Teague P - Search Results

1

Estimating human inbreeding coefficients: comparison of genealogical and marker heterozygosity approaches.

Carothers AD, Rudan I, Kolcic I, Polasek O, Hayward C, Wright AF, Campbell H, Teague P, Hastie ND, Weber JL. Carothers AD, et al. Among authors: teague p. Ann Hum Genet. 2006 Sep;70(Pt 5):666-76. doi: 10.1111/j.1469-1809.2006.00263.x. Ann Hum Genet. 2006. PMID: 16907711

2

Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study design.

Vitart V, Carothers AD, Hayward C, Teague P, Hastie ND, Campbell H, Wright AF. Vitart V, et al. Among authors: teague p. Am J Hum Genet. 2005 May;76(5):763-72. doi: 10.1086/429840. Epub 2005 Mar 24. Am J Hum Genet. 2005. PMID: 15791542 Free PMC article.

3

Pitfalls in homozygosity mapping.

Miano MG, Jacobson SG, Carothers A, Hanson I, Teague P, Lovell J, Cideciyan AV, Haider N, Stone EM, Sheffield VC, Wright AF. Miano MG, et al. Among authors: teague p. Am J Hum Genet. 2000 Nov;67(5):1348-51. doi: 10.1016/S0002-9297(07)62966-8. Epub 2000 Sep 27. Am J Hum Genet. 2000. PMID: 11007652 Free PMC article.

4

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.

Teague PW, Aldred MA, Jay M, Dempster M, Harrison C, Carothers AD, Hardwick LJ, Evans HJ, Strain L, Brock DJ, et al. Teague PW, et al. Am J Hum Genet. 1994 Jul;55(1):105-11. Am J Hum Genet. 1994. PMID: 8023838 Free PMC article.

5

A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease families.

Wright AF, Teague PW, Pound SE, Pignatelli PM, Macnicol AM, Carothers AD, De Mey RJ, Allan PL, Watson ML. Wright AF, et al. Among authors: teague pw. Hum Genet. 1993 Jan;90(5):569-71. doi: 10.1007/BF00217461. Hum Genet. 1993. PMID: 8428756

6

Recombination patterns around the breakpoints of a balanced 1;11 autosomal translocation associated with major mental illness.

He L, Carothers A, Blackwood DH, Teague P, Maclean AW, Brown J, Wright AF, Muir WJ, Porteous DJ, St Clair DM. He L, et al. Among authors: teague p. Psychiatr Genet. 1996 Winter;6(4):201-8. doi: 10.1097/00041444-199624000-00006. Psychiatr Genet. 1996. PMID: 9149326

7

Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa.

Aldred MA, Dry KL, Knight-Jones EB, Hardwick LJ, Teague PW, Lester DH, Brown J, Spowart G, Carothers AD, Raeburn JA, et al. Aldred MA, et al. Among authors: teague pw. Am J Hum Genet. 1994 Nov;55(5):916-22. Am J Hum Genet. 1994. PMID: 7977353 Free PMC article.

8

Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

Aldred MA, Teague PW, Jay M, Bundey S, Redmond RM, Jay B, Bird AC, Bhattacharya SS, Wright AF. Aldred MA, et al. Among authors: teague pw. J Med Genet. 1994 Nov;31(11):848-52. doi: 10.1136/jmg.31.11.848. J Med Genet. 1994. PMID: 7853368 Free PMC article.

9

European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain.

Cox SA, Attwood J, Bryant SP, Bains R, Povey S, Rebello M, Kapsetaki M, Moschonas NK, Grzeschik KH, Otto M, Dixon M, Sudworth HE, Kooy RF, Wright A, Teague P, Terrenato L, Vergnaud G, Monfouilloux S, Weissenbach J, Alibert O, Dib C, Fauré S, Bakker E, Pearson NM, Spurr NK. Cox SA, et al. Among authors: teague p. Ann Hum Genet. 1996 Nov;60(6):447-86. doi: 10.1111/j.1469-1809.1996.tb01614.x. Ann Hum Genet. 1996. PMID: 9024576

10

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF. Bruford EA, et al. Among authors: teague pw. Genomics. 1997 Apr 1;41(1):93-9. doi: 10.1006/geno.1997.4613. Genomics. 1997. PMID: 9126487

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