Dearlove AM[au] - Search Results

Year	Number of Results
1999	3
2000	3
2001	2
2002	2
2003	2
2004	1
2005	1
2024	0

1

High throughput genotyping technologies.

Dearlove AM. Dearlove AM. Brief Funct Genomic Proteomic. 2002 Jul;1(2):139-50. doi: 10.1093/bfgp/1.2.139. Brief Funct Genomic Proteomic. 2002. PMID: 15239900 Review.

2

Mutation in myosin heavy chain 6 causes atrial septal defect.

Ching YH, Ghosh TK, Cross SJ, Packham EA, Honeyman L, Loughna S, Robinson TE, Dearlove AM, Ribas G, Bonser AJ, Thomas NR, Scotter AJ, Caves LS, Tyrrell GP, Newbury-Ecob RA, Munnich A, Bonnet D, Brook JD. Ching YH, et al. Among authors: dearlove am. Nat Genet. 2005 Apr;37(4):423-8. doi: 10.1038/ng1526. Epub 2005 Feb 27. Nat Genet. 2005. PMID: 15735645

3

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.

4

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

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

A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13.

Reid E, Dearlove AM, Osborn O, Rogers MT, Rubinsztein DC. Reid E, et al. Among authors: dearlove am. Am J Hum Genet. 2000 Feb;66(2):728-32. doi: 10.1086/302783. Am J Hum Genet. 2000. PMID: 10677333 Free PMC article.

7

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

8

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

9

The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate.

Reid E, Escayg A, Dearlove AM, Meisler MH, Rubinsztein DC. Reid E, et al. Among authors: dearlove am. J Med Genet. 2001 Jan;38(1):65-7. doi: 10.1136/jmg.38.1.65. J Med Genet. 2001. PMID: 11334010 Free PMC article. No abstract available.

10

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.

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