A quick and simple method for detecting subjects with abnormal genetic background in case-control samples

Annals of Human Genetics

Volumn 66, Issue 3, 2002, Pages 235-244

  Curtis, D ^a   North, B V ^a   Gurling, H M D ^b   Blaveri, E ^b   Sham, P C ^c  

^a ROYAL LONDON HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTIC METHOD; ARTICLE; CASE CONTROL STUDY; COMPUTER PROGRAM; COMPUTER SIMULATION; CONTROLLED STUDY; GENETIC DIFFERENCE; GENETIC DISORDER; GENOTYPE; HETEROZYGOTE DETECTION; HUMAN; MAJOR CLINICAL STUDY; MARKER GENE; PRIORITY JOURNAL; SCHIZOPHRENIA; STATISTICAL ANALYSIS;

CASE-CONTROL STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LIKELIHOOD FUNCTIONS; RESEARCH DESIGN; SAMPLING STUDIES; VARIATION (GENETICS);

EID: 0036562880     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480002001094     Document Type: Article

References (7)

1. New methods employing multilocus genotypes to select or exclude populations as origins of individuals
2. Validation of the AMPFISTR SGM plus system for use in forensic casework
3. Use of siblings as controls in case-control association studies
4. Inference of population structure using multilocus genotype data
5. Association mapping in structured populations
6. The transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
7. Allele frequencies for the four major sub-populations of New Zealand at the 10 AMPFISTR SGM Plus loci