Mélanie Parisot

1.3k total citations
16 papers, 466 citations indexed

About

Mélanie Parisot is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Mélanie Parisot has authored 16 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Immunology. Recurrent topics in Mélanie Parisot's work include Immunodeficiency and Autoimmune Disorders (4 papers), Renal and related cancers (3 papers) and Viral-associated cancers and disorders (3 papers). Mélanie Parisot is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (4 papers), Renal and related cancers (3 papers) and Viral-associated cancers and disorders (3 papers). Mélanie Parisot collaborates with scholars based in France, United States and Switzerland. Mélanie Parisot's co-authors include Patrick Nitschké, Christine Bôle‐Feysot, Corinne Antignac, Rémi Salomon, Jelena Martinović, Marc Jeanpierre, David M. Ornitz, Shuang Chen, Hila Barak and Sung‐Ho Huh and has published in prestigious journals such as Nature Communications, Scientific Reports and Journal of Allergy and Clinical Immunology.

In The Last Decade

Mélanie Parisot

13 papers receiving 463 citations

Peers

Countries citing papers authored by Mélanie Parisot

Since Specialization

Citations

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

Fields of papers citing papers by Mélanie Parisot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mélanie Parisot

This figure shows the co-authorship network connecting the top 25 collaborators of Mélanie Parisot. A scholar is included among the top collaborators of Mélanie Parisot 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 Mélanie Parisot. Mélanie Parisot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech 2025 ·Molecular Autism ·(unknown), (unknown), Karine Siquier-Pernet, Geoffroy Delplancq, Marlène Rio, Mélanie Parisot, Patrick Nitschké, Cristina Rodriguez‐Fontenla, (unknown), (unknown), Émilie Schlumberger, Vincent Cantagrel, Valérie Malan	0
2	Study of the potential role of CASPASE-10 mutations in the development of autoimmune lymphoproliferative syndrome 2024 ·Cell Death and Disease ·(unknown), (unknown), (unknown), Marie‐Claude Stolzenberg, (unknown), Mélanie Parisot, Cécile Masson, N. Neveux, Jérémie Rosain, (unknown), (unknown), Marion Malphettes, Pierre Quartier, Capucine Pïcard, Frédéric Rieux‐Laucat, Aude Magérus	3
3	Overexpression of Egr1 Transcription Regulator Contributes to Schwann Cell Differentiation Defects in Neural Crest-Specific Adar1 Knockout Mice 2024 ·Cells ·(unknown), (unknown), (unknown), (unknown), (unknown), Laurence Richard, Mélanie Parisot, Nicolas Cagnard, Stéphane Mathis, Christine Bole‐Feysot, Mary A. O’Connell, Véronique Pingault, Emilie Dambroise, Liam P. Keegan, J.M. Vallat, Nadège Bondurand	0
4	Fluid shear stress triggers cholesterol biosynthesis and uptake in inner medullary collecting duct cells, independently of nephrocystin-1 and nephrocystin-4 2023 ·Frontiers in Molecular Biosciences ·Meriem Garfa‐Traoré, Federica Roccio, Caterina Miceli, Giulia Ferri, Mélanie Parisot, Nicolas Cagnard, Marie Lhomme, Nicolas Dupont, Alexandre Benmerah, Sophie Saunier, Marion Delous	3
5	Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla 2023 ·Acta Neuropathologica Communications ·Aude Tessier, (unknown), Lucile Boutaud, (unknown), (unknown), Mélanie Parisot, Meriem Garfa‐Traoré, Amale Ichkou, Nadia Elkhartoufi, Christine Bole, Patrick Nitschké, Jeanne Amiel, Jelena Martinović, Férechté Encha‐Razavi, Tania Attié‐Bitach, Sophie Thomas	7
6	Reducing lipid bilayer stress by monounsaturated fatty acids protects renal proximal tubules in diabetes 2022 ·eLife ·(unknown), Suresh Krishna Ramakrishnan, Jiayi Li, Aurélien Dugourd, Martijn R. Molenaar, (unknown), (unknown), (unknown), Mélanie Parisot, Soeren S. Lienkamp, Julio Sáez-Rodríguez, Matias Simons	27
7	BLNK mutation associated with T-cell LGL leukemia and autoimmune diseases: Case report in hematology 2022 ·Frontiers in Medicine ·Guillemette Fouquet, Julien Rossignol, Laure Ricard, Flavia Guillem, Lucile Couronné, Vahid Asnafi, (unknown), Mélanie Parisot, Nicolas Garcelon, Frédéric Rieux‐Laucat, A. Mékinian, Olivier Hermine	0
8	Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith–Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K Signaling 2021 ·Frontiers in Pediatrics ·(unknown), (unknown), (unknown), (unknown), Cécile Masson, Mélanie Parisot, (unknown), Capucine Pïcard, Isabelle André‐Schmutz, Marina Cavazzana, Laurence Perrin, Anne Durandy, Saba Azarnoush, Sven Kracker	9
9	Disruption of pathways regulated by Integrator complex in Galloway–Mowat syndrome due to WDR73 mutations 2021 ·Scientific Reports ·(unknown), Christelle Arrondel, Cérina Chhuon, (unknown), Nicolas Cagnard, Mélanie Parisot, (unknown), Nathalie Lefort, Ida Chiara Guerrera, Christine Bôle‐Feysot, Alexandre Benmerah, Corinne Antignac, Géraldine Mollet	17
10	ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development 2020 ·Nature Communications ·(unknown), (unknown), (unknown), Laurence Richard, Stéphane Mathis, Raj P. Kapur, Mélanie Parisot, Jeanne Amiel, Sylvie Dufour, Pierre de la Grange, Véronique Pingault, J.M. Vallat, Nadège Bondurand	32
11	Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population 2016 ·Orphanet Journal of Rare Diseases ·Hisham Megahed, Michaël Nicouleau, Giulia Barcia, (unknown), Karine Siquier-Pernet, Christine Bôle‐Feysot, Mélanie Parisot, Cécile Masson, Patrick Nitschké, Marlène Rio, Nadia Bahi‐Buisson, Isabelle Desguerre, Arnold Münnich, Nathalie Boddaert, Laurence Colleaux, Vincent Cantagrel	24
12	Deficiency in Mucosa‐associated Lymphoid Tissue Lymphoma Translocation 1 2016 ·Journal of Pediatric Gastroenterology and Nutrition ·Fabienne Charbit‐Henrion, (unknown), Bernadette Bègue, Gašper Markelj, Marianna Parlato, (unknown), Isabelle Callebaut, Marc Bras, Mélanie Parisot, Janez Jazbec, Matjaž Homan, Alojz Ihan, Frédéric Rieux‐Laucat, Marie‐Claude Stolzenberg, (unknown), Frank M. Ruemmele, Tadej Avčin, Nadine Cerf–Bensussan	51
13	Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutation 2015 ·Journal of Allergy and Clinical Immunology ·David Buchbinder, Jeffrey R. Stinson, Diane J. Nugent, Lucie Heurtier, Felipe Suárez, Gauthaman Sukumar, Clifton L. Dalgard, Cécile Masson, Mélanie Parisot, Yu Zhang, Helen Matthews, Helen C. Su, Anne Durandy, Alain Fischer, Sven Kracker, Andrew L. Snow	39
14	FGF9 and FGF20 Maintain the Stemness of Nephron Progenitors in Mice and Man 2012 ·Developmental Cell ·Hila Barak, Sung‐Ho Huh, Shuang Chen, Marc Jeanpierre, Jelena Martinović, Mélanie Parisot, Christine Bôle‐Feysot, Patrick Nitschké, Rémi Salomon, Corinne Antignac, David M. Ornitz, Raphael Kopan	216
15	RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects 2011 ·Journal of Medical Genetics ·Marc Jeanpierre, G. Macé, Mélanie Parisot, Vincent Morinière, (unknown), (unknown), Jelena Martinović, Jeanne Amiel, Tania Attié‐Bitach, Anne‐Lise Delezoide, Philippe Loget, Patricia Blanchet, Dominique Gaillard, M. Gonzalés, Wassila Carpentier, Patrick Nitschké, Frédéric Torès, Laurence Heidet, Corinne Antignac, Rémi Salomon, (unknown)	37
16	[Cardiac involvement in 2 cases of malignant non-Hodgkin's lymphoma. Course of cardiac involvement under chemotherapy]. 1987 ·PubMed ·Gilles Grollier, Xavier Troussard, (unknown), Philippe Commeau, (unknown), (unknown), Mélanie Parisot, (unknown), M Leporrier, (unknown)	1

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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