Nathalie Boddaert

27.0k total citations · 1 hit paper
389 papers, 12.7k citations indexed

About

Nathalie Boddaert is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Neurology. According to data from OpenAlex, Nathalie Boddaert has authored 389 papers receiving a total of 12.7k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Molecular Biology, 79 papers in Pediatrics, Perinatology and Child Health and 68 papers in Neurology. Recurrent topics in Nathalie Boddaert's work include Glioma Diagnosis and Treatment (53 papers), Fetal and Pediatric Neurological Disorders (53 papers) and Metabolism and Genetic Disorders (41 papers). Nathalie Boddaert is often cited by papers focused on Glioma Diagnosis and Treatment (53 papers), Fetal and Pediatric Neurological Disorders (53 papers) and Metabolism and Genetic Disorders (41 papers). Nathalie Boddaert collaborates with scholars based in France, United States and United Kingdom. Nathalie Boddaert's co-authors include Françis Brunelle, Mônica Zilbovicius, Arnold Münnich, Yves Samson, Christian Sainte‐Rose, Isabelle Desguerre, Nadia Chabane, Nadia Bahi‐Buisson, Catherine Barthélémy and Agnès Rötig and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Nathalie Boddaert

372 papers receiving 12.4k citations

Hit Papers

Histone H3F3A and HIST1H3... 2015 2026 2018 2022 2015 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathalie Boddaert France 60 4.4k 2.7k 2.2k 1.8k 1.7k 389 12.7k
Françis Brunelle France 62 1.5k 0.3× 1.5k 0.6× 1.9k 0.8× 768 0.4× 2.0k 1.1× 319 12.6k
Mustafa Şahin United States 62 7.4k 1.7× 3.7k 1.4× 2.3k 1.1× 643 0.3× 995 0.6× 314 15.9k
Ingmar Blümcke Germany 72 5.0k 1.1× 2.1k 0.8× 1.8k 0.8× 3.3k 1.8× 3.3k 1.9× 333 16.0k
Nereo Bresolin Italy 71 10.6k 2.4× 1.6k 0.6× 410 0.2× 3.1k 1.7× 548 0.3× 487 18.1k
Eugenio Mercuri Italy 75 11.0k 2.5× 1.8k 0.7× 745 0.3× 5.9k 3.2× 4.9k 2.8× 608 20.7k
Dennis Shaw United States 40 1.4k 0.3× 1.3k 0.5× 1.5k 0.7× 586 0.3× 871 0.5× 164 5.3k
William B. Dobyns United States 89 13.5k 3.0× 9.9k 3.7× 1.3k 0.6× 1.5k 0.8× 7.7k 4.4× 346 27.8k
Giacomo P. Comi Italy 62 9.0k 2.0× 1.3k 0.5× 631 0.3× 2.7k 1.5× 238 0.1× 570 15.6k
Kon Chu South Korea 62 4.3k 1.0× 693 0.3× 1.2k 0.5× 1.2k 0.6× 1.1k 0.7× 355 14.1k
Eric J. Huang United States 67 8.5k 1.9× 1.4k 0.5× 1.5k 0.7× 1.5k 0.8× 675 0.4× 173 20.9k

Countries citing papers authored by Nathalie Boddaert

Since Specialization
Citations

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

Fields of papers citing papers by Nathalie Boddaert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathalie Boddaert

