Literature DB >> 3957003

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

G M Lathrop, J M Lalouel, R L White.   

Abstract

Methods are given for efficient calculation of the likelihood for multilocus linkage in families comprised of grandparents, parents, and children. Such families are being used in large-scale cooperative efforts to build a detailed linkage map of the human genome. The methods are illustrated by an application to loci on chromosome 13.

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Mesh：

Year:  1986        PMID： 3957003     DOI： 10.1002/gepi.1370030105

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN： 0741-0395            Impact factor:   2.135


  62 in total

1.  X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

Authors:  A L Christianson; R E Stevenson; C H van der Meyden; J Pelser; F W Theron; P L van Rensburg; M Chandler; C E Schwartz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

Review 2.  Gene mapping by linkage and association analysis.

Authors:  R E March
Journal:  Mol Biotechnol       Date:  1999-12-01       Impact factor: 2.695

3.  Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Authors:  C M Greenwood; T M Fujiwara; L J Boothroyd; M A Miller; D Frappier; E A Fanning; E Schurr; K Morgan
Journal:  Am J Hum Genet       Date:  2000-07-05       Impact factor: 11.025

4.  A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Authors:  Simeon A Boyadjiev; Cristina M Justice; Wafaa Eyaid; Victor A McKusick; Ralph S Lachman; Arnab B Chowdry; Monzer Jabak; Johan Zwaan; Alexander F Wilson; Ethylin Wang Jabs
Journal:  Hum Genet       Date:  2003-04-03       Impact factor: 4.132

5.  A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.

Authors:  Lisa A Freed; James S Acierno; Daisy Dai; Maire Leyne; Jane E Marshall; Francesca Nesta; Robert A Levine; Susan A Slaugenhaupt
Journal:  Am J Hum Genet       Date:  2003-04-21       Impact factor: 11.025

6.  Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12.

Authors:  Dwight Stambolian; Grace Ibay; Lauren Reider; Debra Dana; Chris Moy; Melissa Schlifka; Taura Holmes; Elise Ciner; Joan E Bailey-Wilson
Journal:  Am J Hum Genet       Date:  2004-07-23       Impact factor: 11.025

7.  Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer.

Authors:  Deborah W Neklason; Thérèse M Tuohy; Jeffery Stevens; Brith Otterud; Lisa Baird; Richard A Kerber; Wade S Samowitz; Scott K Kuwada; Mark F Leppert; Randall W Burt
Journal:  J Med Genet       Date:  2010-06-03       Impact factor: 6.318

8.  Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Authors:  K A Mills; K H Buetow; Y Xu; T M Ritty; K D Mathews; S E Bodrug; C Wijmenga; I Balazs; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

9.  Independent replication and initial fine mapping of 3p21-24 in Asperger syndrome.

Authors:  K Rehnström; T Ylisaukko-oja; T Nieminen-von Wendt; S Sarenius; T Källman; E Kempas; L von Wendt; L Peltonen; I Järvelä
Journal:  J Med Genet       Date:  2006-02       Impact factor: 6.318

Review 10.  A random walk method for computing genetic location scores.

Authors:  K Lange; E Sobel
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025
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