Igor Vořechovský

10.1k citations

106 papers · 6.2k indexed · 2 hit papers · h-index 39

Impact in

Genetics top 0.5%
- Chronic Lymphocytic Leukemia Research
- Blood disorders and treatments
Immunology top 0.5%
- Immunodeficiency and Autoimmune Disorders
- T-cell and B-cell Immunology

Papers in ⓘ

Immunology 28
- Immunodeficiency and Autoimmune Disorders 24
- Immune Cell Function and Interaction 9
Genetics 12
- Chronic Lymphocytic Leukemia Research 11

Co-authors: Lennart Hammarström (26 shared papers)Smith Rjh (15 shared papers)Jana Královičová (30 shared papers)Paschalis Sideras (5 shared papers)David Vetrie (6 shared papers)D Webster (1 shared paper)Rune Toftgård (6 shared papers)David Bentley (4 shared papers)
Journals: Nucleic Acids Research (17 papers)Human Molecular Genetics (6 papers)The Journal of Immunology (5 papers)Oncogene (5 papers)European Journal of Human Genetics (4 papers)
Partner nations: United Kingdom Sweden United States

In The Last Decade

Igor Vořechovský

103 papers receiving 6.1k citations

Hit Papers

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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases 1993 · 1.1k citations

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 106 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases Nature ·David Vetrie, Igor Vořechovský, Paschalis Sideras, Jill Holland, Angela Davies, Frances Flinter, Lennart Hammarström, Christine Kinnon, Roland J. Levinsky, Martin Bobrow, Smith Rjh, David Bentley Hit paper breakdown →	1993	1134
2	Colocalization of X-Linked Agammaglobulinemia and X-Linked Immunodeficiency Genes Science ·Jeffrey Thomas, Paschalis Sideras, Smith Rjh, Igor Vořechovský, Verne M. Chapman, William E. Paul Hit paper breakdown →	1993	543
3	Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID) Clinical & Experimental Immunology ·Lennart Hammarström, Igor Vořechovský, D Webster	2000	309
4	Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemia Nature Genetics ·Igor Vořechovský, Liping Luo, Martin J.S. Dyer, Daniel Catovsky, P L Amlot, John C. Yaxley, Letizia Foroni, Lennart Hammarström, A. David B. Webster, Martin Yuille	1997	223
5	The FHIT gene at 3p14.2 is abnormal in breast carcinomas. PubMed ·Massimo Negrini, C Monaco, Igor Vořechovský, Masataka Ohta, Teresa Druck, Raffaele Baffa, Kay Huebner, Carlo M. Croce	1996	189
6	Low frequency of alterations of the α (PPP2R1A) and β (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms Oncogene ·George A. Calin, Maria Grazia di Iasio, Elisabetta Caprini, Igor Vořechovský, Pier Giorgio Natali, Gabriella Sozzi, Carlo M. Croce, Giuseppe Barbanti‐Brodano, Giandomenico Russo, Massimo Negrini	2000	183
7	Aberrant 3′ splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization Nucleic Acids Research ·Igor Vořechovský	2006	165
8	A Mammalian patched Homolog Is Expressed in Target Tissues of sonic hedgehog and Maps to a Region Associated with Developmental Abnormalities Journal of Biological Chemistry ·Heidi Hahn, Jeffrey H. Christiansen, Carol Wicking, Peter G. Zaphiropoulos, Abirami Chidambaram, Bernard Gerrard, Igor Vořechovský, A. Bale, Rune Toftgård, Michael Dean, Brandon J. Wainwright	1996	163
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. PubMed ·A. B. Unden, E Holmberg, Barbro Lundh-Rozell, Mona Ståhle‐Bäckdahl, Peter G. Zaphiropoulos, Rune Toftgård, Igor Vořechovský	1996	160
10	Aberrant 5′ splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization Nucleic Acids Research ·Emanuele Buratti, Martin Chivers, Jana Královičová, Maurizio Romano, Marco Baralle, Adrian R. Krainer, Igor Vořechovský	2007	144
