nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Accurate and Scalable Construction of Polygenic Scores in Large Biobank Data Sets
|
Yang, Sheng |
|
|
106 |
5 |
p. 679-693 |
artikel |
2 |
Analysis of U8 snoRNA Variants in Zebrafish Reveals How Bi-allelic Variants Cause Leukoencephalopathy with Calcifications and Cysts
|
Badrock, Andrew P. |
|
|
106 |
5 |
p. 694-706 |
artikel |
3 |
Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases
|
DeBoever, Christopher |
|
|
106 |
5 |
p. 611-622 |
artikel |
4 |
Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities
|
Muir, Alison M. |
|
|
106 |
5 |
p. 623-631 |
artikel |
5 |
De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy
|
Chung, Hyung-lok |
|
|
106 |
5 |
p. 717-725 |
artikel |
6 |
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes
|
Choufani, Sanaa |
|
|
106 |
5 |
p. 596-610 |
artikel |
7 |
Insufficient Evidence for “Autism-Specific” Genes
|
Myers, Scott M. |
|
|
106 |
5 |
p. 587-595 |
artikel |
8 |
Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning
|
Vitsios, Dimitrios |
|
|
106 |
5 |
p. 659-678 |
artikel |
9 |
Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases
|
Cochran, J. Nicholas |
|
|
106 |
5 |
p. 632-645 |
artikel |
10 |
Pleiotropy-Based Decomposition of Genetic Risk Scores: Association and Interaction Analysis for Type 2 Diabetes and CAD
|
Chasman, Daniel I. |
|
|
106 |
5 |
p. 646-658 |
artikel |
11 |
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups
|
Dikilitas, Ozan |
|
|
106 |
5 |
p. 707-716 |
artikel |
12 |
This Month in The Journal
|
Ratzel, Sarah |
|
|
106 |
5 |
p. 585-586 |
artikel |