about
Genomic and epigenetic evidence for oxytocin receptor deficiency in autismAutistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistInvolvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expressionLack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individualsAge-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autismMutations that affect the ability of the vnd/NK-2 homeoprotein to regulate gene expression: transgenic alterations and tertiary structureNeocortical RELN promoter methylation increases significantly after puberty.Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects.Immune transcriptome alterations in the temporal cortex of subjects with autism.Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome.Do mutations of RAG genes have a role in human autoimmunity? The Notarangelo's hypothesis revisited.Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes.Autism genetics: Methodological issues and experimental design.Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features.Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: a nested case-control study.An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE).Decreased serum arylesterase activity in autism spectrum disorders.Association of autism with polyomavirus infection in postmortem brains.Linking genetics to epigenetics: The role of folate and folate-related pathways in neurodevelopmental disordersReelin Gene Polymorphisms in Autistic DisorderAppropriateness of array-CGH in the ADHD clinics: a comparative studyPhenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic reviewGenetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders
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hulumtuese
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հետազոտող
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Carla Lintas
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Carla Lintas
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Carla Lintas
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Carla Lintas
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Carla Lintas
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Carla Lintas
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Carla Lintas
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Carla Lintas
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