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Sun Chen

Showing results (131-140 of 198) with videos related to

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Frontiers in Genetics|June 22, 2026
Exploration of candidate genes associated with rare SNVs in pulmonary stenosis using whole-exome sequencing and machine learningYuting Liu, Sun Chen, Yongzhou Liang, et al.
Nutrients|May 27, 2026
An Exploratory Study of Serum 25-Hydroxyvitamin D Concentration and Psychological Distress Among Aboriginal and Torres Strait Islander Peoples in AustraliaBelinda Neo, Noel Nannup, Dale Tilbrook, et al.
Cureus|December 9, 2024
Diffuse Glioneuronal Tumor With Oligodendroglioma-Like Features and Nuclear Clusters Relapse in a Seven-Year-Old Boy: An Unusual Case Exhibiting Near-Tetraploidy and Chromosome 14 DiploidyFrancis M Torres, Thomas Denapoli, Ping-Sun Chen, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|November 27, 2019
Ambulatory blood pressure monitoring and morning surge in blood pressure in adult black and white South AfricansGavin W Lambert, Geoffrey A Head, Won Sun Chen, et al.
FEBS Open Bio|November 19, 2020
A loss-of-function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF)Jiayu Peng, Qingjie Wang, Zhuo Meng, et al.
Plos Genetics|December 2, 2022
LOF variants identifying candidate genes of laterality defects patients with congenital heart diseaseSijie Liu, Wei Wei, Pengcheng Wang, et al.
Molecular Genetics and Genomics : MGG|March 9, 2022
Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4Baolei Li, Zhuoyan Li, Jianping Yang, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|January 15, 2024
Trends in blood pressure changes and hypertension prevalence in Australian adults before and during the COVID-19 pandemicJanis M Nolde, Fleur Streets, Denny Meyer, et al.
Genomics|July 5, 2023
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencingJiaJun Ye, Yiwei Niu, Yongxuan Peng, et al.
Journal of Translational Medicine|September 23, 2018
A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplicationNanchao Hong, Erge Zhang, Qingjie Wang, et al.
Pageof 20

Showing results (131-140 of 198) with videos related to

Sort By:
Pageof 20
Frontiers in Genetics|June 22, 2026
Exploration of candidate genes associated with rare SNVs in pulmonary stenosis using whole-exome sequencing and machine learningYuting Liu, Sun Chen, Yongzhou Liang, et al.
Nutrients|May 27, 2026
An Exploratory Study of Serum 25-Hydroxyvitamin D Concentration and Psychological Distress Among Aboriginal and Torres Strait Islander Peoples in AustraliaBelinda Neo, Noel Nannup, Dale Tilbrook, et al.
Cureus|December 9, 2024
Diffuse Glioneuronal Tumor With Oligodendroglioma-Like Features and Nuclear Clusters Relapse in a Seven-Year-Old Boy: An Unusual Case Exhibiting Near-Tetraploidy and Chromosome 14 DiploidyFrancis M Torres, Thomas Denapoli, Ping-Sun Chen, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|November 27, 2019
Ambulatory blood pressure monitoring and morning surge in blood pressure in adult black and white South AfricansGavin W Lambert, Geoffrey A Head, Won Sun Chen, et al.
FEBS Open Bio|November 19, 2020
A loss-of-function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF)Jiayu Peng, Qingjie Wang, Zhuo Meng, et al.
Plos Genetics|December 2, 2022
LOF variants identifying candidate genes of laterality defects patients with congenital heart diseaseSijie Liu, Wei Wei, Pengcheng Wang, et al.
Molecular Genetics and Genomics : MGG|March 9, 2022
Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4Baolei Li, Zhuoyan Li, Jianping Yang, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|January 15, 2024
Trends in blood pressure changes and hypertension prevalence in Australian adults before and during the COVID-19 pandemicJanis M Nolde, Fleur Streets, Denny Meyer, et al.
Genomics|July 5, 2023
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencingJiaJun Ye, Yiwei Niu, Yongxuan Peng, et al.
Journal of Translational Medicine|September 23, 2018
A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplicationNanchao Hong, Erge Zhang, Qingjie Wang, et al.
Pageof 20