Curtis D - Search Results

1

Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

Whitehouse WP, Rees M, Curtis D, Sundqvist A, Parker K, Chung E, Baralle D, Gardiner RM. Whitehouse WP, et al. Among authors: curtis d. Am J Hum Genet. 1993 Sep;53(3):652-62. Am J Hum Genet. 1993. PMID: 8352275 Free PMC article.

2

Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variants.

Rees M, Curtis D, Parker K, Sundqvist A, Baralle D, Bespalova IN, Burmeister M, Chung E, Gardiner RM, Whitehouse WP. Rees M, et al. Among authors: curtis d. Neuropediatrics. 1994 Feb;25(1):20-5. doi: 10.1055/s-2008-1071576. Neuropediatrics. 1994. PMID: 8208346

3

Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

Elmslie FV, Rees M, Williamson MP, Kerr M, Kjeldsen MJ, Pang KA, Sundqvist A, Friis ML, Chadwick D, Richens A, Covanis A, Santos M, Arzimanoglou A, Panayiotopoulos CP, Curtis D, Whitehouse WP, Gardiner RM. Elmslie FV, et al. Among authors: curtis d. Hum Mol Genet. 1997 Aug;6(8):1329-34. doi: 10.1093/hmg/6.8.1329. Hum Mol Genet. 1997. PMID: 9259280

4

Genetic evidence for the neuronal nitric oxide synthase gene (NOS1) as a susceptibility locus for infantile pyloric stenosis.

Chung E, Curtis D, Chen G, Marsden PA, Twells R, Xu W, Gardiner M. Chung E, et al. Among authors: curtis d. Am J Hum Genet. 1996 Feb;58(2):363-70. Am J Hum Genet. 1996. PMID: 8571963 Free PMC article.

5

Linkage analysis of chromosome 22q12-13 in a United Kingdom/Icelandic sample of 23 multiplex schizophrenia families.

Kalsi G, Brynjolfsson J, Butler R, Sherrington R, Curtis D, Sigmundsson T, Read T, Murphy P, Sharma T, Petursson H, et al. Kalsi G, et al. Among authors: curtis d. Am J Med Genet. 1995 Aug 14;60(4):298-301. doi: 10.1002/ajmg.1320600407. Am J Med Genet. 1995. PMID: 7485264

6

Model-free linkage analysis using likelihoods.

Curtis D, Sham PC. Curtis D, et al. Am J Hum Genet. 1995 Sep;57(3):703-16. Am J Hum Genet. 1995. PMID: 7668300 Free PMC article.

7

Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

Collier DA, Barrett TG, Curtis D, Macleod A, Arranz MJ, Maassen JA, Bundey S. Collier DA, et al. Among authors: curtis d. Am J Hum Genet. 1996 Oct;59(4):855-63. Am J Hum Genet. 1996. PMID: 8808601 Free PMC article.

8

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D. Gurling HM, et al. Among authors: curtis d. Am J Hum Genet. 2001 Mar;68(3):661-73. doi: 10.1086/318788. Am J Hum Genet. 2001. PMID: 11179014 Free PMC article.

9

Power comparison of parametric and nonparametric linkage tests in small pedigrees.

Sham PC, Lin MW, Zhao JH, Curtis D. Sham PC, et al. Among authors: curtis d. Am J Hum Genet. 2000 May;66(5):1661-8. doi: 10.1086/302888. Epub 2000 Apr 11. Am J Hum Genet. 2000. PMID: 10762550 Free PMC article.

10

Coeliac disease: follow-up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11.

King AL, Fraser JS, Moodie SJ, Curtis D, Dearlove AM, Ellis HJ, Rosen-Bronson S, Ciclitira PJ. King AL, et al. Among authors: curtis d. Ann Hum Genet. 2001 Jul;65(Pt 4):377-86. doi: 10.1017/S0003480001008703. Ann Hum Genet. 2001. PMID: 11592927

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