Martina Müller Nurasyid


Ontology type: schema:Person     


Person Info

NAME

Martina

SURNAME

Müller Nurasyid

Publications in SciGraph latest 50 shown

  • 2019-01-07 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci in MOLECULAR PSYCHIATRY
  • 2018-12 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 in GENOME BIOLOGY
  • 2018-12 PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity in NATURE COMMUNICATIONS
  • 2018-12 Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation in NATURE COMMUNICATIONS
  • 2018-12 Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests in NATURE COMMUNICATIONS
  • 2018-09 Multi-ethnic genome-wide association study for atrial fibrillation 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 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes in NATURE GENETICS
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-01-23 Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 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 CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits in NATURE COMMUNICATIONS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 pulver: an R package for parallel ultra-rapid p-value computation for linear regression interaction terms in BMC BIOINFORMATICS
  • 2017-12 Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium in SCIENTIFIC REPORTS
  • 2017-12 Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes in SCIENTIFIC REPORTS
  • 2017-08-02 Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk in NATURE COMMUNICATIONS
  • 2017-08 Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 2017-06-14 Genetic loci associated with heart rate variability and their effects on cardiac disease risk in NATURE COMMUNICATIONS
  • 2017-06 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 2017-04-26 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits in NATURE COMMUNICATIONS
  • 2017-02 Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index in MOLECULAR PSYCHIATRY
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 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 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2016-10 Genetic variants in RBFOX3 are associated with sleep latency in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-11 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation in NATURE GENETICS
  • 2015-06 The impact of low-frequency and rare variants on lipid levels in NATURE GENETICS
  • 2015-05 Genome-wide association study of kidney function decline in individuals of European descent in KIDNEY INTERNATIONAL
  • 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
  • 2014-10 Controversial association results for INSIG2 on body mass index may be explained by interactions with age and with MC4R in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization 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
  • 2013-06 Common variants at 12q15 and 12q24 are associated with infant head circumference in NATURE GENETICS
  • 2013-05 Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222 in BRITISH JOURNAL OF CANCER
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-01 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2012-09 Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways in NATURE GENETICS
  • 2012-09 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes in NATURE GENETICS
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