Krista Heliö

Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients

M. Gentile, T. Heliö, S. Tuupanen, 2021, BMC Cardiovascular Disorders.

Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.

T. Ojala, M. Gentile, S. Ahonen, 2021, PloS one.

Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients

T. Heliö, S. Myllykangas, J. Koskenvuo, 2023, Frontiers in cardiovascular medicine.

DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma

T. Heliö, J. Koskenvuo, M. Holmström, 2023, Frontiers in Cardiovascular Medicine.

DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy

T. Heliö, S. Myllykangas, J. Koskenvuo, 2020, BMC Medical Genetics.

GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy

K. Nikus, M. Gentile, S. Ahonen, 2021, Frontiers in Genetics.