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MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.
Mašindová I, Šoltýsová A, Varga L, Mátyás P, Ficek A, Hučková M, Sůrová M, Šafka-Brožková D, Anwar S, Bene J, Straka S, Janicsek I, Ahmed ZM, Seeman P, Melegh B, Profant M, Klimeš I, Riazuddin S, Kádasi Ľ, Gašperíková D. Mašindová I, et al. Among authors: klimes i. PLoS One. 2015 Apr 17;10(4):e0124232. doi: 10.1371/journal.pone.0124232. eCollection 2015. PLoS One. 2015. PMID: 25885414 Free PMC article.
[Genetics of monogenic forms of diabetes].
Staník J, Hucková M, Staníková D, Masindová I, Valentínová L, Gasperíková D, Klimes I. Staník J, et al. Among authors: klimes i. Vnitr Lek. 2011 Nov;57(11):937-45. Vnitr Lek. 2011. PMID: 22165700 Review. Slovak.
Melanocortin-4 receptor gene mutations in obese Slovak children.
Stanikova D, Surova M, Ticha L, Petrasova M, Virgova D, Huckova M, Skopkova M, Lobotkova D, Valentinova L, Mokan M, Stanik J, Klimes I, Gasperikova D. Stanikova D, et al. Among authors: klimes i. Physiol Res. 2015;64(6):883-90. doi: 10.33549/physiolres.932968. Epub 2015 Jun 5. Physiol Res. 2015. PMID: 26047380 Free article.
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