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Gilles Thomas

Research Profile

Anatomy

Chromosomes, Human, Pair 22

Concepts & Ideas

Molecular Sequence Data

Chemicals & Drugs

Procedures

Disorders

Genes & Molecular Sequences

Physiology

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Heterozygote

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Sophie Postel-Vinay; Stéphanie Reynaud; Gilles Thomas; Franck Tirode; Amélie S Véron; JAVIER ALONSO; Stelly Ballet; STEPHEN CHANOCK; Françoise Clavel-Chapelon; David G Cox; Brigitte Bressac de Paillerets; Christian Dina; Francois Doz; philippe froguel; Anna González-Neira; Udo Kontny; Heinrich Kovar; Eve Lapouble; Karine Laud; Carlo LUCCHESI; Jean Michon; Odile Oberlin; Ana Patino-Garcia; Piero Picci; Gaelle Pierron; Olivier Delattre
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.
Camille Jung; Marc Lemann; Christian Libersa; Françoise Merlin; Frank M Ruemmele; Nadem Soufir; Gilles Thomas; Dominique Turck; Gwenola Vernier-Massouille; Habib Zouali; Matthieu Allez; Laurent Beaugerie; Jean-Pierre Cezard; Jean-Frédéric Colombel; Jacques Cosnes; Philippe Dieudé; Jean-Pierre Gendre; Jean-Marc Gornet; Jean-Pierre Hugot
Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.
Sylviane Olschwang; Kai Yu; Christine Lasset; Stéphanie Baert-Desurmont; Marie-Pierre Buisine; Qing Wang; Pierre Hutter; Etienne Rouleau; Olivier Caron; Violaine Bourdon; Gilles Thomas
Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers.

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All Publications

2012: Sophie Postel-Vinay; Stéphanie Reynaud; Gilles Thomas; Franck Tirode; Amélie S Véron; JAVIER ALONSO; Stelly Ballet; STEPHEN CHANOCK; Françoise Clavel-Chapelon; David G Cox; Brigitte Bressac de Paillerets; Christian Dina; Francois Doz; philippe froguel; Anna González-Neira; Udo Kontny; Heinrich Kovar; Eve Lapouble; Karine Laud; Carlo LUCCHESI; Jean Michon; Odile Oberlin; Ana Patino-Garcia; Piero Picci; Gaelle Pierron; Olivier Delattre
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.
Nature genetics 2012;44(3):323-7.
2012: Camille Jung; Marc Lemann; Christian Libersa; Françoise Merlin; Frank M Ruemmele; Nadem Soufir; Gilles Thomas; Dominique Turck; Gwenola Vernier-Massouille; Habib Zouali; Matthieu Allez; Laurent Beaugerie; Jean-Pierre Cezard; Jean-Frédéric Colombel; Jacques Cosnes; Philippe Dieudé; Jean-Pierre Gendre; Jean-Marc Gornet; Jean-Pierre Hugot
Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.
PloS one 2012;7(12):e52223.
2009: Sylviane Olschwang; Kai Yu; Christine Lasset; Stéphanie Baert-Desurmont; Marie-Pierre Buisine; Qing Wang; Pierre Hutter; Etienne Rouleau; Olivier Caron; Violaine Bourdon; Gilles Thomas
Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers.
Journal of cancer epidemiology 2009;2009():791754.
2008: Najat Mourra; Guy Zeitoun; Guillaume Portier; Hélène Blanche; Emmanuel Tubacher; Laetitia Gressin; Jean-François Flejou; Emmanuel Tiret; Gilles Thomas; Sylviane Olschwang
High-resolution genotyping of chromosome 8 in colon adenocarcinomas reveals recurrent break point but no gene mutation in the 8p21 region.
Diagnostic molecular pathology : the American journal of surgical pathology, part B 2008;17(2):90-3.
2006: Jesper Graakjaer; Héra Der-Sarkissian; Annette Schmitz; Jan Bayer; Gilles Thomas; Steen Kolvraa; J Arturo Londoño-Vallejo
Allele-specific relative telomere lengths are inherited.
Human genetics 2006;119(3):344-50.
2004: Els C Robanus-Maandag; Marco Giovannini; Martin van der Valk; Michiko Niwa-Kawakita; Vincent Abramowski; Cristina R Antonescu; Gilles Thomas; Anton Berns
Synergy of Nf2 and p53 mutations in development of malignant tumours of neural crest origin.
Oncogene 2004;23(39):6541-7.
2004: Jesper Graakjaer; Leigh Pascoe; Héra Der-Sarkissian; Gilles Thomas; Steen Kolvraa; Kaare Christensen; J Arturo Londoño-Vallejo
The relative lengths of individual telomeres are defined in the zygote and strictly maintained during life.
Aging cell 2004;3(3):97-102.
2002: Héra Der-Sarkissian; Gilles Vergnaud; Yves-Marie Borde; Gilles Thomas; J Arturo Londoño-Vallejo
Segmental polymorphisms in the proterminal regions of a subset of human chromosomes.
Genome research 2002;12(11):1673-8.
2002: Michel Kalamarides; Michiko Niwa-Kawakita; Hélène Leblois; Vincent Abramowski; Michel Perricaudet; Anne Janin; Gilles Thomas; David H Gutmann; Marco Giovannini
Nf2 gene inactivation in arachnoidal cells is rate-limiting for meningioma development in the mouse.
Genes & development 2002;16(9):1060-5.
2001: Alex Duval; Barry Iacopetta; Lin Thorstensen; Gunn Iren Meling; Ragnhild A Lothe; B Thuille; Nirosha Suraweera; Gilles Thomas; Richard Hamelin
Gender difference for mismatch repair deficiency in human colorectal cancer.
Gastroenterology 2001;121(4):1026-7.