11	Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours Oncogene ·Igor Vořechovský, Ola Tingby, Magdalena Hartman‐Petrycka, Bo Strömberg, Monica Nistér, V. Peter Collins, Rune Toftgård	1997	129
12	The ATM gene and susceptibility to breast cancer: analysis of 38 breast tumors reveals no evidence for mutation. PubMed ·Igor Vořechovský, Debora Rasio, Lu Luo, C Monaco, Lennart Hammarström, A D Webster, Jan Žaloudík, G Barbanti-Brodani, Michael R. James, Giandomenico Russo	1996	129
13	Prediction of single‐nucleotide substitutions that result in exon skipping: identification of a splicing silencer inBRCA1exon 6 Human Mutation ·Michela Raponi, Jana Královičová, Ellen Copson, Petr Divina, Diana Eccles, Peter Johnson, Diana Baralle, Igor Vořechovský	2011	106
14	ATM mutations in cancer families. PubMed ·Igor Vořechovský, Liping Luo, Annika Lindblom, Massimo Negrini, A D Webster, C M Croce, Lennart Hammarström	1996	100
15	X‐Linked Agammaglobulinemia and Other Immunoglobulin Deficiencies Immunological Reviews ·Smith Rjh, Khalid B. Islam, Igor Vořechovský, Olle Olerup, Erik Jakob Wallin, Hodjattallah Rabbani, Berivan Baskin, Lennart Hammarström	1994	96
16	Genetic Linkage of IgA Deficiency to the Major Histocompatibility Complex: Evidence for Allele Segregation Distortion, Parent-of-Origin Penetrance Differences, and the Role of Anti-IgA Antibodies in Disease Predisposition The American Journal of Human Genetics ·Igor Vořechovský, A. David B. Webster, Alessandro Plebani, Lennart Hammarström	1999	93
17	Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis. PubMed ·Igor Vořechovský, A B Undén, Bengt Sandstedt, Rune Toftgård, Mona Ståhle‐Bäckdahl	1997	91
18	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 ·Igor Vořechovský, Michael Cullen, Mary Carrington, Lennart Hammarström, A. David B. Webster	2000	90
19	Family and Linkage Study of Selective IgA Deficiency and Common Variable Immunodeficiency Clinical Immunology and Immunopathology ·Igor Vořechovský, Henrik Zetterquist, Roberto Paganelli, Sinikka Koskinen, Anna L. David, Brian Webster, Janne Björkander, Smith Rjh, Lennart Hammarström	1995	87
20	Transposable elements in disease-associated cryptic exons Human Genetics ·Igor Vořechovský	2009	82

About Igor Vořechovský

Igor Vořechovský is a scholar working on Immunology, Genetics, Molecular Biology, Immunology and Allergy and Hematology, having authored 106 papers that have together received 6.2k indexed citations. Recurring topics across this work include RNA Research and Splicing (36 papers), RNA and protein synthesis mechanisms (36 papers), RNA modifications and cancer (30 papers), Immunodeficiency and Autoimmune Disorders (24 papers), Chronic Lymphocytic Leukemia Research (11 papers), DNA Repair Mechanisms (11 papers), Immune Cell Function and Interaction (9 papers) and Cancer-related Molecular Pathways (8 papers). The work is most often cited by research in Genetics (1.3k citations), Immunology (2.5k citations), Genetics (1.6k citations), Hematology (590 citations) and Molecular Biology (3.3k citations). Igor Vořechovský has collaborated with scholars based in United Kingdom, Sweden and United States. Frequent co-authors include Lennart Hammarström, Smith Rjh, Jana Královičová, Paschalis Sideras, David Vetrie, D Webster, Rune Toftgård, David Bentley, Jill Holland and Frances Flinter. Their work appears in journals such as Nucleic Acids Research, Human Molecular Genetics, The Journal of Immunology, Oncogene and European Journal of Human Genetics.

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