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List of works by George P Patrinos

"LRF/ZBTB7A conservation accentuates its potential as a therapeutic target for the hematopoietic disorders"

scientific article published on 02 August 2020

6-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent manner.

scientific article published in February 2012

6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapy ⬇️

scientific article published on September 25, 2012

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

scientific article

A Noninvasive Ocular (Tear) Sampling Method for Genetic Ascertainment of Transgenic Mice and Research Ethics Innovation

scientific article published on 17 May 2019

A Novel Text-Mining Approach for Retrieving Pharmacogenomics Associations From the Literature

scientific article published on 10 November 2020

A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.

scientific article published on 28 April 2008

A call for pharmacogenovigilance and rapid falsification in the age of big data: why not first road test your biomarker?

scientific article published on 29 October 2014

A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and beta-thalassemia compound heterozygotes

scientific article published on 18 December 2001

A critical view of the general public’s awareness and physicians’ opinion of the trends and potential pitfalls of genetic testing in Greece

A dual reporter mouse model of the human β-globin locus: applications and limitations

scientific article

A formalization of one of the main claims of “Cost-effectiveness analysis of pharmacogenomics-guided clopidogrel treatment in Spanish patients undergoing percutaneous coronary intervention” by Fragoulakis et al. 20191

scientific article published in 2022

A note from the editors

scientific article published on 21 June 2018

A pharmacokinetic binding model for bevacizumab and VEGF165 in colorectal cancer patients

scientific article

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

scientific article published in January 2012

A versatile denaturing HPLC approach for human beta-globin gene mutation screening.

scientific article published in February 2007

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software

scientific article published on March 2009

Advancing Global Precision Medicine: An Overview of Genomic Testing and Counseling Services in Malaysia.

scientific article

Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson disease.

scientific article published on June 2010

An Alternative Methodological Approach for Cost-Effectiveness Analysis and Decision Making in Genomic Medicine

scientific article published on 20 April 2016

An Appeal to the Global Health Community for a Tripartite Innovation: An "Essential Diagnostics List," "Health in All Policies," and "See-Through 21(st) Century Science and Ethics".

scientific article

An Exploratory Study of Radiation Dermatitis in Breast Cancer Patients.

scientific article

An Introduction to Pharmacogenomics and Personalized Medicine

An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project

scientific article published on January 2009

An overview of current microarray-based human globin gene mutation detection methods

scientific article published on January 2007

Application of Economic Evaluation to Assess Feasibility for Reimbursement of Genomic Testing as Part of Personalized Medicine Interventions

scientific article published on 02 August 2019

Application of the DruGeVar Database in Cancer Genomics and Pharmacogenomics

scientific article published on 14 July 2017

Ascertainment and critical assessment of the views of the general public and healthcare professionals on nutrigenomics in Greece

article

Assessment of the pharmacogenomics educational environment in Southeast Europe.

scientific article published on 17 October 2014

Association of genome variations in the renin-angiotensin system with physical performance ⬇️

scientific article published on November 24, 2012

Association study of human VN1R1 pheromone receptor gene alleles and gender

scientific article (publication date: 2007)

Bioenergetic Profiling of the Differentiating Human MDS Myeloid Lineage with Low and High Bone Marrow Blast Counts

scientific article published on 26 November 2020

Bridging genomics research between developed and developing countries: the Genomic Medicine Alliance

CYP3A5 Gene-Guided Tacrolimus Treatment of Living-Donor Egyptian Kidney Transplanted Patients

scientific article published on 11 August 2020

Cancer Genomics and Public Health.

scientific article

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project

scientific article

Catalyzing clinical implementation of pharmacogenomics and personalized medicine interventions in Africa

scientific article published on 23 December 2020

Cellular models to study bipolar disorder: A systematic review

scientific article published on 28 May 2015

Clarity and claims in variation/mutation databasing

scientific article published on 8 September 2011

Clinical Applicability of Sequence Variations in Genes Related to Drug Metabolism ⬇️

scientific article published on June 1, 2011

Clinical application of pharmacogenomics: the example of HLA-based drug-induced toxicity

scientific article

Clinical applications of next-generation sequencing: the 2013 human genome variation society scientific meeting

scientific article published on 4 September 2013

Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations

scientific article published on 30 October 2020

Collaborative Crowdsourcing for the Diagnosis of Rare Genetic Syndromes: The DYSCERNE Experience.

