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Cecilia Gunnarsson

MD, Ass Prof

Linköping University

Sweden

Research Interests

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Professors in Sweden Professors in Biostatistics Biostatistics professors in Sweden

Articles (14)

Year:

2026

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2026

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2025

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2025

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2025

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2024

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2024

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2024

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2024

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2024

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2023

Year:

2023

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2023

Year:

2023

Collaborators (12)

Koen Dekkers

Uppsala University

SWEDEN

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Claudia Gonzaga-Jauregui

Associate Professor (with Tenure)

National Autonomous University of Mexico

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Marcus Carlsson

Professor, head of research group

Karolinska Institutet

SWEDEN

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qiaosen Chen

Karolinska Institutet

SWEDEN

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Sanna Gudmundsson

Assistant Professor

Karolinska Institutet

SWEDEN

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Antonios Pantazis

Sr. associate professor of ion channel molecular physiology

Linköping University

SWEDEN

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Göran Bergström

University of Gothenburg

SWEDEN

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Mats Fredrikson

Ass. Professor

Linköping University

SWEDEN

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Mauno Vihinen

Professor of Medical Structural Biology

Lund University

SWEDEN

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Olle Melander

Professor

Lund University Medical Faculty

SWEDEN

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Isabel Tapia-Paez

Karolinska Institutet

SWEDEN

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Henrik Gréen

Professor

Linköping University

SWEDEN

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Cecilia Gunnarsson

Research Interests

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Articles (14)

A Heterozygous Variant in the GABBR2 Gene in a Girl With Clinical Classic Rett Syndrome

Extracting homogenous data from heterogenous diseases: RaraSwed, the Swedish national rare disease quality registry

A genome-wide association study of imaging-defined atherosclerosis

Translation, cross-cultural adaptation, and preliminary validation of a patient-reported outcome measure for genetic counseling outcomes in Sweden

Unravelling the Genotype of the Apical Variant of Hypertrophic Cardiomyopathy in a Swedish Cohort

Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young—FGF-21 Highly Associated with Overt Disease

Spatial QRS-T angle can indicate presence of myocardial fibrosis in pediatric and young adult patients with hypertrophic cardiomyopathy.

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon

Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions

Transcriptome analysis of the aortic coarctation area

Two epilepsy-associated variants in KCNA2 (K<sub>V</sub> 1.2) at position H310 oppositely affect channel functional expression.

Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy

Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome

Whole exome sequencing of FFPE samples—expanding the horizon of forensic molecular autopsies

Collaborators (12)

Koen Dekkers

Claudia Gonzaga-Jauregui

Marcus Carlsson

qiaosen Chen

Sanna Gudmundsson

Antonios Pantazis

Göran Bergström

Mats Fredrikson

Mauno Vihinen

Olle Melander

Isabel Tapia-Paez

Henrik Gréen

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