Stéphanie Gobin

1.2k total citations
27 papers, 778 citations indexed

About

Stéphanie Gobin is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Stéphanie Gobin has authored 27 papers receiving a total of 778 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 4 papers in Rheumatology. Recurrent topics in Stéphanie Gobin's work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (6 papers) and Amino Acid Enzymes and Metabolism (3 papers). Stéphanie Gobin is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (6 papers) and Amino Acid Enzymes and Metabolism (3 papers). Stéphanie Gobin collaborates with scholars based in France, United Kingdom and United States. Stéphanie Gobin's co-authors include Jean‐Paul Bonnefont, Carina Prip‐Buus, J. A. Phillips, Laure Thuillier, Nathalie Boddaert, France Demaugre, Arnold Münnich, Alan J. Paine, Noman Kadhom and Pascale de Lonlay and has published in prestigious journals such as Journal of Biological Chemistry, Annals of Neurology and Biochemical Journal.

In The Last Decade

Stéphanie Gobin

26 papers receiving 759 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stéphanie Gobin France 16 432 321 125 120 95 27 778
Marco Rimoldi Italy 13 621 1.4× 436 1.4× 43 0.3× 79 0.7× 128 1.3× 17 908
Mauro Scarpelli Italy 17 535 1.2× 312 1.0× 42 0.3× 62 0.5× 179 1.9× 34 796
Iris Marquardt Germany 11 347 0.8× 401 1.2× 101 0.8× 20 0.2× 120 1.3× 15 796
Marion Paturneau-Jouas France 14 550 1.3× 263 0.8× 77 0.6× 15 0.1× 171 1.8× 29 788
Liesbeth T. Wintjes Netherlands 12 588 1.4× 173 0.5× 45 0.4× 65 0.5× 127 1.3× 19 847
K. Bartholomé Germany 16 441 1.0× 636 2.0× 102 0.8× 18 0.1× 181 1.9× 27 931
Gianfrancesco Goracci Italy 16 315 0.7× 70 0.2× 34 0.3× 124 1.0× 128 1.3× 30 681
Pascaline Clerc United States 8 789 1.8× 199 0.6× 43 0.3× 35 0.3× 214 2.3× 10 1.0k
Susana Peralta United States 18 953 2.2× 329 1.0× 62 0.5× 24 0.2× 131 1.4× 29 1.1k
Noman Kadhom France 10 1.0k 2.4× 453 1.4× 149 1.2× 10 0.1× 79 0.8× 10 1.2k

Countries citing papers authored by Stéphanie Gobin

Since Specialization
Citations

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

Fields of papers citing papers by Stéphanie Gobin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Gobin

