Allowing for genotyping error in analysis of unmatched case-control studiesRICE, K. M; HOLMANS, P.Annals of human genetics. 2003, Vol 67, Num 2, pp 165-174, issn 0003-4800, 10 p.Article

Assessing optimal neural network architecture for identifying disease-associated multi-marker genotypes using a permutation test, and application to calpain 10 polymorphisms associated with diabetesNORTH, B. V; CURTIS, D; CASSELL, P. G et al.Annals of human genetics. 2003, Vol 67, Num 4, pp 348-356, issn 0003-4800, 9 p.Article

Simultaneous detection of ACP1 and GC genotypes using PCR/SSCPDISSING, J; THYMANN, M; HOPKINSON, D et al.Annals of human genetics. 2003, Vol 67, Num 1, pp 81-85, issn 0003-4800, 5 p.Article

Smith-Lemli-Opitz syndrome and the DHCR7 geneJIRA, P. E; WATERHAM, H. R; WANDERS, R. J. A et al.Annals of human genetics. 2003, Vol 67, Num 3, pp 269-280, issn 0003-4800, 12 p.Article

Using affected sibling pairs to distinguish the direct effect of a susceptibility gene and the indirect effect of linkage disequilibriumLEE, W.-C.Annals of human genetics. 2003, Vol 67, Num 2, pp 185-188, issn 0003-4800, 4 p.Article

A metric linkage disequilibrium map of a human chromosomeTAPPER, W. J; MANIATIS, N; MORTON, N. E et al.Annals of human genetics. 2003, Vol 67, Num 6, pp 487-494, issn 0003-4800, 8 p.Article

Diversity of mitochondrial DNA lineages in South SiberiaDERENKO, M. V; GRZYBOWSKI, T; ZAKHAROV, I. A et al.Annals of human genetics. 2003, Vol 67, Num 5, pp 391-411, issn 0003-4800, 21 p.Article

A quick and simple method for detecting subjects with abnormal genetic background in case-control samplesCURTIS, D; NORTH, B. V; GURLING, H. M. D et al.Annals of human genetics. 2002, Vol 66, Num 3, pp 235-244, issn 0003-4800Article

Determination of probability distribution of diplotype configuration (diplotype distribution) for each subject from genotypic data using the EM algorithmKITAMURA, Y; MORIGUCHI, M; KANEKO, H et al.Annals of human genetics. 2002, Vol 66, Num 3, pp 183-193, issn 0003-4800Article

Extension of conditional model-free likelihood-based linkage analysis to additive and other modelsCURTIS, D; NORTH, B. V; SHAM, P. C et al.Annals of human genetics. 2002, Vol 66, Num 2, pp 157-167, issn 0003-4800Article

Mitochondrial DNA variability in Poles and RussiansMALYARCHUK, B. A; GRZYBOWSKI, T; DERENKO, M. V et al.Annals of human genetics. 2002, Vol 66, Num 4, pp 261-283, issn 0003-4800, 23 p.Article

The expected power of genome-wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low-frequency disease variantOHASHI, J; TOKUNAGA, K.Annals of human genetics. 2002, Vol 66, Num 4, pp 297-306, issn 0003-4800, 10 p.Article

Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populationsFARADZ, Sultana M. H; LEGGO, J; MURRAY, A et al.Annals of human genetics. 2001, Vol 65, pp 127-135, issn 0003-4800, 2Article

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease familiesGRECO, L; BABRON, M. C; GASPARINI, P et al.Annals of human genetics. 2001, Vol 65, pp 35-41, issn 0003-4800, 1Article

Genetic crossover interference in the human genomeLIN, S; CHENG, R; WRIGHT, F. A et al.Annals of human genetics. 2001, Vol 65, pp 79-93, issn 0003-4800, 1Article

Physical mapping : integrating computational and molecular genetic dataLE HELLARD, S; SEMPLE, C. A. M; MORRIS, S. W et al.Annals of human genetics. 2001, Vol 65, pp 221-228, issn 0003-4800, 3Article

Sample size calculations for classical association and TDT-type methods using family dataTREGOUET, D. A; PALLAUD, C; SASS, C et al.Annals of human genetics. 2001, Vol 65, pp 293-312, issn 0003-4800, 3Article

Use of an artificial neural network to detect association between a disease and multiple marker genotypesCURTIS, D; NORTH, B. V; SHAM, P. C et al.Annals of human genetics. 2001, Vol 65, pp 95-107, issn 0003-4800, 1Article

Y chromosome microsatellite variation in three populations of Jerba Island (Tunisia)EL KHIL, H. Khodjet; MARRAKCHI, R. Triki; LOUESLATI, B. Yacoubi et al.Annals of human genetics. 2001, Vol 65, pp 263-270, issn 0003-4800, 3Article

A novel method of two-locus linkage analysis applied to a genome scan for late onset Alzheimer's diseaseCURTIS, D; NORTH, B. V; SHAM, P. C et al.Annals of human genetics. 2001, Vol 65, Num 5, pp 473-482, issn 0003-4800Article

Correcting for multiple analyses in genomewide linkage studiesCAMP, N. J; FARNHAM, J. M.Annals of human genetics. 2001, Vol 65, Num 6, pp 577-582, issn 0003-4800Article

Power of regression and maximum likelihood methods to map QTL from sib-pair and DZ twin dataVISSCHER, P. M; HOPPER, J. L.Annals of human genetics. 2001, Vol 65, Num 6, pp 583-601, issn 0003-4800Article

Replication studies in longevity: puzzling findings in Danish centenarians at the 3'APOB-VNTR locusVARCASIA, O; GARASTO, S; FRANCESCHI, C et al.Annals of human genetics. 2001, Vol 65, pp 371-376, issn 0003-4800, 4Article

Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairsCORDELL, H. J.Annals of human genetics. 2001, Vol 65, Num 5, pp 491-502, issn 0003-4800Article

Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3IROBI, J; NELIS, E; MEULEMAN, J et al.Annals of human genetics. 2001, Vol 65, Num 6, pp 517-529, issn 0003-4800Article