2001: J Arturo Londoño-Vallejo; H DerSarkissian; Lucien Cazes; Gilles Thomas
Differences in telomere length between homologous chromosomes in humans.
Nucleic acids research 2001;29(15):3164-71.
2001: Pierre Laurent-Puig; P Legoix; Olivier Bluteau; Jacques Belghiti; Dominique Franco; F Binot; Geneviève Monges; Gilles Thomas; Paulette Bioulac-Sage; Jessica Zucman-Rossi
Genetic alterations associated with hepatocellular carcinomas define distinct pathways of hepatocarcinogenesis.
Gastroenterology 2001;120(7):1763-73.
2001: Estelle Brault; Alexis Gautreau; M Lamarine; I Callebaut; Gilles Thomas; L Goutebroze
Normal membrane localization and actin association of the NF2 tumor suppressor protein are dependent on folding of its N-terminal domain.
Journal of cell science 2001;114(Pt 10):1901-12.
2001: Alex Duval; S Rolland; Aurore Compoint; Emmanuel Tubacher; Barry Iacopetta; Gilles Thomas; Richard Hamelin
Evolution of instability at coding and non-coding repeat sequences in human MSI-H colorectal cancers.
Human molecular genetics 2001;10(5):513-8.
2001: L Goutebroze; H Der Sarkissian; Estelle Brault; Gilles Thomas
Assignment of the schwannomin-interacting protein 1 (SCHIP1) gene to human chromosome band 3q25 by in situ hybridization and with somatic cell hybrids.
Cytogenetics and cell genetics 2001;94(1-2):96-7.
2000: Alex Duval; S Rolland; Emmanuel Tubacher; H Bui; Gilles Thomas; Richard Hamelin
The human T-cell transcription factor-4 gene: structure, extensive characterization of alternative splicings, and mutational analysis in colorectal cancer cell lines.
Cancer research 2000;60(14):3872-9.
2000: Marco Giovannini; Els C Robanus-Maandag; Martin van der Valk; Michiko Niwa-Kawakita; Vincent Abramowski; L Goutebroze; J M Woodruff; Anton Berns; Gilles Thomas
Conditional biallelic Nf2 mutation in the mouse promotes manifestations of human neurofibromatosis type 2.
Genes & development 2000;14(13):1617-30.
2000: Etienne Baulieu; Gilles Thomas; Sylvie Legrain; Najiba Lahlou; M Roger; B Debuire; V Faucounau; L Girard; M P Hervy; Florence Latour; M C Leaud; A Mokrane; H Pitti-Ferrandi; Christophe Trivalle; O de Lacharrière; S Nouveau; B Rakoto-Arison; J C Souberbielle; J Raison; Yves Le Bouc; A Raynaud; X Girerd; Françoise Forette
Dehydroepiandrosterone (DHEA), DHEA sulfate, and aging: contribution of the DHEAge Study to a sociobiomedical issue.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(8):4279-84.
2000: P Legoix; H D Sarkissian; Lucien Cazes; S Giraud; F Sor; G A Rouleau; G Lenoir; Gilles Thomas; Jessica Zucman-Rossi
Molecular characterization of germline NF2 gene rearrangements.
Genomics 2000;65(1):62-6.
2000: L Goutebroze; Estelle Brault; C Muchardt; Jacques Camonis; Gilles Thomas
Cloning and characterization of SCHIP-1, a novel protein interacting specifically with spliced isoforms and naturally occurring mutant NF2 proteins.
Molecular and cellular biology 2000;20(5):1699-712.
2000: Michiko Niwa-Kawakita; Vincent Abramowski; Michel Kalamarides; Gilles Thomas; Marco Giovannini
Targeted expression of Cre recombinase to myelinating cells of the central nervous system in transgenic mice.
Genesis (New York, N.Y. : 2000) 2000;26(2):127-9.
1999: Olivier Bluteau; P Legoix; Jan Bayer; Paulette Bioulac-Sage; J F Fléjou; F Capron; Geneviève Monges; C Brechot; Gilles Thomas; Pierre Laurent-Puig; Jessica Zucman-Rossi
[Semi-automated quantitative method for detecting the loss of heterozygosity at the long arm of chromosome 4 in hepatocellular carcinoma].
Gastroentérologie clinique et biologique 1999;23(11):1225-32.
1999: Heinrich Kovar; D Jugovic; T Melot; Andreas Zoubek; G Lenoir; F M Fink; I Philip; C Turc-Carel; Gilles Thomas; J Zucman-Rossi
Cryptic exons as a source of increased diversity of Ewing tumor-associated EWS-FLI1 chimeric products.
Genomics 1999;60(3):371-4.
1999: P Legoix; Olivier Bluteau; Jan Bayer; C Perret; Charles Balabaud; Jacques Belghiti; Dominique Franco; Gilles Thomas; Pierre Laurent-Puig; Jessica Zucman-Rossi
Beta-catenin mutations in hepatocellular carcinoma correlate with a low rate of loss of heterozygosity.
Oncogene 1999;18(27):4044-6.
1999: F Lerebours; Sylviane Olschwang; B Thuille; Annette Schmitz; P Fouchet; Bruno Buecher; N Martinet; F Galateau; Gilles Thomas
Fine deletion mapping of chromosome 8p in non-small-cell lung carcinoma.
International journal of cancer. Journal international du cancer 1999;81(6):854-8.
1999: F Lerebours; Sylviane Olschwang; B Thuille; Annette Schmitz; P Fouchet; Pierre Laurent-Puig; Françoise Boman; J F Fléjou; G Monges; François Paraf; P Bedossa; J C Sabourin; Rémy J Salmon; R Parc; Gilles Thomas
Deletion mapping of the tumor suppressor locus involved in colorectal cancer on chromosome band 8p21.
Genes, chromosomes & cancer 1999;25(2):147-53.
