Bengt Persson
Professor at Institutionen för cell- och molekylärbiologi; Beräkningsbiologi och bioinformatik
- Telephone:
- +46 18 471 44 22, +46 70 425 02 30
- E-mail:
- bengt.persson@icm.uu.se
- Visiting address:
- Husargatan 3
752 37 Uppsala - Postal address:
- Box 596
751 24 UPPSALA
Director at Institutionen för cell- och molekylärbiologi; NBIS - National Bioinformatics Infrastructure Sweden
- Telephone:
- +46 18 471 44 22, +46 70 425 02 30
- Visiting address:
- Husargatan 3
75237 Uppsala - Postal address:
- Box 596
75124 Uppsala
- ORCID:
- 0000-0003-3165-5344
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Publications
Recent publications
- Computational analysis of human medium-chain dehydrogenases/ reductases revealing substrate- and coenzyme-binding characteristics (2024)
- Relationship between iron deficiency and expression of genes involved in iron metabolism in human myocardium and skeletal muscle (2023)
- Associations between heredity, height, BMI, diabetes mellitus type 1 or 2 and gene variants in the insulin receptor (INSR) gene in patients with schizophrenia. (2023)
- Baseline characteristics of 547 new onset heart failure patients in the PREFERS heart failure study (2022)
- Extracellular vesicles in heart failure (2022)
All publications
Articles
- Computational analysis of human medium-chain dehydrogenases/ reductases revealing substrate- and coenzyme-binding characteristics (2024)
- Relationship between iron deficiency and expression of genes involved in iron metabolism in human myocardium and skeletal muscle (2023)
- Associations between heredity, height, BMI, diabetes mellitus type 1 or 2 and gene variants in the insulin receptor (INSR) gene in patients with schizophrenia. (2023)
- Baseline characteristics of 547 new onset heart failure patients in the PREFERS heart failure study (2022)
- Extracellular vesicles in heart failure (2022)
- Association between single nucleotide polymorphisms in non-coding regions of the insulin (INS) gene and schizophrenia (2022)
- ELIXIR‐EXCELERATE (2021)
- Increased iron absorption in patients with chronic heart failure and iron deficiency (2020)
- The ELIXIR Core Data Resources: fundamental infrastructure for the life sciences (2020)
- Metabolomic Profile in HFpEF vs HFrEF Patients (2020)
- Transcriptomics of cardiac biopsies reveals differences in patients with or without diagnostic parameters for heart failure with preserved ejection fraction (2019)
- The bio.tools registry of software tools and data resources for the life sciences (2019)
- Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia (2019)
- Leveraging European infrastructures to access 1 million human genomes by 2022 (2019)
- Spatial detection of fetal marker genes expressed at low level in adult human heart tissue (2017)
- Rationale and design of the PREFERS (Preserved and Reduced Ejection Fraction Epidemiological Regional Study) Stockholm heart failure study (2016)
- Functional and Structural Consequences of Nine CYP21A2 Mutations Ranging from Very Mild to Severe Effects (2016)
- Comment (2016)
- Computational studies of human class V alcohol dehydrogenase - the odd sibling (2016)
- In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia (2015)
- The mammalian alcohol dehydrogenase genome shows several gene duplications and gene losses resulting in a large set of different enzymes including pseudoenzymes (2015)
- Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures (2015)
- On an Early Gene for Membrane-Integral Inorganic Pyrophosphatase in the Genome of an Apparently Pre-LUCA Extremophile, the Archaeon Candidatus Korarchaeum cryptofilum (2014)
- A mutation interfering with 5-lipoxygenase domain interaction leads to increased enzyme activity (2014)
- Novel candidate genes for 46,XY gonadal dysgenesis identified by a customized 1 M array-CGH platform (2013)
