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Katalin Farkas, Ph.D. - Publications

Affiliations: 
2005 Semmelweis Egyetem, Hungary 
Area:
Molecular Biology
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37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Pap ÉM, Farkas K, Széll M, Németh G, Rajan N, Nagy N. Identification of putative phenotype-modifying genetic factors associated with phenotypic diversity in Brooke-Spiegler syndrome. Experimental Dermatology. PMID 32744342 DOI: 10.1111/Exd.14161  0.324
2019 Kolossváry E, Ferenci T, Kováts T, Kovács L, Járai Z, Menyhei G, Farkas K. Corrigendum to 'Trends in Major Lower Limb Amputations Related to Peripheral Arterial Disease in Hungary. A Nationwide Study (2004-2012).'[European Journal of Vascular & Endovascular Surgery 50/1 (2015) 78-85]. European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society For Vascular Surgery. PMID 31521487 DOI: 10.1016/J.Ejvs.2019.07.025  0.32
2019 Dávid É, Török D, Farkas K, Nagy N, Horváth E, Kiss Z, Oroszlán G, Balogh M, Széll M. Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: a case report. Bmc Pediatrics. 19: 16. PMID 30635044 DOI: 10.1186/S12887-019-1390-1  0.314
2019 Farkas K, Kolossváry E, Járai Z, Paksy A, Kiss I. LOW ANKLE-BRACHIAL INDEX DOUBLES THE MORTALITY OF HYPERTENSIVE PATIENTS. RESULTS OF THE HUNGARIAN ERV SCREENING PROGRAM Journal of Hypertension. 37: e10. DOI: 10.1097/01.Hjh.0000570464.68834.E7  0.346
2018 Twelves S, Mostafa A, Dand N, Burri E, Farkas K, Wilson R, Cooper HL, Irvine AD, Oon HH, Kingo K, Köks S, Mrowietz U, Puig L, Reynolds N, Sern-Ting Tan E, et al. Clinical and genetic differences between pustular psoriasis subtypes. The Journal of Allergy and Clinical Immunology. PMID 30036598 DOI: 10.1016/J.Jaci.2018.06.038  0.322
2018 Danis J, Göblös A, Gál B, Sulák A, Farkas K, Török D, Varga E, Korom I, Kemény L, Széll M, Bata-Csörgö Z, Nagy N. Nuclear Factor κB Activation in a Type V Pityriasis Rubra Pilaris Patient Harboring Multiple Variants. Frontiers in Immunology. 9: 1564. PMID 30018619 DOI: 10.3389/Fimmu.2018.01564  0.336
2018 Járai Z, Kolossváry E, Szabó I, Kiss I, Farsang C, Farkas K. [The potential role of oscillometric devices for ankle-brachial index measurements in clinical practice]. Orvosi Hetilap. 159: 176-182. PMID 29376424 DOI: 10.1556/650.2018.30957  0.523
2018 Farkas K, Kolossváry E, Járai Z, Paksy A, Kiss I. MORTALITY RATES IN HYPERTENSIVE SUBJECTS WITH PERIPHERAL ARTERIAL DISEASE Journal of Hypertension. 36: e1-e2. DOI: 10.1097/01.Hjh.0000538965.73890.B5  0.324
2017 Nemcsik J, Cseprekál O, Egresits J, Kielstein J, Kümpers P, Lukasz A, Tabák Á, Marton A, Németh ZK, Járai Z, Godina G, Sallai L, Farkas K, Kiss I, Tislér A. The role of laser Doppler flowmetry tests, serum angiopoietin-2, asymmetric and symmetric dimethylarginine to predict outcome in chronic kidney disease. Journal of Hypertension. PMID 28106663 DOI: 10.1097/Hjh.0000000000001256  0.302
2017 Farkas K, Kolossvary E, Jarai Z, Paksy A, Kiss I. P3227Mortality rates in hypertensive subjects with peripheral arterial disease: detection of a J-curve phenomenon European Heart Journal. 38. DOI: 10.1093/Eurheartj/Ehx504.P3227  0.328
2017 Sulák A, Tripolszki K, Farkas K, Széll M, Nagy N. Phenotypic diversity of the recurrent p.Val379Leu missense mutation of the TGM1 gene Dermatologica Sinica. 36: 89-92. DOI: 10.1016/J.Dsi.2017.08.001  0.313
2016 Farkas K, Deák BK, Sánchez LC, Martínez AM, Corell JJ, Botella AM, Benito GM, López RR, Vanecek T, Kazakov DV, Kromosoeto JN, van den Ouweland AM, Varga J, Széll M, Nagy N. The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene. Bmc Genetics. 17: 36. PMID 26861065 DOI: 10.1186/S12863-016-0346-9  0.326
