K
Kristina Holmberg
Researcher at Royal Institute of Technology
Publications - 6
Citations - 1413
Kristina Holmberg is an academic researcher from Royal Institute of Technology. The author has contributed to research in topics: Single-nucleotide polymorphism & SNP genotyping. The author has an hindex of 6, co-authored 6 publications receiving 1238 citations.
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Journal ArticleDOI
The Norway spruce genome sequence and conifer genome evolution.
Björn Nystedt,Nathaniel R. Street,Anna Wetterbom,Andrea Zuccolo,Yao-Cheng Lin,Douglas G. Scofield,Francesco Vezzi,Nicolas Delhomme,Stefania Giacomello,Andrey Alexeyenko,Riccardo Vicedomini,Kristoffer Sahlin,Ellen Sherwood,Malin Elfstrand,Lydia Gramzow,Kristina Holmberg,Jimmie Hällman,Olivier Keech,Lisa Klasson,Maxim Koriabine,Melis Kucukoglu,Max Käller,Johannes Luthman,Fredrik Lysholm,Totte Niittylä,Åke Olson,Nemanja Rilakovic,Carol Ritland,Josep A. Rosselló,Juliana Stival Sena,Thomas Svensson,Carlos Talavera-López,Günter Theißen,Hannele Tuominen,Kevin Vanneste,Zhiqiang Wu,Bo Zhang,Philipp Zerbe,Lars Arvestad,Lars Arvestad,Rishikesh P. Bhalerao,Joerg Bohlmann,Jean Bousquet,Rosario Garcia Gil,Torgeir R. Hvidsten,Torgeir R. Hvidsten,Pieter J. de Jong,John MacKay,Michele Morgante,Kermit Ritland,Björn Sundberg,Stacey Lee Thompson,Yves Van de Peer,Björn Andersson,Ove Nilsson,Pär K. Ingvarsson,Joakim Lundeberg,Stefan Jansson +57 more
TL;DR: The draft assembly of the 20-gigabase genome of Norway spruce (Picea abies), the first available for any gymnosperm, is presented, revealing numerous long (>10,000 base pairs) introns, gene-like fragments, uncharacterized long non-coding RNAs and short RNAs, which opens up new genomic avenues for conifer forestry and breeding.
Journal ArticleDOI
UGT1A polymorphisms in a Swedish cohort and a human diversity panel, and the relation to bilirubin plasma levels in males and females
TL;DR: Investigation of the prevalence of different polymorphisms and haplotypes associated with individual variations in pharmacokinetics and drug toxicity in the uridine-diphosphate glucuronosyl transferase (UGT) 1A gene in a Swedish cohort found several genetic variants in the UGT1A gene are common, but prevalence in a population may differ because of ethnicity.
Journal ArticleDOI
Pyrosequencing analysis of thrombosis-associated risk markers.
TL;DR: A pyrosequencing-based genotyping protocol for parallel analysis of the β-fibrinogen, prothrombin, coagulation factor V Leiden, and endothelial nitric oxide synthase polymorphisms, which modulate the effect of warfarin in antithrombotic therapy is developed.
Journal ArticleDOI
A quality assessment survey of SNP genotyping laboratories.
Päivi Lahermo,Ulrika Liljedahl,Grethe I. Grenaker Alnæs,Tomas Axelsson,Anthony J. Brookes,Anthony J. Brookes,Pekka Ellonen,Per-Henrik Groop,Christer Halldén,Dan Holmberg,Kristina Holmberg,Mauri Keinänen,Katrin Kepp,Juha Kere,Päivi Kiviluoma,Vessela N. Kristensen,Cecilia M. Lindgren,Jacob Odeberg,Pia Osterman,Maija Parkkonen,Janna Saarela,Maria Sterner,Linda Strömqvist,Linda Strömqvist,Ulvi Talas,Maija Wessman,Aarno Palotie,Ann-Christine Syvänen +27 more
TL;DR: In this paper, a joint Nordic quality assessment (QA) round was organized between 11 laboratories in the Nordic and Baltic countries to survey the quality of SNP genotyping, and the results from each laboratory were compared to this genotype.