OOIR: Observatory of International Research

Papers

(The TQCC of Personalized Medicine is 3. 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 2022-08-01 to 2026-08-01.)

Article	Citations
Application of Transcriptomics and Proteomics in Pulmonary Arterial Hypertension	17
Developing the Workplace Learning Social System: considerations for genomics implementation and workforce preparedness	17
A scoping review of the cost-effectiveness of precision treatment in chronic lymphocytic leukemia	15
Perceived understanding and psychosocial outcomes: employees’ responses to learning results of workplace genetic testing	15
Pharmacogenomics education in China and the United States: advancing personalized medicine	13
miR-559 rs58450758 polymorphism is associated with colorectal cancer risk and prognosis in Chinese Han population	11
An evidence gap map of the personalized medicine in bladder cancer	11
Predictive value of miR-132-3p for the onset of sepsis-induced acute kidney injury and its functional role during disease development	10
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
Genetic Predisposition for the Development of Lamotrigine-Induced Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis: a Systematic Review and Meta-Analysis	8
Precision acute medical care through “-omic” analyses: a scoping review	8
Association between IL-6, miRNA-146a, MALAT1 genetic polymorphisms and risk of rheumatoid arthritis	8
Val66Met polymorphism in the BDNF gene and antidepressant response in depression: an updated meta-analysis	7
Knowledge, attitudes and practice regarding pharmacovigilance and adverse drug reaction reporting among physicians and pharmacists in Egypt: a step toward personalized medicine implementation	6
Polygenic risk scores to refine Breast cancer screening and prevention strategies	6
Enhancing Parkinson’s disease prediction using meta-heuristic optimized machine learning models	6
Precision medicine activities and opportunities for shaping maternal and neonatal health in Qatar	6
The effect of RNLS gene polymorphisms on preeclampsia susceptibility: a meta-analysis study	6
MYC variant at 8q24 increases susceptibility to urinary bladder cancer: a meta-analysis of 53,957 individuals	6
Leveraging circulating microRNAs for personalized disease-modifying therapies in type 1 diabetes	5
Identification of novel variants of XPA and POLH/XPV genes in xeroderma pigmentosum patients in Vietnam	5
Association of a common SOD gene variant with ARHL risk: analysis by age, hearing threshold, and enzyme activity	5
Gene expression profiling of peripheral blood in patients with steroid-induced osteonecrosis of the femoral head	5

Looking Back Over 2023 and Welcome to the 21 ^st Issue of Personalized Medicine	5
Digital biomarkers in chronic disease management: a systematic review of personalization and ethical challenges	5
Cost–effectiveness and budget impact analysis of screening strategies for maturity-onset diabetes of the young in three European countries	5
Deciphering the multi-organ anti-fibrotic mechanisms of pirfenidone and nintedanib via network pharmacology	5
Identification of Dpyd Variants and Estimation of Uracil and Dihydrouracil in A Healthy Indian Population	4
Development of Competency-based Online Genomic Medicine Training (COGENT)	4
Genomics and the early diagnosis of lung cancer	4
HEcoPerMed, Personalized Medicine from a Health Economic Perspective: Lessons Learned and Potential Opportunities Ahead	4
Regional disparities in access to gene therapies in the European Union, the United States, Japan, and China	4
Diagnostic Utility of the 23-gene Expression Profile Test for an Atypical Intradermal Melanocytic Proliferation	4
Cost–effectiveness of extended DPYD testing before fluoropyrimidine chemotherapy in metastatic breast cancer in the UK	4
Association of miR-21 gene polymorphisms with cognitive function in patients with systemic lupus erythematosus	4
Machine learning–enabled early risk stratification of β-Iactam–induced electrolyte imbalances	4
Whole-exome sequencing reveals novel variants associated with abnormal uterine bleeding caused by copper intrauterine device	4
Cloud-based Digital Healthcare Development for Precision Medical Hospital Information System	4
Association between CYP11B2 rs1799998 genetic variant with essential hypertension and antihypertensive response	4
Global harmonization in advanced therapeutics: balancing innovation, safety, and access	3
Pharmacogenomics of Lipid-Lowering Agents: the Impact on Efficacy and Safety	3
Genetic and non-genetic factors influencing the therapeutic response of valproic acid in pediatric epileptic patients	3
Recent Advances in Personalized Cancer Immunotherapy with Immune Checkpoint Inhibitors, T Cells and Vaccines	3
The genetic association of IL-17A rs8193036 with the susceptibility to Alzheimer’s disease	3
Lung cancer, platinum analog-based frontline treatment and pharmacogenetic limitations	3
Development of a computer-based tool to obtain a family health history in Vietnam	3
A rare likely pathogenic HLA-DRB1 variant with compromised immunity in severe COVID-19 patient and in-hospital mortality	3
A Real-World Analysis of Tyrosine Receptor Kinase Inhibitor-Related Toxicities in Cancer Treatment	3
Tailoring pediatric vancomycin doses: achieving therapeutic levels and minimizing toxicity in oncology patients	3
Evaluation of pharmacogenomic information in drug labeling: a case study from Jordan	3
Patient-Derived Tumour Organoids (PDOs) may help oncologists in clinical practice	3
The correlation between the polymorphism of lysolecithin acyltransferase (MBOAT7) rs641738 and liver fibrosis	3
The norepinephrine dosing dilemma in septic shock: a narrative review	3
Low Rate of Complications in Nipple-Sparing Mastectomy for Patients with BRCA1 and BRCA2 Mutation	3
Association of miR-21 rs1292037 polymorphism with congenital heart disease susceptibility in Chinese children	3
From genomes to metabolomes: adaptive science in personalized medicine	3