mannens; Egbert J Redeker; Raoul C M Hennekam
High rate of mosaicism in individuals with Cornelia de Lange syndrome.
Journal of medical genetics 2013;50(5):339-44.
2011: Judith B A van de Meerakker; Klaartje van Engelen; Arthur A M Wilde; Marieke J H Baars; Jan Lam; Ronald H Lekanne dit Deprez; marcel mannens; Inge B Mathijssen; Antoon F M Moorman; Barbara J M Mulder; Alex V Postma
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q.
European journal of human genetics : EJHG 2011;19(7):820-6.
2011: Imke Christiaans; Erwin Birnie; Gouke J Bonsel; marcel mannens; Michelle Michels; Daniëlle Majoor-Krakauer; Dennis Dooijes; J Peter van Tintelen; Maarten P van den Berg; Paul G A Volders; Yvonne H Arens; Arthur van den Wijngaard; Douwe E Atsma; Apollonia T J M Helderman-van den Enden; Arjan C Houweling; Karin de Boer; Jasper J van der Smagt; Richard N W Hauer; Carlo L M Marcelis; Janneke Timmermans; Irene M van Langen; Arthur A M Wilde
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.
European heart journal 2011;32(9):1161-70.
2009: Jet Bliek; Marielle Alders; Saskia M Maas; Roelof-Jan Oostra; Deborah M Mackay; Karin van der Lip; Johnatan L Callaway; Alice Brooks; Sandra van 't Padje; Andries Westerveld; Nico J Leschot; marcel mannens
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.
European journal of human genetics : EJHG 2009;17(12):1625-34.
2009: Argelia Medeiros Domingo; Zahurul A Bhuiyan; David J Tester; Nynke Hofman; Hennie Bikker; J Peter van Tintelen; marcel mannens; Arthur A M Wilde; Michael J Ackerman
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis.
Journal of the American College of Cardiology 2009;54(22):2065-74.
2009: Zahurul A Bhuiyan; Jan D H Jongbloed; Jasper van der Smagt; Paola M Lombardi; Ans C P Wiesfeld; Marcel Nelen; Meyke Schouten; Roselie J Jongbloed; Moniek G P J Cox; Marleen van Wolferen; Luz M Rodriguez; Isabelle C Van Gelder; Hennie Bikker; Albert J H Suurmeijer; Maarten P van den Berg; marcel mannens; Richard N W Hauer; Arthur A M Wilde; J Peter van Tintelen
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study.
Circulation. Cardiovascular genetics 2009;2(5):418-27.
2009: Jet Bliek; Gaetano Verde; Jonathan Callaway; Saskia M Maas; Agostina De Crescenzo; Angela Sparago; Flavia Cerrato; Silvia Russo; Serena Ferraiuolo; Maria Michela Rinaldi; Rita Fischetto; Faustina Lalatta; Lucio Giordano; Paola Ferrari; Maria Vittoria Cubellis; Lidia Larizza; I Karen Temple; marcel mannens; Deborah J G Mackay; Andrea Riccio
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.
2009: Marielle Alders; Tamara T Koopmann; Imke Christiaans; Pieter G Postema; Leander Beekman; Michael W T Tanck; Katja Zeppenfeld; Peter Loh; Karel T Koch; Sophie Demolombe; marcel mannens; Connie R Bezzina; Arthur A M Wilde
Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.
American journal of human genetics 2009;84(4):468-76.
2009: Marielle Alders; Jet Bliek; Karin vd Lip; Ruud vd Bogaard; marcel mannens
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.
2008: Antoinet C J Gijsbers; Barbara D'haene; Y Hilhorst-Hofstee; marcel mannens; Beate Albrecht; Joerg Seidel; David R Witt; Melissa K Maisenbacher; Bart Loeys; Ton van Essen; Egbert Bakker; Raoul Hennekam; Martijn H Breuning; Elfride De Baere; Claudia Ruivenkamp
Identification of copy number variants associated with BPES-like phenotypes.
Human genetics 2008;124(5):489-98.
