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Kathryn Lunetta

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TOP 3
Kathryn L Lunetta
Methods for meta-analysis of genetic data.
Tiffany C Hadzi; Audrey E Hendricks; Jeanne C Latourelle; Kathryn L Lunetta; Marcy E MacDonald; Richard H Myers; Jayalakshmi Mysore; L Adrienne Cupples; Tammy Gillis; James F Gusella; Jean-Paul Vonsattel
Assessment of cortical and striatal involvement in 523 Huntington disease brains.
Gyungah Jun; Eric B Larson; Kathryn L Lunetta; Richard Mayeux; Margaret A Pericak-Vance; Gerard D Schellenberg; Badri N Vardarajan; Chang-En Yu; Jacqueline Buros; Paul K Crane; Beth A Dombroski; Jonathan L Haines; Michele V Hawk; Lindsay A Farrer
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.

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All Publications

2013: Kathryn L Lunetta
Methods for meta-analysis of genetic data.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2013;Chapter 1():Unit1.24.
2012: Tiffany C Hadzi; Audrey E Hendricks; Jeanne C Latourelle; Kathryn L Lunetta; Marcy E MacDonald; Richard H Myers; Jayalakshmi Mysore; L Adrienne Cupples; Tammy Gillis; James F Gusella; Jean-Paul Vonsattel
Assessment of cortical and striatal involvement in 523 Huntington disease brains.
Neurology 2012;79(16):1708-15.
2012: Gyungah Jun; Eric B Larson; Kathryn L Lunetta; Richard Mayeux; Margaret A Pericak-Vance; Gerard D Schellenberg; Badri N Vardarajan; Chang-En Yu; Jacqueline Buros; Paul K Crane; Beth A Dombroski; Jonathan L Haines; Michele V Hawk; Lindsay A Farrer
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.
Archives of neurology 2012;69(10):1270-9.
2012: Scott A Melville; Antonio R Parrado; Shannon L Risacher; Andrew J. Saykin; Li Shen; Badri Vardarajan; Clinton T Baldwin; Jacqueline Buros; Charles DeCarli; Lindsay A Farrer; Gyungah Jun; Sungeun Kim; Mark W Logue; Kathryn L Lunetta
Multiple loci influencing hippocampal degeneration identified by genome scan.
Annals of neurology 2012;72(1):65-75.
2012: Porat M Erlich; Carmela R Abraham; Clinton T Baldwin; L Adrienne Cupples; Robert C Green; Kathryn L Lunetta; Lindsay A Farrer
Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.
Neurobiology of aging 2012;33(5):1015.e7-23.
2012: Audrey E Hendricks; Mark W Logue; Josée Dupuis; Mayetri Gupta; Kathryn L Lunetta
A comparison of gene region simulation methods.
PloS one 2012;7(7):e40925.
2011: Mark W Logue; Kathryn L Lunetta; Thomas O Obisesan; Matthew Schu; Rhonna Shatz; Badri N Vardarajan; Clinton T Baldwin; Amy Borenstein; Jacki Buros; L Adrienne Cupples; MARGARET D FALLIN; Lindsay A Farrer; Rodney C P Go; Robert C Green; Patrick Griffith
A comprehensive genetic association study of Alzheimer disease in African Americans.
Archives of neurology 2011;68(12):1569-79.
2011: Usha S Govindarajulu; Haiqun Lin; Kathryn L Lunetta; R B D'Agostino
Frailty models: Applications to biomedical and genetic studies.
Statistics in medicine 2011;30(22):2754-64.
2011: A D Coviello; D Karasik; D P Kiel; Kathryn L Lunetta; Jagadish Ulloor; Ramachandran S Vasan; A Zhang; W V Zhuang; Shalender Bhasin; Joanne M Murabito
Circulating testosterone and SHBG concentrations are heritable in women: the Framingham Heart Study.
The Journal of clinical endocrinology and metabolism 2011;96(9):E1491-5.
