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Publications by Yuwei Fu

Increased Frequency of FBN1 Frameshift and Nonsense Mutations in Marfan Syndrome Patients With Aortic Dissection

Molecular genetics & genomic medicine

Molecular Biology

English

Related publications

Pregnancy, Marfan Syndrome, and Type-B Aortic Dissection

BJOG: An International Journal of Obstetrics and Gynaecology

English

Large Aortic Aneurysm and Dissection in a Patient With Marfan S Syndrome

Clinical & Biomedical Research

English

Re: Peripartum Type B Aortic Dissection in Patients With Marfan Syndrome Who Underwent Aortic Root Replacement: A Case Series Study

BJOG: An International Journal of Obstetrics and Gynaecology

English

A Recurring FBN1 Gene Mutation in Neonatal Marfan Syndrome

Archives of Pediatrics & Adolescent Medicine

English

Family-Based Whole-Exome Sequencing Identifies Novel Loss-Of-Function Mutations of FBN1 for Marfan Syndrome

Molecular Biology

Biological Sciences

English

Correlation of Nonsense and Frameshift Mutations With Severity of Retinal Abnormalities in Neurofibromatosis 2

Archives of Ophthalmology

English

A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

Double Mutant Fibrillin-1 (FBN1) Allele in a Patient With Neonatal Marfan Syndrome.

Journal of Medical Genetics

English

Increased Risk of Aortic Aneurysm and Dissection in Patients With Sjögren’s Syndrome: A Nationwide Population-Based Cohort Study in Taiwan

English