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Patient acceptability of genotypic testing for hemochromatosis in primary care.
Anderson RT, Press N, Tucker DC, Snively BM, Wenzel L, Ellis SD, Hall MA, Walker AP, Thomson EJ, Lewis-Jack O, Acton RT. Anderson RT, et al. Among authors: hall ma. Genet Med. 2005 Oct;7(8):557-63. doi: 10.1097/01.gim.0000177531.53338.65. Genet Med. 2005. PMID: 16247294 Free article. Clinical Trial.
Results communication and patient education after screening for possible hemochromatosis and iron overload: experience from the HEIRS Study of a large ethnically and linguistically diverse group.
Walker AP, Tucker DC, Hall MA, Lohman K, Harrison H, Harrison BW, Reiss J, Acton RT, Adams PC, Diaz S, Holup J, Thomson E, Ellis SD, McLaren CE; Hemochromatosis and Iron Overload Study Research Investigators. Walker AP, et al. Among authors: hall ma. Genet Med. 2007 Nov;9(11):778-91. doi: 10.1097/gim.0b013e318159a303. Genet Med. 2007. PMID: 18007147 Free article.
Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.
McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley MR, Sholinsky P, Dawkins FW, Snively BM, Vogt TM, Eckfeldt JH; Hemochromatosis and Iron Overload Screen (HEIRS) Study Research Investigators. McLaren GD, et al. Can J Gastroenterol. 2008 Nov;22(11):923-30. doi: 10.1155/2008/907356. Can J Gastroenterol. 2008. PMID: 19018338 Free PMC article.
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
Onengut-Gumuscu S, Chen WM, Burren O, Cooper NJ, Quinlan AR, Mychaleckyj JC, Farber E, Bonnie JK, Szpak M, Schofield E, Achuthan P, Guo H, Fortune MD, Stevens H, Walker NM, Ward LD, Kundaje A, Kellis M, Daly MJ, Barrett JC, Cooper JD, Deloukas P; Type 1 Diabetes Genetics Consortium; Todd JA, Wallace C, Concannon P, Rich SS. Onengut-Gumuscu S, et al. Nat Genet. 2015 Apr;47(4):381-6. doi: 10.1038/ng.3245. Epub 2015 Mar 9. Nat Genet. 2015. PMID: 25751624 Free PMC article.
509 results