Andrew Dearlove BSc, MSc, MBA
Bibliography
Kennedy AM, Inada M, Krane SM, Christie PT, Harding B, Lopez-Otin C, Sanchez LM,
Pannett AA, Dearlove A, Hartley C, Byrne MH, Reed AA, Nesbit MA, Whyte MP, Thakker RV.
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMDMO).
J Clin Invest. 2005 Sep 15; [Epub ahead of print]
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.
Mutation in myosin heavy chain 6 causes atrial septal defect. Nat Genet. 37(4): 423-8 (2005).
Curtis D, Brett P, Dearlove AM, McQuillin A, Kalsi G, Robertson MM, Gurling HM.
Genome scan of Tourette syndrome in a single large pedigree shows some support
for linkage to regions of chromosomes 5, 10 and 13. Psychiatr Genet. 14(2): 83-87 (2004).
King AL, Moodie SJ, Fraser JS, Curtis D, Reid E, Dearlove AM, Ciclitira PJ.
Coeliac disease: investigation of proposed causal variants in the CTLA4 gene region.
Eur J Immunogenet. 30(6): 427-32 (2003).
Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM. Familial
vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.
J Med Genet. 40(1): 37-41 (2003).
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.
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia
(SPG10). Am J Hum Genet. 71(5):1189-94 (2002).
Rhodes M, Day J, Dong P, Scafe C, Dailey D, Gilbert G, Wang Y, Laig Webster
N, Su X, Koehle R, AviItshak H, Ziegle J, Wogan L, McMullen I, Spier E,
De La Vega F, Reid E, Brooking J, Dudbridge, Dearlove A, Weaver T, Yuille M.
A validated set of SNPs for linkage mapping studies Am J Hum Genet Suppl 71:442 (2002).
Dearlove AM. High throughput genotyping technologies. Brief Funct Genomic
Proteomic. 1(2):139-50 (2002).
King AL, Moodie SJ, Fraser JS, Curtis D, Reid E, Dearlove AM, Ellis HJ, Ciclitira PJ.
CTLA-4/CD28 gene region is associated with genetic susceptibility to coeliac
disease in UK families. J Med Genet. 39(1):51-4 (2002).
Vulliamy T, Marrone A, Goldman F, Dearlove A, Bessler M, Mason PJ, Dokal I.
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis
congenita. Nature. 27;413(6854):432-5 (2001).
King AL, Fraser JS, Moodie SJ, Curtis D, Dearlove AM, Ellis HJ, Rosen-Bronson S,
Ciclitira PJ.Coeliac disease: follow-up linkage study provides further support
for existence of a susceptibility locus on chromosome 11p11. Ann Hum Genet. 65(4):377-86 (2001).
King AL, Yiannakou JY, Brett PM, Curtis D, Morris MA, Dearlove AM, Rhodes M,
Rosen-Bronson S, Mathew C, Ellis HJ, Ciclitira PJ. A genome-wide family-based
linkage study of coeliac disease. Ann Hum Genet. 64(Pt 6):479-90 (2000).
Baralle D, Dearlove AM, Beach R, Ffrench-Constant C, Reid E.
Benign familial infantile convulsions: report of a UK family and confirmation of
genetic heterogeneity. J Med Genet. 37(10): E31 (2000).
Reid E, Dearlove AM, Osborn O, Rogers MT, Rubinsztein DC. A locus for autosomal
dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13.
Am J Hum Genet. 66(2):728-32 (2000).
Brockington M, Sewry CA, Herrmann R, Naom I, Dearlove A, Rhodes M, Topaloglu H,
Dubowitz V, Voit T, Muntoni F. Assignment of a form of congenital muscular dystrophy
with secondary merosin deficiency to chromosome 1q42. Am J Hum Genet. 66(2):428-35 (2000).
Reid E, Escayg A, Dearlove AM, Meisler MH, Rubinsztein DC. The spastic paraplegia
SPG10 locus: narrowing of critical region and exclusion of sodium channel gene
SCN8A as a candidate. J Med Genet. 38(1):65-7 (2001).
Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC. Autosomal dominant
spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
Neurology. 53(8):1844-9 (1999).
Reid E, Dearlove AM, Rhodes M, Rubinsztein DC. A new locus for autosomal dominant
"pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for
further genetic heterogeneity. Am J Hum Genet. 65(3):757-63 (1999).
Ohadi M, Lalloz MR, Sham P, Zhao J, Dearlove AM, Shiach C, Kinsey S, Rhodes M,
Layton DM. Localization of a gene for familial hemophagocytic lymphohistiocytosis
at chromosome 9q21.3-22 by homozygosity mapping. Am J Hum Genet. 64(1):165-71 (1999).
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.
A high-resolution microsatellite map of the mouse genome. Genome Res. 8(5):531-42 (1998).
Rhodes M, Dearlove A, Straw R, Fernando S, Evans A, Greener M, Lacey T,
Kelly M, Gibson K, Brown SD, Mundy C. High-throughput microsatellite
analysis using fluorescent dUTPs for high-resolution genetic mapping
of the mouse genome. Genome Res. 7(1):81-6 (1997).