Igor Vořechovský

10.1k total citations · 2 hit papers
106 papers, 6.2k citations indexed

About

Igor Vořechovský is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Igor Vořechovský has authored 106 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Molecular Biology, 28 papers in Immunology and 19 papers in Genetics. Recurrent topics in Igor Vořechovský's work include RNA and protein synthesis mechanisms (36 papers), RNA Research and Splicing (36 papers) and RNA modifications and cancer (30 papers). Igor Vořechovský is often cited by papers focused on RNA and protein synthesis mechanisms (36 papers), RNA Research and Splicing (36 papers) and RNA modifications and cancer (30 papers). Igor Vořechovský collaborates with scholars based in United Kingdom, Sweden and United States. Igor Vořechovský's co-authors include Lennart Hammarström, Smith Rjh, Jana Královičová, Paschalis Sideras, David Vetrie, D Webster, Rune Toftgård, David Bentley, Jill Holland and Christine Kinnon and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Igor Vořechovský

103 papers receiving 6.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

1993 1.1k citations Igor Vořechovský, Lennart Hammarström et al. profile →
Colocalization of X-Linked Agammaglobulinemia and X-Linked Immunodeficiency Genes

1993 543 citations Smith Rjh, Igor Vořechovský et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Igor Vořechovský United Kingdom	39	3.3k	2.5k	1.6k	1.3k	785	106	6.2k
Massimo Geuna Italy	32	1.7k 0.5×	1.5k 0.6×	817 0.5×	1.1k 0.8×	1.1k 1.4×	84	4.4k
David Vetrie United Kingdom	32	3.1k 0.9×	1.8k 0.7×	1.1k 0.7×	1.2k 0.9×	407 0.5×	59	5.7k
Tobias Gedde‐Dahl Norway	39	1.8k 0.6×	1.2k 0.5×	1.0k 0.6×	651 0.5×	770 1.0×	225	5.3k
Ivo P. Touw Netherlands	42	1.9k 0.6×	2.6k 1.0×	1.6k 1.0×	734 0.6×	2.0k 2.5×	145	5.7k
Hanno Glimm Germany	36	3.0k 0.9×	704 0.3×	1.6k 1.0×	533 0.4×	1.5k 1.9×	124	4.9k
Kohichiro Tsuji Japan	39	2.2k 0.7×	2.4k 0.9×	608 0.4×	1.3k 1.0×	1.4k 1.8×	112	6.3k
Shigetaka Asano Japan	41	2.3k 0.7×	1.5k 0.6×	706 0.4×	788 0.6×	1.5k 1.9×	207	5.8k
Jean‐Pierre de Villartay France	48	5.1k 1.5×	4.2k 1.7×	1.9k 1.2×	474 0.4×	2.3k 2.9×	160	9.0k
Christine Ambrose United States	29	2.4k 0.7×	4.1k 1.6×	564 0.4×	449 0.3×	834 1.1×	52	7.1k
Stewart D. Lyman United States	38	2.8k 0.9×	4.5k 1.8×	1000 0.6×	893 0.7×	1.5k 2.0×	78	8.5k

Countries citing papers authored by Igor Vořechovský

Since Specialization

Citations

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

Fields of papers citing papers by Igor Vořechovský

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Igor Vořechovský

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Vořechovský, Igor, et al.. (2024). Copper-binding proteins and exonic splicing enhancers and silencers. Metallomics. 16(5). 1 indexed citations

Vořechovský, Igor, et al.. (2023). Alu RNA fold links splicing with signal recognition particle proteins. Nucleic Acids Research. 51(15). 8199–8216. 6 indexed citations

Pengelly, Reuben J., et al.. (2023). Exonic splicing code and coordination of divalent metals in proteins. Nucleic Acids Research. 52(3). 1090–1106. 2 indexed citations

Pengelly, Reuben J., et al.. (2022). Exonic splicing code and protein binding sites for calcium. Nucleic Acids Research. 50(10). 5493–5512. 4 indexed citations

