Profil bibliographique

Senwei Tan

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

32Publications signalées

379Citations signalées

8Affiliations récentes

Institutions déclarées

Union Hospital Central South University Changsha Medical University Hunan University Wuhan Union Hospital Ministry of Education Huazhong University of Science and Technology University of South China

Domaines associés

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomics and Rare DiseasesGenomic variations and chromosomal abnormalitiesCongenital heart defects research

Publications récentes

2026 articleOpenAlex

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features

Susan M. Hiatt, Wenjing Zhao, Zhongqing Wang, Yingjie Wan et autres

0 citationsThe American Journal of Human Genetics

Accès ouvert 2026 articleOpenAlex

X-linked SYTL4 missense variant disrupts RAB27A-dependent vesicle trafficking and synaptic transmission in autism

Yang Liao, Shuju Zhang, Xiaolei Zhang, Senwei Tan et autres

0 citationsProceedings of the National Academy of Sciences

Accès ouvert 2026 articleOpenAlex

Optical coherence tomography for carotid artery plaque: a standardised imaging and analysis methodology

Luojinyun Wang, Jiashuo Lin, Yan Wan, Candong Hong et autres

0 citationsStroke and Vascular Neurology

2026 articleOpenAlex

Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes

Senwei Tan, Yongqing Lyu, Xiaoyue Sun, Ruolan Guo et autres

1 citationMolecular Psychiatry

Accès ouvert 2026 articleOpenAlex

Post‐Omicron cognitive decline is largely reversible: Two‐year multicenter cohort study of domain‐specific outcomes in hospitalized patients

Min Qiu, Mengwen Wang, Shengcai Chen, Wenbo Zuo et autres

0 citationsNeuroprotection/Neuroprotection (Chichester, England. Print)

2026 articleOpenAlex

Evidence supporting the role of GIGYF2 in synapse development and autism

Bin Yu, S M Zhu, Linhu Xiao, Guodong Chen et autres

1 citationMolecular Psychiatry

2026 articleOpenAlex

CHST5 gene mutations contribute to high myopia by disrupting collagen fiber organization

Meining He, Senwei Tan, Furong Huang, Zhe Cheng et autres

0 citationsJournal of genetics and genomics/Journal of Genetics and Genomics

Accès ouvert 2026 articleOpenAlex

MSL2 disruption leads to autism-like behaviors, impairs neurogenesis, and alters histone H4K16 acetylation

Shengjie Luo, Shiyi Qu, Senwei Tan, Zhuo Song et autres

0 citationsCellular and Molecular Life Sciences

Accès ouvert 2026 articleOpenAlex

Beyond Hemoglobin Levels: Integrating Anemia Phenotyping Into Prognostic Models for Patients With Stroke Following Intravenous Thrombolysis

Senwei Tan, Shengcai Chen, Huijuan Jin, Min Qiu et autres

0 citationsJournal of the American Heart Association

Accès ouvert 2026 articleOpenAlex

Two-year trajectory of cognitive decline and neurological sequelae in COVID-19 survivors with acute neurological symptoms

Jiashuo Lin, Shengcai Chen, Lei Zhang, Min Qiu et autres

0 citationsFrontiers in Aging Neuroscience

2026 articleOpenAlex

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder

Jinchen Li, Tengfei Luo, Xue Ren, Songyu Yang et autres

1 citation中国科学通报：英文版

Accès ouvert 2025 articleOpenAlex

Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development

Xiaoxia Peng, Xiangbin Jia, Hanying Wang, Jingjing Chen et autres

2 citationsJournal of Clinical Investigation

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