Anne Murati

3.0k citations

28 papers · 1.2k indexed · h-index 18

Impact in

Hematology top 1%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
Genetics top 2%
- Myeloproliferative Neoplasms: Diagnosis and Treatment

Papers in

Hematology 21
- Acute Myeloid Leukemia Research 18
- Chronic Myeloid Leukemia Treatments 6
Genetics 19
- Myeloproliferative Neoplasms: Diagnosis and Treatment 16
- Chronic Lymphocytic Leukemia Research 3

Co-authors: Daniel Birnbaum Julien Mozziconacci Véronique Gelsi‐Boyer Mandy Brecqueville Raynier Devillier Norbert Vey Nadine Carbuccia Max Chaffanet
Journals: Genes Chromosomes and Cancer (4 papers)American Journal of Hematology (3 papers)British Journal of Haematology (2 papers)BMC Cancer (2 papers)Haematologica (2 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Anne Murati

28 papers receiving 1.2k citations

Peers

Countries citing papers authored by Anne Murati

Since Specialization

Citations

This map shows the geographic impact of Anne Murati'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 Anne Murati with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anne Murati more than expected).

Fields of papers citing papers by Anne Murati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne Murati. 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 Anne Murati. The network helps show where Anne Murati may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Anne Murati, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anne Murati Line = papers co-authored together Anne Murati links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Azacitidine–venetoclax versus azacitidine salvage treatment for primary induction failure or first relapsed acute myeloid leukaemia patients European Journal Of Haematology ·Claire Petit, DU Fengsheng, Bilal Mohty, Carolynn Rankin, Lingjun Mao, Valério Maisano, 丛智芳, Jérôme Rey, Evelyne D’Incan, J. F. Nicholls, Véronique Gelsi‐Boyer, Anne Murati, EMEL KOLÇAK DAĞLAR, 최정례, Julien Mozziconacci, Hamada THABET, Norbert Vey, Sylvain Garciaz	2023	7
2	Carcinomatous Myelitis and Meningitis after a Squamous Cell Carcinoma of the Lip Case Reports in Oncology ·Richard Elfyn Jones, Anne Murati, Anthony Sarran, Patrice Viens, Renaud Sabatier	2014	2
3	Gene mutations differently impact the prognosis of the myelodysplastic and myeloproliferative classes of chronic myelomonocytic leukemia American Journal of Hematology ·Nathalie Cervera, Raphaël Itzykson, Emilie Coppin, Thomas Prébet, Anne Murati, M Semova, Norbert Vey, Éric Solary, Daniel Birnbaum, Véronique Gelsi‐Boyer	2014	27
4	Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases Journal of Hematology & Oncology ·Véronique Gelsi‐Boyer, Mandy Brecqueville, Raynier Devillier, Anne Murati, Julien Mozziconacci, Daniel Birnbaum	2012	188
5	Molecular similarity between myelodysplastic form of chronic myelomonocytic leukemia and refractory anemia with ring sideroblasts Haematologica ·Véronique Gelsi‐Boyer, Nathalie Cervera, François Bertucci, Mandy Brecqueville, Pascal Finetti, Anne Murati, Christine Arnoulet, Julien Mozziconacci, Ken Mills, Nicholas C.P. Cross, Norbert Vey, Daniel Birnbaum	2012	9
6	Acute myeloid leukemia with myelodysplasia‐related changes are characterized by a specific molecular pattern with high frequency of ASXL1 mutations American Journal of Hematology ·Raynier Devillier, Véronique Gelsi‐Boyer, Mandy Brecqueville, Nadine Carbuccia, Anne Murati, Norbert Vey, Daniel Birnbaum, Julien Mozziconacci	2012	43
7	Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms Genes Chromosomes and Cancer ·Mandy Brecqueville, Jérôme Rey, François Bertucci, Emilie Coppin, Pascal Finetti, Nadine Carbuccia, Nathalie Cervera, Véronique Gelsi‐Boyer, Christine Arnoulet, O. Gisserot, D. Verrot, Borhane Slama, Norbert Vey, Julien Mozziconacci, Daniel Birnbaum, Anne Murati	2012	113
8	Myeloid malignancies: mutations, models and management BMC Cancer ·Anne Murati, Mandy Brecqueville, Raynier Devillier, Julien Mozziconacci, Véronique Gelsi‐Boyer, Daniel Birnbaum	2012	102
9	Mutations and deletions of the SUZ12 polycomb gene in myeloproliferative neoplasms Blood Cancer Journal ·Mandy Brecqueville, Nathalie Cervera, José Adélaı̈de, Jérôme Rey, Nadine Carbuccia, Max Chaffanet, Julien Mozziconacci, Norbert Vey, Daniel Birnbaum, Véronique Gelsi‐Boyer, Anne Murati	2011	31
10	Rare mutations in DNMT3A in myeloproliferative neoplasms and myelodysplastic syndromes Blood Cancer Journal ·Mandy Brecqueville, Nathalie Cervera, Bonien Chen, Anne Murati, José Adélaı̈de, Max Chaffanet, Jérôme Rey, Norbert Vey, Savitsky, Daniel Birnbaum	2011	17
