Nadia Bahi‐Buisson

13.3k citations

150 papers · 5.6k indexed · 1 hit paper · h-index 36

Impact in

Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Developmental Neuroscience top 2%

Papers in

Genetics 84
- Genetics and Neurodevelopmental Disorders 66
- Genomic variations and chromosomal abnormalities 23
- Genomics and Rare Diseases 15
Developmental Neuroscience 12

Co-authors: Thierry Bienvenu Nathalie Boddaert Helen Leonard Alan K. Percy John Christodoulou Walter E. Kaufmann Alessandra Renieri Angus Clarke
Journals: Epilepsia (9 papers)European Journal of Medical Genetics (9 papers)Neurogenetics (8 papers)Developmental Medicine & Child Neurology (7 papers)European Journal of Human Genetics (5 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Nadia Bahi‐Buisson

145 papers receiving 5.5k citations

Hit Papers

align trajectories log scale

Rett syndrome: Revised diagnostic criteria and nomenclature 2010 · 990 citations

Peers

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-authors

The 25 scholars most cited alongside Nadia Bahi‐Buisson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nadia Bahi‐Buisson Line = papers co-authored together Nadia Bahi‐Buisson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis Development ·Vicente Elorriaga, Benoît Bouloudi, Elodie Delberghe, Yoann Saillour, J. Morel, Patrick Azzam, Matthieu X. Moreau, Rolf W. Stottmann, Nadia Bahi‐Buisson, Alessandra Pierani, Nathalie Spassky, Frédéric Causeret	2025	0
2	Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial European Journal of Paediatric Neurology ·Jenny Downs, Peter Jacoby, Nicola Specchio, H Cross, S Amin, Nadia Bahi‐Buisson, Rajsekar R. Rajaraman, Bernhard Suter, Orrin Devinsky, A Aimetti, Gregory D. Busse, Heather E. Olson, S Demarest, T A Benke, E Pestana-Knight	2024	6
3	Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry Orphanet Journal of Rare Diseases ·Elise Brimble, Kathryn Reyes, Kopika Kuhathaas, Orrin Devinsky, Maura Ruzhnikov, Xilma R. Ortiz‐González, Ingrid E. Scheffer, Nadia Bahi‐Buisson, Heather E. Olson	2023	7
4	Long‐term treatment with ganaxolone for seizures associated with cyclin‐dependent kinase‐like 5 deficiency disorder: Two‐year open‐label extension follow‐up Epilepsia ·Heather E. Olson, Sam Amin, Nadia Bahi‐Buisson, Orrin Devinsky, Eric D. Marsh, Elia Pestana‐Knight, Rajsekar R. Rajaraman, Alex A. Aimetti, Eva Rybak, Fanhui Kong, Ian Miller, Joseph Hulihan, Scott Demarest	2023	16
5	Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development Nature Communications ·Delfina M. Romero, Karine Poirier, Richard Belvindrah, Imane Moutkine, Anne Houllier, Anne-Gaëlle LeMoing, Florence Petit, Anne Boland, Stephan C. Collins, Mariano Soiza‐Reilly, Binnaz Yalcin, Jamel Chelly, Jean‐François Deleuze, Nadia Bahi‐Buisson, Fiona Francis	2022	4
6	Heterogeneity in defining fetal corpus callosal pathology: systematic review Ultrasound in Obstetrics and Gynecology ·Houman Mahallati, Alexandros Sotiriadis, C. Celestin, A. Millischer, P. Sonigo, D. Grévent, N. O’Gorman, Nadia Bahi‐Buisson, Tania Attié‐Bitach, Y. Ville, L. J. Salomon	2020	19
7	Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features European Journal of Paediatric Neurology ·Lubov Blumkin, Z. Leibovitz, Karina Krajden-Haratz, Ayala Arad, Keren Yosovich, L. Gindes, Ayelet Zerem, Liat Ben‐Sira, Dorit Lev, Andrea Nissenkorn, Dvora Kidron, William B. Dobyns, G. Malinger, Nadia Bahi‐Buisson, Richard J. Leventer, Tally Lerman‐Sagie	2020	12
8	EML1‐associated brain overgrowth syndrome with ribbon‐like heterotopia American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Renske Oegema, George McGillivray, Richard J. Leventer, Anne‐Gaëlle Le Moing, Nadia Bahi‐Buisson, Angela Barnicoat, Simone Mandelstam, David Francis, Fiona Francis, Grazia M.S. Mancini, Sanne M. C. Savelberg, Gijs van Haaften, Kshitij Mankad, Maarten H. Lequin	2019	17
9	Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia Cell Reports ·Ana Uzquiano, Carmen Cifuentes-Díaz, Ammar Jabali, Delfina M. Romero, Anne Houllier, Florent Dingli, Camille Maillard, Anne Boland, Jean‐François Deleuze, Damarys Loew, Grazia M.S. Mancini, Nadia Bahi‐Buisson, Julia Ladewig, Fiona Francis	2019	33
10	Mutations in TBR1 gene leads to cortical malformations and intellectual disability European Journal of Medical Genetics ·Nancy Végas, Mara Cavallin, Tjitske Kleefstra, Lonneke de Boer, Marion Philbert, Camille Maillard, Nathalie Boddaert, Arnold Münnich, Laurence Hubert, Amandine Béry, Claude Besmond, Nadia Bahi‐Buisson	2018	21
