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Elizabeth Hauser

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Jennifer M Wu; Renée M Ward; Kristina L Allen-Brady; Todd L Edwards; Katherine E Hartmann; Elizabeth R Hauser; Peggy A Norton; Digna R Velez Edwards
Phenotyping clinical disorders: lessons learned from pelvic organ prolapse.
Svati H Shah; Robert D Stevens; Jie Lena Sun; Christopher B Newgard; Karen S Pieper; James R Bain; Robert M Califf; Christopher B Granger; Elizabeth R Hauser; Carol Haynes; William E Kraus; Michael J Muehlbauer; L Kristin Newby
Baseline metabolomic profiles predict cardiovascular events in patients at risk for coronary artery disease.
Asad A Shah; Robert C Stevens; Damian M Craig; Christopher B Granger; Elizabeth R Hauser; Carol Haynes; G Chad Hughes; William E Kraus; Michael J Muehlbauer; L Kristin Newby; Christopher B Newgard; Jacqueline K Sebek; Svati H Shah
Metabolic profiles predict adverse events after coronary artery bypass grafting.

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2013: Jennifer M Wu; Renée M Ward; Kristina L Allen-Brady; Todd L Edwards; Katherine E Hartmann; Elizabeth R Hauser; Peggy A Norton; Digna R Velez Edwards
Phenotyping clinical disorders: lessons learned from pelvic organ prolapse.
American journal of obstetrics and gynecology 2013;208(5):360-5.
2012: Svati H Shah; Robert D Stevens; Jie Lena Sun; Christopher B Newgard; Karen S Pieper; James R Bain; Robert M Califf; Christopher B Granger; Elizabeth R Hauser; Carol Haynes; William E Kraus; Michael J Muehlbauer; L Kristin Newby
Baseline metabolomic profiles predict cardiovascular events in patients at risk for coronary artery disease.
American heart journal 2012;163(5):844-850.e1.
2012: Asad A Shah; Robert C Stevens; Damian M Craig; Christopher B Granger; Elizabeth R Hauser; Carol Haynes; G Chad Hughes; William E Kraus; Michael J Muehlbauer; L Kristin Newby; Christopher B Newgard; Jacqueline K Sebek; Svati H Shah
Metabolic profiles predict adverse events after coronary artery bypass grafting.
The Journal of thoracic and cardiovascular surgery 2012;143(4):873-8.
2012: Daniel K Nolan; Jacqueline Sebek; David Seo; Michael H Sketch; Beth Sutton; David R Crosslin; David Crossman; Elaine Dowdy; Pascal J Goldschmidt-Clermont; Christopher B Granger; Simon G Gregory; Elizabeth R Hauser; Chad Haynes; Jessica Johnson; William E Kraus; Svati H Shah
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.
BMC genetics 2012;13():12.
2011: Mollie A Minear; David R Crosslin; Beth S Sutton; Jessica J Connelly; Sarah C Nelson; Shera Gadson-Watson; Tianyuan Wang; David Seo; Jeffery Vance; Michael H Sketch; Chad Haynes; Pascal J Goldschmidt-Clermont; Svati H Shah; William E Kraus; Elizabeth R Hauser; Simon G Gregory
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.
Human genetics 2011;129(6):641-54.
2011: Lori A Orlando; Karen P Powell; Elizabeth R Hauser; Vincent C Henrich; Astrid B Agbaje; Adam H Buchanan; Blair Chesnut; Carol Christianson; Geoffrey Ginsburg
Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system.
BMC health services research 2011;11():264.
2010: Svati H Shah; Christopher B Granger; Elizabeth R Hauser; William E Kraus; Jie Lena Sun; Karen Pieper; Charlotte L Nelson; Elizabeth R DeLong; Robert M Califf; L Kristin Newby
Reclassification of cardiovascular risk using integrated clinical and molecular biosignatures: Design of and rationale for the Measurement to Understand the Reclassification of Disease of Cabarrus and Kannapolis (MURDOCK) Horizon 1 Cardiovascular Disease Study.
