Li‐Ping Tsai - Concepedia

Author

Li‐Ping Tsai

Buddhist Tzu Chi General Hospital ORCID

Also Known As

L P Tsai, L Tsai, L.‐P. Tsai, LI‐PING TSAI, Li-Ping Tsai, Li‐Ping Tsai, Li–Ping Tsai, Shio‐Jean Lin

Publications

774

Citations

H-Index

Concepts

All Affiliations

Buddhist Tzu Chi General Hospital Tzu Chi University Taipei Tzu Chi Hospital National Taiwan University Hospital Mackay Memorial Hospital

About

Li‐Ping Tsai is an author at Buddhist Tzu Chi General Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	238
2	Natural Sciences	2	2	46
3	Public Health	2	2	29
4	Social Sciences	1	1	74
5	Diabetes	1	1	25

Li‐Ping Tsai

Publications

480

Citations

H-Index

Page 1

	Year	Citations
Incidence of severe combined immunodeficiency through newborn screening in a Chinese population Yin‐Hsiu Chien, Shu-Chuan Chiang, Kai‐Ling Chang, Journal of the Formosan Medical Association Primary ImmunodeficiencyMaternal ImmunizationSexual HealthNewborn ScreeningPediatrics	2013	74
Prevalence of theFMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype Ching‐Cherng Tzeng, Li‐Ping Tsai, Wuh‐Liang Hwu, American Journal of Medical Genetics Part A	2005	58
Polysomnographic characteristics in patients with Prader–Willi syndrome Hsiang‐Yu Lin, Ching‐Chi Lin, Li‐Ping Tsai, Pediatric Pulmonology	2007	58
Elevated postvoid residual urine volume predicting recurrence of urinary tract infections in toilet-trained children Shang‐Jen Chang, Li‐Ping Tsai, Chun‐Kai Hsu, Pediatric Nephrology Urinary Tract InfectionsUrologyVoiding DysfunctionUrological ResearchToilet-trained Children	2015	37
Analysis of the CYP21A1P pseudogene: Indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes Li‐Ping Tsai, Ching‐Feng Cheng, Shu-Hua Chuang, Analytical Biochemistry Cyp21a1p PseudogeneNatural SciencesGeneticsGene StructureMolecular Biology	2011	29
Genotype and phenotype in patients with Prader–Willi Syndrome in Taiwan Hsiang‐Yu Lin, Chih‐Kuang Chuang, Ming‐Ren Chen, Acta Paediatrica	2007	28
Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type la Wuh‐Liang Hwu, Shu-Chuan Chuang, Li‐Ping Tsai, Human Molecular Genetics GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	1995	25
Genetic Architecture Associated With Familial Short Stature Ying-Ju Lin, Chi‐Fung Cheng, Chung‐Hsing Wang, The Journal of Clinical Endocrinology & Metabolism Short StatureGeneticsPolygenic RiskGenetic EpidemiologyGenome-wide Association Studies	2020	19
Parenting stress in families of children with Prader–Willi syndrome Shi‐Bing Wong, Tzong‐Shi Wang, Wen‐Hsin Tsai, American Journal of Medical Genetics Part A	2020	19
A Novel 3670-Base Pair Mitochondrial DNA Deletion Resulting in Multi-systemic Manifestations in a Child Hsin-Ming Liu, Li‐Ping Tsai, Yin‐Hsiu Chien, Pediatrics & Neonatology DnaGeneticsMolecular BiologyPathologyMolecular Genetics	2012	17

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