1999: Marco Giovannini; Els C Robanus-Maandag; Michiko Niwa-Kawakita; Martin van der Valk; J M Woodruff; L Goutebroze; Philippe Mérel; Anton Berns; Gilles Thomas
Schwann cell hyperplasia and tumors in transgenic mice expressing a naturally occurring mutant NF2 protein.
Genes & development 1999;13(8):978-86.
1999: P Legoix; M F Legrand; E Ollagnon; G Lenoir; Gilles Thomas; Jessica Zucman-Rossi
Characterisation of 16 polymorphic markers in the NF2 gene: application to hemizygosity detection.
Human mutation 1999;13(4):290-3.
1998: Jessica Zucman-Rossi; P Legoix; Héra Der-Sarkissian; G Cheret; F Sor; A Bernardi; Lucien Cazes; S Giraud; E Ollagnon; G Lenoir; Gilles Thomas
NF2 gene in neurofibromatosis type 2 patients.
Human molecular genetics 1998;7(13):2095-101.
1998: Jessica Zucman-Rossi; P Legoix; J M Victor; B Lopez; Gilles Thomas
Chromosome translocation based on illegitimate recombination in human tumors.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(20):11786-91.
1998: B Deguen; L Goutebroze; Marco Giovannini; C Boisson; R van der Neut; M C Jaurand; Gilles Thomas
Heterogeneity of mesothelioma cell lines as defined by altered genomic structure and expression of the NF2 gene.
International journal of cancer. Journal international du cancer 1998;77(4):554-60.
1998: Rémy J Salmon; Bernard Asselain; Laurent Chauveinc; Bernard Dutrillaux; Marie-Christine Falcou; Jacques Girodet; Richard Hamelin; Pierre Laurent-Puig; Martine Muleris; Sylviane Olschwang; Jean-Yves Pierga; Yurgos Remvikos; Anne de La Rochefordière; Gilles Thomas
[Contributions of genetics in gastroenterology. Has genetic progress changed the therapeutic management of colorectal neoplasms? "Colon" Group of the Curie Institute].
Chirurgie; mémoires de l'Académie de chirurgie 1998;123(3):304-8.
1998: XP Zhou; JM Hoang; Y J Li; Raquel Seruca; F Carneiro; Manuel Sobrinho-Simoes; Ragnhild A Lothe; CM Gleeson; S E Hilary Russell; F Muzeau; Jean-François Fléjou; K Hoang-Xuan; Rosette Lidereau; Gilles Thomas; Richard Hamelin
Determination of the replication error phenotype in human tumors without the requirement for matching normal DNA by analysis of mononucleotide repeat microsatellites.
Genes, chromosomes & cancer 1998;21(2):101-7.
1998: B Deguen; Philippe Mérel; L Goutebroze; Marco Giovannini; H Reggio; Monique Arpin; Gilles Thomas
Impaired interaction of naturally occurring mutant NF2 protein with actin-based cytoskeleton and membrane.
Human molecular genetics 1998;7(2):217-26.
1998: Patrice Morand; Gilles Thomas; C Bungener; Mélanie M Ferreri; R Jouvent
Fava's Anger Attacks Questionnaire: evaluation of the French version in depressed patients.
European psychiatry : the journal of the Association of European Psychiatrists 1998;13(1):41-5.
1997: Sylviane Olschwang; Richard Hamelin; Pierre Laurent-Puig; B Thuille; Yann De Rycke; Y J Li; F Muzeau; Jacques Girodet; Rémy J Salmon; Gilles Thomas
Alternative genetic pathways in colorectal carcinogenesis.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(22):12122-7.
1997: XP Zhou; JM Hoang; Paul-Henri Cottu; Gilles Thomas; Richard Hamelin
Allelic profiles of mononucleotide repeat microsatellites in control individuals and in colorectal tumors with and without replication errors.
Oncogene 1997;15(14):1713-8.
1997: C Desmaze; F Brizard; C Turc-Carel; T Melot; Olivier Delattre; Gilles Thomas; Alain Aurias
Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors.
Cancer genetics and cytogenetics 1997;97(1):12-9.
1997: F Muzeau; Jean-François Fléjou; Gilles Thomas; Richard Hamelin
Loss of heterozygosity on chromosome 9 and p16 (MTS1, CDKN2) gene mutations in esophageal cancers.
International journal of cancer. Journal international du cancer 1997;72(1):27-30.
1997: V Boige; Pierre Laurent-Puig; P Fouchet; J F Fléjou; G Monges; P Bedossa; P Bioulac-Sage; F Capron; Annette Schmitz; Sylviane Olschwang; Gilles Thomas
Concerted nonsyntenic allelic losses in hyperploid hepatocellular carcinoma as determined by a high-resolution allelotype.
Cancer research 1997;57(10):1986-90.
1997: Martine Peter; Jérôme Couturier; Hélène Pacquement; Jean Michon; Gilles Thomas; Henri Magdelenat; Olivier Delattre
A new member of the ETS family fused to EWS in Ewing tumors.
Oncogene 1997;14(10):1159-64.
1997: J Zucman-Rossi; M A Batzer; M Stoneking; Olivier Delattre; Gilles Thomas
Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombination.
Human genetics 1997;99(3):357-63.
1997: JM Hoang; Paul-Henri Cottu; B Thuille; Rémy J Salmon; Gilles Thomas; Richard Hamelin
BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines.
Cancer research 1997;57(2):300-3.
1997: S Olschwang; Gilles Thomas
[A major genetic predisposition to colorectal cancer].
Annales de pathologie 1997;17 Suppl 5():19-22.
1997: C Duriez; Annette Schmitz; P Fouchet; Bruno Buecher; B Thuille; F Lerebours; R Léger; Françoise Boman; J F Fléjou; G Monges; François Paraf; P Bedossa; J C Sabourin; Rémy J Salmon; Pierre Laurent-Puig; Gilles Thomas; Sylviane Olschwang
[Localization of a tumor suppressor gene distal to D22S270 in colorectal cancers].
