Rezultaty - Páll Magnússon
- Rezultaty 1 - 4 Rezultaty od 4
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2
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis od Nigel Williams, Irina Zaharieva, Andrew Martin, K. Langley, Kiran K. Mantripragada, Ragnheiður Fossdal, Hreinn Stefánsson, Hreinn Stefánsson, Páll Magnússon, Ólafur Ó. Guðmundsson, Ómar Gústafsson, Peter Holmans, Michael J. Owen, Michael O’Donovan, Anita Thapar
Wydane 2010Artigo -
3
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder od 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
Wydane 2019Artigo -
4
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia od Richard Anney, Stephan Ripke, Verneri Anttila, Jakob Grove, Peter Holmans, Aiden Corvin, Lambertus Klei, Phil H. Lee, Sarah E. Medland, Benjamin M. Neale, Elise Robinson, Lauren A. Weiss, Lonnie Zwaigenbaum, Timothy W. Yu, Kerstin Wittemeyer, A. Jeremy Willsey, Ellen M. Wijsman, Thomas Werge, Thomas H. Wassink, Regina Waltes, Christopher A. Walsh, Simon Wallace, Jacob Vorstman, Veronica J. Vieland, Astrid M. Vicente, Herman Vanengeland, Kathryn Tsang, Ann Thompson, Peter Szatmari, Oscar Svantesson, Stacy Steinberg, Kāri Stefánsson, Hreinn Stefánsson, Matthew W. State, Latha Soorya, Teimuraz Silagadze, Stephen W. Scherer, Gerard D. Schellenberg, Sven Sandin, Stephan Sanders, Evald Sæmundsen, Guy A. Rouleau, Bernadette Rogé, Kathryn Roeder, Wendy Roberts, Jennifer Reichert, Abraham Reichenberg, Karola Rehnström, Regina Regan, Fritz Poustka, Christopher S. Poultney, Joseph Piven, Dalila Pinto, Margaret A. Pericak‐Vance, Milica Pejović-Milovančević, Marianne Giørtz Pedersen, Carsten Bøcker Pedersen, Andrew D. Paterson, Jeremy Parr, Alistair T. Pagnamenta, Guiomar Oliveira, John I. Nürnberger, Merete Nordentoft, Michael T. Murtha, Susana Mouga, Preben Bo Mortensen, Ole Mors, Eric M. Morrow, Daniel Moreno‐De‐Luca, Anthony P. Monaco, Nancy J. Minshew, Alison Merikangas, William M. McMahon, Susan G. McGrew, Jouko Lönnqvist, Igor Martsenkovsky, Donna M. Martin, Shrikant Mane, Páll Magnússon, Tiago R. Magalhães, Elena Maestrini, Jennifer K. Lowe, Catherine Lord, Pat Levitt, Christa Lese Martin, David H. Ledbetter, Marion Leboyer, Ann S. LeCouteur, Christine Ladd‐Acosta, Alexander Kolevzon, Sabine M. Klauck, Suma Jacob, Bozenna Iliadou, Christina M. Hultman, David M. Hougaard, Irva Hertz‐Picciotto, Robert L. Hendren, Christine Søholm Hansen, Jonathan L. Haines, Stephen J. Guter
Wydane 2017Revisão
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Autism
Medicine
Psychiatry
Autism spectrum disorder
Biology
Gene
Genetics
Schizophrenia (object-oriented programming)
Attention deficit hyperactivity disorder
Clinical psychology
Cognition
Copy-number variation
Environmental health
Genome
Genome-wide association study
Genotype
Population
Psychology
Psychosis
Schizophrenia spectrum
Single-nucleotide polymorphism
Autistic spectrum disorder
Cohort
Cohort study
Epilepsy
Intellectual disability
Intelligence quotient
Internal medicine
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