Sandrine Geffroy

2.1k citations

32 papers · 949 indexed · h-index 14

Co-authors: Claude Preudhomme Aline Renneville Nicolas Boissel Hervé Dombret Olivier Nibourel Bruno Quesnel N Philippe Martin Figeac
Topics: Acute Myeloid Leukemia Research (18 papers)Chronic Myeloid Leukemia Treatments (6 papers)Cancer Genomics and Diagnostics (6 papers)
Cited by: Hematology Genetics Cancer Research
Journals: Journal of Clinical Oncology Blood Clinical Cancer Research
Partner nations: France United States Belgium

In The Last Decade

Sandrine Geffroy

29 papers receiving 938 citations

Peers

Countries citing papers authored by Sandrine Geffroy

Since Specialization

Citations

This map shows the geographic impact of Sandrine Geffroy's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sandrine Geffroy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandrine Geffroy more than expected).

Fields of papers citing papers by Sandrine Geffroy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandrine Geffroy. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sandrine Geffroy. The network helps show where Sandrine Geffroy may publish in the future.

Co-authorship network of co-authors of Sandrine Geffroy

This figure shows the co-authorship network connecting the top 25 collaborators of Sandrine Geffroy. A scholar is included among the top collaborators of Sandrine Geffroy based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sandrine Geffroy. Sandrine Geffroy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Monitoring of measurable residual disease by next‐generation sequencing in patients with acute myeloid leukaemia 2025 ·British Journal of Haematology ·(unknown),(unknown),Delphine Lebon,(unknown),Véronique Harrivel,(unknown),(unknown),Alice Marceau‐Renaut,Sandrine Geffroy,(unknown),(unknown),Laurène Fenwarth,Céline Berthon,Jean‐Pierre Marolleau,Martin Figeac,Claude Preudhomme,Nicolas Duployez	1
2	PB0818 Impact of ABO Blood Group Genotype on VWF Level in Carriers of Type 3 von Willebrand Disease from the French von Willebrand Disease Reference Center 2023 ·Research and Practice in Thrombosis and Haemostasis ·(unknown),Emmanuelle Jeanpierre,Pierre Boisseau,Catherine Ternisien,(unknown),Antoine Rauch,Camille Paris,M. D. Daniel,Sandrine Geffroy,Nicolas Duployez,Jenny Goudemand,Pierre‐Emmanuel Morange,Christophe Zawadzki,Sophie Susen	0
3	Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r 2022 ·BMC Bioinformatics ·(unknown),(unknown),Nicolas Duployez,Martin Figeac,Sandrine Geffroy,Maxime Bucci,Karine Celli‐Lebras,Matthieu Duchmann,(unknown),Laurène Fenwarth,Olivier Nibourel,(unknown),Raphaël Itzykson,Hervé Dombret,Mathilde Hunault,Claude Preudhomme,Mikaël Salson	0
4	SNP-array lesions in core binding factor acute myeloid leukemia 2018 ·Oncotarget ·Nicolas Duployez,(unknown),Christophe Roumier,Nicolas Boissel,Arnaud Petit,Sandrine Geffroy,Nathalie Hélevaut,Karine Celli‐Lebras,Christine Terré,Odile Fenneteau,Wendy Cuccuini,Isabelle Luquet,Hélène Lapillonne,Catherine Lacombe,Pascale Cornillet,Norbert Ifrah,Hervé Dombret,Guy Leverger,Éric Jourdan,Claude Preudhomme	10