Gastroentérologie clinique et biologique 1997;21(5):358-64.
1997: F Muzeau; Jean-François Fléjou; Jacques Belghiti; Gilles Thomas; Richard Hamelin
Infrequent microsatellite instability in oesophageal cancers.
British journal of cancer 1997;75(9):1336-9.
1996: P H Cottu; F Muzeau; A Estreicher; Jean-François Fléjou; Richard D Iggo; Gilles Thomas; Richard Hamelin
Inverse correlation between RER+ status and p53 mutation in colorectal cancer cell lines.
Oncogene 1996;13(12):2727-30.
1996: Jessica Zucman-Rossi; P Legoix; Gilles Thomas
Identification of new members of the Gas2 and Ras families in the 22q12 chromosome region.
Genomics 1996;38(3):247-54.
1996: Martine Peter; F Mugneret; Alain Aurias; Gilles Thomas; Henri Magdelenat; Olivier Delattre
An EWS/ERG fusion with a truncated N-terminal domain of EWS in a Ewing's tumor.
International journal of cancer. Journal international du cancer 1996;67(3):339-42.
1996: S Demczuk; Gilles Thomas; Alain Aurias
Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes.
Human molecular genetics 1996;5(5):633-8.
1996: G Schleiermacher; Olivier Delattre; Martine Peter; Véronique Mosseri; P Delonlay; Philippe Vielh; Gilles Thomas; Jean-Michel Zucker; Henri Magdelénat; Jean Michon
Clinical relevance of loss heterozygosity of the short arm of chromosome 1 in neuroblastoma: a single-institution study.
International journal of cancer. Journal international du cancer 1996;69(2):73-8.
1996: François Doz; Martine Peter; G Schleiermacher; Philippe Vielh; Pierre Validire; M Putterman; V Blanquet; Laurence Desjardins; Jean-Louis Dufier; Jean-Michel Zucker; Véronique Mosseri; Gilles Thomas; Henri Magdelénat; Olivier Delattre
N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma.
European journal of cancer (Oxford, England : 1990) 1996;32A(4):645-9.
1996: J P Hugot; Pierre Laurent-Puig; Corinne Gower-Rousseau; J M Olson; J C Lee; L Beaugerie; I Naom; J L Dupas; A Van Gossum; M Orholm; C Bonaiti-Pellie; J Weissenbach; C G Mathew; J E Lennard-Jones; Antoine Cortot; Jean-Frédéric Colombel; Gilles Thomas
Mapping of a susceptibility locus for Crohn's disease on chromosome 16.
Nature 1996;379(6568):821-3.
1996: P Kleinfinger; Y Labelle; T Melot; Gilles Thomas; Olivier Delattre; Alain Aurias
Localization of TEC to 9q22.3-q31 by fluorescence in situ hybridization.
Annales de génétique 1996;39(4):233-5.
1996: O Maarek; Gilles Thomas; Alain Aurias
[Importance of the DIRVISH technique for detecting microdeletions].
Annales de génétique 1996;39(3):173-5.
1996: F Muzeau; Jean-François Fléjou; F Potet; Jacques Belghiti; Gilles Thomas; Richard Hamelin
[Profile of p53 mutations and abnormal expression of P53 protein in 2 forms of esophageal cancer].
Gastroentérologie clinique et biologique 1996;20(5):430-7.
1996: Gilles Thomas
[Diagnosing predisposition to tumor development by genetic typing].
Gastroentérologie clinique et biologique 1996;20(5 Pt 2):B1-4.
1995: Y J Li; M Sanson; Khê Hoang-Xuan; Jean-Yves Delattre; M Poisson; Gilles Thomas; Richard Hamelin
Incidence of germ-line p53 mutations in patients with gliomas.
International journal of cancer. Journal international du cancer 1995;64(6):383-7.
1995: Bruno Buecher; Annette Schmitz; F Lerebours; B Thuille; Gilles Thomas; Sylviane Olschwang
[Towards an allotype of second generation colon cancer].
Gastroentérologie clinique et biologique 1995;19(12):1004-10.
1995: J P Hugot; P Laurent-Puig; Gilles Thomas
[Genetics of inflammatory bowel diseases].
Gastroentérologie clinique et biologique 1995;19(11):890-8.
1995: Theo J M Hulsebos; D J Gilbert; O Delattre; L J Smink; Carl Bruder; Andries Westerveld; Gilles Thomas; N A Jenkins; N G Copeland
Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.
Genomics 1995;29(3):712-8.
1995: Y J Li; Khê Hoang-Xuan; Jean-Yves Delattre; M Poisson; Gilles Thomas; Richard Hamelin
Frequent loss of heterozygosity on chromosome 9, and low incidence of mutations of cyclin-dependent kinase inhibitors p15 (MTS2) and p16 (MTS1) genes in gliomas.
Oncogene 1995;11(3):597-600.
1995: EK Bijlsma; A M Voesten; EH Bijleveld; Dirk Troost; Andries Westerveld; P Mérel; Gilles Thomas; Theo J M Hulsebos
Molecular analysis of genetic changes in ependymomas.
Genes, chromosomes & cancer 1995;13(4):272-7.
1995: S Demczuk; A Lévy; M Aubry; Marie-Françoise Croquette; N Philip; Marguerite Prieur; U Sauer; Patrice Bouvagnet; Guy Rouleau; Gilles Thomas
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.
Human genetics 1995;96(1):9-13.
1995: EK Bijlsma; P Merel; P Fleury; CJ van Asperen; Andries Westerveld; O Delattre; Gilles Thomas; Theo J M Hulsebos
Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene.
Human genetics 1995;96(1):1-5.
1995: Martine Peter; Henri Magdelenat; Jean Michon; T Melot; O Oberlin; Jean-Michel Zucker; Gilles Thomas; Olivier Delattre
Sensitive detection of occult Ewing's cells by the reverse transcriptase-polymerase chain reaction.
