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1. Full Text Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
by Minshew, Nancy J and Thomas, Kelly and Nurnberger, John I and Crawford, Emily L and Otieno, Frederick and Dawson, Geraldine and Posey, David J and Annaiah, Kiran and Glaberson, Wendy and Wood, Shawn and Meyer, Kacie J and Sleiman, Patrick M. A and Miller, Judith and Munson, Jeffrey and Kim, Cecilia E and Bradfield, Jonathan P and Soorya, Latha and Frackelton, Edward C and Bucan, Maja and Sakurai, Takeshi and Hou, Cuiping and Anagnostou, Evdokia and Piven, Joseph and Schultz, Robert T and Zhang, Haitao and Cook, Edwin H and Schellenberg, Gerard D and Wang, Kai and Flory, James and Rudd, Danielle S and Sweeney, John A and Zurawiecki, Danielle and Grant, Struan F. A and Michaels, Shana and Levy, Susan E and Chiavacci, Rosetta and McMahon, William M and Brune, Camille W and Korvatska, Olena and Klei, Lambertus and Cai, Guiqing and McDougle, Christopher J and Hakonarson, Hakon and Kolevzon, Alexander and Garris, Maria and Silverman, Jeremy M and Wassink, Thomas H and Owley, Thomas and Glessner, Joseph T and Sutcliffe, James S and Reichert, Jennifer and Davis, Lea K and Bernier, Raphael and Game, Rachel M and Devlin, Bernie and Coon, Hilary and Imielinski, Marcin and Estes, Annette and Buxbaum, Joseph D
Nature (London), ISSN 0028-0836, 05/2009, Volume 459, Issue 7246, pp. 569 - 573
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Reproducibility of Results | Gene Regulatory Networks - genetics | Humans | Ubiquitin - metabolism | Genotype | Case-Control Studies | Cell Adhesion Molecules, Neuronal - genetics | Europe - ethnology | Genome, Human - genetics | Polymerase Chain Reaction | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Neurons - metabolism | Cohort Studies | Ubiquitin | Autism | Genetic aspects | Properties | Neurons | Databases | Genomics | Genes | Genetics | Standard deviation | Risk factors | Methods | Cell adhesion & migration | Index Medicus
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2. Full Text Common genetic variants on 5p14.1 associate with autism spectrum disorders
by Schellenberg, Gerard D and Minshew, Nancy J and Korvatska, Olena and Hakonarson, Hakon and Buxbaum, Joseph D and Hutman, Ted and Alvarez Retuerto, Ana I and Sleiman, Patrick M. A and Coon, Hilary and Nurnberger, John I and Kim, Cecilia E and Pericak-Vance, Margaret A and Dong, Hongmei and Bradfield, Jonathan P and Abrahams, Brett S and Gilbert, John R and Munson, Jeffrey and Sonnenblick, Lisa I and Klin, Ami and Levy, Susan E and Herman, Edward I and Ma, Deqiong and Sakurai, Takeshi and Hou, Cuiping and Lajonchere, Clara M and Miller, Judith and Zhang, Haitao and Cook, Edwin H and Estes, Annette and Wang, Kai and State, Matthew W and Haines, Jonathan L and Sweeney, John A and Wassink, Thomas H and Ozonoff, Sally and Piven, Joseph and Chiavacci, Rosetta and Cuccaro, Michael L and Brune, Camille W and Frackelton, Edward and McMahon, William M and Geschwind, Daniel H and Takahashi, Nagahide and Owley, Thomas and Glessner, Joseph T and Salyakina, Daria and Sutcliffe, James S and Dawson, Geraldine and Bucan, Maja and Bernier, Raphael and Imielinski, Marcin and Rappaport, Eric and Sigman, Marian and Cantor, Rita M and Schultz, Robert T and Grant, Struan F. A
Nature (London), ISSN 0028-0836, 05/2009, Volume 459, Issue 7246, pp. 528 - 533
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Autistic Disorder - genetics | Cell Adhesion - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Humans | Genotype | Case-Control Studies | Cell Adhesion Molecules, Neuronal - genetics | Brain - metabolism | Genetic Markers - genetics | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Cadherins - genetics | Chromosomes, Human, Pair 5 - genetics | Cohort Studies | Genetic research | Genetic aspects | Risk factors | Pervasive developmental disorders | Autism | Brain | Genomics | Quality control | Genetics | Software | Kinases | Gene expression | Chromosomes | Index Medicus
