Nicholas A. Furlotte
Statistics and Probability · 2011–2019
A researcher in the Science corpus: 15 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Statistics and Probability — 16 citations into it
Whom Nicholas A. Furlotte trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Nicholas A. Furlotte's perspective
Ordered by how strongly the researchers Nicholas A. Furlotte trusts endorse each paper. Same corpus, a different order for every researcher.
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- Genetic Dissection of Transcriptional Regulation in Budding Yeast (Science)
- Genetics of gene expression surveyed in maize, mouse and man (Nature)
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Demographic history and rare allele sharing among human populations (Proceedings of the National Academy of Sciences of the United States of America)
- Partitioning heritability by functional annotation using genome-wide association summary statistics (Nature Genetics)
- Rcpp: Seamless R and C++ Integration
- Genome-wide genetic data on ~500,000 UK Biobank participants (bioRxiv)
- A direct approach to false discovery rates
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
Their papers
- Mouse genomic variation and its effect on phenotypes and gene regulation (2011) — 1,549 citations
- Comparative Analysis of Proteome and Transcriptome Variation in Mouse (2011) — 637 citations
- Linkage disequilibrium dependent architecture of human complex traits reveals action of negative selection (2016) — 192 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
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) — 1,654 citations
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) — 629 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- Multi-trait analysis of genome-wide association summary statistics using MTAG (2018) — 1,002 citations
- Analysis of shared heritability in common disorders of the brain (2018) — 1,836 citations
- An atlas of genetic influences on osteoporosis in humans and mice (2018) — 681 citations
- Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
- Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
- R/qtl2: Software for Mapping Quantitative Trait Loci with High-Dimensional Data and Multiparent Populations (2018) — 383 citations
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) — 986 citations