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Professor Andrew Read (PhD FRCPath FMedSci) - publications

List of publications

2015

  • Huijben, S., Chan, B. H. K., & Read, A. F. (2015). Relevance of undetectably rare resistant malaria parasites in treatment failure: Experimental evidence from Plasmodium chabaudi. American Journal of Tropical Medicine and Hygiene, 92(6), 1214-1221. DOI: 10.4269/ajtmh.15-0036. Publication link: fd4fff4d-d553-4032-afee-f05413b90eee | PubMed:25940195

2012

  • Blanford, S., Jenkins, N. E., Christian, R., Chan, B. H. K., Nardini, L., Osae, M., ... Thomas, M. B. (2012). Storage and persistence of a candidate fungal biopesticide for use against adult malaria vectors. Malaria Journal, 11, [354]. DOI: 10.1186/1475-2875-11-354. Publication link: bf446200-3d49-4d7a-a8ba-16980598310a | PubMed:23098323
  • Bell, A. S., Huijben, S., Paaijmans, K. P., Sim, D. G., Chan, B. H. K., Nelson, W. A., & Read, A. F. (2012). Enhanced transmission of drug-resistant parasites to mosquitoes following drug treatment in rodent malaria. PLoS ONE, 7(6), [e37172]. DOI: 10.1371/journal.pone.0037172. Publication link: b4083c16-f23c-44cc-9345-c91532b494c3 | PubMed:22701563
  • Barclay, V. C., Sim, D., Chan, B. H. K., Nell, L. A., Rabaa, M. A., Bell, A. S., ... Read, A. F. (2012). The evolutionary consequences of blood-stage vaccination on the rodent malaria Plasmodium chabaudi. PLoS biology, 10(7), 9. [e1001368]. DOI: 10.1371/journal.pbio.1001368. Publication link: d995029d-bd37-401e-ac9a-0b00eb67b077

2008

2007

2006

  • Wargo, A. R., Randle, N., Chan, B. H. K., Thompson, J., Read, A. F., & Babiker, H. A. (2006). Plasmodium chabaudi: Reverse transcription PCR for the detection and quantification of transmission stage malaria parasites. Experimental Parasitology, 112(1), 13-20. DOI: 10.1016/j.exppara.2005.08.013. Publication link: 821024b1-e0b0-40b8-976b-3039fdf61d70 | PubMed:16256988
  • Long, G. H., Chan, B. H. K., Allen, J. E., Read, A. F., & Graham, A. L. (2006). Parasite genetic diversity does not influence TNF-mediated effects on the virulence of primary rodent malaria infections. Parasitology, 133(6), 673-684. DOI: 10.1017/S003118200600117X. Publication link: 7bd7c18a-1c44-4adb-92dd-075cba39ab3a
  • Banerjee, I., Trueman, J. A., Hall, C. M., Price, D. A., Patel, L., Whatmore, A. J., ... Clayton, P. E. (2006). Phenotypic variation in constitutional delay of growth and puberty: Relationship to specific leptin and leptin receptor gene polymorphisms. European Journal of Endocrinology, 155(1), 121-126. DOI: 10.1530/eje.1.02184. Publication link: c6fa8893-89aa-4027-8291-1ca2fa5c93c2

2005

  • Blanford, S., Chan, B. H. K., Jenkins, N., Sim, D., Turner, R. J., Read, A. F., & Thomas, M. B. (2005). Fungal pathogen reduces potential for malaria transmission. Science, 308(5728), 1638-1641. DOI: 10.1126/science.1108423. Publication link: 3673797b-e09d-4486-8f5a-0521a85daf12 | PubMed:15947189
  • Tassabehji, M., Hammond, P., Karmiloff-Smith, A., Thompson, P., Thorgeireson, S. S., Durkin, M. E., ... Donnai, D. (2005). Genetics: GTF2IRD1 in craniofacial development of humans mice. Science, 310(5751), 1184-1187. DOI: 10.1126/science.1116142. Publication link: 1e252cd2-7354-47d8-b0b3-7317978e7370
  • De Roode, J. C., Pansini, R., Cheesman, S. J., Helinski, M. E. H., Huijben, S., Wargo, A. R., ... Read, A. F. (2005). Virulence and competitive ability in genetically diverse malaria infections. Proceedings of the National Academy of Sciences, 102(21), 7624-7628. DOI: 10.1073/pnas.0500078102. Publication link: 802db76f-89ca-4c22-b348-e557ecafe0f6 | PubMed:15894623
  • Sedlmeyer, I. L., Pearce, C. L., Trueman, J. A., Butler, J. L., Bersaglieri, T., Read, A. P., ... Palmert, M. R. (2005). Determination of sequence variation and haplotype structure for the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes: Investigation of role in pubertal timing. Journal of Clinical Endocrinology and Metabolism, 90(2), 1091-1099. DOI: 10.1210/jc.2004-0649. Publication link: cf27b99b-e587-4f01-b5d0-2e91afea9c85
  • Huber, C., Dias-Santagata, D., Glaser, A., O'Sullivan, J., Brauner, R., Wu, K., ... Cormier-Daire, V. (2005). Identification of mutations in CUL7 in 3-M syndrome. Nature Genetics, 37(10), 1119-1124. DOI: 10.1038/ng1628. Publication link: af9e4a2a-9079-413d-b0c1-6ccf2ca7c589

2004

  • Hewitt, C., Wilson, P., McGlinn, E., MacFarlane, G., Papageorgiou, A., Woodwards, R. T. M., ... Thakker, N. (2004). DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinoma. Cancer Letters, 209(2), 207-213. DOI: 10.1016/j.canlet.2003.12.018. Publication link: 94758e0f-d735-463c-80cd-8643eb24cc81 | PubMed:15159023
  • Hewitt, C., McCormick, D., Linden, G., Turk, D., Stern, I., Wallace, I., ... Thakker, N. (2004). The Role of Cathepsin C in Papillon-Lefèvre Syndrome, Prepubertal Periodontitis, and Aggressive Periodontitis. Human Mutation, 23(3), 222-228. DOI: 10.1002/humu.10314. Publication link: 239bf431-7901-4382-94b2-b7a4a3564c68 | PubMed:14974080
  • Hewitt, C., Wu, C. L., Hattab, F. N., Amin, W., Ghaffar, K. A., Toomes, C., ... Thakker, N. S. (2004). Coinheritance of two rare genodermatoses (Papillon-Lefèvre syndrome and oculocutaneous albinism type 1) in two families: A genetic study. British Journal of Dermatology, 151(6), 1261-1265. DOI: 10.1111/j.1365-2133.2004.06237.x. Publication link: 470d5d64-6dd6-4774-a1a2-d1d8a682ab6f | PubMed:15606524

2003

2002

2001

1999

  • Toomes, C., James, J., Wood, A. J., Wu, C. L., McCormick, D., Lench, N., ... Thakker, N. S. (1999). Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis. Nature Genetics, 23(4), 421-424. DOI: 10.1038/70525. Publication link: 25f856ad-730b-4ea3-9da6-cefda935a194 | PubMed:10581027
  • Wu, C. L., Roz, L., McKown, S., Sloan, P., Read, A. P., Holland, S., ... Thakker, N. (1999). DNA studies underestimate the major role of CDKN2A inactivation in oral and oropharyngeal squamous cell carcinomas. Genes Chromosomes and Cancer, 25(1), 16-25. . Publication link: 583557ec-7028-402a-a3fa-003842cdd4bf | PubMed:10221335
  • Tassabehji, M., Metcalfe, K., Karmiloff-Smith, A., Carette, M. J., Grant, J., Dennis, N., ... Donnai, D. (1999). Williams syndrome: Use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes. American Journal of Human Genetics, 64(1), 118-125. DOI: 10.1086/302214. Publication link: fa6be23c-2620-4348-9fab-6565b2d17662

1998

  • Wu, C. L., Thakker, N., Neary, W., Black, G., Lye, R., Ramsden, R. T., ... Evans, D. G. R. (1998). Differential diagnosis of type 2 neurofibromatosis: Molecular discrimination of NF2 and sporadic vestibular schwannomas. Journal of Medical Genetics, 35(12), 973-977. . Publication link: 1ee0a32c-a7ce-443d-8268-c6162641e667 | PubMed:9863591
  • Tassabehji, M., Metcalfe, K., Hurst, J., Ashcroft, G. S., Kielty, C., Wilmot, C., ... Jones, C. J. P. (1998). An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa. Human Molecular Genetics, 7(6), 1021-1028. DOI: 10.1093/hmg/7.6.1021. Publication link: 3352158a-d1e0-455e-9505-ffce42e6c181 | PubMed:9580666

1997

1995

  • Tassabehji, M., Newton, V. E., Liu, X. Z., Brady, A., Donnai, D., Krajewska-Walasek, M., ... Read, A. P. (1995). The mutational spectrum in waardenburg syndrome. Human Molecular Genetics, 4(11), 2131-2137. . Publication link: c5937e59-12c9-4e0a-9c30-f44f15a6820c

1994

  • Tassabehji, M., Newton, V. E., Leverton, K., Turnbull, K., Seemanova, E., Kunze, J., ... Read, A. P. (1994). PAX3 gene structure and mutations: Close analogies between Waardenburg syndrome and the Splotch mouse. Human Molecular Genetics, 3(7), 1069-1074. . Publication link: 80b6d366-14e5-4901-be27-87b6aa105004
  • Tassabehji, M., Newton, V. E., & Read, A. P. (1994). Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nature Genetics, 8(3), 251-255. DOI: 10.1038/ng1194-251. Publication link: 1531e17e-6d42-44fc-a05e-d7a82be0570a

1993

  • Tassabehji, M., Read, A. P., Newton, V. E., Patton, M., Gruss, P., Harris, R., & Strachan, T. (1993). Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2. Nature Genetics, 3(1), 26-30. DOI: 10.1038/ng0193-26. Publication link: 074cbd9f-21c0-4fab-84ad-f2a57ddfbec5