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Runs of homozygosity: windows into population history and trait architecture
Long runs of homozygosity (ROH) arise when identical haplotypes are inherited from each
parent and thus a long tract of genotypes is homozygous. Cousin marriage or inbreeding …
parent and thus a long tract of genotypes is homozygous. Cousin marriage or inbreeding …
Activity-dependent neuronal signalling and autism spectrum disorder
DH Ebert, ME Greenberg - Nature, 2013 - nature.com
Neuronal activity induces the post-translational modification of synaptic molecules, promotes
localized protein synthesis within dendrites and activates gene transcription, thereby …
localized protein synthesis within dendrites and activates gene transcription, thereby …
A NPAS4–NuA4 complex couples synaptic activity to DNA repair
Neuronal activity is crucial for adaptive circuit remodelling but poses an inherent risk to the
stability of the genome across the long lifespan of postmitotic neurons,,,–. Whether neurons …
stability of the genome across the long lifespan of postmitotic neurons,,,–. Whether neurons …
Modeling autism by SHANK gene mutations in mice
Y Jiang, MD Ehlers - Neuron, 2013 - cell.com
Shank family proteins (Shank1, Shank2, and Shank3) are synaptic scaffolding proteins that
organize an extensive protein complex at the postsynaptic density (PSD) of excitatory …
organize an extensive protein complex at the postsynaptic density (PSD) of excitatory …
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing
Autism Spectrum Disorder (ASD) demonstrates high heritability and familial clustering, yet
the genetic causes remain only partially understood as a result of extensive clinical and …
the genetic causes remain only partially understood as a result of extensive clinical and …
Using whole-exome sequencing to identify inherited causes of autism
Despite significant heritability of autism spectrum disorders (ASDs), their extreme genetic
heterogeneity has proven challenging for gene discovery. Studies of primarily simplex …
heterogeneity has proven challenging for gene discovery. Studies of primarily simplex …
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing
Background To facilitate the clinical implementation of genomic medicine by next-generation
sequencing, it will be critically important to obtain accurate and consistent variant calls on …
sequencing, it will be critically important to obtain accurate and consistent variant calls on …
Recessive gene disruptions in autism spectrum disorder
Autism spectrum disorder (ASD) affects up to 1 in 59 individuals. Genome-wide association
and large-scale sequencing studies strongly implicate both common variants,–and rare de …
and large-scale sequencing studies strongly implicate both common variants,–and rare de …
Autism genetics
AM Persico, V Napolioni - Behavioural brain research, 2013 - Elsevier
Autism spectrum disorder (ASD) is a severe neuropsychiatric disease with strong genetic
underpinnings. However, genetic contributions to autism are extremely heterogeneous, with …
underpinnings. However, genetic contributions to autism are extremely heterogeneous, with …
[PDF][PDF] The genetics of autism spectrum disorders
G Huguet, M Benabou, T Bourgeron - A time for metabolism and …, 2016 - library.oapen.org
In the last 30 years, twin studies have indicated a strong genetic contribution to Autism
Spectrum Disorders (ASD). The heritability of ASD is estimated to be 50%, mostly captured …
Spectrum Disorders (ASD). The heritability of ASD is estimated to be 50%, mostly captured …