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authFullName_s : Catherine Henry

Postnatal diagnosis of 9q interstitial imbalances involving PTCH1, resulting from a familial intrachromosomal insertion.

Marina Blanchard , Christèle Dubourg , Laurent Pasquier , Sylvie Odent , Josette Lucas et al.
European Journal of Medical Genetics, 2014, 57 (5), pp.195-9. ⟨10.1016/j.ejmg.2013.12.010⟩
Journal articles hal-01009816v1

Clinical-grade production of human mesenchymal stromal cells: occurrence of aneuploidy without transformation.

Karin Tarte , Julien Gaillard , Jean-Jacques Lataillade , Loic Fouillard , Martine Becker et al.
Blood, 2010, 115 (8), pp.1549-53. ⟨10.1182/blood-2009-05-219907⟩
Journal articles hal-00744192v1
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Dynamic ER Interactomes Control the Estrogen-Responsive Trefoil Factor (TFF) Locus Cell-Specific Activities.

Justine Quintin , Christine Le Péron , Gaëlle Palierne , Maud Bizot , Stéphanie Cunha et al.
Molecular and Cellular Biology, 2014, 34 (13), pp.2418-2436. ⟨10.1128/MCB.00918-13⟩
Journal articles hal-00984591v1

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.

Sylvie Jaillard , Séverine Drunat , Claude Bendavid , Azzedine Aboura , Amandine Etcheverry et al.
European Journal of Medical Genetics, 2010, 53 (2), pp.66-75. ⟨10.1016/j.ejmg.2009.10.002⟩
Journal articles istex inserm-00434932v1
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Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review

Laïla El Khattabi , Sylvie Jaillard , Joris Andrieux , Laurent Pasquier , Laurence Perrin et al.
American Journal of Medical Genetics Part A, 2015, 167 (6), pp.1252--1261. ⟨10.1002/ajmg.a.36932⟩
Journal articles istex hal-01165441v1
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Cytogénétique des carcinomes rénaux [Cytogenetics profiles of renal carcinoma]

Frédéric Dugay , Julien Dagher , Grégory Verhoest , Catherine Henry , Sylvie Jaillard et al.
Morphologie, 2014, 98 (320), pp.1-7. ⟨10.1016/j.morpho.2014.02.006⟩
Journal articles hal-01025708v1

Chromosome marqueur surnuméraire dérivé du 19 en mosaïque : à propos d’un cas

Elouan Chérot , Frédéric Dugay , Christèle Dubourg , Mélanie Fradin , Vincent Jauffret et al.
Morphologie, 2015, 20es Journées du Collège des Histologistes, Embryologistes et Cytogénéticiens - Paris 12-14 mars 2015, 99 (327), pp.166--167. ⟨10.1016/j.morpho.2015.09.039⟩
Journal articles hal-01245005v1

Twelve new patients with 13q deletion syndrome: Genotype-phenotype analyses in progress.

Chloé Quélin , Claude Bendavid , Christèle Dubourg , Céline de La Rochebrochard , Josette Lucas et al.
European Journal of Medical Genetics, 2009, 52 (1), pp.41-6. ⟨10.1016/j.ejmg.2008.10.002⟩
Journal articles istex inserm-00353241v1
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2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?

Sylvie Jaillard , Christèle Dubourg , Marion Gérard-Blanluet , Andrée Delahaye , Laurent Pasquier et al.
Journal of Medical Genetics, 2009, 46 (12), pp.847-55. ⟨10.1136/jmg.2008.058156⟩
Journal articles inserm-00325658v1

Therapeutic approach and outcome of children with Philadelphia chromosome-positive acute lymphoblastic leukemia at first relapse in the era of tyrosine kinase inhibitors: An SFCE retrospective study

Lucie Aubert , Arnaud Petit , Yves Bertrand , Anne-France Ray-Lunven , Marie Angoso et al.
Pediatric Blood and Cancer, 2022, 69 (2), pp.e29441. ⟨10.1002/pbc.29441⟩
Journal articles hal-03510816v1