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3. Full Text A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
by Casey, Jillian P and Casey, Jillian P and Magalhaes, Tiago and Magalhaes, Tiago and Conroy, Judith M and Conroy, Judith M and Regan, Regina and Regan, Regina and Shah, Naisha and Shah, Naisha and Anney, Richard and Anney, Richard and Shields, Denis C and Shields, Denis C and Abrahams, Brett S and Abrahams, Brett S and Almeida, Joana and Almeida, Joana and Bacchelli, Elena and Bacchelli, Elena and Bailey, Anthony J and Bailey, Anthony J and Baird, Gillian and Baird, Gillian and Battaglia, Agatino and Battaglia, Agatino and Berney, Tom and Berney, Tom and Bolshakova, Nadia and Bolshakova, Nadia and Bolton, Patrick F and Bolton, Patrick F and Bourgeron, Thomas and Bourgeron, Thomas and Brennan, Sean and Brennan, Sean and Cali, Phil and Cali, Phil and Correia, Catarina and Correia, Catarina and Corsello, Christina and Corsello, Christina and Coutanche, Marc and Coutanche, Marc and Dawson, Geraldine and Dawson, Geraldine and de Jonge, Maretha and de Jonge, Maretha and Delorme, Richard and Delorme, Richard and Duketis, Eftichia and Duketis, Eftichia and Duque, Frederico and Duque, Frederico and Estes, Annette and Estes, Annette and Farrar, Penny and Farrar, Penny and Fernandez, Bridget A and Fernandez, Bridget A and Folstein, Susan E and Folstein, Susan E and Foley, Suzanne and Foley, Suzanne and Fombonne, Eric and Fombonne, Eric and Freitag, Christine M and Freitag, Christine M and Gilbert, John and Gilbert, John and Gillberg, Christopher and Gillberg, Christopher and Glessner, Joseph T and Glessner, Joseph T and Green, Jonathan and Green, Jonathan and Guter, Stephen J and Guter, Stephen J and Hakonarson, Hakon and Hakonarson, Hakon and Holt, Richard and Holt, Richard and Hughes, Gillian and Hughes, Gillian and Hus, Vanessa and Hus, Vanessa and Igliozzi, Roberta and Igliozzi, Roberta and Kim, Cecilia and Kim, Cecilia and Klauck, Sabine M and Klauck, Sabine M and Kolevzon, Alexander and Kolevzon, Alexander and Lamb, Janine A and Lamb, Janine A and Leboyer, Marion and Leboyer, Marion and Le Couteur, Ann and Le Couteur, Ann and ... and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Human genetics, ISSN 0340-6717, 4/2012, Volume 131, Issue 4, pp. 565 - 579
Gene Function | Human Genetics | Molecular Medicine | Biomedicine | Metabolic Diseases | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Nuclear Family | Genotype | Male | DNA Copy Number Variations | Linkage Disequilibrium | Haplotypes - genetics | Homozygote | Child Development Disorders, Pervasive - genetics | Adult | Female | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Child | Cluster Analysis | Cohort Studies | Autism | Genetic aspects | Genes | Genomics | Genetic polymorphisms | Haplotypes | Fibroblast growth factor 10 | Cognitive ability | Data processing | Genomes | Single-nucleotide polymorphism | Foxp2 protein | Language | genomics | Heritability | Gene mapping | copy number | Communication | Index Medicus | Genetic Predisposition to Disease | Genome-Wide Association Study | Neurons and Cognition | Life Sciences | Child Development Disorders, Pervasive | Original Investigation | Pervasive | Child Development Disorders | Single Nucleotide | Psykiatri | Genetics | Psychiatry | Methods | Polymorphism
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4. Full Text SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research
