Maéva Langouët

799 total citations
9 papers, 462 citations indexed

About

Maéva Langouët is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maéva Langouët has authored 9 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maéva Langouët's work include Genetic Syndromes and Imprinting (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genomics and Rare Diseases (2 papers). Maéva Langouët is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Prenatal Screening and Diagnostics (3 papers) and Genomics and Rare Diseases (2 papers). Maéva Langouët collaborates with scholars based in United States, France and Switzerland. Maéva Langouët's co-authors include Arnold Münnich, Laurence Colleaux, Patrick Nitschké, Avinash Abhyankar, Isabelle Desguerre, Nathalie Boddaert, Giulia Barcia, Olivier Dulac, Maile R. Brown and Haijun Chen and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Science Advances.

In The Last Decade

Maéva Langouët

9 papers receiving 456 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maéva Langouët United States 8 253 226 164 114 48 9 462
Amanda Lindy United States 8 225 0.9× 328 1.5× 146 0.9× 65 0.6× 31 0.6× 13 517
Simone Brusco Italy 6 235 0.9× 118 0.5× 105 0.6× 156 1.4× 9 0.2× 9 377
Bryan Lynch Ireland 13 378 1.5× 217 1.0× 170 1.0× 141 1.2× 79 1.6× 32 659
Miriam Kessi China 11 160 0.6× 143 0.6× 158 1.0× 117 1.0× 33 0.7× 34 440
Édouard Henrion Canada 7 355 1.4× 328 1.5× 36 0.2× 96 0.8× 9 0.2× 9 572
Heidi Löffler Germany 6 169 0.7× 67 0.3× 70 0.4× 117 1.0× 80 1.7× 8 275
Dara McCreary United Kingdom 6 133 0.5× 123 0.5× 89 0.5× 91 0.8× 14 0.3× 8 274
Dimira Tambunan United States 6 176 0.7× 226 1.0× 161 1.0× 93 0.8× 32 0.7× 6 399
Philip H. Iffland United States 11 181 0.7× 99 0.4× 107 0.7× 93 0.8× 11 0.2× 17 377
Marta A. Bayly Australia 9 181 0.7× 399 1.8× 140 0.9× 74 0.6× 9 0.2× 11 588

Countries citing papers authored by Maéva Langouët

Since Specialization
Citations

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

Fields of papers citing papers by Maéva Langouët

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maéva Langouët

This figure shows the co-authorship network connecting the top 25 collaborators of Maéva Langouët. A scholar is included among the top collaborators of Maéva Langouët 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 Maéva Langouët. Maéva Langouët 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.
Langouët, Maéva, Christine Jolicoeur, Awais Javed, et al.. (2022). Mutations inBCOR, a co-repressor ofCRX/OTX2, are associated with early-onset retinal degeneration. Science Advances. 8(36). eabh2868–eabh2868. 7 indexed citations
2.
Langouët, Maéva, Michael Chung, Heather R. Glatt-Deeley, et al.. (2020). Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics. 29(19). 3285–3295. 12 indexed citations
3.
Chung, Michael, Maéva Langouët, Stormy J. Chamberlain, & Gordon Carmichael. (2020). Prader-Willi syndrome: reflections on seminal studies and future therapies. Open Biology. 10(9). 200195–200195. 24 indexed citations
4.
Langouët, Maéva, Heather R. Glatt-Deeley, Michael Chung, et al.. (2017). Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics. 27(3). 505–515. 30 indexed citations
5.
Langouët, Maéva, Dennis Mircsof, Marlène Rio, et al.. (2016). Les mutations du gèneNONOsont responsables d’un nouveau syndrome de déficience intellectuelle lié au dysfonctionnement des synapses inhibitrices. médecine/sciences. 32(6-7). 571–573. 1 indexed citations
6.
Langouët, Maéva, Karine Siquier-Pernet, Sylvia Sanquer, et al.. (2015). Contiguous mutation syndrome in the era of high‐throughput sequencing. Molecular Genetics & Genomic Medicine. 3(3). 215–220. 8 indexed citations
7.
Haag, Andrea, Peter L. Gutiérrez, Qiutan Yang, et al.. (2014). An In Vivo EGF Receptor Localization Screen in C. elegans Identifies the Ezrin Homolog ERM-1 as a Temporal Regulator of Signaling. PLoS Genetics. 10(5). e1004341–e1004341. 27 indexed citations
8.
Langouët, Maéva, Guillaume Rieunier, Sébastien Moutton, et al.. (2013). Mutation in TTI2 Reveals a Role for Triple T Complex in Human Brain Development. Human Mutation. 34(11). 1472–1476. 18 indexed citations
9.
Barcia, Giulia, Matthew R. Fleming, Valeswara‐Rao Gazula, et al.. (2012). De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy. Nature Genetics. 44(11). 1255–1259. 335 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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