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Issue Date	Title	Author(s)	Source	scopus	WOS
2019	Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgia	Huang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Kuo C.-C.	Scientific Reports	2	10
2019	Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgia	Huang C.-W.; Lai H.-J.; Huang P.-Y.; Lee M.-J.; Chung-Chin Kuo	Scientific Reports	2	10
2004	The association between transforming growth factor-β gene promoter C-509T polymorphism and Chinese children with Henoch-Sch?nlein purpura	YAO-HSU YANG ; Lai H.-J.; Kao C.-K.; Lin Y.-T.; Chiang B.-L.	Pediatric Nephrology	36	30
2004	The association between transforming growth factor-β gene promoter C-509T polymorphism and Chinese children with Henoch-Sch?nlein purpura	Yang Y.-H.; Lai H.-J.; Kao C.-K.; YU-TSAN LIN ; Chiang B.-L.	Pediatric Nephrology	36	30
2004	The association between transforming growth factor-β gene promoter C-509T polymorphism and Chinese children with Henoch-Sch?nlein purpura	Yang Y.-H.; Lai H.-J.; Kao C.-K.; Lin Y.-T.; BOR-LUEN CHIANG	Pediatric Nephrology		30
2016	The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia	Huang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Kuo C.-C.	PLoS Biology		4
2016	The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia	Huang C.-W.; Lai H.-J.; Huang P.-Y.; Lee M.-J.; Chung-Chin Kuo	PLoS Biology	5	4
2020	Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser	Lai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; MING-JEN LEE ; Hsieh S.-T.; Chao C.-C.; Yang C.-C.	Journal of the Formosan Medical Association	5	5
2020	Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser	Lai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; Lee M.-J.; Hsieh S.-T.; CHI-CHAO CHAO ; Yang C.-C.	Journal of the Formosan Medical Association	5	5
2020	Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser	Lai H.-J.; Huang K.-C.; Liang Y.-C.; KUO-LIONG CHIEN ; Lee M.-J.; Hsieh S.-T.; Chao C.-C.; Yang C.-C.	Journal of the Formosan Medical Association		5
2019	Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser	Lai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; Lee M.-J.; SUNG-TSANG HSIEH ; Chao C.-C.; Yang C.-C.	Journal of the Formosan Medical Association	2	4
2020	Changes of resurgent Na+ currents in the Nav1.4 channel resulting from an SCN4A mutation contributing to sodium channel myotonia	Huang C.-W.; Lai H.-J.; Lin P.-C.; MING-JEN LEE	International Journal of Molecular Sciences	2	3
2004	Dendritic cells modulated by cytokine-expressing adenoviruses alleviate eosinophilia and airway hyperresponsiveness in an animal model of asthma	Ye Y.-L.; Lee Y.-L.; Chuang Z.-J.; Lai H.-J.; Chen C.-C.; Tao M.-H.; BOR-LUEN CHIANG	Journal of Allergy and Clinical Immunology		10
2012	Early-onset autosomal-recessive parkinsonian-pyramidal syndrome	Lai H.-J.; CHIN-HSIEN LIN ; Wu R.-M.	Acta Neurologica Taiwanica		0
2012	Efficacy, safety and tolerability of ongoing statin plus ezetimibe versus doubling the ongoing statin dose in hypercholesterolemic Taiwanese patients: An open-label, randomized clinical trial	Yu C.-C.; Lai W.-T.; Shih K.-C.; Lin T.-H.; Lu C.-H.; Lai H.-J.; Hanson M.E.; HWANG, JUEY-JEN	BMC Research Notes		0
2012	Efficacy, safety and tolerability of ongoing statin plus ezetimibe versus doubling the ongoing statin dose in hypercholesterolemic Taiwanese patients: An open-label, randomized clinical trial	CHIH-CHIEH YU ; Lai W.-T.; Shih K.-C.; Lin T.-H.; Lu C.-H.; Lai H.-J.; Hanson M.E.; Hwang J.-J.	BMC Research Notes		0
2020	Electrophysiological parameters that contribute to the pathogenesis of familial amyloid polyneuropathy caused by transthyretin mutations	Lai H.-J.; Lai W.-T.; Jin L.; Kuo K.-T.; MING-JEN LEE	Journal of the Neurological Sciences	1	1
2020	Electrophysiological parameters that contribute to the pathogenesis of familial amyloid polyneuropathy caused by transthyretin mutations	Lai H.-J.; Lai W.-T.; Jin L.; KUAN-TING KUO ; Lee M.-J.	Journal of the Neurological Sciences		1
2021	An electrophysiological perspective on Parkinson’s disease: symptomatic pathogenesis and therapeutic approaches	Lee L.-H.N.; Huang C.-S.; Chuang H.-H.; Lai H.-J.; Yang C.-K.; Yang Y.-C.; CHUNG-CHIN KUO	Journal of Biomedical Science		0
2017	Frail phenotype is associated with distinct quantitative electroencephalographic findings among end-stage renal disease patients: An observational study	Chao C.-T.; Lai H.-J.; Tsai H.-B.; Yang S.-Y.; JENQ-WEN HUANG	BMC Geriatrics		7

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