scientific article published on 9 October 2015

Comparative study and meta-analysis of meta-analysis studies for the correlation of genomic markers with early cancer detection.

scientific article published on 05 June 2013

Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription

scientific article published on 20 August 2008

Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia

scientific article published on 01 September 2008

Computational approaches in target identification and drug discovery

scientific article

Continuous pharmacogenomics and genomic medicine education for healthcare professionals through electronic educational courses

scientific article published on 21 May 2019

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

scientific article published on 16 February 2017

Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacy.

scientific article published on 21 October 2016

Cost-effectiveness analysis of pharmacogenomics-guided clopidogrel treatment in Spanish patients undergoing percutaneous coronary intervention

scientific article published on 16 January 2019

Costing Methods as a Means to Measure the Costs of Pharmacogenomics Testing

scientific article published on 01 September 2020

Critical appraisal of the private genetic and pharmacogenomic testing environment in Greece

Critical appraisal of the views of healthcare professionals with respect to pharmacogenomics and personalized medicine in Greece

article

Culturomics: A New Kid on the Block of OMICS to Enable Personalized Medicine

scientific article published on 12 April 2017

David Bowie and the Art of Slow Innovation: A Fast-Second Winner Strategy for Biotechnology and Precision Medicine Global Development

scientific article published on 24 October 2017

Deciphering next-generation pharmacogenomics: an information technology perspective

scientific article

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

scientific article published on 25 August 2013

Delineating significant genome-wide associations of variants with antipsychotic and antidepressant treatment response: implications for clinical pharmacogenomics

scientific article published on 15 January 2020

Development of Rapid Pharmacogenomic Testing Assay in a Mobile Molecular Biology Laboratory (2MoBiL)

scientific article published on 16 October 2020

Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies ⬇️

scientific article

Documentation of clinically relevant genomic biomarker allele frequencies in the next-generation FINDbase worldwide database

scientific article published on 05 April 2020

Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database

scientific article

DruGeVar: an online resource triangulating drugs with genes and genomic biomarkers for clinical pharmacogenomics

scientific article

Drug-Induced Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Call for Optimum Patient Stratification and Theranostics via Pharmacogenomics

scientific article published on 13 April 2018

ETHNOS : A versatile electronic tool for the development and curation of national genetic databases

scientific article

Economic analysis of pharmacogenomic-guided clopidogrel treatment in Serbian patients with myocardial infarction undergoing primary percutaneous coronary intervention

scientific article

Economic evaluation of pharmacogenomics: a value-based approach to pragmatic decision making in the face of complexity

scientific article published on 26 September 2014

Editorial: (Pharmaco)Metabolomics in Drug Discovery and Individualisation of Treatment

scientific article published in January 2017

Erythroid phenotypes associated with KLF1 mutations

scientific article

Estimating the Effectiveness of DPYD Genotyping in Italian Individuals Suffering from Cancer Based on the Cost of Chemotherapy-Induced Toxicity

scientific article published on 30 May 2019

Evidence for association of anACCN1gene variant with response to lithium treatment in Sardinian patients with bipolar disorder

article

Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the betaS/Benin haplotype

scientific article published on September 2005

Exome-Wide Analysis of the DiscovEHR Cohort Reveals Novel Candidate Pharmacogenomic Variants for Clinical Pharmacogenomics

scientific article published on 18 May 2020

Exosomes: A Cancer Theranostics Road Map.

scientific article

Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies

scientific article

Exploring public genomics data for population pharmacogenomics

scientific article

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide

scientific article published on 28 November 2006

FINDbase: a worldwide database for genetic variation allele frequencies updated

scientific article

First Report of Hb A2-NYU (HBD:c.39T>A) in the Hellenic Population ⬇️

scientific article published on January 1, 2011

Functional Analysis of an (A)γ-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress

scientific article published on 16 November 2015

Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin.

scientific article

Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in TPMT gene transcription

scientific article published in April 2010

Gene Conversion in Evolution and Disease

article

Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair

scientific article

Gene conversion: mechanisms, evolution and human disease

scientific article

Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study

scientific article published on 20 April 2020

Generic Cost-Effectiveness Models: A Proof of Concept of a Tool for Informed Decision-Making for Public Health Precision Medicine

scientific article published on 01 January 2018

Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium ⬇️

scientific article published on March 24, 2011

Genetic Databases in Pharmacogenomics: The Frequency of Inherited Disorders Database (FINDbase) ⬇️

scientific article published on January 1, 2013

Genetic Variations Associated with Sleep Disorders in Patients with Schizophrenia: A Systematic Review

scientific article published on 24 March 2018

Genetic databases and their potential in pharmacogenomics

scientific article

Genetic recombination as a major cause of mutagenesis in the human globin gene clusters

scientific article published on 22 July 2009

Genetic tests obtainable through pharmacies: the good, the bad, and the ugly

scientific article published on 8 July 2013

Genetics of myasthenia gravis: a case-control association study in the Hellenic population.

scientific article

Genetics, genomics and society: the responsibilities of scientists for science communication and education

article

Genome-Based Population Clustering: Nuggets of Truth Buried in a Pile of Numbers?

Genomic Medicine Without Borders: Which Strategies Should Developing Countries Employ to Invest in Precision Medicine? A New "Fast-Second Winner" Strategy

scientific article published in November 2017

Genomic rearrangements in inherited disease and cancer

scientific article published on 09 June 2010

Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients

scientific article published on 01 July 2019

Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/β-thalassemia patients

scientific article published on 19 February 2016

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

scientific article published on 8 December 2017

Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy.

scientific article published in April 2013

Genomics and Pharmacogenomics Knowledge, Attitude and Practice of Pharmacists Working in United Arab Emirates: Findings from Focus Group Discussions-A Qualitative Study

scientific article published on 18 September 2020

Global implementation of genomic medicine: We are not alone

scientific article

Golden Helix Pharmacogenomics Days: educational activities on pharmacogenomics and personalized medicine

scientific article published on 01 April 2012

HDAC3 role in medication consumption in medication overuse headache patients: a pilot study

scientific article

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

scientific article

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update

scientific article published in February 2007

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

scientific article published on 01 March 2002

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population

scientific article published in April 2005

Human Variome Project country nodes: documenting genetic information within a country

scientific article published on 18 July 2012

Human genetic factors associated with susceptibility to SARS-CoV-2 infection and COVID-19 disease severity

scientific article published on 22 October 2020

Identical Mutations in the Paralogous Human γ-Globin Genes Leading to Hemoglobin Variants and Nondeletional Hereditary Persistence of Fetal Hemoglobin ⬇️

scientific article published on 01 January 2011

Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia

scientific article published on 07 August 2015

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

scientific article published on 20 June 2015

Impact of ACE and ApoE polymorphisms on myocardial perfusion: correlation with myocardial single photon emission computed tomographic imaging

scientific article published on 28 August 2009

Impact of ZBTB7A hypomethylation and expression patterns on treatment response to hydroxyurea

scientific article published on 01 October 2018

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

scientific article

Increased gamma-globin gene expression in beta-thalassemia intermedia patients correlates with a mutation in 3'HS1

scientific article published on 01 November 2007

Individualizing clozapine and risperidone treatment for schizophrenia patients

scientific article published on January 2014

Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients

scientific article

Institutional Profile: Golden Helix Institute of Biomedical Research: interdisciplinary research and educational activities in pharmacogenomics and personalized medicine

scientific article published on March 2012

Integrating Next-Generation Sequencing in the Clinical Pharmacogenomics Workflow

Introducing dAUTObase: a first step towards the global scale geoepidemiology of autoimmune syndromes and diseases

scientific article

Isolation and characterization of hematopoietic transcription factor complexes by in vivo biotinylation tagging and mass spectrometry.

