Nadège Calmels

1.5k total citations
31 papers, 445 citations indexed

About

Nadège Calmels is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nadège Calmels has authored 31 papers receiving a total of 445 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nadège Calmels's work include DNA Repair Mechanisms (14 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic Neurodegenerative Diseases (7 papers). Nadège Calmels is often cited by papers focused on DNA Repair Mechanisms (14 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic Neurodegenerative Diseases (7 papers). Nadège Calmels collaborates with scholars based in France, United Kingdom and Canada. Nadège Calmels's co-authors include Hélène Puccio, Alain Martelli, Stéphane Schmucker, Manuela Argentini, Vincent Laugel, Cathy Obringer, Laurence Reutenauer, Michel Kœnig, Cécile Bouton and Marie‐Aude Spitz and has published in prestigious journals such as New England Journal of Medicine, PLoS ONE and Scientific Reports.

In The Last Decade

Nadège Calmels

30 papers receiving 442 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nadège Calmels France 12 369 202 117 61 44 31 445
Flavia Palombo Italy 10 226 0.6× 51 0.3× 155 1.3× 27 0.4× 39 0.9× 27 416
C. M. Everett United Kingdom 6 412 1.1× 245 1.2× 84 0.7× 33 0.5× 57 1.3× 9 491
Mahmoud Y. Issa Egypt 15 258 0.7× 47 0.2× 156 1.3× 71 1.2× 28 0.6× 45 482
Ruth Sheffer Israel 14 417 1.1× 61 0.3× 156 1.3× 118 1.9× 12 0.3× 22 627
Marc D’Hooghe Belgium 12 337 0.9× 95 0.5× 63 0.5× 44 0.7× 45 1.0× 18 580
Imen Dorboz France 14 492 1.3× 59 0.3× 94 0.8× 67 1.1× 40 0.9× 30 650
Cathy E. Woodward United Kingdom 13 420 1.1× 100 0.5× 53 0.5× 51 0.8× 65 1.5× 20 566
Liesbeth M. Bleeker-Wagemakers Netherlands 10 415 1.1× 51 0.3× 205 1.8× 74 1.2× 36 0.8× 12 557
Lauren Brady Canada 17 360 1.0× 102 0.5× 120 1.0× 57 0.9× 72 1.6× 40 558
Andrew R.J. Curtis United Kingdom 7 286 0.8× 115 0.6× 41 0.4× 16 0.3× 103 2.3× 8 587

Countries citing papers authored by Nadège Calmels

Since Specialization
Citations

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

Fields of papers citing papers by Nadège Calmels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadège Calmels

This figure shows the co-authorship network connecting the top 25 collaborators of Nadège Calmels. A scholar is included among the top collaborators of Nadège Calmels 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 Nadège Calmels. Nadège Calmels 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.
Buisine, Marie‐Pierre, Christine Bellanné‐Chantelot, Nadège Calmels, et al.. (2025). RNA-based diagnostic studies in genetics: Review and guidance from a multidisciplinary French network. European Journal of Human Genetics. 33(10). 1219–1227.
2.
Schaefer, Élise, et al.. (2024). Recurrent familial case of early childhood sudden death: Complex post mortem genetic investigations. Forensic Science International Genetics. 71. 103028–103028. 1 indexed citations
3.
Wirth, Thomas, Céline Bonnet, David Pellerin, et al.. (2024). Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?. Journal of Neurology. 271(4). 2078–2085. 8 indexed citations
4.
Calmels, Nadège, et al.. (2023). Functional analysis of novel variants identified in cis in the PCCB gene in a patient with propionic acidemia. Gene. 893. 147902–147902. 1 indexed citations
5.
Kraoua, Ichraf, Nadège Calmels, Cathy Obringer, et al.. (2022). Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations. Orphanet Journal of Rare Diseases. 17(1). 121–121. 7 indexed citations
6.
7.
Narayanan, Dhanya Lakshmi, Adam D. McIntyre, Robert A. Hegele, et al.. (2021). Clinical and Mutation Spectra of Cockayne Syndrome in India. Neurology India. 69(2). 362–366. 6 indexed citations
8.
Baer, Sarah, Cathy Obringer, Sophie Julia, et al.. (2020). Early‐onset nucleotide excision repair disorders with neurological impairment: Clues for early diagnosis and prognostic counseling. Clinical Genetics. 98(3). 251–260. 11 indexed citations
9.
Epanchintsev, Alexey, Nadège Calmels, Cathy Obringer, et al.. (2020). Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome. Scientific Reports. 10(1). 1105–1105. 16 indexed citations
10.
Barthélémy, Inès, Nadège Calmels, Robert B. Weiss, et al.. (2020). X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation. Skeletal Muscle. 10(1). 23–23. 13 indexed citations
11.
Spitz, Marie‐Aude, M. Durand, Cathy Obringer, et al.. (2019). Renal disease in Cockayne syndrome. European Journal of Medical Genetics. 63(1). 103612–103612. 6 indexed citations
12.
May, Nicolas Le, et al.. (2018). Xeroderma Pigmentosum Groups C and A in Algerian Patients with Deregulation of both Transcription and DNA Repair. HAL (Le Centre pour la Communication Scientifique Directe). 6(4). 3 indexed citations
13.
Drouot, Nathalie, Cathy Obringer, Hélène Dollfus, et al.. (2018). Deep intronic variation in splicing regulatory element of the ERCC8 gene associated with severe but long-term survival Cockayne syndrome. European Journal of Human Genetics. 26(4). 527–536. 7 indexed citations
14.
Gitiaux, Cyril, Marie Hully, Andoni Echaniz‐Laguna, et al.. (2014). Progressive demyelinating neuropathy correlates with clinical severity in Cockayne syndrome. Clinical Neurophysiology. 126(7). 1435–1439. 12 indexed citations
15.
Sananès, N., Christophe Vayssière, M. Köhler, et al.. (2010). Contribution of 3D ultrasound and fetal face studies to the prenatal diagnosis of Pallister-Killian syndrome. The Journal of Maternal-Fetal & Neonatal Medicine. 23(6). 558–562. 7 indexed citations
16.
Calmels, Nadège, Pascale Saugier-Véber, Françoise Girard‐Lemaire, et al.. (2009). Genetic Compensation in a Human Genomic Disorder. New England Journal of Medicine. 360(12). 1211–1216. 35 indexed citations
17.
Calmels, Nadège, H. Seznec, Pascal Villa, et al.. (2009). Limitations in a frataxin knockdown cell model for Friedreich ataxia in a high-throughput drug screen. BMC Neurology. 9(1). 46–46. 13 indexed citations
18.
Calmels, Nadège, Stéphane Schmucker, Marie Wattenhofer‐Donzé, et al.. (2009). The First Cellular Models Based on Frataxin Missense Mutations That Reproduce Spontaneously the Defects Associated with Friedreich Ataxia. PLoS ONE. 4(7). e6379–e6379. 46 indexed citations
19.
Calmels, Nadège, Françoise Girard‐Lemaire, Éric Guérin, et al.. (2008). Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: A cytogenetic pitfall. European Journal of Medical Genetics. 51(6). 547–557. 3 indexed citations
20.
Schmucker, Stéphane, Manuela Argentini, Nadège Calmels, Alain Martelli, & Hélène Puccio. (2008). The in vivo mitochondrial two-step maturation of human frataxin. Human Molecular Genetics. 17(22). 3521–3531. 111 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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