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Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits
Autism is a highly heritable, heterogeneous, neurodevelopmental condition. Large-scale
genetic studies, predominantly focussing on simplex families and clinical diagnoses of …
genetic studies, predominantly focussing on simplex families and clinical diagnoses of …
Structural models of genome-wide covariance identify multiple common dimensions in autism
L De Hoyos, MT Barendse, F Schlag… - Nature …, 2024 - nature.com
Common genetic variation has been associated with multiple phenotypic features in Autism
Spectrum Disorder (ASD). However, our knowledge of shared genetic factor structures …
Spectrum Disorder (ASD). However, our knowledge of shared genetic factor structures …
Serotonin signaling in the enteric nervous system and connection to autism spectrum disorder: a translational mathematical model
I Kareva - Applied Sciences, 2023 - mdpi.com
While the causes of autism spectrum disorder (ASD) remain unclear, some studies have
shown that serotonin-mediated effects on the enteric nervous system (ENS) correlate with an …
shown that serotonin-mediated effects on the enteric nervous system (ENS) correlate with an …