scientific article

KLF10gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients

article

Key Pharmacogenomic Considerations for Sickle Cell Disease Patients

scientific article published on 09 May 2017

Key challenges for next-generation pharmacogenomics: Science & Society series on Science and Drugs

scientific article

Knowledge and Attitudes of Medical and Health Science Students in the United Arab Emirates toward Genomic Medicine and Pharmacogenomics: A Cross-Sectional Study

scientific article published on 24 October 2020

Knowledge, Attitudes, and Perceived Barriers toward Genetic Testing and Pharmacogenomics among Healthcare Workers in the United Arab Emirates: A Cross-Sectional Study

scientific article published on 09 November 2020

Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants

scientific article

Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central Greece compared to the rest of the country

scientific article

Leukocyte telomere length is reduced in patients with major depressive disorder

scientific article published on 01 November 2019

Lithium-induced differential expression of SAT1 in suicide completers and controls is not correlated with polymorphisms in the promoter region of the gene

scientific article

Locus-specific database domain and data content analysis: evolution and content maturation toward clinical use.

scientific article

Meta-Analysis of Genes in Commercially Available Nutrigenomic Tests Denotes Lack of Association with Dietary Intake and Nutrient-Related Pathologies

scientific article published on September 2015

Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domain

scientific article

Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B

scientific article published on 16 October 2020

Minimum information required for a DMET experiment reporting

scientific article published on 22 August 2016

Molecular characterization and diagnosis of Hb Crete [beta129(H7)Ala-->Pro].

scientific article published in January 2004

Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies

scientific article

Multi-Omics for Biomarker Discovery and Target Validation in Biofluids for Amyotrophic Lateral Sclerosis Diagnosis

scientific article

Multiomics Analysis Coupled with Text Mining Identify Novel Biomarker Candidates for Recurrent Cardiovascular Events

scientific article published on 13 March 2020

Multiple interactions between regulatory regions are required to stabilize an active chromatin hub.

scientific article

Mutation screening in the human epsilon-globin gene using single-strand conformation polymorphism analysis

scientific article published on 01 February 2006

Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants

scientific article published on 16 October 2008

New molecular diagnostic trends and biomarkers for amyotrophic lateral sclerosis

scientific article published on 21 January 2019

Novel genetic risk variants for pediatric celiac disease

scientific article published on 24 October 2016

Novel sequence variations in the CER1 gene are strongly associated with low bone mineral density and risk of osteoporotic fracture in postmenopausal women

scientific article published on 29 April 2012

Nutrigenetics and nutrigenomics: ready for clinical use or still a way to go?

scientific article published on 24 April 2020

Nutrigenomics 2.0: The Need for Ongoing and Independent Evaluation and Synthesis of Commercial Nutrigenomics Tests' Scientific Knowledge Base for Responsible Innovation

scientific article published on 08 December 2015

Nutrigenomics: A controversy

scientific article published on 14 February 2015

Optimizing thiopurine dosing based on TPMT and NUDT15 genotypes: It takes two to tango

scientific article published on 10 April 2019

PARC report: health outcomes and value of personalized medicine interventions: impact on patient care

scientific article published on 08 July 2020

Performance Ratio Based Resource Allocation Decision-Making in Genomic Medicine

scientific article published on 24 January 2017

Personal genomics in Greece: an overview of available direct-to-consumer genomic services and the relevant legal framework

scientific article published on October 2014

Personalized pharmacogenomics profiling using whole-genome sequencing

Pharmacogenetics of lithium effects on glomerular function in bipolar disorder patients under chronic lithium treatment: a pilot study

scientific article published on 3 December 2016

Pharmacogenomics and therapeutics of hemoglobinopathies

scientific article published on January 2008

Pharmacogenomics education and research at the Department of Pharmacy, University of Patras, Greece

scientific article published on 28 October 2016

Pharmacogenomics in pediatric acute lymphoblastic leukemia: promises and limitations

scientific article

Pharmacogenomics: paving the path to personalized medicine

scientific article published in February 2010

Pharmacometabolomics Informs Quantitative Radiomics for Glioblastoma Diagnostic Innovation.

scientific article

Pharmacometabolomics Informs Viromics toward Precision Medicine

scientific article published on 27 October 2016

Pharmacometabolomics-aided Pharmacogenomics in Autoimmune Disease

scientific article

Pharmacomicrobiomics informs clinical pharmacogenomics

scientific article published on 01 July 2019

PhenCode: connecting ENCODE data with mutations and phenotype

scientific article

Planning the human variome project: the Spain report.

scientific article published in April 2009

Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey

scientific article

Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase

article

Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs)

scientific article (publication date: November 2010)

