Dearlove AM - Search Results

1

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

2

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

3

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

4

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

5

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.

6

A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.

Reid E, Dearlove AM, Rhodes M, Rubinsztein DC. Reid E, et al. Among authors: dearlove am. Am J Hum Genet. 1999 Sep;65(3):757-63. doi: 10.1086/302555. Am J Hum Genet. 1999. PMID: 10441583 Free PMC article.

7

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.

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

Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.

Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC. Reid E, et al. Among authors: dearlove am. Neurology. 1999 Nov 10;53(8):1844-9. doi: 10.1212/wnl.53.8.1844. Neurology. 1999. PMID: 10563637

10

High-throughput microsatellite analysis using fluorescent dUTPs for high-resolution genetic mapping of the mouse genome.

Rhodes M, Dearlove A, Straw R, Fernando S, Evans A, Greener M, Lacey T, Kelly M, Gibson K, Brown SD, Mundy C. Rhodes M, et al. Genome Res. 1997 Jan;7(1):81-6. doi: 10.1101/gr.7.1.81. Genome Res. 1997. PMID: 9037606 Free article.

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