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Eden Martin

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Disorders

Procedures

Living Beings

Nuclear Family

Activities & Behaviors

Computer Simulation

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Publications

TOP 3
Edwards Todd L; Pericak-Vance Margaret; Gilbert Johnny R; Haines Jonathan L; Martin Eden R; Ritchie Marylyn D
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
Ma Deqiong; Salyakina Daria; Jaworski James M; Konidari Ioanna; Whitehead Patrice L; Andersen Ashley N; Hoffman Joshua D; Slifer Susan H; Hedges Dale J; Cukier Holly N; Griswold Anthony J; McCauley Jacob L; Beecham Gary W; Wright Harry H; Abramson Ruth K; Martin Eden R; Hussman John P; Gilbert John R; Cuccaro Michael L; Haines Jonathan L; Pericak-Vance Margaret A
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Slifer Michael A; Martin Eden R; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Resolving the relationship between ApolipoproteinE and depression.

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All Publications

2009: Edwards Todd L; Pericak-Vance Margaret; Gilbert Johnny R; Haines Jonathan L; Martin Eden R; Ritchie Marylyn D
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(5):721-35.
2009: Ma Deqiong; Salyakina Daria; Jaworski James M; Konidari Ioanna; Whitehead Patrice L; Andersen Ashley N; Hoffman Joshua D; Slifer Susan H; Hedges Dale J; Cukier Holly N; Griswold Anthony J; McCauley Jacob L; Beecham Gary W; Wright Harry H; Abramson Ruth K; Martin Eden R; Hussman John P; Gilbert John R; Cuccaro Michael L; Haines Jonathan L; Pericak-Vance Margaret A
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Annals of human genetics 2009;73(Pt 3):263-73.
2009: Slifer Michael A; Martin Eden R; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Resolving the relationship between ApolipoproteinE and depression.
Neuroscience letters 2009;455(2):116-9.
2009: Zhang Li; Martin Eden R; Morris Richard W; Li Yi-Ju
Association test for X-linked QTL in family-based designs.
American journal of human genetics 2009;84(4):431-44.
2009: Gao Xiaoyi; Martin Eden R; Liu Yutao; Mayhew Gregory; Vance Jeffery M; Scott William K
Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18.
American journal of human genetics 2009;84(4):499-504.
2009: Liang Xueying; Slifer Michael; Martin Eden R; Schnetz-Boutaud Nathalie; Bartlett Jackie; Anderson Brent; Züchner Stephan; Gwirtsman Harry; Gilbert John R; Pericak-Vance Margaret A; Haines Jonathan L
Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.
Human mutation 2009;30(3):463-71.
2009: Beecham Gary W; Martin Eden R; Li Yi-Ju; Slifer Michael A; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.
American journal of human genetics 2009;84(1):35-43.
2009: Gao Xiaoyi; Martin Eden R
Using allele sharing distance for detecting human population stratification.
Human heredity 2009;68(3):182-91.
2008: Züchner S; Gilbert J R; Martin E R; Leon-Guerrero C R; Xu P-T; Browning C; Bronson P G; Whitehead P; Schmechel D E; Haines J L; Pericak-Vance M A
Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3.
Annals of human genetics 2008;72(Pt 6):725-31.
2008: Chung Ren-Hua; Schmidt Silke; Martin Eden R; Hauser Elizabeth R
Ordered-subset analysis (OSA) for family-based association mapping of complex traits.
Genetic epidemiology 2008;32(7):627-37.
2008: Hancock Dana B; Martin Eden R; Vance Jeffery M; Scott William K
Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
Neurogenetics 2008;9(4):249-62.
2008: Ewens Warren J; Spielman Richard S; Kaplan Norman L; Gao Xiaoyi; Morris Richard W; Martin Eden R
Disease associations and family-based tests.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2008;Chapter 1():Unit 1.12.
2008: Li Y W; Martin E R; Li Y J
EMK: a novel program for family-based allelic and genotypic association tests on quantitative traits.
Annals of human genetics 2008;72(Pt 3):388-96.
2008: Zhang Li; Martin Eden R; Chung Ren-Hua; Li Yi-Ju; Morris Richard W
X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design.
Genetic epidemiology 2008;32(4):370-80.
2008: Gao Xiaoyi; Starmer Joshua; Martin Eden R
A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms.
