Benjamin Cogné

4.5k total citations
18 papers, 222 citations indexed

About

Benjamin Cogné is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Benjamin Cogné has authored 18 papers receiving a total of 222 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Benjamin Cogné's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Benjamin Cogné is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Benjamin Cogné collaborates with scholars based in France, United States and Germany. Benjamin Cogné's co-authors include Pierre Lindenbaum, Adrien Léger, Philippe Moullier, Véronique Blouin, Richard Redon, Magalie Penaud‐Budloo, Achille François, Bertrand Isidor, Otto‐Wilhelm Merten and Matthias Hebben and has published in prestigious journals such as Annals of Neurology, Clinica Chimica Acta and Journal of Medical Genetics.

In The Last Decade

Benjamin Cogné

15 papers receiving 220 citations

Peers

Benjamin Cogné
Gustavo de Alencastro United States
Rossano Butcher United States
K. Gardiner United States
Gou Takahashi Japan
Nachiket Pendse United States
Matthieu Drouyer Australia
Denis A. Reshetov Russia
Zhi Cheng China
Jonas Weinmann Germany
Yann Jouvenot United States
Gustavo de Alencastro United States
Benjamin Cogné
Citations per year, relative to Benjamin Cogné Benjamin Cogné (= 1×) peers Gustavo de Alencastro

Countries citing papers authored by Benjamin Cogné

Since Specialization
Citations

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

Fields of papers citing papers by Benjamin Cogné

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benjamin Cogné

This figure shows the co-authorship network connecting the top 25 collaborators of Benjamin Cogné. A scholar is included among the top collaborators of Benjamin Cogné 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 Benjamin Cogné. Benjamin Cogné is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 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.
Mercier, Sandra, Céline Poirsier, Nathalie Bednarek, et al.. (2025). Commentary on UBTF haploinsufficiency associated with UBTF-related global developmental delay and distinctive facial features without neuroregression. Journal of Medical Genetics. 62(10). 653–655.
3.
Ronce, Nathalie, Benjamin Cogné, Thomas Besnard, et al.. (2024). Identification of a Rare Branch Point Variant in the SMS Gene in a Large Family With a Severe Form of Snyder–Robinson Syndrome. Clinical Genetics. 107(2). 231–233.
4.
Joubert, Madeleine, Claudine Le Vaillant, Pierre‐Emmanuel Séguéla, et al.. (2024). Prenatal Diagnosis of Myhre Syndrome in Two Cases: Further Delineation of the Cardiac and External Phenotype. Prenatal Diagnosis. 44(10). 1268–1272. 1 indexed citations
5.
Bayat, Allan, Zhenjiang Liu, Sheng Luo, et al.. (2023). A new neurodevelopmental disorder linked to heterozygous variants in UNC79. Genetics in Medicine. 25(9). 100894–100894. 13 indexed citations
6.
Isidor, Bertrand, Sandra Mercier, Mathilde Nizon, et al.. (2023). Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders. Journal of Medical Genetics. 61(1). 47–56. 5 indexed citations
7.
Désir, Julie, Damien Haye, Pauline Le Tanno, et al.. (2022). Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis. Clinical Genetics. 103(5). 560–565. 3 indexed citations
8.
Valenzuela, Irene, Ivon Cuscó, Benjamin Cogné, et al.. (2022). Clinical and molecular characterization of five new individuals with WAC‐related intellectual disability: Evidence of pathogenicity for a novel splicing variant. American Journal of Medical Genetics Part A. 188(5). 1396–1406. 3 indexed citations
9.
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
10.
Besnard, Thomas, Mathilde Nizon, Christel Thauvin‐Robinet, et al.. (2021). Loss‐of‐function variants in ARHGEF9 are associated with an X‐linked intellectual disability dominant disorder. Human Mutation. 42(5). 498–505. 2 indexed citations
11.
Cholet, Sophie, Bertrand Isidor, Benjamin Cogné, et al.. (2021). MAN1B1-CDG: Three new individuals and associated biochemical profiles. Molecular Genetics and Metabolism Reports. 28. 100775–100775. 9 indexed citations
12.
Gill, Harinder, Margaret L. McKinnon, Bertrand Isidor, et al.. (2020). SETD1B-associated neurodevelopmental disorder. Journal of Medical Genetics. 58(3). 196–204. 19 indexed citations
13.
Cogné, Benjamin, Jamal-Eddine Bouameur, Xénia Latypova, et al.. (2020). A dominant vimentin variant causes a rare syndrome with premature aging. European Journal of Human Genetics. 28(9). 1218–1230. 20 indexed citations
14.
Vuillaume, Marie‐Laure, Benjamin Cogné, Médéric Jeanne, et al.. (2018). Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability. Clinica Chimica Acta. 485. 218–223. 10 indexed citations
15.
Platzer, Konrad, Benjamin Cogné, Jennifer Hague, et al.. (2018). Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch‐up Development. Annals of Neurology. 84(2). 200–207. 16 indexed citations
16.
Penaud‐Budloo, Magalie, Sylvie Saleün, Alain Roulet, et al.. (2017). Accurate Identification and Quantification of DNA Species by Next-Generation Sequencing in Adeno-Associated Viral Vectors Produced in Insect Cells. Human Gene Therapy Methods. 28(3). 148–162. 37 indexed citations
17.
Cogné, Benjamin, Pierre Lindenbaum, Matthias Hebben, et al.. (2015). Advanced Characterization of DNA Molecules in rAAV Vector Preparations by Single-stranded Virus Next-generation Sequencing. Molecular Therapy — Nucleic Acids. 4. e260–e260. 62 indexed citations
18.
Georger, Christophe, Béatrice Marolleau, Laurence Jeanson-Leh, et al.. (2015). Short-lived recombinant adeno-associated virus transgene expression in dystrophic muscle is associated with oxidative damage to transgene mRNA. Molecular Therapy — Methods & Clinical Development. 2. 15010–15010. 14 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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