Thomas Josse

572 total citations
11 papers, 118 citations indexed

About

Thomas Josse is a scholar working on Rheumatology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Thomas Josse has authored 11 papers receiving a total of 118 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Rheumatology, 4 papers in Molecular Biology and 3 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Thomas Josse's work include Folate and B Vitamins Research (5 papers), Epigenetics and DNA Methylation (2 papers) and Monoclonal and Polyclonal Antibodies Research (2 papers). Thomas Josse is often cited by papers focused on Folate and B Vitamins Research (5 papers), Epigenetics and DNA Methylation (2 papers) and Monoclonal and Polyclonal Antibodies Research (2 papers). Thomas Josse collaborates with scholars based in France, Spain and Italy. Thomas Josse's co-authors include Jean‐Louis Guéant, Céline Chéry, Abderrahim Oussalah, Rosa‐Maria Guéant‐Rodriguez, François Feillet, Antonino Romano, Cédric Hartard, Jean‐Marc Alberto, Philippe Gérard and J.A. Cornejo‐García and has published in prestigious journals such as American Journal of Clinical Nutrition, The Science of The Total Environment and Medicine.

In The Last Decade

Thomas Josse

11 papers receiving 116 citations

Peers

Thomas Josse

RHEUM

PHARM

PPCH

GENET

K. Robin Carder United States

Harry Visser Netherlands

J. González-Ramos Spain

M Oda Japan

Kaarina Heiskanen Finland

Mark M. Fernandez United States

V. Y. Kalashnikov Russia

Manickam Chidambaram India

Algün Polat Ekinci Türkiye

Idit Lachover‐Roth Israel

K. Robin Carder United States

Thomas Josse

30 ×0.6

RHEUM

41 ×1.2

28 ×1.1

PHARM

15 ×0.7

PPCH

39 ×2.1

GENET

Citations per year, relative to Thomas Josse Thomas Josse (= 1×) peers K. Robin Carder

Countries citing papers authored by Thomas Josse

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Josse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Josse

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

All Works

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11 of 11 papers shown

Josse, Thomas, et al.. (2024). First detection of Hepatitis E virus (Rocahepevirus ratti) in French urban wastewater: Potential implications for human contamination. The Science of The Total Environment. 954. 176805–176805. 4 indexed citations

Chéry, Céline, Thomas Josse, Jean–Pierre Bronowicki, et al.. (2023). Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive cases. Human Genomics. 17(1). 5–5. 6 indexed citations

Romano, Antonino, Abderrahim Oussalah, Céline Chéry, et al.. (2021). Next‐generation sequencing and genotype association studies reveal the association of HLA‐DRB3*02:02 with delayed hypersensitivity to penicillins. Allergy. 77(6). 1827–1834. 16 indexed citations

Hartard, Cédric, Sibel Berger, Thomas Josse, Évelyne Schvoerer, & Hélène Jeulin. (2021). Performance evaluation of an automated SARS-CoV-2 Ag test for the diagnosis of COVID-19 infection on nasopharyngeal swabs. Clinical Chemistry and Laboratory Medicine (CCLM). 59(12). 2003–2009. 11 indexed citations

Chéry, Céline, Abderrahim Oussalah, Thomas Josse, et al.. (2019). Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathway. Human Genetics. 138(7). 703–713. 11 indexed citations

Guéant‐Rodriguez, Rosa‐Maria, Jean‐Marc Alberto, Céline Chéry, et al.. (2018). Vitamin B-12 and liver activity and expression of methionine synthase are decreased in fetuses with neural tube defects. American Journal of Clinical Nutrition. 109(3). 674–683. 17 indexed citations

Guéant‐Rodriguez, Rosa‐Maria, Céline Chéry, B. Foliguet, et al.. (2017). Association of combined GIF290T>C heterozygous mutation/FUT2 secretor variant with neural tube defects. Clinical Genetics. 93(1). 191–193. 4 indexed citations

Oussalah, Abderrahim, Rosa‐Maria Guéant‐Rodriguez, Céline Chéry, et al.. (2016). Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populations. Journal of Medical Genetics. 53(12). 828–834. 5 indexed citations

Oussalah, Abderrahim, Paolo Bosco, Guido Anello, et al.. (2015). Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects. Medicine. 94(22). e925–e925. 14 indexed citations

10.

Cornejo‐García, J.A., Antonino Romano, Rosa María Guéant-Rodríguez, et al.. (2015). A non-synonymous polymorphism in galectin-3 lectin domain is associated with allergic reactions to beta-lactam antibiotics. The Pharmacogenomics Journal. 16(1). 79–82. 14 indexed citations

11.

Chéry, Céline, Alain Hehn, Nadir T. Mrabet, et al.. (2013). Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant. Biochimie. 95(5). 995–1001. 16 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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