qmwwallace's linkage [51 articles] Export

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	The significance of not finding a gene. [My Copy] Am J Hum Genet, Vol. 69, No. 3. (September 2001), pp. 660-663. by M. A. Province posted to fisher linkage meta-analysis by qmwwallace on 2007-09-20 12:03:27 as
	Biases and reconciliation in estimates of linkage disequilibrium in the human genome. [My Copy] Am J Hum Genet, Vol. 78, No. 4. (Apr 2006), pp. 588-603. by Itsik Pe'er, Yves R. Chretien, Paul I. W. de Bakker, Jeffrey C. Barrett, Mark J. Daly, David M. Altshuler posted to 16532390 disequilibrium genome human humans linkage combinedbib by qmwwallace on 2007-07-05 14:55:23 as
	A gene for universal congenital alopecia maps to chromosome 8p21-22. [My Copy] Am J Hum Genet, Vol. 62, No. 2. (Feb 1998), pp. 386-390. by M. M. Nöthen, S. Cichon, I. R. Vogt, et al.S. Hemmer, R. Kruse, M. Knapp, T. Höller, Faiyaz, S. Haque, P. Propping, M. Ahmad, M. Rietschel posted to 8p21-22 alopecia linkage by qmwwallace on 2007-07-05 14:55:22 as
	Genetic mapping of a maternal locus responsible for familial hydatidiform moles. [My Copy] Hum Mol Genet, Vol. 8, No. 4. (Apr 1999), pp. 667-671. by Y. B. Moglabey, R. Kircheisen, M. Seoud, El N. Mogharbel, I. Van den Veyver, R. Slim posted to hydatidiform linkage moles by qmwwallace on 2007-07-05 14:55:18 as
	Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. [My Copy] Am J Hum Genet, Vol. 74, No. 5. (May 2004), pp. 886-897. by F. A. Middleton, M. T. Pato, K. L. Gentile, et al.C. P. Morley, X. Zhao, A. F. Eisener, A. Brown, T. L. Petryshen, A. N. Kirby, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M. J. Soares, C. P. Ferreira, M. Lei, M. H. Azevedo, J. L. Kennedy, M. J. Daly, P. Sklar, C. N. Pato posted to bipolar chromosomes combinedbib comparative disorder family female genetics genome genotype govt haplotypes human humans linkage lod male microsatellite non-us nucleotide pair phs polymorphism repeats research score single study support us by qmwwallace on 2007-07-05 14:55:18 as
	Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23. [My Copy] Hum Mol Genet, Vol. 2, No. 7. (Jul 1993), pp. 969-974. by C. M. Mcconville, P. J. Byrd, H. J. Ambrose, et al.T. Stankovic, Y. Ziv, Bar A. Shira, L. Vanagaite, G. Rotman, Y. Shiloh, G. T. Gillett posted to antigens ataxia base cell cells chromosome chromosomes chronic combinedbib complex cystic data deletion diseases dna factor-alpha failure family female fragment fungal gene genetic genetics genome govt haplotypes histocompatibility hla human humans hybrid kidney length library line linkage ma major male mapping markers molecular multigene mutation necrosis non-us pair pedigree polymorphism pping research restriction satellite sequence serotyping sites support tagged telangiectasia testing tumor by qmwwallace on 2007-07-05 14:55:18 as
	Common deletion polymorphisms in the human genome. [My Copy] Nat Genet, Vol. 38, No. 1. (Jan 2006), pp. 86-92. by Steven A. Mccarroll, Tracy N. Hadnott, George H. Perry, et al.Pardis C. Sabeti, Michael C. Zody, Jeffrey C. Barrett, Stephanie Dallaire, Stacey B. Gabriel, Charles Lee, Mark J. Daly, David M. Altshuler, International H. Consortium posted to chain combinedbib continental databases deletion disequilibrium exons fluorescence genetic genome groups homozygote human humans hybridization in linkage models nucleotide polymerase polymorphism population reaction sequence single situ techniques by qmwwallace on 2007-07-05 14:55:18 as
