Emmi Helle

University of Helsinki

Finland

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Articles (19)

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2025

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2025

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2025

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2021

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2021

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2021

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2020

Collaborators (17)

Hanna Ollila

University of Helsinki

FINLAND

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Markku Varjosalo

University of Helsinki

FINLAND

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Johanna Ilvesvuo

University of Helsinki

FINLAND

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Ilari Kuitunen

University of Eastern Finland

FINLAND

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Diego Balboa

University of Helsinki

FINLAND

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Aarno Palotie

University of Helsinki

FINLAND

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Anu Kaskinen

University of Helsinki

FINLAND

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Martin Broberg

University of Helsinki

FINLAND

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Tiina Ojala

Helsinki University Hospital

FINLAND

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Jessica Chong

University of Washington

UNITED STATES

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Peter White

Chief Data Sciences Officer

Nationwide Children's Hospital

UNITED STATES

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Elizabeth Blue

Associate Professor

University of Washington

UNITED STATES

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Santtu Heinonen

University of Helsinki

FINLAND

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Karl Lemström

University of Helsinki

FINLAND

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Riikka Kivelä

University of Helsinki

FINLAND

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Maria Hurskainen

Helsinki University Hospital

FINLAND

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Amanda Ranta

Stanford University

UNITED STATES

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Emmi Helle

Research Interests

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Articles (19)

Association of maternal asthma with congenital heart defects in offspring

The ERBB2 c.1795C&gt;T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans

Prevalence, risk factors, and outcomes of QT prolongation in primary and RASopathy-associated hypertrophic cardiomyopathy

Consequences of electrocardiography screening for prolonged QTc in neonates—A systematic review

Cardiac MRI in patients with Fontan circulation: assessing risk factors for adverse outcomes

Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

Maternal Diabetes and Overweight and Congenital Heart Defects in Offspring

Unravelling associations between maternal health and congenital heart defect risk in the offspring—the FINNPEDHEART study

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome

Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population

Risk factors for mortality in patients with hypoplastic left heart syndrome after the Norwood procedure

Cardiac MRI and Clinical Outcomes in TMEM43 Arrhythmogenic Cardiomyopathy

Risk factors for severe respiratory syncytial virus infection during the first year of life: development and validation of a clinical prediction model

Maternal first trimester metabolic profile in pregnancies with transposition of the great arteries.

Heart Transplantation for Early-Onset Anthracycline-Induced Cardiomyopathy Within 5 Months of Chemotherapy Completion

HiPS-Endothelial Cells Acquire Cardiac Endothelial Phenotype in Co-culture With hiPS-Cardiomyocytes

From Stem Cells to Populations—Using hiPSC, Next-Generation Sequencing, and GWAS to Explore the Genetic and Molecular Mechanisms of Congenital Heart Defects

Single cell transcriptomic analysis of murine lung development on hyperoxia-induced damage.

Rare Variants in Genes Associated With Cardiomyopathy Are Not Common in Hypoplastic Left Heart Syndrome Patients With Myocardial Dysfunction

Collaborators (17)

Hanna Ollila

Markku Varjosalo

Johanna Ilvesvuo

Ilari Kuitunen

Diego Balboa

Aarno Palotie

Anu Kaskinen

Martin Broberg

Tiina Ojala

Jessica Chong

Peter White

Elizabeth Blue

Santtu Heinonen

Karl Lemström

Riikka Kivelä

Maria Hurskainen

Amanda Ranta

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The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans