Céline Garrec

739 citations
28 papers · 532 · h-index 10

Impact in

  • Genetics top 10%
    • Hemoglobinopathies and Related Disorders
    • Myeloproliferative Neoplasms: Diagnosis and Treatment
    • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Nephrology top 10%
    • Renal Diseases and Glomerulopathies

Papers in

  • Genetics 11
    • Myeloproliferative Neoplasms: Diagnosis and Treatment 7
    • BRCA gene mutations in cancer 4
    • Hemoglobinopathies and Related Disorders 4
  • Cancer Research 8
    • Cancer Genomics and Diagnostics 4
    • Cancer, Hypoxia, and Metabolism 4
Co-authors
Stéphane Bezieau (10 shared papers)Alain Stépanian (2 shared papers)Paul Coppo (2 shared papers)Pierre Boisseau (2 shared papers)Agnès Veyradier (2 shared papers)Yahsou Delmas (2 shared papers)Lionel Galicier (1 shared paper)Eric Rondeau (1 shared paper)
Journals
Blood (6 papers)Haematologica (4 papers)New England Journal of Medicine (1 paper)npj Genomic Medicine (1 paper)The American Journal of Human Genetics (1 paper)
Partner nations
FranceSwitzerlandUnited Kingdom

In The Last Decade

Céline Garrec

27 papers receiving 526 citations

Peers

Céline Garrec
Comparison fields: 5 of 44
  • Genetics 174
  • Nephrology 95
  • Hematology 138
  • Immunology 226
  • Cancer Research 68
Replace Yiannis Athanasiou with:
Yiannis Athanasiou Cyprus
Michela Faleschini Italy
Federica Banterla Italy
WH Kane United States
Tiina M. Järvinen Finland
Ashley A. Basiorka United States
Kazuaki Yokoyama Japan
Niv Pencovich Israel
J. Maciejewski United States
DV Faller United States
Céline Garrec relative to Yiannis Athanasiou Cyprus Yiannis Athanasiou's profile →
Citations per field
00.5×2×3.2×
Yiannis Athanasiou · 1×
Citations per year

