Personalized Medicine

Papers
(The median citation count of Personalized Medicine is 1. 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 2020-03-01 to 2024-03-01.)
ArticleCitations
The role of circular RNAs in therapy resistance of patients with solid tumors35
A review of clinical pharmacogenetics Studies in African populations34
The evolution of personalized healthcare and the pivotal role of European regions in its implementation29
Assessment of healthcare professionals’ knowledge, attitudes, and perceived challenges of clinical pharmacogenetic testing in Egypt28
Microsatellite instability testing in colorectal patients with Lynch syndrome: lessons learned from a case report and how to avoid such pitfalls27
Review of policies of companies and databases regarding access to customers’ genealogy data for law enforcement purposes22
Elevated expression of ASF1B correlates with poor prognosis in human lung adenocarcinoma17
International consortium for personalized medicine: an international survey about the future of personalized medicine17
Increase inMEG3, MALAT1, NEAT1significantly predicts the clinical parameters in patients with rheumatoid arthritis14
The United States 2020 Census data: implications for precision medicine and the research landscape14
Pharmacogenomic considerations for repurposing of dexamethasone as a potential drug against SARS-CoV-2 infection13
Gout prevalence in the Hmong: a prime example of health disparity and the role of community-based genetic research12
Sorafenib treatment has the potential to downstage advanced hepatocellular carcinoma before liver resection12
Artificial intelligence in healthcare: a primer for medical education in radiomics11
MiR-452-5p mediates the proliferation, migration and invasion of hepatocellular carcinoma cells via targeting COLEC1011
Promoter region single nucleotide polymorphism of siglec-8 gene associates with susceptibility to allergic asthma10
Engaging community stakeholders in research on best practices for clinical genomic sequencing9
Creating accessible Spanish language materials for Clinical Sequencing Evidence-Generating Research consortium genomic projects: challenges and lessons learned8
Public interest in whole genome sequencing and information needs: an online survey study8
Clinical validity of a gene expression signature in diagnostically uncertain neoplasms8
Intelligent health system for the investigation of consenting COVID-19 patients and precision medicine8
Genetic and genomic learning needs of oncologists and oncology nurses in the era of precision medicine: a scoping review8
Personalized medicine in Latin America8
Clinical significance and functions of miR-203a-3p/AVL9 axis in human non-small-cell lung cancer8
Predictive role of single nucleotide polymorphism (rs11614913) in the development of breast cancer in Pakistani population7
CYP2D6 does not impact on breast cancer-free survival in Southeast Mexican patients under tamoxifen treatment7
Concentration and integrity indexes of urine cell-free DNA as promising biomarkers for early lung cancer diagnosis7
The frequency of majorCYP2C19genetic polymorphisms in women of Asian, Native Hawaiian and Pacific Islander subgroups7
Current advances in the diagnosis and personalized treatment of breast cancer: lessons from tumor biology7
LncRNA ZFAS1, as a poor prognostic indicator, promotes cell proliferation and epithelial–mesenchymal transition in endometrial carcinoma7
Recommendations to researchers for aiding in increasing American Indian representation in genetic research and personalized medicine7
Toward precision health: applying artificial intelligence analytics to digital health biometric datasets7
Clinician perspectives on communication and implementation challenges in precision oncology7
Correlation of miR-600 with WT1 expression and its potential clinical significance in breast cancer6
miR-516a-3P, a potential circulating biomarker in hepatocellular carcinoma, correlated with rs738409 polymorphism in PNPLA36
Clinical significance of serum miR-101-3p expression in patients with neonatal sepsis6
Nudges and the meaningful adoption of digital health6
The role of miR-101 in esophageal and gastric cancer6
Stem cells as therapeutic targets in colorectal cancer6
Assessing the implications of positive genomic screening results6
MiR-455-5p serves as a biomarker of atherosclerosis and inhibits vascular smooth muscle cell proliferation and migration6
The enduring importance of family health history in the era of genomic medicine and risk assessment5
