Dr JEANDIDIER Eric

Fiche personne

Coordonnées

Hôpital Emile Muller
20 avenue du Dr René Laennec
68100 MULHOUSE

+33 3 89 64 87 04

jeandidiere@ch-mulhouse.fr

Territoire

Alsace

Statut

Hospitalier

Affiliation

Groupe hospitalier de la région de Mulhouse et Sud-Alsace (GHRMSA)

Recherche

Expertises :
- Clinique:Génétique Médicale
- Recherche:Biologie Cellulaire
- Cancer:Leucémies
- Cancer:Lymphomes
- Plateforme:Biologie Moléculaire Hospitalière
- Clinique:Cytogénétique
- Clinique:Oncogénétique

Projets

Détection prospective des biomarqueurs émergents dans le cancer du poumon, le cancer colo-recta et le mélanome

2014 - Porteur du projet : Dr GHNASSIA Jean-Pierre - Partenaire : Dr GAUB Marie-Pierre , Dr JEANDIDIER Eric , Pr LESSINGER Jean-Marc

Publications

Telomere Dysfunction in Pediatric Patients with Differences/Disorders of Sexual Development.

Younoussa H, Gadji M, Soumboundou M, Colicchio B, Said A, Ndoye NA, Junker S, Plesch A, Heidingsfelder L, Diagne NR, Dieterlen A, Voisin P, Carde P, Jeandidier E, M'kacher R

Biomedicines. 2024 03 2;12(3):

Trisomy 22: First and second trimester cytogenetic analysis and phenotypic presentation in a series of seven cases.

Minella C, Jeandidier E, Koch A, Antal MC, Favre R, Sananes N, Weingertner AS

Fetal Diagn Ther. 2023 11 3;:

Multi-omics comparison of malignant and normal uveal melanocytes reveals molecular features of uveal melanoma.

Gentien D, Saberi-Ansari E, Servant N, Jolly A, de la Grange P, Némati F, Liot G, Saule S, Teissandier A, Bourc'his D, Girard E, Wong J, Masliah-Planchon J, Narmanli E, Liu Y, Torun E, Goulancourt R, Rodrigues M, Gaudé LV, Reyes C, Bazire M, Chenegros T, Henry E, Rapinat A, Bohec M, Baulande S, M'kacher R, Jeandidier E, Nicolas A, Ciriello G, Margueron R, Decaudin D, Cassoux N, Piperno-Neumann S, Stern MH, Gibcus JH, Dekker J, Heard E, Roman-Roman S, Waterfall JJ

Cell Rep. 2023 09 13;42(9):113132

Extended lifespan and improved genome stability in HepaRG-derived cell lines through reprogramming by high-density stress.

Brun C, Allain C, Ferron PJ, Younoussa H, Colicchio B, Jeandidier E, M'Kacher R, Guguen-Guillouzo C, Bertile F

Proc Natl Acad Sci U S A. 2023 09 5;120(36):e2219298120

High Resolution and Automatable Cytogenetic Biodosimetry Using In Situ Telomere and Centromere Hybridization for the Accurate Detection of DNA Damage: An Overview.

M'Kacher R, Colicchio B, Junker S, El Maalouf E, Heidingsfelder L, Plesch A, Dieterlen A, Jeandidier E, Carde P, Voisin P

Int J Mol Sci. 2023 03 16;24(6):

A Central Role of Telomere Dysfunction in the Formation of a Unique Translocation within the Sub-Telomere Region Resulting in Duplication and Partial Trisomy.

M'Kacher R, Miguet M, Maillard PY, Colicchio B, Scheidecker S, Najar W, Arnoux M, Oudrhiri N, Borie C, Biehler M, Plesch A, Heidingsfelder L, Bennaceur-Griscelli A, Dieterlen A, Voisin P, Junker S, Carde P, Jeandidier E

Genes (Basel). 2022 09 29;13(10):

Patient-Derived iPSCs Reveal Evidence of Telomere Instability and DNA Repair Deficiency in Coats Plus Syndrome.

Oudrhiri N, M'kacher R, Chaker D, Colicchio B, Borie C, Jeandidier E, Dieterlen A, Griscelli F, Bennaceur-Griscelli A, Turhan AG

Genes (Basel). 2022 08 5;13(8):

Lung Fibroblasts from Idiopathic Pulmonary Fibrosis Patients Harbor Short and Unstable Telomeres Leading to Chromosomal Instability.

M'Kacher R, Jaillet M, Colicchio B, Vasarmidi E, Mailleux A, Dieterlen A, Kannengiesser C, Borie C, Oudrhiri N, Junker S, Voisin P, Jeandidier E, Carde P, Fenech M, Bennaceur-Griscelli A, Crestani B, Borie R

Biomedicines. 2022 Jan 28;10(2):

Is Response to Genotoxic Stress Similar in Populations of African and European Ancestry? A Study of Dose-Response After Irradiation.

