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Jean-Michel Dupont

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Céline Dupont; Azzedine Aboura; C Baumann; Brigitte Benzacken; P Bourdoncle; Fabien Guimiot; Dominique Le Tessier; C Lebugle; I Marey; L Perrin; D Smiljkovski; AC Tabet; Jean-Michel Dupont
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
Andreea Cristina Tuţulan-Cuniţă; Géraldine Viot; Dominique Blancho; Magdalena Budişteanu; Jean-Michel Dupont; Aziza Lebbar; Agripina Lungeanu; Sorina Mihaela Papuc; Aurora Arghir
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.
Fatma Abdelhedi; Johanna Corcos; Laurence Cuisset; Dominique Le Tessier; Aziza Lebbar; Julia Tantau; Vassilis Tsatsaris; Jean-Michel Dupont
First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur.

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All Publications

2012: Céline Dupont; Azzedine Aboura; C Baumann; Brigitte Benzacken; P Bourdoncle; Fabien Guimiot; Dominique Le Tessier; C Lebugle; I Marey; L Perrin; D Smiljkovski; AC Tabet; Jean-Michel Dupont
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
Clinical genetics 2012;82(2):187-92.
2012: Andreea Cristina Tuţulan-Cuniţă; Géraldine Viot; Dominique Blancho; Magdalena Budişteanu; Jean-Michel Dupont; Aziza Lebbar; Agripina Lungeanu; Sorina Mihaela Papuc; Aurora Arghir
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.
Psychiatry research 2012;197(3):356-7.
2012: Fatma Abdelhedi; Johanna Corcos; Laurence Cuisset; Dominique Le Tessier; Aziza Lebbar; Julia Tantau; Vassilis Tsatsaris; Jean-Michel Dupont
First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur.
American journal of medical genetics. Part A 2012;158A(3):617-21.
2011: Jörg Tost; Florence Busato; Jean-Michel Dupont; Hinda Hamzaoui; SAMIA MOURAH; Aymeric Neyret; Zhor Bouizar
Methylation of specific CpG sites in the P2 promoter of parathyroid hormone-related protein determines the invasive potential of breast cancer cell lines.
Epigenetics : official journal of the DNA Methylation Society 2011;6(8):1035-46.
2008: Aziza Lebbar; Patrick Callier; Françoise Baverel; Nathalie Marle; Catherine Patrat; Dominique Le Tessier; Francine Mugneret; Jean-Michel Dupont
Two cases of mosaicism for complex chromosome rearrangements (CCRM) associated with secondary infertility.
American journal of medical genetics. Part A 2008;146A(20):2651-6.
2008: Sandrine Leclercq; Aziza Lebbar; Gilles Grange; Vassilis Tsatsaris; Dominique Le Tessier; Jean-Michel Dupont
Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies.
Prenatal diagnosis 2008;28(4):313-8.
2007: Celine Dupont; Aziza Lebbar; Cecile Teinturier; Françoise Baverel; Géraldine Viot; Dominique Le Tessier; Jerome Le Bozec; Laurence Cuisset; Jean-Michel Dupont
First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation.
American journal of medical genetics. Part A 2007;143A(11):1236-43.
2007: Jörg Tost; Hélène Jammes; Jean-Michel Dupont; Christophe Buffat; Brigitte Robert; Thérèse-Marie Mignot; Françoise Mondon; Bruno Carbonne; Umberto Siméoni; Gilles Grangé; Antoine Kerjean; Françoise Ferré; Ivo Gut; Daniel Vaiman
Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.
Nucleic acids research 2007;35(2):701.
2007: Mohammad Pazooki; Aziza Lebbar; Anne Roubergues; Françoise Baverel; Dominique Letessier; Jean-Michel Dupont
Pure familial 6q21q22.1 duplication in two generations.
European journal of medical genetics 2007;50(1):60-5.
2006: Jörg Tost; Hélène Jammes; Jean-Michel Dupont; Christophe Buffat; Brigitte Robert; Thérèse-Marie Mignot; Françoise Mondon; Bruno Carbonne; Umberto Siméoni; Gilles Grangé; Antoine Kerjean; Françoise Ferré; Ivo Gut; Daniel Vaiman
Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.
Nucleic acids research 2006;34(19):5438-48.
2004: Jean-Michel Dupont
[Topographical organisation of the chromatin in human interphase nuclei: architecture meets function].
Morphologie : bulletin de l'Association des anatomistes 2004;88(282):127-34.
2004: Jean-Michel Dupont; Jörg Tost; Hélène Jammes; Ivo Gut
De novo quantitative bisulfite sequencing using the pyrosequencing technology.
Analytical biochemistry 2004;333(1):119-27.
2003: Catherine Dodé; Jacqueline Levilliers; Jean-Michel Dupont; Anne De Paepe; Nathalie Le Dû; Nadia Soussi-Yanicostas; Roney Coimbra; Sedigheh Delmaghani; Sylvie Compain-Nouaille; Françoise Baverel; Christophe Pêcheux; Dominique Le Tessier; Corinne Cruaud; Marc Delpech; Frank Speleman; Stefan Vermeulen; Andrea Amalfitano; Yvan Bachelot; Philippe Bouchard; Sylvie Cabrol; Jean-Claude Carel; Henriette A Delemarre-Van De Waal; Barbara Goulet-Salmon; Marie-Laure Kottler; Odile Richard; Franco Sanchez-Franco; Robert Saura; Jacques Young; Christine Petit; Jean-Pierre Hardelin
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Nature genetics 2003;33(4):463-5.
2002: Aziza Lebbar; Géraldine Viot; S Szpiro-Tapia; Françoise Baverel; Didier Rabineau; Jean-Michel Dupont
Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.
Prenatal diagnosis 2002;22(11):973-5.
2002: Jean-Michel Dupont; Laurence Cuisset; Maryse Cartigny; Dominique Le Tessier; Christian Vasseur; Didier Rabineau; Marc Jeanpierre
Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patient.
American journal of medical genetics 2002;111(4):405-8.
2002: Isabelle Luquet; Francine Mugneret; P D Athis; N Nadal; Bernardine Favre; C Abel; N Chelloug; James Lespinasse; M F Portnoi; Nicole Joyé; Jean-Michel Dupont; Aziza Lebbar; J L Bresson; Florence Fellmann; Jean-Pierre Siffroi; Sandra Chantot-Bastaraud; J Chiesa; F Amblard; F Devillard; Eric Jeandidier; Michelle Boceno; Jean-Marie Rival; V Bellec; H Lallaoui; Bruno Delobel; Marie-Françoise Croquette; Brigitte Benzacken
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature.
Annales de génétique 2002;45(2):77-88.
2002: Yann-Erick Claessens; Didier Bouscary; Jean-Michel Dupont; Françoise Picard; Josiane Melle; Sylvie Gisselbrecht; Catherine Lacombe; François Dreyfus; Patrick Mayeux; Michaëla Fontenay-Roupie
In vitro proliferation and differentiation of erythroid progenitors from patients with myelodysplastic syndromes: evidence for Fas-dependent apoptosis.
Blood 2002;99(5):1594-601.
2001: AC Tabet; Jean-Michel Dupont; Aziza Lebbar; M H Couturier-Turpin; G Feldmann; Didier Rabineau
Heteromorphism 18ph+ : with or without reproductive consequences?
Annales de génétique 2001;44(3):139-42.
2001: Géraldine Viot; Emmanuelle Pannier; L Faivre; Julia Tantau; Catherine Fallet-Bianco; Jean-Michel Dupont; Pierre Jouannet; Marie-Cécile Aubry; Stanislas LYONNET; D Cabrol
A new case of exomphalos, short limbs, and macrogonadism syndrome.
Journal of medical genetics 2001;38(3):E8.
2000: Antoine Kerjean; Jean-Michel Dupont; Christian Vasseur; Dominique Le Tessier; Laurence Cuisset; A Pàldi; Pierre Jouannet; Marc Jeanpierre
Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis.
Human molecular genetics 2000;9(14):2183-7.
2000: Dominique Le Tessier; Jean-Michel Dupont; Serge Fichelson; Didier Bouscary; Aziza Lebbar; François Dreyfus; Didier Rabineau
Clonal chromosomal abnormalities identified by interphase fluorescence in situ hybridization on collagen cultured hematopoietic stem cells.
Leukemia 2000;14(5):949-50.
1999: Jean-Michel Dupont; Dominique Le Tessier; Didier Rabineau; Laurence Cuisset; Christian Vasseur; Marc Jeanpierre; Marc Delpech; F Pinton; Gérard Ponsot; M F Denavit
Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome.
Journal of medical genetics 1999;36(8):652-4.
1998: Michaëla Fontenay-Roupie; Jean-Michel Dupont; Françoise Picard; Serge Fichelson; A Botella; Josiane Melle; Martine Guesnu; Nicole Casadevall; François Dreyfus; Didier Bouscary
Analysis of megakaryocyte growth and development factor (thrombopoietin) effects on blast cell and megakaryocyte growth in myelodysplasia.
Leukemia research 1998;22(6):527-35.
1998: Jean-Michel Dupont; Laurence Cuisset
[Genetic basis of Prader-Willi and Angelman syndromes: implications for the biologic diagnosis].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1998;5(4):418-24.
1998: Jean-Michel Dupont; Michaëla Fontenay-Roupie; O Dupuy; A Lebarr; Dominique Le Tessier; P Auvinet; Didier Rabineau; Serge Fichelson
Fluorescence in situ hybridization on methylcellulose cultured hematopoietic stem cells from myelodysplastic syndromes.
Cancer genetics and cytogenetics 1998;101(1):12-5.
1998: Jean-Michel Dupont; Aziza Lebbar; O Dupuy; N Frydman; D Letessier; P Auvinet; Didier Rabineau
Polymerase Chain reaction generated probes for fluorescence in situ hybridization.
Morphologie : bulletin de l'Association des anatomistes 1998;82(257):21-4.
1997: Jean-Michel Dupont; Dominique Le Tessier; Françoise Baverel; A Rouffet; Didier Rabineau
Mosaic isochromosome 20q and normal outcome: a new case ascertained by fluorescence in situ hybridization and a review of the literature.
Fetal diagnosis and therapy 1997;12(5):283-5.
1997: Laurence Cuisset; C Le Stunff; Jean-Michel Dupont; Christian Vasseur; M Cartigny; F Despert; Marc Delpech; P Bougnere; Marc Jeanpierre
PEG1 expression in maternal uniparental disomy 7.
Annales de génétique 1997;40(4):211-5.