Magnus Ingelman-Sundberg
Pharmacology · 2001–2016
A researcher in the Science corpus: 8 papers; trusts 3 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Pharmacology — 47 citations into it; #65 of 1,112 by trust here, #240 by citations
- Oncology — 22 citations into it; #127 of 1,698 by trust here, #923 by citations
- Genetics — 12 citations into it
- Clinical Biochemistry — 5 citations into it
Whom Magnus Ingelman-Sundberg trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Richard M. Weinshilboum
- William E. Evans
- S. Sim
- Ulrich M. Zanger
- G. Wilkinson
- Mary V. Relling
- T. Bestor
- Barbara E. Stranger
- M. Eichelbaum
- David R. Nelson
Who trusts Magnus Ingelman-Sundberg overall
- Shufeng Zhou
- M. Eichelbaum
- Ulrich M. Zanger
- D. Nebert
- D. Waxman
- S. Sim
- P. Gillman
- M. Schwab
- Jun-Ping Liu
- A. Gomez
Papers from Magnus Ingelman-Sundberg's perspective
Ordered by how strongly the researchers Magnus Ingelman-Sundberg trusts endorse each paper. Same corpus, a different order for every researcher.
- Pharmacogenetics of antidepressants and antipsychotics: the contribution of allelic variations to the phenotype of drug response (Molecular Psychiatry)
- Clinical Significance of the Cytochrome P450 2C19 Genetic Polymorphism (Clinical Pharmacokinetics)
- Pharmacogenetics of cytochrome P450 and its applications in drug therapy: the past, present and future. (TIPS - Trends in Pharmacological Sciences)
- Genetic polymorphisms of cytochrome P450 2D6 (CYP2D6): clinical consequences, evolutionary aspects and functional diversity (The Pharmacogenomics Journal)
- Inheritance and drug response. (New England Journal of Medicine)
- Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression (Nature Genetics)
- The Widespread Impact of Mammalian MicroRNAs on mRNA Repression and Evolution (Science)
- HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol. (Proceedings of the National Academy of Sciences of the United States of America)
- Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy. (Gastroenterology)
- Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis. (Cancer Research)
Their papers
- Genetic polymorphisms of cytochrome P450 2D6 (CYP2D6): clinical consequences, evolutionary aspects and functional diversity (2005) — 1,126 citations
- Characterization of primary human hepatocyte spheroids as a model system for drug-induced liver injury, liver function and disease (2016) — 655 citations
- Influence of cytochrome P450 polymorphisms on drug therapies: pharmacogenetic, pharmacoepigenetic and clinical aspects. (2007) — 1,166 citations
- Pharmacogenomics and individualized drug therapy. (2006) — 673 citations
- A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants (2006) — 778 citations
- Pharmacogenetics of cytochrome P450 and its applications in drug therapy: the past, present and future. (2004) — 671 citations
- Dietary long-chain n-3 fatty acids for the prevention of cancer: a review of potential mechanisms. (2004) — 992 citations
- Metabolic gene polymorphism frequencies in control populations. (2001) — 921 citations