Pages that link to "Q29030218"
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The following pages link to Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations (Q29030218):
Displaying 50 items.
- A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao) (Q21090760) (← links)
- Lamarckian evolution explains human brain evolution and psychiatric disorders (Q21129357) (← links)
- De novo mutations in moderate or severe intellectual disability (Q21144861) (← links)
- Revisiting an old riddle: what determines genetic diversity levels within species? (Q21145734) (← links)
- Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring (Q21146665) (← links)
- CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems (Q21198723) (← links)
- Environmental and state-level regulatory factors affect the incidence of autism and intellectual disability (Q21558515) (← links)
- Mitochondrial dysfunction in Pten haplo-insufficient mice with social deficits and repetitive behavior: interplay between Pten and p53 (Q21560776) (← links)
- From mouse to human: evolutionary genomics analysis of human orthologs of essential genes (Q22065247) (← links)
- Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments (Q23936599) (← links)
- Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology (Q24273406) (← links)
- Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems (Q24294551) (← links)
- Disruptive CHD8 mutations define a subtype of autism early in development (Q24300432) (← links)
- CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors (Q24305288) (← links)
- Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities (Q24338502) (← links)
- De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies (Q24563008) (← links)
- A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP (Q24567998) (← links)
- De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome (Q24600816) (← links)
- Exome sequencing reveals new causal mutations in children with epileptic encephalopathies (Q24604206) (← links)
- In search of low-frequency and rare variants affecting complex traits (Q24618492) (← links)
- De novo mutations in epileptic encephalopathies (Q24621776) (← links)
- Estimating the human mutation rate using autozygosity in a founder population (Q24622247) (← links)
- Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder (Q24624740) (← links)
- Rate of de novo mutations and the importance of father's age to disease risk (Q24632353) (← links)
- Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements (Q26741394) (← links)
- Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology (Q26744368) (← links)
- Somatic mutations in disorders with disrupted brain connectivity (Q26747309) (← links)
- The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder (Q26747333) (← links)
- Using biological networks to integrate, visualize and analyze genomics data (Q26748923) (← links)
- Prenatal Neurogenesis in Autism Spectrum Disorders (Q26750832) (← links)
- Synaptic Wnt/GSK3β Signaling Hub in Autism (Q26765504) (← links)
- A Short Review on the Current Understanding of Autism Spectrum Disorders (Q26765918) (← links)
- Striatal Circuits as a Common Node for Autism Pathophysiology (Q26768226) (← links)
- Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology (Q26770773) (← links)
- Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements (Q26770859) (← links)
- On the Role of Glutamate in Presynaptic Development: Possible Contributions of Presynaptic NMDA Receptors (Q26773295) (← links)
- Functional genomics of human brain development and implications for autism spectrum disorders (Q26778520) (← links)
- Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders (Q26779153) (← links)
- The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential (Q26781422) (← links)
- Characterizing autism spectrum disorders by key biochemical pathways (Q26781645) (← links)
- The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disorders (Q26783008) (← links)
- Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders (Q26783154) (← links)
- Advancing epilepsy genetics in the genomic era (Q26798035) (← links)
- Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseases (Q26822979) (← links)
- The developmental transcriptome of the human brain: implications for neurodevelopmental disorders (Q26824947) (← links)
- From genomes to societies: a holistic view of determinants of human health (Q26827143) (← links)
- Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia (Q26829347) (← links)
- Genome-scale neurogenetics: methodology and meaning (Q26886374) (← links)
- A genetic model for neurodevelopmental disease (Q26860566) (← links)
- Channelopathy pathogenesis in autism spectrum disorders (Q26864726) (← links)