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V. Kučinskas · SciRah

Researcher profile · Semantic Scholar

V. Kučinskas

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V. Kučinskas — researcher profile on SciRah

h-index: 32
Works: 190
Citations: 18K

Most-cited papers

Biological Insights From 108 Schizophrenia-Associated Genetic Loci
S. Ripke, B. Neale, A. Corvin, J. Walters +296 more
2014Nature7,487 citations Open access
Semantic Scholar
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V. Trubetskoy, A. Pardiñas, Ting Qi, G. Panagiotaropoulou +430 more
2022Nature2,385 citations Open access
Semantic Scholar
Analysis of shared heritability in common disorders of the brain
V. Anttila, B. Bulik-Sullivan, H. Finucane, R. Walters +496 more
2018Science1,869 citations Open access
Semantic Scholar
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes
D. Ruderfer, S. Ripke, A. McQuillin, J. Boocock +496 more
2018Cell675 citations Open access
Semantic Scholar
Genomic control process: development and evolution
E. Preiksaitiene, V. Kučinskas
2015European Journal of Human Genetics142 citations Open access
Semantic Scholar
Genetic Heritage of the Balto-Slavic Speaking Populations: A Synthesis of Autosomal, Mitochondrial and Y-Chromosomal Data
A. Kushniarevich, O. Utevska, Marina Chuhryaeva, A. Agdzhoyan +35 more
2015PLoS ONE127 citations Open access
Semantic Scholar
A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics
C. Mizzi, Eleni Dalabira, Judit Kumuthini, N. Dzimiri +46 more
2016PLoS ONE117 citations Open access
Semantic Scholar
The most common technologies and tools for functional genome analysis
Evelina Gasperskaja, V. Kučinskas
2017Acta medica Lituanica69 citations Open access
Semantic Scholar
Association analysis of ACE, ACTN3 and PPARGC1A gene polymorphisms in two cohorts of European strength and power athletes
V. Ginevičienė, A. Jakaitienė, M. Aksenov, A. Aksenova +7 more
2016Biology of Sport68 citations Open access
Semantic Scholar
Variation in the ACE, PPARGC1A and PPARA genes in Lithuanian football players
V. Ginevičienė, A. Jakaitienė, L. Tubelis, V. Kučinskas
2014European Journal of Sport Science67 citations
Semantic Scholar
KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis
L. Gueneau, R. Fish, H. Shamseldin, N. Voisin +35 more
2017American Journal of Human Genetics54 citations Open access
Semantic Scholar
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
J. den Hoed, Elke de Boer, N. Voisin, A. Dingemans +93 more
2020bioRxiv51 citations Open access
Semantic Scholar
Array CGH analysis of a cohort of Russian patients with intellectual disability.
A. Kashevarova, L. Nazarenko, N. Skryabin, O. Salyukova +8 more
2014Gene46 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 Genetics28 citations
Semantic Scholar
Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649)
S. Knappskog, Liv B Gansmo, K. Dibirova, A. Metspalu +33 more
2014OncoTarget26 citations Open access
Semantic Scholar
Age at first birth in women is genetically associated with increased risk of schizophrenia
G. Ni, J. Gratten, N. Wray, Sang-Hong Lee +297 more
2017Scientific Reports25 citations Open access
Semantic Scholar
Patterns of genetic structure and adaptive positive selection in the Lithuanian population from high-density SNP data
A. Urnikytė, A. Flores-Bello, Mayukh Mondal, Alma Molyte +4 more
2019Scientific Reports24 citations Open access
Semantic Scholar
NSD1 duplication in Silver–Russell syndrome (SRS): molecular karyotyping in patients with SRS features
Jana Sachwitz, R. Meyer, G. Fekete, S. Spranger +9 more
2017Clinical Genetics22 citations
Semantic Scholar
The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population
V. Mikštienė, A. Jakaitienė, J. Byčkova, E. Gradauskienė +12 more
2016BMC Genetics22 citations Open access
Semantic Scholar
Recent common origin, reduced population size, and marked admixture have shaped European Roma genomes.
E. Bianco, G. Laval, N. Font-Porterias, C. García-Fernández +11 more
2020Molecular biology and evolution21 citations Open access
Semantic Scholar
Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes
J. Sachwitz, G. Strobl-Wildemann, G. Fekete, L. Ambrozaitytė +4 more
2016BMC Medical Genetics21 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
RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families
I. Domarkienė, A. Pranculis, Š. Germanas, A. Jakaitienė +4 more
2013Balkan Journal of Medical Genetics18 citations Open access
Semantic Scholar
Inflammatory myopathy in a patient with Aicardi-Goutières syndrome.
Birutė Tumienė, N. Voisin, E. Preiksaitiene, D. Petroška +5 more
2017European Journal of Medical Genetics16 citations Open access
Semantic Scholar
Association of BMP4 polymorphisms with non-syndromic cleft lip with or without cleft palate and isolated cleft palate in Latvian and Lithuanian populations.
Inga Kempa, L. Ambrozaitytė, J. Stavusis, I. Akota +6 more
2014Stomatologija16 citations
Semantic Scholar
Sex-biased patterns shaped the genetic history of Roma
C. García-Fernández, N. Font-Porterias, V. Kučinskas, E. Sukarova-Stefanovska +7 more
