E A Lindsay
Overview
Explore the profile of E A Lindsay including associated specialties, affiliations and a list of published articles.
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Articles
55
Citations
1166
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Recent Articles
1.
Lindsay E, Wilson D, Best J, Willms D, Singer J, Gilbert J, et al.
Am J Health Promot
. 2011 Dec;
3(3):11-8.
PMID: 22206330
Abstract This randomized controlled trial investigated the effects of a smoking cessation workshop on physician practices and on patients' smoking behavior. Eighty-three community family physicians were randomly allocated by practice...
2.
Singer J, Lindsay E, Wilson D
Can Fam Physician
. 2011 Jan;
37:2167-73.
PMID: 21229089
The principle barriers preventing health care professionals from promoting physical activity include an incomplete understanding of the evidence linking physical activity and health, difficulty in translating research findings into a...
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Vitelli F, Lindsay E, Baldini A
Cold Spring Harb Symp Quant Biol
. 2003 Jul;
67:327-32.
PMID: 12858556
No abstract available.
6.
Liebana E, Garcia-Migura L, Clouting C, Cassar C, Clifton-Hadley F, Lindsay E, et al.
J Appl Microbiol
. 2002 Oct;
93(5):732-44.
PMID: 12392517
Aims: To assess the degree of genetic diversity among animal Salmonella Dublin UK isolates, and to compare it with the genetic diversity found among human isolates from the same time...
7.
Paylor R, McIlwain K, McAninch R, Nellis A, Yuva-Paylor L, Baldini A, et al.
Hum Mol Genet
. 2001 Dec;
10(23):2645-50.
PMID: 11726551
Del22q11 syndrome is caused by heterozygous deletion of an approximately 3 Mb segment of chromosome 22q11.2. Children diagnosed with del22q11 syndrome commonly have learning difficulties, deficits of motor development, cognitive...
8.
Lindsay E
Nat Rev Genet
. 2001 Nov;
2(11):858-68.
PMID: 11715041
Identifying the genes that underlie the pathogenesis of chromosome deletion and duplication syndromes is a challenge because the affected chromosomal segment can contain many genes. The identification of genes that...
9.
Taddei I, Morishima M, Huynh T, Lindsay E
Proc Natl Acad Sci U S A
. 2001 Sep;
98(20):11428-31.
PMID: 11562466
The del22q11 syndrome is associated with a highly variable phenotype despite the uniformity of the chromosomal deletion that causes the disease in most patients. Df1/+ mice, which model del22q11, present...
10.
Lindsay E, Baldini A
Hum Mol Genet
. 2001 Apr;
10(9):997-1002.
PMID: 11309372
Chromosome 22q11.2 heterozygous deletions cause the most common deletion syndrome, including the DiGeorge syndrome phenotype. Using a mouse model of this deletion (named Df1) we show that the aortic arch...