Resultats de la cerca - Stefan Jonsson
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1
Circulating Protein Signatures and Causal Candidates for Type 2 Diabetes per Valborg Guðmundsdóttir, Shaza B. Zaghlool, Valur Emilsson, Thor Aspelund, Marjan Ilkov, Elías F. Guðmundsson, Stefan Jönsson, Nuno R. Zilhão, John R. Lamb, Karsten Suhre, Lori L. Jennings, Vilmundur Guðnason
Publicat 2020Artigo -
2
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease per Egil Ferkingstad, Ásmundur Oddsson, Sólveig Grétarsdóttir, Stefania Benónísdóttir, Guðmar Þorleifsson, Aimée M. Deaton, Stefan Jonsson, Ólafur Andri Stefánsson, Gudmundur L. Norddahl, Florian Zink, Gudny A. Arnadottir, Bjarni Gunnarsson, Gísli H. Halldórsson, Anna Helgadóttir, Brynjar Ö. Jensson, Ragnar P. Kristjansson, Garðar Sveinbjörnsson, David A. Sverrisson, Gísli Másson, Ísleifur Ólafsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Hilma Hólm, Ingileif Jónsdóttir, Sigurdur Olafsson, Þóra Steingrímsdóttir, Þórunn Rafnar, Einar S. Björnsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Patrick Sulem, Kāri Stefánsson
Publicat 2018Revisão -
3
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation per Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Patrick Sulem, Jonas B. Nielsen, Stefan Jonsson, Gísli H. Halldórsson, Páll Melsted, Erna V. Ivarsdottir, Olafur B. Davidsson, Ragnar P. Kristjansson, Guðmar Þorleifsson, Anna Helgadóttir, Sólveig Grétarsdóttir, Gudmundur L. Norddahl, Sridharan Rajamani, Bjarni Torfason, Atli S. Valgardsson, Jon T. Sverrisson, Vinicius Tragante, Oddgeir L. Holmen, Folkert W. Asselbergs, Dan M. Roden, Dawood Darbar, Terje R. Pedersen, Marc S. Sabatine, Cristen J. Willer, Maja‐Lisa Løchen, Bjarni V. Halldórsson, Ingileif Jónsdóttir, Kristian Hveem, Davíð O. Arnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson
Publicat 2018Artigo -
4
Genetic insight into sick sinus syndrome per Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Hildur M. Aegisdottir, Stefania Benónísdóttir, Lilja Stefánsdóttir, Erna V. Ivarsdottir, Gísli H. Halldórsson, Jon K. Sigurdsson, Christian Torp‐Pedersen, Peter Weeke, Søren Brunak, David Westergaard, Ole Birger Pedersen, Erik Sørensen, Kaspar René Nielsen, Kristoffer Sølvsten Burgdorf, Karina Banasik, Ben Brumpton, Wei Zhou, Ásmundur Oddsson, Vinicius Tragante, Kristján Eldjárn Hjörleifsson, Olafur B. Davidsson, Sridharan Rajamani, Stefan Jonsson, Bjarni Torfason, Atli S. Valgardsson, Guðmundur Þorgeirsson, Michael L. Frigge, Guðmar Þorleifsson, Gudmundur L. Norddahl, Anna Helgadóttir, Sólveig Grétarsdóttir, Patrick Sulem, Ingileif Jónsdóttir, Cristen J. Willer, Kristian Hveem, Henning Bundgaard, Henrik Ullum, Davíð O. Arnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson, Steffen Andersen, Christian Erikstrup, Thomas Hansen, Henrik Hjalgrim, Gregor B. E. Jemec, Poul Jennum, Mette Nyegaard, Mie Topholm Bruun, Mikkel Steen Petersen, Thomas Werge, Pär I. Johansson
Publicat 2021Artigo -
5
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets per Louise V. Wain, Nick Shrine, María Soler Artigas, A. Mesut Erzurumluoglu, Boris Noyvert, Lara Bossini‐Castillo, Ma’en Obeidat, Amanda P. Henry, Michael A. Portelli, Robert J. Hall, Charlotte K. Billington, Tracy L. Rimington, Anthony G. Fenech, Catherine John, Tineka Blake, Victoria E. Jackson, Richard J. Allen, Bram P. Prins, Archie Campbell, David J. Porteous, Marjo‐Riitta Järvelin, Matthias Wielscher, Anthony James, Jennie Hui, Nicholas J. Wareham, Wei Zhao, James F. Wilson, Peter K. Joshi, Beate Stubbe, Rajesh Rawal, Holger Schulz, Medea Imboden, Nicole Probst‐Hensch, Stefan Karrasch, Christian Gieger, Ian J. Deary, Sarah E. Harris, Jonathan Marten, Igor Rudan, Stefan Enroth, Ulf Gyllensten, Shona M. Kerr, Ozren Polašek, Mika Kähönen, Ida Surakka, Véronique Vitart, Caroline Hayward, Terho Lehtimäki, Olli T. Raitakari, David M. Evans, Alex Henderson, Craig E. Pennell, Carol A. Wang, Peter D. Sly, Emily S. Wan, Robert Busch, Brian D. Hobbs, Augusto A. Litonjua, David Sparrow, Amund Gulsvik, Per Bakke, James D. Crapo, Terri H. Beaty, Nadia N. Hansel, Rasika A. Mathias, Ingo Ruczinski, Kathleen C. Barnes, Yohan Bossé, Philippe Joubert, Maarten van den Berge, Corry‐Anke Brandsma, Peter D. Paré, Don D. Sin, David C. Nickle, Ke Hao, Omri Gottesman, Frederick E. Dewey, Shannon Bruse, David J. Carey, H. Lester Kirchner, Stefan Jonsson, Guðmar Þorleifsson, Ingileif Jónsdóttir, Þórarinn Gíslason, Kāri Stefánsson, Claudia Schurmann, Girish N. Nadkarni, Erwin P. Böttinger, Ruth J. F. Loos, Robin Walters, Zhengming Chen, Iona Y. Millwood, Julien Vaucher, Om Kurmi, Liming Li, Anna Hansell, Christopher E. Brightling, Eleftheria Zeggini, Michael H. Cho, Edwin K. Silverman
Publicat 2017Artigo
Eines de cerca:
Matèries relacionades
Medicine
Biology
Gene
Genetics
Genotype
Internal medicine
Bioinformatics
Genetic association
Genome-wide association study
Single-nucleotide polymorphism
Biobank
Disease
Missense mutation
Mutation
Allele
Atrial fibrillation
Bile acid
Blood proteins
COPD
Cardiology
Computational biology
Diabetes mellitus
Endocrinology
Enterohepatic circulation
Exon
Gallstones
Gastroenterology
Genetic variants
Haplotype
Intensive care medicine