Kết quả tìm kiếm - Arnaldur Gylfason
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1
The rate of meiotic gene conversion varies by sex and age Bằng Bjarni V. Halldórsson, Marteinn T. Hardarson, Birte Kehr, Unnur Styrkársdóttir, Arnaldur Gylfason, Guðmar Þorleifsson, Florian Zink, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Patrick Sulem, Gísli Másson, Unnur Þorsteinsdóttir, Agnar Helgason, Augustine Kong, Daníel F. Guðbjartsson, Kāri Stefánsson
Được phát hành 2016Artigo -
2
Detection of sharing by descent, long-range phasing and haplotype imputation Bằng Augustine Kong, Gísli Másson, Michael L. Frigge, Arnaldur Gylfason, Pasha Zusmanovich, Guðmar Þorleifsson, Pall I. Olason, Andrés Ingason, Stacy Steinberg, Þórunn Rafnar, Patrick Sulem, Magali Mouy, Frosti Jónsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hreinn Stefánsson, Kāri Stefánsson
Được phát hành 2008Artigo -
3
Sequence variants from whole genome sequencing a large group of Icelanders Bằng Daníel F. Guðbjartsson, Patrick Sulem, Hannes Helgason, Arnaldur Gylfason, Sigurjón A. Guðjónsson, Florian Zink, Asmundur Oddson, Gísli Magnússon, Bjarni V. Halldórsson, Eirikur Hjartarson, Gunnar Sigurðsson, Augustine Kong, Agnar Helgason, Gísli Másson, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Kāri Stefánsson
Được phát hành 2015Artigo -
4
Complete human recombination maps Bằng Gunnar Pálsson, Marteinn T. Hardarson, Hákon Jónsson, Valgerður Steinthórsdóttir, Ólafur Andri Stefánsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Pall I. Olason, Arnaldur Gylfason, Gísli Másson, Unnur Þorsteinsdóttir, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson
Được phát hành 2025Artigo -
5
Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression Bằng Nauder Faraday, Lisa R. Yanek, Xiao Yang, Rasika A. Mathias, J. Enrique Herrera‐Galeano, Bhoom Suktitipat, Rehan Qayyum, Andrew D. Johnson, Ming‐Huei Chen, Geoffrey H. Tofler, Ingo Ruczinski, Alan D. Friedman, Arnaldur Gylfason, Unnur Þorsteinsdóttir, Paul F. Bray, Christopher J. O’Donnell, Diane M. Becker, Lewis C. Becker
Được phát hành 2011Artigo -
6
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly Bằng Florian Zink, Simon Stacey, Gudmundur L. Norddahl, Michael L. Frigge, Ólafur Þ. Magnússon, Ingileif Jónsdóttir, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Sigurjón A. Guðjónsson, Jūlı́us Guðmundsson, Jón G. Jónasson, Laufey Tryggvadóttír, Þorvaldur Jónsson, Agnar Helgason, Arnaldur Gylfason, Patrick Sulem, Þórunn Rafnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Gísli Másson, Augustine Kong, Kāri Stefánsson
Được phát hành 2017Artigo -
7
Sequence variants affecting the genome-wide rate of germline microsatellite mutations Bằng Snædís Kristmundsdóttir, Hákon Jónsson, Marteinn T. Hardarson, Gunnar Pálsson, Doruk Beyter, Hannes P. Eggertsson, Arnaldur Gylfason, Garðar Sveinbjörnsson, Guillaume Holley, Ólafur Andri Stefánsson, Gísli H. Halldórsson, Sigurgeir Ólafsson, Gudny A. Arnadottir, Pall I. Olason, Ögmundur Eiríksson, Gísli Másson, Unnur Þorsteinsdóttir, Þórunn Rafnar, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson
Được phát hành 2023Artigo -
8
