Curtis D - Search Results

1

Family association studies of markers on chromosome 2q and Type 1 diabetes in subjects from South India.

Ogunkolade WB, Ramachandran A, McDermott MF, Kumarajeewa TR, Curtis D, Snehalatha C, Mohan V, Cassell PG, Eskdale J, Gallagher G, Hitman GA. Ogunkolade WB, et al. Among authors: curtis d. Diabetes Metab Res Rev. 2000 Jul-Aug;16(4):276-80. doi: 10.1002/1520-7560(200007/08)16:4<276::aid-dmrr128>3.0.co;2-w. Diabetes Metab Res Rev. 2000. PMID: 10934456

2

Allelic variation in the vitamin D receptor influences susceptibility to IDDM in Indian Asians.

McDermott MF, Ramachandran A, Ogunkolade BW, Aganna E, Curtis D, Boucher BJ, Snehalatha C, Hitman GA. McDermott MF, et al. Among authors: curtis d. Diabetologia. 1997 Aug;40(8):971-5. doi: 10.1007/s001250050776. Diabetologia. 1997. PMID: 9267994

3

Exclusion of the familial Mediterranean fever locus as a susceptibility region for autosomal dominant familial Hibernian fever.

McDermott MF, McDermott EM, Quane KA, Jones LC, Ogunkolade BW, Curtis D, Waldron-Lynch F, Phelan M, Hitman GA, Molloy MG, Powell RJ. McDermott MF, et al. Among authors: curtis d. J Med Genet. 1998 May;35(5):432-4. doi: 10.1136/jmg.35.5.432. J Med Genet. 1998. PMID: 9610811 Free PMC article.

4

Assessing optimal neural network architecture for identifying disease-associated multi-marker genotypes using a permutation test, and application to calpain 10 polymorphisms associated with diabetes.

North BV, Curtis D, Cassell PG, Hitman GA, Sham PC. North BV, et al. Among authors: curtis d. Ann Hum Genet. 2003 Jul;67(Pt 4):348-56. doi: 10.1046/j.1469-1809.2003.00030.x. Ann Hum Genet. 2003. PMID: 12914569

5

Linkage studies in bipolar affective disorder with markers on chromosome 21.

Vallada H, Craddock N, Vasques L, Curtis D, Kirov G, Lauriano V, Gentil V, Passos-Bueno R, Murray RM, Zatz M, McGuffin P, Powell JF, Gill M, Owen M, Collier DA. Vallada H, et al. Among authors: curtis d. J Affect Disord. 1996 Dec 16;41(3):217-21. doi: 10.1016/s0165-0327(96)00055-9. J Affect Disord. 1996. PMID: 8988454

6

Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia.

Vallada H, Curtis D, Sham PC, Murray RM, McGuffin P, Nanko S, Gill M, Owen M, Collier DA. Vallada H, et al. Among authors: curtis d. Psychiatr Genet. 1995 Fall;5(3):127-30. doi: 10.1097/00041444-199505030-00005. Psychiatr Genet. 1995. PMID: 8746411

7

Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder.

McQuillin A, Lawrence J, Curtis D, Kalsi G, Smyth C, Hannesdottir S, Gurling H. McQuillin A, et al. Among authors: curtis d. Psychol Med. 1999 Nov;29(6):1449-54. doi: 10.1017/s0033291799001166. Psychol Med. 1999. PMID: 10616951

8

Use of siblings as controls in case-control association studies.

Curtis D. Curtis D. Ann Hum Genet. 1997 Jul;61(Pt 4):319-33. doi: 10.1046/j.1469-1809.1998.6210089.x. Ann Hum Genet. 1997. PMID: 9365785

9

Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32.

Lin MW, Curtis D, Williams N, Arranz M, Nanko S, Collier D, McGuffin P, Murray R, Owen M, Gill M, et al. Lin MW, et al. Among authors: curtis d. Psychiatr Genet. 1995 Fall;5(3):117-26. doi: 10.1097/00041444-199505030-00004. Psychiatr Genet. 1995. PMID: 8746410

10

Linkage analysis of manic depression (bipolar affective disorder) in Icelandic and British kindreds using markers on the short arm of chromosome 18.

Kalsi G, Smyth C, Brynjolfsson J, Sherrington RS, O'Neill J, Curtis D, Rifkin L, Murphy P, Petursson H, Gurling HM. Kalsi G, et al. Among authors: curtis d. Hum Hered. 1997 Sep-Oct;47(5):268-78. doi: 10.1159/000154423. Hum Hered. 1997. PMID: 9358015

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