2016 Tripolszki K, Knox R, Parker V, Semple R, Farkas K, Sulák A, Horváth E, Széll M, Nagy N. Somatic mosaicism of the PIK3CA gene identified in a Hungarian girl with macrodactyly and syndactyly. European Journal of Medical Genetics. PMID 26851524 DOI: 10.1016/J.Ejmg.2016.02.002  0.323
2015 Hamon Y, Legowska M, Fergelot P, Dallet-Choisy S, Newell L, Vanderlynden L, Kord Valeshabad A, Acrich K, Kord H, Charalampos T, Morice-Picard F, Surplice I, Zoidakis J, David K, Vlahou A, ... ... Farkas K, et al. Analysis of urinary cathepsin C for diagnosing Papillon-Lefèvre syndrome. The Febs Journal. PMID 26607765 DOI: 10.1111/Febs.13605  0.328
2015 Nemes E, Farkas K, Kocsis-Deák B, Drubi A, Sulák A, Tripolszki K, Dósa P, Ferenc L, Nagy N, Széll M. Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation. Archives of Dermatological Research. 307: 891-5. PMID 26377839 DOI: 10.1007/S00403-015-1597-4  0.339
2015 Sulák A, Tóth L, Farkas K, Tripolszki K, Fábos B, Kemény L, Vályi P, Nagy K, Nagy N, Széll M. One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes. Clinical and Experimental Dermatology. PMID 26205983 DOI: 10.1111/Ced.12710  0.344
2015 Kolossváry E, Ferenci T, Kováts T, Kovács L, Járai Z, Menyhei G, Farkas K. Trends in Major Lower Limb Amputation Related to Peripheral Arterial Disease in Hungary: A Nationwide Study (2004-2012). European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society For Vascular Surgery. 50: 78-85. PMID 25842279 DOI: 10.1016/J.Ejvs.2015.02.019  0.333
2015 Nagy N, Farkas K, Kemény L, Széll M. Phenotype-genotype correlations for clinical variants caused by CYLD mutations. European Journal of Medical Genetics. 58: 271-8. PMID 25782638 DOI: 10.1016/J.Ejmg.2015.02.010  0.337
2015 Kolossváry E, Járai Z, Ludányi A, Kiss I, Farkas K. Pp.41.29: Association Of Blood Pressure Control And Peripheral Arterial Disease In The Evaluation Of Ankle/Brachial Index In Hungarian Hypertensives (Erv) Study Population Journal of Hypertension. 33. DOI: 10.1097/01.Hjh.0000468992.16352.B5  0.332
2014 Horváth E, Farkas K, Herczegfalvi A, Nagy N, Széll M. Identification of a novel missense GLRA1 gene mutation in hyperekplexia: A case report Journal of Medical Case Reports. 8. PMID 24969041 DOI: 10.1186/1752-1947-8-233  0.312
2014 Nagy N, Vályi P, Csoma Z, Sulák A, Tripolszki K, Farkas K, Paschali E, Papp F, Tóth L, Fábos B, Kemény L, Nagy K, Széll M. CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update. Molecular Genetics & Genomic Medicine. 2: 217-28. PMID 24936511 DOI: 10.1002/Mgg3.61  0.307
2014 Kinyó A, Vályi P, Farkas K, Nagy N, Gergely B, Tripolszki K, Török D, Bata-Csörgo Z, Kemény L, Széll M. A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ-Siemens-Touraine syndrome Archives of Dermatological Research. 306: 97-100. PMID 23989902 DOI: 10.1007/S00403-013-1408-8  0.32
2012 Nagy N, Farkas K, Kinyo A, Nemeth IB, Kis E, Varga J, Bata-Csorgo Z, Kemeny L, Szell M. A novel missense mutation of the CYLD gene identified in a Hungarian family with Brooke-Spiegler syndrome. Experimental Dermatology. 21: 967-9. PMID 23171463 DOI: 10.1111/Exd.12040  0.311
2012 Farkas K, Járai Z, Kolossváry E, Ludányi A, Clement DL, Kiss I. High prevalence of peripheral arterial disease in hypertensive patients: the Evaluation of Ankle-Brachial Index in Hungarian Hypertensives screening program. Journal of Hypertension. 30: 1526-32. PMID 22743684 DOI: 10.1097/Hjh.0B013E3283559A6A  0.358
