Florence Coulet

7.9k citations

149 papers · 6.2k · 1 hit paper · h-index 41

Impact in

Genetics top 1%
- Vascular Anomalies and Treatments
- BRCA gene mutations in cancer
- Glioma Diagnosis and Treatment
Cancer Research top 2%
- Cancer Genomics and Diagnostics

Papers in

Pathology and Forensic Medicine 50
- Genetic factors in colorectal cancer 48
Cancer Research 26
- Cancer Genomics and Diagnostics 22

Co-authors: Florent Soubrier (33 shared papers)Marc Humbert (16 shared papers)David Montani (17 shared papers)Barbara Girerd (9 shared papers)Mélanie Eyries (21 shared papers)Olivier SITBON (9 shared papers)Gérald Simonneau (6 shared papers)Chrystelle Colas (21 shared papers)
Journals: Human Mutation (8 papers)Clinical Genetics (8 papers)European Respiratory Journal (6 papers)Journal of Medical Genetics (6 papers)European Journal of Human Genetics (5 papers)
Partner nations: France United States Germany

In The Last Decade

Florence Coulet

140 papers receiving 6.0k citations

Florence Coulet's Hit Papers

align trajectories log scale

Mechanisms and therapeutic implications of hypermutation in gliomas 2020 · 494 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2020 Nature

