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Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report

BMC medical genomics, 2024-04, Vol.17 (1), p.104-104

2024

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Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke

Journal of neuroinflammation, 2012-10, Vol.9 (1), p.235-235, Article 235

2012

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A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency

Journal of the American College of Cardiology, 2014-07, Vol.64 (3), p.267-277

2014

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Effects of Shuanghuanglian oral liquids on patients with COVID-19: a randomized, open-label, parallel-controlled, multicenter clinical trial

Frontiers of medicine, 2021-10, Vol.15 (5), p.704-717

2021

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The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA

BMC medical genetics, 2019-05, Vol.20 (1), p.91-91, Article 91

2019

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Aortic root aortopathy in bicuspid aortic valve associated with high genetic risk

BMC cardiovascular disorders, 2021-08, Vol.21 (1), p.413-413, Article 413

2021

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Numerical simulation and experimental study of gas cyclone–liquid jet separator for fine particle separation

Chinese journal of chemical engineering, 2022-11, Vol.51 (11), p.43-52

2022

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COL5A1 Variants Cause Aortic Dissection by Activating TGF‐β‐Signaling Pathway

Journal of the American Heart Association, 2021-06, Vol.10 (11), p.e019276-e019276

2021

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FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review

Genes, 2022-10, Vol.13 (10), p.1842

2022

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RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy

Canadian journal of cardiology, 2021-11, Vol.37 (11), p.1751-1759

2021

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Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report

BMC medical genetics, 2020-07, Vol.21 (1), p.1-144, Article 144

2020

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MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

Science China. Life sciences, 2020-09, Vol.63 (9), p.1347-1362

2020

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Rare Variants and Polymorphisms of FBN1 Gene May Increase the Risk of Non-Syndromic Aortic Dissection

Frontiers in genetics, 2022-01, Vol.13, p.778806-778806

2022

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Erratum to: MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

Science China. Life sciences, 2022-05, Vol.65 (5), p.1056-1056

2022

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FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations

Connective tissue research, 2024-05, Vol.65 (3), p.214-225

2024

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Case Report: A Novel LAMP2 Splice-Altering Mutation Causes Cardiac-Only Danon Disease

Frontiers in cardiovascular medicine, 2021-11, Vol.8, p.763240

2021

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Machine learning modeling identifies hypertrophic cardiomyopathy subtypes with genetic signature

Frontiers of medicine, 2023-08, Vol.17 (4), p.768-780

2023

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Object Tracking With Structured Metric Learning

IEEE access, 2019, Vol.7, p.161764-161775

2019

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Identification of COL3A1 variants associated with sporadic thoracic aortic dissection: a case--control study

Frontiers of medicine, 2021-06, Vol.15 (3), p.438-447

2021

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Comparison of High-Resolution Melting Analysis, TaqMan Allelic Discrimination Assay, and Sanger Sequencing for Clopidogrel Efficacy Genotyping in Routine Molecular Diagnostics

The Journal of molecular diagnostics : JMD, 2013-09, Vol.15 (5), p.600-606

2013

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Growth of Metal Organic Frameworks on the Surface of Individual Cellulose Nanocrystals

Crystal growth & design, 2024-02, Vol.24 (4), p.1792-1797

2024

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Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection

Science China. Life sciences, 2017, Vol.60 (1), p.57-65

2017

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The Involvement of ALPK3 in Hypertrophic Cardiomyopathy in East Asia

Frontiers in medicine, 2022-06, Vol.9, p.915649-915649

2022

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A laboratory viewpoint of the consensus paper from the European Society of Cardiology regarding the utilization of the American College of Medical Genetics and Genomics pathogenic criteria for cardiomyopathy

European heart journal, 2022-07, Vol.43 (27), p.2636-2637

2022

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Aortic Coarctation Associated With Hypertrophic Cardiomyopathy in a Woman With Hypertension and Syncope: A Case Report With 8-Year Follow-Up

Frontiers in cardiovascular medicine, 2022-01, Vol.8, p.818884

2022

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Waardenburg syndrome type 2 with a de novo variant of the SOX10 gene: a case report

Polymorphism of tumor necrosis factor alpha (TNF-alpha) gene promoter, circulating TNF-alpha level, and cardiovascular risk factor for ischemic stroke

A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency

Effects of Shuanghuanglian oral liquids on patients with COVID-19: a randomized, open-label, parallel-controlled, multicenter clinical trial

The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA

Aortic root aortopathy in bicuspid aortic valve associated with high genetic risk

Numerical simulation and experimental study of gas cyclone–liquid jet separator for fine particle separation

COL5A1 Variants Cause Aortic Dissection by Activating TGF‐β‐Signaling Pathway

FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review

RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy

Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report

MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

Rare Variants and Polymorphisms of FBN1 Gene May Increase the Risk of Non-Syndromic Aortic Dissection

Erratum to: MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

FBN2 pathogenic variants in congenital contractural arachnodactyly with severe cardiovascular manifestations

Case Report: A Novel LAMP2 Splice-Altering Mutation Causes Cardiac-Only Danon Disease

Machine learning modeling identifies hypertrophic cardiomyopathy subtypes with genetic signature

Object Tracking With Structured Metric Learning

Identification of COL3A1 variants associated with sporadic thoracic aortic dissection: a case--control study

Comparison of High-Resolution Melting Analysis, TaqMan Allelic Discrimination Assay, and Sanger Sequencing for Clopidogrel Efficacy Genotyping in Routine Molecular Diagnostics

Growth of Metal Organic Frameworks on the Surface of Individual Cellulose Nanocrystals

Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection

The Involvement of ALPK3 in Hypertrophic Cardiomyopathy in East Asia

A laboratory viewpoint of the consensus paper from the European Society of Cardiology regarding the utilization of the American College of Medical Genetics and Genomics pathogenic criteria for cardiomyopathy

Aortic Coarctation Associated With Hypertrophic Cardiomyopathy in a Woman With Hypertension and Syncope: A Case Report With 8-Year Follow-Up

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