qmwwallace's genetic [38 articles] Export

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	Splicing mutation of the prostacyclin synthase gene in a family associated with hypertension. [My Copy] Biochem Biophys Res Commun, Vol. 297, No. 5. (Oct 2002), pp. 1135-9. by Tomohiro Nakayama, Masayoshi Soma, Yoshiyasu Watanabe, et al.Buaijiaer Hasimu, Mikano Sato, Noriko Aoi, Kotoko Kosuge, Katsuo Kanmatsuse, Shinichiro Kokubun, Jason D. Marrow, John A. Oates posted to 12372404 alleles biosynthesis conformational cytochrome data enzyme exons family female genetic genotype govt health humans hypertension intramolecular introns male models molecular mutation non-us oxidoreductases p-450 pedigree phs polymorphism protein research rna sequence single-stranded splicing support system us combinedbib by qmwwallace on 2007-07-05 14:55:21 as
	Nonsense mutation of prostacyclin synthase gene in a family. [My Copy] Lancet, Vol. 349, No. 9069. (Jun 1997), pp. 1887-8. by T. Nakayama, M. Soma, D. Rahmutula, Y. Izumi, K. Kanmatsuse posted to 9217767 aged alleles biosynthesis cerebral codon conformational cytochrome data enzyme exons family female genetic genotype govt health humans hypertension infarction intramolecular introns isomerases male middle models molecular mutation non-us nonsense oxidoreductases p-450 pedigree phs point polymorphism protein research rna sequence single-stranded splicing support system us combinedbib by qmwwallace on 2007-07-05 14:55:20 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
	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
	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
	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
	Human prostacyclin synthase gene and hypertension : the Suita Study. [My Copy] Circulation, Vol. 100, No. 22. (Nov 1999), pp. 2231-2236. by N. Iwai, T. Katsuya, K. Ishikawa, et al.T. Mannami, J. Ogata, J. Higaki, T. Ogihara, T. Tanabe, S. Baba posted to adult aged analysis ancestry asian base blood chromosomes combinedbib continental cytochrome data diastole disease dna enzyme factors female frequency gene genes genetic genotype group human humans hypertension infarction intramolecular japan male middle minisatellite molecular multivariate mutational myocardial oxidoreductases p-450 pair predisposition pressure repeats reporter risk sequence system systole to 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
	Localization of a susceptibility gene for common forms of stroke to 5q12. [My Copy] Am J Hum Genet, Vol. 70, No. 3. (Mar 2002), pp. 593-603. by Solveig Gretarsdottir, Sigurlaug Sveinbjörnsdottir, Hjörtur H. Jonsson, et al.Finnbogi Jakobsson, Elisabet Einarsdottir, Uggi Agnarsson, Dana Shkolny, Gisli Einarsson, Herdis M. Gudjonsdottir, Einar M. Valdimarsson, Olafur B. Einarsson, Gudmundur Thorgeirsson, Radinka Hadzic, Sif Jonsdottir, Sigridur T. Reynisdottir, Sigrun M. Bjarnadottir, Thorunn Gudmundsdottir, Gudrun J. Gudlaugsdottir, Ramanjit Gill, Klaus Lindpaintner, Jesus Sainz, Helgi H. Hannesson, Gunnar T. Sigurdsson, Michael L. Frigge, Augustine Kong, Vilmundur Gudnason, Kari Stefansson, Jeffrey R. Gulcher posted to 11833004 5 accident alleles cerebrovascular chromosome chromosomes complications diabetes disease factors female genetic genome human humans hypercholesterolemia hypertension iceland lod male mapping markers mellitus pair pedigree predisposition risk score to combinedbib by qmwwallace on 2007-07-05 14:55:04 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
	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
	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
	Rank truncated product of P-values, with application to genomewide association scans. [My Copy] Genet Epidemiol, Vol. 25, No. 4. (Dec 2003), pp. 360-366. by Frank Dudbridge, Bobby P. C. Koeleman posted to algorithms genetic genome human humans markers models statistical 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
	Detecting multiple associations in genome-wide studies. [My Copy] Hum Genomics, Vol. 2, No. 5. (Mar 2006), pp. 310-317. by Frank Dudbridge, Arief Gusnanto, Bobby P. C. Koeleman posted to genetic genome govt human humans mutation non-us of reproducibility research results sample size support techniques combinedbib by qmwwallace on 2007-07-05 14:54:51 as
	A genetic model defines the importance of the atrial natriuretic peptide receptor (guanylyl cyclase-A) in the regulation of kidney function. [My Copy] Proc Natl Acad Sci U S A, Vol. 97, No. 8. (Apr 2000), pp. 4369-4373. by S. K. Dubois, I. Kishimoto, T. O. Lillis, D. L. Garbers posted to 10760303 animals atrial cyclase factor genetic govt guanylate kidney knockout mice models natriuretic non-us receptors research signal sodium support transduction combinedbib by qmwwallace on 2007-07-05 14:54:51 as
	Interacting genetic loci on chromosomes 20 and 10 influence extreme human obesity. [My Copy] Am J Hum Genet, Vol. 72, No. 1. (Jan 2003), pp. 115-24. by Chuanhui Dong, Shuang Wang, Wei D. Li, Ding Li, Hongyu Zhao, Arlen R. Price posted to body chromosome chromosomes combinedbib epistasis genetic govt human humans index loci lod mapping mass obesity pair phs probability quantitative research score siblings support trait us by qmwwallace on 2007-07-05 14:54:51 as
