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Publications by Weixiang Zhong

Whole-Exome Sequencing Reveals Frequent Mutations in Chromatin Remodeling Genes in Mammary and Extramammary Paget’s Diseases

Journal of Investigative Dermatology

English

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Whole-Exome Sequencing Reveals Critical Genes Underlying Metastasis in Oesophageal Squamous Cell Carcinoma

English

Whole-Exome Sequencing Identifies Somatic ATRX Mutations in Pheochromocytomas and Paragangliomas

Nature Communications

English

Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

English

Whole Exome Sequencing in Monogenic Dyslipidemias

Journal of Atherosclerosis and Thrombosis

Biochemistry

Internal Medicine

Cardiovascular Medicine

Cardiology

2015

English

Whole Exome Sequencing Identified Sixty-Five Coding Mutations in Four Neuroblastoma Tumors

Scientific Reports

Multidisciplinary

2017

English

Whole-Exome-Sequencing of Nodal Marginal Zone Lymphomas Identifies Recurrent Molecular Lesions in Genes Involved in Chromatin Remodelling and Notch Signalling

Hematological Oncology

English

Application of Whole Exome Sequencing in the Diagnosis of Hereditary Neurological Diseases

Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova

English

Annotation of Genes Having Candidate Somatic Mutations in Acute Myeloid Leukemia With Whole-Exome Sequencing Using Concept Lattice Analysis

Genomics and Informatics

English

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

2015

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Weixiang Zhong

Whole-Exome Sequencing Reveals Frequent Mutations in Chromatin Remodeling Genes in Mammary and Extramammary Paget’s Diseases

Related publications

Whole-Exome Sequencing Reveals Critical Genes Underlying Metastasis in Oesophageal Squamous Cell Carcinoma

Whole-Exome Sequencing Identifies Somatic ATRX Mutations in Pheochromocytomas and Paragangliomas

Novel Mutations in PRPF31 Causing Retinitis Pigmentosa Identified Using Whole-Exome Sequencing

Whole Exome Sequencing in Monogenic Dyslipidemias

Whole Exome Sequencing Identified Sixty-Five Coding Mutations in Four Neuroblastoma Tumors

Whole-Exome-Sequencing of Nodal Marginal Zone Lymphomas Identifies Recurrent Molecular Lesions in Genes Involved in Chromatin Remodelling and Notch Signalling

Application of Whole Exome Sequencing in the Diagnosis of Hereditary Neurological Diseases

Annotation of Genes Having Candidate Somatic Mutations in Acute Myeloid Leukemia With Whole-Exome Sequencing Using Concept Lattice Analysis

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants