Eden R. Martin

发表

SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies

Michael A. Schmidt, Stephan Züchner, Eden R. Martin, 2010, Bioinform..

Pathway-PDT: a flexible pathway analysis tool for nuclear families

Margaret A. Pericak-Vance, Ren-Hua Chung, Michael A. Schmidt, 2013, BMC Bioinformatics.

CAPL: an efficient association software package using family and case-control data and accounting for population stratification

Ren-Hua Chung, Michael A. Schmidt, Eden R. Martin, 2010, BMC Bioinformatics.

Family-Based Association Test Using Both Common and Rare Variants and Accounting for Directions of Effects for Sequencing Data

Ren-Hua Chung, Wei-Yun Tsai, Eden R. Martin, 2014, PloS one.

Reconsidering Association Testing Methods Using Single-Variant Test Statistics as Alternatives to Pooling Tests for Sequence Data with Rare Variants

Eden R. Martin, Ray E. Hershberger, E. Martin, 2012, PloS one.

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2012, Nature Genetics.

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2020, Nature Communications.

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

Margaret A. Pericak-Vance, Jonathan L. Haines, Lindsay A. Farrer, 2016, Neurology: Genetics.

Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias

Margaret A. Pericak-Vance, Matthew P. Frosch, M. Ilyas Kamboh, 2014, PLoS genetics.

Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis

Margaret A. Pericak-Vance, P. Murali Doraiswamy, Jonathan L. Haines, 2006, Neurogenetics.

A General Framework for Formal Tests of Interaction after Exhaustive Search Methods with Applications to MDR and MDR-PDT

Marylyn D. Ritchie, Scott M. Dudek, Todd L. Edwards, 2010, PloS one.

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

Margaret A. Pericak-Vance, Jonathan L. Haines, John R. Gilbert, 2006, Neurogenetics.

Using Allele Sharing Distance for Detecting Human Population Stratification

Xiaoyi Gao, Eden R. Martin, E. Martin, 2009, Human Heredity.

Evaluation of Current Methods of Testing Differential Gene expression and Beyond

Marcy C. Speer, Eden R. Martin, Yi-Ju Li, 2002 .

Identifying Consensus Disease Pathways in Parkinson's Disease Using an Integrative Systems Biology Approach

Margaret A. Pericak-Vance, Deborah C. Mash, Sawsan Khuri, 2011, PloS one.

Association test for X-linked QTL in family-based designs.

Li Zhang, Eden R. Martin, Yi-Ju Li, 2009, American journal of human genetics.

Linkage Disequilibrium and Association Analysis

Eden R. Martin, E. Martin, 2005, Genetic Analysis of Complex Diseases.

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

Margaret A. Pericak-Vance, Marylyn D. Ritchie, Tricia A. Thornton-Wells, 2016, Neurobiology of Aging.

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

Dana B. Hancock, William K. Scott, Eden R. Martin, 2008, Neurogenetics.

Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing

Margaret A. Pericak-Vance, Silke Schmidt, Marcy C. Speer, 2005, Human Heredity.