Literature DB >> 11713414

A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: a pilot study on myopia.

S Heath1, R Robledo, W Beggs, G Feola, C Parodo, A Rinaldi, L Contu, D Dana, D Stambolian, M Siniscalco.   

Abstract

Autosomal dominant high myopia, a genetic disorder already mapped to region 18p11.31, is common in Carloforte (Sardinia, Italy), an isolated village of 8,000 inhabitants descending from a founder group of 300 in the early 1700s. Fifteen myopic propositi and 36 normal controls were selected for not having ancestors in common at least up to the grandparental generation, although still descendants of the original founders. All subjects were genotyped for 14 markers located on autosome 18 at a resolution of about 10 cM. Allelic distributions were found to be similar at all tested loci in propositi and controls, except for the candidate marker D18S63 known to segregate in close linkage association with high myopia. In particular, the frequency of allele 85 among the propositi was almost double that of the controls (Fisher's exact test, p = 0.037). The association is more striking when the frequency of the genotype 85/85 in the two groups is compared (Fisher's exact test, p = 0.005). This conclusion was further evaluated through a bootstrap analysis by computing the overall probability of the observed data under the null hypothesis (i.e. no difference between the two groups in frequency distributions for the chromosome 18 markers). Again, marker D18S63 was found to have a sample probability lower than 0.004, which is significant at the 0.05 level after correcting for simultaneous testing of multiple loci. The study demonstrates the efficiency of our novel strategy to detect identity by descent (IBD) in small numbers of patients and controls when they are both part of well-defined Mendelian breeding units (MBUs). The iterative application of our strategy in separate MBUs is expected to become the method of choice to evaluate the ever-growing number of reported associations between candidate genes and multifactorial traits and diseases. Copyright 2002 S. Karger AG, Basel

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Year:  2001        PMID: 11713414     DOI: 10.1159/000053375

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  13 in total

1.  Pilot study on schizophrenia in Sardinia.

Authors:  Jurg Ott; Fabio Macciardi; Yuanyuan Shen; Mauro G Carta; Andrea Murru; Riccardo Triunfo; Renato Robledo; Antoniettina Rinaldi; Licinio Contu; Marcello Siniscalco
Journal:  Hum Hered       Date:  2010-06-17       Impact factor: 0.444

2.  Association mapping of complex trait loci with context-dependent effects and unknown context variable.

Authors:  Mikko J Sillanpää; Madhuchhanda Bhattacharjee
Journal:  Genetics       Date:  2006-10-08       Impact factor: 4.562

3.  Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

Authors:  A Thomas; N J Camp; J M Farnham; K Allen-Brady; L A Cannon-Albright
Journal:  Ann Hum Genet       Date:  2007-12-18       Impact factor: 1.670

4.  Analysis of single nucleotide polymorphisms at 13 loci within the transforming growth factor-induced factor gene shows no association with high myopia in Japanese subjects.

Authors:  Yukiko Hasumi; Hidetoshi Inoko; Shuhei Mano; Masao Ota; Eiichi Okada; Jerzy K Kulski; Ritsuko Nishizaki; Jeewon Mok; Akira Oka; Naoki Kumagai; Teruo Nishida; Shigeaki Ohno; Nobuhisa Mizuki
Journal:  Immunogenetics       Date:  2006-10-18       Impact factor: 2.846

5.  Dissecting the genetics of human high myopia: a molecular biologic approach.

Authors:  Terri L Young
Journal:  Trans Am Ophthalmol Soc       Date:  2004

6.  Candidate gene and locus analysis of myopia.

Authors:  Donald O Mutti; Margaret E Cooper; Sarah O'Brien; Lisa A Jones; Mary L Marazita; Jeffrey C Murray; Karla Zadnik
Journal:  Mol Vis       Date:  2007-06-28       Impact factor: 2.367

7.  Molecular genetics of human myopia: an update.

Authors:  Terri L Young
Journal:  Optom Vis Sci       Date:  2009-01       Impact factor: 1.973

8.  An international collaborative family-based whole-genome linkage scan for high-grade myopia.

Authors:  Yi-Ju Li; Jeremy A Guggenheim; Anuradha Bulusu; Ravikanth Metlapally; Diana Abbott; Francois Malecaze; Patrick Calvas; Thomas Rosenberg; Sandrine Paget; Rosalind C Creer; George Kirov; Michael J Owen; Bei Zhao; Tristan White; David A Mackey; Terri L Young
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-03-25       Impact factor: 4.799

9.  Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium.

Authors:  Alun Thomas
Journal:  Genet Epidemiol       Date:  2010-02       Impact factor: 2.135

Review 10.  Myopia genetics: a review of current research and emerging trends.

Authors:  Dana M Hornbeak; Terri L Young
Journal:  Curr Opin Ophthalmol       Date:  2009-09       Impact factor: 3.761

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