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by Pinto, Dalila and Delaby, Elsa and Merico, Daniele and Barbosa, Mafalda and Merikangas, Alison and Klei, Lambertus and Thiruvahindrapuram, Bhooma and Xu, Xiao and Ziman, Robert and Wang, Zhuozhi and Vorstman, Jacob A.S and Thompson, Ann and Regan, Regina and Pilorge, Marion and Pellecchia, Giovanna and Pagnamenta, Alistair T and Oliveira, Guiomar and Oliveira, Bárbara and Marshall, Christian R and Magalhaes, Tiago R and Lowe, Jennifer K and Howe, Jennifer L and Griswold, Anthony J and Gilbert, John and Duketis, Eftichia and Dombroski, Beth A and De Jonge, Maretha V and Cuccaro, Michael and Crawford, Emily L and Correia, Catarina T and Conroy, Judith and Conceição, Inês C and Chiocchetti, Andreas G and Casey, Graham and Casey, Jillian P and Cai, Guiqing and Cabrol, Christelle and Bolshakova, Nadia and Bacchelli, Elena and Anney, Richard and Gallinger, Steven and Cotterchio, Michelle and Zwaigenbaum, Lonnie and Wittemeyer, Kerstin and Wing, Kirsty and Wallace, Simon and van Engeland, Herman and Tryfon, Ana and Thomson, Susanne and Soorya, Latha and Rogé, Bernadette and Roberts, Wendy and Poustka, Fritz and Mouga, Susana and Minshew, Nancy and McInnes, L. Alison and McGrew, Susan G and Lord, Catherine and Leboyer, Marion and Le Couteur, Ann S and Kolevzon, Alexander and Jiménez González, Patricia and Jacob, Suma and Holt, Richard and Guter, Stephen and Green, Jonathan and Green, Andrew and Gillberg, Christopher and Fernandez, Bridget A and Duque, Frederico and Delorme, Richard and Dawson, Geraldine and Chaste, Pauline and Café, Cátia and Brennan, Sean and Bourgeron, Thomas and Bolton, Patrick F and Bölte, Sven and Bernier, Raphael and Baird, Gillian and Bailey, Anthony J and Anagnostou, Evdokia and Almeida, Joana and Wijsman, Ellen M and Vieland, Veronica J and Vicente, Astrid M and Schellenberg, Gerard D and Pericak-Vance, Margaret and Paterson, Andrew D and Parr, Jeremy R and Nurnberger, John I and Monaco, Anthony P and Maestrini, Elena and Klauck, Sabine M and Hakonarson, Hakon and Haines, Jonathan L and Geschwind, Daniel H and Freitag, Christine M and Folstein, Susan E and Ennis, Sean and ... and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
The American Journal of Human Genetics, ISSN 0002-9297, 05/2014, Volume 94, Issue 5, pp. 677 - 694
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 8/2012, Volume 42, Issue 8, pp. 1729 - 1737
Journal Article
by Weiner, Daniel J and Wigdor, Emilie M and Ripke, Stephan and Walters, Raymond K and Kosmicki, Jack A and Grove, Jakob and Samocha, Kaitlin E and Goldstein, Jacqueline I and Okbay, Aysu and Bybjerg-Grauholm, Jonas and Werge, Thomas and Hougaard, David M and Taylor, Jacob and Skuse, David and Devlin, Bernie and Anney, Richard and Sanders, Stephan J and Bishop, Somer and Mortensen, Preben Bo and Børglum, Anders D and Smith, George Davey and Daly, Mark J and Robinson, Elise B and Bækvad-Hansen, Marie and Dumont, Ashley and Hansen, Christine and Hansen, Thomas F and Howrigan, Daniel and Mattheisen, Manuel and Moran, Jennifer and Mors, Ole and Nordentoft, Merete and Nørgaard-Pedersen, Bent and Poterba, Timothy and Poulsen, Jesper and Stevens, Christine and Anttila, Verneri and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A Jeremy and Wijsman, Ellen M and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Van Engeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne G and Pedersen, Carsten B and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Murtha, Michael T and Mouga, Susana and Morrow, Eric M and DeLuca, Daniel Moreno and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and ... and Psychiat Genomics Consortium and iPSYCH-Broad Autism Grp and iPSYCH-Broad Autism Group and Psychiatric Genomics Consortium Autism Group and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 978 - 985
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/2010, Volume 47, Issue 5, pp. 332 - 341
Journal Article
by Anney, Richard J. L and Ripke, Stephan and Anttila, Verneri and Grove, Jakob and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Robinson, Elise and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A.Jeremy and Wijsman, Ellen M and Werge, Thomas and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Vanengeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Sanders, Stephan J and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne Giørtz and Pedersen, Carsten Bøcker and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Nordentoft, Merete and Murtha, Michael T and Mouga, Susana and Mortensen, Preben Bo and Mors, Ole and Morrow, Eric M and Moreno-De-Luca, Daniel and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and McGrew, Susan G and Mattheisen, Manuel and Martsenkovsky, Igor and Martin, Donna M and Mane, Shrikant M and Magnusson, Pall and Magalhaes, Tiago and Maestrini, Elena and Lowe, Jennifer K and Lord, Catherine and Levitt, Pat and Martin, Christa Lese and Ledbetter, David H and Leboyer, Marion and Lecouteur, Ann S and Ladd-Acosta, Christine and Kolevzon, Alexander and Klauck, Sabine M and Jacob, Suma and Iliadou, Bozenna and Hultman, Christina M and Hougaard, David M and Hertz-Picciotto, Irva and Hendren, Robert and Hansen, Christine Søholm and Haines, Jonathan L and Guter, Stephen J and ... and Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Molecular Autism, ISSN 2040-2392, 05/2017, Volume 8, Issue 1, pp. 21 - 17
Background: Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of traits. The success of... 
Gene-set analysis | Genome-wide association study | Genetic correlation | Neurodevelopment | Schizophrenia | Heritability | Autism spectrum disorder | Meta-analysis | MENTAL-RETARDATION | NEUROSCIENCES | FOXP1 | INTELLECTUAL DISABILITY | RISK LOCI | GENETICS & HEREDITY | COMMON | SCAN | COPY NUMBER VARIATION | LINKAGE | GENOME-WIDE ASSOCIATION | REVEALS | Autism Spectrum Disorder - genetics | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Plasma Membrane Calcium-Transporting ATPases - genetics | Membrane Proteins - genetics | Humans | Repressor Proteins - genetics | Male | Genetic Loci | Transcription Factors - genetics | Forkhead Transcription Factors - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Carrier Proteins - genetics | Schizophrenia - genetics | Schizophrenia - diagnosis | Schizophrenia - physiopathology | Female | Autism Spectrum Disorder - diagnosis | Autism Spectrum Disorder - physiopathology | Genetic aspects | Research | Genetic susceptibility | Risk factors | Pervasive developmental disorders | Autism | Genomes | Gene expression | Life Sciences | Genetics | Autism spectrum disorder, Genome-wide association study, Meta-analysis, Genetic correlation, Heritability, Gene-set analysis, Schizophrenia, Neurodevelopment | genetic | Neurologi | asperger-syndrome | resource exchange | Genetics & Heredity | Neurosciences & Neurology | pervasive developmental disorders | Neurology | copy number variation | neuronal migration | risk loci | de-novo mutations | genome-wide association | mental-retardation | intellectual disability
Journal Article
Journal Article