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Author/Creator Geffroy, Sandrine

1. Molecular Profiling Defines Distinct Prognostic Subgroups in Childhood AML: A Report From the French ELAM02 Study Group. Issue 1 (January 2018)

Authors:
Marceau-Renaut, Alice; Duployez, Nicolas; Ducourneau, Benoît; Labopin, Myriam; Petit, Arnaud; Rousseau, Alexandra; Geffroy, Sandrine; Bucci, Maxime; Cuccuini, Wendy; Fenneteau, Odile; Ruminy, Philippe; Nelken, Brigitte; Ducassou, Stéphane; Gandemer, Virginie; Leblanc, Thierry; Michel, Gérard; Ber...
Journal:
HemaSphere
Issue:
Volume 2:Issue 1(2018)
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Record Type:
Journal Article
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2. Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia. (9th November 2017)

Authors:
Duployez, Nicolas; Abou Chahla, Wadih; Lejeune, Sophie; Marceau‐Renaut, Alice; Letizia, Guillaume; Boyer, Thomas; Geffroy, Sandrine; Peyrouze, Pauline; Grardel, Nathalie; Nelken, Brigitte; Michel, Gérard; Bertrand, Yves; Preudhomme, Claude
Journal:
European journal of haematology
Issue:
Volume 100:Number 1(2018)
Page Start:
104
Record Type:
Journal Article
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3. MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome. (27th August 2014)

Authors:
Poulain, Stéphanie; Boyle, Eileen M.; Roumier, Christophe; Demarquette, Hélène; Wemeau, Mathieu; Geffroy, Sandrine; Herbaux, Charles; Bertrand, Elisabeth; Hivert, Bénédicte; Terriou, Louis; Verrier, Albert; Pollet, Jean Paul; Maurage, Claude Alain; Onraed, Brigitte; Morschhauser, Franck; Quesnel,...
Journal:
British journal of haematology
Issue:
Volume 167:Number 4(2014:Nov.)
Page Start:
506
Record Type:
Journal Article
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4. Neurofibromatosis‐1 gene deletions and mutations in de novo adult acute myeloid leukemia. Issue 4 (5th March 2013)

Authors:
Boudry‐Labis, Elise; Roche‐Lestienne, Catherine; Nibourel, Olivier; Boissel, Nicolas; Terre, Christine; Perot, Christine; Eclache, Virginie; Gachard, Nathalie; Tigaud, Isabelle; Plessis, Ghislaine; Cuccuini, Wendy; Geffroy, Sandrine; Villenet, Céline; Figeac, Martin; Leprêtre, Frederic; Rennevill...
Journal:
American journal of hematology
Issue:
Volume 88:Issue 4(2013:Apr.)
Page Start:
306
Record Type:
Journal Article
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5. Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21). Issue 1 (2nd January 2016)

Authors:
Duployez, Nicolas; Micol, Jean-Baptiste; Boissel, Nicolas; Petit, Arnaud; Geffroy, Sandrine; Bucci, Maxime; Lapillonne, Hélène; Renneville, Aline; Leverger, Guy; Ifrah, Norbert; Dombret, Hervé; Abdel-Wahab, Omar; Jourdan, Eric; Preudhomme, Claude
Journal:
Leukemia & lymphoma
Issue:
Volume 57:Issue 1(2016:Jan.)
Page Start:
199
Record Type:
Journal Article
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