Lara Moumné

783 total citations
11 papers, 629 citations indexed

About

Lara Moumné is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Lara Moumné has authored 11 papers receiving a total of 629 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Lara Moumné's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Ubiquitin and proteasome pathways (3 papers). Lara Moumné is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Ubiquitin and proteasome pathways (3 papers). Lara Moumné collaborates with scholars based in France, United States and India. Lara Moumné's co-authors include Reiner A. Veitia, Sandrine Bétuing, Nallathambi Jeyabalan, Frank Batista, Periasamy Sundaresan, Marc Fellous, Elfride De Baere, Jocelyne Caboche, Diane Beysen and Christiane Pagès and has published in prestigious journals such as PLoS ONE, Brain and Biological Psychiatry.

In The Last Decade

Lara Moumné

11 papers receiving 621 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lara Moumné France	11	386	251	178	89	73	11	629
Akiko Takizawa Japan	13	437 1.1×	315 1.3×	131 0.7×	235 2.6×	51 0.7×	33	804
Yu-Lai Wang Japan	9	394 1.0×	129 0.5×	92 0.5×	70 0.8×	26 0.4×	9	598
Elena Panzeri Italy	15	225 0.6×	125 0.5×	140 0.8×	47 0.5×	77 1.1×	33	587
Monique Saunier France	12	448 1.2×	61 0.2×	219 1.2×	46 0.5×	37 0.5×	20	793
Tania Sorg France	15	306 0.8×	120 0.5×	78 0.4×	35 0.4×	36 0.5×	27	571
Grant R. Sutherland Australia	11	346 0.9×	188 0.7×	189 1.1×	20 0.2×	32 0.4×	14	610
Siegmund S. Wolf United Kingdom	15	622 1.6×	147 0.6×	51 0.3×	25 0.3×	77 1.1×	27	852
Hitomi Yamanaka Japan	8	379 1.0×	122 0.5×	127 0.7×	131 1.5×	17 0.2×	11	596
Cécile Mignon‐Ravix France	15	475 1.2×	320 1.3×	62 0.3×	20 0.2×	14 0.2×	26	727
M Poissonnier France	14	324 0.8×	317 1.3×	34 0.2×	221 2.5×	24 0.3×	20	712

Countries citing papers authored by Lara Moumné

Since Specialization

Citations

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

Fields of papers citing papers by Lara Moumné

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lara Moumné

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

All Works

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11 of 11 papers shown

Alves, Sandro, Antonin Lamazière, Anabelle Planques, et al.. (2016). CYP46A1, the rate-limiting enzyme for cholesterol degradation, is neuroprotective in Huntington’s disease. Brain. 139(3). 953–970. 147 indexed citations

Salery, Marine, Marc Dos Santos, Lara Moumné, et al.. (2016). Activity-Regulated Cytoskeleton-Associated Protein Accumulates in the Nucleus in Response to Cocaine and Acts as a Brake on Chromatin Remodeling and Long-Term Behavioral Alterations. Biological Psychiatry. 81(7). 573–584. 44 indexed citations

Moumné, Lara, Sandrine Bétuing, & Jocelyne Caboche. (2013). Multiple Aspects of Gene Dysregulation in Huntington’s Disease. Frontiers in Neurology. 4. 127–127. 55 indexed citations

Beconi, Maria, Omar Aziz, Kim L. Matthews, et al.. (2012). Oral Administration of the Pimelic Diphenylamide HDAC Inhibitor HDACi 4b Is Unsuitable for Chronic Inhibition of HDAC Activity in the CNS In Vivo. PLoS ONE. 7(9). e44498–e44498. 33 indexed citations

Moumné, Lara, et al.. (2012). Genetic Knock-Down of Hdac3 Does Not Modify Disease-Related Phenotypes in a Mouse Model of Huntington's Disease. PLoS ONE. 7(2). e31080–e31080. 52 indexed citations

Beysen, Diane, Lara Moumné, Reiner A. Veitia, et al.. (2008). Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation. Human Molecular Genetics. 17(13). 2030–2038. 66 indexed citations

Jeyabalan, Nallathambi, Paul Laissue, Frank Batista, et al.. (2008). Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients. Human Mutation. 29(8). E123–E131. 22 indexed citations

Moumné, Lara, Frank Batista, Bérénice A. Benayoun, et al.. (2007). The mutations and potential targets of the forkhead transcription factor FOXL2. Molecular and Cellular Endocrinology. 282(1-2). 2–11. 60 indexed citations

Moumné, Lara, Aurélie Dipietromaria, Frank Batista, et al.. (2007). Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development. Human Molecular Genetics. 17(7). 1010–1019. 61 indexed citations

10.

Jeyabalan, Nallathambi, Lara Moumné, Elfride De Baere, et al.. (2006). A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. Human Genetics. 121(1). 107–112. 59 indexed citations

11.

Moumné, Lara, Marc Fellous, & Reiner A. Veitia. (2005). Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation. Human Molecular Genetics. 14(23). 3557–3564. 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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