Genetic epidemiology 2008;32(4):361-9.
2008: Thornton-Wells Tricia A; Moore Jason H; Martin Eden R; Pericak-Vance Margaret A; Haines Jonathan L
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.
Genetic epidemiology 2008;32(3):187-203.
2008: Gao X; Scott W K; Wang G; Mayhew G; Li Y J; Vance J M; Martin E R
Gene-gene interaction between FGF20 and MAOB in Parkinson disease.
Annals of human genetics 2008;72(Pt 2):157-62.
2008: Wang Gaofeng; van der Walt Joelle M; Mayhew Gregory; Li Yi-Ju; Züchner Stephan; Scott William K; Martin Eden R; Vance Jeffery M
Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.
American journal of human genetics 2008;82(2):283-9.
2008: Martin E R; Schmidt M A
The future is now - will the real disease gene please stand up?
Human heredity 2008;66(2):127-35.
2008: Hancock Dana B; Martin Eden R; Mayhew Gregory M; Stajich Jeffrey M; Jewett Rita; Stacy Mark A; Scott Burton L; Vance Jeffery M; Scott William K
Pesticide exposure and risk of Parkinson's disease: a family-based case-control study.
BMC neurology 2008;8():6.
2008: Schmidt Silke; Schmidt Michael A; Qin Xuejun; Martin Eden R; Hauser Elizabeth R
Increased efficiency of case-control association analysis by using allele-sharing and covariate information.
Human heredity 2008;65(3):154-65.
2007: Mei H; Cuccaro M L; Martin E R
Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.
American journal of human genetics 2007;81(6):1251-61.
2007: Hancock Dana B; Martin Eden R; Li Yi-Ju; Scott William K
Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations.
Genetic epidemiology 2007;31(8):883-93.
2007: Liang Xueying; Martin Eden R; Schnetz-Boutaud Nathalie; Bartlett Jackie; Anderson Brent; Züchner Stephan; Gwirtsman Harry; Schmechel Don; Carney Regina; Gilbert John R; Pericak-Vance Margaret A; Haines Jonathan L
Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease.
Human mutation 2007;28(11):1065-73.
2007: Schmidt Silke; Qin Xuejun; Schmidt Michael A; Martin Eden R; Hauser Elizabeth R
Interpreting analyses of continuous covariates in affected sibling pair linkage studies.
Genetic epidemiology 2007;31(6):541-52.
2007: Ashley-Koch Allison E; Jaworski James; Ma De Qiong; Mei Hao; Ritchie Marylyn D; Skaar David A; Robert Delong G; Worley Gordon; Abramson Ruth K; Wright Harry H; Cuccaro Michael L; Gilbert John R; Martin Eden R; Pericak-Vance Margaret A
Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.
Psychiatric genetics 2007;17(4):221-6.
2007: Hancock Dana B; Martin Eden R; Stajich Jeffrey M; Jewett Rita; Stacy Mark A; Scott Burton L; Vance Jeffery M; Scott William K
Smoking, caffeine, and nonsteroidal anti-inflammatory drugs in families with Parkinson disease.
Archives of neurology 2007;64(4):576-80.
2007: Lin Ping-I; Vance Jeffery M; Pericak-Vance Margaret A; Martin Eden R
No gene is an island: the flip-flop phenomenon.
American journal of human genetics 2007;80(3):531-8.
2007: Chung Ren-Hua; Hauser Elizabeth R; Martin Eden R
Interpretation of simultaneous linkage and family-based association tests in genome screens.
Genetic epidemiology 2007;31(2):134-42.
2007: Chung Ren-Hua; Morris Richard W; Zhang Li; Li Yi-Ju; Martin Eden R
X-APL: an improved family-based test of association in the presence of linkage for the X chromosome.
American journal of human genetics 2007;80(1):59-68.
2007: Rampersaud E; Morris R W; Weinberg C R; Speer M C; Martin E R
Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available.
Genetic epidemiology 2007;31(1):18-30.
2007: Schmidt Mike; Qin Xuejun; Martin Eden R; Hauser Elizabeth R; Schmidt Silke
Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies.
BMC proceedings 2007;1 Suppl 1():S138.
2007: Qin Xuejun; Schmidt Silke; Martin Eden; Hauser Elizabeth R
Visualizing genotype x phenotype relationships in the GAW15 simulated data.