5	Clinical relevance of IDH1/2 mutant allele burden during follow-up in acute myeloid leukemia. A study by the French ALFA group 2018 ·Haematologica ·(unknown),Nicolas Boissel,Nathalie Hélevaut,Jordan Madic,Olivier Nibourel,Alice Marceau‐Renaut,Maxime Bucci,Sandrine Geffroy,Karine Celli‐Lebras,Sylvie Castaigné,Xavier Thomas,Christine Terré,Hervé Dombret,Claude Preudhomme,Aline Renneville	34
6	TP53 Mutation and Its Prognostic Significance in Waldenstrom's Macroglobulinemia 2017 ·Clinical Cancer Research ·Stéphanie Poulain,Christophe Roumier,Elisabeth Bertrand,Aline Renneville,(unknown),(unknown),Sandrine Geffroy,Shéhérazade Sebda,Olivier Nibourel,(unknown),Charles Herbaux,Loïc Renaud,Cécile Tomowiak,Stéphanie Guidez,Sabine Tricot,Catherine Roche‐Lestienne,Bruno Quesnel,Claude Preudhomme,Xavier Leleu	62
7	Comprehensive mutational profiling of core binding factor acute myeloid leukemia 2016 ·Blood ·Nicolas Duployez,Alice Marceau‐Renaut,Nicolas Boissel,Arnaud Petit,Maxime Bucci,Sandrine Geffroy,Hélène Lapillonne,Aline Renneville,Christine Ragu,Martin Figeac,Karine Celli‐Lebras,Catherine Lacombe,Jean‐Baptiste Micol,Omar Abdel‐Wahab,Pascale Cornillet,Norbert Ifrah,Hervé Dombret,Guy Leverger,Éric Jourdan,Claude Preudhomme	150
8	Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia 2015 ·Clinical Cancer Research ·Stéphanie Poulain,Christophe Roumier,(unknown),Martin Figeac,Charles Herbaux,Guillemette Marot,(unknown),Elisabeth Bertrand,Sandrine Geffroy,Frédéric Leprêtre,Olivier Nibourel,(unknown),Eileen M. Boyle,Aline Renneville,Sabine Tricot,Agnès Daudignon,Bruno Quesnel,Patrick Duthilleul,Claude Preudhomme,Xavier Leleu	82
9	Genomic Landscape of CXCR4 Mutations in Waldenstrom's Macroglobulinemia 2014 ·Blood ·Stéphanie Poulain,Christophe Roumier,(unknown),Martin Figeac,Aurélie Caillault,Sandrine Geffroy,Olivier Nibourel,Frédéric Leprêtre,Agnès Daudignon,Sabine Tricot,Patrick Duthilleul,Claude Preudhomme,Xavier Leleu	1
10	MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome 2014 ·British Journal of Haematology ·Stéphanie Poulain,Eileen M. Boyle,Christophe Roumier,Hélène Demarquette,Mathieu Wémeau,Sandrine Geffroy,Charles Herbaux,Elisabeth Bertrand,Bénédicte Hivert,Louis Terriou,(unknown),(unknown),Claude Alain Maurage,Brigitte Onraed,Franck Morschhauser,Bruno Quesnel,Patrick Duthilleul,Claude Preudhomme,Xavier Leleu	48
11	Molecular Prognostic Factors in Acute Myeloid Leukemia (AML) Patients Receiving First Line Therapy with Azacytidine (AZA) 2014 ·Blood ·(unknown),Julie Gay,Céline Berthon,Lionel Adès,Jean Pierre Marolleau,Sandrine Geffroy,Isabelle Plantier,Alice Marceau‐Renaut,Nathalie Hélevaut,José Fernandes,(unknown),(unknown),Julien Labreuche,Olivier Nibourel,Christophe Roumier,Martin Figeac,Pierre Fenaux,Bruno Quesnel,Aline Renneville,Claude Preudhomme	2
12	Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations 2014 ·Blood ·Jean‐Baptiste Micol,Nicolas Duployez,Nicolas Boissel,Arnaud Petit,Sandrine Geffroy,Olivier Nibourel,Catherine Lacombe,Hélène Lapillonne,Pascaline Etancelin,Martin Figeac,Aline Renneville,Sylvie Castaigné,Guy Leverger,Norbert Ifrah,Hervé Dombret,Claude Preudhomme,Omar Abdel‐Wahab,Éric Jourdan	69
13	New-generation sequencing (NGS) in hematologic oncology laboratories 2013 ·Hématologie ·Alice Marceau‐Renaut,Aline Renneville,Olivier Nibourel,(unknown),(unknown),Céline Villenet,Sandrine Geffroy,Nathalie Hélevaut,Sabine Quief,(unknown),Nathalie Grardel,Aurélie Caillault,Nicolas Duployez,Thomas Boyer,Christophe Roumier,Frédéric Leprêtre,Meyling Cheok,Nicole Porchet,Martin Figeac,Claude Preudhomme	2
