Chia-shan Hsieh
TPQ 10617, Taiwan
Last Updated: 09/26/2026
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Found 8 publications
Differential whole-genome doubling and homologous recombination deficiencies across breast cancer subtypes from the Taiwanese population.
Journal: Communications biology
Published: August 23, 2020
Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: October 04, 2019
Genome-Wide Copy Number Variation Association Study of Atrial Fibrillation Related Thromboembolic Stroke.
Journal: Journal of clinical medicine
Published: January 17, 2019
Global Expression Profiling Identifies a Novel Hyaluronan Synthases 2 Gene in the Pathogenesis of Lower Extremity Varicose Veins.
Journal: Journal of clinical medicine
Published: October 24, 2018
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.
Journal: Journal of medical genetics
Published: November 14, 2014
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation.
Journal: Nature communications
Published: October 21, 2014
Next-Generation Sequencing in the Genetics of Human Atrial Fibrillation.
Journal: Acta Cardiologica Sinica
Published: July 01, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026