BMC proceedings 2007;1 Suppl 1():S132.
2006: Kang Sun J; Scott William K; Li Yi-Ju; Hauser Michael A; van der Walt Joelle M; Fujiwara Kenichiro; Mayhew Gregory M; West Sandra G; Vance Jeffery M; Martin Eden R
Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease.
Movement disorders : official journal of the Movement Disorder Society 2006;21(12):2175-80.
2006: North B V; Sham P C; Knight J; Martin E R; Curtis D
Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility loci.
Annals of human genetics 2006;70(Pt 6):893-906.
2006: Hancock Dana B; Martin Eden R; Fujiwara Kenichiro; Stacy Mark A; Scott Burton L; Stajich Jeffrey M; Jewett Rita; Li Yi-Ju; Hauser Michael A; Vance Jeffery M; Scott William K
NOS2A and the modulating effect of cigarette smoking in Parkinson's disease.
Annals of neurology 2006;60(3):366-73.
2006: Li Yi-Ju; Scott William K; Zhang Ling; Lin Ping-I; Oliveira Sofia A; Skelly Tara; Doraiswamy Maurali P; Welsh-Bohmer Kathleen A; Martin Eden R; Haines Jonathan L; Pericak-Vance Margaret A; Vance Jeffery M
Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.
Neurobiology of aging 2006;27(8):1087-93.
2006: Lin P I; Martin E R; Bronson P G; Browning-Large C; Small G W; Schmechel D E; Welsh-Bohmer K A; Haines J L; Gilbert J R; Pericak-Vance M A
Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease.
Neurology 2006;67(1):64-8.
2006: Collins Ann L; Ma Deqiong; Whitehead Patrice L; Martin Eden R; Wright Harry H; Abramson Ruth K; Hussman John P; Haines Jonathan L; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.
Neurogenetics 2006;7(3):167-74.
2006: Lin Ping-I; Martin Eden R; Browning-Large Carrie A; Schmechel Donald E; Welsh-Bohmer Kathleen A; Doraiswamy P Murali; Gilbert John R; Haines Jonathan L; Pericak-Vance Margaret A
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis.
Neurogenetics 2006;7(3):157-65.
2006: Schmidt Silke; Schmidt Michael A; Qin Xuejun; Martin Eden R; Hauser Elizabeth R
Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.
Genetic epidemiology 2006;30(5):409-22.
2006: Ashley-Koch A E; Mei H; Jaworski J; Ma D Q; Ritchie M D; Menold M M; Delong G R; Abramson R K; Wright H H; Hussman J P; Cuccaro M L; Gilbert J R; Martin E R; Pericak-Vance M A
An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder.
Annals of human genetics 2006;70(Pt 3):281-92.
2006: Rabionet Raquel; McCauley Jacob L; Jaworski James M; Ashley-Koch Allison E; Martin Eden R; Sutcliffe James S; Haines Jonathan L; DeLong G Robert; Abramson Ruth K; Wright Harry H; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
Lack of association between autism and SLC25A12.
The American journal of psychiatry 2006;163(5):929-31.
2006: Slifer M A; Martin E R; Bronson P G; Browning-Large C; Doraiswamy P M; Welsh-Bohmer K A; Gilbert J R; Haines J L; Pericak-Vance M A
Lack of association between UBQLN1 and Alzheimer disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(3):208-13.
2006: Allen Andrew S; Martin Eden R; Qin Xuejun; Li Yi-Ju
Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring.
Genetic epidemiology 2006;30(3):248-58.
2006: Liang X; Schnetz-Boutaud N; Kenealy S J; Jiang L; Bartlett J; Lynch B; Gaskell P C; Gwirtsman H; McFarland L; Bembe M L; Bronson P; Gilbert J R; Martin E R; Pericak-Vance M A; Haines J L
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.
Molecular psychiatry 2006;11(3):280-5.
2006: Martin E R; Ritchie M D; Hahn L; Kang S; Moore J H
A novel method to identify gene-gene effects in nuclear families: the MDR-PDT.
Genetic epidemiology 2006;30(2):111-23.
2006: Chung Ren-Hua; Hauser Elizabeth R; Martin Eden R
The APL test: extension to general nuclear families and haplotypes and examination of its robustness.
Human heredity 2006;61(4):189-99.
