L. Brooks
Genetics · Nature · 2007–2015
A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 172 citations into it; #4,860 of 6,854 by trust here, #39 by citations
- Molecular Biology — 110 citations into it
Whom L. Brooks trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts L. Brooks overall
Papers from L. Brooks's perspective
Ordered by how strongly the researchers L. Brooks trusts endorse each paper. Same corpus, a different order for every researcher.
- A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Exome sequencing as a tool for Mendelian disease gene discovery
- The Human Gene Mutation Database: 2008 update
- Searching for genetic determinants in the new millennium (Nature)
- Mapping copy number variation by population scale genome sequencing (Nature)
- Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration (Science)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- ClinGen--the Clinical Genome Resource. (2015) — 1,269 citations
- Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
- Replicating genotype–phenotype associations (2007) — 1,394 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- A map of human genome variation from population scale sequencing (2010) — 7,967 citations
- A HapMap harvest of insights into the genetics of common disease. (2008) — 956 citations