Digital Library
Close Browse articles from a journal
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
                                       All articles of the corresponding issues
 
                             18 results found
no title author magazine year volume issue page(s) type
1 A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions Garg, Paras

107 4 p. 654-669
article
2 Bayesian Genome-wide TWAS Method to Leverage both cis- and trans-eQTL Information through Summary Statistics Luningham, Justin M.

107 4 p. 714-726
article
3 De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation Mendoza-Ferreira, Natalia

107 4 p. 763-777
article
4 De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity Cristofoli, Francesca

107 4 p. 753-762
article
5 eQTL Colocalization Analyses Identify NTN4 as a Candidate Breast Cancer Risk Gene Beesley, Jonathan

107 4 p. 778-787
article
6 Generalizability of “GWAS Hits” in Clinical Populations: Lessons from Childhood Cancer Survivors Im, Cindy

107 4 p. 636-653
article
7 Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy Krebs, Kristi

107 4 p. 612-621
article
8 Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project Roman, Tamara S.

107 4 p. 596-611
article
9 Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? Middleton, Anna

107 4 p. 743-752
article
10 Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations Martin, Alicia R.

107 4 p. 788-789
article
11 Inferring Gene-by-Environment Interactions with a Bayesian Whole-Genome Regression Model Kerin, Matthew

107 4 p. 698-713
article
12 Lessons Learned from Bugs in Models of Human History Ragsdale, Aaron P.

107 4 p. 583-588
article
13 Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations Connaughton, Dervla M.

107 4 p. 727-742
article
14 Ovarian Cancer Risk Variants Are Enriched in Histotype-Specific Enhancers and Disrupt Transcription Factor Binding Sites Jones, Michelle R.

107 4 p. 622-635
article
15 Roadmap for Establishing Large-Scale Genomic Medicine Initiatives in Low- and Middle-Income Countries Patrinos, George P.

107 4 p. 589-595
article
16 Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies Galer, Peter D.

107 4 p. 683-697
article
17 This Month in The Journal Ratzel, Sarah

107 4 p. 581-582
article
18 Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation Althari, Sara

107 4 p. 670-682
article
                             18 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands