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Page 1
Analysis of BAFF gene polymorphisms in UK Graves' disease patients.
Lane LC, Allinson KR, Campbell K, Bhatnagar I, Ingoe L, Razvi S, Cheetham T, Cordell HJ, Pearce SH, Mitchell AL. Lane LC, et al. Among authors: cordell hj. Clin Endocrinol (Oxf). 2019 Jan;90(1):170-174. doi: 10.1111/cen.13872. Epub 2018 Nov 5. Clin Endocrinol (Oxf). 2019. PMID: 30281845
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.
Sutherland A, Davies J, Owen CJ, Vaikkakara S, Walker C, Cheetham TD, James RA, Perros P, Donaldson PT, Cordell HJ, Quinton R, Pearce SH. Sutherland A, et al. Among authors: cordell hj. J Clin Endocrinol Metab. 2007 Aug;92(8):3338-41. doi: 10.1210/jc.2007-0173. Epub 2007 May 29. J Clin Endocrinol Metab. 2007. PMID: 17535987 Free PMC article.
A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.
Goodship JA, Hall D, Topf A, Mamasoula C, Griffin H, Rahman TJ, Glen E, Tan H, Palomino Doza J, Relton CL, Bentham J, Bhattacharya S, Cosgrove C, Brook D, Granados-Riveron J, Bu'Lock FA, O'Sullivan J, Stuart AG, Parsons J, Cordell HJ, Keavney B. Goodship JA, et al. Among authors: cordell hj. Circ Cardiovasc Genet. 2012 Jun;5(3):287-92. doi: 10.1161/CIRCGENETICS.111.962035. Epub 2012 Apr 13. Circ Cardiovasc Genet. 2012. PMID: 22503907 Free PMC article.
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
Mamasoula C, Prentice RR, Pierscionek T, Pangilinan F, Mills JL, Druschel C, Pass K, Russell MW, Hall D, Töpf A, Brown DL, Zelenika D, Bentham J, Cosgrove C, Bhattacharya S, Riveron JG, Setchfield K, Brook JD, Bu'Lock FA, Thornborough C, Rahman TJ, Doza JP, Tan HL, O'Sullivan J, Stuart AG, Blue G, Winlaw D, Postma AV, Mulder BJ, Zwinderman AH, van Engelen K, Moorman AF, Rauch A, Gewillig M, Breckpot J, Devriendt K, Lathrop GM, Farrall M, Goodship JA, Cordell HJ, Brody LC, Keavney BD. Mamasoula C, et al. Among authors: cordell hj. Circ Cardiovasc Genet. 2013 Aug;6(4):347-53. doi: 10.1161/CIRCGENETICS.113.000191. Epub 2013 Jul 22. Circ Cardiovasc Genet. 2013. PMID: 23876493 Free PMC article.
Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts.
Mitchell AL, Macarthur KD, Gan EH, Baggott LE, Wolff AS, Skinningsrud B, Platt H, Short A, Lobell A, Kämpe O, Bensing S, Betterle C, Kasperlik-Zaluska A, Zurawek M, Fichna M, Kockum I, Nordling Eriksson G, Ekwall O, Wahlberg J, Dahlqvist P, Hulting AL, Penna-Martinez M, Meyer G, Kahles H, Badenhoop K, Hahner S, Quinkler M, Falorni A, Phipps-Green A, Merriman TR, Ollier W, Cordell HJ, Undlien D, Czarnocka B, Husebye E, Pearce SH. Mitchell AL, et al. Among authors: cordell hj. PLoS One. 2014 Mar 10;9(3):e88991. doi: 10.1371/journal.pone.0088991. eCollection 2014. PLoS One. 2014. PMID: 24614117 Free PMC article.
Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.
Mitchell AL, Bøe Wolff A, MacArthur K, Weaver JU, Vaidya B; Swedish Addision Registry Study Group; Erichsen MM, Darlay R, Husebye ES, Cordell HJ, Pearce SH. Mitchell AL, et al. Among authors: cordell hj. PLoS One. 2015 Jun 4;10(6):e0123550. doi: 10.1371/journal.pone.0123550. eCollection 2015. PLoS One. 2015. PMID: 26042420 Free PMC article. Clinical Trial.
CTLA-4 as a genetic determinant in autoimmune Addison's disease.
Wolff AS, Mitchell AL, Cordell HJ, Short A, Skinningsrud B, Ollier W, Badenhoop K, Meyer G, Falorni A, Kampe O, Undlien D, Pearce SH, Husebye ES. Wolff AS, et al. Among authors: cordell hj. Genes Immun. 2015 Sep;16(6):430-6. doi: 10.1038/gene.2015.27. Epub 2015 Jul 23. Genes Immun. 2015. PMID: 26204230 Free PMC article.
Correction: Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.
Mitchell AL, Bøe Wolff A, MacArthur K, Weaver JU, Vaidya B; Swedish Addison Registry Study Group; Erichsen MM, Darlay R, Husebye ES, Cordell HJ, Pearce SH. Mitchell AL, et al. Among authors: cordell hj. PLoS One. 2015 Sep 18;10(9):e0138844. doi: 10.1371/journal.pone.0138844. eCollection 2015. PLoS One. 2015. PMID: 26382621 Free PMC article. No abstract available.
259 results