A systematic variant annotation approach for ranking genes associated with autism spectrum disorders. - Wikidata - awgldk - TriplyDB

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.

http://www.wikidata.org/entity/Q37358859

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The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings.Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children Editorial: Non-Coding RNAs in Neurodevelopmental Disorders.AutDB: a platform to decode the genetic architecture of autism.ADNP Plays a Key Role in Autophagy: From Autism to Schizophrenia and Alzheimer's Disease.Editorial: Trends in Regulatory Peptides.Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders

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A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.

http://www.wikidata.org/entity/Q37358859

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 21 October 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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A systematic variant annotatio ...... ith autism spectrum disorders.

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A systematic variant annotatio ...... ith autism spectrum disorders.

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A systematic variant annotatio ...... ith autism spectrum disorders.

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A systematic variant annotatio ...... ith autism spectrum disorders.

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A systematic variant annotatio ...... ith autism spectrum disorders.

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A systematic variant annotatio ...... ith autism spectrum disorders.

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S13229-016-0103-Y

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Molecular Autism

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A systematic variant annotatio ...... ith autism spectrum disorders.

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Alan Packer

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Eric Larsen

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Mark N Ziats

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Sharmila Banerjee-Basu

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Wayne Pereanu

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P2860

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Contribution of SHANK3 mutations to autism spectrum disorder

Synaptic, transcriptional and chromatin genes disrupted in autism

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Low load for disruptive mutations in autism genes and their biased transmission

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

A genome-wide scan for common alleles affecting risk for autism

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scholarly article

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10.1186/S13229-016-0103-Y

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Autism spectrum

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