British journal of cancer 1995;72(1):96-100.
1995: S Demczuk; Olivier Delattre; A Vignal; J Weissenbach; Gilles Thomas; Alain Aurias
Physical mapping of 30 CA repeats on human chromosome 22.
Genomics 1995;27(2):345-7.
1995: Sylviane Olschwang; Pierre Laurent-Puig; T Melot; B Thuille; Gilles Thomas
High resolution genetic map of the adenomatous polyposis coli gene (APC) region.
American journal of medical genetics 1995;56(4):413-9.
1995: S Demczuk; R Aledo; J Zucman; Olivier Delattre; C Desmaze; L Dauphinot; P Jalbert; Guy Rouleau; Gilles Thomas; Alain Aurias
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.
Human molecular genetics 1995;4(4):551-8.
1995: Reiner Caspari; Sylviane Olschwang; Waltraut Friedl; M Mandl; Cécile Boisson; T Böker; A Augustin; Martina Kadmon; G Möslein; Gilles Thomas
Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.
Human molecular genetics 1995;4(3):337-40.
1995: Gilles Thomas; Sylviane Olschwang
Genetic predispositions to colorectal cancer.
Pathologie-biologie 1995;43(3):159-64.
1995: Gilles Thomas
[Identification of oncogenes and anti-oncogenes].
Pathologie-biologie 1995;43(3):143-9.
1995: Khê Hoang-Xuan; P Merel; F Vega; J P Hugot; Philippe Cornu; Jean-Yves Delattre; M Poisson; Gilles Thomas; Olivier Delattre
Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas.
International journal of cancer. Journal international du cancer 1995;60(4):478-81.
1995: Y J Li; Pierre Laurent-Puig; Rémy J Salmon; Gilles Thomas; Richard Hamelin
Polymorphisms and probable lack of mutation in the WAF1-CIP1 gene in colorectal cancer.
Oncogene 1995;10(3):599-601.
1995: Rémy J Salmon; Jacques Girodet; Yurgos Remvikos; Martine Muleris; Sylviane Olschwang; Gilles Thomas
[Genetic abnormalities in colorectal cancer].
Annales de gastroentérologie et d'hépatologie 1995;31(1):23-7.
1995: G Schleiermacher; Martine Peter; Jean Michon; Jean-Michel Zucker; Gilles Thomas; Henri Magdelénat; Olivier Delattre
A multiplex PCR assay for routine evaluation of deletion of the short arm of chromosome 1 in neuroblastoma.
European journal of cancer (Oxford, England : 1990) 1995;31A(4):535-8.
1995: Sylviane Olschwang; Cécile Boisson; Stéphane Richard; F Resche; Gilles Thomas
DNA-based presymptomatic diagnosis for the von Hippel-Lindau disease by linkage analysis.
European journal of human genetics : EJHG 1995;3(2):108-15.
1994: Rémy J Salmon; Jacques Girodet; Yurgos Remvikos; Martine Muleris; Sylviane Olschwang; Gilles Thomas
[Genetic anomalies of colorectal cancers].
Journal de chirurgie 1994;131(11):511-6.
1994: Richard Hamelin; Jean-François Fléjou; F Muzeau; F Potet; Pierre Laurent-Puig; F Fékété; Gilles Thomas
TP53 gene mutations and p53 protein immunoreactivity in malignant and premalignant Barrett's esophagus.
Gastroenterology 1994;107(4):1012-8.
1994: B Plougastel; M G Mattei; Gilles Thomas; Olivier Delattre
Cloning and chromosome localization of the mouse Ews gene.
Genomics 1994;23(1):278-81.
1994: EK Bijlsma; P Merel; D Andries Bosch; Andries Westerveld; O Delattre; Gilles Thomas; Theo J M Hulsebos
Analysis of mutations in the SCH gene in schwannomas.
Genes, chromosomes & cancer 1994;11(1):7-14.
1994: J P Hugot; Pierre Laurent-Puig; Corinne Gower-Rousseau; S Caillat-Zucman; L Beaugerie; J L Dupas; A Van Gossum; C Bonäit-Pellie; Antoine Cortot; Gilles Thomas
Linkage analyses of chromosome 6 loci, including HLA, in familial aggregations of Crohn disease. G.E.T.A.I.D.
American journal of medical genetics 1994;52(2):207-13.
1994: G Schleiermacher; Martine Peter; Jean Michon; J P Hugot; Philippe Vielh; Jean-Michel Zucker; Henri Magdelénat; Gilles Thomas; Olivier Delattre
Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma.
Genes, chromosomes & cancer 1994;10(4):275-81.
1994: R Hamelin; F Barichard; I Henry; Claudine Junien; Gilles Thomas
Single base pair germ-line deletion in the p53 gene in a cancer predisposed family.
Human genetics 1994;94(1):88-90.
1994: Gilles Thomas
Advances in the genetics and molecular biology of colorectal tumors.
Current opinion in oncology 1994;6(4):406-12.
1994: C Desmaze; J Zucman; Olivier Delattre; T Melot; Gilles Thomas; Alain Aurias
Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes.
Cancer genetics and cytogenetics 1994;74(1):13-8.
1994: Richard Hamelin; J Zucman; T Melot; Olivier Delattre; Gilles Thomas
p53 mutations in human tumors with chimeric EWS/FLI-1 genes.
International journal of cancer. Journal international du cancer 1994;57(3):336-40.
1994: M H Ruttledge; J Sarrazin; S Rangaratnam; CM Phelan; E Twist; P Merel; Olivier Delattre; Gilles Thomas; Magnus Nordenskjöld; V Peter Collins
Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.
Nature genetics 1994;6(2):180-4.