Soumboundou M, Dossou J, Kalaga Y, Nkengurutse I, Faye I, Guingani A, Gadji M, Yameogo KJ, Zongo H, Mbaye G, Dem A, Diarra M, Adjibade R, Djebou C, Junker S, Oudrhiri N, Hempel WM, Dieterlen A, Jeandidier E, Carde P, El Maalouf E, Colicchio B, Bennaceur-Griscelli A, Fenech M, Voisin P, Rodriguez-Lafrasse C, M'Kacher R

Front Genet. 2021 ;12:657999

Telomere aberrations, including telomere loss, doublets, and extreme shortening, are increased in patients with infertility.

M'kacher R, Colicchio B, Marquet V, Borie C, Najar W, Hempel WM, Heidingsfelder L, Oudrhiri N, Al Jawhari M, Wilhelm-Murer N, Miguet M, Dieterlen A, Deschênes G, Tabet AC, Junker S, Grynberg M, Fenech M, Bennaceur-Griscelli A, Voisin P, Carde P, Jeandidier E, Yardin C

Fertil Steril. 2020 Nov 30;:

Telomere and Centromere Staining Followed by M-FISH Improves Diagnosis of Chromosomal Instability and Its Clinical Utility.

M'kacher R, Colicchio B, Borie C, Junker S, Marquet V, Heidingsfelder L, Soehnlen K, Najar W, Hempel WM, Oudrhiri N, Wilhelm-Murer N, Miguet M, Arnoux M, Ferrapie C, Kerbrat W, Plesch A, Dieterlen A, Girinsky T, Voisin P, Deschenes G, Tabet AC, Yardin C, Bennaceur-Griscelli A, Fenech M, Carde P, Jeandidier E

Genes (Basel). 2020 Apr 27;11(5):

The Use of Natural Agents to Counteract Telomere Shortening: Effects of a Multi-Component Extract of Bunge and Danazol.

Guinobert I, Blondeau C, Colicchio B, Oudrhiri N, Dieterlen A, Jeandidier E, Deschenes G, Bardot V, Cotte C, Ripoche I, Carde P, Berthomier L, M'Kacher R

Biomedicines. 2020 Feb 12;8(2):

Benefit of an association of an antioxidative substrate and a traditional chinese medicine on telomere elongation.

M'kacher R, Breton L, Colicchio B, Puget H, Hempel WM, Al Jawhari M, Jeandidier E, Frey M

Cell. Mol. Biol. (Noisy-le-grand). 2019 Dec 31;65(8):54-58

Biological Dosimetry Network in Africa: Establishment of a Dose-response Curve Using Telomere and Centromere Staining.

Soumboundou M, Nkengurutse I, Dossou J, Colicchio B, Djebou C, Gadji M, Houenon G, Dem A, Dedjan A, Diarra M, Adjibade R, Finot F, Hempel W, Dieterlen A, Jeandidier E, Rodriguez-Lafrasse C, M'kacher R

Health Phys. 2019 Jun 6;:

Design and Validation of an Automated Process for the Expansion of Peripheral Blood-Derived CD34 Cells for Clinical Use After Myocardial Infarction.

Saucourt C, Vogt S, Merlin A, Valat C, Criquet A, Harmand L, Birebent B, Rouard H, Himmelspach C, Jeandidier É, Chartois-Leauté AG, Derenne S, Koehl L, Salem JE, Hulot JS, Tancredi C, Aries A, Judé S, Martel E, Richard S, Douay L, Hénon P

Stem Cells Transl Med. 2019 Apr 29;:

Establishment and Characterization of a Reliable Xenograft Model of Hodgkin Lymphoma Suitable for the Study of Tumor Origin and the Design of New Therapies.

M'kacher R, Frenzel M, Al Jawhari M, Junker S, Cuceu C, Morat L, Bauchet AL, Stimmer L, Lenain A, Dechamps N, Hempel WM, Pottier G, Heidingsfelder L, Laplagne E, Borie C, Oudrhiri N, Jouni D, Bennaceur-Griscelli A, Colicchio B, Dieterlen A, Girinsky T, Boisgard R, Bourhis J, Bosq J, Mehrling T, Jeandidier E, Carde P

Cancers (Basel). 2018 Oct 31;10(11):

Independent Mechanisms Lead to Genomic Instability in Hodgkin Lymphoma: Microsatellite or Chromosomal Instability .

Cuceu C, Colicchio B, Jeandidier E, Junker S, Plassa F, Shim G, Mika J, Frenzel M, Al Jawhari M, Hempel WM, O'Brien G, Lenain A, Morat L, Girinsky T, Dieterlen A, Polanska J, Badie C, Carde P, M'Kacher R

Cancers (Basel). 2018 Jul 13;10(7):

The Transition between Telomerase and ALT Mechanisms in Hodgkin Lymphoma and Its Predictive Value in Clinical Outcomes.