Public Health Genomics joins forces with the Genomic Medicine Alliance

scientific article published on 13 June 2014

RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research

scientific article

Realities and expectations of pharmacogenomics and personalized medicine: impact of translating genetic knowledge into clinical practice

scientific article

Recent advances in genetic predisposition of myasthenia gravis

scientific article published on 5 November 2013

Recent trends on the role of epigenomics, metabolomics and noncoding RNAs in rationalizing mood stabilizing treatment.

scientific article published on 4 December 2017

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection

scientific article

Recording human globin gene variation.

scientific article published in May 2004

Region-specific genetic heterogeneity of HBB mutation distribution in South-Western Greece

scientific article published on 01 January 2010

Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries

scientific article published on 01 October 2020

Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study

scientific article published on 01 January 2019

Screening for the C9ORF72 expansion in Greek Huntington Disease phenocopies and controls and meta-analysis of current data

scientific article published on 12 June 2020

Searching for Clinically Relevant Biomarkers in Geriatric Oncology.

scientific article

Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping

scientific article published on 18 August 2017

Sequence Variations in the FII , FV , F13A1 , FGB and PAI-1 Genes are Associated with Differences in Myocardial Perfusion ⬇️

scientific article published on 01 February 2011

Success stories in genomic medicine from resource-limited countries

scientific article published on 18 June 2015

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

scientific article

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

scientific article published on 28 September 2015

Ten simple rules for international short-term research stays

scientific article published on 7 December 2017

Test Pricing and Reimbursement in Genomic Medicine: Towards a General Strategy

scientific article published on 28 September 2016

The 5' regulatory region of the human fetal globin genes is a gene conversion hotspot

scientific article published in January 2008

The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter

scientific article published on 03 December 2008

The Implications of Metabotypes for Rationalizing Therapeutics in Infants and Children

scientific article (publication date: 2015)

The Israeli National Genetic Database

scientific article

The Israeli National Genetic database: a 10-year experience

scientific article published on 16 March 2017

The New Age of -omics in Urothelial Cancer - Re-wording Its Diagnosis and Treatment

scientific article published on 2 February 2018

The Rise and Rise of Exome Sequencing.

scientific article published on 30 November 2016

The Role of MicroRNAs in Patients with Amyotrophic Lateral Sclerosis

scientific article published on 10 November 2018

The cypriot and Iranian National Mutation Frequency Databases.

scientific article published in June 2006

The importance of adherence to international standards for depositing open data in public repositories

scientific article published on 02 November 2021

The multi-faceted functioning portrait of LRF/ZBTB7A

scientific article published on 10 December 2019

The role of C9orf72 in neurodegenerative disorders: a systematic review, an updated meta-analysis, and the creation of an online database

scientific article published on 24 April 2019

Toward High-Throughput Fungal Electroculturomics and New Omics Methodologies in 21st-Century Microbiology and Ecology

scientific article published on 11 June 2020

Toxicity and Pharmacogenomic Biomarkers in Breast Cancer Chemotherapy

scientific article published on 15 April 2020

Transcriptional Regulation and Pharmacogenomics ⬇️

scientific article published on May 1, 2011

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

scientific article

VEGF-A and ICAM-1 Gene Polymorphisms as Predictors of Clinical Outcome to First-Line Bevacizumab-Based Treatment in Metastatic Colorectal Cancer

scientific article published on 18 November 2019

Variants in TPMT, ITPA, ABCC4 and ABCB1 Genes As Predictors of 6-mercaptopurine Induced Toxicity in Children with Acute Lymphoblastic Leukemia

scientific article published on 01 July 2018

Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations

scientific article published on 04 December 2020

VarioML framework for comprehensive variation data representation and exchange

scientific article (publication date: 3 October 2012)

What Do Students in Pharmacy and Medicine Think About Pharmacogenomics and Personalized Medicine Education? Awareness, Attitudes, and Perceptions in Malaysian Health Sciences

scientific article published on 10 November 2020

Whole genome sequencing in pharmacogenomics

scientific article

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

scientific article published on 23 October 2017

Working towards personalization of Medicine: Genomics in 2014

article

ePGA: A Web-Based Information System for Translational Pharmacogenomics

scientific article

variants as significant predictors of warfarin dose in Emiratis

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