14	Association of TET2 Alterations with NPM1 Mutations and Prognostic Value in De Novo Acute Myeloid Leukemia (AML). 2009 ·Blood ·Olivier Nibourel,Olivier Kosmider,Meyling Cheok,Nicolas Boissel,Aline Renneville,N Philippe,Hervé Dombret,François Dreyfus,Bruno Quesnel,Sandrine Geffroy,Samuel Quentin,Catherine Roche‐Lestienne,Jean‐Michel Cayuela,Christophe Roumier,Pierre Fenaux,William Vainchenker,Olivier Bernard,Jean Soulier,Michaëla Fontenay,Claude Preudhomme	6
15	Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1–PRDM16 fusion in a case of progressive chronic myeloid leukemia: A complex chromosomal rearrangement of underestimated frequency in disease progression? 2008 ·Genes Chromosomes and Cancer ·(unknown),(unknown),Sélim Corm,Agnès Daudignon,Sandrine Geffroy,Sabine Quief,Céline Villenet,Jean‐Pierre Kerckaert,Jean-Luc Laı̈,Claude Preudhomme,Catherine Roche‐Lestienne	13
16	Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis 2007 ·Cancer Genetics and Cytogenetics ·Joris Andrieux,Catherine Roche‐Lestienne,Sandrine Geffroy,Christophe Desterke,Nathalie Grardel,Isabelle Plantier,Dominik Selleslag,Jean‐Loup Demory,Jean-Luc Laı̈,Xavier Leleu,Marie‐Caroline Le Bousse‐Kerdilès,Peter Vandenberghe	8
17	Cryptic 6p21.3 duplications and triplication involving HMGA1 partially masked by add 6p in four cases of myelodysplasia 2005 ·Cancer Genetics and Cytogenetics ·Joris Andrieux,Sandrine Geffroy,Chrystèle Bilhou‐Nabera,Brigitte Dupriez,(unknown),F Bauters,Jean Luc Laı̈,Nicole Dastugue	8
18	Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3) 2005 ·Genes Chromosomes and Cancer ·Frédéric Nicodème,Sandrine Geffroy,Massimo Conti,Bruno Delobel,Valérie Soenen,Nathalie Grardel,Henri Porte,Marie‐Christine Copin,Jean-Luc Laı̈,Joris Andrieux	14
19	The Human Fatty Acid Transport Protein-1 (SLC27A1; FATP-1) cDNA and Gene: Organization, Chromosomal Localization, and Expression 2000 ·Genomics ·Geneviève Martin,Masami Nemoto,Laurent Gelman,Sandrine Geffroy,Jamila Najïb,Jean‐Charles Fruchart,Peter Roevens,Bérengère de Martinville,Samir S. Deeb,Johan Auwerx	45
20	Localization of the Human OB Gene (OBS) to Chromosome 7q32 by Fluorescence in Situ Hybridization 1995 ·Genomics ·Sandrine Geffroy,Piet De Vos,Bart Staels,(unknown),Johan Auwerx,Bérengère de Martinville	24

About Sandrine Geffroy

Sandrine Geffroy is a scholar working on Hematology, Genetics and Cancer Research, having authored 32 papers that have together received 949 indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (18 papers), Chronic Myeloid Leukemia Treatments (6 papers) and Cancer Genomics and Diagnostics (6 papers). The work is most often cited by research in Hematology (578 citations), Genetics (419 citations) and Cancer Research (151 citations). Sandrine Geffroy has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Claude Preudhomme, Aline Renneville, Nicolas Boissel, Hervé Dombret, Olivier Nibourel, Bruno Quesnel, N Philippe, Martin Figeac, Catherine Roche‐Lestienne and Christophe Roumier. Their work appears in journals such as Journal of Clinical Oncology, Blood and Clinical Cancer Research.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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