2005: Martin E R; Bronson P G; Li Y-J; Wall N; Chung R-H; Schmechel D E; Small G; Xu P-T; Bartlett J; Schnetz-Boutaud N; Haines J L; Gilbert J R; Pericak-Vance M A
Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease.
Journal of medical genetics 2005;42(10):787-92.
2005: van der Walt Joelle M; Scott William K; Slifer Susan; Gaskell P C; Martin Eden R; Welsh-Bohmer Kathleen; Creason Marilyn; Crunk Amy; Fuzzell Denise; McFarland Lynne; Kroner Charles C; Jackson C E; Haines Jonathan L; Pericak-Vance Margaret A
Maternal lineages and Alzheimer disease risk in the Old Order Amish.
Human genetics 2005;118(1):115-22.
2005: Ma D Q; Whitehead P L; Menold M M; Martin E R; Ashley-Koch A E; Mei H; Ritchie M D; Delong G R; Abramson R K; Wright H H; Cuccaro M L; Hussman J P; Gilbert J R; Pericak-Vance M A
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.
American journal of human genetics 2005;77(3):377-88.
2005: Slifer Michael A; Martin Eden R; Haines Jonathan L; Pericak-Vance Margaret A
The ubiquilin 1 gene and Alzheimer's disease.
The New England journal of medicine 2005;352(26):2752-3; author reply 2752-3.
2005: Skaar D A; Shao Y; Haines J L; Stenger J E; Jaworski J; Martin E R; DeLong G R; Moore J H; McCauley J L; Sutcliffe J S; Ashley-Koch A E; Cuccaro M L; Folstein S E; Gilbert J R; Pericak-Vance M A
Analysis of the RELN gene as a genetic risk factor for autism.
Molecular psychiatry 2005;10(6):563-71.
2005: Schmidt Mike; Hauser Elizabeth R; Martin Eden R; Schmidt Silke
Extension of the SIMLA package for generating pedigrees with complex inheritance patterns: environmental covariates, gene-gene and gene-environment interaction.
Statistical applications in genetics and molecular biology 2005;4():Article15.
2005: Boyles Abee L; Scott William K; Martin Eden R; Schmidt Silke; Li Yi-Ju; Ashley-Koch Allison; Bass Meredyth P; Schmidt Michael; Pericak-Vance Margaret A; Speer Marcy C; Hauser Elizabeth R
Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
Human heredity 2005;59(4):220-7.
2004: Rabionet Raquel; Jaworski James M; Ashley-Koch Allison E; Martin Eden R; Sutcliffe James S; Haines Jonathan L; Delong G Robert; Abramson Ruth K; Wright Harry H; Cuccaro Michael L; Gilbert John R; Pericak-Vance Margaret A
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Neuroscience letters 2004;372(3):209-14.
2004: Nicodemus Kristin K; Stenger Judith E; Schmechel Donald E; Welsh-Bohmer Kathleen A; Saunders Ann M; Roses Allen D; Gilbert John R; Vance Jeffery M; Haines Jonathan L; Pericak-Vance Margaret A; Martin Eden R
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease.
Neurogenetics 2004;5(4):201-8.
2004: Oliveira Sofia A; Scott William K; Zhang Fengyu; Stajich Jeffrey M; Fujiwara Kenichiro; Hauser Michael; Scott Burton L; Pericak-Vance Margaret A; Vance Jeffery M; Martin Eden R
Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.
Neurogenetics 2004;5(3):147-55.
2004: Kraus V B; Li Y-J; Martin E R; Jordan J M; Renner J B; Doherty M; Wilson A G; Moskowitz R; Hochberg M; Loeser R; Hooper M; Sundseth Scott
Articular hypermobility is a protective factor for hand osteoarthritis.
Arthritis and rheumatism 2004;50(7):2178-83.
2004: van der Walt Joelle M; Dementieva Yulia A; Martin Eden R; Scott William K; Nicodemus Kristin K; Kroner Charles C; Welsh-Bohmer Kathleen A; Saunders Ann M; Roses Allen D; Small Gary W; Schmechel Donald E; Murali Doraiswamy P; Gilbert John R; Haines Jonathan L; Vance Jeffery M; Pericak-Vance Margaret A
Analysis of European mitochondrial haplogroups with Alzheimer disease risk.
Neuroscience letters 2004;365(1):28-32.
2004: Li Y J; Hauser M A; Scott W K; Martin E R; Booze M W; Qin X J; Walter J W; Nance M A; Hubble J P; Koller W C; Pahwa R; Stern M B; Hiner B C; Jankovic J; Goetz C G; Small G W; Mastaglia F; Haines J L; Pericak-Vance M A; Vance J M
Apolipoprotein E controls the risk and age at onset of Parkinson disease.
Neurology 2004;62(11):2005-9.
2004: van der Walt Joelle M; Noureddine Maher A; Kittappa Raja; Hauser Michael A; Scott William K; McKay Ron; Zhang Fengyu; Stajich Jeffrey M; Fujiwara Kenichiro; Scott Burton L; Pericak-Vance Margaret A; Vance Jeffery M; Martin Eden R
Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.
American journal of human genetics 2004;74(6):1121-7.
2004: North B V; Curtis D; Martin E R; Lai E H; Roses A D; Sham P C
Further investigation of linkage disequilibrium SNPs and their ability to identify associated susceptibility loci.
Annals of human genetics 2004;68(Pt 3):240-8.
2004: Raiford K L; Shao Y; Allen I C; Martin E R; Menold M M; Wright H H; Abramson R K; Worley G; DeLong G R; Vance J M; Cuccaro M L; Gilbert J R; Pericak-Vance M A
No association between the APOE gene and autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;125B(1):57-60.
2004: Bass M P; Martin E R; Hauser E R
Pedigree generation for analysis of genetic linkage and association.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2004;():93-103.
2003: Li Yi-Ju; Oliveira Sofia A; Xu Puting; Martin Eden R; Stenger Judith E; Scherzer Clemens R; Hauser Michael A; Scott William K; Small Gary W; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Pahwa Rajesh; Stern Mathew B; Hiner Bradley C; Jankovic Joseph; Goetz Christopher G; Mastaglia Frank; Middleton Lefkos T; Roses Allen D; Saunders Ann M; Schmechel Donald E; Gullans Steven R; Haines Jonathan L; Gilbert John R; Vance Jeffery M; Pericak-Vance Margaret A; Hulette Christine; Welsh-Bohmer Kathleen A
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.
Human molecular genetics 2003;12(24):3259-67.
2003: Ewens Warren J; Spielman Richard S; Kaplan Norman L; Martin Eden R
Disease associations and family-based tests.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2003;Chapter 1():Unit 1.12.
2003: Martin E R; Bass M P; Gilbert J R; Pericak-Vance M A; Hauser E R
Genotype-based association test for general pedigrees: the genotype-PDT.
Genetic epidemiology 2003;25(3):203-13.
2003: Martin Eden R; Bass Meredyth P; Hauser Elizabeth R; Kaplan Norman L
Accounting for linkage in family-based tests of association with missing parental genotypes.
American journal of human genetics 2003;73(5):1016-26.
2003: Oliveira Sofia A; Martin Eden R; Scott William K; Nicodemus Kristin K; Small Gary W; Schmechel Donald E; Doraiswamy P Murali; Roses Allen D; Saunders Ann M; Gilbert John R; Haines Jonathan L; Vance Jeffery M; Pericak-Vance Margaret A
The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease.
Neuroscience letters 2003;347(3):143-6.
2003: Oliveira Sofia A; Scott William K; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Lyons Kelly E; Pahwa Rajesh; Stern Matthew B; Hiner Bradley C; Jankovic Joseph; Ondo William G; Allen Fred H; Scott Burton L; Goetz Christopher G; Small Gary W; Mastaglia Frank L; Stajich Jeffrey M; Zhang Fengyu; Booze Michael W; Reaves Joshua A; Middleton Lefkos T; Haines Jonathan L; Pericak-Vance Margaret A; Vance Jeffery M; Martin Eden R
Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.
Archives of neurology 2003;60(7):975-80.
2003: Caillier S; Barcellos L F; Baranzini S E; Swerdlin A; Lincoln R R; Steinman L; Martin E; Haines J L; Pericak-Vance M; Hauser S L; Oksenberg J R;
Osteopontin polymorphisms and disease course in multiple sclerosis.
Genes and immunity 2003;4(4):312-5.
