Literature DB >> 2884728

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children.

E S Lander, D Botstein.   

Abstract

An efficient strategy for mapping human genes that cause recessive traits has been devised that uses mapped restriction fragment length polymorphisms (RFLPs) and the DNA of affected children from consanguineous marriages. The method involves detection of the disease locus by virtue of the fact that the adjacent region will preferentially be homozygous by descent in such inbred children. A single affected child of a first-cousin marriage is shown to contain the same total information about linkage as a nuclear family with three affected children. Calculations show that it should be practical to map a recessive disease gene by studying DNA from fewer than a dozen unrelated, affected inbred children, given a complete RFLP linkage map. The method should make it possible to map many recessive diseases for which it is impractical or impossible to collect adequate numbers of families with multiple affected offspring.

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Year:  1987        PMID: 2884728     DOI: 10.1126/science.2884728

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  283 in total

1.  Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15.

Authors:  C R Jamieson; C Govaerts; M J Abramowicz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.

Authors:  F E Karet; K E Finberg; A Nayir; A Bakkaloglu; S Ozen; S A Hulton; S A Sanjad; E A Al-Sabban; J F Medina; R P Lifton
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

3.  Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain.

Authors:  K W Broman; J L Weber
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

4.  Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms.

Authors:  Tianhua Niu; Zhaohui S Qin; Xiping Xu; Jun S Liu
Journal:  Am J Hum Genet       Date:  2001-11-26       Impact factor: 11.025

5.  Homozygosity and linkage disequilibrium.

Authors:  Chiara Sabatti; Neil Risch
Journal:  Genetics       Date:  2002-04       Impact factor: 4.562

6.  An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Authors:  Xianhua Piao; Lina Basel-Vanagaite; Rachel Straussberg; P Ellen Grant; Elizabeth W Pugh; Kim Doheny; Betty Doan; Susan E Hong; Yin Yao Shugart; Christopher A Walsh
Journal:  Am J Hum Genet       Date:  2002-02-13       Impact factor: 11.025

Review 7.  Finnish Disease Heritage I: characteristics, causes, background.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

8.  Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus.

Authors:  Arya Mani; Seyed-Mahmoud Meraji; Roozbeh Houshyar; Jayaram Radhakrishnan; Alaleh Mani; Mehrabeh Ahangar; Tayebeh M Rezaie; Mohammad-Ali Taghavinejad; Behrooz Broumand; Hongyu Zhao; Carol Nelson-Williams; Richard P Lifton
Journal:  Proc Natl Acad Sci U S A       Date:  2002-10-30       Impact factor: 11.205

9.  Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome.

Authors:  Randi Burns; Karen Majczenko; Jishu Xu; Weiping Peng; Zuhal Yapici; James J Dowling; Jun Z Li; Margit Burmeister
Journal:  Neurology       Date:  2014-10-31       Impact factor: 9.910

10.  Estimation of the inbreeding coefficient through use of genomic data.

Authors:  Anne-Louise Leutenegger; Bernard Prum; Emmanuelle Génin; Christophe Verny; Arnaud Lemainque; Françoise Clerget-Darpoux; Elizabeth A Thompson
Journal:  Am J Hum Genet       Date:  2003-07-29       Impact factor: 11.025

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