2011: Thomas P Ahern; Mariann Christensen; Deirdre P Cronin-Fenton; Jens Peter Garne; Jennifer Gjerde; Timothy L Lash; Kathryn L Lunetta; Carol L Rosenberg; Rebecca A Silliman; Håvard Søiland; Henrik Toft Sørensen; Stephen Hamilton-Dutoit
Functional polymorphisms in UDP-glucuronosyl transferases and recurrence in tamoxifen-treated breast cancer survivors.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011;20(9):1937-43.
2011: Gina M Peloso; Josée Dupuis; Kathryn L Lunetta
Evaluation of methods accounting for population structure with pedigree data and continuous outcomes.
Genetic epidemiology 2011;35(6):427-36.
2011: Timothy L Lash; Deirdre Cronin-Fenton; Thomas P Ahern; Carol L Rosenberg; Kathryn L Lunetta; Rebecca A Silliman; Jens Peter Garne; Henrik Toft Sørensen; Ylva Hellberg; Mariann Christensen; Lars Pedersen; Stephen Hamilton-Dutoit
CYP2D6 inhibition and breast cancer recurrence in a population-based study in Denmark.
Journal of the National Cancer Institute 2011;103(6):489-500.
2011: Karen T Cuenco; Robert P Friedland; Clinton T Baldwin; Jianping Guo; Badri Vardarajan; Kathryn L Lunetta; L Adrienne Cupples; Robert C Green; Charles DeCarli; Lindsay A Farrer
Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families.
Neurobiology of aging 2011;32(2):249-56.
2011: Gina M Peloso; Kathryn L Lunetta
Choice of population structure informative principal components for adjustment in a case-control study.
BMC genetics 2011;12():64.
2010: Timothy L Lash; Deirdre Cronin-Fenton; Thomas P Ahern; Carol L Rosenberg; Kathryn L Lunetta; Rebecca A Silliman; Stephen Hamilton-Dutoit; Jens Peter Garne; Marianne Ewertz; Henrik Toft Sørensen; Lars Pedersen
Breast cancer recurrence risk related to concurrent use of SSRI antidepressants and tamoxifen.
Acta oncologica (Stockholm, Sweden) 2010;49(3):305-12.
2010: Thomas P Ahern; Mariann Christensen; Deirdre P Cronin-Fenton; Kathryn L Lunetta; Carol L Rosenberg; Henrik Toft Sørensen; Timothy L Lash; Stephen Hamilton-Dutoit
Concordance of metabolic enzyme genotypes assayed from paraffin-embedded, formalin-fixed breast tumors and normal lymphatic tissue.
Clinical epidemiology 2010;2():241-6.
2009: Audrey E Hendricks; Jeanne C Latourelle; Kathryn L Lunetta; L Adrienne Cupples; Vanessa Wheeler; Marcy E MacDonald; James Gusella; Richard H Myers
Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).
American journal of medical genetics. Part A 2009;149A(7):1375-81.
2009: Gina M Peloso; Nadia Timofeev; Kathryn L Lunetta
Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method.
BMC proceedings 2009;3 Suppl 7():S108.
2009: Yan A Meng; Yi Yu; L Adrienne Cupples; Lindsay A Farrer; Kathryn L Lunetta
Performance of random forest when SNPs are in linkage disequilibrium.
BMC bioinformatics 2009;10():78.
2009: Chao-Yu Guo; Kathryn L Lunetta; Anita L DeStefano; L Adrienne Cupples
Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.
Genetic epidemiology 2009;33(1):54-62.
2008: Karen T Cuenco; Kathryn L Lunetta; Clinton T Baldwin; Ann C McKee; Jianping Guo; L Adrienne Cupples; Robert C Green; Peter St George-Hyslop; Helena Chui; Charles DeCarli; Lindsay A Farrer
Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
Archives of neurology 2008;65(12):1640-8.
2008: T L Lash; L Pedersen; D Cronin-Fenton; T P Ahern; Carol L Rosenberg; Kathryn L Lunetta; R A Silliman; Stephen Hamilton-Dutoit; Jens Peter Garne; M Ewertz; Henrik Toft Sørensen
Tamoxifen's protection against breast cancer recurrence is not reduced by concurrent use of the SSRI citalopram.