Multiple transmissions of de novo mutations in families Bằng Hákon Jónsson, Patrick Sulem, Gudny A. Arnadottir, Gunnar Pálsson, Hannes P. Eggertsson, Snædís Kristmundsdóttir, Florian Zink, Birte Kehr, Kristján Eldjárn Hjörleifsson, Brynjar Ö. Jensson, Ingileif Jónsdóttir, Sigurdur Einar Marelsson, Sigurjón A. Guðjónsson, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Simon Stacey, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Bjarni V. Halldórsson, Agnar Helgason, Daníel F. Guðbjartsson, Kāri Stefánsson
Được phát hành 2018Carta -
9
Parental origin of sequence variants associated with complex diseases Bằng Augustine Kong, Valgerður Steinthórsdóttir, Gísli Másson, Guðmar Þorleifsson, Patrick Sulem, Søren Besenbacher, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Kári Kristinsson, Aðalbjörg Jónasdóttir, Michael L. Frigge, Arnaldur Gylfason, Pall I. Olason, Sigurjón A. Guðjónsson, Sverrir T. Sverrisson, Simon Stacey, Bárður Sigurgeirsson, Kristrún R. Benediktsdóttir, Helgi Sigurðsson, Þorvaldur Jónsson, Rafn Benediktsson, Jón Ólafsson, Oskar T. Johannsson, Ástráður B. Hreiðarsson, Gunnar Sigurðsson, Anne C. Ferguson‐Smith, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Kāri Stefánsson
Được phát hành 2009Artigo -
10
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis Bằng Erna V. Ivarsdottir, Hilma Hólm, Stefania Benónísdóttir, Þórhildur Ólafsdóttir, Garðar Sveinbjörnsson, Guðmar Þorleifsson, Hannes P. Eggertsson, Gísli H. Halldórsson, Kristján Eldjárn Hjörleifsson, Páll Melsted, Arnaldur Gylfason, Gudny A. Arnadottir, Ásmundur Oddsson, Brynjar Ö. Jensson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Thorhildur Juliusdottir, Lilja Stefánsdóttir, Vinicius Tragante, Bjarni V. Halldórsson, Hannes Petersen, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Patrick Sulem, Ingibjorg Hinriksdottir, Ingileif Jónsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson
Được phát hành 2021Artigo -
11
A rare variant in MYH6 is associated with high risk of sick sinus syndrome Bằng Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Gísli Másson, Hafdís T. Helgadóttir, Carlo Zanon, Ólafur Þ. Magnússon, Agnar Helgason, Jona Saemundsdottir, Arnaldur Gylfason, Hrafnhildur Stefansdottir, Sólveig Grétarsdóttir, Stefán E. Matthíasson, Gu∂mundur Thorgeirsson, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Hreinn Stefánsson, Thomas Werge, Þórunn Rafnar, Lambertus A. Kiemeney, Babar Parvez, Raafia Muhammad, Dan M. Roden, Dawood Darbar, Guðmar Þorleifsson, G. Bragi Walters, Augustine Kong, Unnur Þorsteinsdóttir, Davíð O. Arnar, Kāri Stefánsson
Được phát hành 2011Artigo -
12
HLA class II sequence variants influence tuberculosis risk in populations of European ancestry Bằng Garðar Sveinbjörnsson, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Karl G. Kristinsson, Magnús Gottfreðsson, Jeffrey C. Barrett, Lárus J. Gudmundsson, Kai Blöndal, Arnaldur Gylfason, Sigurjón A. Guðjónsson, Hafdís T. Helgadóttir, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ari Kárason, Ljiljana Bulat Kardum, Jelena Knežević, Helgi Kristjansson, Már Kristjánsson, Arthur Löve, Yang Luo, Ólafur Þ. Magnússon, Patrick Sulem, Augustine Kong, Gísli Másson, Unnur Þorsteinsdóttir, Zlatko Dembić, Sergey Nejentsev, Þorsteinn Blöndal, Ingileif Jónsdóttir, Kāri Stefánsson
Được phát hành 2016Revisão -
13
