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1دورية أكاديمية
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
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2دورية أكاديمية
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
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3دورية أكاديمية
المؤلفون: Fombonne, Eric, Goin-Kochel, Robin, ORoak, Brian
المصدر: Vaccine. 38(7)
مصطلحات موضوعية: Autism, Autism spectrum disorder, Disorder, Ethnicity, Immunizations, Intellectual disability, Language, Language delay, Psychiatric disorder, Regression, Seizure, Sex, Social factors, Vaccines, Adolescent, Autism Spectrum Disorder, Autistic Disorder, Caregivers, Child, Child, Preschool, Ethnicity, Female, Health Knowledge, Attitudes, Practice, Humans, Male, Minority Groups, Vaccination, Vaccines
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/59z5m6mpTest
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4دورية أكاديمية
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
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5دورية أكاديمية
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
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6دورية أكاديمية
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
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7دورية أكاديمية
المؤلفون: Beckmann, Noam, Hanson, Ellen, Maillard, Anne, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W, Goin-Kochel, Robin, Grant, Ellen, Harewood, Louise, Hunter, Jill, Lebon, Sébastien, Ledbetter, David, Martin, Christa, Männik, Katrin, Martinet, Danielle, Ramocki, Melissa, Spence, Sarah, Steinman, Kyle, Tjernagel, Jennifer, Spiro, John, Reymond, Alexandre, Beckmann, Jacques, Chung, Wendy, Jacquemont, Sébastien, Zufferey, Flore, Mukherjee, Pratik, Sherr, Elliott
المصدر: Journal of Medical Genetics. 49(10)
مصطلحات موضوعية: Adolescent, Adult, Body Mass Index, Child, Child Development Disorders, Pervasive, Chromosome Deletion, Chromosomes, Human, Pair 16, Developmental Disabilities, Female, Gene Order, Heterozygote, Humans, Intelligence Tests, Male, Phenotype, Syndrome, Young Adult
وصف الملف: application/pdf
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8
المؤلفون: Niarchou, Maria, Chawner, Samuel JRA, Doherty, Joanne L, Maillard, Anne M, Jacquemont, Sébastien, Chung, Wendy K, Green-Snyder, LeeAnne, Bernier, Raphael A, Goin-Kochel, Robin P, Hanson, Ellen, Linden, David EJ, Linden, Stefanie C, Raymond, F Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J, Bree, Marianne BM Van Den
المساهمون: Maillard, Anne M [0000-0002-4811-0693], Skuse, David [0000-0002-7891-5732], Owen, Michael J [0000-0003-4798-0862], Apollo - University of Cambridge Repository
المصدر: Translational Psychiatry, Vol 9, Iss 1, Pp 1-8 (2019)
مصطلحات موضوعية: Male, Heterozygote, Adolescent, DNA Copy Number Variations, Autism Spectrum Disorder, lcsh:RC321-571, Attention Deficit Disorder with Hyperactivity, Case-Control Studies, Child, Preschool, Chromosome Duplication, Humans, Female, Child, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, Chromosomes, Human, Pair 16, Sequence Deletion
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::572988528086eef1755d233bacfc7a55Test
https://orca.cardiff.ac.uk/id/eprint/116939/1/Binder1.pdfTest