2008: Zahurul A Bhuiyan; Tarek S Momenah; Ahmad S Amin; Ayman S al-Khadra; Marielle Alders; Arthur A M Wilde; marcel mannens
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.
2008: Jet Bliek; Saskia M Maas; Marielle Alders; Johannes H M Merks; marcel mannens
Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.
The Journal of pediatrics 2008;153(1):95-100.
2008: Zahurul A Bhuiyan; Tarek S Momenah; Qiuming Gong; Ahmad S Amin; Saleh Al Ghamdi; Julene S Carvalho; Tessa Homfray; marcel mannens; Zhengfeng Zhou; Arthur A M Wilde
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.
2008: Egbert J W Redeker; Annette S H de Visser; Arthur A B Bergen; marcel mannens
Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders.
Molecular vision 2008;14():836-40.
2007: Zahurul A Bhuiyan; Maarten P van den Berg; J Peter van Tintelen; Margreet Th E Bink-Boelkens; Ans C P Wiesfeld; Marielle Alders; Alex V Postma; Irene M van Langen; marcel mannens; Arthur A M Wilde
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.
Circulation 2007;116(14):1569-76.
2007: Zahurul A Bhuiyan; Mohamed A Hamdan; Eman T A Shamsi; Alex V Postma; marcel mannens; Arthur A M Wilde; Lihadh Al-Gazali
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.
2007: Mischa G Vrouwe; Elhaam Elghalbzouri-Maghrani; Matty Meijers; Peter Schouten; Barbara C Godthelp; Zahurul A Bhuiyan; Egbert J Redeker; marcel mannens; Leon H F Mullenders; Albert Pastink; Firouz Darroudi
Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair.
Human molecular genetics 2007;16(12):1478-87.
2007: Tamara T Koopmann; Leander Beekman; Marielle Alders; Paola G Meregalli; marcel mannens; Antoon F M Moorman; Arthur A M Wilde; Connie R Bezzina
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.
2007: Zahurul A Bhuiyan; Helen Stewart; Egbert J Redeker; marcel mannens; Raoul Hennekam
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange syndrome.
European journal of human genetics : EJHG 2007;15(4):505-8.
2007: Nynke Hofman; Arthur A M Wilde; Stefan Kääb; Irene M van Langen; Michael W T Tanck; marcel mannens; Martin Hinterseer; britt beckmann; Hanno L Tan
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.
2007: Anouk C Vedder; Gabor E Linthorst; Mariëlle J Van Breemen; Johanna E M Groener; F J Bemelman; Anneke Strijland; marcel mannens; johannes aerts; Carla E M Hollak
The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels.
Journal of inherited metabolic disease 2007;30(1):68-78.
2006: Ralph J Florijn; Willem J P Loves; Liesbeth J J M Maillette de Buy Wenniger-Prick; marcel mannens; Nel Tijmes; Simon P Brooks; Alison J Hardcastle; Arthur A B Bergen
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.
2006: Prince J Kannankeril; Zahurul A Bhuiyan; Dawood Darbar; marcel mannens; Arthur A M Wilde; Dan Mark Roden
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.
2006: Zahurul A Bhuiyan; M Klein; Peter Hammond; A van Haeringen; marcel mannens; I Van Berckelaer-Onnes; Raoul Hennekam
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience.
Journal of medical genetics 2006;43(7):568-75.
2006: J Peter van Tintelen; Mark M Entius; Zahurul A Bhuiyan; Roselie J Jongbloed; Ans C P Wiesfeld; Arthur A M Wilde; Jasper van der Smagt; Ludolf G Boven; marcel mannens; Irene M van Langen; Robert M W Hofstra; Luuk C Otterspoor; Pieter A Doevendans; Luz-Maria Rodriguez; Isabelle C Van Gelder; Richard N W Hauer
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Circulation 2006;113(13):1650-8.
2006: Jet Bliek; Paulien Terhal; Marie-José van den Bogaard; Saskia M Maas; Ben Hamel; Georgette Salieb-Beugelaar; Marleen Simon; Tom Letteboer; Jasper van der Smagt; Hester Kroes; marcel mannens
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.