M'kacher R, Cuceu C, Al Jawhari M, Morat L, Frenzel M, Shim G, Lenain A, Hempel WM, Junker S, Girinsky T, Colicchio B, Dieterlen A, Heidingsfelder L, Borie C, Oudrhiri N, Bennaceur-Griscelli A, Moralès O, Renaud S, Van de Wyngaert Z, Jeandidier E, Delhem N, Carde P

Cancers (Basel). 2018 May 30;10(6):

Transmission of Induced Chromosomal Aberrations through Successive Mitotic Divisions in Human Lymphocytes after In Vitro and In Vivo Radiation.

Kaddour A, Colicchio B, Buron D, El Maalouf E, Laplagne E, Borie C, Ricoul M, Lenain A, Hempel WM, Morat L, Al Jawhari M, Cuceu C, Heidingsfelder L, Jeandidier E, Deschênes G, Dieterlen A, El May M, Girinsky T, Bennaceur-Griscelli A, Carde P, Sabatier L, M'kacher R

Sci Rep. 2017 Jun;7(1):3291

Genotoxic risk of ethyl-paraben could be related to telomere shortening.

Finot F, Kaddour A, Morat L, Mouche I, Zaguia N, Cuceu C, Souverville D, Négrault S, Cariou O, Essahli A, Prigent N, Saul J, Paillard F, Heidingsfelder L, Lafouge P, Al Jawhari M, Hempel WM, El May M, Colicchio B, Dieterlen A, Jeandidier E, Sabatier L, Clements J, M'Kacher R

J Appl Toxicol. 2016 Dec;:

TELOMERE SHORTENING: A NEW PROGNOSTIC FACTOR FOR CARDIOVASCULAR DISEASE POST-RADIATION EXPOSURE.

M'kacher R, Girinsky T, Colicchio B, Ricoul M, Dieterlen A, Jeandidier E, Heidingsfelder L, Cuceu C, Shim G, Frenzel M, Lenain A, Morat L, Bourhis J, Hempel WM, Koscielny S, Paul JF, Carde P, Sabatier L

Radiat Prot Dosimetry. 2014 Oct 1. pii: ncu296.

ONSL and OSKM cocktails act synergistically in reprogramming human somatic cells into induced pluripotent stem cells.

Jung L, Tropel P, Moal Y, Teletin M, Jeandidier E, Gayon R, Himmelspach C, Bello F, Andre C, Tosch A, Mansouri A, Bruant-Rodier C, Bouille P, Viville S

Mol Hum Reprod. 2014 Jun;20(6):538-49

First description of the t(10;11)(q22;q23)/MLL-TET1 translocation in a T-cell lymphoblastic lymphoma, with subsequent lineage switch to acute myelomonocytic myeloid leukemia.

Ittel A, Jeandidier E, Helias C, Perrusson N, Humbrecht C, Lioure B, Mazurier I, Mayeur-Rousse C, Lavaux A, Thiebault S, Lerintiu F, Gervais C, Mauvieux L

Haematologica. 2013 Dec;98(12):e166-8

Complex subclone structure that responds differentially to therapy in a patient with essential thrombocythemia and chronic myeloid leukemia.

Grisouard J, Ojeda-Uribe M, Looser R, Hao-Shen H, Lundberg P, Duek A, Jeandidier E, Karow A, Skoda RC

Blood. 2013 Nov 21;122(22):3694-6

A translocation t(2;8)(q12;p11) fuses FGFR1 to a novel partner gene, RANBP2/NUP358, in a myeloproliferative/myelodysplastic neoplasm.

Gervais C, Dano L, Perrusson N, Helias C, Jeandidier E, Galoisy AC, Ittel A, Herbrecht R, Bilger K, Mauvieux L

Leukemia. 2013 Apr;27(5):1186-8

Therapy-related acute myeloid leukemia (t-AML) with poor-risk cytogenetics in two patients with persistent molecular complete remission of acute promyelocytic leukemia.

Ojeda-Uribe M, Schneider A, Luquet I, Berceanu A, Cornillet-Lefebvre P, Jeandidier E, Lioure B, Ades L, Mauvieux L, Himberlin C

Eur J Haematol. 2012 Sep;89(3):267-72

A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity.

Jeandidier E, Gervais C, Radford-Weiss I, Zink E, Gangneux C, Eischen A, Galoisy AC, Helias C, Dano L, Cammarata O, Jung G, Harzallah I, Guerin E, Martzolff L, Drenou B, Lioure B, Tancredi C, Rimelen V, Mauvieux L

Cancer Genet. 2012 Jul-Aug;205(7-8):365-72

Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.

Schluth C, Cossee M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E

Pathol Biol (Paris). 2007 Feb;55(1):29-36

Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique Hematologique.

Jeandidier E, Dastugue N, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Herens C, Michaux L, Verellen-Dumoulin C, Talmant P, Cornillet-Lefebvre P, Luquet I, Charrin C, Barin C, Collonge-Rame MA, Perot C, Van den Akker J, Gregoire MJ, Jonveaux P, Baranger L, Eclache-Saudreau V, Pages MP, Cabrol C, Terre C, Berger R

Cancer Genet Cytogenet. 2006 Apr 1;166(1):1-11.