Works by Boehnke, Michael
Results: 126
Multi-INTACT: integrative analysis of the genome, transcriptome, and proteome identifies causal mechanisms of complex traits.
- Published in:
- Genome Biology, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s13059-025-03480-2
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- Article
The role of HNF4A variants in the risk of type 2 diabetes.
- Published in:
- Current Diabetes Reports, 2005, v. 5, n. 2, p. 149, doi. 10.1007/s11892-005-0043-y
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- Article
Estimating Hepatic Glucokinase Activity Using a Simple Model of Lactate Kinetics.
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- Diabetes Care, 2012, v. 35, n. 5, p. 1015, doi. 10.2337/dc11-1540
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- Article
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.
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- PLoS Genetics, 2019, v. 15, n. 5, p. 1, doi. 10.1371/journal.pgen.1008130
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- Article
Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes.
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- PLoS Genetics, 2018, v. 14, n. 7, p. 1, doi. 10.1371/journal.pgen.1007452
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- Article
Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis.
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- 2018
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- journal article
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
- Published in:
- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00335-2
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- Article
Finding the missing heritability of complex diseases.
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- Nature, 2009, v. 461, n. 7265, p. 747, doi. 10.1038/nature08494
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- Article
Replicating genotype–phenotype associations.
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- Nature, 2007, v. 447, n. 7145, p. 655, doi. 10.1038/447655a
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- Article
Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns.
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- Human Genetics, 2005, v. 118, n. 2, p. 245, doi. 10.1007/s00439-005-0046-4
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- Article
Revisiting the genome-wide significance threshold for common variant GWAS.
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- G3: Genes | Genomes | Genetics, 2021, v. 11, n. 2, p. 1, doi. 10.1093/g3journal/jkaa056
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- Article
Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies.
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- G3: Genes | Genomes | Genetics, 2018, v. 8, n. 10, p. 3255, doi. 10.1534/g3.118.200502
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- Article
Trans-ancestry Fine Mapping and Molecular Assays Identify Regulatory Variants at the ANGPTL8 HDL-C GWAS Locus.
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- G3: Genes | Genomes | Genetics, 2017, v. 7, n. 9, p. 3217, doi. 10.1534/g3.117.300088
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- Article
FIVEx: an interactive eQTL browser across public datasets.
- Published in:
- Bioinformatics, 2022, v. 38, n. 2, p. 559, doi. 10.1093/bioinformatics/btab614
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- Article
LocusZoom.js: interactive and embeddable visualization of genetic association study results.
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- Bioinformatics, 2021, v. 37, n. 18, p. 3017, doi. 10.1093/bioinformatics/btab186
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- Article
emeraLD: rapid linkage disequilibrium estimation with massive datasets.
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- Bioinformatics, 2019, v. 35, n. 1, p. 164, doi. 10.1093/bioinformatics/bty547
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- Article
LASER server: ancestry tracing with genotypes or sequence reads.
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- Bioinformatics, 2017, v. 33, n. 13, p. 2056, doi. 10.1093/bioinformatics/btx075
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- Article
Genome-wide association studies in diverse populations.
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- 2010
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- journal article
Meta-analysis of Complex Diseases at Gene Level with Generalized Functional Linear Models.
- Published in:
- Genetics, 2016, v. 202, n. 2, p. 457, doi. 10.1534/genetics.115.180869
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- Article
Gene Level Meta-Analysis of Quantitative Traits by Functional Linear Models.
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- Genetics, 2015, v. 200, n. 4, p. 1089, doi. 10.1534/genetics.115.178343
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- Publication type:
- Article
Tissue-specific alternative splicing of TCF7L2.
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- Human Molecular Genetics, 2009, v. 18, n. 20, p. 3795, doi. 10.1093/hmg/ddp321
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- Article
Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.
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- Human Molecular Genetics, 2008, v. 17, n. R2, p. R102, doi. 10.1093/hmg/ddn275
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- Article
Association Analysis and Meta-Analysis of Multi-Allelic Variants for Large-Scale Sequence Data.
- Published in:
- Genes, 2020, v. 11, n. 5, p. 586, doi. 10.3390/genes11050586
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- Article
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans.
- Published in:
- Diabetes, 2010, v. 59, n. 5, p. 1266, doi. 10.2337/DB09-1568
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- Article
Association of 18 Confirmed Susceptibility Loci for Type 2 Diabetes With Indices of Insulin Release, Proinsulin Conversion, and Insulin Sensitivity in 5,327 Nondiabetic Finnish Men.
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- Diabetes, 2009, v. 58, n. 9, p. 2129, doi. 10.2337/db09-0117
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- Article
Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample.
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- Diabetes, 2006, v. 55, n. 9, p. 2649, doi. 10.2337/db06-0341
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- Article
Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort.
