Curtis D - Search Results

1

Haplotype combinations of calpain 10 gene polymorphisms associate with increased risk of impaired glucose tolerance and type 2 diabetes in South Indians.

Cassell PG, Jackson AE, North BV, Evans JC, Syndercombe-Court D, Phillips C, Ramachandran A, Snehalatha C, Gelding SV, Vijayaravaghan S, Curtis D, Hitman GA. Cassell PG, et al. Among authors: curtis d. Diabetes. 2002 May;51(5):1622-8. doi: 10.2337/diabetes.51.5.1622. Diabetes. 2002. PMID: 11978665

2

SPINK1 is a susceptibility gene for fibrocalculous pancreatic diabetes in subjects from the Indian subcontinent.

Hassan Z, Mohan V, Ali L, Allotey R, Barakat K, Faruque MO, Deepa R, McDermott MF, Jackson AE, Cassell P, Curtis D, Gelding SV, Vijayaravaghan S, Gyr N, Whitcomb DC, Khan AK, Hitman GA. Hassan Z, et al. Among authors: curtis d. Am J Hum Genet. 2002 Oct;71(4):964-8. doi: 10.1086/342731. Epub 2002 Aug 16. Am J Hum Genet. 2002. PMID: 12187509 Free PMC article.

3

Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait.

Knight J, North BV, Sham PC, Curtis D. Knight J, et al. Among authors: curtis d. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S74. doi: 10.1186/1471-2156-4-S1-S74. BMC Genet. 2003. PMID: 14975142 Free PMC article.

4

Application of logistic regression to case-control association studies involving two causative loci.

North BV, Curtis D, Sham PC. North BV, et al. Among authors: curtis d. Hum Hered. 2005;59(2):79-87. doi: 10.1159/000085222. Epub 2005 Apr 18. Hum Hered. 2005. PMID: 15838177

5

Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes.

Curtis D. Curtis D. Diabetes Metab Res Rev. 2022 Jan;38(1):e3482. doi: 10.1002/dmrr.3482. Epub 2021 Jul 6. Diabetes Metab Res Rev. 2022. PMID: 34216101

6

Minor differences in haplotype frequency estimates can produce very large differences in heterogeneity test statistics.

Curtis D, Xu K. Curtis D, et al. BMC Genet. 2007 Jun 27;8:38. doi: 10.1186/1471-2156-8-38. BMC Genet. 2007. PMID: 17597526 Free PMC article.

7

Yin yang haplotypes revisited - long, disparate haplotypes observed in European populations in regions of increased homozygosity.

Curtis D, Vine AE. Curtis D, et al. Hum Hered. 2010;69(3):184-92. doi: 10.1159/000289592. Epub 2010 Mar 4. Hum Hered. 2010. PMID: 20203523 Free article.

8

Genetic variation in the miR-708 gene and its binding targets in bipolar disorder.

Fiorentino A, O'Brien NL, Sharp SI, Curtis D, Bass NJ, McQuillin A. Fiorentino A, et al. Among authors: curtis d. Bipolar Disord. 2016 Dec;18(8):650-656. doi: 10.1111/bdi.12448. Epub 2016 Nov 16. Bipolar Disord. 2016. PMID: 27864917 Free PMC article.

9

Identification of specific genes involved in schizophrenia aetiology - what difference does it make?

Curtis D. Curtis D. Br J Psychiatry. 2022 Aug;221(2):437-439. doi: 10.1192/bjp.2021.153. Br J Psychiatry. 2022. PMID: 35382908

10

A new method of linkage analysis using LOD scores for quantitative traits supports linkage of monoamine oxidase activity to D17S250 in the Collaborative Study on the Genetics of Alcoholism pedigrees.

Curtis D, Knight J, Sham PC. Curtis D, et al. Psychiatr Genet. 2005 Sep;15(3):181-7. doi: 10.1097/01.ypg.0000173119.04430.65. Psychiatr Genet. 2005. PMID: 16094252

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