J. Howson
Genetics · 2003–2020
A researcher in the Science corpus: 13 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 231 citations into it
Whom J. Howson trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Chris Wallace (in Genetics)
Papers from J. Howson's perspective
Ordered by how strongly the researchers J. Howson trusts endorse each paper. Same corpus, a different order for every researcher.
- Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
- Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses (Nature)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
- The C‐type lectin‐like domain superfamily (The FEBS Journal)
- A quantitative protein interaction network for the ErbB receptors using protein microarrays (Nature)
- Copy Number Variation in Human Health, Disease, and Evolution (Annual review of genomics and human genetics (Print))
- A global reference for human genetic variation
Their papers
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) — 631 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits (2019) — 481 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) — 244 citations
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) — 401 citations
- Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) — 508 citations
- Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations
- Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac Disease (2008) — 701 citations
- Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes (2007) — 1,532 citations
- Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease (2003) — 2,313 citations