Genetics, statistics and human disease: analytical retooling for complexity
- 1 December 2004
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 20 (12) , 640-647
- https://doi.org/10.1016/j.tig.2004.09.007
Abstract
No abstract availableKeywords
This publication has 72 references indexed in Scilit:
- Ordered subset analysis in genetic linkage mapping of complex traitsGenetic Epidemiology, 2004
- The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings?BioEssays, 2004
- Power of multifactor dimensionality reduction for detecting gene‐gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneityGenetic Epidemiology, 2003
- Trimming, Weighting, and Grouping SNPs in Human Case-Control Association StudiesGenome Research, 2001
- A Combinatorial Partitioning Method to Identify Multilocus Genotypic Partitions That Predict Quantitative Trait VariationGenome Research, 2001
- Neuropathological phenotype and ‘prion protein’ genotype correlation in sporadic Creutzfeldt-Jakob diseaseNeuroscience Letters, 1994
- Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13Annals of Human Genetics, 1994
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991
- Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndromeBiochemical and Biophysical Research Communications, 1989
- Testing for heterogeneity of recombination fraction values in Human GeneticsAnnals of Human Genetics, 1963