	A genome scan for renal function among hypertensives: the HyperGEN study. [My Copy] Am J Hum Genet, Vol. 68, No. 1. (Jan 2001), pp. 136-144. by A. T. Dewan, D. K. Arnett, L. D. Atwood, et al.M. A. Province, C. E. Lewis, S. C. Hunt, J. Eckfeldt posted to african aged americans ancestry body chromosomes combinedbib comparative continental creatine european family female function genetic genotype govt group heritable human humans hypertension index kidney lod male mass middle models nuclear pair phenotype phs quantitative research score software study support tests trait us by qmwwallace on 2007-07-05 14:54:48 as
	Analysis of multilocus models of association. [My Copy] Genet Epidemiol, Vol. 25, No. 1. (Jul 2003), pp. 36-47. by B. Devlin, Kathryn Roeder, Larry Wasserman posted to chromosome data disease genetic govt humans interpretation mapping models non-phs phs predisposition research statistical support to us combinedbib by qmwwallace on 2007-07-05 14:54:47 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
	The HLA-DPB1--associated component of the IDDM1 and its relationship to the major loci HLA-DQB1, -DQA1, and -DRB1. [My Copy] Diabetes, Vol. 50, No. 5. (May 2001), pp. 1200-5. by F. Cucca, F. Dudbridge, M. Loddo, et al.A. P. Mulargia, R. Lampis, E. Angius, S. De Virgiliis, B. P. Koeleman, S. C. Bain, A. H. Barnett, F. Gilchrist, H. Cordell, K. Welsh, J. A. Todd posted to alleles antigens britain chromosome chromosomes combinedbib confidence diabetes disease genetic genetics govt great haplotypes hla-dp hla-dq hla-dr human humans intervals italy mapping mellitus non-us pair predisposition research support to type variation by qmwwallace on 2007-07-05 14:54:44 as
	A high-resolution survey of deletion polymorphism in the human genome. [My Copy] Nat Genet, Vol. 38, No. 1. (Jan 2006), pp. 75-81. by Donald F. Conrad, Daniel T. Andrews, Nigel P. Carter, Matthew E. Hurles, Jonathan K. Pritchard posted to analysis combinedbib cooperation databases deletion extramural genetic genome govt human humans hybridization in international microarray models nih non-us nucleotide of polymorphism reproducibility research results sequence single situ support by qmwwallace on 2007-07-05 14:54:40 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
	The serotonin transporter gene and peer-rated neuroticism. [My Copy] Neuroreport, Vol. 8, No. 5. (Mar 1997), pp. 1301-1304. by D. Ball, L. Hill, B. Freeman, et al.T. C. Eley, J. Strelau, R. Riemann, F. M. Spinath, A. Angleitner, R. Plomin posted to 9175133 adolescent adult aged carrier chi-square disorders distribution frequency gene genetic genotype glycoproteins govt group humans membrane middle nerve neurotic non-us peer polymorphism proteins research serotonin support tissue transport combinedbib by qmwwallace on 2007-07-05 14:54:12 as
	Dopamine markers and general cognitive ability. [My Copy] Neuroreport, Vol. 9, No. 2. (Jan 1998), pp. 347-349. by D. Ball, L. Hill, T. C. Eley, et al.M. J. Chorney, K. Chorney, L. A. Thompson, D. K. Detterman, C. Benbow, D. Lubinski, M. Owen, P. Mcguffin, R. Plomin posted to 9507981 adolescent alleles biological child cognition dna dopamine female genetic genotype heritable humans intelligence male markers polymorphism quantitative tests trait combinedbib by qmwwallace on 2007-07-05 14:54:12 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
	Haplotypic analysis of the TNF locus by association efficiency and entropy. [My Copy] Genome Biol, Vol. 4, No. 4. (2003) by Hans Ackerman, Stanley Usen, Richard Mott, et al.Anna Richardson, Fatoumatta S. Joof, Pauline Katundu, Terrie Taylor, Ryk Ward, Malcolm Molyneux, Margaret Pinder, Dominic P. Kwiatkowski posted to 12702205 adult case-control disease disequilibrium entropy factor-alpha frequency gambia gene genetic govt haplotypes humans linkage malawi necrosis non-us nucleotide polymorphism predisposition recombination research single studies support to tumor combinedbib by qmwwallace on 2007-07-05 14:53:46 as

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britain	1
calcium	1
canada	1
candidate	1
cardiovascular-disease	1
carlo	1
case-only	1
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
cognitive-ability	1
complications	1
computational	1
computer	1
computing	1
confounding	1
converting-enzyme	1
coronary	1
cosmids	1
creatine	1
crossing	1
cultured	1
cyclase	1
d2-dpoamine-receptor	1
deficit	1
demographic-history	1
dependent	1
design	1
diabetes-mellitus	1
diastole	1
diet	1
discordant	1
disorders	1
donovani	1
drd4	1
drug	1
echocardiography	1
electrocardiography	1
encode	1
environment	1
environmental-	1
epidemiologic	1
epoxide	1
europe	1
evolution	1
evolving	1
exclusion	1
extensions	1
factor	1
familial	1
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
poisson	1
polymorphisms	1
potassium	1
pport	1
pred	1
pressure	1
problem	1
properties	1
qtl	1
rat	1
rate	1
rates	1
reaction	1
recessive	1
rectifying	1
reductase	1
region	1
regulation	1
renal-disease	1
repeat	1
reporter	1
reproductive	1
resolution	1
retinitis	1
retrospective	1
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
systole	1
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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