American heart journal 2010;160(3):371-379.e2.
2010: Lisheng Zhang; Jessica J Connelly; Karsten Peppel; Leigh Brian; Svati H Shah; Sarah Nelson; David R Crosslin; Tianyuan Wang; Andrew Allen; William E Kraus; Simon G Gregory; Elizabeth R Hauser; Neil J Freedman
Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.
Human molecular genetics 2010;19(14):2754-66.
2010: Xuejun Qin; Elizabeth R Hauser; Silke Schmidt
Ordered subset analysis for case-control studies.
Genetic epidemiology 2010;34(5):407-17.
2010: Hsiang-Cheng Chen; Virginia B Kraus; Yi-Ju Li; Sarah Nelson; Chad Haynes; Jessica Johnson; Thomas Stabler; Elizabeth R Hauser; Simon G Gregory; William E Kraus; Svati H Shah
Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.
Arthritis and rheumatism 2010;62(3):781-90.
2010: David R Crosslin; Xuejun Qin; Elizabeth R Hauser
Assessment of LD matrix measures for the analysis of biological pathway association.
Statistical applications in genetics and molecular biology 2010;9():Article35.
2009: Tianyuan Wang; Terrence S Furey; Jessica J Connelly; Shihao Ji; Sarah Nelson; Steffen Heber; Simon G Gregory; Elizabeth R Hauser
A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease.
Human genomics 2009;3(3):221-35.
2009: David R Crosslin; Svati H Shah; Sarah C Nelson; CS Haynes; Jessica J Connelly; Shera Gadson; Pascal J Goldschmidt-Clermont; Jeffery Vance; Jason Rose; Chris B Granger; David Seo; Simon G Gregory; William E Kraus; Elizabeth R Hauser
Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
Human genetics 2009;125(2):217-29.
2009: Svati H Shah; Elizabeth R Hauser; James R Bain; Michael J Muehlbauer; Carol Haynes; Robert D Stevens; Brett R Wenner; Z Elaine Dowdy; Christopher B Granger; Geoffrey S Ginsburg; Christopher B Newgard; William E Kraus
High heritability of metabolomic profiles in families burdened with premature cardiovascular disease.
Molecular systems biology 2009;5():258.
2009: Svati H Shah; Neil J Freedman; Lisheng Zhang; David R Crosslin; David H Stone; Chad Haynes; Jessica Johnson; Sarah Nelson; Liyong Wang; Jessica J Connelly; Michael Muehlbauer; Geoffrey S Ginsburg; David C Crossman; Christopher J H Jones; Jeffery Vance; Michael H Sketch; Christopher B Granger; Christopher B Newgard; Simon G Gregory; Pascal J Goldschmidt-Clermont; William E Kraus; Elizabeth R Hauser
Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.
PLoS genetics 2009;5(1):e1000318.
2008: Ren-Hua Chung; Silke Schmidt; Eden R Martin; Elizabeth R Hauser
Ordered-subset analysis (OSA) for family-based association mapping of complex traits.
Genetic epidemiology 2008;32(7):627-37.
2008: Svati H Shah; Elizabeth R Hauser; David R Crosslin; Liyong Wang; Chad Haynes; Jessica Connelly; Sarah Nelson; Jessica Johnson; Shera Gadson; Charlotte L Nelson; David Seo; Simon Gregory; William E Kraus; Christopher B Granger; Pascal J Goldschmidt-Clermont; L Kristin Newby
ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.
Atherosclerosis 2008;201(1):148-54.
2008: Beth S Sutton; David R Crosslin; Svati H Shah; Sarah C Nelson; Anthony Bassil; A Brent Hale; Chad Haynes; Pascal J Goldschmidt-Clermont; Jeffery Vance; David Seo; William E Kraus; Simon G Gregory; Elizabeth R Hauser
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
Human molecular genetics 2008;17(9):1318-28.