11	Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome European Journal of Medical Genetics ·B. Deloison, P. Sonigo, A. Millischer, Thibaud Quibel, Mara Cavallin, G. Benoist, Chloé Quēlin, Pierre‐Simon Jouk, Dorit Lev, Marianne Alison, Clarisse Baumann, C. Beldjord, F. Razavi, B. Bessières, Nathalie Boddaert, Y. Ville, L. J. Salomon, Nadia Bahi‐Buisson	2018	12
12	Prenatal and postnatal presentations of corpus callosum agenesis with polymicrogyria caused by EGP5 mutation American Journal of Medical Genetics Part A ·Camille Maillard, Mara Cavallin, Kevin Piquand, Marion Philbert, Jean Philippe Bault, A. Millischer, Despina Moshous, Marlène Rio, Cyril Gitiaux, Nathalie Boddaert, Cécile Masson, Sophie Thomas, Nadia Bahi‐Buisson	2017	10
13	A critical and previously unsuspected role for doublecortin at the neuromuscular junction in mouse and human Neuromuscular Disorders ·F. Bourgeois, Julien Messéant, Ekaterini Kordeli, Julia Petit, Perrine Delers, Nadia Bahi‐Buisson, Véronique Bernard, Séverine M. Sigoillot, Cyril Gitiaux, Melissa A. Stouffer, Fiona Francis, Claire Legay	2015	14
14	Late onset epileptic spasms is frequent in MECP2 gene duplication: Electroclinical features and long-term follow-up of 8 epilepsy patients European Journal of Paediatric Neurology ·Roseline Caumes, Odile Boespflug‐Tanguy, Nathalie Villeneuve, Laëtitia Lambert, Catherine Delanöe, Bruno Leheup, Nadia Bahi‐Buisson, Stéphane Auvin	2014	18
15	New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum Brain ·Nadia Bahi‐Buisson, Isabelle Souville, Franck J. Fourniol, Aurélie Toussaint, Carolyn A. Moores, Anne Houdusse, Jean Yves Lemaitre, Karine Poirier, Reham Khalaf‐Nazzal, Marie Hully, Pierre Louis Léger, Caroline Elie, Nathalie Boddaert, Chérif Beldjord, Jamel Chelly, Fiona Francis	2013	74
16	Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria European Journal of Human Genetics ·Karine Poirier, Yoann Saillour, Franck J. Fourniol, Fiona Francis, Isabelle Souville, Stéphanie Valence, Isabelle Desguerre, Jean Marie Lepage, Nathalie Boddaert, Marine Line Jacquemont, Chérif Beldjord, Jamel Chelly, Nadia Bahi‐Buisson	2012	50
17	<i>CDKL5</i>-Related Disorders: From Clinical Description to Molecular Genetics Molecular Syndromology ·Nadia Bahi‐Buisson, Thierry Bienvenu	2011	66
18	GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Brain ·Nadia Bahi‐Buisson, Karine Poirier, Nathalie Boddaert, Catherine Fallet‐Bianco, Nicola Specchio, Enrico Bertini, Ahmet Okay Çağlayan, Karine Lascelles, Caroline Elie, Jérôme Rambaud, Michel Baulac, Isabelle An, Patrícia Dias, Vincent des Portes, Marie Laure Moutard, Christine Soufflet, Monique El Maleh, Chérif Beldjord, Laurent Villard, Jamel Chelly	2010	102
19	Novel FOXG1 mutations associated with the congenital variant of Rett syndrome Journal of Medical Genetics ·Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso, Dalila Rondinella, Roberta De Filippis, Nadia Bahi‐Buisson, Juliette Nectoux, R. Rubinsztajn, Thierry Bienvenu, A. Moncla, B. Chabrol, Laurent Villard, Zita Krūmiņa, Judith Armstrong, Ana Roche, M. Pineda, Eva Gak, Francesca Mari, Francesca Ariani, Alessandra Renieri	2009	74
20	The Nonmalformed Hemisphere Is Secondarily Impaired in Young Children with Hemimegalencephaly: A Pre‐ and Postsurgery Study with SPECT and EEG Epilepsia ·Christine Soufflet, Christine Bulteau, Olivier Delalande, Florence Pinton, C Jalin, Perrine Plouin, Nadia Bahi‐Buisson, Olivier Dulac, Catherine Chiron	2004	19

About Nadia Bahi‐Buisson

Nadia Bahi‐Buisson is a scholar working on Genetics, Developmental Neuroscience, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Psychiatry and Mental health, having authored 150 papers that have together received 5.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (66 papers), Fetal and Pediatric Neurological Disorders (25 papers), Genomic variations and chromosomal abnormalities (23 papers), Epilepsy research and treatment (22 papers), Metabolism and Genetic Disorders (17 papers), Autism Spectrum Disorder Research (17 papers), Microtubule and mitosis dynamics (16 papers) and Genomics and Rare Diseases (15 papers). The work is most often cited by research in Genetics (3.1k citations), Developmental Neuroscience (273 citations), Cognitive Neuroscience (1.3k citations), Clinical Biochemistry (395 citations) and Psychiatry and Mental health (701 citations). Nadia Bahi‐Buisson has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Thierry Bienvenu, Nathalie Boddaert, Helen Leonard, Alan K. Percy, John Christodoulou, Walter E. Kaufmann, Alessandra Renieri, Angus Clarke, Mark E.S. Bailey and Michele Zappella. Their work appears in journals such as Epilepsia, European Journal of Medical Genetics, Neurogenetics, Developmental Medicine & Child Neurology and European Journal of Human Genetics.

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