Shengran Liang

发表

Novel phenotypes of NF1 patients from unrelated Chinese families with tibial pseudarthrosis and anemia

S. Banerjee, Dongzhu Lei, Shengran Liang, 2016, Oncotarget.

A novel heterozygous germline deletion in MSH2 gene in a five generation Chinese family with Lynch syndrome.

S. Banerjee, Shengran Liang, B. Wu, 2017, Oncotarget.

A novel pathogenic large germline deletion in adenomatous polyposis coli gene in a Chinese family with familial adenomatous polyposis

S. Banerjee, Shengran Liang, Xipeng Zhang, 2016, Oncotarget.

An LMNB1 Duplication Caused Adult-Onset Autosomal Dominant Leukodystrophy in Chinese Family: Clinical Manifestations, Neuroradiology and Genetic Diagnosis

L. Cui, S. Banerjee, Shengran Liang, 2017, Front. Mol. Neurosci..

A novel pathogenic single nucleotide germline deletion in APC gene in a four generation Chinese family with familial adenomatous polyposis

Guoru Zhao, S. Banerjee, Shengran Liang, 2017, Scientific Reports.

Whole Exome Sequencing Identified a Novel Heterozygous Mutation in HMBS Gene in a Chinese Patient With Acute Intermittent Porphyria With Rare Type of Mild Anemia

S. Banerjee, Shengran Liang, Yongjiang Zheng, 2018, Front. Genet..

Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy‐dystroglycanopathy

Y. Guan, L. Cui, S. Banerjee, 2018, Journal of cellular and molecular medicine.

A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis

Guoru Zhao, S. Banerjee, Shengran Liang, 2017, Oncotarget.

Targeted next generation sequencing identifies two novel mutations in SEPN1 in rigid spine muscular dystrophy 1

Y. Huang, S. Banerjee, Shengran Liang, 2016, Oncotarget.

A novel mutation in NF1 is associated with diverse intra-familial phenotypic variation and astrocytoma in a Chinese family

S. Banerjee, Shengran Liang, Hui Huang, 2016, Journal of Clinical Neuroscience.

Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber’s congenital amaurosis in unrelated Chinese patients

S. Banerjee, Shengran Liang, M. Qi, 2017, Oncotarget.