	The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis. [My Copy] Proc Natl Acad Sci U S A, Vol. 99, No. 4. (Feb 2002), pp. 2228-2233. by N. Maniatis, A. Collins, C. F. Xu, et al.L. C. Mccarthy, D. R. Hewett, W. Tapper, S. Ennis, X. Ke, N. E. Morton posted to chromosome chromosomes combinedbib disequilibrium evolution factors genetic genotype haplotypes human humans linkage mapping models molecular nucleotide pair physical polymorphism single statistical time by qmwwallace on 2007-07-05 14:55:18 as
	Environmental covariates: Effects on the power of sib-pair linkage methods [My Copy] Vol. 17 (1999), pp. S643-S648. by D. M. Mandal, A. J. M. Sorant, E. W. Pugh, et al.S. E. Marcus, A. P. Klein, R. A. Mathias, J. O'Neill, L. F. Temiyakarn, A. F. Wilson, Bailey J. E. Wilson posted to affected-sib-pair complex linkage sib-pair test traits combinedbib by qmwwallace on 2007-07-05 14:55:18 as
	Heterogeneity analysis of breast cancer families by using age at onset as a covariate [My Copy] Vol. 50 (1992), pp. 515-519. by Chantal Mérette, Mary C. King, Jurg Ott posted to linkage combinedbib by qmwwallace on 2007-07-05 14:55:16 as
	Cost-effective analysis of candidate genes using htSNPs: a staged approach. [My Copy] Genes Immun, Vol. 5, No. 4. (Jun 2004), pp. 301-5. by C. E. Lowe, J. D. Cooper, J. M. Chapman, et al.B. J. Barratt, Twells, E. A. Green, D. A. Savage, C. Guja, Ionescu C. Tîrgovi?te, Tuomilehto E. Wolf, J. Tuomilehto, J. A. Todd, D. G. Clayton posted to adolescent and carrier case-control child combinedbib cytoplasmic diabetes disease disequilibrium dna-binding epistasis female genetic genetics genotype glycoproteins govt haplotypes humans interleukin-13 interleukin-4 linkage male markers mellitus membrane models non-us nuclear nucleotide polymorphism population predisposition preschool proteins receptors research single statistical studies support to trans-activators type by qmwwallace on 2007-07-05 14:55:16 as
	Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q. [My Copy] J Clin Invest, Vol. 100, No. 5. (Sep 1997), pp. 1240-7. by A. V. Lembertas, L. Pérusse, Y. C. Chagnon, et al.J. S. Fisler, C. H. Warden, Purcell D. A. Huynh, F. T. Dionne, J. Gagnon, A. Nadeau, A. J. Lusis, C. Bouchard posted to chr20 linkage obesity by qmwwallace on 2007-07-05 14:55:15 as
	Genome scan for human obesity and linkage to markers in 20q13. [My Copy] Am J Hum Genet, Vol. 64, No. 1. (Jan 1999), pp. 196-209. by J. H. Lee, D. R. Reed, W. D. Li, et al.W. Xu, E. J. Joo, R. L. Kilker, E. Nanthakumar, M. North, H. Sakul, C. Bell, R. A. Price posted to african ancestry banding chromosome chromosomes combinedbib continental european frequency gene genetic genetics genotype govt group heritable human humans linkage lod mapping markers non-us obesity pair phenotype phs quantitative research score software support trait us by qmwwallace on 2007-07-05 14:55:15 as
	Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. [My Copy] Genetics, Vol. 121, No. 1. (Jan 1989), pp. 185-199. by E. S. Lander, D. Botstein posted to linkage qtl statistics by qmwwallace on 2007-07-05 14:55:14 as
	Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. [My Copy] Nat Genet, Vol. 11, No. 3. (1995), pp. 241-7. by E. Lander, L. Kruglyak posted to linkage significance by qmwwallace on 2007-07-05 14:55:14 as
	Genomewide scan of multiple sclerosis in Finnish multiplex families. [My Copy] Am J Hum Genet, Vol. 61, No. 6. (Dec 1997), pp. 1379-1387. by S. Kuokkanen, M. Gschwend, J. D. Rioux, et al.M. J. Daly, J. D. Terwilliger, P. J. Tienari, J. Wikström, J. Palo, L. D. Stein, T. J. Hudson, E. S. Lander, L. Peltonen posted to finnish linkage ms by qmwwallace on 2007-07-05 14:55:13 as
	Coverage and power in genomewide association studies. [My Copy] Am J Hum Genet, Vol. 78, No. 5. (May 2006), pp. 884-888. by Eric Jorgenson, John S. Witte posted to chromosome disequilibrium genetics genome heritable human humans linkage mapping models nucleotide polymorphism quantitative single statistical trait variation combinedbib by qmwwallace on 2007-07-05 14:55:11 as
