Shi-lei Sun

1 Jian She East Road
Zhengzhou, 450000, China

Last Updated: 09/26/2026

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Found 14 publications

Shared Genetic Architecture between Parkinson's Disease and Brain Structural Phenotypes.

Shared Genetic Architecture between Parkinson's Disease and Brain Structural Phenotypes.

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

Published: May 10, 2023

Identifying causal genes for migraine by integrating the proteome and transcriptome.

Identifying causal genes for migraine by integrating the proteome and transcriptome.

Journal: The journal of headache and pain

Published: March 07, 2023

Dual antiplatelet therapy reduced stroke risk in transient ischemic attack with positive diffusion weighted imaging.

Dual antiplatelet therapy reduced stroke risk in transient ischemic attack with positive diffusion weighted imaging.

Journal: Scientific reports

Published: December 04, 2019

Association of FOXF2 gene polymorphisms with ischemic stroke in Chinese Han population.

Association of FOXF2 gene polymorphisms with ischemic stroke in Chinese Han population.

Journal: Oncotarget

Published: June 21, 2017

Endothelial Progenitor Cells' Classification and Application in Neurological Diseases.

Endothelial Progenitor Cells' Classification and Application in Neurological Diseases.

Journal: Tissue engineering and regenerative medicine

Published: August 21, 2016

Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.

Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.

Journal: The International journal of neuroscience

Published: December 09, 2015

Calcium intake and the risk of stroke: an up-dated meta-analysis of prospective studies.

Calcium intake and the risk of stroke: an up-dated meta-analysis of prospective studies.

Journal: Asia Pacific journal of clinical nutrition

Published: June 17, 2015

Nerve growth factor for the treatment of spinocerebellar ataxia type 3: an open-label study.

Nerve growth factor for the treatment of spinocerebellar ataxia type 3: an open-label study.

Journal: Chinese medical journal

Published: January 31, 2015

Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation.

Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation.

Journal: Neurology

Published: January 08, 2015

Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes.

Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes.

Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia

Published: April 30, 2014

Validation of ABCD3 score in the predication of stroke risk after transient ischemic attack

Validation of ABCD3 score in the predication of stroke risk after transient ischemic attack

Journal: Zhonghua yi xue za zhi

Published: January 16, 2014

Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia cases.

Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia cases.

Journal: Journal of the neurological sciences

Published: November 07, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026