Thierry Nouspikel

2.6k total citations
34 papers, 1.9k citations indexed

About

Thierry Nouspikel is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Thierry Nouspikel has authored 34 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 9 papers in Cancer Research and 7 papers in Genetics. Recurrent topics in Thierry Nouspikel's work include DNA Repair Mechanisms (17 papers), CRISPR and Genetic Engineering (9 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Thierry Nouspikel is often cited by papers focused on DNA Repair Mechanisms (17 papers), CRISPR and Genetic Engineering (9 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Thierry Nouspikel collaborates with scholars based in Switzerland, United States and United Kingdom. Thierry Nouspikel's co-authors include Philip C. Hanawalt, Patrick B. Iynedjian, Stuart G. Clarkson, Catherine Ucla, Maryam Asfari, Nevila Hyka‐Nouspikel, Amos Bairoch, Daniel Scherly, Thibaud Koessler and Jean‐Louis Blouin and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Thierry Nouspikel

32 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thierry Nouspikel Switzerland 19 1.5k 427 342 275 261 34 1.9k
Axelle Cadoret France 20 1.0k 0.7× 263 0.6× 313 0.9× 165 0.6× 269 1.0× 27 1.7k
Alexandros Tzatsos United States 19 1.6k 1.1× 424 1.0× 297 0.9× 126 0.5× 571 2.2× 25 2.3k
Benjamin Cieply United States 23 1.7k 1.1× 424 1.0× 405 1.2× 157 0.6× 500 1.9× 30 2.4k
Ànna Manzano Spain 22 1.2k 0.8× 876 2.1× 277 0.8× 85 0.3× 263 1.0× 41 1.8k
Jan‐Wilhelm Kornfeld Germany 15 1.1k 0.7× 456 1.1× 234 0.7× 113 0.4× 284 1.1× 26 1.8k
Naomoto Harada Japan 14 1.5k 1.0× 166 0.4× 375 1.1× 241 0.9× 562 2.2× 18 2.2k
Yangjin Bae United States 16 1.1k 0.7× 346 0.8× 133 0.4× 234 0.9× 279 1.1× 22 1.6k
Yi‐Fen Lee United States 26 1.0k 0.7× 328 0.8× 187 0.5× 410 1.5× 165 0.6× 48 1.7k
Mercè Martı́n Spain 15 1.2k 0.8× 800 1.9× 704 2.1× 385 1.4× 344 1.3× 18 2.0k
Polina Iakova United States 21 1.3k 0.9× 191 0.4× 178 0.5× 120 0.4× 284 1.1× 31 1.9k

Countries citing papers authored by Thierry Nouspikel

Since Specialization
Citations

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

Fields of papers citing papers by Thierry Nouspikel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thierry Nouspikel

This figure shows the co-authorship network connecting the top 25 collaborators of Thierry Nouspikel. A scholar is included among the top collaborators of Thierry Nouspikel 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 Thierry Nouspikel. Thierry Nouspikel 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
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Schwitzgebel, Valérie, Jean-Louis Blouin, Claudine Rieubland, et al.. (2024). Enhancing fetal outcomes in GCK-MODY pregnancies: a precision medicine approach via non-invasive prenatal GCK mutation detection. Frontiers in Medicine. 11. 1347290–1347290. 1 indexed citations
3.
4.
Fokstuen, Siv, Lina Quteineh, Valérie Schwitzgebel, et al.. (2023). Noninvasive prenatal diagnosis of Mendelian disorders for consanguineous couples by relative genotype dosage. Clinical Genetics. 104(5). 505–515. 3 indexed citations
5.
Nouspikel, Thierry, et al.. (2021). Precision medicine in diabetes: A non‐invasive prenatal diagnostic test for the determination of fetal glucokinase mutations. Journal of Diabetes Investigation. 13(2). 256–261. 8 indexed citations
6.
Koessler, Thibaud, Salvatore Piscuoglio, Ronny Nienhold, et al.. (2020). Reliability of liquid biopsy analysis: an inter-laboratory comparison of circulating tumor DNA extraction and sequencing with different platforms. Laboratory Investigation. 100(11). 1475–1484. 15 indexed citations
7.
Koessler, Thibaud, Alfredo Addeo, & Thierry Nouspikel. (2019). Implementing circulating tumor DNA analysis in a clinical laboratory: A user manual. Advances in clinical chemistry. 89. 131–188. 9 indexed citations
8.
Hyka‐Nouspikel, Nevila, Joëlle A. Desmarais, Paul J. Gokhale, et al.. (2012). Deficient DNA Damage Response and Cell Cycle Checkpoints Lead to Accumulation of Point Mutations in Human Embryonic Stem Cells. Stem Cells. 30(9). 1901–1910. 43 indexed citations
9.
Lu, Wei-Ting, Kimon Lemonidis, Ross M. Drayton, & Thierry Nouspikel. (2011). The Fanconi anemia pathway is downregulated upon macrophage differentiation through two distinct mechanisms. Cell Cycle. 10(19). 3300–3310. 9 indexed citations
10.
Hyka‐Nouspikel, Nevila & Thierry Nouspikel. (2011). Nucleotide excision repair and B lymphoma: Somatic hypermutation is not the only culprit. Cell Cycle. 10(14). 2276–2280. 2 indexed citations
11.
Nouspikel, Thierry. (2009). DNA Repair in Mammalian Cells. Cellular and Molecular Life Sciences. 66(6). 994–1009. 247 indexed citations
12.
Nouspikel, Thierry. (2008). Nucleotide excision repair and neurological diseases. DNA repair. 7(7). 1155–1167. 51 indexed citations
13.
Hanawalt, Philip C., et al.. (2006). Nucleotide excision repair phenotype of human acute myeloid leukemia cell lines at various stages of differentiation. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 614(1-2). 3–15. 24 indexed citations
14.
Nouspikel, Thierry & Philip C. Hanawalt. (2003). When parsimony backfires: Neglecting DNA repair may doom neurons in Alzheimer's disease. BioEssays. 25(2). 168–173. 60 indexed citations
15.
Nouspikel, Thierry. (2002). DNA repair in terminally differentiated cells. DNA repair. 1(1). 59–75. 200 indexed citations
16.
Nouspikel, Thierry & Philip C. Hanawalt. (2000). Terminally Differentiated Human Neurons Repair Transcribed Genes but Display Attenuated Global DNA Repair and Modulation of Repair Gene Expression. Molecular and Cellular Biology. 20(5). 1562–1570. 157 indexed citations
17.
Ellison, Aaron R., Thierry Nouspikel, Nicolaas G.J. Jaspers, Stuart G. Clarkson, & Dieter C. Gruenert. (1998). Complementation of Transformed Fibroblasts from Patients with Combined Xeroderma Pigmentosum–Cockayne Syndrome. Experimental Cell Research. 243(1). 22–28. 19 indexed citations
18.
Nouspikel, Thierry & Stuart G. Clarkson. (1994). Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient. Human Molecular Genetics. 3(6). 963–967. 47 indexed citations
19.
Nouspikel, Thierry & Patrick B. Iynedjian. (1992). Insulin signalling and regulation of glucokinase gene expression in cultured hepatocytes. European Journal of Biochemistry. 210(1). 365–373. 47 indexed citations
20.
Iynedjian, Patrick B., Thierry Nouspikel, Joseph L. Milburn, et al.. (1989). Differential expression and regulation of the glucokinase gene in liver and islets of Langerhans.. Proceedings of the National Academy of Sciences. 86(20). 7838–7842. 152 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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