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Results 1 - 10 of 35 for Autism
  1. CHD8 gene 
    ... gene mutations have been identified in people with autism spectrum disorder (ASD), a varied condition characterized by ... of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology. Front Neurosci. 2015 Dec 17;9:477. ...
    https://medlineplus.gov/genetics/gene/chd8 - Genetics
  2. DYRK1A gene 
    ... gene mutations have been identified in people with autism spectrum disorder (ASD), a varied condition characterized by ... Wu BB, An Y, Qiu ZL, Wu BL. Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and ...
    https://medlineplus.gov/genetics/gene/dyrk1a - Genetics
  3. SHANK3 gene 
    ... mutations have been found in people who have autism spectrum disorder (ASD), which is a varied condition ... the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet. 2007 Jan;39(1): ...
    https://medlineplus.gov/genetics/gene/shank3 - Genetics
  4. PTEN gene 
    ... large head size and the characteristic features of autism spectrum disorder, which affects communication and social interaction. ... gene are related to the risk of developing autism spectrum disorder. Some of these mutations have also ...
    https://medlineplus.gov/genetics/gene/pten - Genetics
  5. SYNGAP1 gene 
    ... other neurological problems, including recurrent seizures (epilepsy) and autism spectrum disorder, which affects communication and social interaction. ...
    https://medlineplus.gov/genetics/gene/syngap1 - Genetics
  6. ADNP gene 
    ... ADNP syndrome. This condition features intellectual disability and autism spectrum disorder, which is characterized by impaired communication ... brain. These changes likely explain the intellectual disability, autism spectrum disorder, and other diverse signs and symptoms ...
    https://medlineplus.gov/genetics/gene/adnp - Genetics
  7. POGZ gene 
    ... gastrointestinal problems. Most affected individuals have features of autism spectrum disorder (ASD), a varied condition characterized by ... F, Miyake N, Matsumoto N. A case of autism spectrum disorder arising from a de novo missense ...
    https://medlineplus.gov/genetics/gene/pogz - Genetics
  8. MECP2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Autism spectrum disorder More About This Health Condition Mutations ... activity have been reported in some cases of autism spectrum disorder, which affects communication and social interaction. ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  9. SLC6A3 gene 
    ... factors for attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). ADHD, which typically begins in ... A. SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking. Transl ...
    https://medlineplus.gov/genetics/gene/slc6a3 - Genetics
  10. ASH1L gene 
    ... gene mutations have been identified in people with autism spectrum disorder (ASD), a varied condition characterized by ... sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nat Genet. 2017 Apr; ...
    https://medlineplus.gov/genetics/gene/ash1l - Genetics
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