Nelly Burnichon

7.3k total citations · 2 hit papers
63 papers, 4.3k citations indexed

About

Nelly Burnichon is a scholar working on Surgery, Endocrinology, Diabetes and Metabolism and Cancer Research. According to data from OpenAlex, Nelly Burnichon has authored 63 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Surgery, 40 papers in Endocrinology, Diabetes and Metabolism and 38 papers in Cancer Research. Recurrent topics in Nelly Burnichon's work include Adrenal and Paraganglionic Tumors (44 papers), Cancer, Hypoxia, and Metabolism (36 papers) and Hormonal Regulation and Hypertension (27 papers). Nelly Burnichon is often cited by papers focused on Adrenal and Paraganglionic Tumors (44 papers), Cancer, Hypoxia, and Metabolism (36 papers) and Hormonal Regulation and Hypertension (27 papers). Nelly Burnichon collaborates with scholars based in France, United States and Netherlands. Nelly Burnichon's co-authors include Anne‐Paule Gimenez‐Roqueplo, Judith Favier, Jérôme Bertherat, Laurence Amar, Xavier Jeunemaı̂tre, Alexandre Buffet, Pierre‐François Plouin, Paule Bénit, Pierre Rustin and Rossella Libé and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Nelly Burnichon

61 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma

2013 551 citations Éric Letouzé, Nelly Burnichon et al. profile →
SDHA is a tumor suppressor gene causing paraganglioma

2010 491 citations Nelly Burnichon, Jean-Jacques Brière et al. Human Molecular Genetics profile →

Peers

Countries citing papers authored by Nelly Burnichon

Since Specialization

Citations

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

Fields of papers citing papers by Nelly Burnichon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nelly Burnichon