2003: Oliveira Sofia A; Scott William K; Martin Eden R; Nance Martha A; Watts Ray L; Hubble Jean P; Koller William C; Pahwa Rajesh; Stern Matthew B; Hiner Bradley C; Ondo William G; Allen Fred H; Scott Burton L; Goetz Christopher G; Small Gary W; Mastaglia Frank; Stajich Jeffrey M; Zhang Fengyu; Booze Michael W; Winn Michelle P; Middleton Lefkos T; Haines Jonathan L; Pericak-Vance Margaret A; Vance Jeffery M
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
Annals of neurology 2003;53(5):624-9.
2003: van der Walt J M; Martin E R; Scott W K; Zhang F; Nance M A; Watts R L; Hubble J P; Haines J L; Koller W C; Lyons K; Pahwa R; Stern M B; Colcher A; Hiner B C; Jankovic J; Ondo W G; Allen F H; Goetz C G; Small G W; Mastaglia F; Roses A D; Stajich J M; Booze M W; Fujiwara K; Gibson R A; Middleton L T; Scott B L; Pericak-Vance M A; Vance J M
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease.
Neurology 2003;60(7):1189-91.
2003: van der Walt Joelle M; Nicodemus Kristin K; Martin Eden R; Scott William K; Nance Martha A; Watts Ray L; Hubble Jean P; Haines Jonathan L; Koller William C; Lyons Kelly; Pahwa Rajesh; Stern Matthew B; Colcher Amy; Hiner Bradley C; Jankovic Joseph; Ondo William G; Allen Fred H; Goetz Christopher G; Small Gary W; Mastaglia Frank; Stajich Jeffrey M; McLaurin Adam C; Middleton Lefkos T; Scott Burton L; Schmechel Donald E; Pericak-Vance Margaret A; Vance Jeffery M
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.
American journal of human genetics 2003;72(4):804-11.
2003: Hauser Michael A; Li Yi-Ju; Takeuchi Satoshi; Walters Robert; Noureddine Maher; Maready Melinda; Darden Tiffany; Hulette Christine; Martin Eden; Hauser Elizabeth; Xu Hong; Schmechel Don; Stenger Judith E; Dietrich Fred; Vance Jeffery
Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage.
Human molecular genetics 2003;12(6):671-7.
2003: Barcellos L F; Oksenberg J R; Begovich A B; Martin E R; Schmidt S; Vittinghoff E; Goodin D S; Pelletier D; Lincoln R R; Bucher P; Swerdlin A; Pericak-Vance M A; Haines J L; Hauser S L;
HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course.
American journal of human genetics 2003;72(3):710-6.
2003: Rampersaud Evadnie; Allen Andrew; Li Yi-Ju; Shao Yujun; Bass Meredyth; Haynes Carol; Ashley-Koch Allison; Martin Eden R; Schmidt Silke; Hauser Elizabeth R
Adjusting for covariates on a slippery slope: linkage analysis of change over time.
BMC genetics 2003;4 Suppl 1():S50.
2002: Uthoff Sonja M S; Crawford Nigel P S; Eichenberger M Robert; Hamilton Crystal J; Petras Robert E; Martin Eden R; Galandiuk Susan
Association of ulcerative colitis with the inflammatory bowel disease susceptibility locus IBD2 in non-Jewish Caucasians and evidence of genetic heterogeneity among racial and ethnic populations with Crohn disease.
American journal of medical genetics 2002;113(3):242-9.
2002: Haines Jonathan L; Bradford Yuki; Garcia Melissa E; Reed Allison D; Neumeister Elizabeth; Pericak-Vance Margaret A; Rimmler Jacqueline B; Menold Marissa M; Martin Eden R; Oksenberg Jorge R; Barcellos Lisa F; Lincoln Robin; Hauser Stephen L;
Multiple susceptibility loci for multiple sclerosis.
Human molecular genetics 2002;11(19):2251-6.
2002: Schmidt Silke; Barcellos Lisa F; DeSombre Karen; Rimmler Jacqueline B; Lincoln Robin R; Bucher Patricia; Saunders Ann M; Lai Eric; Martin Eden R; Vance Jeffery M; Oksenberg Jorge R; Hauser Stephen L; Pericak-Vance Margaret A; Haines Jonathan L;
Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.
American journal of human genetics 2002;70(3):708-17.
