Search Results - "Eden, Martin"
-
1
A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms
Published in Genetic epidemiology (01-05-2008)“…Multiple testing is a challenging issue in genetic association studies using large numbers of single nucleotide polymorphism (SNP) markers, many of which…”
Get full text
Journal Article -
2
Epigenome-wide meta-analysis of DNA methylation differences in prefrontal cortex implicates the immune processes in Alzheimer’s disease
Published in Nature communications (30-11-2020)“…DNA methylation differences in Alzheimer’s disease (AD) have been reported. Here, we conducted a meta-analysis of more than 1000 prefrontal cortex brain…”
Get full text
Journal Article -
3
Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease
Published in PloS one (07-10-2011)“…miRNAs were recently implicated in the pathogenesis of numerous diseases, including neurological disorders such as Parkinson's disease (PD). miRNAs are…”
Get full text
Journal Article -
4
Cross-tissue analysis of blood and brain epigenome-wide association studies in Alzheimer’s disease
Published in Nature communications (18-08-2022)“…To better understand DNA methylation in Alzheimer’s disease (AD) from both mechanistic and biomarker perspectives, we performed an epigenome-wide meta-analysis…”
Get full text
Journal Article -
5
MethReg: estimating the regulatory potential of DNA methylation in gene transcription
Published in Nucleic acids research (20-05-2022)“…Epigenome-wide association studies often detect many differentially methylated sites, and many are located in distal regulatory regions. To further prioritize…”
Get full text
Journal Article -
6
Explainable machine learning aggregates polygenic risk scores and electronic health records for Alzheimer’s disease prediction
Published in Scientific reports (09-01-2023)“…Alzheimer’s disease (AD) is the most common late-onset neurodegenerative disorder. Identifying individuals at increased risk of developing AD is important for…”
Get full text
Journal Article -
7
Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease
Published in American journal of human genetics (09-01-2009)“…Only Apolipoprotein E polymorphisms have been consistently associated with the risk of late-onset Alzheimer disease (LOAD), but they represent only a minority…”
Get full text
Journal Article -
8
Critical evaluation of the reliability of DNA methylation probes on the Illumina MethylationEPIC v1.0 BeadChip microarrays
Published in Epigenetics (01-12-2024)“…DNA methylation (DNAm) plays a crucial role in a number of complex diseases. However, the reliability of DNAm levels measured using Illumina arrays varies…”
Get full text
Journal Article -
9
coMethDMR: accurate identification of co-methylated and differentially methylated regions in epigenome-wide association studies with continuous phenotypes
Published in Nucleic acids research (26-09-2019)“…Recent technology has made it possible to measure DNA methylation profiles in a cost-effective and comprehensive genome-wide manner using array-based…”
Get full text
Journal Article -
10
Pesticide exposure and risk of Parkinson's disease: a family-based case-control study
Published in BMC neurology (28-03-2008)“…Pesticides and correlated lifestyle factors (e.g., exposure to well-water and farming) are repeatedly reported risk factors for Parkinson's disease (PD), but…”
Get full text
Journal Article -
11
Dry eye symptoms align more closely to non-ocular conditions than to tear film parameters
Published in British journal of ophthalmology (01-08-2015)“…To evaluate the relationship between dry eye symptoms, non-ocular conditions and tear film parameters. Cross-sectional study. The study population consisted of…”
Get more information
Journal Article -
12
Incomplete response to artificial tears is associated with features of neuropathic ocular pain
Published in British journal of ophthalmology (01-06-2016)“…Artificial tears are first-line therapy for patients with dry eye symptoms. It is not known, however, which patient factors associate with a positive response…”
Get more information
Journal Article -
13
A pharmacist-led information technology intervention for medication errors (PINCER): a multicentre, cluster randomised, controlled trial and cost-effectiveness analysis
Published in The Lancet (British edition) (07-04-2012)“…Summary Background Medication errors are common in primary care and are associated with considerable risk of patient harm. We tested whether a pharmacist-led,…”
Get full text
Journal Article -
14
No Gene Is an Island: The Flip-Flop Phenomenon
Published in American journal of human genetics (01-03-2007)“…An increasing number of publications are replicating a previously reported disease-marker association but with the risk allele reversed from the previous…”
Get full text
Journal Article -
15
Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
Published in Annals of human genetics (01-03-2010)“…Summary Parkinson disease (PD) is a chronic neurodegenerative disorder with a cumulative prevalence of greater than one per thousand. To date three independent…”
Get full text
Journal Article -
16
Identification of novel genes for age‐at‐onset of Alzheimer's disease by combining quantitative and survival trait analyses
Published in Alzheimer's & dementia (01-07-2023)“…Introduction Our understanding of the genetic predisposition for age‐at‐onset (AAO) of Alzheimer's disease (AD) is limited. Here, we sought to identify genes…”
Get full text
Journal Article -
17
Profound analgesia is associated with a truncated peptide resulting from tissue specific alternative splicing of DRG CA8-204 regulated by an exon-level cis-eQTL
Published in PLoS genetics (14-06-2019)“…Carbonic anhydrase-8 (CA8) is an intracellular protein that functions as an allosteric inhibitor of inositol trisphosphate receptor-1 (ITPR1) critical to…”
Get full text
Journal Article -
18
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
Published in Human molecular genetics (01-08-2012)“…Autism spectrum disorders (ASDs) are highly heritable, yet relatively few associated genetic loci have been replicated. Copy number variations (CNVs) have been…”
Get full text
Journal Article -
19
Association Between Polymorphisms in DNA Damage Repair Genes and Radiation Therapy–Induced Early Adverse Skin Reactions in a Breast Cancer Population: A Polygenic Risk Score Approach
Published in International journal of radiation oncology, biology, physics (01-04-2020)“…Genetic variations in DNA damage repair (DDR) genes may influence radiation therapy (RT)–induced acute normal tissue toxicity in patients with breast cancer…”
Get full text
Journal Article -
20
Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
Published in American journal of human genetics (11-03-2011)“…Dilated cardiomyopathy commonly causes heart failure and is the most frequent precipitating cause of heart transplantation. Familial dilated cardiomyopathy has…”
Get full text
Journal Article