Juliette Nectoux

2.3k total citations
58 papers, 1.3k citations indexed

About

Juliette Nectoux is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Juliette Nectoux has authored 58 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 29 papers in Genetics and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Juliette Nectoux's work include Genetics and Neurodevelopmental Disorders (23 papers), Genomic variations and chromosomal abnormalities (14 papers) and Prenatal Screening and Diagnostics (12 papers). Juliette Nectoux is often cited by papers focused on Genetics and Neurodevelopmental Disorders (23 papers), Genomic variations and chromosomal abnormalities (14 papers) and Prenatal Screening and Diagnostics (12 papers). Juliette Nectoux collaborates with scholars based in France, United States and Spain. Juliette Nectoux's co-authors include Thierry Bienvenu, Jamel Chelly, Nadia Bahi‐Buisson, Yann Fichou, Benôıt Girard, Nathalie Boddaert, Haydeé Rosas‐Vargas, Chloé Delépine, Marlène Rio and France Leturcq and has published in prestigious journals such as Gastroenterology, PLoS ONE and Brain.

In The Last Decade

Juliette Nectoux

54 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Juliette Nectoux France 23 775 602 207 157 142 58 1.3k
Maria Antonietta Mencarelli Italy 26 1.2k 1.5× 982 1.6× 354 1.7× 44 0.3× 105 0.7× 65 1.9k
Katherine Lachlan United Kingdom 19 659 0.9× 869 1.4× 122 0.6× 78 0.5× 82 0.6× 45 1.4k
Sandrine Passemard France 21 396 0.5× 710 1.2× 59 0.3× 59 0.4× 116 0.8× 42 1.4k
Todd Green United States 6 1.3k 1.7× 623 1.0× 441 2.1× 207 1.3× 125 0.9× 6 1.8k
Amy M. Breman United States 20 713 0.9× 587 1.0× 119 0.6× 139 0.9× 502 3.5× 47 1.4k
Neal Farber United States 10 320 0.4× 615 1.0× 170 0.8× 48 0.3× 49 0.3× 14 1.5k
Shay Ben‐Shachar Israel 18 700 0.9× 592 1.0× 238 1.1× 106 0.7× 145 1.0× 41 1.0k
Greg James United Kingdom 19 401 0.5× 197 0.3× 17 0.1× 264 1.7× 112 0.8× 90 1.2k
Nicole de Leeuw Netherlands 30 2.4k 3.1× 1.4k 2.3× 148 0.7× 170 1.1× 744 5.2× 104 3.2k
María Clara Bonaglia Italy 25 1.1k 1.4× 891 1.5× 226 1.1× 78 0.5× 422 3.0× 61 1.8k

Countries citing papers authored by Juliette Nectoux

Since Specialization
Citations

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

Fields of papers citing papers by Juliette Nectoux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juliette Nectoux

This figure shows the co-authorship network connecting the top 25 collaborators of Juliette Nectoux. A scholar is included among the top collaborators of Juliette Nectoux 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 Juliette Nectoux. Juliette Nectoux 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.
Romo, Lucía, Emily O’Heir, Juliette Nectoux, et al.. (2025). 490PA recurrent non-coding 3’UTR variant as a hidden second hit in 11 families with CAPN3-related limb girdle muscular dystrophy. Neuromuscular Disorders. 53. 105786–105786.
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Pacault, Mathilde, Marie‐Pierre Audrézet, Nathalie Couque, et al.. (2023). Vers une généralisation du diagnostic prénatal non-invasif des maladies monogéniques ? État des lieux et perspectives. Gynécologie Obstétrique Fertilité & Sénologie . 51(10). 463–470.
5.
Nectoux, Juliette, et al.. (2023). The value of plasma cell-free DNA levels as biomarker in patients with eating disorders: A preliminary study. Psychoneuroendocrinology. 160. 106918–106918. 1 indexed citations
6.
Nectoux, Juliette, Benjamin Saintpierre, Nicolas Lebrun, et al.. (2020). MeCP2 is involved in random mono-allelic expression for a subset of human autosomal genes. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(6). 165730–165730. 1 indexed citations
7.
Viollet, Louis, Kathryn J. Swoboda, Rong Mao, et al.. (2020). A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies. European Journal of Medical Genetics. 63(12). 104063–104063. 5 indexed citations
8.
Iliescu, Catrinel, A. Seferian, Svetlana Gataullina, et al.. (2017). DMD and West syndrome. Neuromuscular Disorders. 27(10). 911–913. 4 indexed citations
9.
Khattabi, Laïla El, Dominique Le Tessier, Armelle Luscan, et al.. (2016). Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study. PLoS ONE. 11(5). e0155009–e0155009. 37 indexed citations
10.
Delépine, Chloé, Juliette Nectoux, Franck Letourneur, et al.. (2015). Astrocyte Transcriptome from the Mecp2308-Truncated Mouse Model of Rett Syndrome. NeuroMolecular Medicine. 17(4). 353–363. 29 indexed citations
11.
Rousseaud, Audrey, Chloé Delépine, Juliette Nectoux, Pierre Billuart, & Thierry Bienvenu. (2015). Differential Expression and Regulation of Brain-Derived Neurotrophic Factor (BDNF) mRNA Isoforms in Brain Cells from Mecp2308/y Mouse Model. Journal of Molecular Neuroscience. 56(4). 758–767. 15 indexed citations
12.
Delépine, Chloé, et al.. (2013). Mutations in the C-terminus of CDKL5: proceed with caution. European Journal of Human Genetics. 22(2). 270–272. 13 indexed citations
13.
Nectoux, Juliette, Yann Fichou, Haydeé Rosas‐Vargas, et al.. (2010). Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes. Journal of Cellular and Molecular Medicine. 14(7). 1962–1974. 27 indexed citations
14.
Guen, Tangui Le, Yann Fichou, Juliette Nectoux, et al.. (2010). A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localization. Human Mutation. 32(2). E2026–E2035. 15 indexed citations
15.
Fichou, Yann, Juliette Nectoux, Nadia Bahi‐Buisson, Jamel Chelly, & Thierry Bienvenu. (2010). An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brain. Journal of Human Genetics. 56(1). 52–57. 23 indexed citations
16.
White, Rose, Gladys Ho, Ingrid E. Scheffer, et al.. (2010). Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders. Twin Research and Human Genetics. 13(2). 168–178. 27 indexed citations
17.
Nectoux, Juliette, Yann Fichou, Nicolas Cagnard, et al.. (2010). Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathy. Journal of Molecular Medicine. 89(2). 193–202. 9 indexed citations
18.
Bahi‐Buisson, Nadia, Juliette Nectoux, Benôıt Girard, et al.. (2009). Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant. Neurogenetics. 11(2). 241–249. 57 indexed citations
19.
Mencarelli, Maria Antonietta, Ariele Spanhol-Rosseto, Rosangela Artuso, et al.. (2009). Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Journal of Medical Genetics. 47(1). 49–53. 74 indexed citations
20.
Nectoux, Juliette, Chrystel Leroy, Odile Raguénès, et al.. (2006). A Frequent Large Rearrangement in the CFTR Gene in Cystic Fibrosis Patients from Reunion Island. Genetic Testing. 10(3). 208–214. 3 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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