2008: Jessica J Connelly; Svati H Shah; Jennifer F Doss; Shera Gadson; Sarah Nelson; David R Crosslin; A Brent Hale; Xuemei Lou; Ty Wang; Chad Haynes; David Seo; David C Crossman; Vincent Mooser; Christopher B Granger; Christopher J H Jones; William E Kraus; Elizabeth R Hauser; Simon G Gregory
Genetic and functional association of FAM5C with myocardial infarction.
BMC medical genetics 2008;9():33.
2008: Silke Schmidt; Mike Schmidt; Xuejun Qin; Eden R Martin; Elizabeth R Hauser
Increased efficiency of case-control association analysis by using allele-sharing and covariate information.
Human heredity 2008;65(3):154-65.
2007: Silke Schmidt; Xuejun Qin; Mike Schmidt; Eden R Martin; Elizabeth R Hauser
Interpreting analyses of continuous covariates in affected sibling pair linkage studies.
Genetic epidemiology 2007;31(6):541-52.
2007: Liyong Wang; Elizabeth R Hauser; Svati H Shah; Margaret Pericak-Vance; Chad Haynes; David R Crosslin; Marco Harris; Sarah Nelson; A Brent Hale; Christopher B Granger; Jonathan L Haines; Christopher J H Jones; David C Crossman; David Seo; Simon G Gregory; William E Kraus; Pascal J Goldschmidt-Clermont; Jeffery Vance
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
American journal of human genetics 2007;80(4):650-63.
2007: Xuemei Lou; Silke Schmidt; Elizabeth R Hauser
Comparison of GIST and LAMP on the GAW15 simulated data.
BMC proceedings 2007;1 Suppl 1():S41.
2007: Mike Schmidt; Xuejun Qin; Eden R Martin; Elizabeth R Hauser; Silke Schmidt
Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies.
BMC proceedings 2007;1 Suppl 1():S138.
2007: Xuejun Qin; Silke Schmidt; Eden R Martin; Elizabeth R Hauser
Visualizing genotype x phenotype relationships in the GAW15 simulated data.
BMC proceedings 2007;1 Suppl 1():S132.
2007: Amy P Murtha; Tammy Sinclair; Elizabeth R Hauser; Geeta K Swamy; William N P Herbert; R Phillips Heine
Maternal serum cytokines in preterm premature rupture of membranes.
Obstetrics and gynecology 2007;109(1):121-7.
2006: Amy P Murtha; Angel Nieves; Elizabeth R Hauser; Geeta K Swamy; Bryan Yonish; Tammy R Sinclair; R Phillips Heine
Association of maternal IL-1 receptor antagonist intron 2 gene polymorphism and preterm birth.
American journal of obstetrics and gynecology 2006;195(5):1249-53.
2006: Svati H Shah; William E Kraus; David C Crossman; Christopher B Granger; Jonathan L Haines; Christopher J H Jones; Vincent Mooser; L Huang; Chad Haynes; E Dowdy; G L Vega; S M Grundy; Jeffery Vance; Elizabeth R Hauser
Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.
Annals of human genetics 2006;70(Pt 6):738-48.
2006: Jessica J Connelly; Tianyuan Wang; Julie E Cox; Chad Haynes; Liyong Wang; Svati H Shah; David R Crosslin; A Brent Hale; Sarah Nelson; David C Crossman; Christopher B Granger; Jonathan L Haines; Christopher J H Jones; Jeffery Vance; Pascal J Goldschmidt-Clermont; William E Kraus; Elizabeth R Hauser; Simon G Gregory
GATA2 is associated with familial early-onset coronary artery disease.
PLoS genetics 2006;2(8):e139.
2006: Silke Schmidt; Mike Schmidt; Xuejun Qin; Eden R Martin; Elizabeth R Hauser
Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.
Genetic epidemiology 2006;30(5):409-22.
