Péter L. Nagy

3.8k total citations
58 papers, 2.3k citations indexed

About

Péter L. Nagy is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Péter L. Nagy has authored 58 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 18 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Péter L. Nagy's work include RNA Research and Splicing (11 papers), Genomics and Chromatin Dynamics (10 papers) and Genomics and Rare Diseases (8 papers). Péter L. Nagy is often cited by papers focused on RNA Research and Splicing (11 papers), Genomics and Chromatin Dynamics (10 papers) and Genomics and Rare Diseases (8 papers). Péter L. Nagy collaborates with scholars based in United States, Canada and France. Péter L. Nagy's co-authors include Michael L. Cleary, H Zalkin, Joachim Griesenbeck, Roger D. Kornberg, Jimena Baleriola, John F. Crary, Ying Y. Jean, Carol M. Troy, Ulrich Hengst and Hiroshi Mitsumoto and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Péter L. Nagy

57 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Péter L. Nagy United States 26 1.5k 327 296 249 242 58 2.3k
Rory Kirchner United States 21 994 0.7× 292 0.9× 253 0.9× 181 0.7× 104 0.4× 36 1.8k
Thomas Floß Germany 25 1.8k 1.2× 206 0.6× 457 1.5× 139 0.6× 175 0.7× 44 2.4k
Henna Tyynismaa Finland 30 3.0k 1.9× 187 0.6× 406 1.4× 232 0.9× 405 1.7× 82 3.8k
Holger Hummerich United Kingdom 20 1.2k 0.8× 531 1.6× 214 0.7× 334 1.3× 496 2.0× 40 2.1k
Che-Kun James Shen Taiwan 23 1.1k 0.7× 515 1.6× 179 0.6× 95 0.4× 202 0.8× 43 1.7k
Benoît J. Gentil Canada 22 1.1k 0.7× 257 0.8× 78 0.3× 274 1.1× 236 1.0× 32 1.6k
Marta Biagioli Italy 18 1.5k 1.0× 152 0.5× 238 0.8× 186 0.7× 143 0.6× 28 2.3k
Aldo Pagano Italy 28 1.8k 1.2× 172 0.5× 146 0.5× 100 0.4× 216 0.9× 61 2.4k
Margherita Piccolella Italy 23 763 0.5× 322 1.0× 166 0.6× 348 1.4× 170 0.7× 47 1.6k
Shuji Mita Japan 25 1.4k 1.0× 276 0.8× 154 0.5× 241 1.0× 231 1.0× 70 2.2k

Countries citing papers authored by Péter L. Nagy

Since Specialization
Citations

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

Fields of papers citing papers by Péter L. Nagy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Péter L. Nagy. 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 Péter L. Nagy. The network helps show where Péter L. Nagy may publish in the future.

