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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A calcium-sensing receptor allelic series and underdiagnosis of genetically driven hypocalcemia Chang, Jeremy B.

112 8 p. 1818-1832
artikel
2 A genealogy-based approach for revealing ancestry-specific structures in admixed populations Tang, Ji

112 8 p. 1906-1922
artikel
3 An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome Choufani, Sanaa

112 8 p. 1979
artikel
4 Cross-omics risk scores of inflammation markers are associated with all-cause mortality: The Canadian Longitudinal Study on Aging Yaskolka Meir, Anat

112 8 p. 1892-1905
artikel
5 Data sharing in the PRIMED Consortium: Design, implementation, and recommendations for future policymaking Smith, Johanna L.

112 8 p. 1754-1768
artikel
6 Efficient Mendelian randomization analysis with self-adaptive determination of sample structure and multiple pleiotropic effects Zhang, Liye

112 8 p. 1962-1978
artikel
7 Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing Gold, Jessica I.

112 8 p. 1792-1804
artikel
8 Exploring depression treatment response by using polygenic risk scoring across diverse populations Lapinska, Sandra

112 8 p. 1877-1891
artikel
9 Extracting and calibrating evidence of variant pathogenicity from population biobank data Bhat, Vineel

112 8 p. 1805-1817
artikel
10 Extremely early genomic events and temporal order of esophageal squamous cell carcinogenesis: Longitudinal self-comparison of progressors and non-progressors Liu, Ying

112 8 p. 1864-1876
artikel
11 Genetic predisposition for immunoglobulin E production explains atopic risk in children: Tohoku Medical Megabank cohort study Sutoh, Yoichi

112 8 p. 1852-1863
artikel
12 Genomics-informed drug-repurposing strategy identifies two therapeutic targets for preventing liver disease associated with metabolic dysfunction Seagle, Hannah M.

112 8 p. 1778-1791
artikel
13 Haplotype analysis reveals pleiotropic disease associations in the HLA region Smith, Courtney J.

112 8 p. 1833-1851
artikel
14 Leveraging local ancestry and cross-ancestry genetic architecture to improve genetic prediction of complex traits in admixed populations Zhou, Geyu

112 8 p. 1923-1935
artikel
15 Rare-variant association studies: When are aggregation tests more powerful than single-variant tests? Bose, Debraj

112 8 p. 1948-1961
artikel
16 The evolution of health data ecosystems: An international survey Lerner-Ellis, Jordan P.

112 8 p. 1769-1777
artikel
17 This month in The Journal Hook, Paul W.

112 8 p. 1733-1734
artikel
18 TransferTWAS: A transfer learning framework for cross-tissue transcriptome-wide association study Lai, Daoyuan

112 8 p. 1936-1947
artikel
19 Weighing the evidence on costs and benefits of polygenic risk-based approaches in clinical practice: A systematic review of economic evaluations Siena, Leonardo Maria

112 8 p. 1735-1753
artikel
                             19 gevonden resultaten
 
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