Marie Legendre

5.3k total citations
82 papers, 1.6k citations indexed

About

Marie Legendre is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Marie Legendre has authored 82 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Pulmonary and Respiratory Medicine, 27 papers in Molecular Biology and 21 papers in Genetics. Recurrent topics in Marie Legendre's work include Cystic Fibrosis Research Advances (19 papers), Neonatal Respiratory Health Research (15 papers) and Inflammasome and immune disorders (11 papers). Marie Legendre is often cited by papers focused on Cystic Fibrosis Research Advances (19 papers), Neonatal Respiratory Health Research (15 papers) and Inflammasome and immune disorders (11 papers). Marie Legendre collaborates with scholars based in France, United Kingdom and Morocco. Marie Legendre's co-authors include Serge Amselem, Estelle Escudier, Laure‐Emmanuelle Zaragosi, Hannah M. Mitchison, A. Coste, Dimitri Tchernitchko, Philippe Duquesnoy, Annick Clément, Bruno Copin and Guy Montantin and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Marie Legendre

74 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marie Legendre France	23	741	583	503	202	143	82	1.6k
Éric Bieth France	24	1.1k 1.5×	690 1.2×	383 0.8×	56 0.3×	212 1.5×	72	2.1k
Bénédicte Duriez France	17	698 0.9×	724 1.2×	291 0.6×	63 0.3×	125 0.9×	25	1.5k
Paolo Simi Italy	22	633 0.9×	571 1.0×	201 0.4×	54 0.3×	145 1.0×	82	1.4k
Odile Cohen‐Haguenauer France	16	647 0.9×	527 0.9×	151 0.3×	173 0.9×	141 1.0×	52	1.2k
P. Nagesh Rao United States	26	842 1.1×	625 1.1×	124 0.2×	126 0.6×	249 1.7×	77	2.2k
Güven Lüleci Türkiye	21	750 1.0×	808 1.4×	99 0.2×	134 0.7×	132 0.9×	110	1.7k
Gökçe Törüner United States	19	581 0.8×	376 0.6×	152 0.3×	126 0.6×	101 0.7×	86	1.4k
Mei Cao United States	22	829 1.1×	155 0.3×	296 0.6×	101 0.5×	349 2.4×	69	1.5k
Thomas J. Cunningham United States	27	1.5k 2.0×	329 0.6×	287 0.6×	198 1.0×	205 1.4×	64	2.3k
Takafumi Matsumura Japan	25	752 1.0×	393 0.7×	105 0.2×	175 0.9×	125 0.9×	79	1.7k

Countries citing papers authored by Marie Legendre

Since Specialization

Citations

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

Fields of papers citing papers by Marie Legendre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Legendre

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Legendre. A scholar is included among the top collaborators of Marie Legendre 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 Marie Legendre. Marie Legendre 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

Debray, Marie‐Pierre, Marie Legendre, L Wemeau, et al.. (2024). Chest Wall Deformities in Adults With Fibrotic Interstitial Lung Disease Related to Surfactant-Related Gene Mutations. SHILAP Revista de lepidopterología. 2(4). 100106–100106.

Nathan, Nadia, Camille Louvrier, Marie Legendre, et al.. (2024). Efficacy and safety of CFTR modulators in patients with interstitial lung disease caused by ABCA3 transporter deficiency. ERJ Open Research. 11(2). 701–2024. 2 indexed citations

Mitchell, Valérie, Anne Loyens, Nathalie Rives, et al.. (2023). Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy. Reproductive BioMedicine Online. 47(5). 103328–103328. 4 indexed citations

Assrawi, Eman, Camille Louvrier, Elma El Khouri, et al.. (2022). Mosaic variants in TNFRSF1A: an emerging cause of tumour necrosis factor receptor-associated periodic syndrome. Lara D. Veeken. 62(1). 473–479. 7 indexed citations

Beydon, Nicole, Aline Tamalet, Estelle Escudier, Marie Legendre, & Guillaume Thouvenin. (2021). Breath‐holding and tidal breathing nasal NO to screen children for Primary Ciliary Dyskinesia. Pediatric Pulmonology. 56(7). 2242–2249. 7 indexed citations

Assrawi, Eman, Camille Louvrier, C. Lepelletier, et al.. (2019). Somatic Mosaic NLRP3 Mutations and Inflammasome Activation in Late-Onset Chronic Urticaria. Journal of Investigative Dermatology. 140(4). 791–798.e2. 21 indexed citations

Blanchon, Sylvain, Marie Legendre, Mathieu Bottier, et al.. (2019). Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia. Journal of Medical Genetics. 57(4). 237–244. 22 indexed citations

Béquignon, Émilie, V. Escabasse, Françoise Zerah-Lancner, et al.. (2019). Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference Centers. Journal of Clinical Medicine. 8(9). 1495–1495. 8 indexed citations

Amselem, Serge, et al.. (2019). Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation. Frontiers in Endocrinology. 10. 381–381. 1 indexed citations

10.

Stoupa, Athanasia, Isabelle Flechtner, Graziella Pinto, et al.. (2018). Clinical and Preliminary Molecular Description of a Cohort of Patients with Growth Retardation due to Severe Primary IGF1 Deficiency (GROWPATI Study). HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations

11.

Luongo, Cristina, et al.. (2017). Adult neural stem cell fate is determined by thyroid hormone activation of mitochondrial metabolism. Molecular Metabolism. 6(11). 1551–1561. 39 indexed citations

12.

Legendre, Marie, Florence Dastot, Nathalie Collot, et al.. (2016). Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern. 86. 1 indexed citations

13.

Legendre, Marie, et al.. (2014). Clinical and molecular findings in a Moroccan patient with popliteal pterygium syndrome: a case report. Journal of Medical Case Reports. 8(1). 471–471. 3 indexed citations

14.

Moal, Florence Dastot‐Le, Nathalie Collot, Marie Legendre, et al.. (2012). Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalities. European Journal of Endocrinology. 167(1). 85–91. 8 indexed citations

15.

Frapsauce, Cynthia, Célia Ravel, Marie Legendre, et al.. (2011). Birth after TESE-ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation. Human Reproduction. 26(3). 724–728. 32 indexed citations

16.

Şıklar, Zeynep, Merih Berberoğlu, Marie Legendre, Serge Amselem, & Olcay Evliyaoğlu. (2010). Two Siblings with Isolated GH Deficiency Due to Loss-of-Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation-Case Report. Journal of Clinical Research in Pediatric Endocrinology. 2(4). 164–167. 7 indexed citations

17.

Duquesnoy, Philippe, Estelle Escudier, Laetitia Vincensini, et al.. (2009). Loss-of-Function Mutations in the Human Ortholog of Chlamydomonas reinhardtii ODA7 Disrupt Dynein Arm Assembly and Cause Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 85(6). 890–896. 105 indexed citations

18.

Ratbi, Ilham, Emmanuelle Génin, Marie Legendre, et al.. (2008). Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco. Journal of Cystic Fibrosis. 7(5). 440–443. 15 indexed citations

19.

Ratbi, Ilham, Marie Legendre, Florence Niel, et al.. (2007). Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling. Human Reproduction. 22(5). 1285–1291. 50 indexed citations

20.

Tonnel, André‐Bernard, et al.. (2000). Clinical efficacy and safety of fluticasone propionate 250 microg twice daily administered via a HFA 134a pressurized metered dose inhaler to patients with mild to moderate asthma. French study group.. PubMed. 94 Suppl B. S29–34. 11 indexed citations

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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