Co-authorship network of co-authors of Péter L. Nagy

This figure shows the co-authorship network connecting the top 25 collaborators of Péter L. Nagy. A scholar is included among the top collaborators of Péter L. Nagy 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 Péter L. Nagy. Péter L. Nagy 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.
Rodriguez‐Gil, Jorge L., Péter L. Nagy, & Uta Francke. (2024). Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorder. American Journal of Medical Genetics Part A. 194(12). e63814–e63814. 1 indexed citations
2.
Broeckel, Ulrich, M. Anwar Iqbal, Brynn Levy, et al.. (2024). Detection of Constitutional Structural Variants by Optical Genome Mapping. Journal of Molecular Diagnostics. 26(3). 213–226. 8 indexed citations
3.
Neparáczki, Endre, Zoltán Maróti, Horolma Pamjav, et al.. (2022). The genetic legacy of the Hunyadi descendants. Heliyon. 8(11). e11731–e11731. 2 indexed citations
4.
Fagerberg, Christina, Adrian Taylor, Felix Distelmaier, et al.. (2019). Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 143(1). 94–111. 18 indexed citations
5.
Tóth, Csaba, et al.. (2018). Geoarchaeological Study of Szálka and Vajda Kurgans (Great Hungarian Plain) Based on Radiocarbon and Geophysical Analyses. Radiocarbon. 60(5). 1425–1437. 7 indexed citations
6.
Nagy, Péter L. & Howard J. Worman. (2018). Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins. Methods in molecular biology. 1840. 321–336. 6 indexed citations
7.
Liu, Jin, Fatou Amar, Carlo Corona, et al.. (2018). Brain-Derived Neurotrophic Factor Elevates Activating Transcription Factor 4 (ATF4) in Neurons and Promotes ATF4-Dependent Induction of Sesn2. Frontiers in Molecular Neuroscience. 11. 62–62. 13 indexed citations
8.
Lee‐Messer, Christopher, et al.. (2018). Clinical Transcriptome Sequencing Confirms Activation of a Cryptic Splice Site in Suspected SYNGAP1-Related Disorder. Molecular Syndromology. 9(6). 295–299. 5 indexed citations
9.
Pantazatos, Spiro P., Stuart Andrews, Yung‐yu Huang, et al.. (2015). Isoform-level brain expression profiling of the spermidine/spermine N1-Acetyltransferase1 ( SAT1 ) gene in major depression and suicide. Neurobiology of Disease. 79. 123–134. 29 indexed citations
10.
11.
Wang, Jiyong, Xavier Tadeo, Haitong Hou, et al.. (2014). Tls1 regulates splicing of shelterin components to control telomeric heterochromatin assembly and telomere length. Nucleic Acids Research. 42(18). 11419–11432. 13 indexed citations
12.
Northrop, Lesley E., et al.. (2014). Tetratricopeptide Repeat Domain 7A (TTC7A) Mutation in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency. Journal of Clinical Immunology. 34(6). 607–610. 24 indexed citations
13.
Kallgren, Scott P., Stuart Andrews, Xavier Tadeo, et al.. (2014). The Proper Splicing of RNAi Factors Is Critical for Pericentric Heterochromatin Assembly in Fission Yeast. PLoS Genetics. 10(5). e1004334–e1004334. 24 indexed citations
14.
Dialynas, George, et al.. (2011). LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle. Human Molecular Genetics. 21(7). 1544–1556. 38 indexed citations
15.
Dahdaleh, Fadi S., George W. Woodfield, Sathivel Chinnathambi, et al.. (2010). Discovery of the BMPR1A promoter and germline mutations that cause juvenile polyposis. Human Molecular Genetics. 19(23). 4654–4662. 27 indexed citations
16.
Nagy, Péter L. & David H. Price. (2009). Formaldehyde‐assisted isolation of regulatory elements. WIREs Systems Biology and Medicine. 1(3). 400–406. 10 indexed citations
17.
Nalbant, Demet, Daniel Xia, Bernhard Suter, et al.. (2008). The Glc7 Phosphatase Subunit of the Cleavage and Polyadenylation Factor Is Essential for Transcription Termination on snoRNA Genes. Molecular Cell. 29(5). 577–587. 102 indexed citations
18.
Nagy, Péter L., Iris Schrijver, & James L. Zehnder. (2004). Molecular Diagnosis of Hypercoagulable States. Laboratory Medicine. 35(4). 214–221. 2 indexed citations
19.
Tesařík, Jan, Péter L. Nagy, Roger Abdelmassih, Ermanno Greco, & Carmen Mendoza. (2002). Pharmacological concentrations of follicle-stimulating hormone and testosterone improve the efficacy of in vitro germ cell differentiation in men with maturation arrest. Fertility and Sterility. 77(2). 245–251. 13 indexed citations
20.
Chen, Stephen, Péter L. Nagy, & H Zalkin. (1997). Role of NRF-1 in bidirectional transcription of the human GPAT-AIRC purine biosynthesis locus. Nucleic Acids Research. 25(9). 1809–1816. 24 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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