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Gwendoline Soler

Parallel FISH and Immunohistochemical Studies of ALK Status in 3244 Non–Small-Cell Lung Cancers Reveal Major Discordances
2014 · Florian Cabillic, Audrey Gros, et al. · Journal of Thoracic Oncology · 151
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Prognostic and oncogenic relevance of TLX1/HOX11 expression level in T-ALLs
2007 · Julie Bergeron, Emmanuelle Clappier, et al. · Blood · 77
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PFMG2025–integrating genomic medicine into the national healthcare system in France
2025 · Caroline Abadie, Aldja Abderrahmane, et al. · The Lancet Regional Health - Europe · 59
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Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infants
2011 · Cathy Quelen, Eric Lippert, et al. · Blood · 50
LRRFIP1, a new FGFR1 partner gene associated with 8p11 myeloproliferative syndrome
2009 · G Soler, S Nusbaum, et al. · Leukemia · 50
NUP98–HMGB3: a novel oncogenic fusion
2009 · A Petit, C Ragu, et al. · Leukemia · 39
Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocation
2007 · G Soler, I Radford-Weiss, et al. · Leukemia · 37
NUP98-MLL fusion in human acute myeloblastic leukemia
2010 · Sophie Kaltenbach, Gwendoline Soler, et al. · Blood · 33
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth
2009 · Valérie Malan, Suzanne Chevallier, et al. · European Journal of Human Genetics · 29
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Identification of GSX2 and AF10 as NUP98 partner genes in myeloid malignancies
2013 · G Soler, S Kaltenbach, et al. · Blood Cancer Journal · 24
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Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute Leukemia
2023 · Gwendoline Soler, Zangbéwendé Guy Ouedraogo, et al. · Cancers · 21
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Analysis of alterations of WFDC1, a new putative tumour suppressor gene, in hepatocellular carcinoma
2002 · Raphaël Saffroy, Philippe Riou, et al. · European Journal of Human Genetics · 21
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Functional analysis of the NUP98-CCDC28A fusion protein
2011 · A. Petit, C. Ragu, et al. · Haematologica · 17
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Optical genome mapping for prenatal diagnosis: A prospective study
2023 · Carole Goumy, Zangbéwendé Guy Ouedraogo, et al. · Clinica Chimica Acta · 14
Prenatal diagnosis on chorionic villi using molecular techniques should be performed from mesenchymal core rather than from direct villi
2011 · Jérôme Toutain, Gwendoline Soler, et al. · Prenatal Diagnosis · 10
MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literature
2008 · Gwendoline Soler, Isabelle Radford, et al. · Cancer Genetics and Cytogenetics · 7
Isolated isochromosomes i(X)(p10) and idic(X)(q13) are associated with myeloid malignancies and dysplastic features
2019 · Dominique Penther, Pascaline Etancelin, et al. · American Journal of Hematology · 4
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Bilateral MALT-type ocular adnexal lymphoma with marginal zone lymphoma leukaemic cells and ophthalmological diffuse large B cell lymphoma
2008 · R Sahli, D Canioni, et al. · British Journal of Ophthalmology · 3
Proportion of Parents Agreeing to Delay Fetal Karyotyping until the Third Trimester of Pregnancy in Cases with an Indication
2012 · Jérôme Toutain, Marie-Anne Lemaire-Coustel, et al. · Fetal Diagnosis and Therapy · 2
Molecular landscape of mature B‐cell lymphoproliferative disorders with BCL3‐translocation: A Groupe Francophone de Cytogénétique Hématologique (GFCH)/French Innovative Leukemia Organization (FILO) study
2024 · Lauren Véronèse, Hedi Bensaber, et al. · American Journal of Hematology · 1
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Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination
2023 · Carole Goumy, Zangbéwendé Guy Ouedraogo, et al. · Diagnostics · 1
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Hétérogénéité intraclonale de la dynamique télomérique dans les cellules primaires de leucémie myéloïde chronique au diagnostic
2022 · Andrei Tchirkov, Thomas Tassin, et al. · Morphologie
Faisabilité de la cartographie optique en prénatal et en fœtopathologie : évaluation de l’extraction d’ADN de haut poids moléculaire pour différents types de matrices
2022 · Carole Goumy, Claude Darcha, et al. · Morphologie
Amplification intrachromosomique du chromosome 21 (iAMP(21)) et leucémie aiguë myéloïde : à propos d’un cas de diagnostic difficile
2022 · Lauren Véronèse, Thomas Tassin, et al. · Morphologie
Identification d’un double isodicentrique du bras court du chromosome Y chez un nouveau-né
2019 · Gaëlle Salaun, Eleonore Eymard-Pierre, et al. · Morphologie
Works count: 33
Citation count: 650
H-index: 14
I10-index: 15
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