British journal of cancer 2008;99(4):616-21.
2008: Kathryn L Lunetta
Genetic association studies.
Circulation 2008;118(1):96-101.
2008: D S Lee; Martin G Larson; Kathryn L Lunetta; J Dupuis; J Rong; J F Keaney; I Lipinska; Clinton T Baldwin; Ramachandran S Vasan; Emelia Benjamin
Clinical and genetic correlates of soluble P-selectin in the community.
Journal of thrombosis and haemostasis : JTH 2008;6(1):20-31.
2007: Kathryn L Lunetta; Porat M Erlich; Karen T Cuenco; L Adrienne Cupples; Robert C Green; Lindsay A Farrer; Charles DeCarli
Heritability of magnetic resonance imaging (MRI) traits in Alzheimer disease cases and their siblings in the MIRAGE study.
Alzheimer disease and associated disorders 2007;21(2):85-91.
2007: Chao-Yu Guo; Kathryn L Lunetta; Anita L DeStefano; Jose Ordovas; L Adrienne Cupples
Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.
Genetic epidemiology 2007;31(2):115-33.
2007: Yan Meng; Qiong Yang; Karen T Cuenco; L Adrienne Cupples; Anita L DeStefano; Kathryn L Lunetta
Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks.
BMC proceedings 2007;1 Suppl 1():S56.
2007: Douglas P Kiel; Serkalem Demissie; Josée Dupuis; Kathryn L Lunetta; Joanne M Murabito; David Karasik
Genome-wide association with bone mass and geometry in the Framingham Heart Study.
BMC medical genetics 2007;8 Suppl 1():S14.
2007: Kathryn L Lunetta; Ralph B D'Agostino; David Karasik; Emelia Benjamin; Chao-Yu Guo; Raju Govindaraju; Douglas P Kiel; Margaret Kelly-Hayes; Joseph M Massaro; Michael J Pencina; Sudha Seshadri; Joanne M Murabito
Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.
BMC medical genetics 2007;8 Suppl 1():S13.
2007: Emelia Benjamin; Josée Dupuis; Martin G Larson; Kathryn L Lunetta; Sarah L Booth; Diddahally R Govindaraju; Sekar Kathiresan; John F Keaney; Michelle J Keyes; Jing-Ping Lin; James B Meigs; Sander J Robins; Jian Rong; Renate Schnabel; Joseph A Vita; Thomas J Wang; Peter W F Wilson; Philip A Wolf; Ramachandran S Vasan
Genome-wide association with select biomarker traits in the Framingham Heart Study.
BMC medical genetics 2007;8 Suppl 1():S11.
2006: Abimbola Akomolafe; Kathryn L Lunetta; Porat M Erlich; L Adrienne Cupples; Clinton T Baldwin; Matthew Huyck; Robert C Green; Lindsay A Farrer
Genetic association between endothelial nitric oxide synthase and Alzheimer disease.
Clinical genetics 2006;70(1):49-56.
2006: Amanda M Shearman; Jackie A Cooper; Paul J Kotwinski; George J Miller; Steve E Humphries; Kristin G Ardlie; Barbara Jordan; Kathryn Irenze; Kathryn L Lunetta; Stephanie C E Schuit; André G Uitterlinden; Huibert A P Pols; Serkalem Demissie; L Adrienne Cupples; Michael Mendelsohn; Daniel Levy; David E Housman
Estrogen receptor alpha gene variation is associated with risk of myocardial infarction in more than seven thousand men from five cohorts.
Circulation research 2006;98(5):590-2.
2006: Porat M Erlich; Kathryn L Lunetta; L Adrienne Cupples; Matthew Huyck; Robert C Green; Clinton T Baldwin; Lindsay A Farrer
Polymorphisms in the PON gene cluster are associated with Alzheimer disease.
Human molecular genetics 2006;15(1):77-85.
