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Number of items: 41.

Harper, Peter S. 2018. Activities and initiatives of the renewed European Society of Human Genetics (ESHG) (1992-2017). European Journal of Human Genetics 25 , S2-S5. 10.1038/ejhg.2017.141
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Harper, Peter Stanley 2017. Human genetics in troubled times and places. Hereditas 155 , 7. 10.1186/s41065-017-0042-4
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Harper, Peter 2017. Lysenko and Russian genetics: Reply to Wang & Liu. European Journal of Human Genetics 25 (10) , 1098. 10.1038/ejhg.2017.118
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Harper, Peter 2017. Some pioneers of European human genetics. European Journal of Human Genetics 10.1038/ejhg.2017.47
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Harper, Peter 2017. The European Society of Human Genetics: beginnings, early history and development over its first 25 years. European Journal of Human Genetics 10.1038/ejhg.2017.34
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Harper, Peter 2017. Recorded interviews with human and medical geneticists. Human Genetics 136 (2) , pp. 149-164. 10.1007/s00439-016-1744-9
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McKusick, Victor A. and Harper, Peter Stanley 2013. History of medical genetics. In: Rimoin, David L., Pyeritz, Reed E. and Korf, Bruce eds. Emery and Rimoin's Principles and Practice of Medical Genetics, Elsevier, pp. 1-39. (10.1016/B978-0-12-383834-6.00001-X)

Payne, Y., Williams, M., Cheadle, Jeremy Peter, Stott, N. C. H., Rowlands, M., Shickle, D., West, G., Meredith, Linda, Goodchild, M., Harper, Peter Stanley and Clarke, Angus John 2008. Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales The South Wales Cystic Fibrosis Carrier Screening Research Team. Clinical Genetics 51 (3) , pp. 153-163. 10.1111/j.1399-0004.1997.tb02445.x

Sarangi, Srikant Kumar, Bennert, Kristina, Howell, Lucy, Clarke, Angus John, Harper, Peter Stanley and Gray, Jonathon 2004. Initiation of reflective frames in counselling for Huntington's Disease predictive testing. Journal of Genetic Counselling 13 (2) , pp. 135-155. 10.1023/B:JOGC.0000018823.60761.e0

McEntagart, M, Dunstan, Melanie, Bell, C, Boltshauser, E, Donaghy, M, Harper, Peter, Williams, Nigel Melville, Teare, M. D. and Rahman, N 2002. Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness. Journal of Neurology, Neurosurgery & Psychiatry 73 (6) , p. 762. 10.1136/jnnp.73.6.762

Brain, Katherine Emma, Norman, P., Gray, Jonathon, Rogers, C., Mansel, Robert Edward and Harper, Peter 2002. A randomized trial of specialist genetic assessment: psychological impact on women at different levels of familial breast cancer risk. British Journal of Cancer 86 (2) , pp. 233-238. 10.1038/sj.bjc.6600051

Harper, Peter, Evans, R, Elliston, Linda, Ironside, J. W., Jones, Lesley and Lazarou, L. 2001. Huntington's disease intermediate allele and new variant CJD. American Journal of Human Genetics 69 (4) , p. 547.

Jones, Lesley, Duce, J., Elliston, Linda and Harper, Peter 2001. The involvement of transcriptional repressor proteins in Huntington's disease. Journal of Medical Genetics 38 (Suppl1) , S65-S65.

Sarangi, Srikant Kumar, Howell, Lucy, Bennert, Kristina, Clarke, Angus John, Harper, Peter Stanley and Gray, Jonathon 2001. The negotiation of therapeutic frames in counselling for predictive genetic testing. Journal of Medical Genetics 38 (Sup.1) , S23.

