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プロフィール詳細
Dr. Akbar S.に依頼
United Kingdom
Haemato-oncology expert with 8+ years in translational research, scientific writing, ISO 15189 and biopharma valuation
プロフィール概要
専門分野
サービス
Writing
Clinical Trial Documentation,
Medical Writing,
Non-Medical Regulatory Writing,
Technical Writing,
Copywriting,
Creative Writing,
Newswriting,
General Proofreading & Editing,
Translation
Research
Market Research,
User Research,
Meta-Research,
Fact Checking,
Gap Analysis,
Gray Literature Search,
Scientific and Technical Research,
Systematic Literature Review,
Secondary Data Collection
Consulting
Business Strategy Consulting,
Go-to-Market Strategy Consulting,
Healthcare Consulting,
Scientific and Technical Consulting
Data & AI
Statistical Analysis,
Image Processing,
Image Analysis,
Data Visualization,
Data Mining
職務経験
University of Oxford
- 現在 ![]()
Postdoctoral Research fellow
The University of Oxford
9月 2022 - 現在
学歴
PhD Medicine
The University of St Andrews
9月 2019 - 9月 2022
MRes Biomedical Sciences
The University of Glasgow
9月 2018 - 8月 2019
BSc (Hons) Applied Biomedical Science
Glasgow Caledonian University
9月 2014 - 5月 2018
認定資格
出版物
JOURNAL ARTICLE
Akbar M. Shahid, William Vainchenker, Stefan N. Constantinescu (2025). JCMM Annual Review on Advances in Biotechnology for the Treatment of Haematological Malignancies: A Review of the Latest In‐Patient Developments 2024–2025 . Journal of Cellular and Molecular Medicine.
Akbar M. Shahid, William Vainchenker, Stefan N. Constantinescu (2025). JCMM Annual Review on Advances in Biotechnology for the Treatment of Haematological Malignancies: A Review of the Latest In‐Patient Developments 2024–2025 . Journal of Cellular and Molecular Medicine.
Tomkova M, McClellan MJ, Crevel G, Shahid AM, Mozumdar N, Tomek J, Shepherd E, Cotterill S, Schuster-Böckler B, Kriaucionis S (2024). Human DNA polymerase ε is a source of C>T mutations at CpG dinucleotides . Nature genetics.
Shahid AM, Um IH, Elshani M, Zhang Y, Harrison DJ (2022). NUC-7738 regulates β-catenin signalling resulting in reduced proliferation and self-renewal of AML cells . PloS one.