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P. Olason · SciRah

Researcher profile · Semantic Scholar

P. Olason

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P. Olason — researcher profile on SciRah

h-index: 27
Works: 47
Citations: 8,354

Most-cited papers

Common variants conferring risk of schizophrenia
H. Stefánsson, R. Ophoff, S. Steinberg, O. Andreassen +83 more
2009Nature1,766 citations Open access
Semantic Scholar
A human phenome-interactome network of protein complexes implicated in genetic disorders
K. Lage, E. Karlberg, Zenia M. Størling, P. Olason +8 more
2007Nature Biotechnology953 citations Open access
Semantic Scholar
The genomic landscape of species divergence in Ficedula flycatchers
H. Ellegren, L. Smeds, R. Burri, P. Olason +8 more
2012Nature658 citations Open access
Semantic Scholar
Parental origin of sequence variants associated with complex diseases
A. Kong, V. Steinthorsdottir, G. Másson, G. Thorleifsson +25 more
2009Nature595 citations Open access
Semantic Scholar
Large-scale plasma proteomics comparisons through genetics and disease associations
Grimur Hjorleifsson Eldjarn, E. Ferkingstad, S. Lund, H. Helgason +29 more
2023Nature506 citations Open access
Semantic Scholar
Detection of sharing by descent, long-range phasing and haplotype imputation
A. Kong, G. Másson, M. Frigge, A. Gylfason +13 more
2008Nature Genetics490 citations Open access
Semantic Scholar
Disruption of the neurexin 1 gene is associated with schizophrenia
D. Rujescu, A. Ingason, S. Cichon, O. Pietiläinen +48 more
2008Human Molecular Genetics483 citations Open access
Semantic Scholar
Linked selection and recombination rate variation drive the evolution of the genomic landscape of differentiation across the speciation continuum of Ficedula flycatchers
R. Burri, A. Nater, T. Kawakami, C. Mugal +14 more
2015Genome Research408 citations Open access
Semantic Scholar
The sequences of 150,119 genomes in the UK Biobank
B. Halldórsson, H. Eggertsson, K. Moore, Hannes Hauswedell +52 more
2021Nature395 citations Open access
Semantic Scholar
A high-density linkage map enables a second-generation collared flycatcher genome assembly and reveals the patterns of avian recombination rate variation and chromosomal evolution
T. Kawakami, L. Smeds, N. Backström, A. Husby +4 more
2014Molecular Ecology238 citations Open access
Semantic Scholar
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants
M. Garcia, S. Juhos, M. Larsson, P. Olason +10 more
2020F1000Research236 citations Open access
Semantic Scholar
Genomic consequences of intensive inbreeding in an isolated wolf population
Marty Kardos, M. Åkesson, Toby Fountain, Ø. Flagstad +6 more
2017Nature Ecology & Evolution222 citations Open access
Semantic Scholar
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
A. Ameur, J. Dahlberg, P. Olason, F. Vezzi +23 more
2017European Journal of Human Genetics177 citations Open access
Semantic Scholar
Expanding the range of ZNF804A variants conferring risk of psychosis
S. Steinberg, O. Mors, A. Børglum, O. Gustafsson +68 more
2010Molecular Psychiatry170 citations Open access
Semantic Scholar
Demographic Divergence History of Pied Flycatcher and Collared Flycatcher Inferred from Whole-Genome Re-sequencing Data
K. Nadachowska-Brzyska, R. Burri, P. Olason, T. Kawakami +2 more
2013PLoS Genetics128 citations Open access
Semantic Scholar
TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data
J. Eisfeldt, F. Vezzi, P. Olason, D. Nilsson +1 more
2017F1000Research122 citations Open access
Semantic Scholar
Integrative analysis for finding genes and networks involved in diabetes and other complex diseases
R. Bergholdt, Zenia M. Størling, K. Lage, E. Karlberg +6 more
2007Genome Biology120 citations Open access
Semantic Scholar
Whole-genome sequencing of 490,640 UK Biobank participants
K. Carss, B. Halldórsson, Li-Ping Hou, Jimmy Liu +204 more
2025Nature111 citations Open access
Semantic Scholar
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
S. Saevarsdottir, L. Stefánsdóttir, P. Sulem, G. Thorleifsson +74 more
2022Annals of the Rheumatic Diseases80 citations Open access
Semantic Scholar
Lessons learned from implementing a national infrastructure in Sweden for storage and analysis of next-generation sequencing data
Samuel Lampa, M. Dahlö, P. Olason, Jonas Hagberg +1 more
2013GigaScience74 citations Open access
Semantic Scholar
Estimation of linkage disequilibrium and interspecific gene flow in Ficedula flycatchers by a newly developed 50k single-nucleotide polymorphism array
T. Kawakami, N. Backström, R. Burri, A. Husby +5 more
2014Molecular Ecology Resources58 citations Open access
Semantic Scholar
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data
A. Ameur, Hui-Wen Che, Marcel Martin, I. Bunikis +8 more
