Shuan‐Pei Lin

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

Daniela A. Braun, Jia Rao, Géraldine Mollet et al. · Nature Genetics · 2017 · 212 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +5

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera

Chih‐Ping Chen, Schu‐Rern Chern, Jin-Chern Sheu et al. · Prenatal Diagnosis · 2005 · 101 citations

Clinical Features of Ehlers-Danlos Syndrome

Jui‐Lung Yen, Shuan‐Pei Lin, Ming‐Ren Chen et al. · Journal of the Formosan Medical Association · 2006 · 88 citations · Full text

Ehlers-danlos Syndrome, Autoimmune Disease, Diagnosis +4

A pilot newborn screening program for Mucopolysaccharidosis type I in Taiwan

Shuan‐Pei Lin, Hsiang‐Yu Lin, Tuen-Jen Wang et al. · Orphanet Journal of Rare Diseases · 2013 · 83 citations · Full text

Bioavailability and metabolic pharmacokinetics of rutin and quercetin in rats

Cheng Yong Yang, Su‐Lan Hsiu, K.-C. Wen et al. · Journal of Food and Drug Analysis · 2020 · 69 citations · Full text