Yi-ning N. Su
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 88 publications
Enhancing thalassemia carrier detection: Advancing genetic screening strategies in prenatal care.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: September 18, 2024
Screening for Hearing Impairment in Newborns Using Targeted Genomic Sequencing: A Large Pilot Cohort Study.
Journal: Clinical and experimental otorhinolaryngology
Published: September 13, 2024
Neonatal Filaggrin Genetic Screening and Counseling to Prevent Atopic Dermatitis in High-Risk Infants.
Journal: Dermatitis : contact, atopic, occupational, drug
Published: April 02, 2024
Clinical outcomes of fetuses with chromosome 16 short arm copy number variants.
Journal: Molecular genetics & genomic medicine
Published: January 24, 2023
First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome.
Journal: Taiwanese journal of obstetrics & gynecology
Published: November 20, 2020
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia.
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia.
Journal: Scientific reports
Published: December 26, 2019
TP53 alterations in relapsed childhood acute lymphoblastic leukemia.
Journal: Cancer science
Published: September 18, 2019
Fragile X syndrome carrier screening in pregnant women in Chinese Han population.
Journal: Scientific reports
Published: January 29, 2019
Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith-Wiedemann spectrum.
Journal: American journal of medical genetics. Part A
Published: December 24, 2018
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.
Journal: The Journal of pediatrics
Published: December 21, 2017
Last Updated: 09/26/2026