	Haplotype tagging for the identification of common disease genes. [My Copy] Nat Genet, Vol. 29, No. 2. (Oct 2001), pp. 233-7. by G. C. Johnson, L. Esposito, B. J. Barratt, et al.A. N. Smith, J. Heward, G. Di Genova, H. Ueda, H. J. Cordell, I. A. Eaves, F. Dudbridge, R. C. Twells, F. Payne, W. Hughes, S. Nutland, H. Stevens, P. Carr, Tuomilehto E. Wolf, J. Tuomilehto, S. C. Gough, D. G. Clayton, J. A. Todd posted to 11586306 acid base disease disequilibrium dna genetic govt haplotypes homology humans linkage non-us nucleic nucleotide polymorphism predisposition research sequence single support to combinedbib by qmwwallace on 2007-07-05 14:55:11 as
	Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat. [My Copy] Kidney Int, Vol. 62, No. 4. (Oct 2002), pp. 1143-8. by Steven C. Hunt, Sandra J. Hasstedt, Hilary Coon, et al.Nicola J. Camp, Richard M. Cawthon, Lily L. Wu, Paul N. Hopkins posted to chromosome-10 creatinine-clearance linkage renal-disease by qmwwallace on 2007-07-05 14:55:11 as
	Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees. [My Copy] Am J Hypertens, Vol. 17, No. 6. (Jun 2004), pp. 511-5. by Steven C. Hunt, Hilary Coon, Sandra J. Hasstedt, et al.Richard M. Cawthon, Nicola J. Camp, Lily L. Wu, Paul N. Hopkins posted to accident adult aged cerebrovascular chromosomes combinedbib comparative coronary creatinine disease family female filtration genetic genetics glomerular govt health human humans hypertension linkage lod male markers middle pair pedigree phs predisposition rate research score study support to us utah by qmwwallace on 2007-07-05 14:55:10 as
	Linkage of body mass index to chromosome 20 in Utah pedigrees. [My Copy] Hum Genet, Vol. 109, No. 3. (Sep 2001), pp. 279-85. by S. C. Hunt, V. Abkevich, C. H. Hensel, et al.A. Gutin, C. D. Neff, D. L. Russell, T. Tran, X. Hong, S. Jammulapati, R. Riley, Weaver J. Feldhaus, T. Macalma, M. M. Richards, R. Gress, M. Francis, A. Thomas, G. C. Frech, T. D. Adams, D. Shattuck, S. Stone posted to body centromere chromosomes combinedbib dominant female genes genetic genetics genotype govt human humans index linkage lod male markers mass models non-us obesity pair pedigree phenotype phs recessive research score support us utah by qmwwallace on 2007-07-05 14:55:10 as
	Common deletions and SNPs are in linkage disequilibrium in the human genome. [My Copy] Nat Genet, Vol. 38, No. 1. (Jan 2006), pp. 82-85. by David A. Hinds, Andrew P. Kloek, Michael Jen, Xiyin Chen, Kelly A. Frazer posted to analysis combinedbib continental deletion disequilibrium frequency gene genetic genetics genome groups human humans linkage microarray nucleotide polymorphism population sequence single variation by qmwwallace on 2007-07-05 14:55:09 as
	Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group. [My Copy] Am J Hum Genet, Vol. 53, No. 6. (Dec 1993), pp. 1256-1261. by F. Hildebrandt, Singh I. Sawhney, B. Schnieders, et al.L. Centofante, H. Omran, A. Pohlmann, C. Schmaltz, H. Wedekind, C. Schubotz, C. Antignac posted to 2 8250041 chromosome chromosomes chronic cystic diseases dna failure female genetic genetics govt haplotypes human humans kidney linkage ma male markers non-us pair pedigree pping research satellite support combinedbib by qmwwallace on 2007-07-05 14:55:09 as
	Ordered subset analysis in genetic linkage mapping of complex traits. [My Copy] Genet Epidemiol, Vol. 27, No. 1. (Jul 2004), pp. 53-63. by Elizabeth R. Hauser, Richard M. Watanabe, William L. Duren, Meredyth P. Bass, Carl D. Langefeld, Michael Boehnke posted to linkage osa by qmwwallace on 2007-07-05 14:55:05 as