Whole genome characterization of sequence diversity of 15,220 Icelanders Bằng Hákon Jónsson, Patrick Sulem, Birte Kehr, Snædís Kristmundsdóttir, Florian Zink, Eirikur Hjartarson, Marteinn T. Hardarson, Kristján Eldjárn Hjörleifsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Lucas D. Ward, Gudny A. Arnadottir, Einar A. Helgason, Hannes Helgason, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Þórunn Rafnar, Søren Besenbacher, Michael L. Frigge, Simon Stacey, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Bjarni V. Halldórsson, Agnar Helgason, Daníel F. Guðbjartsson, Kāri Stefánsson
Được phát hành 2017Artigo -
14
Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes Bằng Daníel F. Guðbjartsson, Guðmundur Þorgeirsson, Patrick Sulem, Anna Helgadóttir, Arnaldur Gylfason, Jona Saemundsdottir, Eyþór Björnsson, Gudmundur L. Norddahl, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Hannes P. Eggertsson, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Ólafur S. Indridason, Runólfur Pálsson, Friðbert Jónasson, Ingileif Jónsdóttir, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Ragnar Daníelsen, Stefán E. Matthíasson, Snædís Kristmundsdóttir, Bjarni V. Halldórsson, Ástráður B. Hreiðarsson, Einar Már Valdimarsson, Þórarinn Guðnason, Rafn Benediktsson, Valgerður Steinthórsdóttir, Unnur Þorsteinsdóttir, Hilma Hólm, Kāri Stefánsson
Được phát hành 2019Artigo -
15
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis Bằng Thorunn A. Olafsdottir, Fannar Theódórs, Kristbjörg Bjarnadóttir, Unnur Steina Björnsdóttir, Arna B. Agustsdottir, Ólafur Andri Stefánsson, Erna V. Ivarsdottir, Jon K. Sigurdsson, Stefania Benónísdóttir, Guðmundur I. Eyjólfsson, Davíð Gíslason, Þórarinn Gíslason, Steinunn Guðmundsdóttir, Arnaldur Gylfason, Bjarni V. Halldórsson, Gísli H. Halldórsson, Thorhildur Juliusdottir, Anna M. Kristinsdottir, Dóra Lúðvíksdóttir, Bjórn R. Lúdvíksson, Gísli Másson, Kristján Norland, Páll T. Önundarson, Ísleifur Ólafsson, Ólöf Sigurðardóttir, Lilja Stefánsdóttir, Garðar Sveinbjörnsson, Vinicius Tragante, Daníel F. Guðbjartsson, Guðmar Þorleifsson, Patrick Sulem, Unnur Þorsteinsdóttir, Gudmundur L. Norddahl, Ingileif Jónsdóttir, Kāri Stefánsson
Được phát hành 2020Revisão -
16
Early Spread of SARS-Cov-2 in the Icelandic Population Bằng Daníel F. Guðbjartsson, Agnar Helgason, Hákon Jónsson, Ólafur Þ. Magnússon, Páll Melsted, Gudmundur L. Norddahl, Jona Saemundsdottir, Ásgeir Sigurðsson, Patrick Sulem, Arna B. Agustsdottir, Berglind Eiríksdottir, Rún Friðriksdóttir, Elisabet E Gardarsdottir, G. Georgsson, Olafia S. Gretarsdottir, Kjartan R. Guðmundsson, Thora R Gunnarsdottir, Arnaldur Gylfason, Hilma Hólm, Brynjar Ö. Jensson, Áslaug Jónasdóttir, Frosti Jónsson, Kamilla S. Josefsdottir, Þórður Kristjánsson, Droplaug N. Magnúsdóttir, Louise le Roux, Guðrún Sigmundsdóttir, Garðar Sveinbjörnsson, Kristin E. Sveinsdottir, Maney Sveinsdottir, Emil Aron Thorarensen, Bjarni Thorbjornsson, Arthur Löve, Gísli Másson, Ingileif Jónsdóttir, Alma D. Möller, Þórólfur Guðnason, Karl G. Kristinsson, Unnur Þorsteinsdóttir, Kāri Stefánsson
Được phát hành 2020Pré-impressão -
17
