Genotyping Techniques
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Subject Areas on Research
- 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
- A Common Polymorphism in SCN2A Predicts General Cognitive Ability through Effects on PFC Physiology.
- A Review and Update on Papillary Immature Metaplasia of the Uterine Cervix: A Distinct Subset of Low-Grade Squamous Intraepithelial Lesion, Proposing a Possible Cell of Origin.
- A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.
- A highly efficient strategy to determine genotypes of genetically-engineered mice using genomic DNA purified from hair roots.
- A longitudinal trial comparing chloroquine as monotherapy or in combination with artesunate, azithromycin or atovaquone-proguanil to treat malaria.
- A microarray platform and novel SNP calling algorithm to evaluate Plasmodium falciparum field samples of low DNA quantity.
- A set of microsatellite markers to differentiate Plasmodium falciparum progeny of four genetic crosses.
- Aldose Reductase Polymorphisms, Fasting Blood Glucose, and Age-Related Cortical Cataract.
- Association of CYP2C19 polymorphisms and lansoprazole-associated respiratory adverse effects in children.
- Association of a Novel Mutation in the Plasmodium falciparum Chloroquine Resistance Transporter With Decreased Piperaquine Sensitivity.
- Blood glucose levels and cortical thinning in cognitively normal, middle-aged adults.
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
- Combinations of DIPs and Dprs control organization of olfactory receptor neuron terminals in Drosophila.
- Combined genotype and haplotype tests for region-based association studies.
- Common Genetic Variation and Susceptibility to Ovarian Cancer: Current Insights and Future Directions.
- Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse.
- Cost-effectiveness analysis of genotyping for HLA-B*5801 and an enhanced safety program in gout patients starting allopurinol in Singapore.
- DAOA variants and schizophrenia: influence on diagnosis and treatment outcomes.
- Efficient Genome-Wide Sequencing and Low-Coverage Pedigree Analysis from Noninvasively Collected Samples.
- Endogenous Tagging at the cdh1 Locus for Live Visualization of E-Cadherin Dynamics.
- Ethnic variation in early age-related macular degeneration lesions between white Australians and Singaporean Asians.
- Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease.
- Expansion of CTG18.1 Trinucleotide Repeat in TCF4 Is a Potent Driver of Fuchs' Corneal Dystrophy.
- Factors influencing uptake of pharmacogenetic testing in a diverse patient population.
- Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.
- Gene variants in angiogenesis and lymphangiogenesis and cutaneous melanoma progression.
- Genetic Dissection of Heritable Traits in Yeast Using Bulk Segregant Analysis.
- Genetic architecture of gene expression traits across diverse populations.
- Genetic variation in the prostaglandin E2 pathway is associated with primary graft dysfunction.
- Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
- Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia.
- Human disturbance causes the formation of a hybrid swarm between two naturally sympatric fish species.
- Malaria severity: Possible influence of the E670G PCSK9 polymorphism: A preliminary case-control study in Malian children.
- Matrix metalloproteinase-9 genetic polymorphisms and the risk for advanced pelvic organ prolapse.
- Measures of linkage disequilibrium among neighbouring SNPs indicate asymmetries across the house mouse hybrid zone.
- Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations.
- Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.
- Multiplexed shotgun genotyping resolves species relationships within the North American genus Penstemon.
- Next-generation genotyping of hypervariable loci in many individuals of a non-model species: technical and theoretical implications.
- Overlap Extension Barcoding for the Next Generation Sequencing and Genotyping of Plasmodium falciparum in Individual Patients in Western Kenya.
- Prevalence and severity of fuchs corneal dystrophy in Tangier Island.
- Prolonged tenofovir treatment of macaques infected with K65R reverse transcriptase mutants of SIV results in the development of antiviral immune responses that control virus replication after drug withdrawal.
- Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent.
- RNA-Seq optimization with eQTL gold standards.
- Rapid Molecular Diagnostics, Antibiotic Treatment Decisions, and Developing Approaches to Inform Empiric Therapy: PRIMERS I and II.
- Return of widespread chloroquine-sensitive Plasmodium falciparum to Malawi.
- Risk of geographic atrophy in the comparison of age-related macular degeneration treatments trials.
- Significance of MDM2 and P14 ARF polymorphisms in susceptibility to differentiated thyroid carcinoma.
- Simultaneous Detection of Major Drug Resistance Mutations of HIV-1 Subtype B Viruses from Dried Blood Spot Specimens by Multiplex Allele-Specific Assay.
- Single-Nucleotide Polymorphisms Associated With Age-Related Macular Degeneration and Lesion Phenotypes in the Comparison of Age-Related Macular Degeneration Treatments Trials.
- Specific combinations of donor and recipient KIR-HLA genotypes predict for large differences in outcome after cord blood transplantation.
- Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.
- TOMM40'523 variant and cognitive decline in older persons with APOE ε3/3 genotype.
- The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease.
- The genetic architecture of type 2 diabetes.
- Unisexual reproduction drives meiotic recombination and phenotypic and karyotypic plasticity in Cryptococcus neoformans.
- Using ERDS to infer copy-number variants in high-coverage genomes.
- Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study.
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Keywords of People
- Liu, Yutao, Adjunct Assistant Professor in the Department of Medicine, Medicine, Medical Genetics