Brain, Katherine Emma, Gray, Jonathon, Norman, Paul, France, Elizabeth, Anglim, Cathy, Barton, Garry, Parsons, Evelyn Patricia, Clarke, Alan Richard, Sweetland, Helen Margaret, Tischkowitz, Marc, Myring, Jenny, Stansfield, Kate, Webster, David, Gower-Thomas, Kate, Daoud, Raouf, Gateley, Chris, Montpenny, Ian, Singhal, Hemant, Branston, Lucy, Sampson, Julian Roy, Roberts, Elizabeth, Newcombe, Robert Gordon, Cohen, David, Rogers, Cerilan, Mansel, Robert Edward and Harper, Peter Stanley 2000. Randomized trial of a specialist genetic assessment service for familial breast cancer. Journal of the National Cancer Institute 92 (16) , pp. 1345-1351. 10.1093/jnci/92.16.1345

Gray, Jonathon, Brain, Katherine Emma, Norman, Paul, Anglim, Cathy, France, Liz, Barton, Garry, Branston, Lucy, Parsons, Evelyn Patricia, Clarke, Angus John, Sampson, Julian Roy, Roberts, Elizabeth, Newcombe, Robert Gordon, Cohen, David, Rogers, Cerilan, Mansel, Robert Edward and Harper, Peter 2000. A model protocol evaluating the introduction of genetic assessment for women with a family history of breast cancer. Journal of Medical Genetics 37 (3) , pp. 192-196. 10.1136/jmg.37.3.192

Brain, Katherine Emma, Gray, Jonathon, Norman, Paul, Parsons, Evelyn Patricia, Clarke, Angus John, Rogers, Cerilan, Mansel, Robert and Harper, Peter 2000. Why do women attend familial breast cancer clinics? Journal of Medical Genetics 37 (3) , pp. 197-202. 10.1136/jmg.37.3.197

Procter, A. M., Clarke, Angus John and Harper, Peter Stanley 1999. Attitudes to genetic testing in childhood in England and Wales. American Journal of Human Genetics 65 (4) , A407-A407.

Procter, A., Clarke, Angus John and Harper, Peter Stanley 1999. Survey of genetic testing in childhood. Journal of Medical Genetics 36 (Supp 1) , S73-S73.

Harper, Peter Stanley and Clarke, Angus John 1997. Genetics, society and clinical practice. Garland Science.

Scourfield, J., Soldan, J., Gray, Jonathon, Houlihan, G. and Harper, Peter Stanley 1997. Huntington's disease: psychiatric practice in molecular genetic prediction and diagnosis. British Journal of Psychiatry 170 (2) , pp. 146-149. 10.1192/bjp.170.2.146

Gray, Jonathon Richard, Soldan, J. R. and Harper, Peter Stanley 1996. Special problems of genetic counseling in adult-onset diseases: Huntington’s disease as a model. In: Baker, H. F. and Ridley, R. M. eds. Prion Diseases, Methods in Molecular Medicine, vol. 3. Humana Press, pp. 199-210. (10.1385/0-89603-342-2:199)

Clarke, Angus John, Harper, Peter Stanley, Unsworth, P. F., Scotson, John and Doherty, Peter 1995. Eugenics in China. The Lancet 346 (8973) , pp. 508-509. 10.1016/S0140-6736(95)91358-0

Harper, Peter Stanley and Clarke, Angus John 1995. An ethical debate: testing may be unhelpful. British Medical Journal (BMJ) 310 (6983) , p. 857. 10.1136/bmj.310.6983.857

James, C, Houlihan, G. D., Snell, Russell G., Cheadle, Jeremy Peter and Harper, Peter Stanley 1994. Late-onset Huntington's Disease: a clinical and molecular study. Age and Ageing 23 (6) , pp. 445-448. 10.1093/ageing/23.6.445

Fenton-May, J., Bradley, D. M., Sibert, J. R., Smith, R., Parsons, Evelyn Patricia, Harper, Peter Stanley and Clarke, Angus John 1994. Screening for Duchenne muscular dystrophy. Archives of Disease in Childhood 70 (6) , pp. 551-552. 10.1136/adc.70.6.551

Upadhyaya, Meena, Roberts, S. H., Farnham, J., MacMillan, J.C., Clarke, Angus John, Heath, Jeremy P., Hodges, I. C. G. and Harper, Peter Stanley 1993. Charcot-Marie-Tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2→12. Human Genetics 91 (4) , pp. 392-394. 10.1007/BF00217365

