Výsledky vyhledávání - Andrés Ingason
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1
Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores Autor Lasse Folkersen, Oliver Pain, Andrés Ingason, Thomas Werge, Cathryn M. Lewis, Jehannine Austin
Vydáno 2020Artigo -
2
Neurexin 1 (NRXN1) Deletions in Schizophrenia Autor George Kirov, Dan Rujescu, Andrés Ingason, David Collier, Michael O’Donovan, M J Owen
Vydáno 2009Revisão -
3
Migraine polygenic risk score associates with efficacy of migraine-specific drugs Autor Lisette J. A. Kogelman, Ann-Louise Esserlind, Anne Francke Christensen, Swapnil Awasthi, Stephan Ripke, Andrés Ingason, Olafur B. Davidsson, Christian Erikstrup, Henrik Hjalgrim, Henrik Ullum, Jes Olesen, Thomas Hansen
Vydáno 2019Artigo -
4
Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population Autor Hreinn Stefánsson, Jane Sarginson, Augustine Kong, Phil Yates, Valgerður Steinthórsdóttir, Einar Gudfinnsson, Steinunn Gunnarsdottir, Nicholas Walker, Hannes Pétursson, Caroline Crombie, Andrés Ingason, Jeffrey R. Gulcher, Kāri Stefánsson, David St Clair
Vydáno 2003Artigo -
5
Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia Autor Andrés Ingason, Ina Giegling, Annette M. Hartmann, Just Genius, Bettina Konte, M. Friedl, Stephan Ripke, Patrick F. Sullivan, David St Clair, David Collier, Michael O’Donovan, Károly Mirnics, Dan Rujescu
Vydáno 2015Artigo -
6
Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction Autor Gunnar W. Reginsson, Andrés Ingason, Jack Euesden, Gyða Björnsdóttir, Sigurgeir Ólafsson, Engilbert Sigurðsson, Högni Óskarsson, Þórarinn Tyrfingsson, Valgerður Rúnarsdóttir, Ingunn Hansdóttir, Stacy Steinberg, Hreinn Stefánsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Kāri Stefánsson
Vydáno 2017Artigo -
7
Detection of sharing by descent, long-range phasing and haplotype imputation Autor 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
Vydáno 2008Artigo -
8
Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders Autor Xabier Calle Sánchez, Dorte Helenius, Jonas Bybjerg‐Grauholm, Carsten Bøcker Pedersen, David M. Hougaard, Anders D. Børglum, Merete Nordentoft, Ole Mors, Preben Bo Mortensen, Daniel H. Geschwind, Simone Montalbano, Armin Raznahan, Wesley K. Thompson, Andrés Ingason, Thomas Werge
Vydáno 2021Artigo -
9
Human Disease Variation in the Light of Population Genomics Autor Ana Prohaska, Fernando Racimo, Andrew J. Schork, Martin Sikora, Aaron J. Stern, Melissa Ilardo, Morten E. Allentoft, Lasse Folkersen, Alfonso Buil, J. Víctor Moreno-Mayar, Thorfinn Sand Korneliussen, Daniel H. Geschwind, Andrés Ingason, Thomas Werge, Rasmus Nielsen, Eske Willerslev
Vydáno 2019Revisão -
10
Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study Autor Xabier Calle Sánchez, Simone Montalbano, Morteza Vaez, Morten Dybdahl Krebs, Jonas Byberg-Grauholm, Preben Bo Mortensen, Anders D. Børglum, David M. Hougaard, Merete Nordentoft, Daniel H. Geschwind, Alfonso Buil, Andrew J. Schork, Wesley K. Thompson, Armin Raznahan, Dorte Helenius, Thomas Werge, Andrés Ingason
Vydáno 2023Artigo -
11
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores Autor Clara Albiñana, Zhihong Zhu, Andrew J. Schork, Andrés Ingason, Hugues Aschard, Isabell Brikell, Cynthia M. Bulik, Liselotte Petersen, Esben Agerbo, Jakob Grove, Merete Nordentoft, David M. Hougaard, Thomas Werge, Anders D. Børglum, Preben Bo Mortensen, John J. McGrath, Benjamin M. Neale, Florian Privé, Bjarni J. Vilhjálmsson
