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

Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disorders

识别人类基因组中不稳定的CNG重复序列位点:一种启发式方法及其对神经系统疾病的意义

Suroliya, Varun; Uppili, Bharathram; Kumar, Manish; Jha, Vineet; Srivastava, Achal K; Faruq, Mohammed

SARS-CoV-2 Lineage Tracking, and Evolving Trends Seen during Three Consecutive Peaks of Infection in Delhi, India: a Clinico-Genomic Study

印度德里连续三次感染高峰期间SARS-CoV-2谱系追踪及演变趋势:一项临床基因组学研究

Gautam, Pramod; Paul, Diptanu; Suroliya, Varun; Garg, Rahul; Agarwal, Reshu; Das, Santanu; Kaur, Urvinder S; Pandey, Amit; Bhugra, Arjun; Tarai, Bansidhar; Bihari, Chhagan; Sarin, S K; Gupta, Ekta

Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.

印度人群共济失调的遗传学:来自常用基因筛查工具的综合见解

Sharma Pooja, Sonakar Akhilesh Kumar, Tyagi Nishu, Suroliya Varun, Kumar Manish, Kutum Rintu, Asokchandran Vivekananda, Ambawat Sakshi, Shamim Uzma, Anand Avni, Ahmad Ishtaq, Shakya Sunil, Uppili Bharathram, Mathur Aradhana, Parveen Shaista, Jain Shweta, Singh Jyotsna, Seth Malika, Zahra Sana, Joshi Aditi, Goel Divya, Sahni Shweta, Kamai Asangla, Wadhwa Saruchi, Murali Aparna, Saifi Sheeba, Chowdhury Debashish, Pandey Sanjay, Anand Kuljeet Singh, Narasimhan Ranganathan Lakshmi, Laskar Sanghamitra, Kushwaha Suman, Kumar Mukesh, Shaji Cheruvallill Velayudhan, Srivastava Madakasira Vasantha Padma, Srivastava Achal K, Faruq Mohammed

Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the SAMD12 gene

对印度南部某社区患有常染色体显性遗传性皮质震颤、肌阵挛和癫痫的患者进行基因组分析表明,SAMD12基因中存在创始人重复序列扩增突变。

Mahadevan, Radha; Bhoyar, Rahul C; Viswanathan, Natarajan; Rajagopal, Raskin Erusan; Essaki, Bobby; Suroliya, Varun; Chelladurai, Rachel; Sankaralingam, Saravanan; Shanmugam, Ganesan; Vayanakkan, Sriramakrishnan; Shamim, Uzma; Mathur, Aradhana; Jain, Abhinav; Imran, Mohamed; Faruq, Mohammed; Scaria, Vinod; Sivasubbu, Sridhar; Kalyanaraman, Shantaraman

Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population

脊髓小脑性共济失调10型(SCA10):突变分析和基于常见单倍型的推断表明其在印度人群中较为罕见

Goel, Divya; Suroliya, Varun; Shamim, Uzma; Mathur, Aradhna; Faruq, Mohammed

Tumor necrosis factor-alpha (- 308G/A, + 488G/A, - 857C/T and -1031 T/C) gene polymorphisms and risk of ischemic stroke in north Indian population: A hospital based case-control study

肿瘤坏死因子-α(-308G/A、+488G/A、-857C/T 和 -1031T/C)基因多态性与印度北部人群缺血性卒中风险的关系:一项基于医院的病例对照研究

Kumar, Pradeep; Kumar, Amit; Misra, Shubham; Sagar, Ram; Faruq, Mohammad; Suroliya, Varun; Vivekanandhan, Subiah; Srivastava, Achal Kumar; Prasad, Kameshwar