Anne Moncla

3.3k total citations
38 papers, 1.9k citations indexed

About

Anne Moncla is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anne Moncla has authored 38 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 21 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anne Moncla's work include Genetics and Neurodevelopmental Disorders (20 papers), Genomic variations and chromosomal abnormalities (15 papers) and Epigenetics and DNA Methylation (8 papers). Anne Moncla is often cited by papers focused on Genetics and Neurodevelopmental Disorders (20 papers), Genomic variations and chromosomal abnormalities (15 papers) and Epigenetics and DNA Methylation (8 papers). Anne Moncla collaborates with scholars based in France, United Kingdom and United States. Anne Moncla's co-authors include Laurent Villard, Josette Mancini, Chantal Missirian, Jean‐Christophe Roux, Perrine Malzac, Arnold Münnich, Martine Le Merrer, Nicole Philip, Valérie Cormier‐Daire and Annick Toutain and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and Blood.

In The Last Decade

Anne Moncla

38 papers receiving 1.8k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Anne Moncla 1.3k 1.1k 343 185 146 38 1.9k
Fiorella Gurrieri 1.3k 1.0× 1.4k 1.3× 290 0.8× 345 1.9× 45 0.3× 88 2.4k
Nancy J. Carpenter 1.2k 0.9× 1.0k 1.0× 325 0.9× 292 1.6× 65 0.4× 72 2.2k
Katherina Walz 965 0.7× 1.1k 1.0× 193 0.6× 90 0.5× 40 0.3× 59 1.7k
Jeff M. Milunsky 822 0.6× 704 0.7× 252 0.7× 204 1.1× 123 0.8× 70 1.7k
Valérie Matagne 751 0.6× 702 0.7× 143 0.4× 81 0.4× 145 1.0× 28 1.5k
Bai-Lin Wu 1.4k 1.1× 1.0k 1.0× 646 1.9× 209 1.1× 80 0.5× 43 2.2k
Zohreh Talebizadeh 1.0k 0.8× 973 0.9× 422 1.2× 123 0.7× 38 0.3× 31 1.7k
Bert van der Zwaag 704 0.5× 1.2k 1.2× 200 0.6× 138 0.7× 67 0.5× 44 2.2k
Arti Pandya 413 0.3× 1.3k 1.2× 496 1.4× 131 0.7× 194 1.3× 75 2.7k
Alessandra Murgia 638 0.5× 724 0.7× 254 0.7× 70 0.4× 87 0.6× 76 1.6k

Countries citing papers authored by Anne Moncla

Since Specialization
Citations

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

Fields of papers citing papers by Anne Moncla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Moncla

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

All Works

20 of 20 papers shown
1.
Bonnet, Céline, Asma Ali Khan, Emmanuel Bresso, et al.. (2013). Extended spectrum of MBD5 mutations in neurodevelopmental disorders. European Journal of Human Genetics. 21(12). 1457–1461. 30 indexed citations
2.
Ageeli, Essam Al, Séverine Drunat, Catherine Delanöe, et al.. (2013). Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases. European Journal of Medical Genetics. 57(1). 5–14. 67 indexed citations
3.
Bahi‐Buisson, Nadia, Nathalie Villeneuve, Aurélia Jacquette, et al.. (2012). Recurrent mutations in the CDKL5 gene: Genotype–phenotype relationships. American Journal of Medical Genetics Part A. 158A(7). 1612–1619. 45 indexed citations
4.
Cacciagli, Pierre, Cécile Mignon‐Ravix, Bilal El Waly, et al.. (2010). Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype. European Journal of Human Genetics. 18(12). 1360–1363. 66 indexed citations
5.
Giurgea, Irina, Chantal Missirian, Pierre Cacciagli, et al.. (2008). TCF4Deletions in Pitt-Hopkins Syndrome. Human Mutation. 29(11). E242–E251. 45 indexed citations
6.
Roux, Jean‐Christophe, et al.. (2007). Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome. European Journal of Neuroscience. 25(7). 1915–1922. 107 indexed citations
7.
Mignon‐Ravix, Cécile, D. Depétris, Judith Luciani, et al.. (2007). Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations. European Journal of Human Genetics. 15(4). 432–440. 38 indexed citations
8.
Bienvenu, Thierry, Christophe Philippe, Nicolás de Roux, et al.. (2006). The Incidence of Rett Syndrome in France. Pediatric Neurology. 34(5). 372–375. 41 indexed citations
9.
Cantagrel, Vincent, Steven Lisgo, Chantal Missirian, et al.. (2006). Truncation ofNHEJ1 in a patient with polymicrogyria. Human Mutation. 28(4). 356–364. 28 indexed citations
10.
Viemari, Jean‐Charles, Jean‐Christophe Roux, Andrew K. Tryba, et al.. (2005). Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice. Journal of Neuroscience. 25(50). 11521–11530. 233 indexed citations
11.
Yılmaz, Saliha, Thierry Bienvenu, Anne Moncla, et al.. (2005). Deleterious mutations in exon 1 of MECP2 in Rett syndrome. European Journal of Medical Genetics. 49(4). 313–322. 24 indexed citations
12.
Moncla, Anne, Arlette Kpebe, Chantal Missirian, Josette Mancini, & Laurent Villard. (2002). Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling. European Journal of Human Genetics. 10(1). 86–89. 28 indexed citations
13.
Bonneau, Dominique, et al.. (2000). Les syndromes génétiques avec obésité. 2(6). 56–63. 4 indexed citations
14.
Moncla, Anne, Perrine Malzac, Marie‐Antoinette Voelckel, et al.. (1999). Phenotype–genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients. European Journal of Human Genetics. 7(2). 131–139. 78 indexed citations
15.
Saugier-Véber, Pascale, Cosette Martin, Nathalie Le Meur, et al.. (1998). Identification of novelL1CAM mutations using fluorescence-assisted mismatch analysis. Human Mutation. 12(4). 259–266. 22 indexed citations
16.
Malzac, Perrine, et al.. (1998). Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnoses. American Journal of Medical Genetics. 78(3). 242–244. 6 indexed citations
17.
Cusin, Véronica, Géraldine Viot, Delphine Girlich, et al.. (1998). SHOX mutations in dyschondrosteosis (Leri-Weill syndrome). Nature Genetics. 19(1). 67–69. 257 indexed citations
18.
Jay, Philippe, Claire Rougeulle, Annick Massacrier, et al.. (1997). The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics. 17(3). 357–361. 205 indexed citations
19.
Moncla, Anne, et al.. (1993). Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome. Human Genetics. 90(6). 657–60. 13 indexed citations
20.
Moncla, Anne, Françoise Landon, Marie‐Geneviève Mattéi, & Marie‐Madeleine Portier. (1992). Chromosomal localisation of the mouse and human peripherin genes. Genetics Research. 59(2). 125–129. 12 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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