2006: M Paola Lombardi; Egbert J Redeker; D H M van Gent; K L Smeele; R Weerdesteijn; marcel mannens
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.
2006: Tamara T Koopmann; Marielle Alders; Roselie J Jongbloed; Silvia Guerrero; marcel mannens; Arthur A M Wilde; Connie R Bezzina
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.
2005: Arie O Verkerk; Ronald Wilders; Eric Schulze-Bahr; Leander Beekman; Zahurul A Bhuiyan; Jessica Bertrand; Lars Eckardt; Dongxin Lin; Martin Borggrefe; Günter Breithardt; marcel mannens; Hanno L Tan; Arthur A M Wilde; Connie R Bezzina
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.
2005: Alex V Postma; Isabelle Denjoy; J Kamblock; Marielle Alders; Jean-Marc Lupoglazoff; Guy Vaksmann; L Dubosq-Bidot; Pascale Sebillon; marcel mannens; Pascale Guicheney; Arthur A M Wilde
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
Journal of medical genetics 2005;42(11):863-70.
2005: Arthur A M Wilde; Irene M van Langen; marcel mannens; Reinier A Waalewijn; A Maes
[Sudden death at young age and the importance of molecular-pathologic investigation].
Nederlands tijdschrift voor geneeskunde 2005;149(29):1601-4.
2005: Jeroen P P Smits; Tamara T Koopmann; Ronald Wilders; Marieke W Veldkamp; Tobias Opthof; Zahurul A Bhuiyan; marcel mannens; Jeffrey R Balser; Hanno L Tan; Connie R Bezzina; Arthur A M Wilde
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.
2005: Enno T van der Velde; Velde E T Vander; Joris W J Vriend; marcel mannens; Cuno Uiterwaal; Ronald Brand; Barbara J M Mulder
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.
2004: Jet Bliek; Christine Gicquel; Saskia M Maas; Véronique Gaston; Yves Le Bouc; marcel mannens
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.
2004: Nico J Leschot; marcel mannens
[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.
2004: Chloé Bellocq; Antoni C G van Ginneken; Connie R Bezzina; Marielle Alders; Denis Escande; marcel mannens; Isabelle Baro; Arthur A M Wilde
Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.
Circulation 2004;109(20):2394-7.
2004: Xiaofeng Hu; Astrid S Plomp; Theo G M F Gorgels; Jacoline Ten Brink; Willem J P Loves; marcel mannens; Paulus T V M de Jong; Arthur A B Bergen
Efficient molecular diagnostic strategy for ABCC6 in pseudoxanthoma elasticum.
Genetic testing 2004;8(3):292-300.
2003: Marielle Alders; Roselie J Jongbloed; Wout Deelen; Arthur van den Wijngaard; Pieter A Doevendans; Folkert J Ten Cate; Vera Regitz-Zagrosek; Hans-Peter Vosberg; Irene M van Langen; Arthur Wilde; Dennis Dooijes; marcel mannens
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.
2003: Judith Gianotten; Fulco van der Veen; Marielle Alders; Nico J Leschot; Michael W T Tanck; Jolande A Land; Jan A M Kremer; Lies Hoefsloot; marcel mannens; M Paola Lombardi; Mariëtte J V Hoffer
Chromosomal region 11p15 is associated with male factor subfertility.
Molecular human reproduction 2003;9(10):587-92.
2003: Connie R Bezzina; Arie O Verkerk; Andreas Busjahn; Andreas Jeron; Jeanette Erdmann; Tamara T Koopmann; Zahurul A Bhuiyan; Ronald Wilders; marcel mannens; Hanno L Tan; Friedrich C Luft; Heribert Schunkert; Arthur A M Wilde
A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.
Cardiovascular research 2003;59(1):27-36.
2003: W Antoinette Groenewegen; Connie R Bezzina; J Peter van Tintelen; Theo M Hoorntje; marcel mannens; Arthur A M Wilde; Habo J Jongsma; Martin B Rook
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.
Cardiovascular research 2003;57(4):1072-8.
