Naomi R. Wray
Genetics · 2007–2022
A researcher in the Science corpus: 34 papers; trusts 26 researchers and is trusted by 22 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 647 citations into it; #490 of 6,854 by trust here, #88 by citations
- Molecular Biology — 404 citations into it; #15,340 of 17,773 by trust here, #2,259 by citations
- Computational Biology & Bioinformatics — 43 citations into it; #243 of 660 by trust here, #219 by citations
- Plant Science — 32 citations into it
- Epidemiology — 26 citations into it; #865 of 2,148 by trust here, #759 by citations
- Medical & Health AI — 5 citations into it; #83 of 239 by trust here, #137 by citations
Whom Naomi R. Wray trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Michael E. Goddard
- Jian Yang
- Peter M. Visscher
- Paul M. Vanraden
- Ben J. Hayes
- Sang Hong Lee
- Shaun Purcell
- David Reich
- S. Zollner
- Frank Dudbridge
Who trusts Naomi R. Wray overall
- Frank Dudbridge
- Michael E. Goddard
- Haja N. Kadarmideen
- Bogdan Pasaniuc
- Peter M. Visscher
- Jian Yang
- Sean M. Hoban
- Ben J. Hayes
- Alkes L Price
- Konrad J. Karczewski
Papers from Naomi R. Wray's perspective
Ordered by how strongly the researchers Naomi R. Wray trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Regression Shrinkage and Selection via the Lasso
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
- Principal components analysis corrects for stratification in genome-wide association studies
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Efficient methods to compute genomic predictions. (Journal of Dairy Science)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Accuracy of Predicting the Genetic Risk of Disease Using a Genome-Wide Approach (PLoS ONE)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
Their papers
- Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (2016) — 2,949 citations
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (2017) — 3,277 citations
- DNA methylation age of blood predicts all-cause mortality in later life (2015) — 1,136 citations
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- DNA methylation-based measures of biological age: meta-analysis predicting time to death (2016) — 993 citations
- Epigenetic Signatures of Cigarette Smoking (2016) — 798 citations
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions (2019) — 2,238 citations
- A mega-analysis of genome-wide association studies for major depressive disorder (2012) — 1,096 citations
- Brain age predicts mortality (2017) — 752 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
- Improved polygenic prediction by Bayesian multiple regression on summary statistics (2019) — 484 citations
- Identification of novel risk loci, causal insights, and heritable risk for Parkinson’s disease: a meta-genome wide association study (2019) — 1,651 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- A resource-efficient tool for mixed model association analysis of large-scale data (2019) — 483 citations
- Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits (2018) — 613 citations
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) — 1,432 citations
- Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
- Causal associations between risk factors and common diseases inferred from GWAS summary data (2017) — 942 citations
- Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index (2015) — 781 citations