Ciencias
Campo de conocimiento
Karolinska University Hospital
Estocolmo, SueciaPublicaciones en colaboración con investigadoras/es de Karolinska University Hospital (16)
2024
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Severe steroid-related neuropsychiatric symptoms during paediatric acute lymphoblastic leukaemia therapy—An observational Ponte di Legno Toxicity Working Group Study
British Journal of Haematology, Vol. 205, Núm. 4, pp. 1450-1459
2022
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Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts
International Journal of Obesity, Vol. 46, Núm. 10, pp. 1901-1909
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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X-ray-Based Techniques to Study the Nano-Bio Interface
ACS Nano, Vol. 15, Núm. 3, pp. 3754-3807
2020
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Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education
Scientific Reports, Vol. 10, Núm. 1
2019
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Parental Education and Genetics of BMI from Infancy to Old Age: A Pooled Analysis of 29 Twin Cohorts
Obesity, Vol. 27, Núm. 5, pp. 855-865
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The CODATwins Project: The Current Status and Recent Findings of COllaborative Project of Development of Anthropometrical Measures in Twins
Twin Research and Human Genetics, Vol. 22, Núm. 6, pp. 800-808
2018
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Associations between birth size and later height from infancy through adulthood: An individual based pooled analysis of 28 twin cohorts participating in the CODATwins project
Early Human Development, Vol. 120, pp. 53-60
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Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts
Scientific Reports, Vol. 8, Núm. 1
2017
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Education in Twins and Their Parents Across Birth Cohorts over 100 years: An Individual-Level Pooled Analysis of 42-Twin Cohorts
Twin Research and Human Genetics, Vol. 20, Núm. 5, pp. 395-405
2008
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Refining genetic associations in multiple sclerosis
The Lancet Neurology
2007
2000
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Lack of association between the interferon regulatory factor-1 (IRF1) locus at 5q31.1 and multiple sclerosis in Germany, Northern Italy, Sardinia and Sweden
Genes and Immunity, Vol. 1, Núm. 4, pp. 290-292
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PECAM1, MPO and PRKAR1A at chromosome 17q21-q24 and susceptibility for multiple sclerosis in Sweden and Sardinia
Journal of Neuroimmunology, Vol. 108, Núm. 1-2, pp. 153-159
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Polymorphism analysis suggests that the gelatinase B gene is not a susceptibility factor for multiple sclerosis
Journal of Neuroimmunology, Vol. 105, Núm. 1, pp. 58-63
1999
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Analysis of an IFN-γ gene (IFNG) polymorphism in multiple sclerosis in Europe: Effect of population structure on association with disease
Journal of Interferon and Cytokine Research, Vol. 19, Núm. 9, pp. 1037-1046