1994: C Desmaze; J Zucman; Olivier Delattre; T Melot; Gilles Thomas; Alain Aurias
Precise localization on chromosome 12 of the ATF-1 gene by fluorescence in situ hybridization.
Human genetics 1994;93(2):207-8.
1994: A Munck; Sylviane Olschwang; B Thuille; Jean-François Mougenot; Jean-Pierre Cézard; Latifa Ferkdadji; Christophe Faure; Jean Navarro; Gilles Thomas
[Contribution of genetic typing for the diagnosis of familial adenomatous polyposis in pediatrics].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1994;1(2):147-52.
1994: Richard Hamelin; Pierre Laurent-Puig; Sylviane Olschwang; N Jego; Bernard Asselain; Yurgos Remvikos; Jacques Girodet; Rémy J Salmon; Gilles Thomas
Association of p53 mutations with short survival in colorectal cancer.
Gastroenterology 1994;106(1):42-8.
1994: E C Twist; M H Ruttledge; M Rousseau; M Sanson; L Papi; P Merel; Olivier Delattre; Gilles Thomas; Guy Rouleau
The neurofibromatosis type 2 gene is inactivated in schwannomas.
Human molecular genetics 1994;3(1):147-51.
1994: S Demczuk; C Desmaze; M Aikem; Marguerite Prieur; F Ledeist; M Sanson; Guy Rouleau; Gilles Thomas; Alain Aurias
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.
Annales de génétique 1994;37(2):60-5.
1994: Jean Michon; Olivier Delattre; Jean-Michel Zucker; Martine Peter; P Delonlay; S Luciani; Véronique Mosseri; Philippe Vielh; S Neuenschwander; Gilles Thomas
Prospective evaluation of Nmyc amplification and deletion of the short arm of chromosome 1 in neuroblastoma tumours: a single institution study.
Progress in clinical and biological research 1994;385():11-7.
1994: Gilles Thomas; P Mérel; M Sanson; Khê Hoang-Xuan; J Zucman; C Desmaze; T Melot; Alain Aurias; Olivier Delattre
Neurofibromatosis type 2.
European journal of cancer (Oxford, England : 1990) 1994;30A(13):1981-7.
1994: Gilles Thomas; Olivier Delattre; J Zucman; P Merel; C Desmaze; T Melot; M Sanson; Khê Hoang-Xuan; B Plougastel; P Dejong
Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors.
Cold Spring Harbor symposia on quantitative biology 1994;59():555-64.
1993: Sylviane Olschwang; A Tiret; Pierre Laurent-Puig; Martine Muleris; R Parc; Gilles Thomas
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients.
Cell 1993;75(5):959-68.
1993: B Plougastel; J Zucman; Martine Peter; Gilles Thomas; Olivier Delattre
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation.
Genomics 1993;18(3):609-15.
1993: O Tominaga; Richard Hamelin; V Trouvat; Rémy J Salmon; G Lesec; Gilles Thomas; Yurgos Remvikos
Frequently elevated content of immunochemically defined wild-type p53 protein in colorectal adenomas.
Oncogene 1993;8(10):2653-8.
1993: EK Bijlsma; O Delattre; J A Juyn; T Melot; Andries Westerveld; J P Dumanski; Gilles Thomas; Theo J M Hulsebos
Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2.
Genes, chromosomes & cancer 1993;8(2):112-8.
1993: Martine Muleris; P Laurent-Puig; Rémy J Salmon; Gilles Thomas; Bernard Dutrillaux
Chromosome 12 alterations and c-Ki-ras mutations in colorectal tumors.
Cancer genetics and cytogenetics 1993;69(2):161-2.
1993: M Sanson; F Zhang; S Demczuk; Olivier Delattre; P DeJong; Alain Aurias; Gilles Thomas; Guy Rouleau
Isolation and mapping of 45 NotI linking clones to chromosome 22.
Genomics 1993;17(3):776-9.
1993: J Zucman; Olivier Delattre; C Desmaze; A L Epstein; G Stenman; F Speleman; C D Fletchers; Alain Aurias; Gilles Thomas
EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts.
Nature genetics 1993;4(4):341-5.
1993: M Sanson; Claude Marineau; C Desmaze; M Lutchman; M Ruttledge; C Baron; S Narod; Olivier Delattre; G Lenoir; Gilles Thomas
Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.
Human molecular genetics 1993;2(8):1215-20.
1993: Richard Hamelin; N Jego; Pierre Laurent-Puig; M Vidaud; Gilles Thomas
Efficient screening of p53 mutations by denaturing gradient gel electrophoresis in colorectal tumors.
Oncogene 1993;8(8):2213-20.
1993: Gilles Thomas
[Genetic predisposition to colorectal cancer].
Annales de gastroentérologie et d'hépatologie 1993;29(3):123-4.
1993: Claude Marineau; C Baron; Olivier Delattre; J Zucman; Gilles Thomas; Guy Rouleau
Dinucleotide repeat polymorphism at the D22S268 locus.
Human molecular genetics 1993;2(3):336.
1993: Sylviane Olschwang; Pierre Laurent-Puig; Joanna Groden; Raymond White; Gilles Thomas
Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene.
American journal of human genetics 1993;52(2):273-9.
1993: E A Fon; S Demczuk; Olivier Delattre; Gilles Thomas; Guy Rouleau
Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-->q13.2.
Cytogenetics and cell genetics 1993;64(3-4):201-3.
1993: N Jego; Gilles Thomas; Richard Hamelin
Short direct repeats flanking deletions, and duplicating insertions in p53 gene in human cancers.
Oncogene 1993;8(1):209-13.
1993: Gilles Thomas
[The concept of anti-oncogenes].
Pathologie-biologie 1993;41(1):12.
1993: Anne Vincent-Salomon; Sylviane Olschwang; Richard Hamelin; Yurgos Remvikos; Pierre Laurent-Puig; Gilles Thomas
[Genetic heterogeneity of certain sporadic colorectal cancers].
