Dearlove AM - Search Results

1

Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13.

Curtis D, Brett P, Dearlove AM, McQuillin A, Kalsi G, Robertson MM, Gurling HM. Curtis D, et al. Among authors: dearlove am. Psychiatr Genet. 2004 Jun;14(2):83-7. doi: 10.1097/01.ypg.0000107927.32051.f5. Psychiatr Genet. 2004. PMID: 15167693

2

A genome-wide family-based linkage study of coeliac disease.

King AL, Yiannakou JY, Brett PM, Curtis D, Morris MA, Dearlove AM, Rhodes M, Rosen-Bronson S, Mathew C, Ellis HJ, Ciclitira PJ. King AL, et al. Among authors: dearlove am. Ann Hum Genet. 2000 Nov;64(Pt 6):479-90. doi: 10.1046/j.1469-1809.2000.6460479.x. Ann Hum Genet. 2000. PMID: 11281212

3

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: dearlove am. Ann Hum Genet. 2001 Jul;65(Pt 4):377-86. doi: 10.1017/S0003480001008703. Ann Hum Genet. 2001. PMID: 11592927

4

Coeliac disease: investigation of proposed causal variants in the CTLA4 gene region.

King AL, Moodie SJ, Fraser JS, Curtis D, Reid E, Dearlove AM, Ciclitira PJ. King AL, et al. Among authors: dearlove am. Eur J Immunogenet. 2003 Dec;30(6):427-32. doi: 10.1111/j.1365-2370.2003.00430.x. Eur J Immunogenet. 2003. PMID: 14675397

5

CTLA-4/CD28 gene region is associated with genetic susceptibility to coeliac disease in UK families.

King AL, Moodie SJ, Fraser JS, Curtis D, Reid E, Dearlove AM, Ellis HJ, Ciclitira PJ. King AL, et al. Among authors: dearlove am. J Med Genet. 2002 Jan;39(1):51-4. doi: 10.1136/jmg.39.1.51. J Med Genet. 2002. PMID: 11826026 Free PMC article. No abstract available.

6

Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.

Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM. Ragge NK, et al. Among authors: dearlove am. J Med Genet. 2003 Jan;40(1):37-41. doi: 10.1136/jmg.40.1.37. J Med Genet. 2003. PMID: 12525540 Free PMC article.

7

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping.

Ohadi M, Lalloz MR, Sham P, Zhao J, Dearlove AM, Shiach C, Kinsey S, Rhodes M, Layton DM. Ohadi M, et al. Among authors: dearlove am. Am J Hum Genet. 1999 Jan;64(1):165-71. doi: 10.1086/302187. Am J Hum Genet. 1999. PMID: 9915955 Free PMC article.

8

Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42.

Brockington M, Sewry CA, Herrmann R, Naom I, Dearlove A, Rhodes M, Topaloglu H, Dubowitz V, Voit T, Muntoni F. Brockington M, et al. Am J Hum Genet. 2000 Feb;66(2):428-35. doi: 10.1086/302775. Am J Hum Genet. 2000. PMID: 10677302 Free PMC article.

9

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).

Reid E, Kloos M, Ashley-Koch A, Hughes L, Bevan S, Svenson IK, Graham FL, Gaskell PC, Dearlove A, Pericak-Vance MA, Rubinsztein DC, Marchuk DA. Reid E, et al. Am J Hum Genet. 2002 Nov;71(5):1189-94. doi: 10.1086/344210. Epub 2002 Sep 24. Am J Hum Genet. 2002. PMID: 12355402 Free PMC article.

10

A high-resolution microsatellite map of the mouse genome.

Rhodes M, Straw R, Fernando S, Evans A, Lacey T, Dearlove A, Greystrong J, Walker J, Watson P, Weston P, Kelly M, Taylor D, Gibson K, Mundy C, Bourgade F, Poirier C, Simon D, Brunialti AL, Montagutelli X, Gu'enet JL, Haynes A, Brown SD. Rhodes M, et al. Genome Res. 1998 May;8(5):531-42. doi: 10.1101/gr.8.5.531. Genome Res. 1998. PMID: 9582196 Free article.

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