Patrinos, George P.
George P Patrinos
VIAF ID: 42135198 (Personal)
Permalink: http://viaf.org/viaf/42135198
Preferred Forms
- 100 0 _ ‡a George P Patrinos
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- 100 1 _ ‡a Patrinos, George P
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- 100 1 _ ‡a Patrinos, George P.
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- 100 1 _ ‡a Patrinos, George P.
- 100 1 _ ‡a Patrinos, George P.
- 100 1 _ ‡a Patrinos, George P.
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- 100 1 _ ‡a Patrinos, George P.
4xx's: Alternate Name Forms (5)
5xx's: Related Names (1)
Works
Title | Sources |
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Economic evaluation in genomic medicine | |
Fine-mapping genomic loci refines bipolar disorder risk genes | |
Genome plasticity in health and disease | |
Genomics and the global bioeconomy | |
Introducing dAUTObase: a first step towards the global scale geoepidemiology of autoimmune syndromes and diseases. | |
The Israeli National Genetic database: a 10-year experience | |
Key Pharmacogenomic Considerations for Sickle Cell Disease Patients | |
Knowledge, Attitudes, and Perceived Barriers toward Genetic Testing and Pharmacogenomics among Healthcare Workers in the United Arab Emirates: A Cross-Sectional Study | |
Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants | |
Lithium-induced differential expression of SAT1 in suicide completers and controls is not correlated with polymorphisms in the promoter region of the gene. | |
"LRF/ZBTB7A conservation accentuates its potential as a therapeutic target for the hematopoietic disorders" | |
Meta-Analysis of Genes in Commercially Available Nutrigenomic Tests Denotes Lack of Association with Dietary Intake and Nutrient-Related Pathologies | |
Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B | |
Minimum information required for a DMET experiment reporting | |
Molecular diagnostics | |
The multi-faceted functioning portrait of LRF/ZBTB7A | |
Multi-Omics for Biomarker Discovery and Target Validation in Biofluids for Amyotrophic Lateral Sclerosis Diagnosis. | |
Multiomics Analysis Coupled with Text Mining Identify Novel Biomarker Candidates for Recurrent Cardiovascular Events | |
Multiple interactions between regulatory regions are required to stabilize an active chromatin hub. | |
Mutation screening in the human epsilon-globin gene using single-strand conformation polymorphism analysis | |
Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants | |
The New Age of -omics in Urothelial Cancer - Re-wording Its Diagnosis and Treatment. | |
A Noninvasive Ocular (Tear) Sampling Method for Genetic Ascertainment of Transgenic Mice and Research Ethics Innovation | |
A note from the editors | |
Novel genetic risk variants for pediatric celiac disease | |
Novel sequence variations in the CER1 gene are strongly associated with low bone mineral density and risk of osteoporotic fracture in postmenopausal women | |
Nutrigenetics and nutrigenomics: ready for clinical use or still a way to go? | |
Nutrigenomics 2.0: The Need for Ongoing and Independent Evaluation and Synthesis of Commercial Nutrigenomics Tests' Scientific Knowledge Base for Responsible Innovation | |
Nutrigenomics: A controversy | |
Optimizing thiopurine dosing based on TPMT and NUDT15 genotypes: It takes two to tango | |
An overview of current microarray-based human globin gene mutation detection methods | |
PARC report: health outcomes and value of personalized medicine interventions: impact on patient care | |
Personal genomics in Greece: an overview of available direct-to-consumer genomic services and the relevant legal framework | |
Pharmacogenetics of lithium effects on glomerular function in bipolar disorder patients under chronic lithium treatment: a pilot study. | |
Pharmacogenomics education and research at the Department of Pharmacy, University of Patras, Greece. | |
Pharmacogenomics in pediatric acute lymphoblastic leukemia: promises and limitations | |
A pharmacokinetic binding model for bevacizumab and VEGF165 in colorectal cancer patients | |
Pharmacometabolomics-aided Pharmacogenomics in Autoimmune Disease | |
Pharmacometabolomics Informs Quantitative Radiomics for Glioblastoma Diagnostic Innovation. | |
Pharmacometabolomics Informs Viromics toward Precision Medicine | |
Pharmacomicrobiomics informs clinical pharmacogenomics | |
PhenCode: connecting ENCODE data with mutations and phenotype | |
Planning the human variome project: the Spain report. | |
Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey | |
Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase | |
Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs) | |
Psychiatric genomics | |
Public Health Genomics joins forces with the Genomic Medicine Alliance | |
RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research | |
Recent advances in genetic predisposition of myasthenia gravis | |
Recent trends on the role of epigenomics, metabolomics and noncoding RNAs in rationalizing mood stabilizing treatment. | |
Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection | |
Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece | |
The Rise and Rise of Exome Sequencing. | |
Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries | |
The role of C9orf72 in neurodegenerative disorders: a systematic review, an updated meta-analysis, and the creation of an online database | |
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study | |
The Role of MicroRNAs in Patients with Amyotrophic Lateral Sclerosis | |
Screening for the C9ORF72 expansion in Greek Huntington Disease phenocopies and controls and meta-analysis of current data | |
Searching for Clinically Relevant Biomarkers in Geriatric Oncology. | |
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping. | |
Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion | |
A set of novel mining tools for efficient biological knowledge discovery | |
A single nucleotide polymorphism in the HBBP1 gene in the human β-globin locus is associated with a mild β-thalassemia disease phenotype | |
Success stories in genomic medicine from resource-limited countries | |
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach | |
A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F. | |
Test Pricing and Reimbursement in Genomic Medicine: Towards a General Strategy. | |
Toward High-Throughput Fungal Electroculturomics and New Omics Methodologies in 21st-Century Microbiology and Ecology | |
Toxicity and Pharmacogenomic Biomarkers in Breast Cancer Chemotherapy | |
TPMT gene expression is increased during maintenance therapy in childhood acute lymphoblastic leukemia patients in a TPMT gene promoter variable number of tandem repeat-dependent manner. | |
Translating genes into health | |
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations | |
variants as significant predictors of warfarin dose in Emiratis | |
Variants in TPMT, ITPA, ABCC4 and ABCB1 Genes As Predictors of 6-mercaptopurine Induced Toxicity in Children with Acute Lymphoblastic Leukemia | |
Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations | |
VarioML framework for comprehensive variation data representation and exchange | |
VEGF-A and ICAM-1 Gene Polymorphisms as Predictors of Clinical Outcome to First-Line Bevacizumab-Based Treatment in Metastatic Colorectal Cancer | |
A versatile denaturing HPLC approach for human beta-globin gene mutation screening. | |
What Do Students in Pharmacy and Medicine Think About Pharmacogenomics and Personalized Medicine Education? Awareness, Attitudes, and Perceptions in Malaysian Health Sciences | |
Whole genome sequencing in pharmacogenomics | |
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients | |
Working towards personalization of Medicine: Genomics in 2014 |