Mohamed Imran

ORCID: 0000-0003-4855-3504
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About
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Research Areas
  • SARS-CoV-2 and COVID-19 Research
  • Genomics and Rare Diseases
  • Cardiac electrophysiology and arrhythmias
  • Animal Virus Infections Studies
  • Viral gastroenteritis research and epidemiology
  • Immunodeficiency and Autoimmune Disorders
  • Pharmacogenetics and Drug Metabolism
  • COVID-19 Clinical Research Studies
  • Blood groups and transfusion
  • COVID-19 epidemiological studies
  • Vaccine Coverage and Hesitancy
  • Lipoproteins and Cardiovascular Health
  • Computational Drug Discovery Methods
  • vaccines and immunoinformatics approaches
  • Cancer, Lipids, and Metabolism
  • CRISPR and Genetic Engineering
  • SARS-CoV-2 detection and testing
  • Esophageal Cancer Research and Treatment
  • BRCA gene mutations in cancer
  • Viral Infections and Immunology Research
  • Plant Virus Research Studies
  • Genetic Associations and Epidemiology
  • Chronic Lymphocytic Leukemia Research
  • Genetic factors in colorectal cancer
  • Blood disorders and treatments

Academy of Scientific and Innovative Research
2020-2025

Institute of Genomics and Integrative Biology
2020-2025

Ysbyty Gwynedd Hospital NHS Trust
2021

Council of Scientific and Industrial Research
2020-2021

Fortis Memorial Research Institute
2020

National Institute of Biomedical Genomics
2020

University of Veterinary and Animal Sciences
2019

Delhi, the national capital of India, experienced multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) outbreaks in 2020 and reached population seropositivity >50% by 2021. During April 2021, city became overwhelmed COVID-19 cases fatalities, as a new variant, B.1.617.2 (Delta), replaced B.1.1.7 (Alpha). A Bayesian model explains growth advantage Delta through combination increased transmissibility reduced sensitivity to immune responses generated against earlier variants...

10.1126/science.abj9932 article EN cc-by Science 2021-10-15

The rapid emergence of coronavirus disease 2019 (COVID-19) as a global pandemic affecting millions individuals globally has necessitated sensitive and high-throughput approaches for the diagnosis, surveillance, determining genetic epidemiology SARS-CoV-2. In present study, we used COVIDSeq protocol, which involves multiplex-PCR, barcoding, sequencing samples detection deciphering We approach on 752 clinical in duplicates, amounting to total 1536 could be sequenced single S4 flow cell NovaSeq...

10.1371/journal.pone.0247115 article EN cc-by PLoS ONE 2021-02-17

With the advent of next-generation sequencing, large-scale initiatives for mining whole genomes and exomes have been employed to better understand global or population-level genetic architecture. India encompasses more than 17% world population with extensive diversity, but is under-represented in sequencing datasets. This gave us impetus perform analyze genome 1029 healthy Indian individuals under pilot phase 'IndiGen' program. We generated a compendium 55,898,122 single allelic variants...

10.1093/nar/gkaa923 article EN cc-by-nc Nucleic Acids Research 2020-10-22

Abstract Delhi, the national capital of India, has experienced multiple SARS-CoV-2 outbreaks in 2020 and reached a population seropositivity over 50% by 2021. During April 2021, city became overwhelmed COVID-19 cases fatalities, as new variant B.1.617.2 (Delta) replaced B.1.1.7 (Alpha). A Bayesian model explains growth advantage Delta through combination increased transmissibility partial reduction immunity elicited prior infection (median estimates; ×1.5-fold, 20% reduction). Seropositivity...

10.1101/2021.06.02.21258076 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2021-06-03

Reinfection of SARS-CoV-2 is an apparently rare entity and only a few cases have been reported from across the world with genetic characterization virus, differentiating reinfection persistent virus shedding. These cases, therefore, provide unique insights into long term protective immunity to SARS-CoV-2. The earlier reports suggest that patients were symptomatic in either one or both episodes infection. Here we report case asymptomatic two healthcare workers India identified routine...

