Genome scanning for linkage: an overview.

AS Whittemore - American Journal of Human Genetics, 1996 - ncbi.nlm.nih.gov
Several different methods for linkage analysis are shown to arise from a single likelihood
function L for the observed allele-sharing data at multiple markers in a chromosomal region …

Mapping disease genes: family-based association studies.

G Thomson - American journal of human genetics, 1995 - ncbi.nlm.nih.gov
With recent rapid advances in mapping of the human genome, including highly polymorphic
and closely linked markers, studies of marker associations with disease are increasingly …

HLA disease associations: models for the study of complex human genetic disorders

G Thomson, NJ Cox - Critical reviews in clinical laboratory …, 1995 - Taylor & Francis
The genes of the human leukocyte antigen (HLA) region, the major histocompatibility
complex (MHC) of humans, control a variety of functions involved in immune response and …

HLA–Bw60 increases susceptibility to ankylosing spondylitis in HLA–B27+ patients

WP Robinson, SM Van Der Linden… - … : Official Journal of …, 1989 - Wiley Online Library
We examined the distribution of non‐B27 alleles of the HLA–B locus among B27+ patients
with ankylosing spondylitis (AS), to detect any additional HLA–B locus allele (s) that may act …

Relative predispositional effects (RPEs) of marker alleles with disease: HLA-DR alleles and Graves disease.

H Payami, S Joe, NR Farid, V Stenszky… - American journal of …, 1989 - ncbi.nlm.nih.gov
A method is described to reveal the relative predispositional effects (RPEs)(predisposing,
protective, or neutral) of the HLA alleles or of any other marker system that is associated with …

Sib pair linkage analysis of renin gene haplotypes in human essential hypertension

X Jeunemaitre, B Rigat, A Charru, AM Houot… - Human genetics, 1992 - Springer
Although essential arterial hypertension is believed to have a strong genetic predisposition,
the gene (s) responsible are unknown. The mechanisms underlying the regulation of blood …

Robust methods for the detection of genetic linkage for quantitative data from pedigrees

CI Amos, RC Elston, DC Rao - Genetic Epidemiology, 1989 - Wiley Online Library
The robust method for detecting linkage developed by Haseman and Elston [The
investigation of linkage between a quantitative trait and a marker locus. Behav Genet 2: 3 …

Clustering of albumin excretion rate abnormalities in Caucasian patients with NIDDM

PP Faronato, M Maioli, G Tonolo, E Brocco, F Noventa… - Diabetologia, 1997 - Springer
Proteinuria and nephropathy have been found to cluster in families of non-insulin-
dependent diabetic (NIDDM) Pima Indian, and in Caucasian insulin-dependent diabetic …

Genetic interrelationship between insulin-dependent diabetes mellitus, the autoimmune thyroid diseases, and rheumatoid arthritis.

CP Torfs, MC King, B Huey, J Malmgren… - American journal of …, 1986 - ncbi.nlm.nih.gov
To investigate the possible coinheritance of autoimmune diseases that are associated with
the same HLA antigen, we studied 70 families in which at least two siblings had either type I …

Investigating the HLA component in rheumatoid arthritis: an additive (dominant) mode of inheritance is rejected, a recessive mode is preferred

AS Rigby, AJ Silman, L Voelm, JC Gregory… - Genetic …, 1991 - Wiley Online Library
We examined the mode of inheritance of rheumatoid arthritis (RA) and estimated the genetic
contribution of the HLA‐linked locus to the development of RA using data from 111 multiplex …