Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gudbjorn F Jonsson"'
Autor:
Ana M Valdes, Unnur Styrkarsdottir, Michael Doherty, David L Morris, Massimo Mangino, Agu Tamm, Sally A Doherty, Kalle Kisand, Irina Kerna, Ann Tamm, Margaret Wheeler, Rose A Maciewicz, Weiya Zhang, Kenneth R Muir, Elaine M Dennison, Deborah J Hart, Sarah Metrustry, Ingileif Jonsdottir, Gudbjorn F Jonsson, Helgi Jonsson, Thorvaldur Ingvarsson, Cyrus Cooper, Timothy J Vyse, Tim D Spector, Kari Stefansson, Nigel K Arden
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23371 (2011)
Osteoarthritis (OA) is the most common form of arthritis and a major cause of disability. This study evaluates the association in Caucasian populations of two single nucleotide polymorphisms (SNPs) mapping to the Human Leukocyte Antigen (HLA) region
Externí odkaz:
https://doaj.org/article/e96f0801c8564122b6eb09219f2f8b71
Autor:
Andres Ingason, Stefan Johansson, Hreinn Stefansson, Ester Ingvarsdottir, Gyda S Haraldsdottir, Ted Reichborn-Kjennerud, Omar Gustafsson, Gisli Baldursson, Ole A. Andreassen, Ida E Sønderby, Kari Stefansson, Engilbert Sigurdsson, G. Bragi Walters, Lavinia Athanasiu, Olafur O Gudmundsson, Srdjan Djurovic, Per-Morten Knappskog, Lina Jonsson, Jan Haavik, Gudbjorn F. Jonsson, Páll Magnússon, Ragna Bugge Askeland, Muhammad Nawaz, Katrin Davidsdottir, Tetyana Zayats, Daniel F. Gudbjartsson, Gun Peggy Knudsen
Publikováno v:
Translational psychiatry
Translational Psychiatry, Vol 9, Iss 1, Pp 1-9 (2019)
Translational Psychiatry
Translational Psychiatry, Vol 9, Iss 1, Pp 1-9 (2019)
Translational Psychiatry
Publisher's version (útgefin grein).
Attention-deficit/hyperactivity disorder (ADHD) is a highly heritable common childhood-onset neurodevelopmental disorder. Some rare copy number variations (CNVs) affect multiple neurodevelopmental disorders
Attention-deficit/hyperactivity disorder (ADHD) is a highly heritable common childhood-onset neurodevelopmental disorder. Some rare copy number variations (CNVs) affect multiple neurodevelopmental disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1073eb93160adb892208803093067b5
http://hdl.handle.net/11250/2634369
http://hdl.handle.net/11250/2634369
Autor:
Jeffrey R. Gulcher, Kristleifur Kristjansson, Kristin Thorisdottir, Agnar Helgason, Margaret A. Tucker, Patrick Sulem, Thorunn Rafnar, Jens Kjartansson, Bardur Sigurgeirsson, Jelena Kostic, Gudbjorn F. Jonsson, Gisli Masson, Augustine Kong, Jón Ólafsson, Simon N. Stacey, Unnur Thorsteinsdottir, Kari Stefansson, Rafn Ragnarsson, Alisa M. Goldstein, Kristrun R. Benediktsdottir
Publikováno v:
Journal of Medical Genetics. 45:284-289
Background: Germline CDKN2A mutations have been observed in 20-40% of high-risk melanoma-prone families, however little is known about their prevalence in population-based series of melanoma cases and controls. Methods: We resequenced the CDKN2A gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0d80a9ca0cdac76dc9ce844e6d6a6cd
https://doi.org/10.1136/jmg.2007.055376
https://doi.org/10.1136/jmg.2007.055376
Autor:
Gudbjorn F. Jonsson, Thomas F. Coleman
Publikováno v:
SIAM Journal on Scientific Computing. 20:1430-1437
The advent of robust automatic differentiation tools is an exciting and important development in scientific computing. It is particularly noteworthy that the gradient of a scalar-valued function of many variables can be computed with essentially the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1324e53a394b4ebbddf5afc85e12af5d
https://doi.org/10.1137/s1064827597320794
https://doi.org/10.1137/s1064827597320794
Autor:
Sunna Arnarsdottir, Andreas Meyer-Lindenberg, Johan H. Thygesen, Gyda Bjornsdottir, Heike Tost, Heimir Snorrason, Tine B. Stensbøl, Katrin Morgen, Larus J. Gudmundsson, Michael Didriksen, Gudrun A. Jonsdottir, Orla Doyle, G. Bragi Walters, Evald Saemundsen, Stefan Hreidarsson, Stacy Steinberg, Adam J. Schwarz, Birna Jonsdottir, Solveig Davidsdottir, Isafold Helgadottir, Berglind Stefansdottir, Oliver Grimm, Kari Stefansson, Magnús Haraldsson, Brynja B. Magnusdottir, Shitij Kapur, Michael Brammer, Jonas G. Halldorsson, Engilbert Sigurdsson, Gudbjorn F. Jonsson, Solveig Kristjansdottir, Hreinn Stefansson
