Stéphanie Poulain

MYD88 L265P mutation in Waldenstrom macroglobulinemia

Stéphanie Poulain, Christophe Roumier, Audrey Decambron et al. · Blood · 2013 · 231 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Guideline for the diagnosis, treatment and response criteria for Bing-Neel syndrome

Monique C. Minnema, Eva Kimby, Shirley D’Sa et al. · Haematologica · 2016 · 152 citations · Full text

Medicine, Hematology, Neurology +13

Genomic Landscape of <i>CXCR4</i> Mutations in Waldenström Macroglobulinemia

Stéphanie Poulain, Christophe Roumier, Aurélie Venet-Caillault et al. · Clinical Cancer Research · 2015 · 124 citations

Life Sciences, Genetics, Molecular Genetics +14

<i>TP53</i> Mutation and Its Prognostic Significance in Waldenstrom's Macroglobulinemia

Stéphanie Poulain, Christophe Roumier, Elisabeth Bertrand et al. · Clinical Cancer Research · 2017 · 96 citations

Medicine, Genetics, Molecular Genetics +17

<i><scp>MYD</scp>88</i> L265P mutation contributes to the diagnosis of Bing Neel syndrome

Stéphanie Poulain, Eileen M. Boyle, Christophe Roumier et al. · British Journal of Haematology · 2014 · 78 citations

Life Sciences, Genetics, Neurology +11