Tautvydas Rancelis

Santariskiu Str. 2
Vilnius, VL LT08661, Lithuania

Last Updated: 09/26/2026

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Found 16 publications

Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in Genomics.

Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in Genomics.

Journal: Genes

Published: July 12, 2023

Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.

Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.

Journal: Medicina (Kaunas, Lithuania)

Published: May 26, 2023

Putative protective genomic variation in the Lithuanian population.

Putative protective genomic variation in the Lithuanian population.

Journal: Genetics and molecular biology

Published: February 03, 2023

PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.

PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.

Journal: Medicina (Kaunas, Lithuania)

Published: September 15, 2022

Donor Splice Site Variant in SLC9A6 Causes Christianson Syndrome in a Lithuanian Family: A Case Report.

Donor Splice Site Variant in SLC9A6 Causes Christianson Syndrome in a Lithuanian Family: A Case Report.

Journal: Medicina (Kaunas, Lithuania)

Published: January 26, 2022

CyberGenomics: Application of Behavioral Genetics in Cybersecurity.

CyberGenomics: Application of Behavioral Genetics in Cybersecurity.

Journal: Behavioral sciences (Basel, Switzerland)

Published: September 08, 2021

Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report.

Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report.

Journal: BMC musculoskeletal disorders

Published: May 07, 2021

Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families.

Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families.

Journal: American journal of medical genetics. Part A

Published: July 06, 2019

A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2.

A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2.

Journal: Gene

Published: June 24, 2019

Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family.

Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family.

Journal: Molecular genetics & genomic medicine

Published: May 18, 2019

A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report.

A novel CHD7 variant disrupting acceptor splice site in a patient with mild features of CHARGE syndrome: a case report.

Journal: BMC medical genetics

Published: April 18, 2019

Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort.

Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort.

Journal: Acta medica Lituanic

Published: June 22, 2018

Showing 1-12 of 16

Last Updated: 09/26/2026