| human | Q5 |
| P496 | ORCID iD | 0000-0001-6996-4834 |
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q33297839 | A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease |
| Q33263815 | A comparative analysis of the information content in long and short SAGE libraries |
| Q33969884 | A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. |
| Q42560464 | A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity |
| Q37217180 | Age at onset in two common neurodegenerative diseases is genetically controlled |
| Q100732941 | An exploration of genetic association tests for disease risk and age at onset |
| Q35883321 | An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error. |
| Q36967234 | An international collaborative family-based whole-genome linkage scan for high-grade myopia |
| Q53266856 | Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis. |
| Q31031554 | Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study. |
| Q61554560 | Articular hypermobility is a protective factor for hand osteoarthritis |
| Q28244911 | Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease |
| Q36752987 | Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2. |
| Q37155995 | Association test for X-linked QTL in family-based designs |
| Q40589889 | Baseline Pulse Pressure, Acute Kidney Injury, and Mortality After Noncardiac Surgery. |
| Q35973947 | Biomarkers associated with clinical phenotypes of hand osteoarthritis in a large multigenerational family: the CARRIAGE family study. |
| Q35838094 | Blood Pressure-Lowering Mechanisms of the DASH Dietary Pattern |
| Q37606194 | COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus |
| Q24651845 | Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia |
| Q33871171 | Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays |
| Q49865499 | Correlation of Virtual Reality Simulation and Dry Lab Robotic Technical Skills. |
| Q37432795 | Drawing inferences about the coancestry coefficient |
| Q37593048 | Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders |
| Q37602878 | Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies. |
| Q48854171 | Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism |
| Q36887184 | Factors affecting success of thymus transplantation for complete DiGeorge anomaly |
| Q61809677 | Family-based association tests for rare variants with censored traits |
| Q51780295 | Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease. |
| Q37139997 | Gene signatures of postoperative atrial fibrillation in atrial tissue after coronary artery bypass grafting surgery in patients receiving β-blockers |
| Q34135448 | Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort |
| Q61554500 | Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring |
| Q37384486 | Genetic screen of African Americans with Fuchs endothelial corneal dystrophy |
| Q28943319 | Genetic variants on chromosome 1q41 influence ocular axial length and high myopia |
| Q33904424 | Genome-wide association identifies ATOH7 as a major gene determining human optic disc size |
| Q28943365 | Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese |
| Q37736430 | Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. |
| Q37156208 | Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease |
| Q36733057 | Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery |
| Q34927051 | Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family |
| Q36934059 | Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family |
| Q37267021 | Genome-wide linkage scan in fuchs endothelial corneal dystrophy |
| Q28943360 | Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism |
| Q28257569 | Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra |
| Q28181160 | Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage |
| Q28211511 | Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease |
| Q24531223 | Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease |
| Q36973898 | Inverse association of general joint hypermobility with hand and knee osteoarthritis and serum cartilage oligomeric matrix protein levels |
| Q34612662 | Investigation of the PARK10 gene in Parkinson disease. |
| Q61554190 | Invited Commentary |
| Q36162384 | Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium |
| Q37571849 | Levels of Urinary Metabolites of Organophosphate Flame Retardants, TDCIPP, and TPHP, in Pregnant Women in Shanghai |
| Q53648320 | Leveraging population information in family-based rare variant association analyses of quantitative traits. |
| Q40398032 | Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing |
| Q36925985 | Long-term tolerance to allogeneic thymus transplants in complete DiGeorge anomaly |
| Q38771492 | Maintenance and Representation of Mind Wandering during Resting-State fMRI |
| Q47670427 | Mast cell activation and arterial hypotension during proximal aortic repair requiring hypothermic circulatory arrest. |
| Q31115537 | Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations |
| Q33571775 | Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. |
| Q33943645 | Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy |
| Q33630728 | Molecular clock and recombination in primate Mhc genes. |
| Q24339538 | Mutations in SCO2 are associated with autosomal-dominant high-grade myopia |
| Q37077018 | Myocilin polymorphisms and high myopia in subjects of European origin |
| Q51938289 | NOS2A and the modulating effect of cigarette smoking in Parkinson's disease. |
| Q47889444 | Paleo-demography of the Drosophila melanogaster subgroup: application of the maximum likelihood method. |
| Q38531016 | Paravertebral Block for Inguinal Herniorrhaphy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials |
| Q37292851 | Platelet Counts, Acute Kidney Injury, and Mortality after Coronary Artery Bypass Grafting Surgery |
| Q47554949 | Preterm Delivery and Low Birth Weight Among Neonates Conceived With Intracytoplasmic Sperm Injection Compared With Conventional In Vitro Fertilization. |
| Q33886360 | Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy |
| Q34695965 | Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases |
| Q130682138 | Serum proteomic panel validated for prediction of knee osteoarthritis progression |
| Q36224928 | The Role of Progesterone and a Novel Progesterone Receptor, Progesterone Receptor Membrane Component 1, in the Inflammatory Response of Fetal Membranes to Ureaplasma parvum Infection |
| Q41747119 | The neutral theory and natural selection in the HLA region. |
| Q36718966 | Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein |
| Q35616544 | X-APL: an improved family-based test of association in the presence of linkage for the X chromosome |
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