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Items: 1 to 20 of 128

1.

Search for multifactorial disease susceptibility genes in founder populations.

Bourgain C, Genin E, Quesneville H, Clerget-Darpoux F.

Ann Hum Genet. 2000 May;64(Pt 3):255-65.

PMID:
11409410
2.

Missing data in haplotype analysis: a study on the MILC method.

Bourgain C, Genin E, Ober C, Clerget-Darpoux F.

Ann Hum Genet. 2002 Jan;66(Pt 1):99-108.

PMID:
12022148
3.

Maximum identity length contrast: a powerful method for susceptibility gene detection in isolated populations.

Bourgain C, Génin E, Margaritte-Jeannin P, Clerget-Darpoux F.

Genet Epidemiol. 2001;21 Suppl 1:S560-4.

PMID:
11793738
4.

Use of closely related affected individuals for the genetic study of complex diseases in founder populations.

Bourgain C, Génin E, Holopainen P, Mustalahti K, Mäki M, Partanen J, Clerget-Darpoux F.

Am J Hum Genet. 2001 Jan;68(1):154-159. Epub 2000 Nov 30.

5.

Finding genes underlying risk of complex disease by linkage disequilibrium mapping.

Clark AG.

Curr Opin Genet Dev. 2003 Jun;13(3):296-302. Review.

PMID:
12787793
6.

Finding genes influencing susceptibility to complex diseases in the post-genome era.

Rannala B.

Am J Pharmacogenomics. 2001;1(3):203-21. Review.

PMID:
12083968
7.

Identifying susceptibility genes using linkage and linkage disequilibrium analysis in large pedigrees.

Meng Z, Zaykin DV, Karnoub MC, Sreekumar GP, St Jean PL, Ehm MG.

Genet Epidemiol. 2001;21 Suppl 1:S453-8.

PMID:
11793718
8.

Properties of the transmission-disequilibrium test in the presence of inbreeding.

Génin E, Todorov AA, Clerget-Darpoux F.

Genet Epidemiol. 2002 Feb;22(2):116-27.

PMID:
11788958
9.
11.
12.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.

13.

Detecting susceptibility genes in case-control studies using set association.

Kim S, Zhang K, Sun F.

BMC Genet. 2003 Dec 31;4 Suppl 1:S9.

14.

The role of genes in disease: beware of simplistic interpretations!

[No authors listed]

Prescrire Int. 2009 Dec;18(104):279-82.

PMID:
20027720
15.

Mapping genes of complex psychiatric diseases in Daghestan genetic isolates.

Bulayeva KB, Leal SM, Pavlova TA, Kurbanov RM, Glatt SJ, Bulayev OA, Tsuang MT.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):76-84.

PMID:
15389762
16.
17.

Not all isolates are equal: linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations.

Angius A, Bebbere D, Petretto E, Falchi M, Forabosco P, Maestrale B, Casu G, Persico I, Melis PM, Pirastu M.

Hum Genet. 2002 Jul;111(1):9-15. Epub 2002 Jun 18.

PMID:
12136230
18.

Further investigation of linkage disequilibrium SNPs and their ability to identify associated susceptibility loci.

North BV, Curtis D, Martin ER, Lai EH, Roses AD, Sham PC.

Ann Hum Genet. 2004 May;68(Pt 3):240-8.

19.

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
20.

Two-stage designs to identify the effects of SNP combinations on complex diseases.

Kang G, Yue W, Zhang J, Huebner M, Zhang H, Ruan Y, Lu T, Ling Y, Zuo Y, Zhang D.

J Hum Genet. 2008;53(8):739-46. doi: 10.1007/s10038-008-0307-x. Epub 2008 Jun 27.

PMID:
18584117

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