Eva-Lena Stattin

Senior lecturer (associate professor) at Department of Medical Biosciences
Medical and Clinical Genetics

Publications

Author

Title

Year sorteringsordning

Fulltext

Wisten, Aase
Krantz, Peter
Stattin, Eva-Lena

Sudden cardiac death among the young in Sweden from 2000 to 2010: an autopsy-based study
Europace, 19(8): 1327-1334

2017

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Stattin, Eva-Lena
Henning, Petra
Klar, Joakim; et al.

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts
Scientific Reports, 7

2017

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Wang, Zheng
Iida, Aritoshi
Miyake, Noriko; et al.

Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations
PLoS ONE, 11(3)

2016

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Hannuksela, Matias
Stattin, Eva-Lena
Klar, Joakim; et al.

A novel variant in MYLK causes thoracic aortic dissections: genotypic and phenotypic description
BMC Medical Genetics, 17

2016

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Stattin, Eva-Lena
Westin, Ida Maria
Cederquist, Kristina; et al.

Genetic screening in sudden cardiac death in the young can save future lives
International journal of legal medicine (Print), 130(1): 59-66

2016

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Hannuksela, Matias
Stattin, Eva-Lena
Johansson, Bengt; et al.

Screening for familial thoracic aortic aneurysms with aortic imaging does not detect all potential aarriers of the disease
Aorta, 3(1): 1-8

2015

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Winbo, Annika
Stattin, Eva-Lena
Nordin, Charlotte; et al.

Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families
BMC Cardiovascular Disorders, 14: 22-

2014

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Hannuksela, Matias
Stattin, Eva-Lena
Nyberg, Peter; et al.

Familära torakala aortaaneurysm och dissektioner: flera former finns
Läkartidningen, 111(9-10): 399-403

2014

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Sukalo, Maja
Fiedler, Ariane
Guzman, Celina; et al.

Mutations in the Human UBR1 Gene and the Associated Phenotypic Spectrum
Human Mutation, 35(5): 521-531

2014

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Renard, Marjolijn
Callewaert, Bert
Baetens, Machteld; et al.

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGF beta signaling in FTAAD
International Journal of Cardiology, 165(2): 314-321

2013

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