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Anne-Paule Gimenez-Roqueplo

Anne-Paule Gimenez-Roqueplo

D-Index & Metrics

Medicine

D-Index
79
Citations
29398
World Ranking
17401
National Ranking
579

Overview

Anne-Paule Gimenez-Roqueplo is affiliated with Université Paris Cité in France and has a substantial publication record primarily in the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their research focuses extensively on endocrinology, cancer research, surgery, molecular biology, and genetics.

Their work centers on several key topics including:

  • Adrenal and Paraganglionic Tumors
  • Cancer, Hypoxia, and Metabolism
  • Hormonal Regulation and Hypertension
  • Pituitary Gland Disorders and Treatments
  • Neuroblastoma Research and Treatments
  • Metabolomics and Mass Spectrometry Studies
  • Mitochondrial Function and Pathology

Frequent co-authors contributing alongside Anne-Paule Gimenez-Roqueplo include Laurence Amar, Nelly Burnichon, Alexandre Buffet, Judith Favier, and Mercedes Robledo.

Most of their publications appear in the following venues, indicating a focused contribution to endocrinology and clinical sciences:

  • The Journal of Clinical Endocrinology & Metabolism
  • Annales d Endocrinologie
  • Nature Reviews Endocrinology
  • Journal of the Endocrine Society
  • Endocrine Related Cancer

Recent notable publications by Anne-Paule Gimenez-Roqueplo cover a range of topics related to genetic studies and clinical management of pheochromocytoma and paraganglioma, reflecting the integration of genetics with clinical endocrinology:

  • Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension, 2020, Journal of Hypertension
  • An overview of 20 years of genetic studies in pheochromocytoma and paraganglioma, 2020, Best Practice & Research Clinical Endocrinology & Metabolism
  • International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers, 2021, Nature Reviews Endocrinology
  • TET-Mediated Hypermethylation Primes SDH-Deficient Cells for HIF2α-Driven Mesenchymal Transition, 2020, Cell Reports
  • Sino-European Differences in the Genetic Landscape and Clinical Presentation of Pheochromocytoma and Paraganglioma, 2020, The Journal of Clinical Endocrinology & Metabolism

Anne-Paule Gimenez-Roqueplo's work involves cross-disciplinary approaches integrating genetics, molecular biology, and clinical endocrinology to address complex diseases related to adrenal and neuroendocrine tumors. Their prolific output and collaboration network highlight an active role in advancing knowledge on hormonal regulation, genetic mutations, and their implications for diagnosis and treatment.

Best Publications

  • Oncogenic Signaling Pathways in The Cancer Genome Atlas

    Francisco Sanchez-Vega;Marco Mina;Joshua Armenia;Walid K. Chatila

  • Pheochromocytoma and paraganglioma: An endocrine society clinical practice guideline

    Jacques W.M. Lenders;Quan Yang Duh;Graeme Eisenhofer;Anne Paule Gimenez-Roqueplo

  • Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer.

    Katherine A. Hoadley;Christina Yau;Christina Yau;Toshinori Hinoue;Denise M. Wolf

  • Comprehensive Characterization of Cancer Driver Genes and Mutations.

    Matthew H Bailey;Collin Tokheim;Eduard Porta-Pardo;Sohini Sengupta

  • Genomic and Functional Approaches to Understanding Cancer Aneuploidy

    Alison M. Taylor;Alison M. Taylor;Juliann Shih;Gavin Ha;Gavin Ha;Galen F. Gao

  • A Call to Action and a Lifecourse Strategy to Address the Global Burden of Raised Blood Pressure on Current and Future Generations: The Lancet Commission on Hypertension

    Michael H. Olsen;Michael H. Olsen;Sonia Y. Angell;Samira Asma;Pierre Boutouyrie

  • Pathogenic Germline Variants in 10,389 Adult Cancers

    Kuan-Lin Huang;R Jay Mashl;Yige Wu;Deborah I Ritter

  • Pheochromocytoma: recommendations for clinical practice from the First International Symposium

    Karel Pacak;Graeme Eisenhofer;Håkan Ahlman;Stefan R Bornstein

  • Genetic Testing in Pheochromocytoma or Functional Paraganglioma

    Laurence Amar;Jérôme Bertherat;Eric Baudin;Christiane Ajzenberg

  • SDHA is a tumor suppressor gene causing paraganglioma

    Nelly Burnichon;Jean-Jacques Brière;Rossella Libé;Laure Vescovo

  • SDH mutations establish a hypermethylator phenotype in paraganglioma.

    Eric Letouzé;Cosimo Martinelli;Cosimo Martinelli;Céline Loriot;Céline Loriot;Nelly Burnichon;Nelly Burnichon

  • Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma syndromes.

    Diana E. Benn;Anne Paule Gimenez-Roqueplo;Jennifer R. Reilly;Jérôme Bertherat

  • An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.

    Francien H van Nederveen;José Gaal;Judith Favier;Esther Korpershoek

  • Mutations in the SDHB Gene Are Associated with Extra-adrenal and/or Malignant Phaeochromocytomas

    Anne-Paule Gimenez-Roqueplo;Judith Favier;Pierre Rustin;Claudine Rieubland

  • Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

    Lauren Fishbein;Lauren Fishbein;Ignaty Leshchiner;Ignaty Leshchiner;Vonn Walter;Vonn Walter;Ludmila Danilova;Ludmila Danilova

  • Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD.

    Barbara Pasini;Sarah R. McWhinney;Thalia Bei;Ludmila Matyakhina

  • Erratum: Comprehensive Characterization of Cancer Driver Genes and Mutations (ARTICLE (2018) 173(2) (371–385), (S009286741830237X), (10.1016/j.cell.2018.02.060))

    Matthew H. Bailey;Collin Tokheim;Eduard Porta-Pardo;Sohini Sengupta

  • The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway.

    Anne-Paule Gimenez-Roqueplo;Judith Favier;Pierre Rustin;Jean-Jacques Mourad

  • Succinate Dehydrogenase B Gene Mutations Predict Survival in Patients with Malignant Pheochromocytomas or Paragangliomas

    Laurence Amar;Eric Baudin;Nelly Burnichon;Séverine Peyrard

  • Paraganglioma and phaeochromocytoma: from genetics to personalized medicine

    Judith Favier;Laurence Amar;Anne-Paule Gimenez-Roqueplo

Frequent Co-Authors

Xavier Jeunemaitre
Xavier Jeunemaitre Université Paris Cité
Pierre-François Plouin
Pierre-François Plouin Université Paris Cité
Jérôme Bertherat
Jérôme Bertherat Université Paris Cité
Massimo Mannelli
Massimo Mannelli University of Florence
Felix Beuschlein
Felix Beuschlein University of Zurich
Eric Baudin
Eric Baudin Institut Gustave Roussy
Karel Pacak
Karel Pacak National Institutes of Health
Martin Fassnacht
Martin Fassnacht University of Würzburg
Pierre Corvol
Pierre Corvol Collège de France

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