Harper, Peter Stanley and Clarke, Angus John 1993. Screening for hypertrophic cardiomyopathy. British Medical Journal (BMJ) 306 (6881) , pp. 859-860. 10.1136/bmj.306.6881.859-c

MacMillan, J. C., Snell, R. G., Tyler, A., Houlihan, G. D., Fenton, I., Cheadle, Jeremy Peter, Lazarou, L. P., Shaw, J. D. and Harper, Peter Stanley 1993. Molecular analysis and clinical correlations of the Huntington's disease mutation. The Lancet 342 (8877) , pp. 954-958. 10.1016/0140-6736(93)92002-B

Snell, Russell G., MacMillan, John C., Cheadle, Jeremy Peter, Fenton, Iain, Lazarou, Lazarus P., Davies, Peter, MacDonald, Marcy E., Gusella, James F., Harper, Peter Stanley and Shaw, Duncan J. 1993. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nature Genetics 4 (4) , pp. 393-397. 10.1038/ng0893-393

al-Jader, Layla N., Meredith, Alison L., Ryley, Henry Charles, Cheadle, Jeremy P., Maguire, S., Owen, G., Goodchild, M. C. and Harper, Peter Stanley 1992. Severity of chest disease in cystic fibrosis patients in relation to their genotypes. Journal of Medical Genetics 29 (12) , pp. 883-887. 10.1136/jmg.29.12.883

Clarke, Angus John and Harper, Peter Stanley 1992. Genetic testing for hypertrophic cardiomyopathy. New England Journal of Medicine 327 (16) , pp. 1175-1176. 10.1056/NEJM199210153271616

Zonana, J., Jones, M., Browne, D, Kramer, P., Litt, M., Barker, D., Clarke, Angus John, Thomas, Nicholas Stuart Tudor and Harper, Peter Stanley 1991. Fine mapping of the X-linked hypohidrotic ectodermal dysplasia locus (EDA). American Journal of Human Genetics 49 (4) , p. 209.

Clarke, Angus John, Cole, J. and Harper, Peter Stanley 1991. Testing of children for genetic-disorders. American Journal of Human Genetics 49 (4) , p. 179.

Harper, Peter Stanley and Clarke, Angus John 1990. Should we test children for "adult" genetic diseases? The Lancet 335 (8699) , pp. 1205-1206. 10.1016/0140-6736(90)92713-R

Zonana, Jonathan, Sarfarazi, Mansoor, Thomas, Nicholas Stuart Tudor, Clarke, Angus John, Marymee, Kathi and Harper, Peter Stanley 1989. Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis. The Journal of Pediatrics 114 (3) , pp. 392-399. 10.1016/S0022-3476(89)80556-6

Zonana, J., Clarke, Angus John, Thomas, Nicholas Stuart Tudor, Sarfarazi, M., Roberts, K., Marymee, K. and Harper, Peter Stanley 1988. Linkage analysis of x-linked hypohidrotic ectodermal dysplasia: implications for carrier detection and prenatal diagnosis. Journal of Medical Genetics 25 (4) , p. 274. 10.1136/jmg.25.4.274

Zonana, J., Clarke, Angus John, Sarfarazi, M., Thomas, Nicholas Stuart Tudor, Roberts, K., Marymee, K. and Harper, Peter Stanley 1988. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis. American Journal of Human Genetics 43 (1) , pp. 75-85.

Clarke, Angus John, Phillips, D. I., Brown, R. and Harper, Peter Stanley 1987. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia. Archives of Disease in Childhood 62 (10) , pp. 989-996. 10.1136/adc.62.10.989

Clarke, Angus John, Sarfarazi, M., Thomas, Nicholas Stuart Tudor, Roberts, K. and Harper, Peter Stanley 1987. X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization. Human Genetics 75 (4) , pp. 378-380. 10.1007/BF00284112

Clarke, Angus John, Roberts, S. H., Thomas, Nicholas Stuart Tudor, Whitfield, A., Williams, J. and Harper, Peter Stanley 1986. Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies. Journal of Medical Genetics 23 (6) , pp. 501-508. 10.1136/jmg.23.6.501

This list was generated on Thu Dec 12 09:49:26 2019 GMT.