Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gudmundur A. Hardarson"'
Autor:
Kari M Ersland, Andrea Christoforou, Christine Stansberg, Thomas Espeseth, Manuel Mattheisen, Morten Mattingsdal, Gudmundur A Hardarson, Thomas Hansen, Carla P D Fernandes, Sudheer Giddaluru, René Breuer, Jana Strohmaier, Srdjan Djurovic, Markus M Nöthen, Marcella Rietschel, Astri J Lundervold, Thomas Werge, Sven Cichon, Ole A Andreassen, Ivar Reinvang, Vidar M Steen, Stephanie Le Hellard
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e31687 (2012)
BackgroundDespite its estimated high heritability, the genetic architecture leading to differences in cognitive performance remains poorly understood. Different cortical regions play important roles in normal cognitive functioning and impairment. Rec
Externí odkaz:
https://doaj.org/article/8fc382b6d0cf4619a980614c796de04e
Autor:
Mads Melbye, Peter Alexandersen, Elinborg J Olafsdottir, Unnur Thorsteinsdottir, André L. M. Verbeek, Margret Jakobsdottir, Daniel F. Gudbjartsson, Gudridur H Olafsdottir, Nel Roeleveld, Laufey Tryggvadottir, Valgerdur Steinthorsdottir, Heather A. Boyd, Aslaug Jonasdottir, Lambertus A. Kiemeney, Thorunn Rafnar, Unnur Styrkarsdottir, Thorvaldur Jonsson, Hilma Holm, Augustine Kong, Katja K.H. Aben, Ari Karason, Patrick Sulem, Jeffrey R. Gulcher, Julius Gudmundsson, Gudmundur A. Hardarson, Simon N. Stacey, Claus Christiansen, Kari Stefansson, Gudmar Thorleifsson, Bjarke Feenstra
Publikováno v:
Nature Genetics, 41, 6, pp. 734-738
Nature Genetics, 41, 734-738
Nature Genetics, 41, 734-738
Earlier menarche correlates with shorter adult height and higher childhood body fat. We conducted a genome-wide association study of age at menarche (AAM) on 15,297 Icelandic women. Combined analysis with replication sets from Iceland, Denmark and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d006cb8a2bc380a4d6d92ce7b2ada1
https://doi.org/10.1038/ng.383
https://doi.org/10.1038/ng.383
Autor:
Daniel F. Gudbjartsson, Michael L. Frigge, Agnar Helgason, Unnur Thorsteinsdottir, Gudrun M. Jonsdottir, Theodora Thorlacius, Aslaug Jonasdottir, Gisli Masson, Stefan T Palsson, Augustine Kong, Sverrir T. Sverrisson, Hreinn Stefansson, Gudmundur A. Hardarson, Sigurjon A. Gudjonsson, Jeffrey R. Gulcher, Kari Stefansson, Gudmar Thorleifsson
Publikováno v:
Science. 319:1398-1401
The genome-wide recombination rate varies between individuals, but the mechanism controlling this variation in humans has remained elusive. A genome-wide search identified sequence variants in the 4p16.3 region correlated with recombination rate in b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a6e49445962f3ce2f8e5c6466c0e916
https://doi.org/10.1126/science.1152422
https://doi.org/10.1126/science.1152422
Autor:
Arsaell Arnarsson, Thorlakur Jonsson, Daniel F. Gudbjartsson, Adalbjorg Jonasdottir, Gudmundur A. Hardarson, Jeffrey R. Gulcher, Kristinn P. Magnusson, Unnur Thorsteinsdottir, Fridbert Jonasson, Hreinn Stefansson, Mehdi Motallebipour, Kari Stefansson, Aslaug Jonasdottir, Augustine Kong, Ola Wallerman, Gudmar Thorleifsson, Gisli Masson, G. Bragi Walters, Claes Wadelius, Gerdur Stefansdottir, H. Petursson, Patrick Sulem
Publikováno v:
Science. 317:1397-1400
Glaucoma is a leading cause of irreversible blindness. A genome-wide search yielded multiple single-nucleotide polymorphisms (SNPs) in the 15q24.1 region associated with glaucoma. Further investigation revealed that the association is confined to exf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d36d1c4f8c42174e6416de6c0ef84edd