2001: Brinker K G; Martin E; Borron P; Mostaghel E; Doyle C; Harding C V; Wright J R
Surfactant protein D enhances bacterial antigen presentation by bone marrow-derived dendritic cells.
American journal of physiology. Lung cellular and molecular physiology 2001;281(6):L1453-63.
2001: Kaplan N L; Martin E R
Power calculations for a general class of tests of linkage and association that use nuclear families with affected and unaffected sibs.
Theoretical population biology 2001;60(3):193-201.
2001: Martin E R; Scott W K; Nance M A; Watts R L; Hubble J P; Koller W C; Lyons K; Pahwa R; Stern M B; Colcher A; Hiner B C; Jankovic J; Ondo W G; Allen F H; Goetz C G; Small G W; Masterman D; Mastaglia F; Laing N G; Stajich J M; Ribble R C; Booze M W; Rogala A; Hauser M A; Zhang F; Gibson R A; Middleton L T; Roses A D; Haines J L; Scott B L; Pericak-Vance M A; Vance J M
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.
JAMA : the journal of the American Medical Association 2001;286(18):2245-50.
2001: Pericak-Vance M A; Rimmler J B; Martin E R; Haines J L; Garcia M E; Oksenberg J R; Barcellos L F; Lincoln R; Goodkin D E; Hauser S L
Linkage and association analysis of chromosome 19q13 in multiple sclerosis.
Neurogenetics 2001;3(4):195-201.
2001: de Silva R; Weiler M; Morris H R; Martin E R; Wood N W; Lees A J
Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy.
Neuroscience letters 2001;311(3):145-8.
2001: Martin E R; Bass M P; Kaplan N L
Correcting for a potential bias in the pedigree disequilibrium test.
American journal of human genetics 2001;68(4):1065-7.
2001: Menold M M; Shao Y; Wolpert C M; Donnelly S L; Raiford K L; Martin E R; Ravan S A; Abramson R K; Wright H H; Delong G R; Cuccaro M L; Pericak-Vance M A; Gilbert J R
Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.
Journal of neurogenetics 2001;15(3-4):245-59.
2001: Schmidt S; Shao Y; Hauser E R; Slifer S H; Martin E R; Scott W K; Speer M C; Pericak-Vance M A
Life after the screen: making sense of many P-values.
Genetic epidemiology 2001;21 Suppl 1():S546-51.
2001: Hardy S W; Weir B S; Kaplan N L; Martin E R
Analysis of single nucleotide polymorphisms in candidate genes using the pedigree disequilibrium test.
Genetic epidemiology 2001;21 Suppl 1():S441-6.
2001: Czika W A; Weir B S; Edwards S R; Thompson R W; Nielsen D M; Brocklebank J C; Zinkus C; Martin E R; Hobler K E
Applying data mining techniques to the mapping of complex disease genes.
Genetic epidemiology 2001;21 Suppl 1():S435-40.
2000: Martin E R; Lai E H; Gilbert J R; Rogala A R; Afshari A J; Riley J; Finch K L; Stevens J F; Livak K J; Slotterbeck B D; Slifer S H; Warren L L; Conneally P M; Schmechel D E; Purvis I; Pericak-Vance M A; Roses A D; Vance J M
SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.
American journal of human genetics 2000;67(2):383-94.
2000: McIntyre L M; Martin E R; Simonsen K L; Kaplan N L
Circumventing multiple testing: a multilocus Monte Carlo approach to testing for association.
Genetic epidemiology 2000;19(1):18-29.
2000: Martin E R; Monks S A; Warren L L; Kaplan N L
A test for linkage and association in general pedigrees: the pedigree disequilibrium test.
American journal of human genetics 2000;67(1):146-54.
2000: Blanton S H; Kolle B S; Hecht J T; Mulliken J B; Martin E R
No evidence supporting MTHFR as a risk factor in the development of familial NSCLP.
American journal of medical genetics 2000;92(5):370-1.
2000: Martin E R; Menold M M; Wolpert C M; Bass M P; Donnelly S L; Ravan S A; Zimmerman A; Gilbert J R; Vance J M; Maddox L O; Wright H H; Abramson R K; DeLong G R; Cuccaro M L; Pericak-Vance M A
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.
American journal of medical genetics 2000;96(1):43-8.
