Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease
出版年份 2018 全文链接
标题
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease
作者
关键词
-
出版物
Nature Communications
Volume 9, Issue 1, Pages -
出版商
Springer Nature
发表日期
2018-04-18
DOI
10.1038/s41467-018-03911-8
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Genetic Association of Waist-to-Hip Ratio With Cardiometabolic Traits, Type 2 Diabetes, and Coronary Heart Disease
- (2017) Connor A. Emdin et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Monosynaptic retrograde tracing of neurons expressing the G-protein coupled receptor Gpr151 in the mouse brain
- (2017) Jonas Broms et al. JOURNAL OF COMPARATIVE NEUROLOGY
- ANGPTL3 Deficiency and Protection Against Coronary Artery Disease
- (2017) Nathan O. Stitziel et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Rare and low-frequency coding variants alter human adult height
- (2017) Eirini Marouli et al. NATURE
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
- (2017) Valérie Turcot et al. NATURE GENETICS
- Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
- (2017) Helen R Warren et al. NATURE GENETICS
- Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease
- (2017) Marc S. Sabatine et al. NEW ENGLAND JOURNAL OF MEDICINE
- Cardiovascular and Metabolic Effects of ANGPTL3 Antisense Oligonucleotides
- (2017) Mark J. Graham et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
- (2017) Frederick E. Dewey et al. NEW ENGLAND JOURNAL OF MEDICINE
- Mast cell and eosinophil surface receptors as targets for anti-allergic therapy
- (2017) Roopesh Singh Gangwar et al. PHARMACOLOGY & THERAPEUTICS
- A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma
- (2017) Dirk Smith et al. PLoS Genetics
- Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
- (2016) Amit V. Khera et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
- (2016) Praveen Surendran et al. NATURE GENETICS
- Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants
- (2016) Ying Jin et al. NATURE GENETICS
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
- (2016) NEW ENGLAND JOURNAL OF MEDICINE
- GSDMB induces an asthma phenotype characterized by increased airway responsiveness and remodeling without lung inflammation
- (2016) Sudipta Das et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
- (2015) Philip E. Stuart et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Vaccination against IL-33 Inhibits Airway Hyperresponsiveness and Inflammation in a House Dust Mite Model of Asthma
- (2015) Ying Lei et al. PLoS One
- Targeted disruption of PDE3B, but not PDE3A, protects murine heart from ischemia/reperfusion injury
- (2015) Youn Wook Chung et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
- (2014) Ron Do et al. NATURE
- MC4R-expressing glutamatergic neurons in the paraventricular hypothalamus regulate feeding and are synaptically connected to the parabrachial nucleus
- (2014) B. P. Shah et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Beyond GWASs: Illuminating the Dark Road from Association to Function
- (2013) Stacey L. Edwards et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts
- (2013) Faer S Morrison et al. BMC GENOMICS
- A Role for Phosphodiesterase 3B in Acquisition of Brown Fat Characteristics by White Adipose Tissue in Male Mice
- (2013) Emilia Guirguis et al. ENDOCRINOLOGY
- Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
- (2011) Georg B. Ehret et al. NATURE
- Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
- (2010) William McLaren et al. BIOINFORMATICS
- Epidemiology of Atopic Dermatitis and Atopic March in Children
- (2010) Jonathan M. Spergel IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA
- Exome Sequencing,ANGPTL3Mutations, and Familial Combined Hypolipidemia
- (2010) Kiran Musunuru et al. NEW ENGLAND JOURNAL OF MEDICINE
- A Large-Scale, Consortium-Based Genomewide Association Study of Asthma
- (2010) Miriam F. Moffatt et al. NEW ENGLAND JOURNAL OF MEDICINE
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
- (2009) S. Nejentsev et al. SCIENCE
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