Vydáno 2023Artigo -
12
Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants Autor Morteza Vaez, Simone Montalbano, Xabier Calle Sánchez, Kajsa-Lotta Georgii Hellberg, Saeid Rasekhi Dehkordi, Morten Dybdahl Krebs, Joeri Meijsen, John Shorter, Jonas Bybjerg‐Grauholm, Preben Bo Mortensen, Anders D. Børglum, David M. Hougaard, Merete Nordentoft, Daniel H. Geschwind, Alfonso Buil, Andrew J. Schork, Dorte Helenius, Armin Raznahan, Wesley K. Thompson, Thomas Werge, Andrés Ingason, Anders D. Børglum, David M. Hougaard, Merete Nordentoft, Ole Mors, Preben Bo Mortensen, Thomas Werge, Jakob Grove, Thomas D. Als, Alfonso Buil, Anders Rosengren, Andrés Ingason, Andrew J. Schork, Dorte Helenius, Jesper R. Gådin, Richard Zetterberg, Vivek Appadurai, Joeri Meijsen, Kajsa-Lotta Georgii Hellberg, Bjarni J. Vilhjálmsson, Carsten Bøcker Pedersen, Esben Agerbo, Jakob Christensen, Liselotte Petersen, Marianne Gjørtz Pedersen, Jonas Byberg-Grauholm, Marie Bækvad‐Hansen
Vydáno 2024Artigo -
13
Quantifying the relative importance of genetics and environment on the comorbidity between mental and cardiometabolic disorders using 17 million Scandinavians Autor Joeri Meijsen, Kejia Hu, Morten Dybdahl Krebs, Georgios Athanasiadis, Sarah Washbrook, Richard Zetterberg, Raquel Nogueira Avelar e Silva, John Shorter, Jesper R. Gådin, Jacob Bergstedt, David M. Howard, Weimin Ye, Yi Lu, Unnur Valdimarsdóttir, Andrés Ingason, Dorte Helenius, Oleguer Plana‐Ripoll, John J. McGrath, Nadia Micali, Ole A. Andreassen, Thomas Werge, Fang Fang, Alfonso Buil
Vydáno 2024Artigo -
14
A Genetic Risk Factor for Periodic Limb Movements in Sleep Autor Hreinn Stefánsson, David B. Rye, Andrew A. Hicks, Hjörvar Pétursson, Andrés Ingason, Thorgeir E. Thorgeirsson, Stefan Palsson, Thordur Sigmundsson, Albert P. Sigurdsson, Ingibjörg Eiríksdóttir, Emilia Söebech, Donald L. Bliwise, Joseph M. Beck, Ami Rosen, Salina P. Waddy, Lynn Marie Trotti, Àlex Iranzo, Madhav Thambisetty, Gudmundur A. Hardarson, Kristleifur Kristjánsson, Lárus J. Gudmundsson, Unnur Þorsteinsdóttir, Augustine Kong, Jeffrey R. Gulcher, Daníel F. Guðbjartsson, Kāri Stefánsson
Vydáno 2007Artigo -
15
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder Autor Ólafur Ó. Guðmundsson, G. Bragi Walters, Andrés Ingason, Stefan Johansson, Tetyana Zayats, Lavinia Athanasiu, Ida E. Sønderby, Ómar Gústafsson, Muhammad Sulaman Nawaz, Guðbjörn F. Jónsson, Lina Jönsson, Per-Morten Knappskog, Ester Ingvarsdottir, Katrín Davíðsdóttir, Srdjan Djurovic, Gun Peggy Knudsen, Ragna Bugge Askeland, Gyða S. Haraldsdóttir, Gísli Baldursson, Páll Magnússon, Engilbert Sigurðsson, Daníel F. Guðbjartsson, Hreinn Stefánsson, Ole A. Andreassen, Jan Haavik, Ted Reichborn‐Kjennerud, Kāri Stefánsson
Vydáno 2019Artigo -
16
Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder Autor Sonja LaBianca, Isabell Brikell, Dorte Helenius, Robert Loughnan, Joel Mefford, Clare E. Palmer, Rebecca L. Walker, Jesper R. Gådin, Morten Dybdahl Krebs, Vivek Appadurai, Morteza Vaez, Esben Agerbo, Marianne Giørtz Pedersen, Anders D. Børglum, David M. Hougaard, Ole Mors, Merete Nordentoft, Preben Bo Mortensen, Kenneth S. Kendler, Terry L. Jernigan, Daniel H. Geschwind, Andrés Ingason, Andrew Dahl, Noah Zaitlen, Søren Dalsgaard, Thomas Werge, Andrew J. Schork
