Struan F. A. Grant
Nature · 2004–2021
A researcher in the Science corpus: 9 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Who trusts Struan F. A. Grant overall
Papers from Struan F. A. Grant's perspective
Ordered by how strongly the researchers Struan F. A. Grant trusts endorse each paper. Same corpus, a different order for every researcher.
- Detection of large-scale variation in the human genome (Nature Genetics)
- Fine-scale structural variation of the human genome (Nature Genetics)
- Large-Scale Copy Number Polymorphism in the Human Genome (Science)
- A tiling resolution DNA microarray with complete coverage of the human genome (Nature Genetics)
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Next-generation genotype imputation service and methods (Nature Genetics)
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
- Global and societal implications of the diabetes epidemic (Nature)
- Mapping and sequencing of structural variation from eight human genomes (Nature)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
Their papers
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes (2006) — 2,333 citations
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007) — 1,861 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes (2009) — 1,451 citations
- High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. (2009) — 374 citations
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (2009) — 1,008 citations
- The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke (2004) — 970 citations