2005: Evadnie Rampersaud; William Scott; Elizabeth R Hauser; Marcy C Speer
Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs.
Journal of medical genetics 2005;42(12):e68.
2005: Hong Xu; Simon G Gregory; Elizabeth R Hauser; Judith E Stenger; Margaret Pericak-Vance; Jeffery Vance; Stephan Zuchner; Michael A Hauser
SNPselector: a web tool for selecting SNPs for genetic association studies.
Bioinformatics (Oxford, England) 2005;21(22):4181-6.
2005: R Rand Allingham; Janey L Wiggs; Elizabeth R Hauser; Karen Larocque-Abramson; Cecilia Santiago-Turla; Bob Broomer; Elizabeth A Del Bono; Felicia L Graham; Jonathan L Haines; Margaret Pericak-Vance; Michael A Hauser
Early adult-onset POAG linked to 15q11-13 using ordered subset analysis.
Investigative ophthalmology & visual science 2005;46(6):2002-5.
2005: Mike Schmidt; Elizabeth R Hauser; Eden R Martin; Silke Schmidt
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: Svati H Shah; Mike Schmidt; Hao Mei; William Scott; Elizabeth R Hauser; Silke Schmidt
Searching for epistatic interactions in nuclear families using conditional linkage analysis.
BMC genetics 2005;6 Suppl 1():S148.
2005: Abee L Boyles; William Scott; Eden R Martin; Silke Schmidt; Yi-Ju Li; Allison Ashley-Koch; Meredyth P Bass; Mike Schmidt; Margaret Pericak-Vance; Marcy C Speer; Elizabeth R Hauser
Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
Human heredity 2005;59(4):220-7.
2005: Judith E Stenger; Hong Xu; Chad Haynes; Elizabeth R Hauser; Margaret Pericak-Vance; Pascal J Goldschmidt-Clermont; Jeffery Vance
Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.
BMC bioinformatics 2005;6():95.
2004: Silke Schmidt; William Scott; Eric A Postel; Anita Agarwal; Elizabeth R Hauser; Monica A De La Paz; John Gilbert; Daniel E Weeks; Michael B Gorin; Jonathan L Haines; Margaret Pericak-Vance
Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.
BMC genetics 2004;5():18.
2004: Elizabeth R Hauser; Richard Watanabe; William L Duren; Meredyth P Bass; Carl D Langefeld; Michael Boehnke
Ordered subset analysis in genetic linkage mapping of complex traits.
Genetic epidemiology 2004;27(1):53-63.
2004: Meredyth P Bass; Eden R Martin; Elizabeth R Hauser
Pedigree generation for analysis of genetic linkage and association.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2004;():93-103.
2003: William Scott; Elizabeth R Hauser; Donald E Schmechel; Kathleen A Welsh-Bohmer; Gary W Small; Allen D Roses; Ann M Saunders; John Gilbert; Jeffery Vance; Jonathan L Haines; Margaret Pericak-Vance
Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.
American journal of human genetics 2003;73(5):1041-51.
2003: Eden R Martin; Meredyth P Bass; John Gilbert; Margaret Pericak-Vance; Elizabeth R Hauser
Genotype-based association test for general pedigrees: the genotype-PDT.
Genetic epidemiology 2003;25(3):203-13.
2003: Eden R Martin; Meredyth P Bass; Elizabeth R Hauser; Norman L Kaplan
Accounting for linkage in family-based tests of association with missing parental genotypes.
American journal of human genetics 2003;73(5):1016-26.
2003: M Louise Markert; Marcella Sarzotti; Daniel A Ozaki; Gregory D Sempowski; Maria E Rhein; Laura P Hale; Françoise Le Deist; Marilyn J Alexieff; Jie Li; Elizabeth R Hauser; Barton F Haynes; Henry E Rice; Michael A Skinner; Samuel M Mahaffey; James Jaggers; Leonard Stein; Michael R Mill
Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients.
