Gilles Morin

2.7k total citations
22 papers, 463 citations indexed

About

Gilles Morin is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Gilles Morin has authored 22 papers receiving a total of 463 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Gilles Morin's work include Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (3 papers) and Porphyrin Metabolism and Disorders (2 papers). Gilles Morin is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (3 papers) and Porphyrin Metabolism and Disorders (2 papers). Gilles Morin collaborates with scholars based in France, Italy and United States. Gilles Morin's co-authors include Mislen Bauer, Nancy D. Leslie, Daniel Gruskin, Deya Corzo, Michael Beck, Susan Richards, Rossella Parini, Ans van der Ploeg, Priya S. Kishnani and Claire Morgan and has published in prestigious journals such as SHILAP Revista de lepidopterología, Pediatric Research and Human Mutation.

In The Last Decade

Gilles Morin

20 papers receiving 442 citations

Peers

Gilles Morin

PHYSI

RHEUM

GENET

Hernán Amartino Argentina

F. A. Beemer Netherlands

Alessandra Zanetti Italy

Ai-Chu Huang Taiwan

Claudio Semplicini Italy

Patrick A. Lundquist United States

Anne Chun-Hui Tsai United States

Céline Cluzeau United States

An Dang United States

Helena Jahnová Czechia

Hernán Amartino Argentina

Gilles Morin

400 ×1.8

PHYSI

102 ×0.6

195 ×1.3

RHEUM

103 ×1.4

GENET

115 ×1.9

Citations per year, relative to Gilles Morin Gilles Morin (= 1×) peers Hernán Amartino

Countries citing papers authored by Gilles Morin

Since Specialization

Citations

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

Fields of papers citing papers by Gilles Morin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gilles Morin

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

Lamireau, Delphine, Pascale de Lonlay, Aude Servais, et al.. (2023). Systemic primary carnitine deficiency induces severe arrhythmia due to shortening of QT interval. Molecular Genetics and Metabolism. 140(4). 107733–107733. 4 indexed citations

Ranza, Emmanuelle, Anne Guimier, Alain Verloès, et al.. (2020). Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants. Clinical Genetics. 98(1). 10–18. 10 indexed citations

Morin, Gilles, Valérie Biancalana, Andoni Echaniz‐Laguna, et al.. (2019). Tubular aggregate myopathy and Stormorken syndrome: Mutation spectrum and genotype/phenotype correlation. Human Mutation. 41(1). 17–37. 33 indexed citations

Leclerc, Julie, Lucie Delattre, Emilie Ait‐Yahya, et al.. (2018). Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation. Genetics in Medicine. 20(12). 1589–1599. 23 indexed citations

Morin, Gilles, Catherine Vincent‐Delorme, Rosalie Cabry, et al.. (2017). New intragenic rearrangements in non‐Finnish mulibrey nanism. American Journal of Medical Genetics Part A. 173(10). 2782–2788. 8 indexed citations

Gérard, Marion, Gilles Morin, A. Bourillon, et al.. (2015). Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorder. European Journal of Medical Genetics. 58(3). 148–153. 21 indexed citations

Brémond‐Gignac, Dominique, Gilles Morin, Guillaume Jedraszak, et al.. (2015). Cat eye syndrome. Journal Français d Ophtalmologie. 38(4). 368–369. 1 indexed citations

Jedraszak, Guillaume, Bénédicte Demeer, Michèle Mathieu‐Dramard, et al.. (2015). Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients. American Journal of Medical Genetics Part A. 167(3). 504–511. 17 indexed citations

Morin, Gilles, et al.. (2015). Stormorken syndrome or York platelet syndrome: A clinician's dilemma. SHILAP Revista de lepidopterología. 2. 80–80. 6 indexed citations

10.

Jedraszak, Guillaume, Aline Receveur, Joris Andrieux, et al.. (2015). Severe Psychomotor Delay in a Severe Presentation of Cat-Eye Syndrome. SHILAP Revista de lepidopterología. 2015. 1–4. 3 indexed citations

11.

Crépin, Michel, Sophie Lejeune, Fabienne Escande, et al.. (2011). Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility. Human Mutation. 33(1). 180–188. 47 indexed citations

12.

Katzaki, Eleni, Gilles Morin, Marzia Pollazzon, et al.. (2010). Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients. American Journal of Medical Genetics Part A. 152A(7). 1711–1717. 19 indexed citations

13.

Kishnani, Priya S., Deya Corzo, Nancy D. Leslie, et al.. (2009). Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe Disease. Pediatric Research. 66(3). 329–335. 232 indexed citations

14.

Morin, Gilles, et al.. (2008). Additional familial case of subtotal leukonychia and sebaceous cysts (Bauer syndrome): Belong the nervous tumours to the phenotype?. European Journal of Medical Genetics. 51(5). 436–443. 4 indexed citations

15.

Morin, Gilles, Jean Gekas, Jean Gondry, et al.. (2001). Cerebro‐costo‐mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission. Prenatal Diagnosis. 21(10). 890–893. 8 indexed citations

16.

Morin, Gilles. (1990). Seasonal affective disorder, the depression of winter: A literature review and description from a nursing perspective. Archives of Psychiatric Nursing. 4(3). 182–187. 5 indexed citations

17.

Gastaut, H, Gilles Morin, & N Lesèvre. (1955). [Behavior of psychomotor epileptics between seizures; disorders of general activity and sociability].. PubMed. 113 1(1). 1–27. 5 indexed citations

18.

Morin, Gilles, et al.. (1954). Caractères et mécanismes de l'hypertension artérielle produite par la stimulation du cortex cérébral péricrucial chez le chat.. 46(1). 1 indexed citations

19.

Morin, Gilles, et al.. (1952). [Is hypertension induced by stimulation of the motor cortex of the brain always related to the production of an epileptic state in the curarized dog].. PubMed. 146(17-18). 1361–3. 1 indexed citations

20.

Morin, Gilles, et al.. (1951). [Variations of excitability cycle of visual receptor areas in cat, caused by pharmacodynamic agents].. PubMed. 43(4). 820–4.

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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