Spread of SARS-CoV-2 in the Icelandic Population Bằng Daníel F. Guðbjartsson, Agnar Helgason, Hákon Jónsson, Ólafur Þ. Magnússon, Páll Melsted, Gudmundur L. Norddahl, Jona Saemundsdottir, Ásgeir Sigurðsson, Patrick Sulem, Arna B. Agustsdottir, Berglind Eiríksdottir, Rún Friðriksdóttir, Elisabet E Gardarsdottir, G. Georgsson, Olafia S. Gretarsdottir, Kjartan R. Guðmundsson, Thora R Gunnarsdottir, Arnaldur Gylfason, Hilma Hólm, Brynjar Ö. Jensson, Áslaug Jónasdóttir, Frosti Jónsson, Kamilla S. Josefsdottir, Þórður Kristjánsson, Droplaug N. Magnúsdóttir, Louise le Roux, Guðrún Sigmundsdóttir, Garðar Sveinbjörnsson, Kristin E. Sveinsdottir, Maney Sveinsdottir, Emil Aron Thorarensen, Bjarni Thorbjornsson, Arthur D. Love, Gísli Másson, Ingileif Jónsdóttir, Alma D. Möller, Þórólfur Guðnason, Karl G. Kristinsson, Unnur Þorsteinsdóttir, Kāri Stefánsson
Được phát hành 2020Artigo -
18
Sequence diversity lost in early pregnancy Bằng Gudny A. Arnadottir, Hákon Jónsson, Tanja Schlaikjær Hartwig, Jennifer R. Gruhn, Peter Möller, Arnaldur Gylfason, David Westergaard, Andrew C. Chan, Ásmundur Oddsson, Lilja Stefánsdóttir, Louise le Roux, Valgerður Steinthórsdóttir, Kristjan H. S. Moore, Sigurgeir Ólafsson, Pall I. Olason, Hannes P. Eggertsson, Gísli H. Halldórsson, G. Bragi Walters, Hreinn Stefánsson, Sigurjón A. Guðjónsson, Gunnar Pálsson, Brynjar Ö. Jensson, Rún Friðriksdóttir, Jesper Friis Petersen, Agnar Helgason, Gudmundur L. Norddahl, Palle Duun Rohde, Jona Saemundsdottir, Ólafur Þ. Magnússon, Bjarni V. Halldórsson, Sofie Bliddal, Karina Banasik, Daníel F. Guðbjartsson, Mette Nyegaard, Patrick Sulem, Unnur Thorsteinsdottir, Eva R. Hoffmann, Henriette Svarre Nielsen, Kāri Stefánsson
Được phát hành 2025Artigo -
19
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Bằng Jūlı́us Guðmundsson, Patrick Sulem, Daníel F. Guðbjartsson, Thórarinn Blöndal, Arnaldur Gylfason, Bjarni A. Agnarsson, Kristrún R. Benediktsdóttir, Droplaug N. Magnúsdóttir, Gudbjorg Orlygsdottir, Margret Jakobsdottir, Simon Stacey, Ásgeir Sigurðsson, Tiina Wahlfors, Teuvo L.J. Tammela, Joan P. Breyer, Kate M. McReynolds, Kevin M. Bradley, Berta Sáez, Javier Godino, Sebastián Navarrete, Fernando Fuertes, Laura Murillo, Eduardo Polo, Katja K.H. Aben, Inge M. van Oort, Brian K. Suarez, Brian T. Helfand, Donghui Kan, Carlo Zanon, Michael L. Frigge, Kristleifur Kristjánsson, Jeffrey R. Gulcher, Guðmundur Einarsson, Eiríkur Jónsson, William J. Catàlona, José Mayordomo, Lambertus A. Kiemeney, Jeffrey R. Smith, Johanna Schleutker, Rósa B. Barkardóttir, Augustine Kong, Unnur Þorsteinsdóttir, Þórunn Rafnar, Kāri Stefánsson
Được phát hành 2009Artigo -
20
Copy number variations of chromosome 16p13.1 region associated with schizophrenia Bằng Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, L. Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair
Được phát hành 2009Artigo
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Biology
Gene
Genetics
Genotype
Medicine
Single-nucleotide polymorphism
Genome
Genome-wide association study
Internal medicine
Mutation
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Environmental health
Missense mutation
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Whole genome sequencing
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Copy-number variation
Coronavirus disease 2019 (COVID-19)
Genetic association
Imputation (statistics)
Indel
Infectious disease (medical specialty)
Missing data
Pathology
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Schizophrenia (object-oriented programming)