Yi‐Ning Su

East China University of Science and Technology — China

Medicine · Health Sciences

34h-index4.0kcitations213works0.82yr avg
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Research Topics

Prenatal Screening and Diagnostics(56), Genomic variations and chromosomal abnormalities(39), RNA modifications and cancer(15), Congenital Anomalies and Fetal Surgery(15), Connective tissue disorders research(14)

Publications213 total

Material hardship, not household income, predicts impaired punishment learning: a computational reinforcement learning perspective
Frontiers in Psychology·2025Open Access
Parental involvement and school engagement reduce adolescent aggressive behaviors: a three wave cross-lagged model
Frontiers in Public Health·2025· 2 citedOpen Access
Operationalizing Microaffirmations for Queer and Transgender People of Color
The Professional Counselor·2025Open Access
Construction of a self-assembled duplexed aptasensor for the simultaneous detection of haemoglobin and glycated haemoglobin
Sensors & Diagnostics·2025· 2 citedOpen Access
Neonatal Filaggrin Genetic Screening and Counseling to Prevent Atopic Dermatitis in High-Risk Infants
Dermatitis·2024
The effects of a Journey of the Brave Counseling Program on anxiety, well-being, and life adjustment in Taiwanese children
BMC Psychiatry·2023Open Access
Clinical outcomes of fetuses with chromosome 16 short arm copy number variants
Molecular Genetics & Genomic Medicine·2023· 11 citedOpen Access
The Effects of a Journey of the Brave Counseling Program on Anxiety, Well-Being, and Life Adjustment in Taiwanese Children
Research Square (Research Square)·2023Open Access
Clinical outcomes of fetuses with chromosome 16 short arm copy number variants
2022Open Access
First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome
Taiwanese Journal of Obstetrics and Gynecology·2022· 3 citedOpen Access
The Prenatal Diagnosis and Clinical Outcomes of Fetuses With 15q11.2 Copy Number Variants: A Case Series of 36 Patients
Frontiers in Medicine·2021· 7 citedOpen Access
Applying the ICF-CY framework to examine biological and environmental factors in early childhood development
UNC Libraries·2021· 1 citedOpen Access
The prenatal diagnosis and clinical outcomes of fetuses with 15q11.2 copy number variants: a case series of 36 patients
2021Open Access
<i>TP53</i> alterations in relapsed childhood acute lymphoblastic leukemia
Cancer Science·2019· 35 citedOpen Access
Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum
American Journal of Medical Genetics Part A·2019· 7 cited
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan
The Journal of Pediatrics·2018· 37 cited
Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan
PLoS ONE·2017· 5 citedOpen Access
Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan
PLoS ONE·2017· 43 citedOpen Access
Carbetocin in prevention of postpartum hemorrhage: Experience in a tertiary medical center of Taiwan
Taiwanese Journal of Obstetrics and Gynecology·2016· 20 citedOpen Access
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion
Taiwanese Journal of Obstetrics and Gynecology·2016· 8 citedOpen Access
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Frequent Co-authors

Wu‐Shiun Hsieh(15), Chien‐Nan Lee(14), Chia‐Cheng Hung(12), Chih‐Ping Chen(10), Wen‐Fang Cheng(9), Pau‐Chung Chen(8), Po‐Nien Tsao(8), Suh‐Fang Jeng(7), Chi‐An Chen(7), Wayseen Wang(7), Hua‐Fang Liao(6), Chia‐Jung Hsieh(6), Fon‐Jou Hsieh(6), Shu‐Chen Wei(6), Shin‐Yu Lin(6), Schu‐Rern Chern(5), Yu‐Ting Chang(4), Ming‐Chu Chang(4), Chang‐Yao Hsieh(4), Hung‐Chieh Chou(4)