10.31219/osf.io/4fmrg preprint EN 2020-09-15

In the last few months, there has been a global catastrophic outbreak of severe acute respiratory syndrome disease caused by novel coronavirus SARS-CoV-2 affecting millions people worldwide. Early diagnosis and isolation are key to contain rapid spread virus. Towards this goal, we report simple, sensitive method detect virus using targeted mass spectrometric approach, which can directly presence from naso-oropharyngeal swabs. Using multiple reaction monitoring two peptides specific in 2.3...

10.1007/s42485-020-00044-9 article EN other-oa Journal of Proteins and Proteomics 2020-08-31

Abstract During the course of COVID-19 pandemic, large-scale genome sequencing SARS-CoV-2 has been useful in tracking its spread and identifying variants concern (VOC). Viral host factors could contribute to variability within a that can be captured next-generation reads as intra-host single nucleotide variations (iSNVs). Analysing 1347 samples collected till June 2020, we recorded 16 410 iSNV sites throughout genome. We found ∼42% reported SNVs by 30 September 2020 consensus sequences...

10.1093/nar/gkab1297 article EN cc-by Nucleic Acids Research 2022-01-13

Introduction Genetic variants contribute to differential responses non-insulin antidiabetic drugs (NIADs), and consequently variable plasma glucose control. Optimal control of is paramount minimizing type 2 diabetes-related long-term complications. India’s distinct genetic architecture its exploding burden diabetes warrants a population-specific survey NIAD-associated pharmacogenetic (PGx) variants. The recent availability large-scale whole genomes from the Indian population provides unique...

10.1136/bmjdrc-2023-003769 article EN cc-by BMJ Open Diabetes Research & Care 2024-03-01

Abstract Emerging reports of SARS‐CoV‐2 breakthrough infections entail methodical genomic surveillance for determining the efficacy vaccines. This study elaborates analysis isolates from following vaccination with AZD1222/Covishield and BBV152/Covaxin. Variants concern B.1.617.2 B.1.1.7 responsible cases surge in April–May 2021 Delhi, were predominant lineages among infections.

10.1002/jmv.27461 article EN Journal of Medical Virology 2021-11-17
James Bundred Sivesh K. Kamarajah K Siaw-Acheampong Dmitri Nepogodiev B. Jefferies and 95 more Pritam Singh Richard Evans Ewen A. Griffiths Derek Alderson James Gossage S McKay Mohamed Imran Richard van Hillegersberg Ravinder Vohra Kasun Wanigsooriya Tony Whitehouse Aleksandras Bagajevas Abebe Bekele Ruth Blanco‐Colino Anna Da Roit Jihene El Kafsi‐Mawley Arben Gjata Ines Gockel Raul Guevara Castro Tomáš Haruštiak Po‐Kuei Hsu Arda Işık Aristotelis Kechagias Andrew Kennedy Biniam Kidane Hans Alexander Mahendran Loreli Mejia J Moreno Ionuț Negoi Azagra Juan Santiago Raza Sayyed Paul M. Schneider António Sampaio Soares Mariana S. Sousa Flávio Roberto Takeda Stephanie Vanstraten Bengt Wallner Bas P. L. Wijnhoven Michael Patrick Achiam Tita Agustin Ali Akbar Ahmad Al‐Bahrani Waleed Al‐Khyatt Markus Albertsmeier Essa AlGhunaim Bilal Alkhaffaf William Allum Fernando Am Nelson Adami Andreollo Andrew Arndt Richard Babor José Pedro Barbosa Romeo Bardini Duncan Beardsmore Grant Beban António Bernardes Richard Berrisford Alessandro Bianchi Miloš Bjelović Alex Boddy Ciprian Bolca Luigi Bonavina Gavin Bryce Richard Byrom Rui Casaca David Chan Alexandros Charalabopoulos Edward Cheong Franco Ciotola Elif Çolak Chris Collins S Constantinoiu Rita Costa Marc H. Dahlke Gail Darling Kahled Dawas Giovanni De Manzoni Adel Denewer Michael Devadas Simon Dexter Sarunas Dikinis Dimitrios Theodorou James P. Dolan Cuong Duong Jan‐Hendrik Egberts Y Elgharably Muhammed Elhadi S. Elmahi Fernando Amézquita Farias Enver Fekaj Jesús Fernández Matthew Forshaw José Paulo Freire Daniel French Goran Gačevski

