New statistical methods for analysis of the genetic component of complex familial diseases are needed in order to determine the relative contribution of environment and hereditary to a variety of traits, and to elucidate the specifics of these determinants. We have been focusing of the problem of genetic linkage studies in complex disorders (e.g. arthritis, other autoimmune diseases, mitochondrial diseases) when certain usual conditions of analysis are not met (e.g. known mendelian model, large sample size, non-normally-distributed quantitative trait measurements).
| Kovach, M J; Lin, J P; Boyadjiev, S et al. (1999) A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness. Am J Hum Genet 64:1580-93 |
