Tuomo Maatta
Kajaani, Finland
Last Updated: 09/26/2026
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Found 9 publications
Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders.
Journal: Scientific reports
Published: January 04, 2024
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 05, 2021
Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders.
Journal: Molecular genetics & genomic medicine
Published: January 13, 2021
Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland.
Journal: Human genetics
Published: December 12, 2020
Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Journal: European journal of human genetics : EJHG
Published: September 12, 2019
Outcome of Chair-Side Dental Fear Treatment: Long-Term Follow-Up in Public Health Setting.
Journal: International journal of dentistry
Published: February 20, 2019
Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Journal: European journal of human genetics : EJHG
Published: September 28, 2018
Identification of C12orf4 as a gene for autosomal recessive intellectual disability.
Journal: Clinical genetics
Published: April 14, 2016
Laser fluorescence in monitoring the influence of targeted tooth brushing on remineralization of initial caries lesions on newly erupted molar teeth - RCT.
Journal: International journal of dental hygiene
Published: December 21, 2015
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Last Updated: 09/26/2026