Pages that link to "Q40045934"
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The following pages link to Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system. (Q40045934):
Displayed 15 items.
- A common loss-of-function variant is associated with lower vitamin B concentration in African Americans (Q56356408) (← links)
- Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland (Q57255465) (← links)
- Understanding the Hidden Complexity of Latin American Population Isolates (Q58618781) (← links)
- The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE (Q64111276) (← links)
- Augmented intelligence with natural language processing applied to electronic health records for identifying patients with non-alcoholic fatty liver disease at risk for disease progression (Q77790627) (← links)
- Population Histories of the United States Revealed through Fine-Scale Migration and Haplotype Analysis (Q90110283) (← links)
- A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank (Q90127350) (← links)
- Rapid, Phase-free Detection of Long Identity-by-Descent Segments Enables Effective Relationship Classification (Q90516160) (← links)
- Analysis of the genetic basis of height in large Jewish nuclear families (Q91709417) (← links)
- Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits (Q92180471) (← links)
- RaPID: ultra-fast, powerful, and accurate detection of segments identical by descent (IBD) in biobank-scale cohorts (Q92180634) (← links)
- A Syrian patient with Steel syndrome due to compound heterozygous COL27A1 mutations with colobomata of the eye (Q92492874) (← links)
- Personalized Medicine and the Power of Electronic Health Records (Q92555536) (← links)
- Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems (Q92643089) (← links)
- Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide (Q94592250) (← links)