	Incorporation of covariates into genome scanning using sib-pair analysis in bipolar affective disorder [My Copy] Vol. 14, No. 6. (1997), pp. 635-640. by C. M. T. Greenwood, S. B. Bull posted to allele chromosome-18 heterogeneity imprinting linkage markers of origin parent regression sharing traits combinedbib by qmwwallace on 2007-07-05 14:55:04 as
	Analysis of affected sib pairs, with covariates - with and without constraints [My Copy] Vol. 64, No. 3. (1999), pp. 871-885. by C. M. T. Greenwood, S. B. Bull posted to analysis disease distribution epidemiology evolving extensions genes ibd linkage methods susceptibility traits combinedbib by qmwwallace on 2007-07-05 14:55:03 as
	Inclusion of risk factor covariates in a segregation analysis of a population-based sample of 426 breast cancer families [My Copy] Vol. 16, No. 2. (1999), pp. 150-164. by D. M. Grabrick, V. E. Anderson, R. A. King, L. H. Kushi, T. A. Sellers posted to age analysis brca2 breast cancer frequency gene genetics health linkage models mutations onset ovarian-cancer penetrance susceptibility combinedbib by qmwwallace on 2007-07-05 14:55:03 as
	Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4 [My Copy] Vol. 68 (2001), pp. 1197-1206. by Katrina A. B. Goddard, John S. Witte, Brian K. Suarez, William J. Catalona, Jane M. Olson posted to 1q24- 1q422-43 25 androgen asymptotic families gene genome high-risk linkage locus pair properties receptor repeat susceptibility combinedbib by qmwwallace on 2007-07-05 14:55:02 as
	Impact of family structure on the power of linkage tests using sib-pair methods. [My Copy] Genet Epidemiol, Vol. 17, No. Suppl 1. (1999), pp. S575-9. by K. A. Goddard, E. L. Goode, L. S. Rozek, G. P. Jarvik posted to 10597495 family genetic genetics govt humans linkage lod markers models non-us phs research score software statistical support us combinedbib by qmwwallace on 2007-07-05 14:55:02 as
	Genomewide linkage analysis to serum creatinine, GFR, and creatinine clearance in a community-based population: the Framingham Heart Study. [My Copy] J Am Soc Nephrol, Vol. 15, No. 9. (Sep 2004), pp. 2457-61. by Caroline S. Fox, Qiong Yang, Adrienne L. Cupples, et al.Chao Y. Guo, Martin G. Larson, Eric P. Leip, Peter W. F. Wilson, Daniel Levy posted to creatinine creatinine-clearance gfr linkage by qmwwallace on 2007-07-05 14:54:56 as
	Accuracy of haplotype reconstruction from haplotype-tagging single-nucleotide polymorphisms. [My Copy] Am J Hum Genet, Vol. 76, No. 3. (Mar 2005), pp. 438-48. by Julian Forton, Dominic Kwiatkowski, Kirk Rockett, Gaia Luoni, Martin Kimber, Jeremy Hull posted to 15660292 biometry comparative disequilibrium female genetic genomics genotype govt haplotypes humans linkage male markers models non-us nucleotide polymorphism research single study support combinedbib by qmwwallace on 2007-07-05 14:54:56 as
	Introduction and overview [My Copy] Vol. 9, No. 6. (2000), pp. 527-541. by R. C. Elston posted to analysis complex data disease linkage loci models pedigree quantitative regressive segregation sib-pair tests traits transmission-disequilibrium combinedbib by qmwwallace on 2007-07-05 14:54:54 as
	The emerging importance of genetics in epidemiologic research III. Bioinformatics and statistical genetic methods [My Copy] Vol. 9, No. 4. (1999), pp. 207-224. by D. L. Ellsworth, T. A. Manolio posted to analysis bioinformatics biology cardiovascular-disease computational converting-enzyme discordant environmental- epidemiologic epidemiology gene genetic genetics influences linkage loci methods methylenetetrahydrofolate molecular myocardial-infarction pairs polymorphisms quantitative reductase segregation sib single-nucleotide statistical trait combinedbib by qmwwallace on 2007-07-05 14:54:53 as
	Statistical methods for mapping quantitative trait loci from a dense set of markers. [My Copy] Genetics, Vol. 151, No. 1. (1999), pp. 373-86. by J. Dupuis, D. Siegmund posted to chromosome computing crossing functions genetic genetics govt heritable likelihood linkage mappingmethods markers mathematical models non-phs over phs quantitative support trait us combinedbib by qmwwallace on 2007-07-05 14:54:52 as
	A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans [My Copy] Vol. 68, No. 5. (2001), pp. 1149-1164. by R. Duggirala, J. Blangero, L. Almasy, et al.R. Arya, T. D. Dyer, K. L. Williams, R. J. Leach, P. O'Connell, M. P. Stern posted to affected analysis assessment autosomal cardiovascular dependent diabetes-mellitus genomic glycoprotein homeostasis linkage locus membrane model multipoint pairs pc-1 quantitative risk-factors scan sib susceptibility trait variance-components combinedbib by qmwwallace on 2007-07-05 14:54:51 as
	Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies. [My Copy] Am J Hum Genet, Vol. 75, No. 3. (Sep 2004), pp. 424-435. by Frank Dudbridge, Bobby P. C. Koeleman posted to association chromosome databases disequilibrium genetic genetics genome genotype govt human humans linkage mapping markers models non-us nucleotide polymorphism research single statistical statistics support techniques combinedbib by qmwwallace on 2007-07-05 14:54:51 as
	Genomic MHC haplotyping of mutant cell lines using a novel marker. [My Copy] Eur J Immunogenet, Vol. 20, No. 5. (Oct 1993), pp. 373-380. by Degli M. A. Esposti, J. F. Williamson, G. K. Tay, et al.B. Salmon, G. A. Joseph, A. A. Morley, R. L. Dawkins posted to 2 9098405 antigens cell chromosome chromosomes chronic complex cystic deletion diseases dna factor-alpha failure family female fragment gene genetic genetics genome govt haplotypes histocompatibility hla human humans kidney length line linkage ma major male markers multigene mutation necrosis non-us pair pedigree polymorphism pping research restriction satellite serotyping support testing tumor combinedbib by qmwwallace on 2007-07-05 14:54:46 as
	Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups. [My Copy] Cytogenet Cell Genet, Vol. 50, No. 4. (1989), pp. 181-187. by S. P. Daiger, M. M. Humphries, N. Giesenschlag, et al.E. Sharp, P. Mcwilliam, J. Farrer, D. Bradley, P. Kenna, D. J. Mcconnell, R. S. Sparkes posted to acid adolescent adult aged amino antigens ataxia atrophy autoantibodies base blotting cell cells chains child chromosome chromosomes chronic combinedbib complex cosmids cultured cystic data deletion diseases dna dominant factor-alpha failure family female fragment fungal gene genes genetic genetics genome genomic govt haplotypes heavy histocompatibility hla human humans hybrid immunoglobulin interpretation kidney length library line linkage ma major male mapping markers middle molecular multigene muscular mutation necrosis non-us pair pedigree pigmentosa polymorphism pping recombination region research restriction retinitis satellite sequence serotyping sites southern spinal statistical support tagged telangiectasia testing transformed tumor variable by qmwwallace on 2007-07-05 14:54:44 as
	Unraveling the genetic component of multifactorial diseases: Dream or reality [My Copy] Vol. 68, No. 1. (2000), pp. 45-51. by Clerget F. Darpoux posted to analysis candidate complex diseases disequilibrium exclusion factors gene genes genetic genome linkage markers method multifactorial pedigree-member risk screen strategies strategy susceptibility test traits transmissiondisequilibrium whole- combinedbib by qmwwallace on 2007-07-05 14:54:40 as
	Use of unphased multilocus genotype data in indirect association studies. [My Copy] Genet Epidemiol, Vol. 27, No. 4. (Dec 2004), pp. 415-28. by David Clayton, Juliet Chapman, Jason Cooper posted to adolescent case-control child combinedbib diabetes disease disequilibrium dna-binding epistasis female genetic genetics genotype govt haplotypes humans interleukin-13 interleukin-4 linkage male markers mellitus models non-us nucleotide polymorphism population predisposition preschool proteins research single statistical studies support to trans-activators type by qmwwallace on 2007-07-05 14:54:39 as
	Ascertainment bias in studies of human genome-wide polymorphism. [My Copy] Genome Res, Vol. 15, No. 11. (Nov 2005), pp. 1496-1502. by Andrew G. Clark, Melissa J. Hubisz, Carlos D. Bustamante, Scott H. Williamson, Rasmus Nielsen posted to 16251459 algorithms alleles analysis chromatin chromosome comparative cooperation design disease disequilibrium dna drug entropy epoxide expression extramural frequency gene genetic genetics genome govt haplotypes human humans hydrolases ii immunoprecipitation industry international isposition laboratories linkage mapping markers nih non-us nucleotide pharmacogenetics phenotype phs polymerase polymorphism pport pred predisposition regulation research rna selection sequence single study su support to us variation combinedbib by qmwwallace on 2007-07-05 14:54:38 as
	Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power. [My Copy] Hum Hered, Vol. 56, No. 1-3. (2003), pp. 18-31. by Juliet M. Chapman, Jason D. Cooper, John A. Todd, David G. Clayton posted to adolescent analysis and carrier case-control child combinedbib cytoplasmic data diabetes disease disequilibrium dna-binding epistasis female genetic genetics genotype glycoproteins govt haplotypes humans interleukin-13 interleukin-4 interpretation linkage male markers mellitus membrane models multivariate non-us nuclear nucleotide polymorphism population predisposition preschool proteins receptors research single statistical studies support to trans-activators type by qmwwallace on 2007-07-05 14:54:37 as
	Genome-wide mapping of human loci for essential hypertension. [My Copy] Lancet, Vol. 361, No. 9375. (Jun 2003), pp. 2118-23. by Mark Caulfield, Patricia Munroe, Janine Pembroke, et al.Nilesh Samani, Anna Dominiczak, Morris Brown, Nigel Benjamin, John Webster, Peter Ratcliffe, Suzanne O'Shea, Jeanette Papp, Elizabeth Taylor, Richard Dobson, Joanne Knight, Stephen Newhouse, Joel Hooper, Wai Lee, Nick Brain, David Clayton, Mark G. Lathrop, Martin Farrall, John Connell, m posted to 12826435 aged chromosome disease female genetic genetics genotype humans hypertension linkage lod male mapping middle phenotype predisposition score siblings to combinedbib by qmwwallace on 2007-07-05 14:54:36 as
	Identification of a genetic locus for familial atrial fibrillation. [My Copy] N Engl J Med, Vol. 336, No. 13. (Mar 1997), pp. 905-911. by R. Brugada, T. Tapscott, G. Z. Czernuszewicz, et al.A. J. Marian, A. Iglesias, L. Mont, J. Brugada, J. Girona, A. Domingo, L. L. Bachinski, R. Roberts posted to 10q22 atrial fibrilation linkage by qmwwallace on 2007-07-05 14:54:28 as
	Ascertainment corrections based on smaller family units [My Copy] Vol. 63, No. 4. (1998), pp. 1202-1215. by G. E. Bonney posted to analysis complex data likelihood linkage models pedigree problem regressive resolution sampling segregation traits combinedbib by qmwwallace on 2007-07-05 14:54:27 as
	Complex segregation analysis of nonsyndromic cleft lip/palate in a Chilean population [My Copy] Vol. 21, No. 1. (1998), pp. 139-144. by R. Blanco, Arcos M. Burgos, M. Paredes, et al.H. Palomino, L. Jara, H. Carreno, V. Obreque, M. A. Munoz posted to association autosomal evidence families genetic-variation growth-factor-alpha inheritance linkage lip locus major no palate combinedbib by qmwwallace on 2007-07-05 14:54:26 as
	Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22. [My Copy] Neurology, Vol. 52, No. 3. (Feb 1999), pp. 510-515. by K. Bejaoui, Mckenna D. Yasek, B. A. Hosler, et al.Burns E. Deater, L. M. Deater, G. O'Neill, J. L. Haines, R. H. Brown posted to 9q22 linkage neuropathy sensory by qmwwallace on 2007-07-05 14:54:19 as
	Association studies for quantitative traits in structured populations. [My Copy] Genet Epidemiol, Vol. 22, No. 1. (Jan 2002), pp. 78-93. by Silviu A. Bacanu, Bernie Devlin, Kathryn Roeder posted to 11754475 algorithms alleles analysis bias carlo case-control chains chi-square chromosome comparative computer confidence confounding disease disequilibrium distribution epidemiology factors genetic genetics genome genotype govt heritable heterogeneity human humans intervals linkage mapping markers markov method models monte mutation non-phs phenotype phs poisson polymorphism population predisposition probability quantitative recombination regression research simulation statistical statistics studies study support theoretical to trait us combinedbib by qmwwallace on 2007-07-05 14:54:11 as
	Epidemiologic and genetic approaches in the study of gene- environment interaction: an overview of available methods [My Copy] Vol. 20, No. 2. (1998), pp. 137-147. by N. Andrieu, A. M. Goldstein posted to analysis breast- cancer case-control complex factors family history linkage logistic-regression lung-cancer nested quantitative reproductive risk-factors segregation traits combinedbib by qmwwallace on 2007-07-05 14:53:54 as
	Genetic linkage analysis of simulated complex disease data [My Copy] Vol. 17 (1999), pp. S461-S466. by M. Alarcón, Y. P. Wang, J. I. Rotter, H. Y. Yang posted to environment interaction linkage multipoint stratification combinedbib by qmwwallace on 2007-07-05 14:53:47 as

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combinedbib	529
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dopamine	2
entropy	2
european	2
evidence	2
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families	2
fungal	2
genomic	2
gfr	2
groups	2
heterogeneity	2
hybrid	2
hybridization	2
hypercholesterolemia	2
in	2
infarction	2
international	2
intervals	2
introns	2
italy	2
library	2
likelihood	2
lung-cancer	2
method	2
methods	2
microarray	2
multipoint	2
multivariate	2
nah-exchanger	2
natriuretic-peptide	2
nih	2
no	2
pairs	2
phosphoproteins	2
polymerase	2
probability	2
receptor	2
regression	2
repeats	2
reproducibility	2
results	2
risk-factors	2
sampling	2
self	2
sib	2
siblings	2
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simulation	2
single-stranded	2
sites	2
situ	2
splicing	2
stratification	2
stroke	2
synthase	2
tagged	2
telangiectasia	2
test	2
transmissiondisequilibrium	2
utah	2
zonulin	2
10597495	1
10760303	1
10q22	1
11586306	1
11754475	1
11833004	1
11q13	1
12372404	1
12702205	1
12826435	1
15660292	1
15809660	1
15882546	1
16006589	1
16103984	1
16251459	1
16532390	1
16715099	1
16736010	1
1q24-	1
1q422-43	1
25	1
5	1
7p	1
8250041	1
8p21-22	1
9098405	1
9175133	1
9217767	1
9507981	1
9q22	1
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alu	1
americans	1
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asian	1
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banding	1
bardet-biedl	1
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biological	1
biology	1
biometry	1
bipolar	1
blocks	1
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bp	1
brca2	1
breast	1
breast-	1
bright	1
britain	1
calcium	1
canada	1