Gastroentérologie clinique et biologique 1993;17(10):733-9.
1992: Gilles Thomas
[Genes and colorectal cancer development].
Pathologie-biologie 1992;39(9):920.
1992: Martine Peter; Jean Michon; Philippe Vielh; S Neuenschwander; Y Nakamura; E Sonsino; Jean-Michel Zucker; Gilles Vergnaud; Gilles Thomas; Olivier Delattre
PCR assay for chromosome 1p deletion in small neuroblastoma samples.
International journal of cancer. Journal international du cancer 1992;52(4):544-8.
1992: Yurgos Remvikos; O Tominaga; Pascal Hammel; Pierre Laurent-Puig; Rémy J Salmon; B Dutrillaux; Gilles Thomas
Increased p53 protein content of colorectal tumours correlates with poor survival.
British journal of cancer 1992;66(4):758-64.
1992: Sylviane Olschwang; Pierre Laurent-Puig; B Thuille; Gilles Thomas
Frequent polymorphism in the 13th exon of the adenomatous polyposis coli gene.
Human genetics 1992;90(1-2):161-3.
1992: M Aubry; Claude Marineau; F R Zhang; L Zahed; D Figlewicz; Olivier Delattre; Gilles Thomas; P J de Jong; Jean-Pierre Julien; Guy Rouleau
Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2).
Genomics 1992;13(3):641-8.
1992: J Zucman; Olivier Delattre; C Desmaze; C Azambuja; Guy Rouleau; P De Jong; Alain Aurias; Gilles Thomas
Rapid isolation of cosmids from defined subregions by differential Alu-PCR hybridization on chromosome 22-specific library.
Genomics 1992;13(2):395-401.
1992: C Desmaze; J F Deleuze; Anne-Marie Dutrillaux; Gilles Thomas; michelle hadchouel; Alain Aurias
Screening of microdeletions of chromosome 20 in patients with Alagille syndrome.
Journal of medical genetics 1992;29(4):233-5.
1992: C Desmaze; J Zucman; Olivier Delattre; Gilles Thomas; Alain Aurias
In situ hybridization of PCR amplified inter-Alu sequences from a hybrid cell line.
Human genetics 1992;88(5):541-4.
1992: Sylviane Olschwang; R Fabre; Pierre Laurent-Puig; A Vassal; B Hamelin; Y Nakamura; Gilles Thomas
Detection by DGGE of a new polymorphism closely linked to the adenomatous polyposis coli region.
Human genetics 1992;88(6):658-60.
1992: M Sanson; S Richard; Olivier Delattre; M Poliwka; J Mikol; J Philippon; Gilles Thomas
Allelic loss on chromosome 22 correlates with histopathological predictors of recurrence of meningiomas.
International journal of cancer. Journal international du cancer 1992;50(3):391-4.
1992: O Tominaga; Richard Hamelin; Yurgos Remvikos; Rémy J Salmon; Gilles Thomas
p53 from basic research to clinical applications.
Critical reviews in oncogenesis 1992;3(3):257-82.
1992: Rémy J Salmon; Yurgos Remvikos; Martine Muleris; Gilles Thomas
[Genetic abnormalities in "sporadic" colorectal cancers].
Journal de chirurgie 1992;129(1):3-8.
1992: Sylviane Olschwang; Pierre Laurent-Puig; T Melot; B Thuille; A Vassal; R Parc; R Salmon; Gilles Thomas
[Familial adenomatous polyposis: early diagnosis by genetic mapping].
Gastroentérologie clinique et biologique 1992;16(3):205-9.
1991: Pierre Laurent-Puig; Sylviane Olschwang; Olivier Delattre; Pierre Validire; T Melot; Véronique Mosseri; Rémy J Salmon; Gilles Thomas
Association of Ki-ras mutation with differentiation and tumor-formation pathways in colorectal carcinoma.
International journal of cancer. Journal international du cancer 1991;49(2):220-3.
1991: Rémy J Salmon; Yurgos Remvikos; Martine Muleris; Gilles Thomas
[Genetic abnormalities in "sporadic" colorectal cancers].
Acta gastro-enterologica Belgica 1991;54(5-6):360-7.
1991: Olivier Delattre; C J Azambuja; Alain Aurias; J Zucman; Martine Peter; F Zhang; M C Hors-Cayla; Guy Rouleau; Gilles Thomas
Mapping of human chromosome 22 with a panel of somatic cell hybrids.
Genomics 1991;9(4):721-7.
1991: Sylviane Olschwang; Pierre Laurent-Puig; A Vassal; Rémy J Salmon; Gilles Thomas
Characterization of a frequent polymorphism in the coding sequence of the Tp53 gene in colonic cancer patients and a control population.
Human genetics 1991;86(4):369-70.
1990: M Sanson; Olivier Delattre; Jérôme Couturier; J Philippon; J Cophignon; P Derome; Guy Rouleau; Gilles Thomas
Parental origin of chromosome 22 alleles lost in meningioma.
American journal of human genetics 1990;47(5):877-80.
1990: F R Zhang; R Heilig; Gilles Thomas; Alain Aurias
A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes.
Chromosoma 1990;99(6):436-9.
1990: F R Zhang; Alain Aurias; Olivier Delattre; M H Stern; J Benitez; Guy Rouleau; Gilles Thomas
Mapping of human chromosome 22 by in situ hybridization.
Genomics 1990;7(3):319-24.
1990: Yurgos Remvikos; Pierre Laurent-Puig; Rémy J Salmon; G Frelat; Bernard Dutrillaux; Gilles Thomas
Simultaneous monitoring of P53 protein and DNA content of colorectal adenocarcinomas by flow cytometry.
International journal of cancer. Journal international du cancer 1990;45(3):450-6.
1990: Jérôme Couturier; Olivier Delattre; M Kujas; J Philippon; Martine Peter; Guy Rouleau; Alain Aurias; Gilles Thomas
Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses.
Cancer genetics and cytogenetics 1990;45(1):55-62.
1990: F R Zhang; Olivier Delattre; Guy Rouleau; Jérôme Couturier; Gilles Thomas; Alain Aurias
The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.
Genomics 1990;6(1):174-7.
1990: Martine Muleris; Olivier Delattre; Sylviane Olschwang; Anne-Marie Dutrillaux; Yurgos Remvikos; Rémy J Salmon; Gilles Thomas; Bernard Dutrillaux
Cytogenetic and molecular approaches of polyploidization in colorectal adenocarcinomas.
Cancer genetics and cytogenetics 1990;44(1):107-18.
1990: Pierre Laurent-Puig; Olivier Delattre; Sylviane Olschwang; Yurgos Remvikos; T Melot; Rémy J Salmon; G Frelat; Gilles Thomas
[A joint study of mutation of the Ki-ras oncogene and overexpression of the Tp53 oncogene in colorectal cancer].
Gastroentérologie clinique et biologique 1990;14(4):347-51.
1990: F Zhang; J F Deleuze; Alain Aurias; Anne-Marie Dutrillaux; R N Hugon; D Alagille; Gilles Thomas; michelle hadchouel
Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome).
The Journal of pediatrics 1990;116(1):73-7.
1989: D Lefrançois; Sylviane Olschwang; Olivier Delattre; Martine Muleris; Anne-Marie Dutrillaux; Gilles Thomas; Bernard Dutrillaux
Preservation of chromosome and DNA characteristics of human colorectal adenocarcinomas after passage in nude mice.
International journal of cancer. Journal international du cancer 1989;44(5):871-8.
1989: Olivier Delattre; Sylviane Olschwang; David J Law; T Melot; Yurgos Remvikos; Rémy J Salmon; Xavier Sastre; Pierre Validire; Andrew P Feinberg; Gilles Thomas
Multiple genetic alterations in distal and proximal colorectal cancer.
Lancet 1989;2(8659):353-6.
1989: Sylviane Olschwang; Gilles Thomas
Temperature gradient increases FIGE resolution.
Nucleic acids research 1989;17(6):2363.
1989: Olivier Delattre; F R Zhang; M S Gross; V C N'guyen; Gilles Thomas
RFLP identified by the anonymous DNA segment OLVIIF5 at 21q22.1-22.3 [HGM9 no.D21S143].
Nucleic acids research 1989;17(4):1790.
1989: F G Zhang; A Aurias; M F de Taud; M S Gross; V C N'guyen; Gilles Thomas
RFLP identified by the anonymous DNA segment FZ IV E11 at 1p23 [HGM9 no.D1S87].
Nucleic acids research 1989;17(4):1788.
1989: Olivier Delattre; M S Gross; M F de Taud; V C N'guyen; Gilles Thomas
RFLP identified by the anonymous DNA segment OLVIID1 on chromosome 6 [HGM9 no.D6S47].
Nucleic acids research 1989;17(4):1789.
1989: F R Zhang; Alain Aurias; Olivier Delattre; Gilles Thomas
RFLP identified by the anonymous DNA segment FZ V D11 at 22q13 [HGM9 no.D22S80].
Nucleic acids research 1989;17(4):1791.
1988: M H Stern; F R Zhang; Gilles Thomas; C Griscelli; Alain Aurias
Molecular characterization of ataxia telangiectasia T cell clones. III. Mapping the 14q32.1 distal breakpoint.
Human genetics 1988;81(1):18-22.
1988: E Viegas-Pequignot; Bernard Dutrillaux; Gilles Thomas
Inactive X chromosome has the highest concentration of unmethylated Hha I sites.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(20):7657-60.
1988: David J Law; Sylviane Olschwang; J P Monpezat; D Lefrançois; D Jagelman; N J Petrelli; Gilles Thomas; Andrew P Feinberg
Concerted nonsyntenic allelic loss in human colorectal carcinoma.
Science (New York, N.Y.) 1988;241(4868):961-5.
1988: F Zhang; M H Stern; Gilles Thomas; Alain Aurias
Molecular characterization of ataxia telangiectasia T cell clones. II. The clonal inv(14) in ataxia telangiectasia differs from the inv(14) in T cell lymphoma.
Human genetics 1988;78(4):316-9.
1988: F R Zhang; J P Monpezat; Olivier Delattre; Alain Aurias; Gilles Thomas
RFLP identified by the anonymous DNA segment FZ VI A2 at 22q11.2 [HGM no. D22S20].
Nucleic acids research 1988;16(6):2739.
1988: J P Monpezat; Olivier Delattre; A Bernard; D Grunwald; Yurgos Remvikos; Martine Muleris; Rémy J Salmon; G Frelat; Bernard Dutrillaux; Gilles Thomas
Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas.
International journal of cancer. Journal international du cancer 1988;41(3):404-8.
1988: Olivier Delattre; M Grunwald; A Bernard; D Grunwald; Gilles Thomas; G Frelat; Alain Aurias
Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridization.
Human genetics 1988;78(2):140-3.
1988: M H Stern; F R Zhang; C Griscelli; Gilles Thomas; Alain Aurias
Molecular characterization of different ataxia telangiectasia T-cell clones. I. A common breakpoint at the 14q11.2 band splits the T-cell receptor alpha-chain gene.
Human genetics 1988;78(1):33-6.
1988: Gilles Thomas
[Genes of hereditary diseases that predispose to tumors].
Bulletin du cancer 1988;75(9):871-8.
1987: J Remvikos; Martine Muleris; Philippe Vielh; Brigitte Zafrani; Gilles Thomas; Bernard Dutrillaux; Jacques Girodet; Rémy J Salmon
[Ploidy in colorectal cancer].
Gastroentérologie clinique et biologique 1987;11(10):681-5.