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Page 1
Overweight and obesity on the island of Ireland: an estimation of costs.
Dee A, Callinan A, Doherty E, O'Neill C, McVeigh T, Sweeney MR, Staines A, Kearns K, Fitzgerald S, Sharp L, Kee F, Hughes J, Balanda K, Perry IJ. Dee A, et al. Among authors: mcveigh t. BMJ Open. 2015 Mar 16;5(3):e006189. doi: 10.1136/bmjopen-2014-006189. BMJ Open. 2015. PMID: 25776042 Free PMC article.
A comparison of physical activity, physical fitness levels, BMI and blood pressure of adults with intellectual disability, who do and do not take part in Special Olympics Ireland programmes: Results from the SOPHIE study.
Walsh D, Belton S, Meegan S, Bowers K, Corby D, Staines A, McVeigh T, McKeon M, Hoey E, Trépel D, Griffin P, Sweeney MR. Walsh D, et al. Among authors: mcveigh t. J Intellect Disabil. 2018 Jun;22(2):154-170. doi: 10.1177/1744629516688773. Epub 2017 Jan 27. J Intellect Disabil. 2018. PMID: 28125943
Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK).
Garrett A, Allen S, Durkie M, Burghel GJ, Robinson R, Callaway A, Field J, Frugtniet B, Palmer-Smith S, Grant J, Pagan J, McDevitt T, Rowlands CF, McVeigh T, Hanson H, Turnbull C; CanVIG-UK. Garrett A, et al. Among authors: mcveigh t. Genet Med. 2024 Oct 24;27(2):101305. doi: 10.1016/j.gim.2024.101305. Online ahead of print. Genet Med. 2024. PMID: 39489894 Free article.
Using cancer phenotype sex-specificity to enable unbiased penetrance estimation of SMARCA4 pathogenic variants for small cell carcinoma of the ovary, hypercalcemic type (SCCOHT).
Wade I, Witkowski L, Ahmed A, Rowlands CF, Banerjee S, Pressey JG, McVeigh TP, Tischkowitz MD, Foulkes WD, Turnbull C; SCCOHT-SMARCA4 Registry Consortium. Wade I, et al. Among authors: mcveigh tp. Genet Med. 2024 Oct 2;27(1):101287. doi: 10.1016/j.gim.2024.101287. Online ahead of print. Genet Med. 2024. PMID: 39367739
Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10 G>T at the intron 9/exon 10 of the MAPT gene.
Olszewska DA, Fearon C, McGuigan C, McVeigh TP, Houlden H, Polke JM, Lawlor B, Coen R, Hutchinson M, Hutton M, Beausang A, Delon I, Brett F, Sevastou I, Seto-Salvia N, de Silva R, Lynch T. Olszewska DA, et al. Among authors: mcveigh tp. Neurobiol Aging. 2025 Feb;146:79. doi: 10.1016/j.neurobiolaging.2024.09.011. Epub 2024 Sep 23. Neurobiol Aging. 2025. PMID: 39317514 No abstract available.
109 results