Santasree Banerjee

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Venues

Journal of cellular and molecular medicine

The application of clinical genetics

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Nan Du, Xiaolei Wang, Zhaohui Wang, Hongwei Liu, Hui Liu, Hongfang Duan, Shaozhi Zhao, Santasree Banerjee, Xinwen Zhang
Identification of a Novel Homozygous Mutation in MTMR2 Gene Causes Very Rare Charcot-Marie-Tooth Disease Type 4B1. The application of clinical genetics 17 (2024)
Nan Du, Xiaolei Wang, Zhaohui Wang, Hongwei Liu, Hui Liu, Hongfang Duan, Shaozhi Zhao, Santasree Banerjee, Xinwen Zhang
Identification of a Novel Homozygous Mutation in MTMR2 Gene Causes Very Rare Charcot-Marie-Tooth Disease Type 4B1. The application of clinical genetics 17 (2024)
Peng Han, Guohong Wei, Ke Cai, Xi Xiang, Wang Ping Deng, Yan Bing Li, Shan Kuang, Zhanying Dong, Tianyu Zheng, Yonglun Luo, Junnian Liu, Yuanning Guan, Chen Li, Subrata Kumar Dey, Zhihong Liao, Santasree Banerjee
Identification and functional characterization of mutations in LPL gene causing severe hypertriglyceridaemia and acute pancreatitis. Journal of cellular and molecular medicine 24 (2) (2020)
Rui Zhang, Shaoyun Chen, Peng Han, Fangfang Chen, Shan Kuang, Zhuo Meng, Junnian Liu, Ruliang Sun, Zhiwei Wang, Xiaohong He, Yong Li, Yuanning Guan, Zhengfang Yue, Chen Li, Subrata Kumar Dey, Yuanfang Zhu, Santasree Banerjee
Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome. Journal of cellular and molecular medicine 24 (2) (2019)
Jianchao Zheng, Hongyun Zhang, Santasree Banerjee, Yun Li, Junyu Zhou, Qian Yang, Xuemei Tan, Peng Han, Qinmei Fu, Xiaoli Cui, Yuying Yuan, Meiyan Zhang, Ruiqin Shen, Haifeng Song, Xiuqing Zhang, Lijian Zhao, Zhiyu Peng, Wei Wang, Ye Yin
A comprehensive assessment of Next-Generation Sequencing variants validation using a secondary technology. Molecular genetics & genomic medicine 7 (7) (2019)
Yi Dai, Shengran Liang, Xue Dong, Yanhuan Zhao, Haitao Ren, Yuzhou Guan, Haifang Yin, Chen Li, Lin Chen, Liying Cui, Santasree Banerjee
Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy. Journal of cellular and molecular medicine 23 (2) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Santasree Banerjee