Nutrigenetics and nutrigenomics: ready for clinical use or still a way to go?5
Exploring the usefulness of plasma level determination and pharmacogenetics for patients treated with clozapine5
Expanded carrier screening in Flanders (Belgium): an online survey on the perspectives of nonpregnant reproductive-aged women5
Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications5
‘It’s much more grey than black and white’: clinical geneticists’ views on the oversight of consumer genomics in Europe5
Defining the role of pharmacists in medication-related genetic counseling4
Mini-gut feelings: perspectives of people with cystic fibrosis on the ethics and governance of organoid biobanking4
Prioritizing pharmacogenomics implementation initiates: a survey of healthcare professionals4
Association study of genetic polymorphisms inGABRDwith treatment response and dose in methadone maintenance treatment4
Alignment of health plan coverage policies for somatic multigene panel testing with clinical guidelines in select solid tumors4
Views on genomic research result delivery methods and informed consent: a review4
PON1 polymorphisms can predict generalized anxiety and depressed mood in patients with multiple chemical sensitivity4
Association ofPON-1polymorphism with susceptibility to and severity of ischemic stroke in the Chinese population3
Personalized therapy: can it tame the COVID-19 monster?3
Guanylyl cyclase C as a diagnostic and therapeutic target in colorectal cancer3
Budget impact and transferability of cost–effectiveness of DPYD testing in metastatic breast cancer in three health systems3
SARS-CoV-2 variant identification using a genome tiling array and genotyping probes3
Positive association of SCD1 genetic variation and metabolic syndrome in dialysis patients in China3
Role of precision nutrition in improving military performance3
An international genomics health workforce education priorities assessment3
miR-938 rs2505901 T>C polymorphism increases Hirschsprung disease risk: a case–control study of Chinese children3
The interplay between pharmacogenetics, concomitant drugs and blood levels of amitriptyline and its main metabolites3
Cost–effectiveness of extended DPYD testing before fluoropyrimidine chemotherapy in metastatic breast cancer in the UK3
Long noncoding RNA polymorphisms and hepatocellular carcinoma and pancreatic cancer risk3
Healthcare professionals' knowledge, attitudes and future expectations towards personalized medicine3
Attitudes of Costa Rican individuals towards donation of personal genetic data for research3
Omics technologies in personalized combination therapy for cardiovascular diseases: challenges and opportunities3
Rs739837 affects the severity of asthma by disrupting the binding of microRNA-8853
Personalized medicine in Austria: expectations and limitations3
Targeting molecular alterations in non-small-cell lung cancer: what's next?3
Universal tumor screening for lynch syndrome: perspectives of patients regarding willingness and informed consent3
Application of transcriptomics and proteomics in pulmonary arterial hypertension3
Cost–effectiveness of genetic-based screening strategies for maturity-onset diabetes of the young3
The integration of personalized medicine into health systems: progress and a path forward3
Cost–effectiveness and budget impact analysis of screening strategies for maturity-onset diabetes of the young in three European countries2
From personalized to precision cancer medicine2
A GRIN3A polymorphism may be associated with glucocorticoid-induced symptomatic osteonecrosis in children with acute lymphoblastic leukemia2
Predictive value of leukocyte telomere length for the severity of coronary artery disease2
Provider preferences for resolving uncertainty and avoiding harms in precision medicine: a discrete choice experiment2
SKA3, negatively regulated by miR-128-3p, promotes the progression of non-small-cell lung cancer2
Identification of unique long non-coding RNAs as putative biomarkers for chromophobe renal cell carcinoma2
Genetic polymorphisms of miRNA machinery genes in bicuspid aortic valve and associated aortopathy2
A consensus on collaboration: reviewing the 15th Annual Personalized Medicine Conference at Harvard Medical School2
The role of metabolomics in personalized medicine for diabetes2
Development and evaluation of an exome sequencing training course for medical interpreters2
RNA-based next-generation sequencing in non-small-cell lung cancer in a routine setting: an experience from an Italian referral center2
Medical geneticists, genetic diseases and services in Brazil in the age of personalized medicine2
