Mark I Mccarthy


Ontology type: schema:Person     


Person Info

NAME

Mark I

SURNAME

Mccarthy

Publications in SciGraph latest 50 shown

  • 2019-02 A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria in DIABETOLOGIA
  • 2018-12 Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels in NATURE COMMUNICATIONS
  • 2018-12 Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference 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
  • 2018-09 Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition in NATURE GENETICS
  • 2018-08 Type 2 diabetes risk alleles in PAM impact insulin release from human pancreatic β-cells in NATURE GENETICS
  • 2018-07 Patterns of differential gene expression in a cellular model of human islet development, and relationship to type 2 diabetes predisposition in DIABETOLOGIA
  • 2018-07 Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation 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
  • 2018-05 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 Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition 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 Metabolite ratios as potential biomarkers for type 2 diabetes: a DIRECT study in DIABETOLOGIA
  • 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 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 Human disease genomics: from variants to biology in GENOME BIOLOGY
  • 2017-07-12 Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness in NATURE COMMUNICATIONS
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Erratum to: Painting a new picture of personalised medicine for diabetes in DIABETOLOGIA
  • 2017-05 Painting a new picture of personalised medicine for diabetes 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
  • 2017-04 How Can Genetic Studies Help Us to Understand Links Between Birth Weight and Type 2 Diabetes? in CURRENT DIABETES REPORTS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2017-02 Genetics of T2DM in 2016: Biological and translational insights from T2DM genetics in NATURE REVIEWS ENDOCRINOLOGY
  • 2017-01 Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity in NATURE
  • 2017-01 Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance in NATURE GENETICS
  • 2016-12 Erratum to: A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studies in GENOME BIOLOGY
  • 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 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-10 Genome-wide associations for birth weight and correlations with adult disease in NATURE
  • 2016-10 A reference panel of 64,976 haplotypes for genotype imputation in NATURE GENETICS
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2016-09 Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin in NATURE GENETICS
  • 2016-09 Tensor decomposition for multiple-tissue gene expression experiments in NATURE GENETICS
  • 2016-09 Trans-ethnic study design approaches for fine-mapping in EUROPEAN JOURNAL OF HUMAN 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
  • 2016-07 Evaluation of type 2 diabetes genetic risk variants in Chinese adults: findings from 93,000 individuals from the China Kadoorie Biobank in DIABETOLOGIA
  • 2016-04 Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 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 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations in NATURE COMMUNICATIONS
  • 2015-12 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels in NATURE COMMUNICATIONS
  • 2015-12 Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases in SCIENTIFIC REPORTS
  • 2015-12 Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants in NATURE COMMUNICATIONS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation in GENOME BIOLOGY
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