Marlène Rio

10.4k total citations
112 papers, 3.5k citations indexed

About

Marlène Rio is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Marlène Rio has authored 112 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 61 papers in Genetics and 19 papers in Clinical Biochemistry. Recurrent topics in Marlène Rio's work include Mitochondrial Function and Pathology (33 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Genomic variations and chromosomal abnormalities (23 papers). Marlène Rio is often cited by papers focused on Mitochondrial Function and Pathology (33 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Genomic variations and chromosomal abnormalities (23 papers). Marlène Rio collaborates with scholars based in France, United States and Switzerland. Marlène Rio's co-authors include Arnold Münnich, Nathalie Boddaert, Laurence Colleaux, Agnès Rötig, Nadia Bahi‐Buisson, Stanislas Lyonnet, Jeanne Amiel, Valérie Cormier‐Daire, Perrine Plouin and Isabelle Desguerre and has published in prestigious journals such as Science, Cell and Brain.

In The Last Decade

Marlène Rio

106 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marlène Rio France 33 2.2k 1.7k 525 263 237 112 3.5k
Fernando Kok Brazil 31 2.1k 0.9× 1.1k 0.6× 315 0.6× 290 1.1× 544 2.3× 177 3.9k
Helger G. Yntema Netherlands 35 2.7k 1.3× 2.6k 1.6× 167 0.3× 357 1.4× 372 1.6× 100 4.9k
Cynthia J. Tifft United States 30 1.9k 0.9× 1.2k 0.7× 158 0.3× 176 0.7× 318 1.3× 111 4.0k
Lina Basel‐Vanagaite Israel 32 1.9k 0.9× 1.4k 0.9× 104 0.2× 497 1.9× 468 2.0× 111 3.6k
Annick Raas‐Rothschild Israel 34 1.7k 0.8× 898 0.5× 190 0.4× 197 0.7× 262 1.1× 108 3.8k
Anna‐Elina Lehesjoki Finland 39 2.1k 1.0× 1.6k 0.9× 142 0.3× 273 1.0× 435 1.8× 126 4.9k
Katrin Õunap Estonia 25 1.0k 0.5× 857 0.5× 249 0.5× 264 1.0× 91 0.4× 106 1.8k
Jun Tohyama Japan 29 1.2k 0.5× 992 0.6× 243 0.5× 458 1.7× 520 2.2× 108 2.8k
Nathalie Drouot France 18 1.9k 0.9× 1.4k 0.9× 94 0.2× 156 0.6× 532 2.2× 36 3.5k
Kerstin Kutsche Germany 32 2.3k 1.0× 1.3k 0.8× 96 0.2× 198 0.8× 358 1.5× 118 3.6k

Countries citing papers authored by Marlène Rio

Since Specialization
Citations

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

Fields of papers citing papers by Marlène Rio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marlène Rio

This figure shows the co-authorship network connecting the top 25 collaborators of Marlène Rio. A scholar is included among the top collaborators of Marlène Rio 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 Marlène Rio. Marlène Rio 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.
Garcelon, Nicolas, Bernard Bénichou, Jeanne Amiel, et al.. (2025). Evaluation of a New Inclusive Next‐Generation Synthetic Face Tool for Dysmorphology. American Journal of Medical Genetics Part A. 200(3). 685–694. 1 indexed citations
2.
Barcia, Giulia, Marlène Rio, Cyril Gitiaux, et al.. (2024). Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisal. European Journal of Medical Genetics. 72. 104979–104979.
3.
Hennocq, Quentin, Corinne Collet, Jeanne Amiel, et al.. (2024). AI-based diagnosis and phenotype – Genotype correlations in syndromic craniosynostoses. Journal of Cranio-Maxillofacial Surgery. 52(10). 1172–1187. 7 indexed citations
4.
Hennocq, Quentin, D. Ramachandra Rao, Jeanne Amiel, et al.. (2024). Next Generation Phenotyping and Synthetic Faces in Coffin Siris Syndrome. Clinical Genetics. 107(5). 495–504. 1 indexed citations
5.
Grévent, D., Mélodie Aubart, Manoëlle Kossorotoff, et al.. (2023). Clinical and radiological description of 120 pediatric stroke‐like episodes. European Journal of Neurology. 30(7). 2051–2061. 2 indexed citations
6.
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
7.
Tsujita, Maki, Marlène Rio, Céline Huber, et al.. (2022). Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome. Journal of Medical Genetics. 60(4). 359–367. 9 indexed citations
8.
Laroche-Raynaud, Cécile, Anne‐Sophie Lia, Franck Sturtz, et al.. (2020). Pharmacoresistant Epilepsy in Childhood: Think of the Cerebral Folate Deficiency, a Treatable Disease. Brain Sciences. 10(11). 762–762. 9 indexed citations
9.
Rötig, Agnès, Charles‐Joris Roux, R. Lévy, et al.. (2020). Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?. Journal of Medical Genetics. 59(2). 204–208. 5 indexed citations
10.
Barcia, Giulia, Marlène Rio, Zahra Assouline, et al.. (2020). Novel FARS2 variants in patients with early onset encephalopathy with or without epilepsy associated with long survival. European Journal of Human Genetics. 29(3). 533–538. 8 indexed citations
11.
Huber, Céline, Caroline Michot, Federico Di Rocco, et al.. (2019). Expanding the phenotype in Adams–Oliver syndrome correlating with the genotype. American Journal of Medical Genetics Part A. 182(1). 29–37. 14 indexed citations
12.
Grévent, D., Marlène Rio, Isabelle Desguerre, et al.. (2018). High predictive value of brain MRI imaging in primary mitochondrial respiratory chain deficiency. Journal of Medical Genetics. 55(6). 378–383. 12 indexed citations
13.
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
14.
Ségalas-Milazzo, Isabelle, Marie Crahès, Florian Renosi, et al.. (2015). Lethal Neonatal Progression of Fetal Cardiomegaly Associated to ACAD9 Deficiency. JIMD Reports. 1–10. 9 indexed citations
15.
Assouline, Zahra, Marguerite Jambou, Marlène Rio, et al.. (2012). A constant and similar assembly defect of mitochondrial respiratory chain complex I allows rapid identification of NDUFS4 mutations in patients with Leigh syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(6). 1062–1069. 44 indexed citations
16.
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
17.
Rio, Marlène, Adeline Vigouroux, Matthias Titeux, et al.. (2008). Confirmation of RAX gene involvement in human anophthalmia. Clinical Genetics. 74(4). 392–395. 34 indexed citations
18.
Bahi‐Buisson, Nadia, Anna Kamińska, Nathalie Boddaert, et al.. (2008). The three stages of epilepsy in patients with CDKL5 mutations. Epilepsia. 49(6). 1027–1037. 139 indexed citations
19.
Molinari, Florence, Annick Raas‐Rothschild, Marlène Rio, et al.. (2005). Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy. The American Journal of Human Genetics. 76(2). 334–339. 115 indexed citations
20.
Baujat, Geneviève, Marlène Rio, Sylvie Rossignol, et al.. (2004). Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome. The American Journal of Human Genetics. 74(4). 715–720. 88 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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