Betty Gardie

3.1k citations

36 papers · 1.3k indexed · h-index 15

Cancer Research top 5%
- Cancer, Hypoxia, and Metabolism 12
Genetics top 5%
- Myeloproliferative Neoplasms: Diagnosis and Treatment 8
- Hemoglobinopathies and Related Disorders 6
Hematology top 10%
- Acute Myeloid Leukemia Research 5
Molecular Biology top 10%
- Epigenetics and DNA Methylation 5
- Kruppel-like factors research 5
Endocrinology, Diabetes and Metabolism top 10%
Physiology
- Erythrocyte Function and Pathophysiology 8
Pulmonary and Respiratory Medicine
- Renal cell carcinoma treatment 4

Co-authors: Richard J. Kahnoski Sophie Gad François Sigaux Jean‐Michel Cayuela M Leporrier Romain Carcenac Jean Feunteun Jacques Pouysségur
Cited by: Cancer Research Genetics Hematology
Journals: New England Journal of Medicine (1 paper)SHILAP Revista de lepidopterología (1 paper)Blood (7 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Betty Gardie

34 papers receiving 1.3k citations

Peers

Countries citing papers authored by Betty Gardie

Since Specialization

Citations

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

Fields of papers citing papers by Betty Gardie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	EGLN1 mutations in Cis can induce congenital erythrocytosis with thromboses by increasing protein instability British Journal of Haematology ·Serge Carillo,Marine Delamare,Laurent Henry,Nada Maaziz,Hana Safraou,Betty Gardie,Thierry Lavabre‐Bertrand	2025	0
2	Germline JAK2 E846D Substitution as the Cause of Erythrocytosis? Genes ·Nada Maaziz,Céline Garrec,Fabrice Airaud,Victor Bobée,Nathalie Contentin,Émilie Cayssials,Antoine Rimbert,Bernard Aral,Stéphane Bezieau,Betty Gardie,François Girodon	2023	2
3	Update of the UMD-VHL database: classification of 164 challenging variants based on genotype–phenotype correlation among 605 entries Journal of Medical Genetics ·Grégory Mougel,Amira Mohamed,Nelly Burnichon,Sophie Giraud,Pascal Pigny,Brigitte Bressac–de Paillerets,Delphine Mirebeau‐Prunier,Alexandre Buffet,Frédérique Savagner,Pauline Romanet,Yannick Arlot,Betty Gardie,Anne‐Paule Gimenez‐Roqueplo,Christophe Béroud,Richard J. Kahnoski,Anne Barlier	2023	2
4	Clinical and molecular diagnosis of hereditary and idiopathic erythrocytosis Hématologie ·Betty Gardie,Nada Maaziz,François Girodon	2022	0
5	FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells STAR Protocols ·Amandine Caillaud,Antoine Lévêque,Aurélie Thedrez,Aurore Girardeau,Robin Canac,Lise Bray,Manon Baudic,Julien Barc,Nathalie Gaborit,Guillaume Lamirault,Betty Gardie,Salam Idriss,Antoine Rimbert,Cédric Le May,Bertrand Cariou,Karim Si‐Tayeb	2022	8
6	Germline mutation in the NBR1 gene involved in autophagy detected in a family with renal tumors Cancer Genetics ·Florine Adolphe,Sophie Ferlicot,Virginie Verkarre,Katia Posseme,Sophie Couvé,Pauline Garnier,Nathalie Droin,Marc Deloger,Bastien Job,Sophie Giraud,Brigitte Bressac–de Paillerets,Betty Gardie,Richard J. Kahnoski,Flore Renaud,Sophie Gad	2021	7
7	Involvement of PBRM1 in VHL disease‑associated clear cell renal cell carcinoma and its putative relationship with the HIF pathway Oncology Letters ·Sophie Gad,Gwénaël Le Teuff,Baptiste Nguyen,Virginie Verkarre,Véronique Duchatelle,Vincent Molinié,Katia Posseme,Benjamin Grandon,Mélanie Da Costa,Bastien Job,Guillaume Meurice,Nathalie Droin,Arnaud Méjean,Sophie Couvé,Flore Renaud,Betty Gardie,Bin Tean Teh,Richard J. Kahnoski,Sophie Ferlicot	2021	7
8	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,G Vignon,Philippe Mottaz,J Labrousse,Franck Lellouche	2020	1
9	Absence of <b><i>CALR</i></b> Mutations in Idiopathic Erythrocytosis Patients with Low Serum Erythropoietin Levels Acta Haematologica ·Mark Catherwood,Amy Graham,Robert J.G. Cuthbert,Céline Garrec,Betty Gardie,François Girodon,Sophie Laird,Nicholas C.P. Cross,Mary Frances McMullin	2018	3
10	Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers Clinical Genetics ·Marie Müller,Sophie Ferlicot,Marine Guillaud‐Bataille,Gwénaël Le Teuff,Catherine Genestie,Scott DeVeaux,Abdelhamid Slama,Nicolas Poulalhon,B. Escudier,Laurence Albigès,Nadem Soufir,Avril Mf,Betty Gardie,C. Saldana,Yves Allory,Anne‐Paule Gimenez‐Roqueplo,Brigitte Bressac–de Paillerets,Richard J. Kahnoski,Patrick R. Benusiglio	2017	93
11	Update on hypoxia-inducible factors and hydroxylases in oxygen regulatory pathways: from physiology to therapeutics PubMed ·Peter J. Ratcliffe,Peppi Koivunen,Johanna Myllyharju,Jiannis Ragoussis,Judith V.M.G. Bovée,Ines Batinić‐Haberle,Claire Vinatier,Valérie Trichet,Florence Robriquet,Lisa Oliver,Betty Gardie	2017	27
12	Pathogenesis of Myeloproliferative Neoplasms: Role and Mechanisms of Chronic Inflammation Mediators of Inflammation ·Sylvie Hermouet,Edith Bigot‐Corbel,Betty Gardie	2015	76
13	The role of PHD2 mutations in the pathogenesis of erythrocytosis PubMed ·Betty Gardie,Melanie J. Percy,David Hoogewijs,Rasheduzzaman Chowdhury,Celeste Bento,Mary Frances McMullin,Christopher J. Schofield,Frank S. Lee,Richard J. Kahnoski,Patrick R. Arsenault,Helena Almeida,Joanne Ewing,Frédéric Lambert	2014	37
14	Identification of TET1 Partners That Control Its DNA-Demethylating Function Genes & Cancer ·Pierre‐François Cartron,Arulraj Nadaradjane,Fiona Le Pape,Lisenn Lalier,Betty Gardie,François M. Vallette	2013	58
15	Von Hippel–Lindau: How a rare disease illuminates cancer biology Seminars in Cancer Biology ·Richard J. Kahnoski,Betty Gardie,Sophie Couvé,Sophie Gad	2012	73
16	Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia Haematologica ·Christophe Ladroue,David Hoogewijs,Sophie Gad,Romain Carcenac,Federica Storti,Michel Barrois,Anne‐Paule Gimenez‐Roqueplo,M Leporrier,Nicole Casadevall,Olivier Hermine,Jean‐Jacques Kiladjian,André Baruchel,F. Fakhoury,Brigitte Bressac–de Paillerets,Jean Feunteun,Nathalie M. Mazure,Jacques Pouysségur,Roland H. Wenger,Richard J. Kahnoski,Betty Gardie	2011	38
17	An Antioxidant Response Phenotype Shared between Hereditary and Sporadic Type 2 Papillary Renal Cell Carcinoma Cancer Cell ·Aikseng Ooi,Jing-Chii Wong,David Petillo,Douglas H. Roossien,Victoria Perrier-Trudova,Douglas Whitten,Bernice H. Wong,Min-Han Tan,Zhongfa Zhang,Ximing J. Yang,Ming Zhou,Betty Gardie,Vincent Molinié,Richard J. Kahnoski,Puay Hoon Tan,Bin Tean Teh,Kyle A. Furge	2011	314
18	PHD2 Mutation and Congenital Erythrocytosis with Paraganglioma New England Journal of Medicine ·Charline Ladroue,Romain Carcenac,M Leporrier,Sophie Gad,C. Le Hello,Françoise Galateau-Sallé,Jean Feunteun,Jacques Pouysségur,Richard J. Kahnoski,Betty Gardie	2008	242
19	A study of 36 unrelated cases with pure erythrocytosis revealed three new mutations in the erythropoietin receptor gene Haematologica ·Maha Al-Sheikh,Elodie Mazurier,Betty Gardie,Nicole Casadevall,Frédéric Galactéros,Michel Goossens,H. Wajcman,Claude Préhu,Valérie Ugo	2008	22
20	Raf-1-induced growth arrest in human mammary epithelial cells is p16-independent and is overcome in immortal cells during conversion Oncogene ·Catherine L. Olsen,Betty Gardie,Paul Yaswen,Martha R. Stampfer	2002	71

About Betty Gardie

Betty Gardie is a scholar working on Genetics, Cancer Research and Aging, having authored 36 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cancer, Hypoxia, and Metabolism (12 papers), Erythrocyte Function and Pathophysiology (8 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers), Hemoglobinopathies and Related Disorders (6 papers), Acute Myeloid Leukemia Research (5 papers), Epigenetics and DNA Methylation (5 papers), Kruppel-like factors research (5 papers) and Renal cell carcinoma treatment (4 papers). The work is most often cited by research in Cancer Research (516 citations), Genetics (172 citations) and Hematology (139 citations). Betty Gardie has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Richard J. Kahnoski, Sophie Gad, François Sigaux, Jean‐Michel Cayuela, M Leporrier, Romain Carcenac, Jean Feunteun, Jacques Pouysségur, Edith Bigot‐Corbel and Sylvie Hermouet. Their work appears in journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Blood.

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