This figure shows the co-authorship network connecting the top 25 collaborators of Nelly Burnichon. A scholar is included among the top collaborators of Nelly Burnichon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nelly Burnichon. Nelly Burnichon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Insights from 2057 germline genetic tests in renal cell carcinoma patients support revisiting testing criteria 2026 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Alexandre Buffet, (unknown), (unknown), (unknown), Judith Favier, (unknown), Sophie Giraud, Nelly Burnichon	0
2	Pancreatic Neuroendocrine Tumors in French VHL Mutation Carriers 2024 ·The Journal of Clinical Endocrinology & Metabolism ·Marie Müller, Pascal Hammel, Anne Couvelard, Anne‐Laure Védié, Jérôme Cros, Nelly Burnichon, (unknown), Alain Sauvanet, Richard J. Kahnoski, Louis de Mestier	3
3	EPAS1 ‐mutated paragangliomas associated with haemoglobin disorders 2024 ·British Journal of Haematology ·(unknown), Alexandre Buffet, (unknown), Laurence Amar, Charlotte Lussey‐Lepoutre, Lise Crinière, Éric Baudin, Tchao Méatchi, Anne‐Paule Gimenez‐Roqueplo, Judith Favier, Nelly Burnichon	3
4	Impact of gender on self-assessment accuracy among fourth-year French medical students on faculty’s online Objective Structured Clinical Examinations 2024 ·BMC Medical Education ·Sylvain Bodard, Donia Bouzid, Valentine Marie Ferré, (unknown), Joëlle Kivits, Yann Nguyen, Michaël Thy, Ugo Marchèse, Bénédicte Oulès, Lina Khider, Christian de Tymowski, Nelly Burnichon, Tristan Mirault, Albert Faye, Laura Levi	0
5	Minors at risk of von Hippel-Lindau disease: 10 years’ experience of predictive genetic testing and follow-up adherence 2022 ·European Journal of Human Genetics ·(unknown), Khadija Lahlou‐Laforêt, (unknown), Valérie Krivosic, Thomas Blanc, Laurence Amar, Nelly Burnichon, Caroline Abadie, Richard J. Kahnoski, Anne‐Paule Gimenez‐Roqueplo	6
6	Low-grade oncocytic renal tumor (LOT): mutations in mTOR pathway genes and low expression of FOXI1 2021 ·Modern Pathology ·(unknown), (unknown), Marc‐Olivier Timsit, Mathilde Sibony, Viorel Vasiliu, Anne‐Paule Gimenez‐Roqueplo, Judith Favier, Cécile Badoual, Arnaud Méjean, Nelly Burnichon, Virginie Verkarre	37
7	Functional Characterization of TMEM127 Variants Reveals Novel Insights into Its Membrane Topology and Trafficking 2020 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Yilun Deng, (unknown), (unknown), (unknown), Afaf Saliba, (unknown), Nelly Burnichon, Anne‐Paule Gimenez‐Roqueplo, Exing Wang, Ricardo C.T. Aguiar, Patricia L. M. Dahia	7
8	Screening of a Large Cohort of Asymptomatic SDHx Mutation Carriers in Routine Practice 2020 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Alexandre Buffet, J. Abeillon, D. Drui, Sophie Leboulleux, Jérôme Bertherat, Delphine Zénaty, Caroline Storey, Françoise Borson‐Chazot, Nelly Burnichon, (unknown), Judith Favier, Éric Baudin, Sophie Giraud, Anne‐Paule Gimenez‐Roqueplo, Laurence Amar, Charlotte Lussey‐Lepoutre	8
9	MET alterations in biphasic squamoid alveolar papillary renal cell carcinomas and clinicopathological features 2020 ·Modern Pathology ·Thomas Denize, (unknown), Mathilde Sibony, Hélène Blons, Marc‐Olivier Timsit, (unknown), (unknown), Chloé Broudin, (unknown), Thierry Jo Molina, Yann Vano, (unknown), Richard J. Kahnoski, Arnaud Méjean, Anne‐Paule Gimenez‐Roqueplo, Nelly Burnichon, Virginie Verkarre	18
10	Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas 2019 ·The Journal of Clinical Endocrinology & Metabolism ·Sylvie Job, Adrien Georges, Nelly Burnichon, Alexandre Buffet, Laurence Amar, Jérôme Bertherat, Nabila Bouatia‐Naji, Aurélien de Reyniès, D. Drui, Charlotte Lussey‐Lepoutre, Judith Favier, Anne‐Paule Gimenez‐Roqueplo, Luis Jaime Castro‐Vega	13
11	Telomerase Activation and ATRX Mutations Are Independent Risk Factors for Metastatic Pheochromocytoma and Paraganglioma 2018 ·Clinical Cancer Research ·Sylvie Job, Irena Drašković, Nelly Burnichon, Alexandre Buffet, Jérôme Cros, (unknown), Annabelle Vénisse, Estelle Robidel, Virginie Verkarre, Tchao Méatchi, Mathilde Sibony, Laurence Amar, Jérôme Bertherat, Aurélien de Reyniès, Arturo Londoño‐Vallejo, Judith Favier, Luis Jaime Castro‐Vega, Anne‐Paule Gimenez‐Roqueplo	83
12	Germline Mutations in the Mitochondrial 2-Oxoglutarate/Malate Carrier SLC25A11 Gene Confer a Predisposition to Metastatic Paragangliomas 2018 ·Cancer Research ·Alexandre Buffet, Aurélie Morin, Luis-Jaime Castro-Vega, Florence Habarou, Charlotte Lussey‐Lepoutre, Éric Letouzé, Hervé Lefèbvre, Isabelle Guilhem, Magalie Haissaguerre, I. Raingeard, (unknown), (unknown), (unknown), Jérôme Bertherat, Laurence Amar, Chris Ottolenghi, Nelly Burnichon, Anne‐Paule Gimenez‐Roqueplo, Judith Favier	99
13	Pheochromocytoma and paraganglioma 2015 ·Current Opinion in Oncology ·Nelly Burnichon, Alexandre Buffet, Anne‐Paule Gimenez‐Roqueplo	34
14	Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma 2011 ·Human Molecular Genetics ·Nelly Burnichon, Laure Vescovo, Laurence Amar, Rossella Libé, Aurélien de Reyniès, Annabelle Vénisse, Elodie Jouanno, Ingrid Laurendeau, Béatrice Parfait, Jérôme Bertherat, Pierre‐François Plouin, Xavier Jeunemaı̂tre, Judith Favier, Anne‐Paule Gimenez‐Roqueplo	220
15	SDHA is a tumor suppressor gene causing paraganglioma breakdown → 2010 ·Human Molecular Genetics ·Nelly Burnichon, Jean-Jacques Brière, Rossella Libé, Laure Vescovo, Julie Rivière, Frédérique Tissier, Elodie Jouanno, Xavier Jeunemaı̂tre, Paule Bénit, Alexander Tzagoloff, Pierre Rustin, Jérôme Bertherat, Judith Favier, Anne‐Paule Gimenez‐Roqueplo	491
16	A novel TMEM127 mutation in a patient with familial bilateral pheochromocytoma 2010 ·European Journal of Endocrinology ·Nelly Burnichon, Charlotte Lussey‐Lepoutre, Julien Laffaire, (unknown), Vincent Molinié, A. Hernigou, Pierre‐François Plouin, Xavier Jeunemaı̂tre, Judith Favier, Anne‐Paule Gimenez‐Roqueplo	32
17	The Warburg Effect Is Genetically Determined in Inherited Pheochromocytomas 2009 ·PLoS ONE ·Judith Favier, Jean-Jacques Brière, Nelly Burnichon, Julie Rivière, Laure Vescovo, Paule Bénit, Isabelle Giscos-Douriez, Aurélien de Reyniès, Jérôme Bertherat, Cécile Badoual, Frédérique Tissier, Laurence Amar, Rossella Libé, Pierre‐François Plouin, Xavier Jeunemaı̂tre, Pierre Rustin, Anne‐Paule Gimenez‐Roqueplo	187
18	Apports de COMETE à la génétique du phéochromocytome 2008 ·Bulletin de l Académie Nationale de Médecine ·Anne‐Paule Gimenez‐Roqueplo, Nelly Burnichon, Laurence Amar, Judith Favier, Xavier Jeunemaı̂tre, Pierre‐François Plouin	2
19	Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network 2007 ·Genetics in Medicine ·Gaëtan Lesca, Carla Olivieri, Nelly Burnichon, Fabio Pagella, Marie‐France Carette, Brigitte Gilbert‐Dussardier, Cyril Goizet, J. Roume, Muriel Rabilloud, Jean‐Christophe Saurin, Vincent Cottin, Jérôme Honnorat, Florence Coulet, Sophie Giraud, Alain Calender, Cesare Danesino, Elisabetta Buscarini, Henri Plauchu	157
20	A New α Chain Hemoglobin Variant: Hb Al-Hammadi Riyadh [α75(EF4)Asp→Val (α2)] 2006 ·Hemoglobin ·Nelly Burnichon, (unknown), Michel Becchi, Isabelle Zanella‐Cléon, (unknown), (unknown), (unknown), Alain Francina	3

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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