Lianshu Han

Newborn screening in China: phenylketonuria, congenital hypothyroidism and expanded screening.

Xuefan Gu, Zhiguo Wang, Jun Ye et al. · PubMed · 2008 · 73 citations

Early Diagnosis, Neonatal Screening, Newborn Screening +13

Analysis of genetic mutations in Chinese patients with systemic primary carnitine deficiency

Lianshu Han, Fei Wang, Yu Wang et al. · European Journal of Medical Genetics · 2014 · 31 citations

Genetic Mutations, Mendelian Disorder, Genetic Disorder +9

A new case of malonyl‐CoA decarboxylase deficiency with mild clinical features

Huan Liu, Dongqiong Tan, Lianshu Han et al. · American Journal of Medical Genetics Part A · 2016 · 11 citations

In vitro residual activities in 20 variants of phenylalanine hydroxylase and genotype-phenotype correlation in phenylketonuria patients

Xia Zhang, Jun Ye, Nan Shen et al. · Gene · 2019 · 11 citations

Urology, Inherited Metabolic Disease, Pathology +5