Syndrome myéloprolifératif avec polyglobulie et translocation t(6;8)(q27;p11) : cas clinique et revue de la littérature

Aurélie Chauveau , Catherine Henry , Erika Launay , Serge Eloit , Bruno Berdin et al.
Hématologie, 2012, 18 (5), pp.294-8. ⟨10.1684/hma.2012.0738⟩
Journal articles hal-01117525v1

MLL-SEPT5 fusion transcript in infant acute myeloid leukemia with t(11;22)(q23;q11).

Erika Launay , Catherine Henry , Claus Meyer , Céline Chappé , Sophie Taque et al.
Leukemia & lymphoma, 2014, 55 (3), pp.662-7. ⟨10.3109/10428194.2013.809528⟩
Journal articles hal-01010758v1
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Pan-HDAC Inhibitors Restore PRDM1 Response to IL21 in CREBBP-Mutated Follicular Lymphoma

Fabienne Desmots , Mikael Roussel , Céline Pangault , Francisco Llamas-Gutierrez , Cedric Pastoret et al.
Clinical Cancer Research, 2019, 25 (2), pp.735-746. ⟨10.1158/1078-0432.CCR-18-1153⟩
Journal articles hal-01952302v1
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Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia

Saloua Toujani , Elena J Tucker , Linda Akloul , Laura Mary , Céline Pimentel et al.
Cytogenetic and Genome Research, 2022, 162 (3), pp.124-131. ⟨10.1159/000524388⟩
Journal articles hal-03714551v1

Involvement of germline DDX1-MYCN duplication in inherited nephroblastoma.

Alice Fievet , Marc-Antoine Belaud-Rotureau , Frédéric Dugay , Caroline Abadie , Catherine Henry et al.
European Journal of Medical Genetics, 2013, 56 (12), pp.643-7. ⟨10.1016/j.ejmg.2013.10.004⟩
Journal articles hal-00933759v1

Histologic prognostic factors associated with chromosomal imbalances in a contemporary series of 89 clear cell renal cell carcinomas.

Julien Dagher , Frederic Dugay , Gregory Verhoest , Florian Cabillic , Sylvie Jaillard et al.
Human Pathology, 2013, 44 (10), pp.2106-15. ⟨10.1016/j.humpath.2013.03.018⟩
Journal articles hal-00937633v1
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Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia

Virginie Gandemer , Anne-Gaëlle Rio , Marie De Tayrac , Vonnick Sibut , Stéphanie Mottier et al.
BMC Genomics, 2007, 8, pp.385. ⟨10.1186/1471-2164-8-385⟩
Journal articles hal-01068393v1
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Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.

Caroline Schluth-Bolard , Bruno Delobel , Damien Sanlaville , Odile Boute , Jean-Marie Cuisset et al.
European Journal of Medical Genetics, 2009, 52 (5), pp.291-6. ⟨10.1016/j.ejmg.2009.05.011⟩
Journal articles inserm-00405484v1
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Multicolor-FISH Characterization of a Prenatal Mosaicism for a Chromosomal Rearrangement Undetected by Molecular Cytogenetics

Laura Mary , Philippe Loget , Sylvie Odent , Dominique Aussel , Gwenaëlle Le Bouar et al.
Cytogenetic and Genome Research, 2021, 161 (3-4), pp.143-152. ⟨10.1159/000514592⟩
Journal articles hal-03215883v1
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Mesenchymal stromal cells orchestrate follicular lymphoma cell niche through the CCL2-dependent recruitment and polarization of monocytes.

Fabien Guilloton , Gersende Caron , Cédric Ménard , Céline Pangault , Patricia Amé-Thomas et al.
Blood, 2012, 119 (11), pp.2556-67. ⟨10.1182/blood-2011-08-370908⟩
Journal articles inserm-00665887v1