Michael Boehnke


Ontology type: schema:Person     


Person Info

NAME

Michael

SURNAME

Boehnke

Publications in SciGraph latest 50 shown

  • 2019-12 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity in NATURE COMMUNICATIONS
  • 2019-01-07 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci in MOLECULAR PSYCHIATRY
  • 2019-01 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals in NATURE GENETICS
  • 2018-12 Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes in NATURE COMMUNICATIONS
  • 2018-12 Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans in NATURE COMMUNICATIONS
  • 2018-12 Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS in NATURE COMMUNICATIONS
  • 2018-12 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-12 Author Correction: Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS in NATURE COMMUNICATIONS
  • 2018-11 Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps in NATURE GENETICS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-07 Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium in NATURE NEUROSCIENCE
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12 Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2017-12 Whole genome sequencing in psychiatric disorders: the WGSPD consortium in NATURE NEUROSCIENCE
  • 2017-12 Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-09 Genetic risk scores in the prediction of plasma glucose, impaired insulin secretion, insulin resistance and incident type 2 diabetes in the METSIM study in DIABETOLOGIA
  • 2017-04-26 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits in NATURE COMMUNICATIONS
  • 2017-03 Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-12 New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk in NATURE COMMUNICATIONS
  • 2016-12 A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans in BMC ENDOCRINE DISORDERS
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
  • 2016-10 Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19 in BMC PROCEEDINGS
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-10 A reference panel of 64,976 haplotypes for genotype imputation in NATURE GENETICS
  • 2016-10 Next-generation genotype imputation service and methods in NATURE GENETICS
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2016-08 Analysis of protein-coding genetic variation in 60,706 humans in NATURE
  • 2016-06-29 The genetic regulatory signature of type 2 diabetes in human skeletal muscle in NATURE COMMUNICATIONS
  • 2016 Epilogue: What the Future Holds: Genomic Medicine at the Heart of Diabetes Management in THE GENETICS OF TYPE 2 DIABETES AND RELATED TRAITS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-12 Biological interpretation of genome-wide association studies using predicted gene functions in NATURE COMMUNICATIONS
  • 2015-08 Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity in NATURE GENETICS
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2015-02 Genetic studies of body mass index yield new insights for obesity biology in NATURE
  • 2015-02 New genetic loci link adipose and insulin biology to body fat distribution in NATURE
  • 2014-11 Defining the role of common variation in the genomic and biological architecture of adult human height in NATURE GENETICS
  • 2014-04 Loss-of-function mutations in SLC30A8 protect against type 2 diabetes in NATURE GENETICS
  • 2014-04 Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk in NATURE GENETICS
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2013-11 Common variants associated with plasma triglycerides and risk for coronary artery disease in NATURE GENETICS
  • 2013-11 Discovery and refinement of loci associated with lipid levels in NATURE GENETICS
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
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