Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Steffan Daniel Bos"'
Autor:
Christian Magnus Page, Sergio E Baranzini, Bjørn-Helge Mevik, Steffan Daniel Bos, Hanne F Harbo, Bettina Kulle Andreassen
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0139642 (2015)
Genotyping chips for rare and low-frequent variants have recently gained popularity with the introduction of exome chips, but the utility of these chips remains unclear. These chips were designed using exome sequencing data from mainly American-Europ
Externí odkaz:
https://doaj.org/article/866bd0af6eb94b89ba771bba630fed73
Autor:
Tone, Berge, Anna, Eriksson, Ina Skaara, Brorson, Einar August, Høgestøl, Pål, Berg-Hansen, Anne, Døskeland, Olav, Mjaavatten, Steffan Daniel, Bos, Hanne F, Harbo, Frode, Berven
Publikováno v:
Clinical Proteomics
Background Multiple sclerosis (MS) is an autoimmune, neuroinflammatory disease, with an unclear etiology. However, T cells play a central role in the pathogenesis by crossing the blood–brain-barrier, leading to inflammation of the central nervous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a1a349e6e148deea0fc3f21dd01705f2
https://pubmed.ncbi.nlm.nih.gov/31080378
https://pubmed.ncbi.nlm.nih.gov/31080378
Autor:
Dana Horáková, Matthew S. Gillman, Nicholas Wood, Colin Palmer, Vincent Damotte, Robert Plomin, Pierre-Antoine Gourraud, Sergio Baranzini, Céline Bellenguez, Finn Sellebjerg, Loukas Moutsianas, Panos Deloukas, Ingrid Kockum, Christopher George Mathew, Jim Stankovich, Frauke Zipp, Steffan Daniel Bos, Janna Saarela, Mohamed EL BEHI, Nikolaos Patsopoulos, William Bush, An Goris, Manuel Comabella Lopez, Tomas Olsson
Publikováno v:
Genes & Immunity. 15:126-132
Genome-wide association studies (GWASs) perform per-SNP association tests to identify variants involved in disease or trait susceptibility. However, such an approach is not powerful enough to unravel genes that are not individually contributing to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81dcc558d8274e0dd8c14fa50b7f9ff6
https://doi.org/10.1038/gene.2013.70
https://doi.org/10.1038/gene.2013.70
Autor:
Harbo, Hanne, Isobe, Noriko, Berg-Hansen, Pal, Steffan Daniel Bos, Cailler, Stacy, Gustavsen, Marte, Mero, Inger-Lise, Celius, Elisabeth Guloswen, Hauser, Stephen, Oksenberg, Jorge, Gourraud, Pierre-Antoine
Publikováno v:
Harbo, HF; Isobe, N; Berg-Hansen, P; Bos, SD; Caillier, SJ; Gustavsen, MW; et al.(2014). Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis. Multiple Sclerosis Journal, 20(6), 660-668. doi: 10.1177/1352458513506503. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/5mv4c5wf
ResearcherID
ResearcherID
Background: Many genetic risk variants are now well established in multiple sclerosis (MS), but the impact on clinical phenotypes is unclear. Objective: To investigate the impact of established MS genetic risk variants on MS phenotypes, in well-chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::58cdc6e68aff9215c707e16a66dd621a
http://www.escholarship.org/uc/item/5mv4c5wf
http://www.escholarship.org/uc/item/5mv4c5wf
Autor:
Sigurgeir Olafsson, Pernilla Stridh, Steffan Daniël Bos, Andres Ingason, Jack Euesden, Patrick Sulem, Gudmar Thorleifsson, Omar Gustafsson, Ari Johannesson, Arni J. Geirsson, Arni V. Thorsson, Bardur Sigurgeirsson, Bjorn Runar Ludviksson, Elias Olafsson, Helga Kristjansdottir, Jon G. Jonasson, Jon Hjaltalin Olafsson, Kjartan B. Orvar, Rafn Benediktsson, Ragnar Bjarnason, Sjofn Kristjansdottir, Thorarinn Gislason, Trausti Valdimarsson, Evgenia Mikaelsdottir, Snaevar Sigurdsson, Stefan Jonsson, Thorunn Rafnar, Dag Aarsland, Srdjan Djurovic, Tormod Fladby, Gun Peggy Knudsen, Elisabeth G. Celius, Kjell-Morten Myhr, Gerdur Grondal, Kristjan Steinsson, Helgi Valdimarsson, Sigurdur Bjornsson, Unnur S. Bjornsdottir, Einar S Bjornsson, Bjorn Nilsson, Ole A. Andreassen, Lars Alfredsson, Jan Hillert, Ingrid Skelton Kockum, Gisli Masson, Unnur Thorsteinsdottir, Daniel F. Gudbjartsson, Hreinn Stefansson, Haukur Hjaltason, Hanne F. Harbo, Tomas Olsson, Ingileif Jonsdottir, Kari Stefansson
Publikováno v:
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-12 (2017)
Multiple sclerosis: Sequence variants discovered by meta-analysis informed by genetic correlation Combining studies and comparing across diseases turned up 14 novel gene variants linked to multiple sclerosis (MS). A team led by Kári Stefánsson and
Externí odkaz:
https://doaj.org/article/9096113a85cf464487746a5332bdc34b
Autor:
Steffan Daniel Bos, Ramos, Y. F., Breggen, R., Duijnisveld, B. J., Bovee, J. V., Goeman, J. J., Nelissen, R. G., Slagboom, P. E., Meulenbelt, I.
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::231ee6e6bda0e28920da31368d64728d
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000209001600374&KeyUID=WOS:000209001600374
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000209001600374&KeyUID=WOS:000209001600374
Autor:
Steffan Daniel Bos, Suchiman, E. H. E. D., Kloppenburg, M. M., Kroon, H. H. M., Slagboom, E. P. E., Meulenbelt, I. I.
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3774216ff14214a546decc444db42118
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000253101100398&KeyUID=WOS:000253101100398
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000253101100398&KeyUID=WOS:000253101100398