Blood 2003;102(3):1121-30.
2003: Elizabeth R Hauser; Vincent Mooser; David C Crossman; Jonathan L Haines; Christopher H Jones; Bernhard R Winkelmann; Silke Schmidt; William Scott; Allen D Roses; Margaret Pericak-Vance; Christopher B Granger; William E Kraus
Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study.
American heart journal 2003;145(4):602-13.
2003: Michael A Hauser; Yi-Ju Li; Satoshi Takeuchi; Robert Walters; Maher A Noureddine; Melinda Maready; Tiffany Darden; Christine M Hulette; Eden R Martin; Elizabeth R Hauser; Hong Xu; Donald E Schmechel; Judith E Stenger; Fred S Dietrich; Jeffery Vance
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: Yujun Shao; Michael Cuccaro; Elizabeth R Hauser; Kimberly L Raiford; Marisa M Menold; Chantelle M Wolpert; Sarah A Ravan; L Elston; K Decena; Shannon L Donnelly; Ruth K Abramson; Harry H Wright; G Robert DeLong; John Gilbert; Margaret Pericak-Vance
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
American journal of human genetics 2003;72(3):539-48.
2003: Evadnie Rampersaud; Andrew Allen; Yi-Ju Li; Yujun Shao; Meredyth Bass; Chad Haynes; Allison Ashley-Koch; Eden R Martin; Silke Schmidt; Elizabeth R Hauser
Adjusting for covariates on a slippery slope: linkage analysis of change over time.
BMC genetics 2003;4 Suppl 1():S50.
2003: Elizabeth R Hauser; Fang-Chi Hsu; Denise Daley; Jane M Olson; Evadnie Rampersaud; Jing-Ping Lin; Andrew D Paterson; Laila M Poisson; Gary A Chase; Gerlinde Dahmen; Andreas Ziegler
Effects of covariates: a summary of Group 5 contributions.
Genetic epidemiology 2003;25 Suppl 1():S43-9.
2001: Elizabeth R Hauser; Daniel E Weeks
Pedigree selection and information content.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 1():Unit 1.2.
2001: Silke Schmidt; Y Shao; Elizabeth R Hauser; Susan H Slifer; Eden R Martin; William Scott; Marcy C Speer; Margaret Pericak-Vance
Life after the screen: making sense of many P-values.
Genetic epidemiology 2001;21 Suppl 1():S546-51.
2000: Richard Watanabe; S Ghosh; Carl D Langefeld; Timo T Valle; Elizabeth R Hauser; Victoria L Magnuson; Karen L Mohlke; Kaisa Silander; DS Ally; Peter S Chines; J Blaschak-Harvan; Julie A Douglas; William L Duren; Michael P Epstein; Tasha E Fingerlin; H S Kaleta; Ethan M Lange; C Li; Richard C McEachin; Heather M Stringham; Edward H Trager; P P White; J Balow Jr; G Birznieks; J Chang; W Eldridge
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.
American journal of human genetics 2000;67(5):1186-200.
2000: S Ghosh; Richard Watanabe; Timo T Valle; Elizabeth R Hauser; Victoria L Magnuson; Carl D Langefeld; DS Ally; Karen L Mohlke; Kaisa Silander; K Kohtamäki; Peter S Chines; J Balow Jr; G Birznieks; J Chang; W Eldridge; Michael R Erdos; ZE Karanjawala; JI Knapp; K Kudelko; C Martin; A Morales-Mena; A Musick; T Musick; C Pfahl; R Porter; JB Rayman
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.
American journal of human genetics 2000;67(5):1174-85.
2000: Elizabeth R Hauser; Margaret Pericak-Vance
Genetic analysis for common complex disease.
American heart journal 2000;140(4):S36-44.
