{ "items": [ "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures\n

\n \n \n \n \n\n \n \n \n

Ben-Shalom R. et al, (2017), Biological Psychiatry, 82, 224 - 232

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Appreciating the Population-wide Impact of Copy Number Variants on Cognition\n

\n \n \n \n \n\n \n \n \n

An JY. and Sanders SJ., (2017), Biological Psychiatry, 82, 78 - 80

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium\n

\n \n \n \n \n\n \n \n \n

Sanders SJ. et al, (2017)

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.\n

\n \n \n \n \n\n \n \n \n

Weiner DJ. et al, (2017), Nat Genet, 49, 978 - 985

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Identification of developmental and behavioral markers associated with genetic abnormalities in autism spectrum disorder\n

\n \n \n \n \n\n \n \n \n

Bishop SL. et al, (2017), American Journal of Psychiatry, 174, 576 - 585

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n De Novo Coding Variants Are Strongly Associated with Tourette Disorder\n

\n \n \n \n \n\n \n \n \n

Willsey AJ. et al, (2017), Neuron, 94, 486 - 499.e9

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.\n

\n \n \n \n \n\n \n \n \n

K\u00fcry S. et al, (2017), Am J Hum Genet, 100

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Peabody Picture Vocabulary Test: Proxy for Verbal IQ in Genetic Studies of Autism Spectrum Disorder\n

\n \n \n \n \n\n \n \n \n

Krasileva KE. et al, (2017), Journal of Autism and Developmental Disorders, 47, 1073 - 1085

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples\n

\n \n \n \n \n\n \n \n \n

Kosmicki JA. et al, (2017), Nature Genetics, 49, 504 - 510

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome\n

\n \n \n \n \n\n \n \n \n

Collins RL. et al, (2017), Genome Biology, 18

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.\n

\n \n \n \n \n\n \n \n \n

K\u00fcry S. et al, (2017), Am J Hum Genet, 100, 352 - 363

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n \n
\n \n \n

\n International Collaborative OCD Network (iCON)\n

\n \n \n \n \n\n \n \n \n

Grice D. et al, (2017), NEUROPSYCHOPHARMACOLOGY, 42, S337 - S337

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.\n

\n \n \n \n \n\n \n \n \n

Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium None., (2017), Mol Autism, 8

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n \n
\n \n \n

\n Parental age explains the majority of variation in de novo mutation rate within families.\n

\n \n \n \n \n\n \n \n \n

Sanders SJ. et al, (2017), ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 58, S38 - S38

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Wnt/beta-Catenin Pathway Contributions to Dendritic Spine and Glutamatergic Synapse Formation Responsive to Lithium-Mediated GSK3 Inhibition\n

\n \n \n \n \n\n \n \n \n

Stanley R. et al, (2017), BIOLOGICAL PSYCHIATRY, 81, S286 - S286

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Intergenerational Neuroimaging of Human Brain Circuitry\n

\n \n \n \n \n\n \n \n \n

Ho TC. et al, (2016), Trends in Neurosciences, 39, 644 - 648

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families\n

\n \n \n \n \n\n \n \n \n

Leppa VM. et al, (2016), American Journal of Human Genetics, 99, 540 - 554

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Autism Spectrum Disorder: Genes to Pathways to Circuits\n

\n \n \n \n \n\n \n \n \n

Muhle RA. et al, (2016), Genomics, Circuits, and Pathways in Clinical Neuropsychiatry, 443 - 465

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n The Newly Emerging View of the Genome\n

\n \n \n \n \n\n \n \n \n

Sanders SJ. and Mason CE., (2016), Genomics, Circuits, and Pathways in Clinical Neuropsychiatry, 3 - 26

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n", "\n\n
\n\n
\n\n \n\n
\n \n \n
\n
\n
\n \n \n

\n Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population\n

\n \n \n \n \n\n \n \n \n

Robinson EB. et al, (2016), Nature Genetics, 48, 552 - 555

\n \n \n \n

\n \n

\n \n \n
\n\n
\n\n
\n\n\n" ], "more": "\n\n \n \n Load More\n \n \n\n", "msg": "" }