Erwin P Bottinger


Ontology type: schema:Person     


Person Info

NAME

Erwin P

SURNAME

Bottinger

Publications in SciGraph latest 50 shown

  • 2019-12 Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies 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
  • 2018-11 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
  • 2018-10 Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations in HUMAN 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 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-03 Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI in INTERNATIONAL JOURNAL OF OBESITY
  • 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 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function in SCIENTIFIC REPORTS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-10 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease in NATURE GENETICS
  • 2017-09 Association analyses based on false discovery rate implicate new loci for coronary artery disease in NATURE GENETICS
  • 2017-06 Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci in HUMAN GENETICS
  • 2017-05-26 Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function in SCIENTIFIC REPORTS
  • 2017-05-25 Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve in NATURE COMMUNICATIONS
  • 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 Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets in NATURE GENETICS
  • 2017-03 Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk in NATURE GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-12 No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis in SCIENTIFIC REPORTS
  • 2016-10 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci in NATURE GENETICS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2016-08 Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits in NATURE GENETICS
  • 2016-06 A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough in THE PHARMACOGENOMICS JOURNAL
  • 2016-05 Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs in SCIENTIFIC REPORTS
  • 2016-05 Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public in GENETICS IN MEDICINE
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function 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 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-12 The IGNITE network: a model for genomic medicine implementation and research in BMC MEDICAL GENOMICS
  • 2015-10 A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease 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
  • 2015-01 Defective fatty acid oxidation in renal tubular epithelial cells has a key role in kidney fibrosis development in NATURE MEDICINE
  • 2014-12 Erratum to: Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians in GERIATRIC NEPHROLOGY AND UROLOGY
  • 2014-11 Defining the role of common variation in the genomic and biological architecture of adult human height in NATURE GENETICS
  • 2014-10 Design and Anticipated Outcomes of the eMERGE‐PGx Project: A Multicenter Pilot for Preemptive Pharmacogenomics in Electronic Health Record Systems in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2013-10 Opportunities for genomic clinical decision support interventions in GENETICS IN MEDICINE
  • 2013-10 The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future in GENETICS IN MEDICINE
  • 2013-08 The CLIPMERGE PGx Program: Clinical Implementation of Personalized Medicine Through Electronic Health Records and Genomics–Pharmacogenomics in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2013-06 A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry in NATURE GENETICS
  • 2013-04 Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians in GERIATRIC NEPHROLOGY AND UROLOGY
  • 2013-04 Implementing genomic medicine in the clinic: the future is here in GENETICS IN MEDICINE
  • 2013-01 Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans in KIDNEY INTERNATIONAL
  • 2010-10 A novel approach for the generation of genetically modified mammary epithelial cell cultures yields new insights into TGFβ signaling in the mammary gland in BREAST CANCER RESEARCH
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