Peers

Countries citing papers authored by Florence Coulet

Since Specialization

Citations

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

Fields of papers citing papers by Florence Coulet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Florence Coulet, 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 Florence Coulet Line = papers co-authored together Florence Coulet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 149 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mechanisms and therapeutic implications of hypermutation in gliomas Nature ·Mehdi Touat, Yvonne Y. Li, Adam N. Boynton, Liam Flinn Spurr, Julian Bryan Iorgulescu, Craig L. Bohrson, Isidro Cortés‐Ciriano, Cristina Birzu Hit paper breakdown →	2020	494
2	EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension Nature Genetics ·Mélanie Eyries, David Montani, Barbara Girerd, Claire Perret, Anne Leroy, Christine Lonjou, Nadjim Chelghoum, Florence Coulet	2013	336
3	Mutations of the TGF-β type II receptorBMPR2 in pulmonary arterial hypertension Human Mutation ·Rajiv D. Machado, Micheala A. Aldred, Victoria H. James, Rachel E. Harrison, Bhakti Patel, Ed C. Schwalbe, Ekkehard Gruenig, Bart J. Janssen	2006	326
4	Clinical Outcomes of Pulmonary Arterial Hypertension in Patients Carrying an ACVRL1 ( ALK1 ) Mutation American Journal of Respiratory and Critical Care Medicine ·Barbara Girerd, David Montani, Florence Coulet, Benjamin Sztrymf, Azzeddine Yaici, Xavier Jaïs, David‐Alexandre Trégouët, Abílio Reis	2010	237
5	Clinical Outcomes of Pulmonary Arterial Hypertension in Carriers of BMPR2 Mutation American Journal of Respiratory and Critical Care Medicine ·Benjamin Sztrymf, Florence Coulet, Barbara Girerd, Azzedine Yaïci, Xavier Jaïs, Olivier SITBON, David Montani, Rogério Souza	2008	227
6	Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants Human Mutation ·Claude Houdayer, Virginie Caux‐Moncoutier, Sophie E. Krieger, Michel Barrois, Françoise Bonnet, Violaine Bourdon, Myriam Bronner, Monique Buisson	2012	199
7	Identification of Hypoxia-response Element in the Human Endothelial Nitric-oxide Synthase Gene Promoter Journal of Biological Chemistry ·Florence Coulet, Sophie Nadaud, Monique Agrapart, Florent Soubrier	2003	182
8	Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network Genetics in Medicine ·Gaëtan Lesca, Carla Olivieri, Nelly Burnichon, Fabio Pagella, Marie‐France Carette, Brigitte Gilbert‐Dussardier, Cyril Goizet, J. Roume	2007	180
9	Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies The Lancet ·Hanna Dêbiec, Jeroen Nauta, Florence Coulet, Mirjam van der Burg, Vincent Guigonis, Thierry Schurmans, Emile de Heer, Florent Soubrier	2004	174
10	Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension Human Mutation ·Talat Nasim, Takeshi Ogo, Mohammad Ejaz Ahmed, Rebecca A. Randall, Hasnin M. Chowdhury, Katie M.G. Snape, Teisha Y. Bradshaw, Laura Southgate	2011	145
11	CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study Journal of Medical Genetics ·Patrick R. Benusiglio, David Malka, Étienne Rouleau, Antoine De Pauw, Bruno Buecher, Catherine Noguès, Emmanuelle Fourme, Chrystelle Colas	2013	126
12	p53 Gene Status as a Predictor of Tumor Response to Induction Chemotherapy of Patients With Locoregionally Advanced Squamous Cell Carcinomas of the Head and Neck Journal of Clinical Oncology ·Stéphane Temam, Antoine Flahault, Sophie Périé, Guy Monceaux, Florence Coulet, P Callard, Jean‐François Bernaudin, Jean Lacau St Guily	2000	125
13	Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort Journal of Medical Genetics ·Noémie Lavoine, Chrystelle Colas, Martine Muleris, Sahra Bodo, Alex Duval, Natacha Entz‐Werlé, Florence Coulet, Odile Cabaret	2015	108
14	Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors Familial Cancer ·Isabelle Sourrouille-Gervais, Florence Coulet, Jérémie H. Lefèvre, Chrystelle Colas, Mélanie Eyries, Magali Svrcek, Armelle Bardier–Dupas, Yann R. Parc	2012	106
15	Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based ApproachVersusMolecular Screening The American Journal of Gastroenterology ·Catherine Julié, Christophe Trésallet, Antoine Brouquet, Céline Vallot, Ute S. Zimmermann, Emmanuel Mitry, François Radvanyi, Étienne Rouleau	2008	104
16	Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France Human Mutation ·Gaëtan Lesca, Henri Plauchu, Florence Coulet, Sylvain Lefèbvre, Ghislaine Plessis, Sylvie Odent, Sophie Rivière, Bruno Leheup	2004	100
17	Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents Gastroenterology ·Sahra Bodo, Chrystelle Colas, Olivier Buhard, Ada Collura, Julie Tinat, Noémie Lavoine, Agathe Guilloux, Alexandra Chalastanis	2015	89
18	Discordance between immunochemistry of mismatch repair proteins and molecular testing of microsatellite instability in colorectal cancer ESMO Open ·Astrid Guyot d’Asnières de Salins, Gaëlle Tachon, Romain Cohen, L. Karayan-Tapon, Audelaure Junca, É. Frouin, Julie Godet, Camille Evrard	2021	89
19	Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension Nature Genetics ·Marine Germain, Mélanie Eyries, David Montani, Odette Poirier, Barbara Girerd, Peter Dorfmüller, Florence Coulet, Sophie Nadaud	2013	87
20	Droplet digital PCR of circulating tumor cells from colorectal cancer patients can predict KRAS mutations before surgery Molecular Oncology ·Jérôme Alexandre Denis, Alexia Patroni, Erell Guillerm, Dominique Pépin, Naoual Benali-Furet, Janine Wechsler, Gilles Manceau, Maguy Bernard	2016	87

About Florence Coulet

Florence Coulet is a scholar working on Pathology and Forensic Medicine, Cancer Research, Oncology, Genetics and Pulmonary and Respiratory Medicine, having authored 149 papers that have together received 6.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (48 papers), Cancer Genomics and Diagnostics (22 papers), Pulmonary Hypertension Research and Treatments (19 papers), BRCA gene mutations in cancer (19 papers), DNA Repair Mechanisms (13 papers), Colorectal Cancer Treatments and Studies (10 papers), Vascular Anomalies and Treatments (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). The work is most often cited by research in Genetics (1.1k citations), Cancer Research (1.0k citations), Pathology and Forensic Medicine (1.3k citations), Pulmonary and Respiratory Medicine (2.1k citations) and Oncology (1.0k citations). Florence Coulet has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Florent Soubrier, Marc Humbert, David Montani, Barbara Girerd, Mélanie Eyries, Olivier SITBON, Gérald Simonneau, Chrystelle Colas, Sophie Nadaud and Benjamin Sztrymf. Their work appears in journals such as Human Mutation, Clinical Genetics, European Respiratory Journal, Journal of Medical Genetics and European Journal of Human Genetics.

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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Florence Coulet's Hit Papers

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