Živilė Čiuladaitė

Relatives with Opposite Chromosome Constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a Familial Pericentric Inversion

Živilė Čiuladaitė, Eglė Preikšaitienė, Algirdas Utkus et al. · Cytogenetic and Genome Research · 2014 · 42 citations

Cytogenetics, Genetics, Large Pericentric Inversions +16

Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome

Biruté Tumiene, Živilė Čiuladaitė, Eglė Preikšaitienė et al. · Journal of Applied Genetics · 2017 · 32 citations

Phenotype Comparison, Gene Deletion Data, Developmental Biology +9

A new single gene deletion on 2q34: <i>ERBB4</i> is associated with intellectual disability

Jūratė Kasnauskienė, Živilė Čiuladaitė, Eglė Preikšaitienė et al. · American Journal of Medical Genetics Part A · 2013 · 31 citations

Clinical and molecular characterization of a second case of 7p22.1 microduplication

Eglė Preikšaitienė, Jūratė Kasnauskienė, Živilė Čiuladaitė et al. · American Journal of Medical Genetics Part A · 2012 · 23 citations · Full text

Genetics, Pathology, Molecular Genetics +18

A single gene deletion on 4q28.3: PCDH18 – A new candidate gene for intellectual disability?

Jūratė Kasnauskienė, Živilė Čiuladaitė, Eglė Preikšaitienė et al. · European Journal of Medical Genetics · 2012 · 21 citations · Full text

Gene Deletion Data, Genetic Disorder, Genetics +6