2012 Farkas K, Nagy N, Kinyó A, Kemény L, Széll M. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities. Archives of Dermatological Research. 304: 679-81. PMID 22584530 DOI: 10.1007/S00403-012-1244-2  0.305
2011 Farkas K, Járai Z, Kolossváry E, Ludányi A, Kiss I. METABOLIC SYNDROME AND THE RISK OF PERIPHERAL ARTERIAL DISEASE: DATA FROM THE EVALUATION OF ANKLE/BRACHIAL INDEX IN HUNGARIAN HYPERTENSIVES (ERV) SCREENING PROGRAM. Journal of Hypertension. 29: e435. DOI: 10.1097/00004872-201106001-01302  0.317
2011 Farkas K, Fábián E, Kolossváry E, Járai Z, Farsang C. Noninvasive assessment of endothelial dysfunction in essential hypertension: Comparison of the forearm microvascular reactivity with flow-mediated dilatation of the brachial artery International Journal of Angiology. 12: 224-228. DOI: 10.1007/S00547-003-1000-8  0.572
2010 Farkas K, Járai Z, Kolossváry E, Ludányi A, Kiss I. THE PREVALENCE OF PERIPHERAL ARTERIAL DISEASE IS LOWER IN PATIENTS WITH CONTROLLED HYPERTENSION: RESULTS OF THE HUNGARIAN ANKLE/BRACHIAL INDEX SCREENING PROGRAM (ERV): PP.19.221 Journal of Hypertension. 28: e315. DOI: 10.1097/01.Hjh.0000379147.52532.43  0.343
2009 Boda Z, Udvardy M, Rázsó K, Farkas K, Tóth J, Jámbor L, Oláh Z, Ilonczai P, Szarvas M, Kappelmayer J, Veréb Z, Rajnavölgyi E. Stem cell therapy: a promising and prospective approach in the treatment of patients with severe Buerger's disease. Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 15: 552-60. PMID 18818231 DOI: 10.1177/1076029608319882  0.311
2008 Farkas K, Fábián E, Nagy L. Quinapril improves endothelial function in postmenopausal hypertensive patients. Kidney & Blood Pressure Research. 31: 226-33. PMID 18587241 DOI: 10.1159/000141927  0.337
2007 Nemcsik J, Farkas K, Kolossváry E, Járai Z, Egresits J, Borgulya G, Kiss I, Lengyel M. Intracardiac calcification is a marker of generalized atherosclerosis. Angiology. 58: 413-9. PMID 17875954 DOI: 10.1177/0003319706291112  0.363
2006 Nemcsik J, Egresits J, Borvendég J, Kolossváry E, Finta E, Farkas K, Kiss I. P.051 Evaluation Of Endothelial Function With Non-Invasive Methods In Different Cardiovascular Diseases Artery Research. 1. DOI: 10.1016/S1872-9312(07)70074-1  0.306
2005 Farkas K, Nemcsik J, Kolossváry E, Járai Z, Borvendég J, Nádory E, Farsang C, Kiss I. [Noninvasive assessment of endothelial function in hemodialyzed hypertensive patients by laser Doppler flowmetry]. Orvosi Hetilap. 146: 2589-94. PMID 16468613  0.581
2005 Kolossváry E, Kollár A, Pintér H, Erényi E, Kiséry I, Péter H, Farkas K, Mogán L, Farsang C, Kiss I. Bilateral axillobrachial and external carotid artery manifestation of giant cell arteritis: important role of color duplex ultrasonography in the diagnosis. International Angiology : a Journal of the International Union of Angiology. 24: 202-5. PMID 15997226  0.53
2005 Farkas K, Nemcsik J, Kolossváry E, Járai Z, Nádory E, Farsang C, Kiss I. Impairment of skin microvascular reactivity in hypertension and uraemia. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 20: 1821-7. PMID 15985514 DOI: 10.1093/Ndt/Gfh944  0.609
2004 Farkas K, Kolossváry E, Járai Z, Nemcsik J, Farsang C. Non-invasive assessment of microvascular endothelial function by laser Doppler flowmetry in patients with essential hypertension. Atherosclerosis. 173: 97-102. PMID 15177128 DOI: 10.1016/J.Atherosclerosis.2003.11.015  0.595
2004 Farkas K, Nemcsik J, Kolossváry E, Járai Z, Borvendég J, Farsang CS, Kiss I. SKIN MICROVASCULAR REACTIVITY IN HYPERTENSIVE PATIENTS WITH AND WITHOUT END STAGE RENAL DISEASE Journal of Hypertension. 22: S194. DOI: 10.1097/00004872-200406002-00672  0.584
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