Vydáno 2023Artigo -
17
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort Autor Birgitte Bertelsen, Hreinn Stefánsson, Lars R. Jensen, Linea Melchior, Nanette Mol Debes, Camilla Groth, Liselotte Skov, Thomas Werge, Iordanis Karagiannidis, Zsanett Tárnok, Csaba Barta, Péter Nagy, Luca Farkas, Karen Brøndum‐Nielsen, Renata Rizzo, Mariangela Gulisano, Dan Rujescu, Lambertus A. Kiemeney, Sarah Tosato, Muhammad Sulaman Nawaz, Andrés Ingason, Unnur Unnsteinsdóttir, Stacy Steinberg, Pétur Lúðvígsson, Kāri Stefánsson, Andreas W. Kuß, Peristera Paschou, Daniëlle C. Cath, Pieter J. Hoekstra, Kirsten Müller‐Vahl, Manfred Stuhrmann, Asli Silahtaroglu, Rolph Pfundt, Zeynep Tümer
Vydáno 2015Artigo -
18
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease Autor Stacy Steinberg, Hreinn Stefánsson, Thorlákur Jónsson, Hrefna Johannsdottir, Andrés Ingason, Hannes Helgason, Patrick Sulem, Ólafur Þ. Magnússon, Sigurjón A. Guðjónsson, Unnur Unnsteinsdóttir, Augustine Kong, Seppo Helisalmi, Hilkka Soininen, James J. Lah, DemGene, Dag Aarsland, Tormod Fladby, Ingun Ulstein, Srdjan Djurovic, Sigrid Botne Sando, Linda R White, Gun-Peggy Knudsen, Lars T. Westlye, Geir Selbæk, Ina Giegling, Harald Hampel, Mikko Hiltunen, Allan I. Levey, Ole A Andreassen, Dan Rujescu, Pálmi V. Jónsson, Sigurbjörn Björnsson, Jón Snædal, Hreinn Stefánsson
Vydáno 2015Revisão -
19
Neuregulin 1 and Susceptibility to Schizophrenia Autor Hreinn Stefánsson, Hannes Pétursson, Engilbert Sigurðsson, Valgerður Steinthórsdóttir, Soley Bjornsdottir, Thordur Sigmundsson, Shyamali Ghosh, Jon Brynjolfsson, Steinunn Gunnarsdottir, Omar Ivarsson, Thomas T. Chou, Ómar Hjaltason, Birgitta Birgisdottir, Helgi Jónsson, Vala G Gudnadottir, Elsa Gudmundsdottir, Ásgeir Björnsson, Brynjolfur Ingvarsson, Andrés Ingason, Sigmundur Sigfússon, Hrönn Harðardóttir, Richard P. Harvey, Donna Lai, Mingdong Zhou, Daniela Brunner, Vincent Mutel, Acuna Gonzalo, Greg Lemke, Jesús Sainz, G Jóhannesson, Þorkell Andrésson, Daníel F. Guðbjartsson, Andrei Manolescu, Michael L. Frigge, Mark E. Gurney, Augustine Kong, Jeffrey R. Gulcher, Kāri Stefánsson
Vydáno 2002Artigo -
20
The selection landscape and genetic legacy of ancient Eurasians Autor Evan K. Irving-Pease, Alba Refoyo-Martínez, William Barrie, Andrés Ingason, Alice Pearson, Anders Fischer, Karl-Göran Sjögren, Alma Halgren, Ruairidh Macleod, Fabrice Demeter, Rasmus Amund Henriksen, Tharsika Vimala, Hugh McColl, Andrew H. Vaughn, Leo Speidel, Aaron J. Stern, Gabriele Scorrano, Abigail Ramsøe, Andrew J. Schork, Anders Rosengren, Lei Zhao, Kristian Kristiansen, Astrid K. N. Iversen, Lars Fugger, Peter H. Sudmant, Daniel J. Lawson, Richard Durbin, Thorfinn Sand Korneliussen, Thomas Werge, Morten E. Allentoft, Martin Sikora, Rasmus Nielsen, Fernando Racimo, Eske Willerslev
Vydáno 2024Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Psychiatry
Internal medicine
Genotype
Schizophrenia (object-oriented programming)
Single-nucleotide polymorphism
Psychology
Computational biology
Population
Genome
Bioinformatics
Demography
Genetic association
Genome-wide association study
Sociology
Disease
Psychosis
Copy-number variation
Environmental health
Evolutionary biology
Geography
Neuroscience
Phenotype
Allele
Autism
Computer science
Migraine