Evidence map›Paper›PMID 40213198›Full record

ReviewAnnals of medicine and surgery (2012)2025

Genomic medicine and personalized treatment: a narrative review.

Adil Khan, Anchal Ramesh Barapatre, Nadir Babar, Joy Doshi, Mohamd Ghaly, Kirtan Ghanshyam Patel, Shayan Nawaz, Uswa Hasana, Swara Punit Khatri, Shilpa Pathange and 4 more

Abstract readReview
In one paragraph

Review in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Genomic Medicine and Individual Autonomy: Reflections on Knowledge Societies and Governmentality.International journal of environmental research and public health · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Adil KhanNowshera Medical College Nowshera, Khyber Pakhtunkhwa, Pakistan.
Anchal Ramesh BarapatreN.K.P Salve Institute of Medical Sciences and Research Centre, Nagpur, India.
Nadir BabarCMH Lahore Medical College, Lahore, Pakistan.
Joy DoshiUniversity Hospital Lewisham, Lewisham & Greenwich NHS Trust, London, United Kingdom.
Mohamd GhalyUniversity of Sharjah, Dubai, United Arab Emirates.
Kirtan Ghanshyam PatelGovernment Medical College, Surat, India.
Shayan NawazUniversity College of Medicine and Dentistry, Lahore, Pakistan.
Uswa HasanaFatima Jinnah Medical University, Lahore, Pakistan.
Swara Punit KhatriGujarat Cancer Society Medical College, Hospital and Research Center, Ahmedabad, India.
Shilpa PathangeSVS Medical College Mahabubnagar, Telangana, India.
Abhinya Reddy PesaruKakatiya Medical College, Warangal, India.
Chaitanya Swaroop PuvvadaGayatri Vidya Parishad Institute of Health Care and Medical Technology, Visakhapatnam, India.
Marium BillooJinnah Sindh Medical University, Karachi, Pakistan.
Usama JamilMedicine, Kabul University, Kabul, Afghanistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic medicine, which integrates genomics and bioinformatics into clinical care and diagnostics, is transforming healthcare by enabling personalized treatment approaches. Advances in technologies such as DNA sequencing, proteomics, and computational power have laid the foundation for individualized therapies that account for genetic variations influencing disease risk, progression, and treatment response. This review explores the historical milestones leading to current applications of genomic medicine, such as targeted therapies, gene therapies, and precision medicine, in fields including cardiovascular diseases, oncology, and rare genetic disorders. It highlights the use of next-generation sequencing and third-generation sequencing to improve diagnostic accuracy and treatment outcomes, emphasizing the role of genomic data in advancing personalized treatments. Furthermore, emerging therapies such as CRISPR/Cas-based genome editing and adeno-associated viral vectors showcase the potential of gene therapy in addressing complex diseases, including rare genetic disorders. Despite promising advancements, challenges remain in fully integrating genomic medicine into routine clinical practice, including cost barriers, data interpretation complexities, and the need for widespread genomic literacy among healthcare professionals. The future of genomic medicine holds transformative potential for revolutionizing the diagnosis, treatment, and management of both common and rare diseases.

Indexed as

cardiologygenomic medicinegenomics

Identifiers

PMID40213198
PMCPMC11981433

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.