Related Articles for PubMed (Select 11532206)

Complex genetic diseases: controversy over the Croesus code.

Wright AF, Hastie ND.

Genome Biol. 2001;2(8):COMMENT2007. Epub 2001 Aug 1.

PMID: 11532206 [PubMed - indexed for MEDLINE]

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The common variants/multiple disease hypothesis of common complex genetic disorders.

Becker KG.

Med Hypotheses. 2004;62(2):309-17.

PMID: 14962646 [PubMed - indexed for MEDLINE]

A haplotype map of the human genome.

Olivier M.

Physiol Genomics. 2003 Mar 18;13(1):3-9. Epub 2003 Mar 18. No abstract available.

PMID: 12644628 [PubMed - indexed for MEDLINE]

Are rare variants responsible for susceptibility to complex diseases?

Pritchard JK.

Am J Hum Genet. 2001 Jul;69(1):124-37. Epub 2001 Jun 12.

PMID: 11404818 [PubMed - indexed for MEDLINE]

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Epialleles and common disease.

Peedicayil J.

Med Hypotheses. 2005;64(1):215. No abstract available.

PMID: 15533644 [PubMed - indexed for MEDLINE]

On selecting markers for association studies: patterns of linkage disequilibrium between two and three diallelic loci.

Garner C, Slatkin M.

Genet Epidemiol. 2003 Jan;24(1):57-67. Review.

PMID: 12508256 [PubMed - indexed for MEDLINE]

The allelic spectra of common diseases may resemble the allelic spectrum of the full genome.

Wang WY, Pike N.

Med Hypotheses. 2004;63(4):748-51.

PMID: 15325027 [PubMed - indexed for MEDLINE]

Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia.

Bonnen PE, Pe'er I, Plenge RM, Salit J, Lowe JK, Shapero MH, Lifton RP, Breslow JL, Daly MJ, Reich DE, Jones KW, Stoffel M, Altshuler D, Friedman JM.

Nat Genet. 2006 Feb;38(2):214-7. Epub 2006 Jan 22.

PMID: 16429162 [PubMed - indexed for MEDLINE]

Pharmacogenetics and genotyping: on the trail of SNPs.

Melton L.

Nature. 2003 Apr 24;422(6934):917, 919, 921, 923. No abstract available.

PMID: 12712209 [PubMed - indexed for MEDLINE]

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What genome-wide association studies can do for medicine.

Christensen K, Murray JC.

N Engl J Med. 2007 Mar 15;356(11):1094-7. No abstract available.

PMID: 17360987 [PubMed - indexed for MEDLINE]

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Genomics and medicine. Dissecting human disease in the postgenomic era.

Peltonen L, McKusick VA.

Science. 2001 Feb 16;291(5507):1224-9. No abstract available.

PMID: 11233446 [PubMed - indexed for MEDLINE]

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Mapping the new frontier: complex genetic disorders.

Mayeux R.

J Clin Invest. 2005 Jun;115(6):1404-7. Review.

PMID: 15931374 [PubMed - indexed for MEDLINE]

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Introduction to SNPs: discovery of markers for disease.

Weiner MP, Hudson TJ.

Biotechniques. 2002 Jun;Suppl:4-7, 10, 12-3. No abstract available.

PMID: 12083396 [PubMed - indexed for MEDLINE]

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On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.

Morris RW, Kaplan NL.

Genet Epidemiol. 2002 Oct;23(3):221-33.

PMID: 12384975 [PubMed - indexed for MEDLINE]

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Localization of the Q1 mutation by cladistic analysis.

Zhu X, Cooper RS, Chen G, Luke A, Elston RC.

Genet Epidemiol. 2001;21 Suppl 1:S594-9.

PMID: 11793744 [PubMed - indexed for MEDLINE]

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Definition and clinical importance of haplotypes.

Crawford DC, Nickerson DA.

Annu Rev Med. 2005;56:303-20. Review.

PMID: 15660514 [PubMed - indexed for MEDLINE]

17:

Life, diversity and the pursuit of haplotypes.

McCarthy J.

Nat Biotechnol. 2005 Nov;23(11):1376-7. No abstract available.

PMID: 16273067 [PubMed - indexed for MEDLINE]

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Generalized T2 test for genome association studies.

Xiong M, Zhao J, Boerwinkle E.

Am J Hum Genet. 2002 May;70(5):1257-68. Epub 2002 Mar 29.

PMID: 11923914 [PubMed - indexed for MEDLINE]

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Advances in genetics: spiralling into trouble?

Nevin NC.

Med Leg J. 2001;69(Pt 1):4-12. No abstract available.

PMID: 11388070 [PubMed - indexed for MEDLINE]

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Structural variation in the human genome.

Lupski JR.

N Engl J Med. 2007 Mar 15;356(11):1169-71. No abstract available.

PMID: 17360997 [PubMed - indexed for MEDLINE]

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