Gábor Mátyás

4.4k total citations
52 papers, 1.7k citations indexed

About

Gábor Mátyás is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gábor Mátyás has authored 52 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 21 papers in Molecular Biology and 18 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Gábor Mátyás's work include Connective tissue disorders research (26 papers), Aortic Disease and Treatment Approaches (16 papers) and Cardiac Valve Diseases and Treatments (10 papers). Gábor Mátyás is often cited by papers focused on Connective tissue disorders research (26 papers), Aortic Disease and Treatment Approaches (16 papers) and Cardiac Valve Diseases and Treatments (10 papers). Gábor Mátyás collaborates with scholars based in Switzerland, United States and Germany. Gábor Mátyás's co-authors include Janine Meienberg, Beat Steinmann, Rémy Bruggmann, Konrad Oexle, Christoph Sperisen, Wolfgang Berger, Thierry Carrel, Daniela Baumgartner, U. Büchler and Félix Gugerli and has published in prestigious journals such as Nucleic Acids Research, Circulation and International Journal of Molecular Sciences.

In The Last Decade

Gábor Mátyás

50 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gábor Mátyás Switzerland	26	892	697	479	283	173	52	1.7k
Sergei G. Tevosian United States	27	879 1.0×	1.9k 2.8×	246 0.5×	182 0.6×	207 1.2×	59	2.7k
Pieter de Jong United States	17	600 0.7×	1.8k 2.6×	1.1k 2.3×	295 1.0×	327 1.9×	27	3.1k
Jian Xiao China	14	391 0.4×	802 1.2×	298 0.6×	187 0.7×	439 2.5×	43	1.9k
Benito Fraile Spain	33	468 0.5×	1.2k 1.8×	556 1.2×	71 0.3×	443 2.6×	117	2.9k
Rémi Houlgatte France	31	619 0.7×	1.3k 1.8×	135 0.3×	125 0.4×	386 2.2×	89	3.0k
Zhan Yin China	27	636 0.7×	1.4k 1.9×	99 0.2×	159 0.6×	204 1.2×	93	2.5k
Juliette Hadchouel France	29	337 0.4×	2.3k 3.3×	530 1.1×	226 0.8×	159 0.9×	55	2.7k
Peggy D. Robertson United States	9	855 1.0×	946 1.4×	74 0.2×	228 0.8×	272 1.6×	12	1.7k
Piotr Kozłowski Poland	33	706 0.8×	2.1k 3.1×	219 0.5×	168 0.6×	759 4.4×	124	3.5k
José Xavier‐Neto Brazil	22	256 0.3×	1.1k 1.6×	95 0.2×	184 0.7×	85 0.5×	40	1.6k

Countries citing papers authored by Gábor Mátyás

Since Specialization

Citations

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

Fields of papers citing papers by Gábor Mátyás

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gábor Mátyás

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

All Works

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20 of 20 papers shown

Smith, Jeffrey D., Szilamér Ferenczi, Krisztina Kovács, et al.. (2024). Novel Insights into the Aortic Mechanical Properties of Mice Modeling Hereditary Aortic Diseases. Thrombosis and Haemostasis. 125(2). 142–152. 1 indexed citations

Ágg, Bence, Miklós Pólos, Gábor Mátyás, et al.. (2021). Potential predictors of severe cardiovascular involvement in Marfan syndrome: the emphasized role of genotype–phenotype correlations in improving risk stratification—a literature review. Orphanet Journal of Rare Diseases. 16(1). 245–245. 10 indexed citations

Bors, András, Bence Ágg, Miklós Pólos, et al.. (2020). Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement. Orphanet Journal of Rare Diseases. 15(1). 290–290. 21 indexed citations

Najafi, Arash, et al.. (2019). Variant filtering, digenic variants, and other challenges in clinical sequencing: a lesson from fibrillinopathies. Clinical Genetics. 97(2). 235–245. 18 indexed citations