Countries citing papers authored by Céline Garrec

Since Specialization
Citations

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

Fields of papers citing papers by Céline Garrec

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura
Blood ·Marie Moatti-Cohen, Céline Garrec, Martine Wolf, Pierre Boisseau, Lionel Galicier, Élie Azoulay, Alain Stépanian, Yahsou Delmas
2012195
2
Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease
Blood ·Marion Lenglet, Florence Robriquet, Klaus Schwarz, Carme Camps, Anne Couturier, David Hoogewijs, Alexandre Buffet, Samantha J.L. Knight
201875
3
BRCA Share: A Collection of Clinical BRCA Gene Variants
Human Mutation ·Christophe Béroud, Stanley I. Letovsky, Corey D. Braastad, Sandrine M. Caputo, Olivia Beaudoux, Yves Jean Bignon, Brigitte Bressac–de Paillerets, Myriam Bronner
201651
4
ADAMTS13 Gene Mutations Influence ADAMTS13 Conformation and Disease Age-Onset in the French Cohort of Upshaw–Schulman Syndrome
Thrombosis and Haemostasis ·Bérangère S. Joly, Pierre Boisseau, Elien Roose, Alain Stépanian, Nathalie Biebuyck, François Provôt, Yahsou Delmas, Céline Garrec
201846
5
Increased incidence of germline PIEZO1 mutations in individuals with idiopathic erythrocytosis
Blood ·Mathilde Filser, Muriel Giansily‐Blaizot, Mélanie Grenier, David Monedero Alonso, Guillaume Bouyer, Laurent Pérès, Stéphane Égée, Bernard Aral
202027
6
Deep Learning for Detecting BRCA Mutations in High-Grade Ovarian Cancer Based on an Innovative Tumor Segmentation Method From Whole Slide Images
Modern Pathology ·Raphaël Bourgade, Noémie Rabilloud, Tanguy Perennec, Thierry Pécot, Céline Garrec, Alexis F. Guédon, Capucine Delnatte, Stéphane Bezieau
202326
7
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach
The American Journal of Human Genetics ·Sandrine M. Caputo, Lisa Golmard, Mélanie Léoné, Francesca Damiola, Marine Guillaud-Bataille, Françoise Révillion, Etienne Rouleau, Nicolas Derive
202122
8
High HFE mutation incidence in idiopathic erythrocytosis
British Journal of Haematology ·Bénédicte Burlet, Valentin Bourgeois, Céline Buriller, Bernard Aral, Fabrice Airaud, Céline Garrec, Stéphane Bezieau, Betty Gardie
201813
9
Low incidence of EPOR mutations in idiopathic erythrocytosis
Haematologica ·Mathilde Filser, Bernard Aral, Fabrice Airaud, Aurélie Chauveau, Aisha A. K. Bruce, Yann Polfrit, Anne Thiébaut, Martin Gauthier
202012
10
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis
Haematologica ·Marine Delamare, Amandine Le Roy, Mathilde Pacault, Loïc Schmitt, Céline Garrec, Nada Maaziz, Matti Myllykoski, Antoine Rimbert
202310
11
Performance of multiplicom's BRCA MASTR Dx kit on the detection of BRCA1 and BRCA2 mutations in fresh frozen ovarian and breast tumor samples
Oncotarget ·Cindy Badoer, Céline Garrec, Dirk Goossens, Gillian Ellison, JOHN S. MILLS, Mélina Dzial, Hakim El Housni, Sarah Berwouts
20169
12
Comprehensive in silico and functional studies for classification of EPAS1/HIF2A genetic variants identified in patients with erythrocytosis
Haematologica ·Valéna Karaghiannis, Darko Maric, Céline Garrec, Nada Maaziz, Alexandre Buffet, Loïc Schmitt, Vincent Antunes, Fabrice Airaud
20238
13
Diagnosis of exon 12‐positive polycythemia vera rescued by NGS
Clinical Case Reports ·Antoine Geay, Bernard Aral, Valentin Bourgeois, Pauline Martin, Fabrice Airaud, Céline Garrec, Stéphane Bezieau, Betty Gardie
20207
14
Gene panel sequencing in idiopathic erythrocytosis
Haematologica ·François Girodon, Fabrice Airaud, Céline Garrec, Stéphane Bezieau, Betty Gardie
20165
15
TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing
Cancers ·Fabienne Lesueur, Séverine Eon‐Marchais, Sarah Bonnet-Boissinot, Juana Beauvallet, Marie‐Gabrielle Dondon, Lisa Golmard, Etienne Rouleau, Céline Garrec
20215
16
Absence of CALR Mutations in Idiopathic Erythrocytosis Patients with Low Serum Erythropoietin Levels
Acta Haematologica ·Mark Alexander Catherwood, Amy Graham, Robert J.G. Cuthbert, Céline Garrec, Betty Gardie, François Girodon, Sophie Laird, Nicholas C.P. Cross
20183
17
Sensitive detection methods are key to identify secondary EGFR c.2369C>T p.(Thr790Met) in non-small cell lung cancer tissue samples
BMC Cancer ·Cleo Keppens, Els M.C. Dequeker, Étienne Rouleau, Nils ’t Hart, Lukas Bubendorf, Kelly Dufraing, Céline Garrec, Paul Guéguen
20203
18
Identification of Hepatic-like EPO as a Cause of Polycythemia
New England Journal of Medicine ·Laurent Martin, Darko Maric, Salam Idriss, Marine Delamare, Amandine Le Roy, Nada Maaziz, Amandine Caillaud, Karim Si‐Tayeb
20253
19
Polyglobulie rare par mutation du gène EGLN1 : à propos d’un cas et revue de la littérature
La Revue de Médecine Interne ·A. Bonnin, Betty Gardie, François Girodon, Fabrice Airaud, Céline Garrec, Stéphane Bezieau, Guillaume Vignon, Philippe Mottaz
20202
20
A de novo pathogenic variant in the MSH6 gene in a 52 years-old woman
Familial Cancer ·Elise Pierre-Noël, Fabrice Airaud, Estelle Cauchin, Céline Garrec, Ricordeau Ingrid, Clémence Michon, Olivier Kerdraon, Stéphane Bezieau
20212

About Céline Garrec

Céline Garrec is a scholar working on Genetics, Cancer Research, Hematology, Physiology and Genetics, having authored 28 papers that have together received 532 indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (8 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (7 papers), Cancer Genomics and Diagnostics (4 papers), BRCA gene mutations in cancer (4 papers), Hemoglobinopathies and Related Disorders (4 papers), Cancer, Hypoxia, and Metabolism (4 papers), Acute Myeloid Leukemia Research (3 papers) and Kruppel-like factors research (3 papers). The work is most often cited by research in Genetics (174 citations), Nephrology (95 citations), Hematology (138 citations), Immunology (226 citations) and Cancer Research (68 citations). Céline Garrec has collaborated with scholars based in France, Switzerland and United Kingdom. Frequent co-authors include Stéphane Bezieau, Alain Stépanian, Paul Coppo, Pierre Boisseau, Agnès Veyradier, Yahsou Delmas, Lionel Galicier, Eric Rondeau, Martine Wolf and Élie Azoulay. Their work appears in journals such as Blood, Haematologica, New England Journal of Medicine, npj Genomic Medicine and The American 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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