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- 2002
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- journal article
The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences.
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- 2001
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- journal article
Evaluation of polygenic risk scores to differentiate between type 1 and type 2 diabetes.
- Published in:
- Genetic Epidemiology, 2023, v. 47, n. 4, p. 303, doi. 10.1002/gepi.22521
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- Article
Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations.
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- Genetic Epidemiology, 2020, v. 44, n. 6, p. 537, doi. 10.1002/gepi.22326
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- Article
Power loss due to testing association between covariate‐adjusted traits and genetic variants.
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- Genetic Epidemiology, 2020, v. 44, n. 6, p. 579, doi. 10.1002/gepi.22325
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- Article
Combining sequence data from multiple studies: Impact of analysis strategies on rare variant calling and association results.
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- Genetic Epidemiology, 2020, v. 44, n. 1, p. 41, doi. 10.1002/gepi.22261
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- Article
Multi‐SKAT: General framework to test for rare‐variant association with multiple phenotypes.
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- Genetic Epidemiology, 2019, v. 43, n. 1, p. 4, doi. 10.1002/gepi.22156
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- Article
Methods for meta-analysis of multiple traits using GWAS summary statistics.
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- Genetic Epidemiology, 2018, v. 42, n. 2, p. 134, doi. 10.1002/gepi.22105
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- Article
A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.
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- Genetic Epidemiology, 2017, v. 41, n. 1, p. 18, doi. 10.1002/gepi.22014
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- Article
Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome.
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- Genetic Epidemiology, 2015, v. 39, n. 7, p. 499, doi. 10.1002/gepi.21935
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- Article
Pleiotropy Analysis of Quantitative Traits at Gene Level by Multivariate Functional Linear Models.
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- Genetic Epidemiology, 2015, v. 39, n. 4, p. 259, doi. 10.1002/gepi.21895
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- Article
The Role of Environmental Heterogeneity in Meta-Analysis of Gene-Environment Interactions With Quantitative Traits.
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- Genetic Epidemiology, 2014, v. 38, n. 5, p. 416, doi. 10.1002/gepi.21810
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- Article
Recommended Joint and Meta-Analysis Strategies for Case-Control Association Testing of Single Low-Count Variants.
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- Genetic Epidemiology, 2013, v. 37, n. 6, p. 539, doi. 10.1002/gepi.21742
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- Article
Importance of Different Types of Prior Knowledge in Selecting Genome-Wide Findings for Follow-Up.
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- Genetic Epidemiology, 2013, v. 37, n. 2, p. 205, doi. 10.1002/gepi.21705
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- Article
SNP Prioritization Using a Bayesian Probability of Association.
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- Genetic Epidemiology, 2013, v. 37, n. 2, p. 214, doi. 10.1002/gepi.21704
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- Article
Identifying Plausible Genetic Models Based on Association and Linkage Results: Application to Type 2 Diabetes.
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- Genetic Epidemiology, 2012, v. 36, n. 8, p. 820, doi. 10.1002/gepi.21668
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- Article
Quantifying and correcting for the winner's curse in quantitative-trait association studies.
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- Genetic Epidemiology, 2011, v. 35, n. 3, p. 133, doi. 10.1002/gepi.20551
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- Article
Meta-analysis of genetic association studies and adjustment for multiple testing of correlated SNPs and traits.
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- Genetic Epidemiology, 2010, v. 34, n. 7, p. 739, doi. 10.1002/gepi.20538
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- Publication type:
- Article
Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies.
- Published in:
- Genetic Epidemiology, 2009, v. 33, n. 6, p. 508, doi. 10.1002/gepi.20403
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- Article
Quantifying and correcting for the winner's curse in genetic association studies.
- Published in:
- Genetic Epidemiology, 2009, v. 33, n. 5, p. 453, doi. 10.1002/gepi.20398
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- Publication type:
- Article
Optimal designs for two-stage genome-wide association studies.
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- Genetic Epidemiology, 2007, v. 31, n. 7, p. 776, doi. 10.1002/gepi.20240
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- Article
Using sex‐averaged genetic maps in multipoint linkage analysis when identity‐by‐descent status is incompletely known.
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- Genetic Epidemiology, 2006, v. 30, n. 5, p. 384, doi. 10.1002/gepi.20151
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- Article
Haplotype association analysis for late onset diseases using nuclear family data.
- Published in:
- Genetic Epidemiology, 2006, v. 30, n. 3, p. 220, doi. 10.1002/gepi.20139
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- Publication type:
- Article
Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database.
- Published in:
- Genetic Epidemiology, 2006, v. 30, n. 2, p. 180, doi. 10.1002/gepi.20131
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- Publication type:
- Article