H
Henrik B. Rasmussen
Researcher at Copenhagen University Hospital
Publications - 90
Citations - 5250
Henrik B. Rasmussen is an academic researcher from Copenhagen University Hospital. The author has contributed to research in topics: Endogenous retrovirus & Carboxylesterase 1. The author has an hindex of 28, co-authored 90 publications receiving 4515 citations. Previous affiliations of Henrik B. Rasmussen include Roskilde University.
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Patients’ perception of pain during axillary and humeral blocks using multiple nerve stimulations
TL;DR: This double-blind study identified which of the three main components of the procedure (repeated needle passes, local anesthetic injections, or electrical stimulations) is most painful, quantified its intensity, and recorded patients' preferences for a future anesthetic.
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The impact of CES1 genotypes on the pharmacokinetics of methylphenidate in healthy Danish subjects.
Claus Stage,Gesche Jürgens,Louise Schow Guski,Ragnar Thomsen,Ditte Bjerre,Laura Ferrero-Miliani,Yassine Kamal Lyauk,Henrik B. Rasmussen,Kim Dalhoff +8 more
TL;DR: The 143E allele resulted in an increased AUC, suggesting a significantly decreased CES1 enzyme activity, which was also the case in subjects with homozygous duplication of CES1, perhaps reflecting an undiscovered mutation affecting the activity of the enzyme.
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Expression of endogenous retroviruses in blood mononuclear cells and brain tissue from multiple sclerosis patients.
Henrik B. Rasmussen,C. Geny,L. Deforges,Hervé Perron,W. Tourtelotte,A. Heltberg,Jørgen Clausen +6 more
TL;DR: Some endogenous retroviruses are normally transcribed in white blood cells and brain tissue and the significance of those findings, which concerned the composite transcripts of the zinc finger sequence and its associated endogenous retrovirus, is uncertain.
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Genetic susceptibility to multiple sclerosis: detection of polymorphic nucleotides and an intron in the 3′ untranslated region of the major histocompatibility complex class II transactivator gene
TL;DR: Polymorphism screening based upon detection of single strand conformational changes followed by sequencing revealed six single nucleotide variations, namely one in the promoter utilized by B cells and five in the 3' untranslated region (UTR) of the human CIITA gene.
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Serotonin transporter: evolution and impact of polymorphic transcriptional regulation.
TL;DR: This study addresses the possible impact of the variable number of tandem repeats (VNTR) to behavior and disease by examining the evolutionary origin and mechanisms of differential transcriptional regulation of SERT.