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphanie Gobin. A scholar is included among the top collaborators of Stéphanie Gobin 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 Stéphanie Gobin. Stéphanie Gobin 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.
Imbard, Apolline, Hortense de Calbiac, Pascal Laforêt, et al.. (2024). Circulatory response to exercise relative to oxygen uptake assessed in the follow‐up of patients with fatty acid beta‐oxidation disorders. Journal of Inherited Metabolic Disease. 48(1). e12819–e12819. 2 indexed citations
2.
Pons, Linda, Cécile Acquaviva, Julie Steffann, et al.. (2020). Intrafamilial Variability in <b><i>LPIN1</i></b>-Related Rhabdomyolysis. Molecular Syndromology. 11(3). 153–156. 1 indexed citations
3.
Bouchemal, Nadia, Lisa Ouss, Anaïs Brassier, et al.. (2019). Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: 1H NMR spectroscopy and genetic testing. Orphanet Journal of Rare Diseases. 14(1). 222–222. 9 indexed citations
4.
Kuster, Alice, Jean‐Baptiste Arnoux, Magalie Barth, et al.. (2017). Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles. Journal of Inherited Metabolic Disease. 41(1). 129–139. 11 indexed citations
5.
Estève, Emmanuel, Pauline Krug, Aurélie Hummel, et al.. (2017). Renal involvement in lysinuric protein intolerance: contribution of pathology to assessment of heterogeneity of renal lesions. Human Pathology. 62. 160–169. 14 indexed citations
6.
Brassier, Anaïs, Stéphanie Gobin, Vassili Valayannopoulos, et al.. (2015). Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients. Orphanet Journal of Rare Diseases. 10(1). 60 indexed citations
7.
Barcia, Giulia, Nicole Chémaly, Stéphanie Gobin, et al.. (2013). Early epileptic encephalopathies associated with STXBP1 mutations: Could we better delineate the phenotype?. European Journal of Medical Genetics. 57(1). 15–20. 42 indexed citations
8.
Rio, Marlène, Stéphanie Gobin, Catherine Ozilou, et al.. (2012). Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH. Clinical Genetics. 84(1). 31–36. 23 indexed citations
9.
Kruer, Michael C., Coro Paisán‐Ruíz, Nathalie Boddaert, et al.. (2010). Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA). Annals of Neurology. 68(5). 611–618. 163 indexed citations
10.
Barth, Magalie, Chris Ottolenghi, Laurence Hubert, et al.. (2010). Multiple sources of metabolic disturbance inETHE1‐related ethylmalonic encephalopathy. Journal of Inherited Metabolic Disease. 33(S3). 443–453. 24 indexed citations
11.
Becdelièvre, Alix de, Marie Legendre, Jacqueline Vigneron, et al.. (2010). Notable contribution of large CFTR gene rearrangements to the diagnosis of cystic fibrosis in fetuses with bowel anomalies. European Journal of Human Genetics. 18(10). 1166–1169. 3 indexed citations
12.
Rio, Marlène, Valérie Malan, Sarah Boissel, et al.. (2009). Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition. European Journal of Human Genetics. 18(3). 285–290. 29 indexed citations
13.
Bensidhoum, Morad, Stéphanie Gobin, Alain Chapel, et al.. (2005). Potentiel thérapeutique des cellules souches mésenchymateuses humaines dans les lésions cutanées radioinduites. Journal de la Société de Biologie. 199(4). 337–341. 22 indexed citations
14.
Gobin, Stéphanie, Laure Thuillier, G. Jogl, et al.. (2003). Functional and Structural Basis of Carnitine Palmitoyltransferase 1A Deficiency. Journal of Biological Chemistry. 278(50). 50428–50434. 58 indexed citations
15.
Thuillier, Laure, Hidayeth Rostane, France Demaugre, et al.. (2003). Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency. Human Mutation. 21(5). 493–501. 80 indexed citations
16.
Gobin, Stéphanie, Jean‐Paul Bonnefont, Carina Prip‐Buus, et al.. (2002). Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia. Human Genetics. 111(2). 179–189. 41 indexed citations
17.
Prip‐Buus, Carina, Laure Thuillier, Chitra Prasad, et al.. (2001). Molecular and Enzymatic Characterization of a Unique Carnitine Palmitoyltransferase 1A Mutation in the Hutterite Community. Molecular Genetics and Metabolism. 73(1). 46–54. 47 indexed citations
18.
Gobin, Stéphanie, R.F. Legg, & Alan J. Paine. (1992). The role of lymphocyte production and migration in the lymphopenia caused by 2-acetyl-4-tetrahydroxy-butyl imidazole. International Journal of Immunopharmacology. 14(4). 687–697. 9 indexed citations
19.
Phillips, J. A., Stéphanie Gobin, & Alan J. Paine. (1990). The Effects of Dietary Vitamin B6 on the Lymphopenic Effects of THI, a Constituent of Ammonia Caramel. Annals of the New York Academy of Sciences. 587(1). 311–312.
20.
Gobin, Stéphanie, R.F. Legg, Alan J. Paine, & J. A. Phillips. (1989). The effect of 2-acetyl-4-tetrahydroxybutylimidazole on lymphocyte subsets in peripheral blood of the rat. International Journal of Immunopharmacology. 11(8). 937–946. 17 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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