Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales
Haralambos, K, Whatley, S.D, Edwards, R, Gingell, R, Townsend, D, Ashfield-Watt, P, Lansberg, P, Datta, D.B.N, McDowell, I.F.W
Published in Atherosclerosis (01.05.2015)
Published in Atherosclerosis (01.05.2015)
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High-throughput sequence analysis reveals structural diversity and improved potency among RNA inhibitors of HIV reverse transcriptase
Ditzler, Mark A, Lange, Margaret J, Bose, Debojit, Bottoms, Christopher A, Virkler, Katherine F, Sawyer, Andrew W, Whatley, Angela S, Spollen, William, Givan, Scott A, Burke, Donald H
Published in Nucleic acids research (01.02.2013)
Published in Nucleic acids research (01.02.2013)
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Molecular epidemiology of erythropoietic protoporphyria in the U.K
Whatley, S.D., Mason, N.G., Holme, S.A., Anstey, A.V., Elder, G.H., Badminton, M.N.
Published in British journal of dermatology (1951) (01.03.2010)
Published in British journal of dermatology (1951) (01.03.2010)
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A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases
Katugampola, R.P., Anstey, A.V., Finlay, A.Y., Whatley, S., Woolf, J., Mason, N., Deybach, J.C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X., Badminton, M.N.
Published in British journal of dermatology (1951) (01.10.2012)
Published in British journal of dermatology (1951) (01.10.2012)
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Journal Article
Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases
Katugampola, R.P., Badminton, M.N., Finlay, A.Y., Whatley, S., Woolf, J., Mason, N., Deybach, J.C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X., Anstey, A.V.
Published in British journal of dermatology (1951) (01.10.2012)
Published in British journal of dermatology (1951) (01.10.2012)
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A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress
Marchbanks, R.M., Ryan, Margaret, Day, I.N.M., Owen, M., McGuffin, P., Whatley, S.A.
Published in Schizophrenia research (01.12.2003)
Published in Schizophrenia research (01.12.2003)
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Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease
Whatley, S D, Mason, N G, Khan, M, Zamiri, M, Badminton, M N, Missaoui, W N, Dailey, T A, Dailey, H A, Douglas, W S, Wainwright, N J, Elder, G H
Published in Journal of medical genetics (01.08.2004)
Published in Journal of medical genetics (01.08.2004)
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X-linked dominant protoporphyria: a new porphyria
Seager, M. J., Whatley, S. D., Anstey, A. V., Millard, T. P.
Published in Clinical and experimental dermatology (01.01.2014)
Published in Clinical and experimental dermatology (01.01.2014)
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Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients
Archer, H L, Whatley, S D, Evans, J C, Ravine, D, Huppke, P, Kerr, A, Bunyan, D, Kerr, B, Sweeney, E, Davies, S J, Reardon, W, Horn, J, MacDermot, K D, Smith, R A, Magee, A, Donaldson, A, Crow, Y, Hermon, G, Miedzybrodzka, Z, Cooper, D N, Lazarou, L, Butler, R, Sampson, J, Pilz, D T, Laccone, F, Clarke, A J
Published in Journal of medical genetics (01.05.2006)
Published in Journal of medical genetics (01.05.2006)
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Journal Article
Potent Inhibition of HIV-1 Reverse Transcriptase and Replication by Nonpseudoknot, “UCAA-motif” RNA Aptamers
Whatley, Angela S, Ditzler, Mark A, Lange, Margaret J, Biondi, Elisa, Sawyer, Andrew W, Chang, Jonathan L, Franken, Joshua D, Burke, Donald H
Published in Molecular therapy. Nucleic acids (01.02.2013)
Published in Molecular therapy. Nucleic acids (01.02.2013)
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Journal Article
Genetic testing of familial hypercholesterolaemia at BGL– a four year audit
Yarram, L, Greenslade, M, Bayly, G, Balasubramani, M, Taylor, A, Day, A, Whatley, S, McDowell, I, Williams, M
Published in Atherosclerosis (01.12.2013)
Published in Atherosclerosis (01.12.2013)
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Journal Article
Genotyping of patients with familial hypercholesterolaemia from lipid clinics in Wales
Wilson, V.C, Haralambos, K, Whatley, S, Halcox, J.P.J, Mcdowell, I.F.W
Published in Atherosclerosis (01.10.2011)
Published in Atherosclerosis (01.10.2011)
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Journal Article
The impact of routine next generation sequencing testing for familial hypercholesterolaemia – 5 months service experience
Yarram-Smith, L, Dean, P, O'Shea, S, Dennis, G, Bayly, G, Taylor, A, Day, A, Watson, M, Giles, P, Ayling, R, Haralambos, K, Whatley, S, McDowell, I, Williams, M
Published in Atherosclerosis (01.10.2014)
Published in Atherosclerosis (01.10.2014)
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Biochemical, inhibition and inhibitor resistance studies of xenotropic murine leukemia virus-related virus reverse transcriptase
Ndongwe, Tanyaradzwa P., Adedeji, Adeyemi O., Michailidis, Eleftherios, Ong, Yee Tsuey, Hachiya, Atsuko, Marchand, Bruno, Ryan, Emily M., Rai, Devendra K., Kirby, Karen A., Whatley, Angela S., Burke, Donald H., Johnson, Marc, Ding, Shilei, Zheng, Yi-Min, Liu, Shan-Lu, Kodama, Ei-Ichi, Delviks-Frankenberry, Krista A., Pathak, Vinay K., Mitsuya, Hiroaki, Parniak, Michael A., Singh, Kamalendra, Sarafianos, Stefan G.
Published in Nucleic acids research (01.01.2012)
Published in Nucleic acids research (01.01.2012)
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Journal Article
Implementation of a comprehensive gene screening test for familial hypercholesterolaemia using next generation sequencing
Dean, P, Yarram, L, Dennis, G, Bayly, G, Taylor, A, Day, A, Haralambos, K, Whatley, S, McDowell, I, Roberts, E, Greenslade, M, Williams, M
Published in Atherosclerosis (01.12.2013)
Published in Atherosclerosis (01.12.2013)
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