| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genealogical estimate of genetic relationships
|
Fan, Caoqi
|
|
|
109 |
5 |
p. 812-824
|
artikel
|
| 2 |
Analyzing and reconciling colocalization and transcriptome-wide association studies from the perspective of inferential reproducibility
|
Hukku, Abhay
|
|
|
109 |
5 |
p. 825-837
|
artikel
|
| 3 |
Combining evidence from Mendelian randomization and colocalization: Review and comparison of approaches
|
Zuber, Verena
|
|
|
109 |
5 |
p. 767-782
|
artikel
|
| 4 |
De novo variants in ATP2B1 lead to neurodevelopmental delay
|
Rahimi, Meer Jacob
|
|
|
109 |
5 |
p. 944-952
|
artikel
|
| 5 |
Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries
|
Smith, Samuel Pattillo
|
|
|
109 |
5 |
p. 871-884
|
artikel
|
| 6 |
Genetic modifiers of Huntington disease differentially influence motor and cognitive domains
|
Lee, Jong-Min
|
|
|
109 |
5 |
p. 885-899
|
artikel
|
| 7 |
Germline MBD4 deficiency causes a multi-tumor predisposition syndrome
|
Palles, Claire
|
|
|
109 |
5 |
p. 953-960
|
artikel
|
| 8 |
Leveraging LD eigenvalue regression to improve the estimation of SNP heritability and confounding inflation
|
Song, Shuang
|
|
|
109 |
5 |
p. 802-811
|
artikel
|
| 9 |
METRO: Multi-ancestry transcriptome-wide association studies for powerful gene-trait association detection
|
Li, Zheng
|
|
|
109 |
5 |
p. 783-801
|
artikel
|
| 10 |
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk
|
Willcox, Jon A.L.
|
|
|
109 |
5 |
p. 961-966
|
artikel
|
| 11 |
Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk
|
Schaid, Daniel J.
|
|
|
109 |
5 |
p. 900-908
|
artikel
|
| 12 |
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program
|
Hu, Xiaowei
|
|
|
109 |
5 |
p. 857-870
|
artikel
|
| 13 |
Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization
|
Jiang, Lin
|
|
|
109 |
5 |
p. 838-856
|
artikel
|
| 14 |
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations
|
Devane, John
|
|
|
109 |
5 |
p. 928-943
|
artikel
|
| 15 |
Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation
|
Coolen, Marion
|
|
|
109 |
5 |
p. 909-927
|
artikel
|
| 16 |
Response to Mörseburg et al.
|
Wyckelsma, Victoria L.
|
|
|
109 |
5 |
p. 973
|
artikel
|
| 17 |
Response to Wyckelsma et al.: Loss of α-actinin-3 during human evolution provides superior cold resilience and muscle heat generation
|
Mörseburg, Alexander
|
|
|
109 |
5 |
p. 967-972
|
artikel
|
| 18 |
This month in The Journal
|
Spencer, Kylee L.
|
|
|
109 |
5 |
p. 765-766
|
artikel
|
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