S M Forrest
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Explore the profile of S M Forrest including associated specialties, affiliations and a list of published articles.
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61
Citations
1120
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Recent Articles
1.
Lorenzo D, Forrest S, Ikeda Y, Dick K, Ranum L, Knight M
Neurology
. 2006 Dec;
67(11):2084-5.
PMID: 17159129
No abstract available.
2.
Van Agtmael T, Forrest S, Williamson R
Laterality
. 2004 Oct;
6(2):149-64.
PMID: 15513167
Although several genes that determine left-right asymmetry for structural syndromes such as situs inversus have been characterised in recent years (Supp, Witte, Potter, & Brueckner, 1997), there has been little...
3.
Solomon N, Ross S, Morgan T, Belsky J, Hol F, Karnes P, et al.
J Med Genet
. 2004 Sep;
41(9):669-78.
PMID: 15342697
Introduction: Array comparative genomic hybridisation (array CGH) is a powerful method that detects alteration of gene copy number with greater resolution and efficiency than traditional methods. However, its ability to...
4.
Nasioulas S, Jones I, St John D, Scott R, Forrest S, Gardner R
Fam Cancer
. 2003 Oct;
1(1):3-7.
PMID: 14574009
The attenuated form of familial adenomatous polyposis coli (AAPC) is associated with mutations in the adenomatous polyposis coli (APC) gene which cluster in the 5' region of the gene. It...
5.
Efron D, Delatycki M, de Silva M, Langbein A, Slaghuis W, Larson A, et al.
J Med Genet
. 2003 Feb;
40(2):E15.
PMID: 12566533
No abstract available.
6.
Hand P, Gardner R, Knight M, Forrest S, Storey E
Mov Disord
. 2001 Dec;
16(5):938-9.
PMID: 11746627
No abstract available.
7.
Storey E, Gardner R, Knight M, Kennerson M, Tuck R, Forrest S, et al.
Neurology
. 2001 Nov;
57(10):1913-5.
PMID: 11723290
A kindred is described with a dominantly inherited "pure" cerebellar ataxia in which the currently known spinocerebellar ataxias have been excluded. In the eight subjects studied, a notable clinical feature...
8.
Wangerek L, Dahl H, Senden T, Carlin J, Jans D, Dunstan D, et al.
J Gene Med
. 2001 Mar;
3(1):72-81.
PMID: 11269338
Background: Cationic liposomes represent an important gene delivery system due to their low immunogenicity, but are relatively inefficient, with optimisation of DNA-liposome complexes (lipoplexes) for transfection necessary for each cell...
9.
Forrest S, Knight M, Akerman B, Cashman J, Treacy E
Pharmacogenetics
. 2001 Mar;
11(2):169-74.
PMID: 11266081
Mutations of the flavin-containing monooxygenase type 3 gene (FMO3) that encode the major functional form present in adult human liver, have been shown to cause trimethylaminuria. We now report a...
10.
Storey E, Du Sart D, Shaw J, Lorentzos P, Kelly L, McKinley Gardner R, et al.
Am J Med Genet
. 2001 Feb;
95(4):351-7.
PMID: 11186889
The frequencies of various genetically defined spinocerebellar ataxias (SCAs) vary in different populations presumably due to founder effects. No data have been published on the Australian population. Although predominantly of...