Francis Ramond

866 total citations
16 papers, 389 citations indexed

About

Francis Ramond is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Francis Ramond has authored 16 papers receiving a total of 389 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Francis Ramond's work include Genetic Neurodegenerative Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Muscle Physiology and Disorders (3 papers). Francis Ramond is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Muscle Physiology and Disorders (3 papers). Francis Ramond collaborates with scholars based in France, United States and Italy. Francis Ramond's co-authors include Alexandre Méjat, Laurent Schaeffer, Saadi Khochbin, Rhonda Bassel‐Duby, Eric N. Olson, Arnaud Ferry, Alban Vignaud, Christophe Hourdé, Gillian Butler‐Browne and Andreas Keller and has published in prestigious journals such as Journal of Biological Chemistry, Nature Neuroscience and Annals of Neurology.

In The Last Decade

Francis Ramond

14 papers receiving 388 citations

Peers

Francis Ramond

CMN

PHYSI

GENET

CCM

Wenqi Han China

Zachary T. McEachin United States

Francesco Tomassoni‐Ardori United States

Manuel Haas Germany

Thomas Lapointe Canada

Luca Chiveri Italy

Huanyu Gu China

Ilaria Musante Italy

Monica Traverso Italy

Wenqi Han China

Francis Ramond

260 ×0.8

70 ×1.0

CMN

27 ×0.5

PHYSI

44 ×1.0

GENET

55 ×1.4

CCM

Citations per year, relative to Francis Ramond Francis Ramond (= 1×) peers Wenqi Han

Countries citing papers authored by Francis Ramond

Since Specialization

Citations

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

Fields of papers citing papers by Francis Ramond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francis Ramond

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

All Works

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16 of 16 papers shown

Harzallah, Inès, et al.. (2024). Expanding the clinical spectrum of Coffin-Siris syndrome with anorectal malformations: Case report and review of the literature. European Journal of Medical Genetics. 69. 104948–104948.

Marelli, Cécilia, Francis Ramond, Catherine Vignal, et al.. (2024). Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia. Journal of Neurology. 271(9). 6038–6044. 1 indexed citations

Madinier, G., et al.. (2024). Compound Heterozygous WARS2 Variants Including a Hypomorphic Allele Cause a Milder Phenotype of Complex Dopa Responsive Dystonia: Case Report and Review of the Literature. The Cerebellum. 23(6). 2616–2621.

Ramond, Francis, et al.. (2022). Startle Disease. Neurology Genetics. 8(6). e200039–e200039. 7 indexed citations

Mazzola, Laure, Karen Oliver, Audrey Labalme, et al.. (2020). Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS. Annals of Neurology. 89(2). 402–407. 2 indexed citations

Ramond, Francis, Marlène Rio, Bénédicte Héron, et al.. (2020). AICA‐ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long‐term update on the first case. Journal of Inherited Metabolic Disease. 43(6). 1254–1264. 26 indexed citations

Ramond, Francis, et al.. (2019). Arthritis associated to cardio-facio-cutaneous syndrome related to a MAP2K1 mutation. Joint Bone Spine. 87(2). 169–169. 1 indexed citations

Poreau, Brice, Francis Ramond, Radu Harbuz, et al.. (2019). Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis. American Journal of Medical Genetics Part A. 179(4). 650–654. 5 indexed citations

Ramond, Francis, et al.. (2019). Predictive testing for Huntington disease over 24 years: Evolution of the profile of the participants and analysis of symptoms. Molecular Genetics & Genomic Medicine. 7(10). e00881–e00881. 8 indexed citations

10.

Ramond, Francis, Sébastien Duband, Pierre Croisille, et al.. (2017). Expanding the cardiac spectrum of Noonan syndrome with RIT1 variant: Left main coronary artery atresia causing sudden death. European Journal of Medical Genetics. 60(6). 299–302. 13 indexed citations

11.

Giraud, Antoine, et al.. (2016). Le phénotype complexe du syndrome ARC : une nouvelle observation. Archives de Pédiatrie. 24(2). 131–134. 1 indexed citations

12.

Ramond, Francis, Alexandre Janin, Sylvie Di Filippo, et al.. (2016). Homozygous PKP2 deletion associated with neonatal left ventricle noncompaction. Clinical Genetics. 91(1). 126–130. 23 indexed citations

13.

Ratti, Francesca, Francis Ramond, Vincent Moncollin, et al.. (2014). Histone Deacetylase 6 Is a FoxO Transcription Factor-dependent Effector in Skeletal Muscle Atrophy. Journal of Biological Chemistry. 290(7). 4215–4224. 32 indexed citations

14.

Ramond, Francis, Aderbal S. Aguiar, Caroline Chevarin, et al.. (2012). RNA splicing and editing modulation of 5-HT2C receptor function: relevance to anxiety and aggression in VGV mice. Molecular Psychiatry. 18(6). 656–665. 67 indexed citations

15.

Vignaud, Alban, Francis Ramond, Christophe Hourdé, et al.. (2007). Diabetes Provides an Unfavorable Environment for Muscle Mass and Function after Muscle Injury in Mice. Pathobiology. 74(5). 291–300. 63 indexed citations

16.

Méjat, Alexandre, Francis Ramond, Rhonda Bassel‐Duby, et al.. (2005). Histone deacetylase 9 couples neuronal activity to muscle chromatin acetylation and gene expression. Nature Neuroscience. 8(3). 313–321. 140 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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