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Maria Johansson Soller

Karolinska Institutet

Sweden

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Research Interests

Epidemiology

10%

Biostatistics

20%

Rare Disease

20%

Medical Science

20%

Genomic

20%

Genetic Epidemiology

10%

Precision Medicine

10%

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Articles4

A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population

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Year:

2022

DLG4-related synaptopathy: a new rare brain disorder

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Year:

2021

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

Article Link

Year:

2021

Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

Article Link

Year:

2020

Collaborators4

Anders Jemt

KTH Royal Institute of Technology

SWEDEN

Magnus Nordenskjöld

Professor of Clinical Genetics

Karolinska Institutet

SWEDEN

Rolf Zetterström

Karolinska Institutet

SWEDEN

Daniel Nilsson

Karolinska Institutet

SWEDEN

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