Maud Blanluet

662 total citations
8 papers, 170 citations indexed

About

Maud Blanluet is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maud Blanluet has authored 8 papers receiving a total of 170 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maud Blanluet's work include Acute Myeloid Leukemia Research (1 paper), DNA Repair Mechanisms (1 paper) and Neurological and metabolic disorders (1 paper). Maud Blanluet is often cited by papers focused on Acute Myeloid Leukemia Research (1 paper), DNA Repair Mechanisms (1 paper) and Neurological and metabolic disorders (1 paper). Maud Blanluet collaborates with scholars based in France, Lebanon and Egypt. Maud Blanluet's co-authors include Tarik Asselah, Dominique Valla, Philippe Broët, Emilie Estrabaud, Simon De Muynck, Qian Zhang, Michelle Martinot-Peignoux, Pierre Bédossa, Ivan Bièche and Martine Lapalus and has published in prestigious journals such as Journal of Hepatology, Neuro-Oncology and American Journal of Medical Genetics Part A.

In The Last Decade

Maud Blanluet

7 papers receiving 167 citations

Peers

Countries citing papers authored by Maud Blanluet

Since Specialization

Citations

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

Fields of papers citing papers by Maud Blanluet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maud Blanluet

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Description of Copy Number Variations in a Series of Children and Adolescents with FASD in Reunion Island 2023 ·Children ·(unknown), Susie Guilly, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Stéphanie Robin, (unknown), (unknown), (unknown), Michel Spodenkiewicz, Jean‐Luc Alessandri, (unknown), Maud Blanluet, Paul Guéguen, (unknown)	0
2	Infantile‐onset parkinsonism, dyskinesia, and developmental delay: do not forget polyglutamine defects! 2023 ·Annals of Clinical and Translational Neurology ·(unknown), (unknown), Nicolas Leboucq, Vincent Procaccio, Maud Blanluet, Pierre Meyer, Marie‐Claire Malinge, (unknown), (unknown), David Geneviève, Cécilia Marelli, Agathe Roubertie	1
3	Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings 2021 ·American Journal of Medical Genetics Part A ·Maud Blanluet, Sandra Chantot‐Bastaraud, Pascal Chambon, Kévin Cassinari, Gabriella Vera, Alice Goldenberg, Boris Keren, Nathalie Le Meur, Didier Hannequin, Bertrand Macé, Jean‐Pierre Siffroi, Thierry Frébourg, Gaël Nicolas, Géraldine Joly‐Hélas	1
4	Recurrent FAN1 p.W707X Pathogenic Variant Originating Before ad 1800 Underlies High Frequency of Karyomegalic Interstitial Nephritis in South Pacific Islands 2021 ·Kidney International Reports ·(unknown), (unknown), Maud Blanluet, Hervé Sartelet, (unknown), Catherine Dubois d’Enghien, Lisa Golmard, Dominique Stoppa‐Lyonnet, (unknown), Stanislas Faguer	4
5	Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes 2020 ·Journal of Pediatric Hematology/Oncology ·Roula Farah, Pratibha Nair, (unknown), Tony Yammine, (unknown), (unknown), (unknown), Claudia Djambas Khayat, (unknown), Éliane Chouery, Maud Blanluet, Stephany El‐Hayek, Dominique Stoppa‐Lyonnet, André Mégarbané	4
6	MBRS-47. RAPID MOLECULAR SUBGROUPING OF MEDULLOBLASTOMA BASED ON DNA METHYLATION BY NANOPORE SEQUENCING 2020 ·Neuro-Oncology ·Julien Masliah‐Planchon, Elodie Girard, Philipp Euskirchen, (unknown), Delphine Lequin, Maud Blanluet, (unknown), François Doz, Franck Bourdeaut, Olivier Delattre	2
7	Ovarian Clear Cell Carcinoma in Cowden Syndrome 2019 ·Journal of the National Comprehensive Cancer Network ·Kévin Yauy, (unknown), Virginie Bubien, (unknown), (unknown), Hélène Perrochia, Gaëtan MacGrogan, Michel Longy, D. Bessis, Julie Tinat, Stéphanie Baert‐Desurmont, Maud Blanluet, (unknown), (unknown), Pascal Pujol, Carole Corsini	8
8	IL28B polymorphism is associated with treatment response in patients with genotype 4 chronic hepatitis C 2011 ·Journal of Hepatology ·Tarik Asselah, Simon De Muynck, Philippe Broët, Julien Masliah‐Planchon, Maud Blanluet, Ivan Bièche, Martine Lapalus, Michelle Martinot-Peignoux, Olivier Lada, Emilie Estrabaud, Qian Zhang, Ahmed El Ray, Dominique Vidaud, Marie–Pierre Ripault, Nathalie Boyer, Pierre Bédossa, Dominique Valla, Michel Vidaud, Patrick Marcellin	150

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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