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Items: 17


Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb.

Johanneson B, McDonnell SK, Karyadi DM, Hebbring SJ, Wang L, Deutsch K, McIntosh L, Kwon EM, Suuriniemi M, Stanford JL, Schaid DJ, Ostrander EA, Thibodeau SN.

Hum Genet. 2008 Feb;123(1):65-75. Epub 2007 Dec 8.


Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy.

Orr A, Dubé MP, Marcadier J, Jiang H, Federico A, George S, Seamone C, Andrews D, Dubord P, Holland S, Provost S, Mongrain V, Evans S, Higgins B, Bowman S, Guernsey D, Samuels M.

PLoS One. 2007 Aug 1;2(8):e685.


Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb.

Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA.

Prostate. 2007 Sep 15;67(13):1456-64.


Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics.

Schaid DJ, McDonnell SK, Zarfas KE, Cunningham JM, Hebbring S, Thibodeau SN, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Badzioch M, Bishop DT, Evans C, Edwards S, Meitz J, Bullock S, Hope Q, Guy M, Hsieh CL, Halpern J, Balise RR, Oakley-Girvan I, Whittemore AS, Xu J, Dimitrov L, Chang BL, Adams TS, Turner AR, Meyers DA, Friedrichsen DM, Deutsch K, Kolb S, Janer M, Hood L, Ostrander EA, Stanford JL, Ewing CM, Gielzak M, Isaacs SD, Walsh PC, Wiley KE, Isaacs WB, Lange EM, Ho LA, Beebe-Dimmer JL, Wood DP, Cooney KA, Seminara D, Ikonen T, Baffoe-Bonnie A, Fredriksson H, Matikainen MP, Tammela TL, Bailey-Wilson J, Schleutker J, Maier C, Herkommer K, Hoegel JJ, Vogel W, Paiss T, Wiklund F, Emanuelsson M, Stenman E, Jonsson BA, Grönberg H, Camp NJ, Farnham J, Cannon-Albright LA, Catalona WJ, Suarez BK, Roehl KA.

Hum Genet. 2006 Nov;120(4):471-85. Epub 2006 Aug 25.


Relaxed significance criteria for linkage analysis.

Chen L, Storey JD.

Genetics. 2006 Aug;173(4):2371-81. Epub 2006 Jun 18.


Description of the International Consortium For Prostate Cancer Genetics, and failure to replicate linkage of hereditary prostate cancer to 20q13.

Schaid DJ, Chang BL; International Consortium For Prostate Cancer Genetics.

Prostate. 2005 May 15;63(3):276-90.


Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis.

Klein AP, Kovac I, Sorant AJ, Baffoe-Bonnie A, Doan BQ, Ibay G, Lockwood E, Mandal D, Santhosh L, Weissbecker K, Woo J, Zambelli-Weiner A, Zhang J, Naiman DQ, Malley J, Bailey-Wilson JE.

BMC Genet. 2003 Dec 31;4 Suppl 1:S73.


Power of maximum HLOD tests to detect linkage to obesity genes.

Yoo YJ, Huo Y, Ning Y, Gordon D, Finch S, Mendell NR.

BMC Genet. 2003 Dec 31;4 Suppl 1:S16.


Genetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13.

Strauch K, Golla A, Wilcox MA, Baur MP.

Genet Epidemiol. 2003;25 Suppl 1:S5-17.


Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees.

Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC.

Hypertension. 2003 Sep;42(3):322-8. Epub 2003 Jul 21.


Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Abecasis GR, Cherny SS, Cookson WO, Cardon LR.

Nat Genet. 2002 Jan;30(1):97-101. Epub 2001 Dec 3.


Allele-sharing models: LOD scores and accurate linkage tests.

Kong A, Cox NJ.

Am J Hum Genet. 1997 Nov;61(5):1179-88.


A new test for linkage in the presence of locus heterogeneity.

MacLean CJ, Ploughman LM, Diehl SR, Kendler KS.

Am J Hum Genet. 1992 Jun;50(6):1259-66.

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