Literature DB >> 2896152

DNA polymorphism and the study of disease associations.

D N Cooper1, J F Clayton.   

Abstract

Recombinant DNA approaches to disease analysis may be as applicable to studies of disease association as they are to the analysis and diagnosis of single-gene defects. Population and/or family association analyses, using restriction fragment length polymorphisms around candidate genes as markers, have been employed to study conditions such as atherosclerosis and disease with an HLA-association. Progress made to date in disease-association studies using recombinant DNA methodology is reviewed, the rationale behind such studies is examined and associated problems and pitfalls discussed.

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Year:  1988        PMID: 2896152     DOI: 10.1007/bf00291724

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  152 in total

1.  A systematic study of HLA class II-beta DNA restriction fragments in insulin-dependent diabetes mellitus.

Authors:  O Cohen-Haguenauer; E Robbins; C Massart; M Busson; I Deschamps; J Hors; J M Lalouel; J Dausset; D Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

2.  HLA class II genes in chronic progressive and in relapsing/remitting multiple sclerosis.

Authors:  O Olerup; S Fredrikson; T Olsson; S Kam-Hansen
Journal:  Lancet       Date:  1987-08-08       Impact factor: 79.321

3.  DNA polymorphisms and the apolipoprotein B gene.

Authors:  P Talmud; S Humphries
Journal:  Lancet       Date:  1986-07-12       Impact factor: 79.321

4.  DR2-negative narcolepsy.

Authors:  A Andreas-Zietz; E Keller; S Scholz; E D Albert; B Roth; S Nevsimalova; K Sonka; P Docekal; E Ivaskova; H Schulz
Journal:  Lancet       Date:  1986-09-20       Impact factor: 79.321

5.  Genetic polymorphisms of apolipoprotein C-III and insulin in survivors of myocardial infarction.

Authors:  G A Ferns; J Stocks; C Ritchie; D J Galton
Journal:  Lancet       Date:  1985-08-10       Impact factor: 79.321

6.  Molecular genetics of lipoprotein disorders.

Authors:  J L Breslow
Journal:  Circulation       Date:  1984-06       Impact factor: 29.690

Review 7.  The molecular genetics of cellular oncogenes.

Authors:  H E Varmus
Journal:  Annu Rev Genet       Date:  1984       Impact factor: 16.830

8.  DNA sequences flanking the insulin gene on chromosome 11 confer risk of atherosclerosis.

Authors:  T Mandrup-Poulsen; D Owerbach; S A Mortensen; K Johansen; H Meinertz; H Sørensen; J Nerup
Journal:  Lancet       Date:  1984-02-04       Impact factor: 79.321

Review 9.  Eukaryotic DNA methylation.

Authors:  D N Cooper
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

10.  Presence of an allelic EcoRI restriction fragment of the c-mos locus in leukocyte and tumor cell DNAs of breast cancer patients.

Authors:  R Lidereau; D Mathieu-Mahul; C Theillet; M Renaud; M Mauchauffé; J Gest; C J Larsen
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

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  21 in total

1.  Fluorescence polarization in homogeneous nucleic acid analysis.

Authors:  X Chen; L Levine; P Y Kwok
Journal:  Genome Res       Date:  1999-05       Impact factor: 9.043

2.  Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus.

Authors:  P Jedlicka; S Greer; D S Millar; C B Grundy; E Jenkins; M Mitchell; R S Mibashan; V V Kakkar; D N Cooper
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

3.  Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11.

Authors:  P Benlian; C Boileau; N Loux; D Pastier; J Masliah; M Coulon; M Nigou; A Ragab; J Guimard; J B Ruidavets
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

4.  Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster.

Authors:  M B Haviland; A M Kessling; J Davignon; C F Sing
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

5.  Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.

Authors:  J Reiss; D N Cooper; J Bal; R Slomski; G R Cutting; M Krawczak
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

Review 6.  Dissecting the genetic contribution to coronary heart disease.

Authors:  J W MacCluer; C M Kammerer
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

7.  Effective testing of gene-disease associations.

Authors:  M Swift; L L Kupper; C L Chase
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

Review 8.  Gene environment interaction.

Authors:  H Campbell
Journal:  J Epidemiol Community Health       Date:  1996-08       Impact factor: 3.710

9.  Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencing.

Authors:  D W Yandell; T P Dryja
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

Review 10.  Diagnosis of genetic disease using recombinant DNA. Second edition.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1989-11       Impact factor: 4.132

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