2005: Catarina D Campbell; Elizabeth L Ogburn; Kathryn L Lunetta; Helen N Lyon; Matthew L Freedman; Leif C Groop; David Altshuler; Kristin G Ardlie; Joel N Hirschhorn
Demonstrating stratification in a European American population.
Nature genetics 2005;37(8):868-72.
2005: Alexandre Bureau; Josée Dupuis; Kathleen Falls; Kathryn L Lunetta; Brooke Hayward; Tim P Keith; Paul Van Eerdewegh
Identifying SNPs predictive of phenotype using random forests.
Genetic epidemiology 2005;28(2):171-82.
2005: Chao-Yu Guo; Anita L DeStefano; Kathryn L Lunetta; Josée Dupuis; L Adrienne Cupples
Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios.
Human heredity 2005;59(3):125-35.
2004: Kathryn L Lunetta; L Brooke Hayward; Jonathan Segal; Paul Van Eerdewegh
Screening large-scale association study data: exploiting interactions using random forests.
BMC genetics 2004;5():32.
2002: Kristin G Ardlie; Kathryn L Lunetta; Mark Seielstad
Testing for population subdivision and association in four case-control studies.
American journal of human genetics 2002;71(2):304-11.
2001: J M Robins; Jordan W Smoller; Kathryn L Lunetta
On the validity of the TDT test in the presence of comorbidity and ascertainment bias.
Genetic epidemiology 2001;21(4):326-36.
2001: Ian Krop; Dennis C Sgroi; Dale A Porter; Kathryn L Lunetta; R LeVangie; Pankaj Seth; Carolyn M Kaelin; Esther Rhei; Marcus W Bosenberg; Stuart J Schnitt; Jeffrey R Marks; Z Pagon; D Belina; J Razumovic; Kornelia Polyak
HIN-1, a putative cytokine highly expressed in normal but not cancerous mammary epithelial cells.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(17):9796-801.
2001: S R Wallace; Martin M Oken; Kathryn L Lunetta; A Panoskaltsis-Mortari; A M Masellis
Abnormalities of bone marrow mesenchymal cells in multiple myeloma patients.
Cancer 2001;91(7):1219-30.
2000: Pankaj Seth; Kathryn L Lunetta; D W Bell; H Gray; S M Nasser; Esther Rhei; Carolyn M Kaelin; D J Iglehart; Jeffrey R Marks; Judy E Garber; D A Haber; Kornelia Polyak
Phenol sulfotransferases: hormonal regulation, polymorphism, and age of onset of breast cancer.
Cancer research 2000;60(24):6859-63.
2000: Jordan W Smoller; Kathryn L Lunetta; J Robins
Implications of comorbidity and ascertainment bias for identifying disease genes.
American journal of medical genetics 2000;96(6):817-22.
2000: JJ Yeh; Kathryn L Lunetta; Nathalie J van Orsouw; F D Moore; George L Mutter; Jan Vijg; Patricia Dahia; Charis Eng
Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours.
Oncogene 2000;19(16):2060-6.
2000: Kathryn L Lunetta; Stephen Faraone; J Biederman; N M Laird
Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions.
American journal of human genetics 2000;66(2):605-14.
1999: Deborah J Marsh; JB Kum; Kathryn L Lunetta; M J Bennett; RJ Gorlin; S F Ahmed; J Bodurtha; C Crowe; M A Curtis; Majed Dasouki; T Dunn; H Feit; M T Geraghty; J M Graham; Shirley V Hodgson; A Hunter; Bruce Korf; D Manchester; S Miesfeldt; Victoria Murday; Katherine L Nathanson; M Parisi; B Pober; Corrado Romano; Charis Eng
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
Human molecular genetics 1999;8(8):1461-72.
1999: Marsha A. Wilcox; Jordan W Smoller; Kathryn L Lunetta; D Neuberg
Using recursive partitioning for exploration and follow-up of linkage and association analyses.
Genetic epidemiology 1999;17 Suppl 1():S391-6.