10.1007/s00268-019-05080-1 article EN World Journal of Surgery 2019-07-22

Ever since the breakout of COVID-19 disease, ceaseless genomic research to inspect epidemiology and evolution pathogen has been undertaken globally. Large scale viral genome sequencing analysis have uncovered functional impact numerous genetic variants in disease pathogenesis transmission. Emerging evidence mutations spike protein domains escaping antibody neutralization is reported. We built a database with precise collation manually curated SARS-CoV-2 from literature potential escape...

10.1093/nar/gkab895 article EN Nucleic Acids Research 2021-10-10

Ethnic differences in pharmacogenomic (PGx) variants have been well documented literature and could significantly impact variability response adverse events to therapeutics. India is a large country with diverse ethnic populations of distinct genetic architecture. India's national genome sequencing initiative (IndiGen) provides unique opportunity explore the landscape PGx using population-scale whole sequences. We analyzed IndiGen variation dataset (N = 1029 genomes) along global population...

10.1111/cts.13153 article EN Clinical and Translational Science 2022-03-26

Abstract The rapid emergence of coronavirus disease 2019 (COVID-19) as a global pandemic affecting millions individuals globally has necessitated sensitive and high-throughput approaches for the diagnosis, surveillance determining genetic epidemiology SARS-CoV-2. In present study, we used COVIDSeq protocol, which involves multiplex-PCR, barcoding sequencing samples detection deciphering We approach on 752 clinical in duplicates, amounting to total 1536 could be sequenced single S4 flow cell...

10.1101/2020.08.10.242677 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2020-08-10

Abstract Many antibody and immune escape variants in SARS-CoV-2 are now documented literature. The availability of genome sequences enabled us to investigate the occurrence genetic epidemiology globally. Our analysis suggests that a number associated with have emerged global populations.

10.1101/2020.12.24.424332 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-12-26

Coronavirus disease 2019 (COVID-19) rapidly spread from a city in China to almost every country the world, affecting millions of individuals. The rapid increase COVID-19 cases state Kerala India has necessitated understanding SARS-CoV-2 genetic epidemiology. We sequenced 200 samples patients using COVIDSeq protocol amplicon-based sequencing. analysis identified 166 high-quality single-nucleotide variants encompassing four novel and 89 new Indian isolated SARS-CoV-2. Phylogenetic haplotype...

10.3389/fgene.2021.630542 article EN cc-by Frontiers in Genetics 2021-03-17

Sequencing of SARS-CoV-2 genomes is crucial for understanding the genetic epidemiology COVID-19 pandemic. It also critical evolution virus and rapid development diagnostic tools. The present protocol a modification Illumina COVIDSeq test. We describe an amplicon-based next-generation sequencing approach with short turnaround time, adapted bench-top sequencers like MiSeq, iSeq, MiniSeq. For complete details on use execution this protocol, please refer to Bhoyar et al. (2021).

10.1016/j.xpro.2021.100755 article EN cc-by-nc-nd STAR Protocols 2021-08-02

Emerging reports of SARS-CoV-2 breakthrough infections entail methodical genomic surveillance for determining efficacy vaccines. This study elaborates analysis isolates from following vaccination with AZD1222/Covishield and BBV152/Covaxin.Variants concern B.1.617.2 B.1.1.7 responsible cases surge in April-May 2021 Delhi, were the predominant lineages among infections.

10.31219/osf.io/fgd4x preprint EN 2021-06-03
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