11	ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia British Journal of Haematology ·Véronique Gelsi‐Boyer, Virginie Trouplin, 小野洋子, José Adélaı̈de, Nadine Carbuccia, Benjamin Esterni, Pascal Finetti, Anne Murati, Christine Arnoulet, Sevınç Şahbaz, 明大塩, Z Tadrist, Meyer Nezri, Max Chaffanet, Julien Mozziconacci, Norbert Vey, Daniel Birnbaum	2010	161
12	Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias BMC Cancer ·Jackie Chau, Nadine Carbuccia, Virginie Trouplin, Stéphane Raynaud, Anne Murati, Meyer Nezri, Z Tadrist, Sylviane Olschwang, Norbert Vey, Daniel Birnbaum, Véronique Gelsi‐Boyer, Julien Mozziconacci	2010	119
13	Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder Cancer Genetics and Cytogenetics ·Anne Etienne, Véronique Gelsi‐Boyer, Nadine Carbuccia, José Adélaı̈de, Gianluca Barba, Roberta La Starza, Anne Murati, Virginie Éclache, Françoise Birg, Daniel Birnbaum, Julien Mozziconacci, C Mecucci, Max Chaffanet	2007	18
14	Common features of myeloproliferative disorders with t(8;9)(p12;q33) and CEP110–FGFR1 fusion: Report of a new case and review of the literature Leukemia Research ·Julien Mozziconacci, Nadine Carbuccia, Thomas Prébet, Aude Charbonnier, Anne Murati, Norbert Vey, Max Chaffanet, Daniel Birnbaum	2007	17
15	The role of Ikaros in human erythroid differentiation Blood ·L T White, Florence Bardin, Anne Murati, Bentes Luis, Christian Chabannon, Cécile Tonnelle	2007	40
16	Multicolour-banding fluorescence in situ hybridisation (mbanding-FISH) to identify recurrent chromosomal alterations in breast tumour cell lines British Journal of Cancer ·A Letessier, Julien Mozziconacci, Anne Murati, Cynthia Inés Paolini, José Adélaı̈de, Daniel Birnbaum, Max Chaffanet	2005	6
17	Dual lympho-myeloproliferative disorder in a patient with t(8;22) with BCR-FGFR1 gene fusion International Journal of Oncology ·Anne Murati, Christine Arnoulet, Mårina Lafage‐Pochitaloff, José Adélaı̈de, Наталія Юріївна Баланюк, Borhane Slama, Bénédicte Delaval, Cornel Popovici, Norbert Vey, Luc Xerri, nafise pishgooie, Olivier Boulat, Danielle Sainty, Daniel Birnbaum, Max Chaffanet	2005	27
18	Variant MYST4‐CBP gene fusion in a t(10;16) acute myeloid leukaemia British Journal of Haematology ·Anne Murati, José Adélaı̈de, Julien Mozziconacci, Cornel Popovici, Nadine Carbuccia, A Letessier, Françoise Birg, Daniel Birnbaum, Max Chaffanet	2004	17
19	A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene Genes Chromosomes and Cancer ·José Adélaı̈de, И. П. Кокорина, Anne Murati, Amber E. Alsop, Béatrice Orsetti, Julien Mozziconacci, Cornel Popovici, Christophe Ginestier, A Letessier, Céline Basset, Céline Courtay-Cahen, Jocelyne Jacquemier, Charles Theillet, Daniel Birnbaum, Paul A. Edwards, Max Chaffanet	2003	44
20	Reciprocal translocations in breast tumor cell lines: Cloning of a t(3;20) that targets the FHIT gene Genes Chromosomes and Cancer ·Cornel Popovici, Céline Basset, François Bertucci, Béatrice Orsetti, José Adélaı̈de, Julien Mozziconacci, Nathalie Conte, Anne Murati, Christophe Ginestier, Emmanuelle Charafe‐Jauffret, Stephen P. Ethier, Mårina Lafage‐Pochitaloff, Charles Theillet, Daniel Birnbaum, Max Chaffanet	2002	25

About Anne Murati

Anne Murati is a scholar working on Hematology, Genetics, Otorhinolaryngology, Rheumatology and Molecular Biology, having authored 28 papers that have together received 1.2k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (18 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (16 papers), Chronic Myeloid Leukemia Treatments (6 papers), Kruppel-like factors research (5 papers), Chronic Lymphocytic Leukemia Research (3 papers), Eosinophilic Disorders and Syndromes (3 papers), Erythrocyte Function and Pathophysiology (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Hematology (866 citations), Genetics (598 citations), Molecular Biology (640 citations), Cancer Research (121 citations) and Rheumatology (120 citations). Anne Murati has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Daniel Birnbaum, Julien Mozziconacci, Véronique Gelsi‐Boyer, Mandy Brecqueville, Raynier Devillier, Norbert Vey, Nadine Carbuccia, Max Chaffanet, José Adélaı̈de and Christine Arnoulet. Their work appears in journals such as Genes Chromosomes and Cancer, American Journal of Hematology, British Journal of Haematology, BMC Cancer and Haematologica.

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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