by Feliciano, Pamela and Daniels, Amy M and Green Snyder, LeeAnne and Beaumont, Amy and Camba, Alexies and Esler, Amy and Gulsrud, Amanda G and Mason, Andrew and Gutierrez, Anibal and Nicholson, Amy and Paolicelli, Anna Marie and McKenzie, Alexander P and Rachubinski, Angela L and Stephens, Alexandra N and Simon, Andrea R and Stedman, Amy and Shocklee, Amanda D and Swanson, Amy and Finucane, Brenda and Hilscher, Brittani A and Hauf, Brenda and O’Roak, Brian J and McKenna, Brooke and Robertson, Beverly E and Rodriguez, Barbara and Vernoia, Brianna M and Van Metre, Bonnie and Bradley, Catherine and Cohen, Cheryl and Erickson, Craig A and Harkins, Christina and Hayes, Caitlin and Lord, Catherine and Martin, Christa Lese and Ortiz, Crissy and Ochoa-Lubinoff, Cesar and Peura, Christine and Rice, Catherine E and Rosenberg, Cordelia R and Smith, Christopher J and Thomas, Carrie and Taylor, Cora M and White, Loran Casey and Walston, Corrie H and Amaral, David G and Coury, Daniel Lee and Sarver, Dustin E and Istephanous, Dalia and Li, Deana and Nugyen, Dzung Cong and Fox, Emily A and Butter, Eric M and Berry-Kravis, Elizabeth and Courchesne, Eric and Fombonne, Eric J and Hofammann, Eugenia and Lamarche, Elena and Wodka, Ericka L and Matthews, Emily T and O’Connor, Eirene and Palen, Emily and Miller, Fiona and Dichter, Gabriel S and Marzano, Gabriela and Stein, Gail and Hutter, Hanna and Kaplan, Hannah E and Li, Hai and Lechniak, Holly and Schneider, Hoa Lam and Zaydens, Hana and Arriaga, Ivette and Gerdts, Jennifer A and Cubells, Joseph F and Cordova, Jeanette M and Gunderson, Jaclyn and Lillard, Joseph and Manoharan, Julie and McCracken, James T and Michaelson, Jacob J and Neely, Jason and Orobio, Jessica and Pandey, Juhi and Piven, Joseph and Scherr, Jessica and Sutcliffe, James S and Tjernagel, Jennifer and Wallace, Jermel and Callahan, Kristen and Dent, Katherine and Schweers, Kathryn A and Hamer, Kira E and Law, J. Kiely and Lowe, Kathryn and O’Brien, Kaela and Smith, Kaitlin and Pawlowski, Katherine G and Pierce, Karen L and Roeder, Katherine and Abbeduto, Leonard J and ... and The SPARK Consortium and SPARK Consortium and SPARK Consortium. Electronic address: pfeliciano@simonsfoundation.org
Neuron (Cambridge, Mass.), ISSN 0896-6273, 02/2018, Volume 97, Issue 3, pp. 488 - 493
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Autism Spectrum Disorder - genetics | Genetic Predisposition to Disease | Autism Spectrum Disorder - epidemiology | United States | Humans | Biomedical Research | Gene-Environment Interaction | Cohort Studies | Patient Selection | Autism | Family | Congenital diseases | Working groups | Genomics | Genes | Families & family life | Systematic review | Genomes | Research | Environmental risk | Meta-analysis | Studies | Consortia | Researchers | Mutation | Pollutants | Index Medicus
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5. Full Text Functional impact of global rare copy number variation in autism spectrum disorders
by Gillberg, Christopher and Kolevzon, Alexander and Nelson, Stanley F and Sansom, Katherine and Casallo, Guillermo and Miller, Judith and Brennan, Sean and Leboyer, Marion and Bacchelli, Elena and Delorme, Richard and Fombonne, Eric and Hallmayer, Joachim and Green, Jonathan and Pickles, Andrew and Heron, Elizabeth A and Salt, Jeff and Battaglia, Agatino and Klauck, Sabine M and McDougle, Christopher J and Mahoney, William and Noor, Abdul and Cytrynbaum, Cheryl and Sato, Daisuke and Almeida, Joana and Korvatska, Olena and Dawson, Geraldine and Bierut, Laura J and Coon, Hilary and Rickaby, Jessica and Freitag, Christine M and Roeder, Kathryn and Bader, Gary D and Wijsman, Ellen M and Vincent, John B and Hakonarson, Hakon and Segurado, Ricardo and Paton, Tara and Roge, Bernadette and Ennis, Sean and Kim, Cecilia and Monaco, Anthony P and Paterson, Andrew D and Crossett, Andrew and McGrath, Jane and Carson, Andrew R and Le Couteur, Ann and Cook, Edwin H and Chung, Brian H.Y and Cuccaro, Michael L and Van Engeland, Herman and Conroy, Judith and Holt, Richard and Strawbridge, Christina and Kustanovich, Vlad and Migita, Ohsuke and Stoppioni, Vera and Igliozzi, Roberta and Poustka, Fritz and Stein, Olaf and Posey, David J and Sheffield, Val C and Duque, Frederico and Parrini, Barbara and Berney, Tom and Hus, Vanessa and Baird, Gillian and Duketis, Eftichia and Soorya, Latha and Corsello, Christina and Drmic, Irene and Sousa, Inês and Abrahams, Brett S and Thomson, Susanne and Lajonchere, Clara M and Tsiantis, John and Pinto, Dalila and