2018bioRxiv57 citations Open access
Semantic Scholar
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
G. Bjornsdottir, M. A. Chalmer, L. Stefánsdóttir, A. Skuladóttir +90 more
2023Nature Genetics51 citations Open access
Semantic Scholar
Mitochondrial DNA variation in the Viking age population of Norway
Maja Krzewińska, G. Bjørnstad, P. Skoglund, P. Olason +3 more
2015Philosophical Transactions of the Royal Society B: Biological Sciences38 citations Open access
Semantic Scholar
Complete human recombination maps
G. Pálsson, M. Hardarson, Hákon Jónsson, V. Steinthorsdottir +12 more
2025Nature34 citations Open access
Semantic Scholar
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants
M. Garcia, S. Juhos, M. Larsson, P. Olason +9 more
2018bioRxiv32 citations Open access
Semantic Scholar
Sequence variants affecting the genome-wide rate of germline microsatellite mutations
Snaedis Kristmundsdottir, Hákon Jónsson, M. Hardarson, G. Pálsson +19 more
2023Nature Communications31 citations Open access
Semantic Scholar
Integrating protein annotation resources through the Distributed Annotation System
P. Olason
2005Nucleic Acids Res.26 citations Open access
Semantic Scholar
Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk
T. Ólafsdóttir, S. Stacey, G. Sveinbjornsson, G. Thorleifsson +35 more
2021Cancer Research23 citations Open access
Semantic Scholar
Sequence diversity lost in early pregnancy
G. Arnadottir, Hákon Jónsson, T. Hartwig, J. Gruhn +35 more
2025Nature17 citations Open access
Semantic Scholar
Germline variants at SOHLH2 influence multiple myeloma risk
Laura Duran-Lozano, G. Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Abhishek Niroula +23 more
2021Blood Cancer Journal14 citations Open access
Semantic Scholar
A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy
A. Skuladóttir, G. Bjornsdottir, G. Thorleifsson, G. Walters +29 more
2021Scientific Reports13 citations Open access
Semantic Scholar
A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis
M. Rentoft, Daniel Svensson, A. Sjödin, P. Olason +11 more
2019PLoS ONE11 citations Open access
Semantic Scholar
Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations
Grimur Hjorleifsson Eldjarn, E. Ferkingstad, S. Lund, H. Helgason +29 more
2024Nature10 citations Open access
Semantic Scholar
Genomic Characterization of the Barnacle Balanus improvisus Reveals Extreme Nucleotide Diversity in Coding Regions
Magnus Alm Rosenblad, A. Abramova, Ulrika Lind, P. Olason +3 more
2021Marine Biotechnology8 citations Open access
Semantic Scholar
SweGen: A whole-genome map of genetic variability in a cross-section of the Swedish population
A. Ameur, J. Dahlberg, P. Olason, F. Vezzi +16 more
2016bioRxiv7 citations Open access
Semantic Scholar
Missense variants in FRS3 affect body mass index in populations of diverse ancestries
Andrea B. Jonsdottir, G. Sveinbjornsson, Rosa B. Thorolfsdottir, Max Tamlander +71 more
2025Nature Communications3 citations Open access
Semantic Scholar
Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease
Grimur Hjorleifsson Eldjarn, E. Ferkingstad, S. Lund, H. Helgason +28 more
2022bioRxiv2 citations Open access
Semantic Scholar
A whole-genome sequenced control population in northern Sweden reveals subregional genetic differences
Daniel Svensson, M. Rentoft, A. Dahlin, Emma Lundholm +6 more
2020bioRxiv2 citations Open access
Semantic Scholar
African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk
G. Thorlacius, Erna V. Ivarsdottir, S. Saevarsdottir, K. Moore +25 more
2025Nature Genetics1 citations Open access
Semantic Scholar
An Icelandic pangenome reference
Guillaume Holley, H. Eggertsson, Snaedis Kristmundsdottir, Doruk Beyter +13 more
2026Nature0 citations Open access
Semantic Scholar
Sequence Diversity Lost in Early Pregnancy.
G. Arnadottir, Hakon Johnsson, Tanja Schlaikjær Hartwig, J. Gruhn +35 more
2025Obstetrical and Gynecological Survey0 citations
Semantic Scholar
Title: The sequences of 150,119 genomes in the UK biobank
B. Halldórsson, H. Eggertsson, K. Moore, Hannes +54 more
20210 citations
Semantic Scholar
Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk
Laura Duran-Lozano, G. Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Abhishek Niroula +23 more
2021Blood Cancer Journal0 citations Open access
Semantic Scholar
CAW - Cancer Analysis Workflow to process normal/tumor WGS data
M. Garcia, S. Juhos, M. Larsson, T. D. de Ståhl +6 more
20180 citations
Semantic Scholar
Data mining and data integration in biology
P. Olason, S. Brunak
20080 citations
Semantic Scholar
Hyperphagia modifies FA profiles of plasma phospholipids, plasma FFA, and adipose tissue TAG
G. Skuladottir, P. Olason, L. Jonsson, J. Skarphedinsson +4 more
2003Lipids0 citations
Semantic Scholar

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