Publikováno v:
Nature. 505(7483)
To access publisher's full text version of this article click on the hyperlink at the bottom of the page In a small fraction of patients with schizophrenia or autism, alleles of copy-number variants (CNVs) in their genomes are probably the strongest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dad2a256454bef8a349b81240ed9df6e
https://pubmed.ncbi.nlm.nih.gov/24352232
https://pubmed.ncbi.nlm.nih.gov/24352232
Autor:
Agu Tamm, Kari Stefansson, Irina Kerna, Deborah J. Hart, Thorvaldur Ingvarsson, Gudbjorn F. Jonsson, Ingileif Jonsdottir, Kenneth Muir, Unnur Styrkarsdottir, Sarah Metrustry, Tim D. Spector, Sally Doherty, Ana M. Valdes, Helgi Jonsson, Kalle Kisand, Timothy J. Vyse, Nigel K Arden, Elaine M. Dennison, Margaret Wheeler, Massimo Mangino, Ann Tamm, Weiya Zhang, Cyrus Cooper, David L. Morris, Rose A. Maciewicz, Michael Doherty
Publikováno v:
PLoS ONE
PLoS ONE; Vol 6
PLoS ONE, Vol 6, Iss 8, p e23371 (2011)
PLoS ONE; Vol 6
PLoS ONE, Vol 6, Iss 8, p e23371 (2011)
Osteoarthritis (OA) is the most common form of arthritis and a major cause of disability. This study evaluates the association\ud in Caucasian populations of two single nucleotide polymorphisms (SNPs) mapping to the Human Leukocyte Antigen (HLA)\ud r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bb1ea444f80e0e48aa585df2462c47e
http://wrap.warwick.ac.uk/36899/1/WRAP_MUIR_journal.pone.0023371.pdf
http://wrap.warwick.ac.uk/36899/1/WRAP_MUIR_journal.pone.0023371.pdf
Autor:
Daniel F. Gudbjartsson, Agnar Helgason, Derek Middleton, Jeffrey R. Gulcher, Palmi V. Jonsson, Conrado Martinez, Thorlakur Jonsson, Birgir Hrafnkelsson, Nanna Vidarsdottir, Sigurbjorn Bjornsson, Hreinn Stefansson, Jon Snaedal, Valgerdur Steinthorsdottir, Sverrir Thorvaldsson, Kari Stefansson, Gudbjorn F. Jonsson, Henning S. Petersen
Publikováno v:
Annals of human genetics. 74(3)
Summary We propose two methods to evaluate the statistical significance of differences in linkage disequilibrium (LD) between populations, where LD is measured by the standardised parameter D′. The first method is based on bootstrapping individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14df835735adf251b1f37dd03a728875
https://pubmed.ncbi.nlm.nih.gov/20529015
https://pubmed.ncbi.nlm.nih.gov/20529015
Autor:
Jon Thor Bergthorsson, Eduardo Nagore, Kristrun R. Benediktsdottir, Kari Stefansson, Veronica Höiom, Yolanda Gilaberte, Rafn Ragnarsson, Theodora Thorlacius, Johan Hansson, Rajesh Kumar, Agnar Helgason, Francisco José Carapeto, Frank Geller, Simon N. Stacey, Jona Saemundsdottir, Eugene Gurzau, Daniel F. Gudbjartsson, Jón Ólafsson, Gudbjorn F. Jonsson, Asgeir Sigurdsson, Steinunn Thorlacius, Aslaug Jonasdottir, Rafael Botella-Estrada, Margret Jakobsdottir, Patrick Sulem, Jose I. Mayordomo, Thorarinn Blondal, Steinunn G Sveinsdottir, Bardur Sigurgeirsson, Unnur Thorsteinsdottir, Gyda Bjornsdottir, Pablo Juberías, Dominique Scherer, Magali Mouy, Gudmar Thorleifsson, Pilar Tabuenca, Virtudes Soriano, Thorunn Rafnar, Kristin Thorisdottir, Augustine Kong, Matilde Grasa, Kvetoslava Koppova, Peter Rudnai, Kristleifur Kristjansson, Julius Gudmundsson, Sigurjon A. Gudjonsson
Publikováno v:
Nature genetics. 40(11)
To search for new sequence variants that confer risk of cutaneous basal cell carcinoma (BCC), we conducted a genome-wide SNP association study of 930 Icelanders with BCC and 33,117 controls. After analyzing 304,083 SNPs, we observed signals from loci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47e469c59a513a0534532348b8a7f4fc
https://pubmed.ncbi.nlm.nih.gov/18849993
https://pubmed.ncbi.nlm.nih.gov/18849993