S. Lindstrom
Genetics · with Kraft · 2014–2018
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 49 citations into it
Whom S. Lindstrom trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from S. Lindstrom's perspective
Ordered by how strongly the researchers S. Lindstrom trusts endorse each paper. Same corpus, a different order for every researcher.
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- Bayesian refinement of association signals for 14 loci in 3 common diseases
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (Nature)
- Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (Nature Genetics)
- Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (bioRxiv)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (American Journal of Human Genetics)
- Integrating Functional Data to Prioritize Causal Variants in Statistical Fine-Mapping Studies
- Bayesian variable selection regression for genome-wide association studies and other large-scale problems
- On the limited memory BFGS method for large scale optimization
- LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies (Nature Genetics)
Their papers
- Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
- Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (2018) — 797 citations
- Integrating Functional Data to Prioritize Causal Variants in Statistical Fine-Mapping Studies (2014) — 492 citations