Maud Langeois

643 total citations
13 papers, 207 citations indexed

About

Maud Langeois is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Maud Langeois has authored 13 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Pulmonary and Respiratory Medicine, 10 papers in Genetics and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Maud Langeois's work include Aortic Disease and Treatment Approaches (8 papers), Connective tissue disorders research (8 papers) and Cardiac Valve Diseases and Treatments (6 papers). Maud Langeois is often cited by papers focused on Aortic Disease and Treatment Approaches (8 papers), Connective tissue disorders research (8 papers) and Cardiac Valve Diseases and Treatments (6 papers). Maud Langeois collaborates with scholars based in France, Morocco and Lebanon. Maud Langeois's co-authors include Guillaume Jondeau, Olivier Milleron, Cathérine Boileau, Florence Arnoult, Pauline Arnaud, Nadine Hanna, Laurent Gouya, Jacques Ropers, Ludivine Eliahou and Marie Cotillon and has published in prestigious journals such as Journal of the American College of Cardiology, Scientific Reports and European Heart Journal.

In The Last Decade

Maud Langeois

13 papers receiving 205 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maud Langeois France	8	151	140	91	30	22	13	207
Ilse Luyckx Belgium	8	122 0.8×	138 1.0×	62 0.7×	55 1.8×	41 1.9×	14	232
H. Pannu United States	6	240 1.6×	269 1.9×	102 1.1×	78 2.6×	58 2.6×	7	391
Simone Salemink Netherlands	5	97 0.6×	75 0.5×	41 0.5×	42 1.4×	17 0.8×	5	171
Victoria Cañadas Spain	7	126 0.8×	223 1.6×	214 2.4×	21 0.7×	83 3.8×	11	347
Alex R. Dalal United States	7	73 0.5×	114 0.8×	43 0.5×	51 1.7×	35 1.6×	27	185
Ludivine Eliahou France	8	91 0.6×	79 0.6×	87 1.0×	115 3.8×	21 1.0×	23	236
Guoyan Zhu China	7	69 0.5×	79 0.6×	25 0.3×	56 1.9×	20 0.9×	17	169
Bo Wen Cai China	4	83 0.5×	110 0.8×	29 0.3×	39 1.3×	38 1.7×	5	204
Rocío Mena Spain	7	75 0.5×	48 0.3×	16 0.2×	65 2.2×	20 0.9×	16	182
Salma Adham France	8	157 1.0×	58 0.4×	26 0.3×	35 1.2×	46 2.1×	23	213

Countries citing papers authored by Maud Langeois

Since Specialization

Citations

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

Fields of papers citing papers by Maud Langeois

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maud Langeois

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

All Works

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13 of 13 papers shown

Édouard, Thomas, Marie‐Christine Picot, Fernanda Bajanca, et al.. (2024). Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study. Orphanet Journal of Rare Diseases. 19(1). 180–180. 2 indexed citations

Rendu, John, Laurence Michel‐Calemard, Rita Menassa, et al.. (2023). Muscular phenotype description of abnormal THOC2 splicing. Neuromuscular Disorders. 33(12). 978–982. 2 indexed citations

Marcheix, Bertrand, Yves Dulac, Thomas Édouard, et al.. (2021). A +3 variant at a donor splice site leads to a skipping of the MYH11 exon 32, a recurrent RNA defect causing Heritable Thoracic Aortic Aneurysm and Dissection and/or Patent Ductus Arteriosus. Molecular Genetics & Genomic Medicine. 9(11). e1814–e1814. 5 indexed citations

Arnaud, Pauline, Olivier Milleron, Nadine Hanna, et al.. (2021). Clinical relevance of genotype–phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants. Genetics in Medicine. 23(7). 1296–1304. 69 indexed citations

Milleron, Olivier, Florence Arnoult, G Delorme, et al.. (2020). Pathogenic FBN1 Genetic Variation and Aortic Dissection in Patients With Marfan Syndrome. Journal of the American College of Cardiology. 75(8). 843–853. 31 indexed citations

Édouard, Thomas, Yves Dulac, Hélène Colineaux, et al.. (2020). Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature. Molecular Genetics & Genomic Medicine. 8(5). e1132–e1132. 12 indexed citations

Grange, Thomas, Mélodie Aubart, Maud Langeois, et al.. (2020). Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability. Genes. 11(5). 574–574. 13 indexed citations

Milleron, Olivier, Jacques Ropers, Florence Arnoult, et al.. (2019). Clinical Significance of Aortic Root Modification Associated With Bicuspid Aortic Valve in Marfan Syndrome. Circulation Cardiovascular Imaging. 12(3). e008129–e008129. 14 indexed citations

Bouleti, Claire, Martin Flamant, Brigitte Escoubet, et al.. (2018). Risk of Ascending Aortic Aneurysm in Patients With Autosomal Dominant Polycystic Kidney Disease. The American Journal of Cardiology. 123(3). 482–488. 18 indexed citations

10.

Extramiana, Fabrice, Olivier Milleron, Sandy Elbitar, et al.. (2018). High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations. Scientific Reports. 8(1). 13019–13019. 3 indexed citations

11.

Flamant, Martin, Brigitte Escoubet, Florence Arnoult, et al.. (2017). P5245Autosomal polycystic kidney disease carries an increased risk of aortic root aneurysm. European Heart Journal. 38(suppl_1). 1 indexed citations

12.

Frank, Michael, et al.. (2016). Phenotypic variability and diffuse arterial lesions in a family with Loeys–Dietz syndrome type 4. Clinical Genetics. 91(3). 458–462. 7 indexed citations

13.

Arnaud, Pauline, Nadine Hanna, Mélodie Aubart, et al.. (2016). Homozygous and compound heterozygous mutations in the FBN1 gene: unexpected findings in molecular diagnosis of Marfan syndrome. Journal of Medical Genetics. 54(2). 100–103. 30 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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