Yuchen Xu

Hunan Provincial Key Laboratory Of Crop Germplasm Innovation And Utilization And College Of Agronomy
Changsha, China

Last Updated: 09/26/2026

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Found 12 publications

Grin1 Y 647 S/+ Mice: A Preclinical Model of GRIN1 -Related Neurodevelopmental Disorder.

Grin1 Y 647 S/+ Mice: A Preclinical Model of GRIN1 -Related Neurodevelopmental Disorder.

Journal: bioRxiv : the preprint server for biology

Published: September 04, 2024

Identification of two novel rice S genes through combination of association and transcription analyses with gene-editing technology.

Identification of two novel rice S genes through combination of association and transcription analyses with gene-editing technology.

Journal: Plant biotechnology journal

Published: June 29, 2022

DNAH14 variants are associated with neurodevelopmental disorders.

DNAH14 variants are associated with neurodevelopmental disorders.

Journal: Human mutation

Published: December 28, 2021

A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.

A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.

Journal: Frontiers in genetics

Published: April 12, 2021

Recurrent seizure-related GRIN1 variant: Molecular mechanism and targeted therapy.

Recurrent seizure-related GRIN1 variant: Molecular mechanism and targeted therapy.

Journal: Annals of clinical and translational neurology

Published: April 05, 2021

A Frameshift Variant in the SEMA6B Gene Causes Global Developmental Delay and Febrile Seizures.

A Frameshift Variant in the SEMA6B Gene Causes Global Developmental Delay and Febrile Seizures.

Journal: Neuroscience bulletin

Published: November 27, 2020

CpG methylation signature defines human temporal lobe epilepsy and predicts drug-resistant.

CpG methylation signature defines human temporal lobe epilepsy and predicts drug-resistant.

Journal: CNS neuroscience & therapeutics

Published: February 15, 2020

A conjoint analysis of epilepsy and migraine through network-and-pathway-based method.

A conjoint analysis of epilepsy and migraine through network-and-pathway-based method.

Journal: Annals of palliative medicine

Published: December 29, 2019

The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus.

The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 27, 2019

De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.

De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.

Journal: Human mutation

Published: March 25, 2019

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Journal: Brain : a journal of neurology

Published: January 14, 2019

Sex-differential DNA methylation and associated regulation networks in human brain implicated in the sex-biased risks of psychiatric disorders.

Sex-differential DNA methylation and associated regulation networks in human brain implicated in the sex-biased risks of psychiatric disorders.

Journal: Molecular psychiatry

Published: November 08, 2018

Showing 1-12 of 12

Last Updated: 09/26/2026