2003: Connie R Bezzina; Martin B Rook; W Antoinette Groenewegen; Lucas J Herfst; Allard C van der Wal; Jan Lam; Habo J Jongsma; Arthur A M Wilde; marcel mannens
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.
2002: Alex V Postma; Isabelle Denjoy; Theo M Hoorntje; Jean-Marc Lupoglazoff; Antoine Da Costa; Pascale Sebillon; marcel mannens; Arthur A M Wilde; Pascale Guicheney
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia.
Circulation research 2002;91(8):e21-6.
2002: Corstiaan C Breugem; Marielle Alders; Georgette B Salieb-Beugelaar; marcel mannens; Chantal M A M van der Horst; Raoul Hennekam
A locus for hereditary capillary malformations mapped on chromosome 5q.
Human genetics 2002;110(4):343-7.
2001: Jet Bliek; Saskia M Maas; J M Ruijter; Raoul Hennekam; Marielle Alders; Andries Westerveld; marcel mannens
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.
2000: R van den Bogaard; Cees A P Fijen; M G Schipper; L de Galan; Ed J Kuijper; marcel mannens
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.
2000: Nico J Leschot; marcel mannens
[Decoding of the human genome: a milestone, but not the end of the road].
Nederlands tijdschrift voor geneeskunde 2000;144(23):1093-6.
2000: A V Postma; Connie R Bezzina; J F de Vries; A A Wilde; Antoon F M Moorman; marcel mannens
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.
Human genetics 2000;106(6):614-9.
2000: Marielle Alders; A Ryan; M Hodges; Jet Bliek; Andrew P Feinberg; O Privitera; Andries Westerveld; P F Little; marcel mannens
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.
American journal of human genetics 2000;66(5):1473-84.
2000: MJ Steenman; Andries Westerveld; marcel mannens
Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.
Genes, chromosomes & cancer 2000;28(1):1-13.
2000: M Paola Lombardi; Egbert J Redeker; Joep C Defesche; Sylvia W A Kamerling; Mieke D Trip; marcel mannens; Louis M Havekes; John J P Kastelein
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands.
Clinical genetics 2000;57(2):116-24.
2000: Cora M Aalfs; G B Salieb-Beugelaar; R J Wanders; marcel mannens; F A Wijburg
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.
2000: MJ Steenman; N Zijlstra; D L Kruitbosch; C Wiesmeijer; L Larizza; Paul A Voûte; Andries Westerveld; marcel mannens
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.
1999: Connie R Bezzina; Marieke W Veldkamp; Maarten P van den Berg; Alex V Postma; Martin B Rook; J W Viersma; Irene M van Langen; G Tan-Sindhunata; Margreet Th E Bink-Boelkens; Annemarie H Van Der Hout; marcel mannens; Arthur A M Wilde
A single Na(+) channel mutation causing both long-QT and Brugada syndromes.
Circulation research 1999;85(12):1206-13.
1999: Martin B Rook; C Bezzina Alshinawi; W Antoinette Groenewegen; I C van Gelder; Antoni C G van Ginneken; Habo J Jongsma; marcel mannens; Arthur A M Wilde
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
Cardiovascular research 1999;44(3):507-17.
1999: TM Hoorntje; Marielle Alders; P van Tintelen; K van der Lip; Narayanswami Sreeram; Allard C van der Wal; marcel mannens; Arthur Wilde
Homozygous premature truncation of the HERG protein : the human HERG knockout.
Circulation 1999;100(12):1264-7.
1999: Cees A P Fijen; R van den Bogaard; M Schipper; marcel mannens; M Schlesinger; F G Nordin; Jacob Dankert; Mohamed R Daha; Anders G Sjöholm; Lennart Truedsson; Ed J Kuijper
Properdin deficiency: molecular basis and disease association.
Molecular immunology 1999;36(13-14):863-7.
1999: Jean-Jacques Schott; C Alshinawi; Florence Kyndt; Vincent Probst; Theo M Hoorntje; M Hulsbeek; Arthur A M Wilde; Denis Escande; marcel mannens; Hervé Le Marec
Cardiac conduction defects associate with mutations in SCN5A.
