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The genetic and phenotypic spectra of adult genetic leukoencephalopathies in a cohort of 309 patients

Brain (London, England : 1878), 2023-06, Vol.146 (6), p.2364-2376

2023

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Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia

Frontiers in neurology, 2022-04, Vol.13, p.872927-872927

2022

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Two Novel Myelin Protein Zero Mutations in a Group of Chinese Patients

Frontiers in neurology, 2021-12, Vol.12, p.734515-734515

2021

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Intracranial Large Artery Abnormalities and Association With Cerebral Small Vessel Disease in CADASIL

Frontiers in neurology, 2020-08, Vol.11, p.726-726

2020

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TIPE2 suppresses progression and tumorigenesis of esophageal carcinoma via inhibition of the Wnt/β-catenin pathway

Journal of translational medicine, 2018-01, Vol.16 (1), p.7-10, Article 7

2018

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Novel Alanyl-tRNA Synthetase 2 Pathogenic Variants in Leukodystrophies

Frontiers in neurology, 2019-12, Vol.10, p.1321-1321

2019

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Reply to: “Inappropriate interpretation of non‐pathogenic HTRA1 variant as pathogenic”

Annals of clinical and translational neurology, 2023-07, Vol.10 (7), p.1263-1263

2023

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Dystonia, spastic tetraplegia, and ataxia due to a novel mutation in the dynamin domain of OPA1

Annals of clinical and translational neurology, 2024-03, Vol.11 (3), p.800-805

2024

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Novel mutations in HTRA1‐related cerebral small vessel disease and comparison with CADASIL

Annals of clinical and translational neurology, 2022-10, Vol.9 (10), p.1586-1595

2022

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Clinical Features and Classification of Neuronal Intranuclear Inclusion Disease

Neurology. Genetics, 2023-04, Vol.9 (2), p.e200057-e200057

2023

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MRI Lesion Load of Cerebral Small Vessel Disease and Cognitive Impairment in Patients With CADASIL

Frontiers in neurology, 2018-10, Vol.9, p.862-862

2018

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Fotemustine-based therapy in combination with rituximab as a first-line induction chemotherapy followed by WBRT for newly diagnosed primary central nervous system lymphoma: a prospective phase II trial

Cancer biology & medicine, 2021-10, Vol.19 (7), p.1089-1099

2021

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A Class of Amide Ligands Enable Cu-Catalyzed Coupling of (Hetero)aryl Halides with Sulfinic Acid Salts under Mild Conditions

Journal of organic chemistry, 2018-06, Vol.83 (12), p.6589-6598

2018

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Pd-Catalyzed Dimethylation of Tyrosine-Derived Picolinamide for Synthesis of (S)‑N‑Boc-2,6-dimethyltyrosine and Its Analogues

Organic letters, 2017-01, Vol.19 (1), p.246-249

2017

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[Retracted] MicroRNA‑664 targets paired box protein 6 to inhibit the oncogenicity of pancreatic ductal adenocarcinoma

International journal of oncology, 2022-08, Vol.61 (2), Article 90

2022

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Genotypic and phenotypic characteristics of juvenile/adult onset vanishing white matter: a series of 14 Chinese patients

Neurological sciences, 2022-08, Vol.43 (8), p.4961-4977

2022

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c‐Myc mediated upregulation of long noncoding RNA SNHG12 regulates proliferation and drug sensitivity in natural killer/T‐cell lymphoma

Journal of cellular biochemistry, 2019-08, Vol.120 (8), p.12628-12637

2019

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Clinical and pathological study of SORD-related distal motor neuropathy caused by novel compound heterozygous mutations in a Chinese patient

Clinical neurology and neurosurgery, 2022-02, Vol.213, p.107118-107118, Article 107118

2022

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Genotypic and Phenotypic Characteristics of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy from China

European neurology, 2021-07, Vol.84 (4), p.237-245

2021

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A patient with SCA17 featuring 41 CAG repeats presents with spastic paraplegia and involuntary movement

Parkinsonism & related disorders, 2021-08, Vol.89, p.87-89

2021

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MicroRNA-664 targets paired box protein 6 to inhibit the oncogenicity of pancreatic ductal adenocarcinoma

International journal of oncology, 2019-05, Vol.54 (5), p.1884-1896

2019

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Clinical and therapeutical significances of the cluster and signature based on oxidative stress for osteosarcoma

Aging (Albany, NY.), 2023-12, Vol.15 (24), p.15360-15381

2023

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Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC

Neurological sciences, 2023-05, Vol.44 (5), p.1769-1772

2023

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Three novel mutations in a group of Chinese patients with X-linked Charcot-Marie-Tooth disease

Clinical neurology and neurosurgery, 2019-09, Vol.184, p.105430-105430, Article 105430

2019

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Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP)

Journal of clinical neuroscience, 2018-02, Vol.48, p.133-137

2018

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The genetic and phenotypic spectra of adult genetic leukoencephalopathies in a cohort of 309 patients

Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia

Two Novel Myelin Protein Zero Mutations in a Group of Chinese Patients

Intracranial Large Artery Abnormalities and Association With Cerebral Small Vessel Disease in CADASIL

TIPE2 suppresses progression and tumorigenesis of esophageal carcinoma via inhibition of the Wnt/β-catenin pathway

Novel Alanyl-tRNA Synthetase 2 Pathogenic Variants in Leukodystrophies

Reply to: “Inappropriate interpretation of non‐pathogenic HTRA1 variant as pathogenic”

Dystonia, spastic tetraplegia, and ataxia due to a novel mutation in the dynamin domain of OPA1

Novel mutations in HTRA1‐related cerebral small vessel disease and comparison with CADASIL

Clinical Features and Classification of Neuronal Intranuclear Inclusion Disease

MRI Lesion Load of Cerebral Small Vessel Disease and Cognitive Impairment in Patients With CADASIL

Fotemustine-based therapy in combination with rituximab as a first-line induction chemotherapy followed by WBRT for newly diagnosed primary central nervous system lymphoma: a prospective phase II trial

A Class of Amide Ligands Enable Cu-Catalyzed Coupling of (Hetero)aryl Halides with Sulfinic Acid Salts under Mild Conditions

Pd-Catalyzed Dimethylation of Tyrosine-Derived Picolinamide for Synthesis of (S)‑N‑Boc-2,6-dimethyltyrosine and Its Analogues

[Retracted] MicroRNA‑664 targets paired box protein 6 to inhibit the oncogenicity of pancreatic ductal adenocarcinoma

Genotypic and phenotypic characteristics of juvenile/adult onset vanishing white matter: a series of 14 Chinese patients

c‐Myc mediated upregulation of long noncoding RNA SNHG12 regulates proliferation and drug sensitivity in natural killer/T‐cell lymphoma

Clinical and pathological study of SORD-related distal motor neuropathy caused by novel compound heterozygous mutations in a Chinese patient

Genotypic and Phenotypic Characteristics of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy from China

A patient with SCA17 featuring 41 CAG repeats presents with spastic paraplegia and involuntary movement

MicroRNA-664 targets paired box protein 6 to inhibit the oncogenicity of pancreatic ductal adenocarcinoma

Clinical and therapeutical significances of the cluster and signature based on oxidative stress for osteosarcoma

Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC

Three novel mutations in a group of Chinese patients with X-linked Charcot-Marie-Tooth disease

Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP)

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