K. Balogh

First detection of the melanoma-predisposing proline-48-threonine mutation of p16 in Hungarians: was there a common founder either in Italy or in Hungary?

L. Kemény, A. Dobozy, M. Széll, 2007, Melanoma research.

Melanoma-Predisposing CDKN2A Mutations in Association with Breast Cancer: A Case-Study and Review of the Literature

L. Kemény, L. Haracska, G. Lázár, 2011 .

Detection of a rare CDKN2A intronic mutation in a Hungarian melanoma‐prone family and its role in splicing regulation

F. Pagani, L. Kemény, M. Széll, 2012, The British journal of dermatology.

CDKN2A gene mutations and genetic interactions in the pathogenesis of melanoma

K. Balogh, Klára Balogh, 2013 .

Genomic and molecular biology investigations in multifactorial skin diseases.

L. Kemény, K. Szegedi, M. Széll, 2009 .

Neonatal Blue Light Phototherapy and Melanocytic Nevi: A Twin Study

L. Kemény, H. Orvos, M. Széll, 2011, Pediatrics.