Nadia Bahi‐Buisson

13.3k total citations · 1 hit paper
150 papers, 5.6k citations indexed

About

Nadia Bahi‐Buisson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nadia Bahi‐Buisson has authored 150 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Genetics, 65 papers in Molecular Biology and 33 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nadia Bahi‐Buisson's work include Genetics and Neurodevelopmental Disorders (66 papers), Fetal and Pediatric Neurological Disorders (25 papers) and Genomic variations and chromosomal abnormalities (23 papers). Nadia Bahi‐Buisson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (66 papers), Fetal and Pediatric Neurological Disorders (25 papers) and Genomic variations and chromosomal abnormalities (23 papers). Nadia Bahi‐Buisson collaborates with scholars based in France, United States and United Kingdom. Nadia Bahi‐Buisson's co-authors include Thierry Bienvenu, Nathalie Boddaert, Helen Leonard, Alan K. Percy, John Christodoulou, Walter E. Kaufmann, Alessandra Renieri, Angus Clarke, Jeffrey L. Neul and Michele Zappella and has published in prestigious journals such as Cell, Nature Communications and PLoS ONE.

In The Last Decade

Nadia Bahi‐Buisson

145 papers receiving 5.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rett syndrome: Revised diagnostic criteria and nomenclature

2010 990 citations John Christodoulou, Nadia Bahi‐Buisson et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nadia Bahi‐Buisson France	36	3.1k	2.4k	1.3k	747	743	150	5.6k
Thierry Bienvenu France	38	3.2k 1.0×	2.4k 1.0×	944 0.7×	393 0.5×	206 0.3×	200	5.6k
Vincent des Portes France	30	2.1k 0.7×	2.2k 0.9×	881 0.7×	417 0.6×	492 0.7×	91	4.1k
Heather C. Mefford United States	38	3.8k 1.2×	2.6k 1.1×	686 0.5×	688 0.9×	223 0.3×	110	5.6k
Tjitske Kleefstra Netherlands	38	3.7k 1.2×	3.4k 1.4×	696 0.6×	344 0.5×	446 0.6×	131	5.7k
Bruria Ben‐Zeev Israel	33	994 0.3×	1.3k 0.5×	530 0.4×	514 0.7×	241 0.3×	105	3.4k
Dawna Armstrong United States	20	2.1k 0.7×	3.0k 1.2×	793 0.6×	360 0.5×	222 0.3×	33	4.2k
Susan L. Christian United States	33	3.2k 1.0×	2.3k 0.9×	920 0.7×	997 1.3×	233 0.3×	53	4.4k
Sakkubai Naidu United States	33	1.0k 0.3×	3.2k 1.3×	645 0.5×	171 0.2×	381 0.5×	80	4.4k
Dimitrios Avramopoulos United States	37	1.5k 0.5×	1.5k 0.6×	745 0.6×	293 0.4×	149 0.2×	114	4.1k
Daniel G. Glaze United States	53	6.8k 2.2×	2.8k 1.2×	4.8k 3.8×	681 0.9×	147 0.2×	164	8.9k

Countries citing papers authored by Nadia Bahi‐Buisson

Since Specialization

Citations

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

Fields of papers citing papers by Nadia Bahi‐Buisson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nadia Bahi‐Buisson. 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 Nadia Bahi‐Buisson. The network helps show where Nadia Bahi‐Buisson may publish in the future.

Co-authorship network of co-authors of Nadia Bahi‐Buisson

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

All Works

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20 of 20 papers shown

Saillour, Yoann, Rolf W. Stottmann, Nadia Bahi‐Buisson, et al.. (2025). Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis. Development. 152(9).

Brimble, Elise, Pamela Ventola, Christopher E. Hart, et al.. (2025). Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome. Journal of Neurodevelopmental Disorders. 17(1). 64–64.

Downs, Jenny, Peter Jacoby, Nicola Specchio, et al.. (2024). Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial. European Journal of Paediatric Neurology. 51. 140–146. 6 indexed citations

Brimble, Elise, Orrin Devinsky, Maura Ruzhnikov, et al.. (2023). Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry. Orphanet Journal of Rare Diseases. 18(1). 149–149. 7 indexed citations

Olson, Heather E., Sam Amin, Nadia Bahi‐Buisson, et al.. (2023). Long‐term treatment with ganaxolone for seizures associated with cyclin‐dependent kinase‐like 5 deficiency disorder: Two‐year open‐label extension follow‐up. Epilepsia. 65(1). 37–45. 16 indexed citations

Poirier, Karine, Richard Belvindrah, Imane Moutkine, et al.. (2022). Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development. Nature Communications. 13(1). 2746–2746. 4 indexed citations

Mahallati, Houman, Alexandros Sotiriadis, A. Millischer, et al.. (2020). Heterogeneity in defining fetal corpus callosal pathology: systematic review. Ultrasound in Obstetrics and Gynecology. 58(1). 11–18. 19 indexed citations

Oegema, Renske, George McGillivray, Richard J. Leventer, et al.. (2019). EML1‐associated brain overgrowth syndrome with ribbon‐like heterotopia. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(4). 627–637. 17 indexed citations

Uzquiano, Ana, Carmen Cifuentes-Díaz, Ammar Jabali, et al.. (2019). Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia. Cell Reports. 28(6). 1596–1611.e10. 33 indexed citations

10.

Cavallin, Mara, Tjitske Kleefstra, Lonneke de Boer, et al.. (2018). Mutations in TBR1 gene leads to cortical malformations and intellectual disability. European Journal of Medical Genetics. 61(12). 759–764. 21 indexed citations

11.

Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations

12.

Cavallin, Mara, A. Millischer, Despina Moshous, et al.. (2017). Prenatal and postnatal presentations of corpus callosum agenesis with polymicrogyria caused by EGP5 mutation. American Journal of Medical Genetics Part A. 173(3). 706–711. 10 indexed citations

13.

Brassier, Anaïs, Vassili Valayannopoulos, Nadia Bahi‐Buisson, et al.. (2015). Two new cases of serine deficiency disorders treated with l-serine. European Journal of Paediatric Neurology. 20(1). 53–60. 29 indexed citations

14.

Bahi‐Buisson, Nadia & Thierry Bienvenu. (2011). <i>CDKL5</i>-Related Disorders: From Clinical Description to Molecular Genetics. Molecular Syndromology. 2(3-5). 137–152. 66 indexed citations

15.

Bahi‐Buisson, Nadia, Karine Poirier, Nathalie Boddaert, et al.. (2010). GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. Brain. 133(11). 3194–3209. 102 indexed citations

16.

Roubertie, Agathe, et al.. (2010). Traitement des dystonies de l’enfant. Archives de Pédiatrie. 17(5). 540–553. 3 indexed citations

17.

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

18.

Bebbington, Ami, Alan K. Percy, John Christodoulou, et al.. (2009). Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Journal of Medical Genetics. 47(4). 242–248. 54 indexed citations

19.

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

20.

Bahi‐Buisson, Nadia, Vicente Villanueva, Christine Bulteau, et al.. (2007). Long term response to steroid therapy in Rasmussen encephalitis. Seizure. 16(6). 485–492. 32 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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