https://doi.org/10.1126/science.1146554
https://doi.org/10.1126/science.1146554
Autor:
Thordur Sigmundsson, Larus J. Gudmundsson, Augustine Kong, Ingibjorg Eiriksdottir, Daniel F. Gudbjartsson, Thorgeir E. Thorgeirsson, Emilia Soebech, Salina P. Waddy, Madhav Thambisetty, Ami Rosen, Stefan T Palsson, David B. Rye, H. Petursson, Albert P. Sigurdsson, Joseph M. Beck, Andres Ingason, Unnur Thorsteinsdottir, Hreinn Stefansson, Jeffrey R. Gulcher, Kari Stefansson, Gudmundur A. Hardarson, Andrew A. Hicks, Kristleifur Kristjansson, Alex Iranzo, Donald L. Bliwise, Lynn Marie Trotti
Publikováno v:
New England Journal of Medicine. 357:639-647
The restless legs syndrome (RLS) is a common neurologic disorder characterized by an irresistible urge to move the legs. It is a major cause of sleep disruption. Periodic limb movements in sleep are detectable in most patients with RLS and represent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6252151fbd095d730d8486fff0b58546
https://doi.org/10.1056/nejmoa072743
https://doi.org/10.1056/nejmoa072743
Autor:
Daniel F. Gudbjartsson, Kari Stefansson, Steven M. Greenberg, Gudmundur Thorgeirsson, Ronald C.W. Ma, Calum A. MacRae, Gudmar Thorleifsson, Michelle Sale, Patrick Sulem, Arnar Palsson, Maggie C.Y. Ng, Solveig Gretarsdottir, Ka Sing Wong, Kristleifur Kristjansson, Valgerdur M Backman, Augustine Kong, Ebba Palsdottir, Runa Sigurjonsdottir, Eric E. Smith, Jeffrey R. Gulcher, Karen L. Furie, Patrick T. Ellinor, Gudmundur A. Hardarson, Peter J. Kelly, Thorarinn Blondal, Hilma Holm, Konstantinos Kostulas, Jonathan Rosand, Jan Hillert, Anna Helgadottir, Agnar Helgason, Unnur Thorsteinsdottir, Adam Baker, Jon Th. Sverrisson, Adalbjorg Jonasdottir, Wing-Yee So, David O. Arnar, Larry Baum, Asgeir Sigurdsson, Juliana C.N. Chan
Publikováno v:
Nature. 448(7151)
Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia in humans and is characterized by chaotic electrical activity of the atria. It affects one in ten individuals over the age of 80 years, causes significant morbidity and is an in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1b17c6e1ca351927872727f4567ff25
https://pubmed.ncbi.nlm.nih.gov/17603472
https://pubmed.ncbi.nlm.nih.gov/17603472
Autor:
Carla P. D. Fernandes, Christine Stansberg, Vidar M. Steen, Manuel Mattheisen, Jana Strohmaier, Marcella Rietschel, Ivar Reinvang, Markus M. Nöthen, Andrea Christoforou, Thomas Werge, Gudmundur A. Hardarson, René Breuer, Thomas Espeseth, Sven Cichon, Morten Mattingsdal, Srdjan Djurovic, Kari Merete Ersland, Thomas Hansen, Sudheer Giddaluru, Astri J. Lundervold, Ole A. Andreassen, Stephanie Le Hellard
Publikováno v:
PLOS ONE 7(2), e31687 (2012). doi:10.1371/journal.pone.0031687
PLoS ONE, Vol 7, Iss 2, p e31687 (2012)
PLoS ONE
PLoS one 7(2), e31687 (2012). doi:10.1371/journal.pone.0031687
PLoS ONE, Vol 7, Iss 2, p e31687 (2012)
PLoS ONE
PLoS one 7(2), e31687 (2012). doi:10.1371/journal.pone.0031687
BackgroundDespite its estimated high heritability, the genetic architecture leading to differences in cognitive performance remains poorly understood. Different cortical regions play important roles in normal cognitive functioning and impairment. Rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca33b85b27ee47b61962a4363cc74858
https://doi.org/10.1371/journal.pone.0031687
https://doi.org/10.1371/journal.pone.0031687