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Ž. Čiuladaitė · SciRah

Researcher profile · Semantic Scholar

Ž. Čiuladaitė

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Ž. Čiuladaitė — researcher profile on SciRah

h-index: 9
Works: 18
Citations: 202

Most-cited papers

A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability
J. Kasnauskienė, Ž. Čiuladaitė, E. Preiksaitiene, A. Utkus +2 more
2013American Journal of Medical Genetics. Part A30 citations
Semantic Scholar
Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
Birutė Tumienė, Ž. Čiuladaitė, E. Preiksaitiene, R. Mameniškienė +2 more
2017Journal of Applied Genetics28 citations
Semantic Scholar
Clinical and molecular characterization of a second case of 7p22.1 microduplication
E. Preiksaitiene, J. Kasnauskienė, Ž. Čiuladaitė, Birutė Tumienė +2 more
2012American Journal of Medical Genetics. Part A22 citations Open access
Semantic Scholar
Considering specific clinical features as evidence of pathogenic copy number variants
E. Preiksaitiene, Alma Molyte, J. Kasnauskienė, Ž. Čiuladaitė +3 more
2014Journal of Applied Genetics21 citations Open access
Semantic Scholar
A single gene deletion on 4q28.3: PCDH18--a new candidate gene for intellectual disability?
J. Kasnauskienė, Ž. Čiuladaitė, E. Preiksaitiene, A. Matulevičienė +6 more
2012European Journal of Medical Genetics21 citations Open access
Semantic Scholar
Mental retardation and autism associated with recurrent 16p11.2 microdeletion: incomplete penetrance and variable expressivity
Ž. Čiuladaitė, J. Kasnauskienė, L. Cimbalistienė, E. Preiksaitiene +2 more
2011Journal of Applied Genetics18 citations Open access
Semantic Scholar
A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features.
E. Preiksaitiene, K. Männik, V. Dirsė, A. Utkus +4 more
2012European Journal of Medical Genetics14 citations Open access
Semantic Scholar
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
Ž. Čiuladaitė, E. Preiksaitiene, A. Utkus, V. Kučinskas
2014Cytogenetic and Genome Research13 citations
Semantic Scholar
De novo 5q35.5 duplication with clinical presentation of Sotos syndrome
J. Kasnauskienė, L. Cimbalistienė, Ž. Čiuladaitė, E. Preiksaitiene +5 more
2011American Journal of Medical Genetics. Part A12 citations Open access
Semantic Scholar
Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
E. Preiksaitiene, E. Benušienė, Ž. Čiuladaitė, Vytautas Šliužas +2 more
2016Taiwanese Journal of Obstetrics & Gynecology8 citations Open access
Semantic Scholar
Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome
Birutė Tumienė, Ž. Čiuladaitė, E. Preiksaitiene, R. Mameniškienė +2 more
2017Journal of Applied Genetics5 citations
Semantic Scholar
Clinical, cytogenetic and molecular study of a case of ring chromosome 10
Ž. Čiuladaitė, B. Burnytė, Danutė Vansevičiūtė, Evelina Dagytė +2 more
2015Molecular Cytogenetics5 citations Open access
Semantic Scholar
Two New de novo Interstitial Duplications Covering 2p14–p22.1: Clinical and Molecular Analysis
J. Kasnauskienė, L. Cimbalistienė, A. Utkus, Ž. Čiuladaitė +3 more
2012Cytogenetic and Genome Research4 citations
Semantic Scholar
Familial Distal Monosomy 5p15.3-pter With Trisomy 12q24.2-qter Resulting in Neurodevelopmental Delay and Dysmorphic Features
Ž. Čiuladaitė, A. Matulevičienė, Aušra Bandanskytė, A. Brazaitis +2 more
2014Journal of Child Neurology1 citations
Semantic Scholar
Establishing the Genetic Diagnosis in Patients with Intellectual Disability: a Case Report of Phelan-Mcdermid Syndrome
E. Preiksaitiene, A. Utkus, Ž. Čiuladaitė, J. Kasnauskienė +1 more
20120 citations
Semantic Scholar
Molecular Karyotyping and Genetic Etiology of Intellectual Disability: Case Reports
Ž. Čiuladaitė, E. Preiksaitiene, J. Kasnauskienė, A. Utkus +7 more
20120 citations
Semantic Scholar
Subtelomeric fluorescence in situ hybridization in clinical cytogenetics: results of analysis of Lithuanian patients
V. Dirsė, Vytautas Šliužas, Ž. Čiuladaitė, B. Aleksiūnienė +1 more
20110 citations Open access
Semantic Scholar
Diversity of human chromosome structural rearrangements identified at the Center for Medical Genetics in 2002–2007
Vytautas Šliužas, Ž. Čiuladaitė, V. Kučinskas
20080 citations
Semantic Scholar

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