Nature genetics 1999;23(1):20-1.
1999: marcel mannens; Marielle Alders
Genomic imprinting: concept and clinical consequences.
Annals of medicine 1999;31(1):4-11.
1999: Patrick Gaudray; Georges F Carle; D S Gerhard; M Gessler; marcel mannens; Maria Athanasiou; Jet Bliek; A Calender; L V Debelenko; M Devignes; Glen A Evans; R Favier; S Forbes; G Gaudray; B Gawin; M Gordon; Sean M Grimmond; Paul D Grossfeld; J Harris; M Hattori; F Hosoda; Holger Hummerich; M James; Jörg Kalla; Nicholas Katsanis
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.
1999: MJ Steenman; Gail Tomlinson; Andries Westerveld; marcel mannens
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.
1998: Rolf G Boot; G Herma Renkema; Marri Verhoek; Anneke Strijland; Jet Bliek; T M de Meulemeester; marcel mannens; johannes aerts
The human chitotriosidase gene. Nature of inherited enzyme deficiency.
The Journal of biological chemistry 1998;273(40):25680-5.
1998: Howard E Henderson; S M Bijvoet; marcel mannens; T Bruin; D W Erkelens; Michael R Hayden; John J P Kastelein
Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo event.
American journal of medical genetics 1998;78(4):313-6.
1998: Irene M van Langen; Arthur A M Wilde; marcel mannens
[Sudden death in young men due to arrhythmogenic right ventricular dysplasia].
Nederlands tijdschrift voor geneeskunde 1998;142(13):739-40.
1998: Sophie Demolombe; Isabelle Baro; Yann Péréon; Jet Bliek; R Mohammad-Panah; H Pollard; S Morid; marcel mannens; Arthur Wilde; Jacques Barhanin; Flavien Charpentier; Denis Escande
A dominant negative isoform of the long QT syndrome 1 gene product.
The Journal of biological chemistry 1998;273(12):6837-43.
1998: Frank Speleman; E van den Berg; C Dhooge; W Oosterhuis; Bert Redeker; Christian R De Potter; R Y Tamminga; Nadine Van Roy; marcel mannens
Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma.
Genes, chromosomes & cancer 1998;21(3):265-9.
1997: Cees B M Oudejans; Bart A Westerman; Evert-Jan van Elk; Andrea A M Könst; Monique A M Mulders; Marielle Alders; John M G van Vugt; Inge J van Wijk; marcel mannens
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.
1997: M Andrew Nesbit; M D Hodges; L Campbell; T M de Meulemeester; Marielle Alders; NR Rodrigues; Kevin Talbot; AM Theodosiou; marcel mannens; Y Nakamura; P F Little; Kay E Davies
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.
1997: Marielle Alders; M Hodges; Anna-Katerina Hadjantonakis; J Postmus; Inge J van Wijk; Jet Bliek; M de Meulemeester; Andries Westerveld; F Guillemot; Cees B M Oudejans; P Little; marcel mannens
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.
1997: Arthur A M Wilde; marcel mannens
[Iatrogenic collapse; can this be prevented?].
Nederlands tijdschrift voor geneeskunde 1997;141(16):796-7.
1997: marcel mannens; Arthur Wilde
KVLQT1, the rhythm of imprinting.
Nature genetics 1997;15(2):113-5.
1997: Rolf G Boot; Carla E M Hollak; Marri Verhoek; P Sloof; B J H M Poorthuis; Wim J Kleijer; Ron A Wevers; Marinus H J van Oers; marcel mannens; johannes aerts; Sonja van Weely
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value.
Human mutation 1997;10(5):348-58.
1997: MJ Steenman; Bert Redeker; M de Meulemeester; K Wiesmeijer; Paul A Voûte; Andries Westerveld; R Slater; marcel mannens
Comparative genomic hybridization analysis of Wilms tumors.
Cytogenetics and cell genetics 1997;77(3-4):296-303.
1996: M de Meulemeester; A Vink; M Jakobs; Mario A J A Hermsen; MJ Steenman; Rosalyn Slater; A Dietrich; marcel mannens
The application of microwave denaturation in comparative genomic hybridization.