2000: Martin E R; Gilbert J R; Lai E H; Riley J; Rogala A R; Slotterbeck B D; Sipe C A; Grubber J M; Warren L L; Conneally P M; Saunders A M; Schmechel D E; Purvis I; Pericak-Vance M A; Roses A D; Vance J M
Analysis of association at single nucleotide polymorphisms in the APOE region.
Genomics 2000;63(1):7-12.
2000: Martin E R; Kaplan N L
A Monte Carlo procedure for two-stage tests with correlated data.
Genetic epidemiology 2000;18(1):48-62.
1999: Skammelsrud N; Martin E R; Murphy P; Khuu C; Frengen E; Kolstø A B
The gene for human transcription factor TCF11 is located telomeric to D17S1827, BTR and HP1Hsbeta on chromosome 17q22.
Genetic analysis : biomolecular engineering 1999;15(6):217-22.
1999: Joshi D; Barnabas R; Martin E R; Parihar V; Kanojiya M
Aging alters properties of the circadian pacemaker controlling the locomotor activity rhythm in males of Drosophila nasuta.
Chronobiology international 1999;16(6):751-8.
1999: Grubber J M; Saunders A M; Crane-Gatherum A R; Scott W K; Martin E R; Haynes C S; Conneally P M; Small G W; Roses A D; Haines J L; Pericak-Vance M A
Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K).
Neuroscience letters 1999;269(2):115-9.
1999: Allison D B; Heo M; Kaplan N; Martin E R
Sibling-based tests of linkage and association for quantitative traits.
American journal of human genetics 1999;64(6):1754-63.
1999: Rogaeva E A; Premkumar S; Grubber J; Serneels L; Scott W K; Kawarai T; Song Y; Hill D L; Abou-Donia S M; Martin E R; Vance J J; Yu G; Orlacchio A; Pei Y; Nishimura M; Supala A; Roberge B; Saunders A M; Roses A D; Schmechel D; Crane-Gatherum A; Sorbi S; Bruni A; Small G W; Conneally P M; Haines J L; Van Leuven F; St George-Hyslop P H; Farrer L A; Pericak-Vance M A
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.
Nature genetics 1999;22(1):19-22.
1999: Monks S A; Martin E R; Umbach D M; Kaplan N L
Two tests of association for a susceptibility locus for families of variable size: an example using two sampling strategies.
Genetic epidemiology 1999;17 Suppl 1():S655-60.
1999: Anderson J L; Hauser E R; Martin E R; Scott W K; Ashley-Koch A; Kim K J; Monks S A; Haynes C S; Speer M C; Pericak-Vance M A
Complete genomic screen for disease susceptibility loci in nuclear families.
Genetic epidemiology 1999;17 Suppl 1():S473-8.
1998: Haines J L; Terwedow H A; Burgess K; Pericak-Vance M A; Rimmler J B; Martin E R; Oksenberg J R; Lincoln R; Zhang D Y; Banatao D R; Gatto N; Goodkin D E; Hauser S L
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.
Human molecular genetics 1998;7(8):1229-34.
1998: Kaplan N L; Martin E R; Morris R W; Weir B S
Marker selection for the transmission/disequilibrium test, in recently admixed populations.
American journal of human genetics 1998;62(3):703-12.
1997: Martin E R; Kaplan N L; Weir B S
Tests for linkage and association in nuclear families.
American journal of human genetics 1997;61(2):439-48.
1997: Kaplan N L; Martin E R; Weir B S
Power studies for the transmission/disequilibrium tests with multiple alleles.
American journal of human genetics 1997;60(3):691-702.
1997: Simonsen K L; Kaplan N L; Martin E R
A Monte Carlo permutation approach to choosing an affection status model for bipolar affective disorder.
Genetic epidemiology 1997;14(6):681-6.
1990: Martin E R; Brenner B M; Ballermann B J
Heterogeneity of cell surface endothelin receptors.
The Journal of biological chemistry 1990;265(23):14044-9.
1989: Martin E R; Lewicki J A; Scarborough R M; Ballermann B J
Expression and regulation of ANP receptor subtypes in rat renal glomeruli and papillae.
The American journal of physiology 1989;257(4 Pt 2):F649-57.
1989: Martin E R; Marsden P A; Brenner B M; Ballermann B J
Identification and characterization of endothelin binding sites in rat renal papillary and glomerular membranes.
Biochemical and biophysical research communications 1989;162(1):130-7.

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