Investigating underlying human immunity genes, implicated diseases and their relationship to COVID-192
Polymorphisms in genes involved in breast cancer among Iranian patients2
How can we address the uncertainties regarding the potential clinical utility of polygenic score-based tests?2
Association of NQO1Pro187Ser polymorphism with clinical outcomes and survival of lung cancer patients treated with platinum chemotherapy2
miR-369-3p serves as prognostic factor and regulates cancer progression of hepatocellular carcinoma2
Racial and ethnic minority patient participation in N-of-1 trials: perspectives of healthcare providers and patients2
Attitudes toward pharmacogenetics in patients undergoing CYP2C19 testing following percutaneous coronary intervention2
Personalized medicine in lipid-modifying therapy2
Cost–effectiveness of alternative NTRK testing strategies in cancer patients followed by histology-independent therapy with entrectinib: an analysis of three European countries2
Big data in severe mental illness: the role of electronic monitoring tools and metabolomics2
State-of-the-art knowledge on the regulation of advanced therapy medicinal products2
HER2 in gastric adenocarcinoma: where do we stand today?1
Seven non-differentially expressed ‘dark biomarkers’ show transcriptional dysregulation in chronic lymphocytic leukemia1
Texas health educators’ practice in basic genomics education and services1
Investigation ofDPYD,MTHFRandTYMSpolymorphisms on 5-fluorouracil related toxicities in colorectal cancer1
Blood direct PCR: impact of CYP2C19 and CYP4F2 variants for bleeding prediction in ST-elevation myocardial infarction patients with ticagrelor1
Correlation between plasma lncRNA CASC11 and malignancy in lung adenocarcinoma patients and the prognostic value of lncRNA CASC111
Deliberations about clinical pharmacogenetic testing in pediatric oncology1
Challenges and opportunities in building a health economic framework for personalized medicine in oncology1
The use of molecular biomarker tests: an interview study with healthcare providers about a molecular biomarker test for prostate cancer1
Genetic predisposition for the development of lamotrigine-induced Stevens–Johnson syndrome/toxic epidermal necrolysis: a systematic review and meta-analysis1
Biomarker-driven immunotherapy for precision medicine in prostate cancer1
A roadmap for precision medicine research recruitment: empirical assessment of the public's willingness to participate1
A sociogenomic paradigm to replace the racial paradigm1
Epithelioid sarcoma as the prototype for personalized therapy in soft tissue sarcoma1
Lessons learned from the application of the HEcoPerMed guidance to three modeling case studies1
A precision medicine approach to stress testing using metabolomics and microribonucleic acids1
Financial incentives to promote personalized medicine in Europe: an overview and guidance for implementation1
Therapeutic drug monitoring guided fluconazole therapy in a patient with cholangitis sepsis1
COVID-19 telehealth preparedness: a cross-sectional assessment of cardiology practices in the USA1
Developing and validating noninvasive prenatal testing for de novo autosomal dominant monogenic diseases in Vietnam1
The pharmacogenetics of mycophenolate mofetil in Tunisian renal transplant patients1
ABCB1 and SLCO1B1 gene polymorphisms predict methotrexate-resistant for low-risk gestational trophoblastic neoplasia1
Developing new frameworks to value genomic information: accounting for complexity1
Pharmacogenomic testing for mental health (Part I): documenting early adopter perceptions of use for eight scenarios1
Avoiding “toxic knowledge”: the importance of framing personalized risk information in clinical decision-making1
Individualizing pharmacogenomic test results in the context of the microbiome1
Patient views on genetics and functional imaging for precision medicine: a willingness-to-pay analysis1
Biomarker testing in patients diagnosed with advanced/metastatic medullary thyroid cancer in the USA1
Guideline-recommended incorporation of biomarker testing results in metastatic colorectal cancer therapy1
HEcoPerMed, personalized medicine from a health economic perspective: lessons learned and potential opportunities ahead1
Prophylactic lymph node dissection in clinically N0 differentiated thyroid carcinoma: example of personalized treatment1
A personalized approach to pancreatic ductal adenocarcinoma and its application in surgical practice1
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