Linkage mapping of CVD risk traits in the isolated Norfolk Island populationBELLIS, C; COX, H. C; DYER, T. D et al.Human genetics. 2008, Vol 124, Num 5, pp 543-552, issn 0340-6717, 10 p.Article

Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian populationELLIS, Justine A; SCURRAH, Katrina J; DUNCAN, Anna E et al.Human genetics. 2007, Vol 121, Num 2, pp 213-222, issn 0340-6717, 10 p.Article

Power comparison of generalizations of the mean test for affected sib pairs in case of incompletely informative markersKNAPP, Michael.Genetic epidemiology. 2006, Vol 30, Num 4, pp 314-319, issn 0741-0395, 6 p.Article

Confirmation of linkage to chromosome 1q for spine bone mineral density in southern ChineseCHEUNG, Ching-Lung; HUANG, Qing-Yang; NG, Mandy Y. M et al.Human genetics. 2006, Vol 120, Num 3, pp 354-359, issn 0340-6717, 6 p.Article

How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkageWILTSHIRE, Steven; MORRIS, Andrew P; MCCARTHY, Mark I et al.Genetic epidemiology. 2005, Vol 28, Num 1, pp 1-10, issn 0741-0395, 10 p.Article

Multilocus linkage disequilibrium mapping by the decay of haplotype sharing with samples of related individualsJIAN ZHANG; SCHNEIDER, Daniel; OBER, Carole et al.Genetic epidemiology. 2005, Vol 29, Num 2, pp 128-140, issn 0741-0395, 13 p.Article

Testing association and linkage using affected-sib-parent study designsMILLSTEIN, Joshua; SIEGMUND, Kimberly D; CONTI, David V et al.Genetic epidemiology. 2005, Vol 29, Num 3, pp 225-233, issn 0741-0395, 9 p.Article

Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformationKANO, Hiroki; KUROSAWA, Kenji; HORII, Emiko et al.Human genetics. 2005, Vol 118, Num 3-4, pp 477-483, issn 0340-6717, 7 p.Article

Dissection of heterogeneous phenotypes for quantitative trait mappingBICKEBÖLLER, Heike; BAILEY, Julia N; PAPANICOLAOU, George J et al.Genetic epidemiology. 2005, Vol 29, Num SUP1, pp S41-S47, issn 0741-0395Conference Paper

Association mapping : Methodologies, strategies, and issuesHAVILL, Lorena M; DYER, Thomas D.Genetic epidemiology. 2005, Vol 29, Num SUP1, pp S77-S85, issn 0741-0395Conference Paper

Bounds and normalization of the composite linkage disequilibrium coefficientZAYKIN, Dmitri V.Genetic epidemiology. 2004, Vol 27, Num 3, pp 252-257, issn 0741-0395, 6 p.Article

Quantitative trait linkage analysis by generalized estimating equations: Unification of variance components and Haseman-Elston regressionCHEN, Wei-Min; BROMAN, Karl W; LIANG, Kung-Yee et al.Genetic epidemiology. 2004, Vol 26, Num 4, pp 265-272, issn 0741-0395, 8 p.Article

Genomic organization of the genes Gtf2ird1, Gtf2i, and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical regionBAYARSAIHAN, Dashzeveg; DUNAI, Judit; GREALLY, John M et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 1, pp 137-143, issn 0888-7543Article

Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysisWINES, Mary E; LEE, Lance; KATARI, Manpreet S et al.Genomics (San Diego, Calif.). 2001, Vol 72, Num 1, pp 88-98, issn 0888-7543Article

The gene encoding TBC1D1 with homology to the tre-2/USP6 oncogene, BUB2, and cdc16 maps to mouse chromosome 5 and human chromosome 4WHITE, R. A; PASZTOR, L. M; RICHARDSON, P. M et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 272-275, issn 0301-0171Article

PCR conditions and DNA denaturants affect reproducibility of single-strand conformation polymorphism patterns for BCRA1 mutationsHENNESSY, L. K; TEARE, J; KO, C et al.Clinical chemistry (Baltimore, Md.). 1998, Vol 44, Num 4, pp 879-882, issn 0009-9147Article

A multimarker regression-based test of linkage for affected sib-pairs at two linked lociBARBER, Mathew J; TODD, John A; CORDELL, Heather J et al.Genetic epidemiology. 2006, Vol 30, Num 3, pp 191-208, issn 0741-0395, 18 p.Article

A tree-based model for allele-sharing-based linkage analysis in human complex diseasesXU, W; SCHULZE, T. G; DEPAULO, J. R et al.Genetic epidemiology. 2006, Vol 30, Num 2, pp 155-169, issn 0741-0395, 15 p.Article

Estimating the power of variance component linkage analysis in large pedigreesCHEN, Wei-Min; ABECASIS, Goncalo R.Genetic epidemiology. 2006, Vol 30, Num 6, pp 471-484, issn 0741-0395, 14 p.Article

Genomewide scan in Ashkenazi jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36WOJCIECHOWSKI, Robert; MOY, Chris; CINER, Elise et al.Human genetics. 2006, Vol 119, Num 4, pp 389-399, issn 0340-6717, 11 p.Article

Microsatellites versus single-nucleotide polymorphisms in confidence interval estimation of disease lociPAPACHRISTOU, Charalampos; SHILI LIN.Genetic epidemiology. 2006, Vol 30, Num 1, pp 3-17, issn 0741-0395, 15 p.Article

A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection arrayHOLMES, S. E; WENTZELL, J. S; SEIXAS, A. I et al.Human genetics. 2006, Vol 120, Num 2, pp 193-200, issn 0340-6717, 8 p.Article

Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, MicronesiaKLEI, Lambertus; BACANU, Silviu-Alin; MYLES-WORSLEY, Marina et al.Human genetics. 2005, Vol 117, Num 4, pp 349-356, issn 0340-6717, 8 p.Article

Power and robustness of linkage tests for quantitative traits in general pedigreesCHEN, Wei-Min; BROMAN, Karl W; LIANG, Kung-Yee et al.Genetic epidemiology. 2005, Vol 28, Num 1, pp 11-23, issn 0741-0395, 13 p.Article

QTL mapping with discordant and concordant sibling pairs : New statistics and new design strategiesSZATKIEWICZ, Jin P; FEINGOLD, Eleanor.Genetic epidemiology. 2005, Vol 28, Num 4, pp 326-340, issn 0741-0395, 15 p.Article