المؤلفون: Donna M. Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An, Brooke Sheppard, Minshi Peng, Zhen Li, Claudia Dastmalchi, Gabriel Santpere, André M.M. Sousa, Andrew T.N. Tebbenkamp, Navjot Kaur, Forrest O. Gulden, Michael S. Breen, Lindsay Liang, Michael C. Gilson, Xuefang Zhao, Shan Dong, Lambertus Klei, A. Ercument Cicek, Joseph D. Buxbaum, Homa Adle-Biassette, Jean-Leon Thomas, Kimberly A. Aldinger, Diana R. O’Day, Ian A. Glass, Noah A. Zaitlen, Michael E. Talkowski, Kathryn Roeder, Matthew W. State, Bernie Devlin, Stephan J. Sanders, Nenad Sestan

المصدر: Cell Reports, Vol 31, Iss 1, Pp - (2020)

مصطلحات موضوعية: Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2211124720303673; https://doaj.org/toc/2211-1247

URL الوصول: https://doaj.org/article/659cb161cbb744e39a67fefdafb36d56

المؤلفون: Michael C. Gilson, Forrest O. Gulden, Zhen Li, Jean-Leon Thomas, Claudia Dastmalchi, Stephen Sanders, Joseph D. Buxbaum, Matthew W. State, Donna M. Werling, Minshi Peng, Navjot Kaur, André M. M. Sousa, Kathryn Roeder, Ian A. Glass, Michael E. Talkowski, Lambertus Klei, Diana R. O’Day, Shan Dong, Lindsay Liang, Xuefang Zhao, Sirisha Pochareddy, Kimberly A. Aldinger, Brooke Sheppard, Bernie Devlin, Gabriel Santpere, A. Ercument Cicek, Homa Adle-Biassette, Joon Yong An, Andrew T.N. Tebbenkamp, Jinmyung Choi, Noah Zaitlen, Michael S. Breen, Nenad Sestan

المساهمون: Çiçek, A. Ercüment

المصدر: Cell reports, vol 31, iss 1
Cell Reports
Cell Reports, Vol 31, Iss 1, Pp-(2020)
Cell reports

مصطلحات موضوعية: 0301 basic medicine, PsychENCODE, Medical Physiology, DLPFC, Genome, Whole Exome Sequencing, Transcriptome, 0302 clinical medicine, fetal transition, Databases, Genetic, Gene expression, 2.1 Biological and endogenous factors, Aetiology, Prefrontal cortex, lcsh:QH301-705.5, Pediatric, Genetics, dorsolateral prefrontal cortex, 0303 health sciences, Brain, Genomics, Single Nucleotide, Human Fetal Tissue, Phenotype, medicine.anatomical_structure, prenatal eQTL, Prenatal eQTL, mTOR, Dorsolateral prefrontal cortex, BrainVar, Haploinsufficiency, Sequence Analysis, Neurotypical, Biotechnology, Quantitative Trait Loci, Prefrontal Cortex, LOC101926933 RP11-298I3.1 AL132780.1 ENSG00000257285, Biology, Polymorphism, Single Nucleotide, Article, General Biochemistry, Genetics and Molecular Biology, Databases, 03 medical and health sciences, Genetic, Exome Sequencing, medicine, Humans, Genetic Predisposition to Disease, RHEBL1, Polymorphism, Gene, 030304 developmental biology, Whole genome sequencing, Base Sequence, Whole Genome Sequencing, Sequence Analysis, RNA, Human Genome, Neurosciences, Computational Biology, Genetic Variation, Fetal transition, Brain Disorders, 030104 developmental biology, lcsh:Biology (General), Expression quantitative trait loci, RNA, Biochemistry and Cell Biology, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e40d256ff3c529add55836204edbc202
https://doi.org/10.1101/585430

المؤلفون: A. Jeremy Willsey, Lindsay Liang, Aaron R. Quinlan, Clif Duhn, Bernie Devlin, Benjamin Currall, Stephen Sanders, Gabor T. Marth, Xuefang Zhao, Kathryn Roeder, Shan Dong, Donna M. Werling, Lingxue Zhu, Mark J. Daly, Joon Yong An, Claudia Dastmalchi, Lambertus Klei, Michael C. Gilson, Harrison Brand, Young Shin Kim, Matthew W. State, Eirene Markenscoff-Papadimitriou, Sirisha Pochareddy, Benjamin M. Neale, Kevin Lin, John L.R. Rubenstein, Nenad Sestan, Harold Z. Wang, Michael E. Talkowski, Jeanselle Dea, Ryan L. Collins, Grace Schwartz, Hilary Coon, Joseph D. Buxbaum, Nadav Ahituv

المصدر: Science (New York, N.Y.), vol 362, iss 6420

مصطلحات موضوعية: 0301 basic medicine, Risk, General Science & Technology, Autism Spectrum Disorder, Intellectual and Developmental Disabilities (IDD), Autism, DNA Mutational Analysis, Context (language use), Biology, medicine.disease_cause, Genome, Article, Conserved sequence, Promoter Regions, 03 medical and health sciences, Genetic, Genetic variation, Genetics, medicine, 2.1 Biological and endogenous factors, Humans, Aetiology, Promoter Regions, Genetic, Conserved Sequence, Pediatric, Mutation, Multidisciplinary, Binding Sites, Human Genome, Genetic Variation, medicine.disease, Brain Disorders, Pedigree, DNA binding site, Mental Health, 030104 developmental biology, Autism spectrum disorder, Genetic Loci, Biotechnology, Transcription Factors

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7a71cc886e120c5f150aba58999f650
https://europepmc.org/articles/PMC6432922/

المؤلفون: Veronica Searles Quick, Shan Dong, Lindsay Liang, Claudia Dastmalchi, Robert Asarnow, Stephan Sanders

المصدر: Journal of the American Academy of Child & Adolescent Psychiatry. 59:S261

مصطلحات موضوعية: Psychiatry and Mental health, Developmental and Educational Psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::db587f7e15b273e8fc13c99a07de4100
https://doi.org/10.1016/j.jaac.2020.08.452