Z. Vlčková

Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly

N. Tommerup, Z. Sedlacek, Z. Zemanová, 2018, Human mutation.

Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis

T. Haaf, E. Seemanová, R. Ullmann, 2007, Cytogenetic and Genome Research.

The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

B. Bonanni, M. Urioste, J. Benítez, 2020, Cancers.

Array comparative genome hybridization in patients with developmental delay: two example cases.

Z. Sedlacek, P. Hedvičáková, M. Vlčková, 2012, New biotechnology.

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

James M. Hodge, E. Burnside, Y. Kamatani, 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.