المؤلفون: Chawner, Samuel JRA, Doherty, Joanne L, Anney, Richard JL, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne BM

المصدر: American Journal of Psychiatry. 178(1)

مصطلحات موضوعية: Clinical Research, Genetics, Prevention, Human Genome, Intellectual and Developmental Disabilities (IDD), Behavioral and Social Science, Autism, Pediatric, Brain Disorders, Mental Health, Genetic Testing, Aetiology, 2.1 Biological and endogenous factors, Autistic Disorder, Child, DNA Copy Number Variations, Gene Deletion, Genetic Association Studies, Genetic Predisposition to Disease, Heterozygote, Humans, Interview, Psychological, Male, Prevalence, Risk Factors, Severity of Illness Index, IMAGINE-ID Consortium, Copy Number Variants, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/97g4x8h8Test

المؤلفون: Kim, So Hyun, Green‐Snyder, LeeAnne, Lord, Catherine, Bishop, Somer, Steinman, Kyle J, Bernier, Raphael, Hanson, Ellen, Goin‐Kochel, Robin P, Chung, Wendy K

المصدر: American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(6)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Clinical Sciences, Neurosciences, Clinical Research, Behavioral and Social Science, Autism, Intellectual and Developmental Disabilities (IDD), Mental Health, Brain Disorders, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Mental health, Adolescent, Adult, Autism Spectrum Disorder, Autistic Disorder, Child, Child, Preschool, Chromosome Deletion, Chromosome Disorders, Chromosome Duplication, Chromosomes, Human, Pair 16, Cognitive Dysfunction, DNA Copy Number Variations, Family, Female, Heterozygote, Humans, Intellectual Disability, Language, Male, Middle Aged, Siblings, Speech, Verbal Behavior, Young Adult, 16p11, deletion, duplication, autism, genetics, language profiles, 16p11.2 deletion, 16p11.2 duplication, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6h67t169Test

المؤلفون: Bernier, Raphael, Steinman, Kyle J, Reilly, Beau, Wallace, Arianne Stevens, Sherr, Elliott H, Pojman, Nicholas, Mefford, Heather C, Gerdts, Jennifer, Earl, Rachel, Hanson, Ellen, Goin-Kochel, Robin P, Berry, Leandra, Kanne, Stephen, Snyder, LeeAnne Green, Spence, Sarah, Ramocki, Melissa B, Evans, David W, Spiro, John E, Martin, Christa L, Ledbetter, David H, Chung, Wendy K, Simons VIP consortium

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 18(4)

مصطلحات موضوعية: Simons VIP consortium, Chromosomes, Human, Pair 1, Humans, Chromosome Disorders, Chromosome Deletion, Registries, Neuropsychological Tests, Phenotype, Adult, Middle Aged, Child, Child, Preschool, Female, Male, Young Adult, DNA Copy Number Variations, Chromosome Duplication, Autism, Intellectual and Developmental Disabilities (IDD), Mental Health, Pediatric, Genetics, Neurosciences, Genetic Testing, Clinical Research, Brain Disorders, Behavioral and Social Science, Mental health, autism spectrum disorder, copy-number variation, developmental disability, 1q21.1 deletion, 1q21.1 duplication, Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6j06n700Test

المؤلفون: D’Angelo, Debra, Lebon, Sébastien, Chen, Qixuan, Martin-Brevet, Sandra, Snyder, LeeAnne Green, Hippolyte, Loyse, Hanson, Ellen, Maillard, Anne M, Faucett, W Andrew, Macé, Aurélien, Pain, Aurélie, Bernier, Raphael, Chawner, Samuel JRA, David, Albert, Andrieux, Joris, Aylward, Elizabeth, Baujat, Genevieve, Caldeira, Ines, Conus, Philippe, Ferrari, Carrina, Forzano, Francesca, Gérard, Marion, Goin-Kochel, Robin P, Grant, Ellen, Hunter, Jill V, Isidor, Bertrand, Jacquette, Aurélia, Jønch, Aia E, Keren, Boris, Lacombe, Didier, Le Caignec, Cédric, Martin, Christa Lese, Männik, Katrin, Metspalu, Andres, Mignot, Cyril, Mukherjee, Pratik, Owen, Michael J, Passeggeri, Marzia, Rooryck-Thambo, Caroline, Rosenfeld, Jill A, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Van Haelst, Mieke, Shen, Yiping, Draganski, Bogdan, Sherr, Elliott H, Ledbetter, David H, van den Bree, Marianne BM, Beckmann, Jacques S, Spiro, John E, Reymond, Alexandre, Jacquemont, Sébastien, Chung, Wendy K

المصدر: JAMA Psychiatry. 73(1)

مصطلحات موضوعية: Biological Psychology, Psychology, Intellectual and Developmental Disabilities (IDD), Behavioral and Social Science, Mental Health, Pediatric, Clinical Research, Brain Disorders, Autism, Aetiology, 2.1 Biological and endogenous factors, Mental health, Adolescent, Adult, Autism Spectrum Disorder, Autistic Disorder, Case-Control Studies, Cerebellum, Child, Child, Preschool, Chromosome Deletion, Chromosome Disorders, Chromosome Duplication, Chromosomes, Human, Pair 16, Cognition, Cohort Studies, Comorbidity, DNA Copy Number Variations, Developmental Disabilities, Epilepsy, Female, Humans, Intellectual Disability, Male, Microcephaly, Middle Aged, Nervous System Malformations, Schizophrenia, Schizophrenic Psychology, Young Adult, Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, 16p11.2 European Consortium, Simons Variation in Individuals Project (VIP) Consortium, Other Medical and Health Sciences, Cognitive Sciences, Clinical sciences, Clinical and health psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/0x58q3tqTest

المؤلفون: Hanson, Ellen, Bernier, Raphael, Porche, Ken, Jackson, Frank I, Goin-Kochel, Robin P, Snyder, LeeAnne Green, Snow, Anne V, Wallace, Arianne Stevens, Campe, Katherine L, Zhang, Yuan, Chen, Qixuan, D’Angelo, Debra, Moreno-De-Luca, Andres, Orr, Patrick T, Boomer, KB, Evans, David W, Kanne, Stephen, Berry, Leandra, Miller, Fiona K, Olson, Jennifer, Sherr, Elliot, Martin, Christa L, Ledbetter, David H, Spiro, John E, Chung, Wendy K, Consortium, on behalf of the Simons Variation in Individuals Project

المصدر: Biological Psychiatry. 77(9)

مصطلحات موضوعية: Clinical Research, Mental Health, Genetic Testing, Brain Disorders, Autism, Behavioral and Social Science, Pediatric, Genetics, Intellectual and Developmental Disabilities (IDD), Detection, screening and diagnosis, 4.2 Evaluation of markers and technologies, Mental health, Adolescent, Child, Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 16, Cognition, Developmental Disabilities, Heterozygote, Humans, Intelligence, Mental Disorders, Phenotype, Young Adult, 16p11.2 Deletion, Autism spectrum disorder, Developmental disability, Psychiatric diagnosis, Simons Variation in Individuals Project Consortium, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/73m062wgTest