Sulak A, Toth L, Farkas K, Tripolszki K, Fabos B, Kemeny L, Valyi P, Nagy K, Nagy N, Szell M: One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes, CLINICAL AND EXPERIMENTAL DERMATOLOGY 41: (2) pp. 190-195. type of document: Journal paper/Article number of independent citations: 1 language: English URL
2016
from data base, 2016. IX. 29.
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 59: (4) pp. 223-226. type of document: Journal paper/Article language: English URL
2015
from data base, 2016. IX. 29.
Nemes E, Farkas K, Kocsis-Deak B, Drubi A, Sulak A, Tripolszki K, Dosa P, Ferenc L, Nagy N, Szell M: Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation., ARCHIVES OF DERMATOLOGICAL RESEARCH 307: (10) pp. 891-895. type of document: Journal paper/Article language: English DOI
2014
from data base, 2016. IX. 29.
Nagy Nikoletta, Valyi Peter, Csoma Zsanett, Sulak Adrienn, Tripolszki Kornelia, Farkas Katalin, Paschali Ekaterine, Papp Ferenc, Toth Lola, Fabos Beata, Kemeny Lajos, Nagy Katalin, Szell Marta: CTSC and Papillon–Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update, MOLECULAR GENETICS AND GENOMIC MEDICINE 2: (3) pp. 217-228. type of document: Journal paper/Review paper number of independent citations: 9 language: English URL
2014
from data base, 2016. IX. 29.
Nagy N, Farkas K, Tripolszki K, Sulák A, Kemény L, Széll M: A cylindromatosis gén mutációi által okozott genodermatosisok, BŐRGYÓGYÁSZATI ÉS VENEROLÓGIAI SZEMLE 90: (5) pp. 185-193. type of document: Journal paper/Article language: Hungarian DOI
Number of independent citations to these publications:
publications not in Hungarian, published in Hungary, meeting the accreditation criteria:
0
number of independent citations to scientific publications and creative works:
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