2020Scientific Reports13 citations Open access
Semantic Scholar
Insights Into de novo Mutation Variation in Lithuanian Exome
Laura Pranckėnienė, A. Jakaitienė, L. Ambrozaitytė, Ingrida Kavaliauskienė +1 more
2018Frontiers in Genetics13 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
Classical rather than genetic risk factors account for high cardiovascular disease prevalence in Lithuania: A cross-sectional population study.
N. Burokienė, I. Domarkienė, L. Ambrozaitytė, Ingrida Uktverytė +6 more
2017Advances in Medical Sciences12 citations
Semantic Scholar
Distinct genetic liability profiles define clinically relevant patient strata across common diseases
L. Trastulla, Georgii V. Dolgalev, S. Moser, Laura Jimenez-Barron +306 more
2023Nature Communications11 citations Open access
Semantic Scholar
CNV analysis in the Lithuanian population
A. Urnikytė, I. Domarkienė, S. Stoma, L. Ambrozaitytė +5 more
2016BMC Genetics11 citations Open access
Semantic Scholar
Y‐Chromosomal Lineages of Latvians in the Context of the Genetic Variation of the Eastern‐Baltic Region
L. Pliss, Līga Timša, S. Rootsi, K. Tambets +10 more
2015Annals of Human Genetics11 citations
Semantic Scholar
De novo splice site variant of ARID1B associated with pathogenesis of Coffin–Siris syndrome
Laura Pranckėnienė, Evelina Siavrienė, L. Gueneau, E. Preiksaitiene +3 more
2019Molecular Genetics & Genomic Medicine10 citations Open access
Semantic Scholar
Ophthalmic phenotypes associated with biallelic loss‐of‐function PCDH12 variants
F. Mattioli, N. Voisin, E. Preiksaitiene, I. Kozlovskaja +2 more
2021American Journal of Medical Genetics. Part A9 citations
Semantic Scholar
Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies
Inna Inashkina, E. Jankevics, J. Stavusis, I. Vasiljeva +11 more
2016BMC Musculoskeletal Disorders9 citations Open access
Semantic Scholar
A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome
E. Preiksaitiene, Alfonso Caro, E. Benušienė, S. Oltra +8 more
2015American Journal of Medical Genetics. Part A9 citations
Semantic Scholar
R368X mutation in MID1 among recurrent mutations in patients with X-linked Opitz G/BBB syndrome
E. Preiksaitiene, N. Krasovskaja, A. Utkus, J. Kasnauskienė +4 more
2015Clinical Dysmorphology9 citations
Semantic Scholar
Genome-Wide Landscape of North-Eastern European Populations: A View from Lithuania
A. Urnikytė, Alma Molyte, V. Kučinskas
2021Genes8 citations Open access
Semantic Scholar
A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report
Evelina Siavrienė, Gunda Petraitytė, V. Mikštienė, Tautvydas Rančelis +6 more
2019BMC Medical Genetics8 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
A de novo 13q31.3 microduplication encompassing the miR-17∼92 cluster results in features mirroring those associated with Feingold syndrome 2.
Evelina Siavrienė, E. Preiksaitiene, Živilė Maldžienė, V. Mikštienė +5 more
2020Gene7 citations
Semantic Scholar
Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families
E. Preiksaitiene, N. Voisin, L. Gueneau, E. Benušienė +6 more
2019American Journal of Medical Genetics. Part A7 citations
Semantic Scholar
Analysis of pathogenic variants from the ClinVar database in healthy people using next-generation sequencing.
Tautvydas Rančelis, Justas Arasimavičius, L. Ambrozaitytė, Ingrida Kavaliauskienė +4 more
2017Genetics Research7 citations Open access
Semantic Scholar
SOX9 p.Lys106Glu mutation causes acampomelic campomelic dysplasia: Prenatal and postnatal clinical findings
E. Preiksaitiene, E. Benušienė, A. Matulevičienė, Kristina Grigalionienė +2 more
2016American Journal of Medical Genetics. Part A7 citations
Semantic Scholar
Frame shift mutations of the ZMPSTE24 gene in two siblings with restrictive dermopathy
A. Matulevičienė, R. Meškienė, Aušra Morkūnienė, L. Ambrozaitytė +5 more
2016Clinical Dysmorphology7 citations
Semantic Scholar
Causes of preterm birth: Genetic factors in preterm birth and preterm infant phenotypes
Svetlana Dauengauer-Kirlienė, I. Domarkienė, I. Pilypienė, Gabrielė Žukauskaitė +2 more
2022The journal of obstetrics and gynaecology research6 citations
Semantic Scholar
Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report
Evelina Siavrienė, Gunda Petraitytė, B. Burnytė, Aušra Morkūnienė +5 more
2021BMC Musculoskeletal Disorders6 citations Open access
Semantic Scholar
Recent effective population size estimated from segments of identity by descent in the Lithuanian population
A. Urnikytė, Alma Molyte, V. Kučinskas
20176 citations Open access
Semantic Scholar
Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics
C. Mizzi, Eleni Dalabira, Judit Kumuthini, N. Dzimiri +46 more
2017PLoS ONE6 citations Open access
Semantic Scholar
A de novo Pericentric Inversion in Chromosome 4 Associated with Disruption of PITX2 and a Microdeletion in 4p15.2 in a Patient with Axenfeld-Rieger Syndrome and Developmental Delay
Živilė Maldžienė, E. Preiksaitiene, Salomėja Ignotienė, Natalija Kapitanova +2 more
2017Cytogenetic and Genome Research6 citations
Semantic Scholar

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