List of works - Eden R Martin

A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT.

scientific article

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

scientific article

ABCA7 frameshift deletion associated with Alzheimer disease in African Americans.

scientific article

APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation

scientific article

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

scientific article

Adjusting for covariates on a slippery slope: linkage analysis of change over time

scientific article

An exploration of genetic association tests for disease risk and age at onset

scientific article published on 19 October 2020

Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations

scientific article published on 05 December 2018

Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.

scientific article

Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis

scientific article (publication date: March 2002)

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

scientific article

Comparison of three targeted enrichment strategies on the SOLiD sequencing platform

scientific article (publication date: 29 April 2011)

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

scientific article

DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient

scientific article

Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities

scientific journal article

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

scientific article

Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention

scientific article

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

scientific article

Exome sequencing of a multigenerational human pedigree

scientific article (publication date: 14 December 2009)

Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data

scientific article

Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data

scientific article

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

scientific article

Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias

scientific article

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

scientific article

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease

scientific article published on January 2009

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

scientific article

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

scientific article

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

scientific article (publication date: 15 March 2003)

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

scientific article

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease

scientific article (publication date: 15 December 2003)

Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach

scientific article

Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease

scientific article

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

scientific article

Lack of association between autism and SLC25A12

scientific article (publication date: May 2006)

Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes

scientific article

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

scientific article

Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations

scientific article

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

scientific article (publication date: April 2003)

Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease

scientific article published on 29 July 2008

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

scientific article

Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants

scientific article published on 14 January 2016

PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease

scientific article

Pesticide exposure and risk of Parkinson's disease: a family-based case-control study

scientific article

Properties of global- and local-ancestry adjustments in genetic association tests in admixed populations.

scientific article published on 30 December 2017

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

scientific article

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy ⬇️

scientific article published on January 1, 2011

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

scientific article

Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians ⬇️

scientific article published on October 27, 2012

Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

scientific article published on 14 January 2016

Smoking, caffeine, and nonsteroidal anti-inflammatory drugs in families with Parkinson disease

scientific article (publication date: April 2007)

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

scientific article

Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies

scientific article

Visualizing genotype x phenotype relationships in the GAW15 simulated data

scientific article

Vitamin D from different sources is inversely associated with Parkinson disease

scientific article

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

scientific article published on 13 February 2013

List of works by Eden R Martin

A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT.

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

ABCA7 frameshift deletion associated with Alzheimer disease in African Americans.

APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

Adjusting for covariates on a slippery slope: linkage analysis of change over time

An exploration of genetic association tests for disease risk and age at onset

Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations

Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.

Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

Comparison of three targeted enrichment strategies on the SOLiD sequencing platform

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient

Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

Exome sequencing of a multigenerational human pedigree

Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data

Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease

Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach

Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

Lack of association between autism and SLC25A12

Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants

PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease

Pesticide exposure and risk of Parkinson's disease: a family-based case-control study

Properties of global- and local-ancestry adjustments in genetic association tests in admixed populations.

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

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy ⬇️

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians ⬇️

Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

Smoking, caffeine, and nonsteroidal anti-inflammatory drugs in families with Parkinson disease

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies

Visualizing genotype x phenotype relationships in the GAW15 simulated data

Vitamin D from different sources is inversely associated with Parkinson disease

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease