Tiia Kontio-Kangas
Espoo, Finland
Last Updated: 09/26/2026
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Found 8 publications
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Journal: Orphanet journal of rare diseases
Published: February 18, 2022
Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Journal: Orphanet journal of rare diseases
Published: July 16, 2021
Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.
Journal: PloS one
Published: June 18, 2020
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.
Journal: BMC cardiovascular disorders
Published: May 24, 2020
Clinical and ultrastructural findings in an ataxic variant of Kufor-Rakeb syndrome.
Journal: Folia neuropathologica
Published: October 08, 2019
Impaired HDL2-mediated cholesterol efflux is associated with metabolic syndrome in families with early onset coronary heart disease and low HDL-cholesterol level.
Journal: PloS one
Published: December 31, 2015
Plasma levels of antibodies against oxidized LDL are inherited but not associated with HDL-cholesterol level in families with early coronary heart disease.
Journal: Atherosclerosis
Published: February 02, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026