M.L. Moutard

860 total citations
9 papers, 490 citations indexed

About

M.L. Moutard is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, M.L. Moutard has authored 9 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pediatrics, Perinatology and Child Health, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in M.L. Moutard's work include Fetal and Pediatric Neurological Disorders (6 papers), Prenatal Screening and Diagnostics (3 papers) and Cerebrospinal fluid and hydrocephalus (2 papers). M.L. Moutard is often cited by papers focused on Fetal and Pediatric Neurological Disorders (6 papers), Prenatal Screening and Diagnostics (3 papers) and Cerebrospinal fluid and hydrocephalus (2 papers). M.L. Moutard collaborates with scholars based in France, Belgium and Italy. M.L. Moutard's co-authors include Isabelle Desguerre, G Ponsot, J. Motte, Stefano Ricci, V. des Portes, I. Snoeck, Olivier Dulac, F. Capron, Linda C. Meiners and J.-M. Pinard and has published in prestigious journals such as Human Molecular Genetics, Ultrasound in Obstetrics and Gynecology and Journal of Inherited Metabolic Disease.

In The Last Decade

M.L. Moutard

8 papers receiving 477 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M.L. Moutard France 7 184 169 128 97 82 9 490
Laurence E. Walsh United States 11 214 1.2× 53 0.3× 191 1.5× 114 1.2× 24 0.3× 32 598
Seher Başaran Türkiye 17 278 1.5× 215 1.3× 305 2.4× 97 1.0× 11 0.1× 73 814
Chantal Missirian France 16 404 2.2× 100 0.6× 418 3.3× 41 0.4× 19 0.2× 39 720
Elisabetta Lapi Italy 18 534 2.9× 131 0.8× 477 3.7× 80 0.8× 91 1.1× 48 957
Monika Cohen Germany 11 551 3.0× 98 0.6× 488 3.8× 113 1.2× 30 0.4× 13 859
S. Ghariani Belgium 12 176 1.0× 88 0.5× 234 1.8× 70 0.7× 9 0.1× 27 600
Renske Oegema Netherlands 13 245 1.3× 147 0.9× 217 1.7× 75 0.8× 10 0.1× 21 534
Anne-Marie Bridoux France 10 359 2.0× 67 0.4× 388 3.0× 58 0.6× 23 0.3× 11 712
Tiziana Filippi Italy 9 207 1.1× 157 0.9× 374 2.9× 41 0.4× 19 0.2× 10 539
Krzysztof Szczałuba Poland 15 328 1.8× 69 0.4× 369 2.9× 63 0.6× 11 0.1× 57 638

Countries citing papers authored by M.L. Moutard

Since Specialization
Citations

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

Fields of papers citing papers by M.L. Moutard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.L. Moutard. 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 M.L. Moutard. The network helps show where M.L. Moutard may publish in the future.

Co-authorship network of co-authors of M.L. Moutard

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

All Works

9 of 9 papers shown
1.
Maurice, P, Lucie Guilbaud, J.-M. Garel, et al.. (2020). Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions. Ultrasound in Obstetrics and Gynecology. 57(5). 783–789. 24 indexed citations
2.
Massoud, Mona, Cathérine Garel, N. Varene, et al.. (2013). Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis. Ultrasound in Obstetrics and Gynecology. 44(4). 447–454. 37 indexed citations
3.
Blondiaux, Éléonore, Chiara Siléo, M.L. Moutard, et al.. (2012). Periventricular nodular heterotopia on prenatal ultrasound and magnetic resonance imaging. Ultrasound in Obstetrics and Gynecology. 42(2). 149–155. 23 indexed citations
4.
Damaj, Léna, Bertrand Bruneau, M.L. Moutard, et al.. (2010). Pediatric outcome of children with the prenatal diagnosis of isolated septal agenesis. Prenatal Diagnosis. 30(12-13). 1143–1150. 26 indexed citations
5.
Anselem, Olivia, Anne Bazin, Charlotte Mechler, et al.. (2010). Prenatal Diagnosis of 18q-Syndrome: A Case of Fetal Mosaicism with a Normal Karyotype in Chorionic Villi. Fetal Diagnosis and Therapy. 28(3). 180–185. 1 indexed citations
6.
Carré, Aurore, Gabor Szinnai, Mireille Castanet, et al.. (2009). Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case. Human Molecular Genetics. 18(12). 2266–2276. 145 indexed citations
7.
Adamsbaum, C., S. Ferey, & M.L. Moutard. (2005). IRM cérébrale : corrélations pré et post-natales. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 34(1). 7–13.
8.
Portes, V. des, Fiona Francis, J.-M. Pinard, et al.. (1998). Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH). Human Molecular Genetics. 7(7). 1063–1070. 209 indexed citations
9.
Degoul, Françoise, D. François, Monique Diry, et al.. (1997). A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues. Journal of Inherited Metabolic Disease. 20(1). 49–53. 25 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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