Amélie Piton

9.2k total citations · 1 hit paper
48 papers, 2.6k citations indexed

About

Amélie Piton is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Amélie Piton has authored 48 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 30 papers in Genetics and 5 papers in Cognitive Neuroscience. Recurrent topics in Amélie Piton's work include Genetics and Neurodevelopmental Disorders (20 papers), Genomics and Rare Diseases (15 papers) and Genomic variations and chromosomal abnormalities (12 papers). Amélie Piton is often cited by papers focused on Genetics and Neurodevelopmental Disorders (20 papers), Genomics and Rare Diseases (15 papers) and Genomic variations and chromosomal abnormalities (12 papers). Amélie Piton collaborates with scholars based in France, Canada and United States. Amélie Piton's co-authors include Fabrice Morel, André Guillouzo, Jean‐Louis Mandel, Sophie Langouët, Christiane Guguen‐Guillouzo, Claire Redin, Caroline Aninat, Denise Glaise, Guy A. Rouleau and Julie Gauthier and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Bioinformatics.

In The Last Decade

Amélie Piton

44 papers receiving 2.6k 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.

EXPRESSION OF CYTOCHROMES P450, CONJUGATING ENZYMES AND NUCLEAR RECEPTORS IN HUMAN HEPATOMA HepaRG CELLS

2005 533 citations Amélie Piton, Sophie Langouët et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amélie Piton France	21	1.4k	1.3k	468	328	254	48	2.6k
Mojgan Rastegar Canada	35	1.7k 1.3×	1.1k 0.8×	377 0.8×	194 0.6×	40 0.2×	69	2.8k
Ueli Schibler Switzerland	10	1.6k 1.2×	589 0.5×	88 0.2×	230 0.7×	165 0.6×	11	3.3k
Moyra Smith United States	26	1.2k 0.9×	698 0.6×	448 1.0×	211 0.6×	145 0.6×	60	2.9k
Diana Hall Switzerland	23	1.5k 1.1×	799 0.6×	257 0.5×	589 1.8×	126 0.5×	49	2.5k
Akiko Murayama Japan	31	1.8k 1.3×	680 0.5×	261 0.6×	461 1.4×	52 0.2×	63	3.6k
Yijing Su United States	22	3.3k 2.4×	876 0.7×	158 0.3×	330 1.0×	94 0.4×	36	4.2k
Christopher R. Mueller Canada	29	1.8k 1.3×	604 0.5×	78 0.2×	378 1.2×	47 0.2×	59	2.9k
Philip J. Ebert United States	22	1.1k 0.8×	634 0.5×	571 1.2×	454 1.4×	19 0.1×	36	2.3k
Orna Levran United States	32	1.8k 1.3×	646 0.5×	101 0.2×	751 2.3×	203 0.8×	75	3.4k

Countries citing papers authored by Amélie Piton

Since Specialization

Citations

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

Fields of papers citing papers by Amélie Piton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amélie Piton

This figure shows the co-authorship network connecting the top 25 collaborators of Amélie Piton. A scholar is included among the top collaborators of Amélie Piton 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 Amélie Piton. Amélie Piton 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

Baer, Sarah, Marie‐Aude Spitz, Édouard Hirsch, et al.. (2025). Explosive onset focal epilepsies without cortical malformation: A review of a pediatric cohort with pathogenic variations in the GATOR1 complex (DEPDC5, NPRL3 and NPRL2). Seizure. 129. 25–28.

Panzade, Ganesh, et al.. (2024). Modeling neurodevelopmental disorder-associated humanAGO1mutations inCaenorhabditis elegansArgonautealg-1. Proceedings of the National Academy of Sciences. 121(10). e2308255121–e2308255121. 8 indexed citations

Piton, Amélie, et al.. (2024). The role of DEAD- and DExH-box RNA helicases in neurodevelopmental disorders. Frontiers in Molecular Neuroscience. 17. 1414949–1414949. 1 indexed citations

Quartier, Angélique, Nathalie Drouot, Damien Plassard, et al.. (2023). Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome. Molecular Psychiatry. 29(2). 287–296. 4 indexed citations

Schaefer, Élise, Pauline Burger, Sarah Baer, et al.. (2022). Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders: the DYRK1A and the Wiedemann–Steiner syndromes. Clinical Genetics. 102(4). 296–304. 11 indexed citations

Patat, Olivier, Sandra Whalen, Lionel Arnaud, et al.. (2021). Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome. Journal of Medical Genetics. 59(5). 505–510. 8 indexed citations

Schaefer, Élise, Christèle Dubourg, Wilfrid Carré, et al.. (2021). Skraban‐Deardorff syndrome: Six new cases of WDR 26 ‐related disease and expansion of the clinical phenotype. Clinical Genetics. 99(5). 732–739. 4 indexed citations

Estrada‐Cuzcano, Alejandro, Christelle Etard, Corinne Stoetzel, et al.. (2019). NovelIQCEvariations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish. Human Mutation. 41(1). 240–254. 5 indexed citations

Geoffroy, Véronique, Yvan Herenger, Arnaud Kress, et al.. (2018). AnnotSV: an integrated tool for structural variations annotation. Bioinformatics. 34(20). 3572–3574. 207 indexed citations

10.

Vears, Danya F., Karine Sénécal, Angus Clarke, et al.. (2017). Points to consider for laboratories reporting results from diagnostic genomic sequencing. European Journal of Human Genetics. 26(1). 36–43. 53 indexed citations

11.

Mattioli, Francesca, Amélie Piton, Bénédicte Gérard, et al.. (2016). Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidism. American Journal of Medical Genetics Part A. 170(6). 1626–1629. 20 indexed citations

12.

Piton, Amélie, Claire Redin, & Jean‐Louis Mandel. (2013). XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing. The American Journal of Human Genetics. 93(2). 368–383. 165 indexed citations

13.

Corradi, Anna, Manuela Fadda, Amélie Piton, et al.. (2013). SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth. Human Molecular Genetics. 23(1). 90–103. 65 indexed citations

14.

Hamdan, Fadi F., Hussein Daoud, Amélie Piton, et al.. (2011). De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism. Biological Psychiatry. 69(9). 898–901. 130 indexed citations

15.

Myers, Rachel A., Ferrán Casals, Julie Gauthier, et al.. (2011). A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing. PLoS Genetics. 7(2). e1001318–e1001318. 68 indexed citations

16.

Hamdan, Fadi F., Hussein Daoud, Daniel Rochefort, et al.. (2010). De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment. The American Journal of Human Genetics. 87(5). 671–678. 170 indexed citations

17.

Piton, Amélie, Claudine Rauch, Sophie Langouët, André Guillouzo, & Fabrice Morel. (2009). Involvement of pregnane X receptor in the regulation of CYP2B6 gene expression by oltipraz in human hepatocytes. Toxicology in Vitro. 24(2). 452–459. 12 indexed citations

18.

Hamdan, Fadi F., Amélie Piton, Julie Gauthier, et al.. (2009). De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. Annals of Neurology. 65(6). 748–753. 108 indexed citations

19.

Morel, Fabrice, Claudine Rauch, Amélie Piton, et al.. (2004). Gene and Protein Characterization of the Human Glutathione S-Transferase Kappa and Evidence for a Peroxisomal Localization. Journal of Biological Chemistry. 279(16). 16246–16253. 125 indexed citations

20.

Piton, Amélie. (2004). Oltipraz regulates different categories of genes relevant to chemoprevention in human hepatocytes. Carcinogenesis. 26(2). 343–351. 10 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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