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carlo	1
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centromere	1
cerebral	1
chain	1
channels	1
characteristics	1
chr20	1
chromatin	1
chromos	1
chromosome-1	1
chromosome-10	1
chromosome-18	1
codon	1
cognition	1
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computer	1
computing	1
confounding	1
converting-enzyme	1
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cosmids	1
creatine	1
crossing	1
cultured	1
cyclase	1
d2-dpoamine-receptor	1
deficit	1
demographic-history	1
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design	1
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donovani	1
drd4	1
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electrocardiography	1
encode	1
environment	1
environmental-	1
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europe	1
evolution	1
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exclusion	1
extensions	1
factor	1
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fibrilation	1
filtration	1
finnish	1
fisher	1
fluorescence	1
function	1
functions	1
gambia	1
genetics-hypertension	1
genetic-variation	1
genomics	1
glomerular	1
gly972-arg	1
glycoprotein	1
great	1
growth-factor-alpha	1
guanylate	1
gwa	1
gwa-association	1
h-11-linked	1
haplotype-blocks	1
haploview	1
hapmap	1
heavy	1
high-risk	1
history	1
hla-dp	1
hla-dq	1
hla-dr	1
homeostasis	1
homology	1
homozygote	1
host-resistance	1
human-genome	1
hydatidiform	1
hydrolases	1
hyperactivity	1
hypertrophy	1
ibd	1
iceland	1
ii	1
il13	1
il4	1
il4ra	1
immunoglobulin	1
immunoprecipitation	1
imprinting	1
industry	1
infection	1
influences	1
inheritance	1
intelligence	1
interaction	1
inwardly	1
irs1	1
irs-1	1
islets	1
isomerases	1
isposition	1
japan	1
knockout	1
laboratories	1
langerhans	1
ld	1
ldu	1
left	1
leishmaniasis	1
lip	1
logistic	1
logistic-regression	1
lsh-ity-bcg	1
malawi	1
mappingmethods	1
markov	1
mathematical	1
methylenetetrahydrofolate	1
mhc	1
mice	1
microsatellite	1
minisatellite	1
mixed-model	1
model	1
moles	1
monte	1
mouse	1
ms	1
multifactorial	1
muscular	1
mutational	1
mutations	1
myocardial	1
myocardial-infarction	1
natriuretic	1
natriuretic-peptide-clearance-receptor	1
natriuretic-peptide-receptor	1
natural-resistance	1
nerve	1
nested	1
neuropathy	1
neurotic	1
nhe8	1
nonsense	1
npr-c	1
nucleic	1
nuisance	1
oligogenic	1
omes	1
onset	1
origin	1
osa	1
ovarian-cancer	1
over	1
palate	1
parameters	1
parent	1
pc-1	1
pca	1
pde4d	1
pedigree-member	1
pedigrees	1
peer	1
penetrance	1
pharmacogenetics	1
physical	1
pigmentosa	1
point	1
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potassium	1
pport	1
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pressure	1
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properties	1
qtl	1
rat	1
rate	1
rates	1
reaction	1
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region	1
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renal-disease	1
repeat	1
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resolution	1
retinitis	1
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review	1
robustness	1
salt	1
sample	1
scan	1
screen	1
selection	1
selective-genotyping	1
semiparametric	1
sensory	1
sequencing	1
serotonin	1
sharing	1
signal	1
significance	1
single-locus	1
single-nucleotide	1
size	1
sma	1
sodium	1
southern	1
spinal	1
strategies	1
strategy	1
structure	1
su	1
substitution	1
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tagging	1
theoretical	1
time	1
tissue	1
transcription	1
transduction	1
transformed	1
transmission	1
transmission-disequilibrium	1
transport	1
transporter	1
usher	1
variable	1
variance-components	1
ventricular	1
visceral	1
whole-	1
wnk1	1
wtccc	1

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