Green, Andrew and Hughes, Gillian and Mantoulan, Carine and Betancur, Catalina and Volkmar, Fred and Poustka, Annemarie and Shah, Naisha and Bryson, Susan E and Munson, Jeff and Tancredi, Raffaella and Nygren, Gudrun and Wittemeyer, Kerstin and Merikangas, Alison and Oliveira, Guiomar and Farrar, Penny and Maestrini, Elena and Liu, Xiao-Qing and Gallagher, Louise and McConachie, Helen and Zurawiecki, Danielle and Schellenberg, Gerard D and Glessner, Joseph T and Lord, Catherine and Piven, Joseph and ... and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature, ISSN 0028-0836, 07/2010, Volume 466, Issue 7304, pp. 368 - 372
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Medical sciences | Child clinical studies | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Signal Transduction | Child Development Disorders, Pervasive - pathology | Humans | Child Development Disorders, Pervasive - physiopathology | DNA Copy Number Variations - genetics | Case-Control Studies | Europe - ethnology | Child Development Disorders, Pervasive - genetics | Social Behavior | Child | Cell Movement | Cytoprotection | Confidence intervals | Autism | Genetics | Genes | Quality control | Reproduction | Disorders | Disabilities | Arrays | Loci | Index Medicus | Genetic Predisposition to Disease | Europe | Gene Dosage | DNA Copy Number Variations | Life Sciences | Child Development Disorders, Pervasive | Pervasive | Child Development Disorders | Ethnology | Physiopathology | Pathology | Psykiatri | Psychiatry
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6. Full Text Individual common variants exert weak effects on the risk for autism spectrum disorderspi
by Anney, Richard and Klei, Lambertus and Pinto, Dalila and Almeida, Joana and Bacchelli, Elena and Baird, Gillian and Bolshakova, Nadia and Boelte, Sven and Bolton, Patrick F and Bourgeron, Thomas and Brennan, Sean and Brian, Jessica and Casey, Jillian and Conroy, Judith and Correia, Catarina and Corsello, Christina and Crawford, Emily L and de Jonge, Maretha and Delorme, Richard and Duketis, Eftichia and Duque, Frederico and Estes, Annette and Farrar, Penny and Fernandez, Bridget A and Folstein, Susan E and Fombonne, Eric and Gilbert, John and Gillberg, Christopher and Glessner, Joseph T and Green, Andrew and Green, Jonathan and Guter, Stephen J and Heron, Elizabeth A and Holt, Richard and Howe, Jennifer L and Hughes, Gillian and Hus, Vanessa and Igliozzi, Roberta and Jacob, Suma and Kenny, Graham P and Kim, Cecilia and Kolevzon, Alexander and Kustanovich, Vlad and Lajonchere, Clara M and Lamb, Janine A and Law-Smith, Miriam and Leboyer, Marion and Le Couteur, Ann and Leventhal, Bennett L and Liu, Xiao-Qing and Lombard, Frances and Lord, Catherine and Lotspeich, Linda and Lund, Sabata C and Magalhaes, Tiago R and Mantoulan, Carine and McDougle, Christopher J and Melhem, Nadine M and Merikangas, Alison and Minshew, Nancy J and Mirza, Ghazala K and Munson, Jeff and Noakes, Carolyn and Nygren, Gudrun and Papanikolaou, Katerina and Pagnamenta, Alistair T and Parrini, Barbara and Paton, Tara and Pickles, Andrew and Posey, David J and Poustka, Fritz and Ragoussis, Jiannis and Regan, Regina and Roberts, Wendy and Roeder, Kathryn and Roge, Bernadette and Rutter, Michael L and Schlitt, Sabine and Shah, Naisha and Sheffield, Val C and Soorya, Latha and Sousa, Ines and Stoppioni, Vera and Sykes, Nuala and Tancredi, Raffaella and Thompson, Ann P and Thomson, Susanne and Tryfon, Ana and Tsiantis, John and Van Engeland, Herman and Vincent, John B and Volkmar, Fred and Vorstman, J. A. S and Wallace, Simon and Wing, Kirsty and Wittemeyer, Kerstin and Wood, Shawn and Zurawiecki, Danielle and Zwaigenbaum, Lonnie and Bailey, Anthony J and ...
Human molecular genetics, ISSN 0964-6906, 11/2012, Volume 21, Issue 21, pp. 4781 - 4792
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Developmental disorders | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Child clinical studies
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