Yuduo Wu
Beijing, 100029, China
Last Updated: 09/26/2026
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Found 11 publications
Analysis of Echocardiography and Risk Factors Related to Prognosis in Adult Patients with Isolated Congenitally Corrected Transposition of the Great Arteries.
Journal: Journal of clinical medicine
Published: May 20, 2025
Mitochondrial DNA mutations as a potential modifier for the clinical variability of marfan syndrome.
Mitochondrial DNA mutations as a potential modifier for the clinical variability of marfan syndrome.
Journal: QJM : monthly journal of the Association of Physicians
Published: July 29, 2024
Clinical and genetic characteristics of 12 cases of Loeys-Dietz syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 29, 2023
Bibliometric Analysis of Health Technology Research: 1990~2020.
Journal: International journal of environmental research and public health
Published: May 24, 2022
Association between placental DNA methylation and fetal congenital heart disease.
Journal: Molecular genetics and genomics : MGG
Published: March 28, 2022
Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects.
Journal: Frontiers in genetics
Published: February 17, 2022
Simultaneous Segmentation of Four Cardiac Chambers in Fetal Echocardiography.
Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference
Published: December 11, 2021
Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid-capture next-generation sequencing.
Journal: Molecular genetics & genomic medicine
Published: February 07, 2021
Analysis of ascending aortic diameter and long-term prognosis in patients with ascending aortic dissection.
Journal: Echocardiography (Mount Kisco, N.Y.)
Published: October 12, 2020
Marfan syndrome: whole-exome sequencing reveals de novo mutations, second gene and genotype-phenotype correlations in the Chinese population.
Journal: Bioscience reports
Published: October 01, 2020
A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome.
Journal: Hereditas
Published: September 06, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026