Tobin MD - Search Results

1

Cohort profile: Extended Cohort for E-health, Environment and DNA (EXCEED).

John C, Reeve NF, Free RC, Williams AT, Ntalla I, Farmaki AE, Bethea J, Barton LM, Shrine N, Batini C, Packer R, Terry S, Hargadon B, Wang Q, Melbourne CA, Adams EL, Bee CE, Harrington K, Miola J, Brunskill NJ, Brightling CE, Barwell J, Wallace SE, Hsu R, Shepherd DJ, Hollox EJ, Wain LV, Tobin MD. John C, et al. Among authors: tobin md. Int J Epidemiol. 2019 Oct 1;48(5):1734. doi: 10.1093/ije/dyz175. Int J Epidemiol. 2019. PMID: 31365084 Free PMC article. No abstract available.

2

Adjusting for bias and unmeasured confounding in Mendelian randomization studies with binary responses.

Palmer TM, Thompson JR, Tobin MD, Sheehan NA, Burton PR. Palmer TM, et al. Among authors: tobin md. Int J Epidemiol. 2008 Oct;37(5):1161-8. doi: 10.1093/ije/dyn080. Epub 2008 May 7. Int J Epidemiol. 2008. PMID: 18463132

3

Common variation in the WNK1 gene and blood pressure in childhood: the Avon Longitudinal Study of Parents and Children.

Tobin MD, Timpson NJ, Wain LV, Ring S, Jones LR, Emmett PM, Palmer TM, Ness AR, Samani NJ, Smith GD, Burton PR. Tobin MD, et al. Hypertension. 2008 Nov;52(5):974-9. doi: 10.1161/HYPERTENSIONAHA.108.118414. Epub 2008 Sep 22. Hypertension. 2008. PMID: 18809789

4

Genomic copy number variation, human health, and disease.

Wain LV, Armour JA, Tobin MD. Wain LV, et al. Among authors: tobin md. Lancet. 2009 Jul 25;374(9686):340-50. doi: 10.1016/S0140-6736(09)60249-X. Epub 2009 Jun 15. Lancet. 2009. PMID: 19535135 Free article. Review.

5

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.

Wain LV, Pedroso I, Landers JE, Breen G, Shaw CE, Leigh PN, Brown RH, Tobin MD, Al-Chalabi A. Wain LV, et al. Among authors: tobin md. PLoS One. 2009 Dec 4;4(12):e8175. doi: 10.1371/journal.pone.0008175. PLoS One. 2009. PMID: 19997636 Free PMC article.

6

DataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the data.

Wolfson M, Wallace SE, Masca N, Rowe G, Sheehan NA, Ferretti V, LaFlamme P, Tobin MD, Macleod J, Little J, Fortier I, Knoppers BM, Burton PR. Wolfson M, et al. Among authors: tobin md. Int J Epidemiol. 2010 Oct;39(5):1372-82. doi: 10.1093/ije/dyq111. Epub 2010 Jul 14. Int J Epidemiol. 2010. PMID: 20630989 Free PMC article.

7

Copy number variation.

Wain LV, Tobin MD. Wain LV, et al. Among authors: tobin md. Methods Mol Biol. 2011;713:167-83. doi: 10.1007/978-1-60327-416-6_13. Methods Mol Biol. 2011. PMID: 21153619

8

Genome-wide association studies in lung disease.

Soler Artigas M, Wain LV, Tobin MD. Soler Artigas M, et al. Among authors: tobin md. Thorax. 2012 Mar;67(3):271-3, 280. doi: 10.1136/thoraxjnl-2011-200724. Epub 2011 Aug 19. Thorax. 2012. PMID: 21856699 Review.

9

Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study.

Kerr SM, Campbell A, Murphy L, Hayward C, Jackson C, Wain LV, Tobin MD, Dominiczak A, Morris A, Smith BH, Porteous DJ. Kerr SM, et al. Among authors: tobin md. BMC Med Genet. 2013 Mar 22;14:38. doi: 10.1186/1471-2350-14-38. BMC Med Genet. 2013. PMID: 23521772 Free PMC article.

10

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).

Glover M, Ware JS, Henry A, Wolley M, Walsh R, Wain LV, Xu S, Van't Hoff WG, Tobin MD, Hall IP, Cook S, Gordon RD, Stowasser M, O'Shaughnessy KM. Glover M, et al. Among authors: tobin md. Clin Sci (Lond). 2014 May;126(10):721-6. doi: 10.1042/CS20130326. Clin Sci (Lond). 2014. PMID: 24266877 Free PMC article.

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