1999: Kathryn L Lunetta; M Wilcox; Jordan W Smoller; D Neuberg
Exploring linkage for alcoholism using affection status and quantitative event related potential phenotypes.
Genetic epidemiology 1999;17 Suppl 1():S241-6.
1998: Deborah J Marsh; V Coulon; Kathryn L Lunetta; P Rocca-Serra; Patricia Dahia; Z Zheng; D Liaw; S Caron; B Duboué; A Y Lin; Andrea L Richardson; J M Bonnetblanc; J M Bressieux; A Cabarrot-Moreau; Agnès Chompret; L Demange; RA Eeles; A M Yahanda; Eric R Fearon; J P Fricker; RJ Gorlin; Shirley V Hodgson; S Huson; D Lacombe; Charis Eng
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.
Human molecular genetics 1998;7(3):507-15.
1998: Kathryn L Lunetta; J J Rogus
Strategy for mapping minor histocompatibility genes involved in graft-versus-host disease: a novel application of discordant sib pair methodology.
Genetic epidemiology 1998;15(6):595-607.
1997: Deborah J Marsh; S Roth; Kathryn L Lunetta; Akseli Hemminki; Patricia Dahia; Pertti Sistonen; Z Zheng; S Caron; Nathalie J van Orsouw; Walter F Bodmer; SE Cottrell; Malcolm G Dunlop; Diana Eccles; Shirley V Hodgson; Heikki Järvinen; Ilmo Kellokumpu; D Markie; Kay Neale; Robin Phillips; P Rozen; Sapna Syngal; Jan Vijg; Ian P M Tomlinson; Lauri A Aaltonen; Charis Eng
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.
Cancer research 1997;57(22):5017-21.
1997: Garry P Larson; G Zhang; Shaofeng Ding; K Foldenauer; Nitin Udar; Richard A Gatti; D Neuberg; Kathryn L Lunetta; John Ruckdeschel; J Longmate; S Flanagan; Theodore G Krontiris
An allelic variant at the ATM locus is implicated in breast cancer susceptibility.
Genetic testing 1997;1(3):165-70.
1996: William C Nichols; Joseph H Antin; Kathryn L Lunetta; Valeri Terry; C E Hertel; M A Wheatley; N D Arnold; DR Siemieniak; Michael Boehnke; David Ginsburg
Polymorphism of adhesion molecule CD31 is not a significant risk factor for graft-versus-host disease.
Blood 1996;88(12):4429-34.
1996: Kathryn L Lunetta; Michael Boehnke; K Lange; D R Cox
Selected locus and multiple panel models for radiation hybrid mapping.
American journal of human genetics 1996;59(3):717-25.
1996: Y C Hou; Julia E Richards; Eve L Bingham; H Pawar; K Scott; M Segal; Kathryn L Lunetta; Michael Boehnke; Paul Sieving
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.
Human heredity 1996;46(4):211-20.
1995: Kathryn L Lunetta; Michael Boehnke; K Lange; D R Cox
Experimental design and error detection for polyploid radiation hybrid mapping.
Genome research 1995;5(2):151-63.
1995: K Lange; Michael Boehnke; D R Cox; Kathryn L Lunetta
Statistical methods for polyploid radiation hybrid mapping.
Genome research 1995;5(2):136-50.
1995: H Pawar; Eve L Bingham; Kathryn L Lunetta; M Segal; Julia E Richards; Michael Boehnke; Paul Sieving
Refined genetic mapping of juvenile X-linked retinoschisis.
Human heredity 1995;45(4):206-10.
1994: Kathryn L Lunetta; Michael Boehnke
Multipoint radiation hybrid mapping: comparison of methods, sample size requirements, and optimal study characteristics.
Genomics 1994;21(1):92-103.
1991: J P Vuchetich; J Dunnette; Kathryn L Lunetta; R M Weinshilboum; Arlen Price
Inheritance of human plasma dopamine-beta-hydroxylase thermal stability.
Genetic epidemiology 1991;8(4):237-51.