Elizabeth T. Cirulli
Genetics · 2010–2018
A researcher in the Science corpus: 4 papers; trusts 5 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 79 citations into it; #5,922 of 6,854 by trust here, #1,848 by citations
- Molecular Biology — 57 citations into it
Whom Elizabeth T. Cirulli trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- J. K. Pritchard
- David B. Goldstein
- David Reich
- B. Maher
- John A. Todd
- Y. Wong
- Teri Manolio
- Pawel Stankiewicz
- David Botstein
- Eric S. Lander
Who trusts Elizabeth T. Cirulli overall
Papers from Elizabeth T. Cirulli's perspective
Ordered by how strongly the researchers Elizabeth T. Cirulli trusts endorse each paper. Same corpus, a different order for every researcher.
- On the allelic spectrum of human disease. (Trends in Genetics)
- Common genetic variation and human traits. (New England Journal of Medicine)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
- The Human Gene Mutation Database: 2008 update
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
- Mutations of optineurin in amyotrophic lateral sclerosis (Nature)
- A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21 (Nature Genetics)
- The allelic architecture of human disease genes: common disease-common variant...or not? (Human Molecular Genetics)
- Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease (Nature Genetics)
- Common and rare variants in multifactorial susceptibility to common diseases (Nature Genetics)
Their papers
- Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2018) — 630 citations
- Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways (2015) — 948 citations
- Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis (2012) — 618 citations
- Uncovering the roles of rare variants in common disease through whole-genome sequencing (2010) — 1,175 citations