Genetic analysis : biomolecular engineering 1996;13(5):129-33.
1996: Marielle Alders; Jet Bliek; B Redeker; A Ryan; Andrew P Feinberg; Andries Westerveld; P Little; marcel mannens
Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.
Medical and pediatric oncology 1996;27(5):495-7.
1996: marcel mannens; Marielle Alders; B Redeker; Jet Bliek; MJ Steenman; C Wiesmeyer; M de Meulemeester; A Ryan; Linda M Kalikin; T Voûte; Jan de Kraker; Jan M N Hoovers; Rosalyn Slater; Andrew P Feinberg; P Little; Andries Westerveld
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
Medical and pediatric oncology 1996;27(5):490-4.
1996: Cees A P Fijen; R van den Bogaard; Mohamed R Daha; Jacob Dankert; marcel mannens; Ed J Kuijper
Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families.
European journal of clinical investigation 1996;26(10):902-6.
1995: Jan M N Hoovers; Linda M Kalikin; L A Johnson; Marielle Alders; B Redeker; David J Law; Jet Bliek; MJ Steenman; M Benedict; Joop Wiegant; Christoph Lengauer; P Taillon-Miller; David Schlessinger; M C Edwards; Stephen J Elledge; Alasdair Ivens; Andries Westerveld; P Little; marcel mannens; Andrew P Feinberg
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.
1995: Cora M Aalfs; Jan M N Hoovers; M A Nieste-Otter; marcel mannens; Raoul Hennekam; Nico J Leschot
Further delineation of the partial proximal trisomy 10q syndrome.
Journal of medical genetics 1995;32(12):968-71.
1995: E Austruy; S Candon; I Henry; G Gyapay; M F Tournade; marcel mannens; D Callen; Claudine Junien; Cécile Jeanpierre
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis.
Genes, chromosomes & cancer 1995;14(4):285-94.
1995: Cees A P Fijen; B H Derkx; Ed J Kuijper; marcel mannens; swibertus rudolfus poort; Marjolein Peters; Mohamed R Daha; Jacob Dankert
Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency.
Clinical and experimental immunology 1995;102(2):290-6.
1995: Judy A Fantes; B Redeker; M Breen; Shelagh Boyle; J Brown; J Fletcher; S Jones; Wendy A Bickmore; Y Fukushima; marcel mannens
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.
Human molecular genetics 1995;4(3):415-22.
1995: E Redeker; Marielle Alders; Jan M N Hoovers; C W Richard; Andries Westerveld; marcel mannens
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.
1994: marcel mannens; Jan M N Hoovers; E Redeker; M Verjaal; Andrew P Feinberg; P Little; M Boavida; N Coad; MJ Steenman; Jet Bliek
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.
1993: marcel mannens; Jan M N Hoovers; EM Bleeker-Wagemakers; Maija Mäntyjärvi; Kari Tuppurainen
The importance of DNA analysis in sporadic aniridia.
Acta ophthalmologica 1993;71(6):841-5.
1993: E Redeker; C J Van Moorsel; Andrew P Feinberg; marcel mannens
TaqI and RsaI polymorphisms in the H19 gene (D11S813E).
Human molecular genetics 1993;2(6):823.
1993: H Caron; P van Sluis; M van Hoeve; Jan de Kraker; J Bras; Rosalyn Slater; marcel mannens; Paul A Voûte; Andries Westerveld; Rogier Versteeg
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.
1993: I Henry; Jan M N Hoovers; F Barichard; M F Berthéas; A Puech; F Prieur; Manfred Gessler; G Bruns; marcel mannens; Claudine Junien
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family.
Genes, chromosomes & cancer 1993;7(1):57-62.
1993: Yoshimitsu Fukushima; Jan M N Hoovers; marcel mannens; Keiko Wakui; Hirofumi Ohashi; T Ohno; Y Ueoka; N Niikawa
Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.
Human genetics 1993;91(3):205-9.
