Ciencias de la Salud
Field of knowledge
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University of Tampere
Tampere, FinlandiaPublications in collaboration with researchers from University of Tampere (13)
2024
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Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
Brain : a journal of neurology, Vol. 147, Núm. 5, pp. 1887-1898
2023
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Surgeons’ perspectives on artificial intelligence to support clinical decision-making in trauma and emergency contexts: results from an international survey
World Journal of Emergency Surgery, Vol. 18
2021
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DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan
Molecular Psychiatry, Vol. 26, Núm. 6, pp. 2148-2162
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Growth and development of islet autoimmunity and type 1 diabetes in children genetically at risk
Diabetologia, Vol. 64, Núm. 4, pp. 826-835
2020
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Genotype–phenotype correlations in recessive titinopathies
Genetics in Medicine, Vol. 22, Núm. 12, pp. 2029-2040
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New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
Brain, Vol. 143, Núm. 9, pp. 2696-2708
2018
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DNA methylation in childhood asthma: an epigenome-wide meta-analysis
The Lancet Respiratory Medicine, Vol. 6, Núm. 5, pp. 379-388
2017
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Global, regional, and national age-sex specifc mortality for 264 causes of death, 1980-2016: A systematic analysis for the Global Burden of Disease Study 2016
The Lancet, Vol. 390, Núm. 10100, pp. 1151-1210
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Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970-2016: A systematic analysis for the Global Burden of Disease Study 2016
The Lancet, Vol. 390, Núm. 10100, pp. 1084-1150
2016
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Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy
Nature Communications, Vol. 7
2015
2012
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Angiogenesis-related gene expression analysis in celiac disease
Autoimmunity, Vol. 45, Núm. 3, pp. 264-270
2011
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Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy
Nature Medicine, Vol. 17, Núm. 6, pp. 720-725