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Author Details

Bengt Persson
Karolinska Institutet
1962
540
74
Timothy Clark (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36931226Associations between heredity, height, BMI, diabetes mellitus type 1 or 2 and gene variants in the insulin receptor (INSR) gene in patients with schizophrenia.Neuro Endocrinol Lett2023
36931398Relationship between iron deficiency and expression of genes involved in iron metabolism in human myocardium and skeletal muscle.Int J Cardiol2023
36931226Associations between heredity, height, BMI, diabetes mellitus type 1 or 2 and gene variants in the insulin receptor (INSR) gene in patients with schizophrenia.Neuro Endocrinol Lett2023
36931398Relationship between iron deficiency and expression of genes involved in iron metabolism in human myocardium and skeletal muscle.Int J Cardiol2023
36330003Extracellular vesicles in heart failure - A study in patients with heart failure with preserved ejection fraction or heart failure with reduced ejection fraction characteristics undergoing elective coronary artery bypass grafting.Front Cardiovasc Med2022
36330003Extracellular vesicles in heart failure - A study in patients with heart failure with preserved ejection fraction or heart failure with reduced ejection fraction characteristics undergoing elective coronary artery bypass grafting.Front Cardiovasc Med2022
35403374Baseline characteristics of 547 new onset heart failure patients in the PREFERS heart failure study.ESC Heart Fail2022
35403374Baseline characteristics of 547 new onset heart failure patients in the PREFERS heart failure study.ESC Heart Fail2022
32165346Increased iron absorption in patients with chronic heart failure and iron deficiency.J Card Fail2020
32165346Increased iron absorption in patients with chronic heart failure and iron deficiency.J Card Fail2020
32750486Metabolomic Profile in HFpEF vs HFrEF Patients.J Card Fail2020
32750486Metabolomic Profile in HFpEF vs HFrEF Patients.J Card Fail2020
30816197Transcriptomics of cardiac biopsies reveals differences in patients with or without diagnostic parameters for heart failure with preserved ejection fraction.Sci Rep2019
31520075Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
30816197Transcriptomics of cardiac biopsies reveals differences in patients with or without diagnostic parameters for heart failure with preserved ejection fraction.Sci Rep2019
31455890Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
31405382The bio.tools registry of software tools and data resources for the life sciences.Genome Biol2019
30890711Addendum: The FAIR Guiding Principles for scientific data management and stewardship.Sci Data2019
31344365Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia.Clin Biochem2019
31520075Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
31405382The bio.tools registry of software tools and data resources for the life sciences.Genome Biol2019
31455890Leveraging European infrastructures to access 1 million human genomes by 2022.Nat Rev Genet2019
31344365Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia.Clin Biochem2019
30890711Addendum: The FAIR Guiding Principles for scientific data management and stewardship.Sci Data2019
29947537Endothelin A receptor blockade improves endothelium-dependent relaxation in obese woman.Physiol Res2018
29947537Endothelin A receptor blockade improves endothelium-dependent relaxation in obese woman.Physiol Res2018
29021611Spatial detection of fetal marker genes expressed at low level in adult human heart tissue.Sci Rep2017
29021611Spatial detection of fetal marker genes expressed at low level in adult human heart tissue.Sci Rep2017
26818892Gestational diabetes: Glycaemic predictors for fetal macrosomia and maternal risk of future diabetes.Diabetes Res Clin Pract2016
26978244The FAIR Guiding Principles for scientific data management and stewardship.Sci Data2016
27384611Rationale and design of the PREFERS (Preserved and Reduced Ejection Fraction Epidemiological Regional Study) Stockholm heart failure study: an epidemiological regional study in Stockholm county of 2.1 million inhabitants.Eur J Heart Fail2016
26818892Gestational diabetes: Glycaemic predictors for fetal macrosomia and maternal risk of future diabetes.Diabetes Res Clin Pract2016
27455956Computational studies of human class V alcohol dehydrogenase - the odd sibling.BMC Biochem2016
27634392Maternal and Neonatal Morbidity for Women Who Would Be Added to the Diagnosis of GDM Using IADPSG Criteria: A Secondary Analysis of the Hyperglycemia and Adverse Pregnancy Outcome Study.Diabetes Care2016
27721825Functional and Structural Consequences of Nine <i>CYP21A2</i> Mutations Ranging from Very Mild to Severe Effects.Int J Endocrinol2016
27634392Maternal and Neonatal Morbidity for Women Who Would Be Added to the Diagnosis of GDM Using IADPSG Criteria: A Secondary Analysis of the Hyperglycemia and Adverse Pregnancy Outcome Study.Diabetes Care2016
27721825Functional and Structural Consequences of Nine <i>CYP21A2</i> Mutations Ranging from Very Mild to Severe Effects.Int J Endocrinol2016
27455956Computational studies of human class V alcohol dehydrogenase - the odd sibling.BMC Biochem2016
27384611Rationale and design of the PREFERS (Preserved and Reduced Ejection Fraction Epidemiological Regional Study) Stockholm heart failure study: an epidemiological regional study in Stockholm county of 2.1 million inhabitants.Eur J Heart Fail2016
26978244The FAIR Guiding Principles for scientific data management and stewardship.Sci Data2016
24953648In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia.Clin Endocrinol (Oxf)2015
25479062The mammalian alcohol dehydrogenase genome shows several gene duplications and gene losses resulting in a large set of different enzymes including pseudoenzymes.Chem Biol Interact2015
26222270Randomized controlled study in pregnancy on treatment of marked hyperglycemia that is short of overt diabetes.Acta Obstet Gynecol Scand2015
26333769Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures.Nat Commun2015
24953648In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia.Clin Endocrinol (Oxf)2015
26333769Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures.Nat Commun2015
26222270Randomized controlled study in pregnancy on treatment of marked hyperglycemia that is short of overt diabetes.Acta Obstet Gynecol Scand2015
25479062The mammalian alcohol dehydrogenase genome shows several gene duplications and gene losses resulting in a large set of different enzymes including pseudoenzymes.Chem Biol Interact2015
24477828On an early gene for membrane-integral inorganic pyrophosphatase in the genome of an apparently pre-luca extremophile, the archaeon Candidatus Korarchaeum cryptofilum.J Mol Evol2014
24480307A mutation interfering with 5-lipoxygenase domain interaction leads to increased enzyme activity.Arch Biochem Biophys2014
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Collaborators

Co-authored papers 53
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CSC - IT Center for Science Ltd
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Josep Carreras Leukaemia Research Institute (IJC)
Co-authored papers 3
Karolinska Institutet
Co-authored papers 3
Co-authored papers 3
Vrije Universiteit Amsterdam (VU)
Co-authored papers 3
Wageningen University and Research
Co-authored papers 2
Pfizer Ltd
Co-authored papers 2
Co-authored papers 2
European Bioinformatics Institute
Co-authored papers 2
Foundation Lygature
Co-authored papers 2
Erasmus Medical Center
Co-authored papers 2
University of Manchester
Co-authored papers 2
BGI Hong Kong Tech Co Ltd.
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Leiden University Medical Center
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Leiden Institute of Advanced Computer Science, Leiden University
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