Bakker, Erik N.T.P., Ed VanBavel, Urs Ziegler, et al.. (2019). Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers–Danlos syndrome. Cardiovascular Research. 116(2). 457–465. 28 indexed citations

Ágg, Bence, Gábor Mátyás, Bálint Szilveszter, et al.. (2015). Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Thrombosis and Haemostasis. 114(10). 748–756. 15 indexed citations

Jost, Christine H. Attenhofer, Matthias Greutmann, Heidi M. Connolly, et al.. (2014). Medical Treatment of Aortic Aneurysms in Marfan Syndrome and other Heritable Conditions. Current Cardiology Reviews. 10(2). 161–171. 29 indexed citations

Curjuric, Ivan, Medea Imboden, Christian Schindler, et al.. (2010). HMOX1 and GST variants modify attenuation of FEF25-75% decline due to PM10 reduction. European Respiratory Journal. 35(3). 505–514. 25 indexed citations

Meienberg, Janine, Marianne Rohrbach, Stefan Neuenschwander, et al.. (2010). Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency. European Journal of Human Genetics. 18(12). 1315–1321. 28 indexed citations

10.

Niedrist, Dunja, Franziska Joncourt, Gábor Mátyás, & Andreas Müller. (2009). Severe phenotype with cis‐acting heterozygous PMP22 mutations. Clinical Genetics. 75(3). 286–289. 4 indexed citations

11.

Maćaš, Ervin, et al.. (2009). Polar body biopsy for Curschmann–Steinert disease and successful pregnancy following embryo vitrification. Reproductive BioMedicine Online. 18(6). 815–820. 2 indexed citations

12.

Jamsheer, Aleksander, Jolanta Wierzba, Bart Loeys, et al.. (2009). A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in theTGFBR2 gene substantiates interindividual clinical variability. Journal of Applied Genetics. 50(4). 405–410. 13 indexed citations

13.

Dündar, Munis, Kuddusi Erkılıç, Ahmet Okay Çağlayan, et al.. (2008). Scoliosis, blindness and arachnodactyly in a large Turkish family: Is it a new syndrome?. PubMed. 19(3). 319–30.

14.

Imboden, Medea, Sara H. Downs, Oliver Senn, et al.. (2007). Glutathione S-transferase genotypes modify lung function decline in the general population: SAPALDIA cohort study. Respiratory Research. 8(1). 2–2. 64 indexed citations

15.

Baumgartner, Daniela, Christian Baumgärtner, Ulrich Schweigmann, et al.. (2006). Different patterns of aortic wall elasticity in patients with Marfan syndrome: A noninvasive follow-up study. Journal of Thoracic and Cardiovascular Surgery. 132(4). 811–819. 36 indexed citations

16.

Bartholdi, Deborah, Andrea Klein, M Weissert, et al.. (2006). Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene. Clinical Genetics. 69(4). 319–326. 13 indexed citations

17.

Zeitz, Christina, Barbara Kloeckener‐Gruissem, U. Förster, et al.. (2006). Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness. The American Journal of Human Genetics. 79(4). 657–667. 123 indexed citations

18.

Baumgartner, Daniela, Christian Baumgärtner, Gábor Mátyás, et al.. (2005). Diagnostic power of aortic elastic properties in young patients with Marfan syndrome. Journal of Thoracic and Cardiovascular Surgery. 129(4). 730–739. 50 indexed citations

19.

Baumgärtner, Christian, Gábor Mátyás, Beat Steinmann, et al.. (2005). A bioinformatics framework for genotype–phenotype correlation in humans with Marfan syndrome caused by FBN1 gene mutations. Journal of Biomedical Informatics. 39(2). 171–183. 9 indexed citations

20.

Sperisen, Christoph, U. Büchler, Félix Gugerli, et al.. (2001). Tandem repeats in plant mitochondrial genomes: application to the analysis of population differentiation in the conifer Norway spruce. Molecular Ecology. 10(1). 257–263. 103 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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