1993: Jan M N Hoovers; E Redeker; Frank Speleman; J W Höppener; S Bhola; Jet Bliek; Nadine Van Roy; Nico J Leschot; Andries Westerveld; marcel mannens
High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.
Genomics 1993;15(3):525-9.
1993: Melissa H Little; K A Williamson; marcel mannens; A Kelsey; C Gosden; Nicholas D Hastie; Veronica van Heyningen
Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
Human molecular genetics 1993;2(3):259-64.
1993: I Henry; Veronica van Heyningen; A Puech; H Scrable; P Augereau; T Boehm; T Rabbitts; marcel mannens; H Rochefort; C Jones
Reassessment of breakpoints in chromosome 11p15.
Cytogenetics and cell genetics 1993;62(1):52-3.
1993: I Henry; A Puech; A Riesewijk; L Ahnine; marcel mannens; C Beldjord; P Bitoun; M F Tournade; P Landrieu; Claudine Junien
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.
1992: Ans M W van den Ouweland; M Verdijk; marcel mannens; BA van Oost
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.
1992: R M Slater; marcel mannens
Cytogenetics and molecular genetics of Wilms' tumor of childhood.
Cancer genetics and cytogenetics 1992;61(2):111-21.
1992: Jan M N Hoovers; A J Dietrich; marcel mannens
Imprinting and Beckwith-Wiedemann syndrome.
Lancet 1992;339(8803):1228.
1992: I J Heding; Alasdair Ivens; J Wilson; M Strivens; S Gregory; Jan M N Hoovers; marcel mannens; B Redeker; D Porteous; Veronica van Heyningen
The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.
Genomics 1992;13(1):89-94.
1992: Claudine Junien; Veronica van Heyningen; G Evans; P Little; marcel mannens
Report of the second chromosome 11 workshop.
Genomics 1992;12(3):620-5.
1992: Jan M N Hoovers; marcel mannens; R John; Jet Bliek; Veronica van Heyningen; D J Porteous; Nico J Leschot; Andries Westerveld; PF Little
High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.
Genomics 1992;12(2):254-63.
1991: F D Verbraak; marcel mannens; E J Redeker; G F Saunders; EM Bleeker-Wagemakers
DNA diagnosis in a family with autosomal dominant aniridia.
Ophthalmic paediatrics and genetics 1991;12(4):165-70.
1991: marcel mannens; Jan M N Hoovers; EM Bleeker-Wagemakers; E Redeker; Jet Bliek; M Overbeeke-Melkert; G Saunders; B Williams; Veronica van Heyningen; C Junien
The distal region of 11p13 and associated genetic diseases.
Genomics 1991;11(2):284-93.
1991: Peter Devilee; M van den Broek; marcel mannens; Rosalyn Slater; Cees J Cornelisse; Andries Westerveld; PM Khan
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.
1991: Frank Speleman; marcel mannens; B Redeker; M Vercruyssen; P Van Oostveldt; J Leroy; Rosalyn Slater
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.
1990: marcel mannens; Peter Devilee; Jet Bliek; I Mandjes; Jan de Kraker; Christa Heyting; R M Slater; Andries Westerveld
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.
1989: A Bout; Jan M N Hoovers; E Bakker; marcel mannens; A Geurts van Kessel; Andries Westerveld; J M Tager; Rob Benne
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.
1989: marcel mannens; EM Bleeker-Wagemakers; Jet Bliek; Jan M N Hoovers; I Mandjes; S van Tol; R R Frants; Christa Heyting; Andries Westerveld; R M Slater
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.
1988: marcel mannens; R M Slater; Christa Heyting; Jet Bliek; Jan de Kraker; N Coad; P de Pagter-Holthuizen; P L Pearson
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.
Human genetics 1988;81(1):41-8.
1988: Anthony de Ronde; marcel mannens; R M Slater; Jan M N Hoovers; Christa Heyting; EM Bleeker-Wagemakers; Nico J Leschot; A van Strien; Cees Sol; Jan ter Schegget
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.
1987: marcel mannens; R M Slater; Christa Heyting; A Geurts van Kessel; E Goedde-Salz; R R Frants; G J Van Ommen; P L Pearson
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.