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A GENOME-WIDE META-ANALYSIS OF PLASMA CLUSTERIN LEVELS IN THE CHARGE CONSORTIUM

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

artículo científico publicado en 2014

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes

artículo científico publicado en 2008

CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses

artículo científico publicado en 2006

Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy

artículo científico publicado en 2005

Co-regulatory networks of human serum proteins link genetics to disease

scientific article published in Science

Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype

artículo científico publicado en 2012

Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility

artículo científico publicado en 2011

Estimating prevalence, false-positive rate, and false-negative rate with use of repeated testing when true responses are unknown

artículo científico publicado en 2007

Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease

artículo científico publicado en 2016

Exome-wide association study of plasma lipids in >300,000 individuals

artículo científico publicado en 2017

G-STRATEGY: Optimal Selection of Individuals for Sequencing in Genetic Association Studies

artículo científico publicado en 2016

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

artículo científico publicado en 2014

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

artículo científico publicado en 2010

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

artículo científico publicado en 2019

Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment

artículo científico publicado en 2019

Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

artículo científico publicado en 2009

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

MASTOR: mixed-model association mapping of quantitative traits in samples with related individuals

artículo científico publicado en 2013

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

artículo científico publicado en 2016

Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.

artículo científico publicado en 2016

PLD3 variants in population studies

artículo científico publicado en 2015

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

artículo científico publicado en 2016

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Susceptibility genes for age-related maculopathy on chromosome 10q26

artículo científico publicado en 2005

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

The impact of APOE genotype on survival: Results of 38,537 participants from six population-based cohorts (E2-CHARGE)

artículo científico publicado en 2019

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

artículo científico publicado en 2014

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