Igor Vořechovský

10.1k citations
122 papers · 8.8k · 2 hit papers · h-index 42

Impact in

  • Immunology top 0.5%
    • Immunodeficiency and Autoimmune Disorders
    • T-cell and B-cell Immunology
  • Genetics top 2%
    • BRCA gene mutations in cancer

Papers in

    • Immunodeficiency and Autoimmune Disorders 31
    • RNA Research and Splicing 41
    • DNA Repair Mechanisms 13
    • Hedgehog Signaling Pathway Studies 7

Igor Vořechovský

120 papers receiving 8.4k citations

Igor Vořechovský's Hit Papers

Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome 1996 · 1.7k citations
1.7k0+11+22Years since publication5001k1.5k

Peers

Igor Vořechovský
Comparison fields: 5 of 105
  • Immunology 2.5k
  • Genetics 580
  • Molecular Biology 3.5k
  • Genetics 1.1k
  • Pathology and Forensic Medicine 414
Replace Peter Besmer with:
Peter Besmer United States
Tessa Crompton United Kingdom
Annick Itié Canada
Robert K. Rottapel Canada
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G Rovera United States
Stephen G. Emerson United States
Jung San Huang United States
Joost van den Oord Belgium
Massimo Geuna Italy
Igor Vořechovský relative to Peter Besmer United States Peter Besmer's profile →
Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside Igor Vořechovský, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Igor Vořechovský Line = papers co-authored together Igor Vořechovský links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 122 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome
Hit paper breakdown →
19961657
2
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
Hit paper breakdown →
19931246
3 1993546
4 2000334
5 1994264
6 1997227
7 2000190
8
The FHIT gene at 3p14.2 is abnormal in breast carcinomas.
1996184
9
Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.
1996178
10 2006175
11 1996172
12 2007159
13 1997140
14
The ATM gene and susceptibility to breast cancer: analysis of 38 breast tumors reveals no evidence for mutation.
1996135
15 2011119
16
ATM mutations in cancer families.
1996117
17 1995104
18 1999102
19 2000102
20 199495

About Igor Vořechovský

Igor Vořechovský is a scholar working on Immunology, Molecular Biology, Genetics, Genetics and Nephrology, having authored 122 papers that have together received 8.8k indexed citations. Recurring topics across this work include RNA Research and Splicing (41 papers), Immunodeficiency and Autoimmune Disorders (31 papers), DNA Repair Mechanisms (13 papers), Genetic Associations and Epidemiology (8 papers), Hedgehog Signaling Pathway Studies (7 papers), BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (4 papers) and Chronic Lymphocytic Leukemia Research (4 papers). The work is most often cited by research in Immunology (2.5k citations), Genetics (580 citations), Molecular Biology (3.5k citations), Genetics (1.1k citations) and Pathology and Forensic Medicine (414 citations). Igor Vořechovský has collaborated with scholars based in United Kingdom, Sweden and United States. Frequent co-authors include Lennart L G Hammarström, Jana Královičová, Paschalis Sideras, A. D. B. WEBSTER, David Webster, David L.P. Vetrie, Jill Holland, David Bentley, Rune Toftgård and Christine Kinnon. Their work appears in journals such as Nucleic Acids Research, Human Molecular Genetics, The Journal of Immunology, Oncogene and Human Mutation.

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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