Královičová, Jana, Reuben J. Pengelly, Pavel Abaffy, et al.. (2021). Restriction of an intron sizeen routeto endothermy. Nucleic Acids Research. 49(5). 2460–2487. 7 indexed citations

Giannoulatou, Eleni, et al.. (2020). Transposon clusters as substrates for aberrant splice-site activation. RNA Biology. 18(3). 354–367. 10 indexed citations

Ennis, Sarah, et al.. (2019). Heterogeneity in the extent of linkage disequilibrium among exonic, intronic, non-coding RNA and intergenic chromosome regions. European Journal of Human Genetics. 27(9). 1436–1444. 3 indexed citations

Nozu, Kandai, Igor Vořechovský, Hiroshi Kaito, et al.. (2014). X-Linked Alport Syndrome Caused by Splicing Mutations in COL4A5. Clinical Journal of the American Society of Nephrology. 9(11). 1958–1964. 22 indexed citations

Divina, Petr, et al.. (2009). Ab initio prediction of mutation-induced cryptic splice-site activation and exon skipping. European Journal of Human Genetics. 17(6). 759–765. 51 indexed citations

10.

Královičová, Jana & Igor Vořechovský. (2006). Position-Dependent Repression and Promotion of DQB1 Intron 3 Splicing by GGGG Motifs. The Journal of Immunology. 176(4). 2381–2388. 29 indexed citations

11.

Královičová, Jana, Lennart Hammarström, Alessandro Plebani, A. David B. Webster, & Igor Vořechovský. (2003). Fine-Scale Mapping at IGAD1 and Genome-Wide Genetic Linkage Analysis Implicate HLA-DQ/DR as a Major Susceptibility Locus in Selective IgA Deficiency and Common Variable Immunodeficiency. The Journal of Immunology. 170(5). 2765–2775. 78 indexed citations

12.

Tischkowitz, Marc, Neil V. Morgan, S V Hodgson, et al.. (2001). Mutation analysis of the Fanconi Anaemia group A, C, E, F and G genes in sporadic acute myeloid leukaemia. Journal of Medical Genetics. 38.

13.

Vořechovský, Igor, Michael Cullen, Mary Carrington, Lennart Hammarström, & A. David B. Webster. (2000). Fine Mapping of IGAD1 in IgA Deficiency and Common Variable Immunodeficiency: Identification and Characterization of Haplotypes Shared by Affected Members of 101 Multiple-Case Families. The Journal of Immunology. 164(8). 4408–4416. 90 indexed citations

14.

Kallassy, Mireille, Rune Toftgård, Masahiro Ueda, et al.. (1997). Patched (ptch)-associated preferential expression of smoothened (smoh) in human basal cell carcinoma of the skin.. PubMed. 57(21). 4731–5. 44 indexed citations

15.

Vořechovský, Igor, et al.. (1997). Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis.. PubMed. 57(21). 4677–81. 91 indexed citations

16.

Vihinen, Mauno, Robert N. Haire, Elke Holinski‐Feder, et al.. (1997). BTKbase, mutation database for X-linked agammaglobulinemia (XLA). Nucleic Acids Research. 25(1). 166–171. 37 indexed citations

17.

Vořechovský, Igor, Ola Tingby, Magdalena Hartman‐Petrycka, et al.. (1997). Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours. Oncogene. 15(3). 361–366. 129 indexed citations

18.

Negrini, Massimo, C Monaco, Igor Vořechovský, et al.. (1996). The FHIT gene at 3p14.2 is abnormal in breast carcinomas.. PubMed. 56(14). 3173–9. 189 indexed citations

19.

Vořechovský, Igor, Henrik Zetterquist, Roberto Paganelli, et al.. (1995). Family and Linkage Study of Selective IgA Deficiency and Common Variable Immunodeficiency. Clinical Immunology and Immunopathology. 77(2). 185–192. 87 indexed citations

20.

Vořechovský, Igor. (1994). SSCP at the BTK locus. Human Molecular Genetics. 3(6). 1031–1031. 1 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.

Explore authors with similar magnitude of impact