2000: Meredyth P Bass; Marisa M Menold; Chantelle M Wolpert; Shannon L Donnelly; Sarah A Ravan; Elizabeth R Hauser; Lee Maddox; Jeffery Vance; Ruth K Abramson; Harry H Wright; John Gilbert; Michael Cuccaro; G Robert DeLong; Margaret Pericak-Vance
Genetic studies in autistic disorder and chromosome 15.
Neurogenetics 2000;2(4):219-26.
1999: Richard Watanabe; Timo T Valle; Elizabeth R Hauser; S Ghosh; Johan Eriksson; K Kohtamäki; C Ehnholm; Jaakko Tuomilehto; Francis S Collins; Richard N Bergman; Michael Boehnke
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators.
Human heredity 1999;49(3):159-68.
1999: S Ghosh; Carl D Langefeld; DS Ally; Richard Watanabe; Elizabeth R Hauser; Victoria L Magnuson; SJ Nylund; Timo T Valle; Johan Eriksson; Richard N Bergman; Jaakko Tuomilehto; Francis S Collins; Michael Boehnke
The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sample.
Diabetologia 1999;42(2):238-44.
1999: JL Anderson; Elizabeth R Hauser; Eden R Martin; William Scott; Allison Ashley-Koch; K J Kim; Stephanie A Monks; CS Haynes; Marcy C Speer; Margaret Pericak-Vance
Complete genomic screen for disease susceptibility loci in nuclear families.
Genetic epidemiology 1999;17 Suppl 1():S473-8.
1998: Elizabeth R Hauser; Michael Boehnke
Genetic linkage analysis of complex genetic traits by using affected sibling pairs.
Biometrics 1998;54(4):1238-46.
1998: S Ghosh; Elizabeth R Hauser; Victoria L Magnuson; Timo T Valle; DS Ally; ZE Karanjawala; JB Rayman; JI Knapp; A Musick; J Tannenbaum; C Te; W Eldridge; S Shapiro; T Musick; C Martin; A So; A Witt; J B Harvan; Richard Watanabe; William Hagopian; Johan Eriksson; SJ Nylund; K Kohtamaki; Eva Tuomilehto-Wolf; Michael Boehnke
A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter.
The Journal of clinical investigation 1998;102(4):704-9.
1998: Timo T Valle; Jaakko Tuomilehto; Richard N Bergman; S Ghosh; Elizabeth R Hauser; Johan Eriksson; SJ Nylund; K Kohtamäki; L Toivanen; G Vidgren; Eva Tuomilehto-Wolf; C Ehnholm; J Blaschak; Carl D Langefeld; Richard Watanabe; Victoria L Magnuson; DS Ally; William Hagopian; E Ross; Thomas A Buchanan; Francis S Collins; Michael Boehnke
Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study.
Diabetes care 1998;21(6):949-58.
1997: S Ghosh; ZE Karanjawala; Elizabeth R Hauser; DS Ally; JI Knapp; JB Rayman; A Musick; J Tannenbaum; C Te; S Shapiro; W Eldridge; T Musick; C Martin; J R Smith; J D Carpten; M J Brownstein; J I Powell; R Whiten; Peter S Chines; SJ Nylund; Victoria L Magnuson; Michael Boehnke; Francis S Collins
Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group.
Genome research 1997;7(2):165-78.
1996: Elizabeth R Hauser; Michael Boehnke; S W Guo; N Risch
Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations.
Genetic epidemiology 1996;13(2):117-37.
1995: Fergus J. Couch; Judy E Garber; S Kiousis; Kathleen A Calzone; Elizabeth R Hauser; Sofia D Merajver; T S Frank; Michael Boehnke; Jeffrey S Chamberlain; Francis S Collins
Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations.
Journal of the National Cancer Institute. Monographs 1995;(17):9-14.
1993: Jeffrey S Chamberlain; Michael Boehnke; T S Frank; S Kiousis; Jianfeng Xu; S W Guo; Elizabeth R Hauser; R A Norum; E A Helmbold; Dorene S Markel
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.
American journal of human genetics 1993;52(4):792-8.