المؤلفون: Berman, JI, Chudnovskaya, D, Blaskey, L, Kuschner, E, Mukherjee, P, Buckner, R, Nagarajan, S, Chung, WK, Sherr, EH, Roberts, TPL

المصدر: American Journal of Neuroradiology. 37(6)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Biomedical Imaging, Mental Health, Clinical Research, Neurosciences, Pediatric, Intellectual and Developmental Disabilities (IDD), Genetics, Autism, Brain Disorders, Auditory Pathways, Child, Chromosome Deletion, Chromosome Duplication, Chromosomes, Human, Pair 16, Developmental Disabilities, Evoked Potentials, Auditory, Female, Humans, Magnetoencephalography, Male, Nuclear Medicine & Medical Imaging, Clinical sciences, Physical chemistry

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2q72s58cTest

المؤلفون: Jenkins, Julian, Chow, Vivian, Blaskey, Lisa, Kuschner, Emily, Qasmieh, Saba, Gaetz, Leah, Edgar, J Christopher, Mukherjee, Pratik, Buckner, Randall, Nagarajan, Srikantan S, Chung, Wendy K, Spiro, John E, Sherr, Elliott H, Berman, Jeffrey I, Roberts, Timothy PL

المصدر: Cerebral Cortex. 26(5)

مصطلحات موضوعية: Brain Disorders, Pediatric, Intellectual and Developmental Disabilities (IDD), Clinical Research, Autism, Basic Behavioral and Social Science, Behavioral and Social Science, Mental Health, 2.1 Biological and endogenous factors, Aetiology, Acoustic Stimulation, Adolescent, Auditory Cortex, Autistic Disorder, Child, Chromosome Deletion, Chromosome Disorders, Chromosome Duplication, Chromosomes, Human, Pair 16, Evoked Potentials, Auditory, Female, Genotype, Humans, Intellectual Disability, Magnetoencephalography, Male, Neuropsychological Tests, autism spectrum disorder, 16p112 deletion, 16p112 duplication, M100, magnetoencephalography, Neurosciences, Psychology, Cognitive Sciences, Experimental Psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/53j9w2cdTest

المؤلفون: Spreafico, Filippo, Ciceri, Sara, Gamba, Beatrice, Torri, Federica, Terenziani, Monica, Collini, Paola, Macciardi, Fabio, Radice, Paolo, Perotti, Daniela

المصدر: Oncotarget. 7(8)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Cancer, Clinical Research, Rare Diseases, Human Genome, Genetics, Biomarkers, Tumor, Child, Child, Preschool, Chromosome Aberrations, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 3, Female, High-Throughput Nucleotide Sequencing, Homeodomain Proteins, Humans, Infant, Kidney Neoplasms, Male, Mutation, Neoplasm Recurrence, Local, Neoplasm Staging, Prognosis, RNA, Messenger, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Ribonuclease III, Survival Rate, Wilms Tumor, Wilms tumor, recurrence, chromosomal anomalies, SIX1, miRNA processor genes, Oncology and carcinogenesis

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5rq8s395Test

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: Yang, Mu, Lewis, Freeman C, Sarvi, Michael S, Foley, Gillian M, Crawley, Jacqueline N

المصدر: Learning & Memory. 22(12)

مصطلحات موضوعية: Brain Disorders, Basic Behavioral and Social Science, Neurosciences, Intellectual and Developmental Disabilities (IDD), Behavioral and Social Science, Mental Health, 2.1 Biological and endogenous factors, Aetiology, Mental health, Animals, Autistic Disorder, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 16, Cognition Disorders, Conditioning, Psychological, Cues, Discrimination, Psychological, Fear, Female, Heterozygote, Intellectual Disability, Learning, Learning Disabilities, Male, Mice, Transgenic, Psychological Tests, Recognition, Psychology, Reversal Learning, Social Perception, Spatial Memory, Swimming, Visual Perception, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/45s1d724Test

المؤلفون: Kusenda, Mary, Vacic, Vladimir, Malhotra, Dheeraj, Rodgers, Linda, Pavon, Kevin, Meth, Jennifer, Kumar, Ravinesh A, Christian, Susan L, Peeters, Hilde, Cho, Shawn S, Addington, Anjene, Rapoport, Judith L, Sebat, Jonathan

المصدر: Journal of Child Neurology. 30(14)

مصطلحات موضوعية: Brain Disorders, Human Genome, Neurosciences, Biotechnology, Mental Health, Genetics, Genetic Testing, 2.1 Biological and endogenous factors, Aetiology, Autism Spectrum Disorder, Cell Line, Chromosomes, Human, Pair 16, DNA Copy Number Variations, Gene Duplication, Gene Expression, Head, Herpesvirus 4, Human, Humans, Lymph Nodes, Microarray Analysis, Organ Size, Real-Time Polymerase Chain Reaction, Schizophrenia, Sequence Deletion, Transcriptome, 16p11.2, autism spectrum disorders, copy number variation, gene expression, schizophrenia, Clinical Sciences, Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/64v9k9dqTest

المؤلفون: Yang, Mu, Mahrt, Elena J, Lewis, Freeman, Foley, Gillian, Portmann, Thomas, Dolmetsch, Ricardo E, Portfors, Christine V, Crawley, Jacqueline N

المصدر: Autism Research. 8(5)

مصطلحات موضوعية: Brain Disorders, Basic Behavioral and Social Science, Autism, Behavioral and Social Science, Rare Diseases, Intellectual and Developmental Disabilities (IDD), Mental Health, Neurosciences, 2.1 Biological and endogenous factors, Aetiology, Mental health, Animals, Autistic Disorder, Behavior, Animal, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 16, Disease Models, Animal, Intellectual Disability, Male, Mice, Social Behavior, Vocalization, Animal, mouse model of autism, 16p11.2 deletion, ultrasonic vocalization, social Interaction, autism, Clinical Sciences, Psychology, Developmental & Child Psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5609p7dtTest

المؤلفون: Dean, Eric, Hu, Donglei, Martino, Alessandro, Serie, Daniel, Curtin, Karen, Campa, Daniele, Aftab, Blake, Bracci, Paige, Buda, Gabriele, Zhao, Yi, Caswell-Jin, Jennifer, Diasio, Robert, Dumontet, Charles, Dudziński, Marek, Greenberg, Alexandra, Huntsman, Scott, Jamroziak, Krzysztof, Jurczyszyn, Artur, Kumar, Shaji, Atanackovic, Djordje, Glenn, Martha, Cannon-Albright, Lisa, Jones, Brandt, Lee, Adam, Marques, Herlander, Martin, Thomas, Martinez-Lopez, Joaquin, Rajkumar, Vincent, Sainz, Juan, Vangsted, Annette, Wątek, Marzena, Wolf, Jeffrey, Slager, Susan, Camp, Nicola, Canzian, Federico, Vachon, Celine, Ziv, Elad, Fejerman, Laura

مصطلحات موضوعية: Chromosomes, Human, Pair 16, Genome-Wide Association Study, Humans, Kaplan-Meier Estimate, Multiple Myeloma, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/684505m2Test

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

المؤلفون: Shen, J, Chen, Y, Zhang, T, Zhang, J, Choy, K, Wang, J, Wang, Q, Li, S, Zhou, W, Guo, J, Wang, Y, Zhang, C, Zhao, Hong, An, Yu, Zhao, Yu, Liu, Z, Zuo, Y, Tian, Y, Weng, X, Sutton, V, Wang, H, Ming, Y, Kulkarni, S, Zhong, T, Giampietro, P, Dunwoodie, S, Cheung, S, Zhang, X, Jin, L, Lupski, J, Qiu, G, Zhang, F, Wu, N, Ming, X, Xiao, J, Wu, Z, Chen, X, Shinawi, M, Shen, Y, Yu, G, Liu, J, Xie, H, Gucev, Z, Liu, S, Yang, N, Al-Kateb, H, Chen, J, Hauser, N, Tasic, V, Liu, P, Su, X, Pan, X, Liu, C, Wang, L, Shen, Joseph

المصدر: The New England Journal of Medicine. 372(4)

مصطلحات موضوعية: Adolescent, Asian People, Child, Child, Preschool, Chromosomes, Human, Pair 16, DNA Copy Number Variations, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Mutation, Pedigree, Phenotype, Radiography, Scoliosis, Sequence Deletion, Spine, T-Box Domain Proteins

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4v9775d7Test