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 |