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「"Day-Williams AG "[Author]」の検索結果

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Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease.

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts.

Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts.

PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variants.

Phenome-wide association studies across large population cohorts support drug target validation.

A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica.

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis.

The genetic architecture of type 2 diabetes.

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study.

Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape.

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.

Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalopathy.

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.

Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases.

ARIEL and AMELIA: Testing for an Accumulation of Rare Variants Using Next-Generation Sequencing Data.

An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studies.

A Variant in MCF2L Is Associated with Osteoarthritis.

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