Personalized medicine and human genetic diversity

scientific article

Personalized medicine and human genetic diversity is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1101/CSHPERSPECT.A008581
P3181OpenCitations bibliographic resource ID536157
P932PMC publication ID4143101
P698PubMed publication ID25059740
P5875ResearchGate publication ID264248449

P50authorGianpiero L. CavalleriQ46969101
P2093author name stringD. B. Goldstein
M. Angrist
Y.-F. Lu
P2860cites workAn evolutionary approach to the high frequency of the Delta F508 CFTR mutation in European populations.Q47411485
Gene Differences between Caucasian, Negro, and Japanese PopulationsQ70417098
Finding the missing heritability of complex diseasesQ22122198
A population-genetic test of founder effects and implications for Ashkenazi Jewish diseasesQ24534086
Genetic variation in IL28B and spontaneous clearance of hepatitis C virusQ24596340
Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish populationQ24606497
A map of human genome variation from population-scale sequencingQ24617794
De novo mutations in epileptic encephalopathiesQ24621776
The population genetics of the Jewish peopleQ24633199
Evaluating candidate agents of selective pressure for cystic fibrosisQ24654240
Global epidemiology of hepatitis C virus infectionQ27860799
Cystic fibrosisQ28212180
Protective effects of the sickle cell gene against malaria morbidity and mortalityQ28215309
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearanceQ28255243
IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapyQ29614896
Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis CQ29619541
Diagnosis, management, and treatment of hepatitis C: an updateQ29619682
The 1000 Genomes Project: new opportunities for research and social challengesQ33693714
Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE reviewQ33900242
The natural history of hepatitis C virus infection: host, viral, and environmental factorsQ33974693
Tay-Sachs diseaseQ34347943
Genetic and geographical variability in cystic fibrosis: evolutionary considerations.Q34399381
Natural history of Ashkenazi intelligenceQ34551013
Next generation disparities in human genomics: concerns and remediesQ35008340
Clinical implications of human population differences in genome-wide rates of functional genotypesQ36361047
Genomics for the worldQ37003231
Uncovering the roles of rare variants in common disease through whole-genome sequencingQ37755970
Recent developments in the genetics of autism spectrum disordersQ38093928
Pegylated interferon-alpha-2a plus ribavirin for treatment-naive Asian patients with hepatitis C virus genotype 1 infection: a multicenter, randomized controlled trial.Q42981999
P433issue9
P407language of work or nameEnglishQ1860
P921main subjectgenetic diversityQ585259
personalized medicineQ2072214
P304page(s)a008581
P577publication date2014-07-24
P1433published inCold Spring Harbor Perspectives in MedicineQ21042440
P1476titlePersonalized medicine and human genetic diversity
P478volume4

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cites work (P2860)
Q92898086A Clinician's Perspective on Biomarkers
Q93086744A core collection of pan-schizophrenia genes allows building cohort-specific signatures of affected brain
Q38593055A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.
Q49385295Activation of Nrf2 signaling by natural products-can it alleviate diabetes?
Q38656488An Integrative Computational Approach to Evaluate Genetic Markers for Bipolar Disorder.
Q64235258Analysis of Benefit of Intensive Care Unit Transfer for Deteriorating Ward Patients: A Patient-Centered Approach to Clinical Evaluation
Q91866776Artificial intelligence-assisted prediction of preeclampsia: Development and external validation of a nationwide health insurance dataset of the BPJS Kesehatan in Indonesia
Q90164481Can education be personalised using pupils' genetic data?
Q50060353Dielectrophoretic analysis of treated cancer cells for rapid assessment of treatment efficacy
Q38665568Evaluation of Quality Assessment Protocols for High Throughput Genome Resequencing Data
Q50123812Full genetic analysis for genome-wide association study of Fangji: a powerful approach for effectively dissecting the molecular architecture of personalized traditional Chinese medicine.
Q31154892Genomics pipelines and data integration: challenges and opportunities in the research setting.
Q95642983Germline Polymorphisms and Length of Survival of Nasopharyngeal Carcinoma: An Exome-Wide Association Study in Multiple Cohorts
Q26749581How to Predict Molecular Interactions between Species?
Q39788339INPS-MD: a web server to predict stability of protein variants from sequence and structure
Q48071853Imaging biobanks in oncology: European perspective
Q38651944Implications of human genetic variation in CRISPR-based therapeutic genome editing
Q28829827Influence of chelator and near-infrared dye labeling on biocharacteristics of dual-labeled trastuzumab-based imaging agents
Q92481647Innovation in Oncology Drug Development
Q64230189Integrated Microfluidic Devices Fabricated in Poly (Methyl Methacrylate) (PMMA) for On-site Therapeutic Drug Monitoring of Aminoglycosides in Whole Blood
Q30389939Large scale analysis of protein stability in OMIM disease related human protein variants
Q38817013Linking neuroimaging signals to behavioral responses in single cases: Challenges and opportunities.
Q47215897MPLasso: Inferring microbial association networks using prior microbial knowledge
Q47870167Mapping the Schizophrenia Genes by Neuroimaging: The Opportunities and the Challenges
Q48139814Modeling the therapeutic efficacy of NFκB synthetic decoy oligodeoxynucleotides (ODNs).
Q41145493Neanderthal and Denisova tooth protein variants in present-day humans
Q92956020Patient similarity by joint matrix trifactorization to identify subgroups in acute myeloid leukemia
Q38578746Perspectives on Human Variation through the Lens of Diversity and Race
Q26765823Population Genomics and the Statistical Values of Race: An Interdisciplinary Perspective on the Biological Classification of Human Populations and Implications for Clinical Genetic Epidemiological Research
Q89519652Precise hepatectomy in the intelligent digital era
Q42315922Precision Medicine in Cats: Novel Niemann-Pick Type C1 Diagnosed by Whole-Genome Sequencing
Q57683879Precision Medicine: An Introduction
Q59810611Prevention genetics program is an efficient model for precision medicine
Q39287356Prostate cancer molecular profiling: the Achilles heel for the implementation of precision medicine
Q39222032RNA Bioinformatics for Precision Medicine
Q33870511Self-reported race and ethnicity of US biobank participants compared to the US Census
Q37250779Serum γ-Glutamyltransferase, Alanine Aminotransferase and Aspartate Aminotransferase Activity in Healthy Blood Donor of Different Ethnic Groups in Gorgan
Q28073967Toward precision medicine of breast cancer
Q28067740Understanding rare and common diseases in the context of human evolution
Q26750460Use of systems biology to decipher host-pathogen interaction networks and predict biomarkers