Reid S - Search Results

1

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.

Rahman N, Seal S, Thompson D, Kelly P, Renwick A, Elliott A, Reid S, Spanova K, Barfoot R, Chagtai T, Jayatilake H, McGuffog L, Hanks S, Evans DG, Eccles D; Breast Cancer Susceptibility Collaboration (UK); Easton DF, Stratton MR. Rahman N, et al. Among authors: reid s. Nat Genet. 2007 Feb;39(2):165-7. doi: 10.1038/ng1959. Epub 2006 Dec 31. Nat Genet. 2007. PMID: 17200668 Free PMC article.

2

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.

Reid S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, Neveling K, Kelly P, Seal S, Freund M, Wurm M, Batish SD, Lach FP, Yetgin S, Neitzel H, Ariffin H, Tischkowitz M, Mathew CG, Auerbach AD, Rahman N. Reid S, et al. Nat Genet. 2007 Feb;39(2):162-4. doi: 10.1038/ng1947. Epub 2006 Dec 31. Nat Genet. 2007. PMID: 17200671

3

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour.

Reid S, Renwick A, Seal S, Baskcomb L, Barfoot R, Jayatilake H, Pritchard-Jones K, Stratton MR, Ridolfi-Lüthy A, Rahman N; Breast Cancer Susceptibility Collaboration (UK); Familial Wilms Tumour Collaboration. Reid S, et al. J Med Genet. 2005 Feb;42(2):147-51. doi: 10.1136/jmg.2004.022673. J Med Genet. 2005. PMID: 15689453 Free PMC article. No abstract available.

4

Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B.

Hanks S, Coleman K, Reid S, Plaja A, Firth H, Fitzpatrick D, Kidd A, Méhes K, Nash R, Robin N, Shannon N, Tolmie J, Swansbury J, Irrthum A, Douglas J, Rahman N. Hanks S, et al. Among authors: reid s. Nat Genet. 2004 Nov;36(11):1159-61. doi: 10.1038/ng1449. Epub 2004 Oct 10. Nat Genet. 2004. PMID: 15475955 Free article.

5

PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations.

McConville C, Reid S, Baskcomb L, Douglas J, Rahman N. McConville C, et al. Among authors: reid s. Am J Med Genet A. 2006 Jun 15;140(12):1297-301. doi: 10.1002/ajmg.a.31278. Am J Med Genet A. 2006. PMID: 16691592

6

Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24.

McEntagart ME, Reid SL, Irrthum A, Douglas JB, Eyre KE, Donaghy MJ, Anderson NE, Rahman N. McEntagart ME, et al. Ann Neurol. 2005 Feb;57(2):293-7. doi: 10.1002/ana.20375. Ann Neurol. 2005. PMID: 15668982

7

Multiple effects of genetic background on variegated transgene expression in mice.

Opsahl ML, McClenaghan M, Springbett A, Reid S, Lathe R, Colman A, Whitelaw CB. Opsahl ML, et al. Among authors: reid s. Genetics. 2002 Mar;160(3):1107-12. doi: 10.1093/genetics/160.3.1107. Genetics. 2002. PMID: 11901126 Free PMC article.

8

Corrigendum to: Taking a value based commissioning approach to non-clinical and clinical support services.

Kinsman T, Reid S, Arnott H. Kinsman T, et al. Among authors: reid s. Aust Health Rev. 2024 Jun;48(3):334. doi: 10.1071/AH23278_CO. Aust Health Rev. 2024. PMID: 38843082 No abstract available.

9

Evaluating the new family medicine internship programmes in the Western Cape, South Africa.

Hutton LN, Jenkins LS, Mash R, Von Pressentin K, Reid S, Morgan J, Kapp P. Hutton LN, et al. Among authors: reid s. S Afr Fam Pract (2004). 2024 May 10;66(1):e1-e8. doi: 10.4102/safp.v66i1.5837. S Afr Fam Pract (2004). 2024. PMID: 38832386 Free PMC article.

10

Rapid mortality in captive bush dogs (Speothos venaticus) caused by influenza A of avian origin (H5N1) at a wildlife collection in the United Kingdom.

Falchieri M, Reid SM, Dastderji A, Cracknell J, Warren CJ, Mollett BC, Peers-Dent J, Schlachter AD, Mcginn N, Hepple R, Thomas S, Ridout S, Quayle J, Pizzi R, Núñez A, Byrne AMP, James J, Banyard AC. Falchieri M, et al. Among authors: reid sm. Emerg Microbes Infect. 2024 Dec;13(1):2361792. doi: 10.1080/22221751.2024.2361792. Epub 2024 Jun 5. Emerg Microbes Infect. 2024. PMID: 38828793 Free article.

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