Michael Boehnke
Genetics · 2003–2022
A researcher in the Science corpus: 56 papers; trusts 13 researchers and is trusted by 7 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 986 citations into it; #3,167 of 6,854 by trust here, #41 by citations
- Molecular Biology — 651 citations into it
- Statistics and Probability — 38 citations into it; #6,148 of 12,932 by trust here, #9,233 by citations
Whom Michael Boehnke trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Michael Boehnke overall
Papers from Michael Boehnke's perspective
Ordered by how strongly the researchers Michael Boehnke trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
- 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)
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
- Common and rare variants in multifactorial susceptibility to common diseases (Nature Genetics)
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
- A method and server for predicting damaging missense mutations
- Fast and accurate long-range phasing in a UK Biobank cohort
- New approaches to population stratification in genome-wide association studies
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Next-generation genotype imputation service and methods (2016) — 3,622 citations
- Biological interpretation of genome-wide association studies using predicted gene functions (2015) — 821 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- Identification of ten loci associated with height highlights new biological pathways in human growth (2008) — 644 citations
- Genome-wide association studies in diverse populations (2010) — 591 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome (2003) — 2,182 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- Replicating genotype–phenotype associations (2007) — 1,394 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- So many correlated tests, so little time! Rapid adjustment of P values for multiple correlated tests. (2007) — 477 citations
- The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2012) — 551 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- Quantifying penetrance in a dominant disease gene using large population control cohorts (2016) — 400 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) — 1,485 citations
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations