Pages that link to "Q28250812"
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The following pages link to The contribution of de novo coding mutations to autism spectrum disorder (Q28250812):
Displaying 50 items.
- Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority (Q21146621) (← links)
- Where Do Epigenetics and Developmental Origins Take the Field of Developmental Psychopathology? (Q24289474) (← links)
- The Interaction between the Immune System and Epigenetics in the Etiology of Autism Spectrum Disorders (Q26741427) (← links)
- Somatic mutations in disorders with disrupted brain connectivity (Q26747309) (← links)
- RELN Mutations in Autism Spectrum Disorder (Q26750436) (← links)
- Prenatal Neurogenesis in Autism Spectrum Disorders (Q26750832) (← links)
- Synaptic Wnt/GSK3β Signaling Hub in Autism (Q26765504) (← links)
- Research advances in the role of vitamin D in autism spectrum disorders (Q26768300) (← links)
- Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology (Q26770773) (← links)
- The PsychENCODE project (Q26775498) (← links)
- Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders (Q26779153) (← links)
- Genetics and genomics of psychiatric disease (Q26781213) (← links)
- Behavioral phenotypes of genetic mouse models of autism (Q26781456) (← links)
- Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders (Q26783154) (← links)
- Somatic mosaicism in the human genome (Q26823199) (← links)
- Brain-specific transcriptional regulator T-brain-1 controls brain wiring and neuronal activity in autism spectrum disorders (Q27001037) (← links)
- From trans to cis: transcriptional regulatory networks in neocortical development (Q27002416) (← links)
- The promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disorders (Q27005952) (← links)
- FoxP1 orchestration of ASD-relevant signaling pathways in the striatum (Q27322723) (← links)
- Brinp1(-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density (Q27322895) (← links)
- Mutation of the CH1 Domain in the Histone Acetyltransferase CREBBP Results in Autism-Relevant Behaviors in Mice (Q27332438) (← links)
- Advancing the understanding of autism disease mechanisms through genetics (Q28069757) (← links)
- New insights into the generation and role of de novo mutations in health and disease (Q28073446) (← links)
- Wnt signaling networks in autism spectrum disorder and intellectual disability (Q28074740) (← links)
- The role of sex-differential biology in risk for autism spectrum disorder (Q28077103) (← links)
- Brain connectivity in autism spectrum disorder (Q28077372) (← links)
- A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons. (Q28079929) (← links)
- Next-Generation Sequencing in Intellectual Disability (Q28080074) (← links)
- The Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and Treatment (Q28081659) (← links)
- Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms (Q28087577) (← links)
- Identification of the BRD1 interaction network and its impact on mental disorder risk (Q28114916) (← links)
- SeqHBase: a big data toolset for family based sequencing data analysis (Q28255525) (← links)
- Low load for disruptive mutations in autism genes and their biased transmission (Q28267714) (← links)
- Schizophrenia risk from complex variation of complement component 4 (Q28272545) (← links)
- Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder (Q28277540) (← links)
- The serotonin system in autism spectrum disorder: From biomarker to animal models (Q28391614) (← links)
- Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics (Q28394524) (← links)
- Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons (Q28510104) (← links)
- Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase (Q28543984) (← links)
- Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder (Q28553061) (← links)
- Structural Basis of Diverse Homophilic Recognition by Clustered α- and β-Protocadherins (Q28590490) (← links)
- Challenges of Identifying Clinically Actionable Genetic Variants for Precision Medicine (Q28596030) (← links)
- Neurogenomics and the role of a large mutational target on rapid behavioral change (Q28596081) (← links)
- Progress in methods for rare variant association (Q28601645) (← links)
- Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid Genomes (Q28607530) (← links)
- A comprehensive meta-analysis of common genetic variants in autism spectrum conditions (Q28608366) (← links)
- JAKMIP1, a Novel Regulator of Neuronal Translation, Modulates Synaptic Function and Autistic-like Behaviors in Mouse (Q28771493) (← links)
- Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures (Q29147423) (← links)
- De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome (Q29147448) (← links)
- An expanded sequence context model broadly explains variability in polymorphism levels across the human genome (Q29307337) (← links)