𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Factors influencing the identification of major genes in a complex disease genome scan

✍ Scribed by Huiying Yang; Yaping Wang; Darlene R. Goldstein; Zhiming Li; Hita Vora; Rita M. Cantor


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
52 KB
Volume
14
Category
Article
ISSN
0741-0395

No coin nor oath required. For personal study only.

✦ Synopsis


A two-stage linkage strategy was employed to identify major genes for a simulated complex disease via a genome scan. The importance of several approaches for improving the ability to locate major genes has been illustrated. These approaches are: adjusting for covariates, ascertaining through multiple affected family members, increasing the sample size, and using multipoint linkage analysis.


πŸ“œ SIMILAR VOLUMES


Genome scan of idiopathic generalized ep
✍ Martina Durner; Mehdi A. Keddache; Livia Tomasini; Shlomo Shinnar; Stanley R. Re πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 203 KB

## Abstract Idiopathic generalized epilepsy (IGE) is a common, complex disease with an almost exclusively genetic etiology but with variable phenotypes. Clinically, IGE can be divided into different syndromes. Varying lines of evidence point to the involvement of several interacting genes in the et

A Genome-Wide Linkage Scan for Quantitat
✍ Richard J. Sherwood; Dana L. Duren; Michael C. Mahaney; John Blangero; Thomas D. πŸ“‚ Article πŸ“… 2011 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 381 KB

## Abstract The genetic architecture of the craniofacial complex has been the subject of intense scrutiny because of the high frequency of congenital malformations. Numerous animal models have been used to document the early development of the craniofacial complex, but few studies have focused dire

Molecular diagnosis of McArdle disease:
✍ Christian Kubisch; Eva M. Wicklein; Thomas J. Jentsch πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 213 KB πŸ‘ 2 views

McArdle disease is a rare autosomal recessive disorder of the muscle glycogen metabolism caused by mutations in the muscle glycogen phosphorylase gene. Until now, a total number of 11 different mutations in the coding region or splice sites of the myophosphorylase gene have been identified. In contr

Identification of complex genomic breakp
✍ Heidi Gill Super; Pamela L. Strissel; Olatoyosi M. Sobulo; Dennis Burian; Shalin πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 154 KB πŸ‘ 1 views

The MLL gene at chromosome 11, band q23, is involved in translocations with as many as 40 different chromosomal bands. Virtually all breakpoints occur within an 8.3 kb BamHI fragment and result in 5' MLL fused to partner genes in a 5'-3' orientation. The translocation t(9;11)(p22;q23), which results

The fate of duplicated major histocompat
✍ BΓ©nΓ©dicte Sammut; Anne Marcuz; Louis Du Pasquier πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 364 KB

The dodecaploid anuran amphibian Xenopus ruwenzoriensis represents the only polyploid species of Xenopus in which the full silencing of the extra copies of the major histocompatibility complex (MHC) has not occurred. Xenopus ruwenzoriensis is a recent polyploid that has evolved within one of the two

Nutritional and occupational factors inf
✍ Per-Arne Fall; Mats Fredrikson; Olav Axelson; Ann-Kathrine GranΓ©rus πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 57 KB πŸ‘ 2 views

## Purpose and methods: To investigate the possible impact of nutritional and environmental risk factors for idiopathic parkinson's disease (ip), a case-control study was performed in the county of ostergΓΆtland in southeastern sweden. the study involved 113 cases of ip and 263 control subjects. die