This figure shows the co-authorship network connecting the top 25 collaborators of Nathalie Boddaert. A scholar is included among the top collaborators of Nathalie Boddaert 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 Nathalie Boddaert. Nathalie Boddaert 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.
Masutani, Evan, Sílvia Montserrat, S Prat, et al.. (2025). Characteristics of left ventricular dysfunction in repaired tetralogy of Fallot: A multi-institutional deep learning analysis of regional strain and dyssynchrony. Journal of Cardiovascular Magnetic Resonance. 27(1). 101886–101886.
2.
Boddaert, Nathalie, et al.. (2025). The influence of closed sutures on cranial morphology in Apert and Crouzon syndromes: A quantitative analysis. Journal of Anatomy. 248(1). 40–52.
3.
Lévy, R., Arnault Tauziède‐Espariat, Jean‐François Hak, et al.. (2025). MRI‐Based Score to Recognize Thalamic Glioma Grade in Children: Morphology, Diffusion, and Arterial‐Spin‐Labeling Perfusion. Pediatric Blood & Cancer. 72(7). e31704–e31704.
4.
Siquier-Pernet, Karine, Pauline Marzin, Christine Bôle‐Feysot, et al.. (2024). LSM7 variants involving key amino acids for LSM complex function cause a neurodevelopmental disorder with leukodystrophy and cerebellar atrophy. Human Genetics and Genomics Advances. 6(1). 100372–100372.
5.
Tauziède‐Espariat, Arnault, Aurore Siegfried, Yvan Nicaise, et al.. (2023). PLAG1 fusions extend the spectrum of PLAG(L)-altered CNS tumors. Acta Neuropathologica. 146(6). 841–844. 4 indexed citations
6.
Lesage, Alan M., Volodia Dangouloff‐Ros, R. Lévy, et al.. (2023). Arterial Spin-Labeling in the Assessment of Pediatric Nontraumatic Orbital Lesions. American Journal of Neuroradiology. 44(10). 1219–1223. 1 indexed citations
7.
Liebig, Patrick, Laura Mancini, Sotirios Bisdas, et al.. (2023). Fluid suppression in amide proton transfer‐weighted (APTw) CEST imaging: New theoretical insights and clinical benefits. Magnetic Resonance in Medicine. 91(4). 1354–1367. 10 indexed citations
8.
Dorval, Guillaume, Sandrine Marlin, Isabelle De Bie, et al.. (2023). Investigating genotype‐to‐phenotype correlation in CHARGE syndrome by deep phenotyping and multiparametric clustering. Clinical Genetics. 104(4). 466–471. 1 indexed citations
9.
Lemaître, Hervé, Ana Saitovitch, Ludovic Fillon, et al.. (2020). Rest Functional Brain Maturation during the First Year of Life. Cerebral Cortex. 31(3). 1776–1785. 15 indexed citations
10.
Garzelli, Lorenzo, Eimad Shotar, Thomas Blauwblomme, et al.. (2020). Risk Factors for Early Brain AVM Rupture: Cohort Study of Pediatric and Adult Patients. American Journal of Neuroradiology. 41(12). 2358–2363. 19 indexed citations
11.
Demily, Caroline, Alice Poisson, Julien Plasse, et al.. (2019). Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin–Siris syndrome. Psychiatric Genetics. 29(6). 237–242. 10 indexed citations
12.
Barret, E., Gwénaël Le Teuff, Jane Merlevede, et al.. (2019). TP53 Pathway Alterations Drive Radioresistance in Diffuse Intrinsic Pontine Gliomas (DIPG). Clinical Cancer Research. 25(22). 6788–6800. 62 indexed citations
13.
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
14.
Goya-Outi, Jessica, Fanny Orlhac, Raphaël Calmon, et al.. (2018). Computation of reliable textural indices from multimodal brain MRI: suggestions based on a study of patients with diffuse intrinsic pontine glioma. Physics in Medicine and Biology. 63(10). 105003–105003. 26 indexed citations
15.
Ozanne, Augustin, et al.. (2017). Patient radiation doses and reference levels in pediatric interventional radiology. European Radiology. 27(9). 3983–3990. 9 indexed citations
16.
Borck, Guntram, et al.. (2009). Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. European Journal of Medical Genetics. 52(4). 180–184. 20 indexed citations
17.
Rocco, Federico Di, Matthew Garnett, Nathalie Boddaert, et al.. (2007). Pediatric infratentorial gangliogliomas: a retrospective series. Journal of Neurosurgery Pediatrics. 107(4). 286–291. 36 indexed citations
18.
Zilbovicius, Mônica, Isabelle Meresse, Nadia Chabane, et al.. (2006). Autism, the superior temporal sulcus and social perception. Trends in Neurosciences. 29(7). 359–366. 284 indexed citations
19.
Portes, Vincent des, Nathalie Boddaert, Silvia Sacco, et al.. (2003). Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin‐1 gene. American Journal of Medical Genetics Part A. 124A(4). 364–371. 45 indexed citations
20.
Cachia, Arnaud, Jean‐François Mangin, Denis Rivière, et al.. (2003). A primal sketch of the cortex mean curvature: A morphogenesis based approach to study the variability of the folding patterns. IEEE Transactions on Medical Imaging. 22(6). 754–765. 108 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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