日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Dissecting trophoblastic heterogeneity in abnormal pregnancy: Insights from comparative analysis of twin-pregnancy with hydatidiform mole and coexisting live fetus

剖析异常妊娠中滋养层细胞的异质性：来自葡萄胎合并活胎双胎妊娠比较分析的启示

期刊:Genes and Diseases
影响因子:
doi:10.1016/j.gendis.2025.101651
Li, Chen; Chen, Jiandong; Wu, Hao; Zhang, Songfa; Yu, Na; Chen, Zhiang; Lu, Bingjian; Banerjee, Santasree; Lu, Weiguo; Qin, Jiale
细胞生物学
发表日期：2026
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Identification and functional characterization of a novel Acinetobacter pittii bacteriophage-encoded depolymerase

对一种新型鲍氏不动杆菌噬菌体编码的解聚酶进行鉴定和功能表征

期刊:Frontiers in Cellular and Infection Microbiology
影响因子:4.8
doi:10.3389/fcimb.2025.1608526
Zhang, Na; Li, Wei; Du, Xue; Daniyal, Danish; Feng, Meng-Ai; Xu, Jiaoyang; Yang, Ziqin; Jiang, Hailin; Sheraz, Muhammad; Huang, Honglan; Banerjee, Santasree; Shi, Hongyan
发表日期：2025
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Correction: Identification and functional characterization of a novel Acinetobacter pittii bacteriophage-encoded depolymerase

更正：鉴定和功能表征一种新型的皮氏不动杆菌噬菌体编码的解聚酶

期刊:Frontiers in Cellular and Infection Microbiology
影响因子:4.8
doi:10.3389/fcimb.2025.1722705
Zhang, Na; Li, Wei; Du, Xue; Daniyal, Danish; Feng, Meng-Ai; Xu, Jiaoyang; Yang, Ziqin; Jiang, Hailin; Sheraz, Muhammad; Huang, Honglan; Banerjee, Santasree; Shi, Hongyan
发表日期：2025
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Genetic variants of SLC6A4 and risk of coronary artery disease: insights from North Indian population

SLC6A4基因变异与冠状动脉疾病风险：来自北印度人群的启示

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-03761-w
Raina, Jyotdeep Kour; Sharma, Minakashee; Sharma, Ravi; Bhardwaj, Rohit; Kumar, Parvinder; Banerjee, Santasree; Panjaliya, Rakesh Kumar
发表日期：2025
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Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the SPTB gene that causes hereditary spherocytosis with hemolytic anemia.

病例报告：SPTB 基因中一种新的杂合剪接供体 (c.647+1G>A) 位点突变的鉴定和功能表征，该突变导致遗传性球形红细胞症伴溶血性贫血。

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2025.1626155
Cao Ke, Luo Xiaojuan, Liu Lianlian, Mao Xiaoning, Liu Ruping, Chen Yunsheng, Banerjee Santasree
红细胞
细胞生物学
贫血
代谢
发表日期：2025
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Identification of a Novel Homozygous Mutation in MTMR2 Gene Causes Very Rare Charcot-Marie-Tooth Disease Type 4B1

MTMR2基因中一种新的纯合突变的发现导致非常罕见的夏科-马里-图斯病4B1型

期刊:Application of Clinical Genetics
影响因子:2.8
doi:10.2147/TACG.S448084
Du, Nan; Wang, Xiaolei; Wang, Zhaohui; Liu, Hongwei; Liu, Hui; Duan, Hongfang; Zhao, Shaozhi; Banerjee, Santasree; Zhang, Xinwen
发表日期：2024
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Editorial: Developmental delay and intellectual disability

社论：发育迟缓和智力障碍

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2022.934815
Banerjee, Santasree; Munshi, Anjana; Li, Chen; Ayub, Muhammad
发育与干细胞
发表日期：2022
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KVarPredDB: a database for predicting pathogenicity of missense sequence variants of keratin genes associated with genodermatoses

KVarPredDB：一个用于预测与遗传性皮肤病相关的角蛋白基因错义序列变异致病性的数据库。

期刊:Human Genomics
影响因子:4.3
doi:10.1186/s40246-020-00295-z
Ying, Yuyi; Lu, Lu; Banerjee, Santasree; Xu, Lizhen; Zhao, Qiang; Wu, Hao; Li, Ruiqi; Xu, Xiao; Yu, Hua; Neculai, Dante; Xi, Yongmei; Yang, Fan; Qin, Jiale; Li, Chen
发表日期：2020
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Identification and functional characterization of mutations in LPL gene causing severe hypertriglyceridaemia and acute pancreatitis

鉴定和功能表征导致严重高甘油三酯血症和急性胰腺炎的LPL基因突变

期刊:Journal of Cellular and Molecular Medicine
影响因子:4.2
doi:10.1111/jcmm.14768
Han, Peng; Wei, Guohong; Cai, Ke; Xiang, Xi; Deng, Wang Ping; Li, Yan Bing; Kuang, Shan; Dong, Zhanying; Zheng, Tianyu; Luo, Yonglun; Liu, Junnian; Guan, Yuanning; Li, Chen; Dey, Subrata Kumar; Liao, Zhihong; Banerjee, Santasree
胰腺炎
发表日期：2020
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Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy

全外显子组测序在一例罕见、轻度、晚发性肌营养不良-肌糖蛋白病患者中发现了一种新的DAG1基因突变。

期刊:Journal of Cellular and Molecular Medicine
影响因子:4.2
doi:10.1111/jcmm.13979
Dai, Yi; Liang, Shengran; Dong, Xue; Zhao, Yanhuan; Ren, Haitao; Guan, Yuzhou; Yin, Haifang; Li, Chen; Chen, Lin; Cui, Liying; Banerjee, Santasree
DAG1
发表日期：2019
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