OOIR: Observatory of International Research

Papers

(The TQCC of Personalized Medicine is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-08-01 to 2025-08-01.)

Article	Citations
The Integration of Personalized Medicine Into Health Systems: Progress and a Path Forward	58
Pharmacogenomics education in China and the United States: advancing personalized medicine	29
Microsatellite Instability Testing in Colorectal Patients with Lynch Syndrome: Lessons Learned from a Case Report and How to Avoid Such Pitfalls	20
Genetic Predisposition for the Development of Lamotrigine-Induced Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis: a Systematic Review and Meta-Analysis	17
An evidence gap map of the personalized medicine in bladder cancer	15
miR-559 rs58450758 polymorphism is associated with colorectal cancer risk and prognosis in Chinese Han population	14
The Pharmacogenetics of Mycophenolate Mofetil in Tunisian Renal Transplant Patients	14
Application of Transcriptomics and Proteomics in Pulmonary Arterial Hypertension	12
Developing the Workplace Learning Social System: considerations for genomics implementation and workforce preparedness	12
Perceived understanding and psychosocial outcomes: employees’ responses to learning results of workplace genetic testing	9
The interplay between pharmacogenetics, concomitant drugs and blood levels of amitriptyline and its main metabolites	8
Association between IL-6, miRNA-146a, MALAT1 genetic polymorphisms and risk of rheumatoid arthritis	8
A scoping review of the cost-effectiveness of precision treatment in chronic lymphocytic leukemia	8
Personalized approach in arrhythmology by genetic-based data: a case report	8
Precision acute medical care through “-omic” analyses: a scoping review	8
Prevalence of Protective Haplotypes of the SLCO1B1 Gene for Statin Transport in Mexican Populations	8
Refining Personalized Diagnosis, Treatment and Exploitation of Hypothyroidism Related to Solid Nonthyroid Cancer	8
Mutational signatures in appendiceal adenocarcinomas: potential for future personalization in hyperthermic intraperitoneal chemotherapy?	8
The rs2275738 variant of the adiponectin receptor 1 gene is associated with biopsy-proven nonalcoholic fatty liver disease	8
How can we address the uncertainties regarding the potential clinical utility of polygenic score-based tests?	7
miR-938 rs2505901 T>C Polymorphism Increases Hirschsprung Disease Risk: A Case–Control Study of Chinese Children	7
Enhancing Parkinson’s disease prediction using meta-heuristic optimized machine learning models	7
The effect of RNLS gene polymorphisms on preeclampsia susceptibility: a meta-analysis study	7
Welcome to the 19th Volume of Personalized Medicine	6
Knowledge, attitudes and practice regarding pharmacovigilance and adverse drug reaction reporting among physicians and pharmacists in Egypt: a step toward personalized medicine implementation	6

Precision medicine activities and opportunities for shaping maternal and neonatal health in Qatar	6
Role of precision nutrition in improving military performance	6
Omics Technologies in Personalized Combination Therapy for Cardiovascular Diseases: Challenges and Opportunities	6
The Frequency of Major CYP2C19 Genetic Polymorphisms in Women of Asian, Native Hawaiian and Pacific Islander Subgroups	6
Gene expression profiling of peripheral blood in patients with steroid-induced osteonecrosis of the femoral head	5
Cost–effectiveness of extended DPYD testing before fluoropyrimidine chemotherapy in metastatic breast cancer in the UK	5
Looking Back Over 2023 and Welcome to the 21 ^st Issue of Personalized Medicine	5
A Personalized Approach to Pancreatic Ductal Adenocarcinoma and its Application in Surgical Practice	5
Cloud-based Digital Healthcare Development for Precision Medical Hospital Information System	5
Cost–effectiveness and budget impact analysis of screening strategies for maturity-onset diabetes of the young in three European countries	5
Development of Competency-based Online Genomic Medicine Training (COGENT)	5
Regional disparities in access to gene therapies in the European Union, the United States, Japan, and China	5
Identification of Dpyd Variants and Estimation of Uracil and Dihydrouracil in A Healthy Indian Population	5
Identification of novel variants of XPA and POLH/XPV genes in xeroderma pigmentosum patients in Vietnam	5
Low Rate of Complications in Nipple-Sparing Mastectomy for Patients with BRCA1 and BRCA2 Mutation	4
The Use of Molecular Biomarker Tests: An Interview Study with Healthcare Providers about a Molecular Biomarker Test for Prostate Cancer	4
Clinical Significance of Serum miR-101-3p Expression in Patients with Neonatal Sepsis	4
Association of miR-21 gene polymorphisms with cognitive function in patients with systemic lupus erythematosus	4
Diagnostic Utility of the 23-gene Expression Profile Test for an Atypical Intradermal Melanocytic Proliferation	4
Whole-exome sequencing reveals novel variants associated with abnormal uterine bleeding caused by copper intrauterine device	4
HEcoPerMed, Personalized Medicine from a Health Economic Perspective: Lessons Learned and Potential Opportunities Ahead	4
Recent Advances in Personalized Cancer Immunotherapy with Immune Checkpoint Inhibitors, T Cells and Vaccines	4
Genomics and the early diagnosis of lung cancer	4
Exploring the usefulness of plasma level determination and pharmacogenetics for patients treated with clozapine	4
A Real-World Analysis of Tyrosine Receptor Kinase Inhibitor-Related Toxicities in Cancer Treatment	4
Evaluation of pharmacogenomic information in drug labeling: a case study from Jordan	4