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Scholar Results 1 - 10 of about 477 citing Bell: A polymorphic locus near the human insulin gene is associated with insulin-dependent.... (0.10 sec) 

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent …

- nih.gov [PDF] 
RS Spielman, RE McGinnis, WJ Ewens - American Journal of Human Genetics, 1993 - pubmedcentral.nih.gov
Page 1. Am. J. Hum. Genet. 52:506-516, 1993 Transmission Test for Linkage
Disequilibrium: The Insulin Gene Region and Insulin-dependent Diabetes Mellitus ( ...
Cited by 2893 - Related articles - BL Direct - All 10 versions

[PDF] A genome-wide search for human type 1 diabetes susceptibility genes


JL Davies, Y Kawaguchi, ST Bennett, JB … - Nature, 1994 - cms1.daegu.ac.kr
ARTICLES A genome-wide search for human type 1 diabetes susceptibility genes
June L. Davies, Yoshihiko Kawaguchi, Simon T. Bennett, James B. Copeman, Heather
J. Cornell, Lynn E. Pritchard, Peter W. Reed, Stephen CL Gough, Suzanne C. ...
Cited by 1060 - Related articles - BL Direct - All 7 versions

Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension

- ahajournals.org [PDF] 
A Bonnardeaux, E Davies, X Jeunemaitre, I … - Hypertension, 1994 - Am Heart Assoc
Abstract We conducted the present study to determine whether the angiotensin II
type I receptor (AT,) gene might be implicated in human essential hypertension
by using case-control and linkage studies. The entire coding and 3' ...
Cited by 618 - Related articles - BL Direct - All 5 versions

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium …

- nih.gov [PDF] 
RS Spielman, WJ Ewens - The American Journal of Human Genetics, 1998 - Elsevier
Linkage analysis with genetic markers has been successful in the localization of
genes for many monogenic human diseases. In studies of complex diseases,
however, tests that rely on linkage disequilibrium (the simultaneous ...
Cited by 533 - Related articles - BL Direct - All 13 versions

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at …


ST Bennett, AM Lucassen, SCL Gough, EE … - Nature Genetics, 1995 - nature.com
The IDDM2 locus encoding susceptibility to type 1 diabetes was mapped previously
to a 4.1−kb region spanning the insulin gene and a minisatellite or variable
number of tandem repeats (VNTR) locus on human chromosome 11p15.5. By ...
Cited by 530 - Related articles - All 3 versions

The insulin gene is transcribed in the human thymus and transcription levels correlate with …


A Pugliese, M Zeller, A Fernandez, LJ Zalcberg … - Nature genetics, 1997 - nature.com
Cited by 447 - Related articles - BL Direct - All 4 versions

The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 …

- oxfordjournals.org
L Nistico, R Buzzetti, LE Pritchard, B Van … - Human Molecular Genetics, 1996 - Oxford Univ Press
Susceptibility to autoimmune insulin-dependent (type 1) diabetes mellitus is
determined by a combination of environmental and genetic factors, which include
variation in MHC genes on chromosome 6p21 (IDDM1) and the insulin gene on ...
Cited by 440 - Related articles - BL Direct - All 3 versions

The transmission/disequilibrium test: history, subdivision, and admixture.

- nih.gov [PDF] 
WJ Ewens, RS Spielman - American Journal of Human Genetics, 1995 - pubmedcentral.nih.gov
Summary Disease association with a genetic marker is often taken as a
preliminary indication of linkage with disease sus- ceptibility. However,
population subdivision and ad- mixture may lead to disease association even ...
Cited by 413 - Related articles - BL Direct - All 9 versions

Assessing the role of HLA-linked and unlinked determinants of disease.

- nih.gov [PDF] 
N Risch - American journal of human genetics, 1987 - pubmedcentral.nih.gov
SUMMARY The relationship between increased risk in relatives over population
prevalence (XR = KRIK) and probability of sharing zero marker alleles identical
by descent (ibd) at a linked locus (such as HLA) by an affected relative ...
Cited by 409 - Related articles - All 5 versions

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma


BR Seizinger, RL Martuza, JF Gusella, 1986 - nature.com
The application of recombinant DNA techniques has identified two fundamental
mechanisms of tumorigenesis in man. The first involves a qualitative or
quantitative change in an oncogene (see ref. 1 for review). In the second, ...
Cited by 318 - Related articles - All 4 versions


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