Downes, SM., Fitzke, FW., Holder, GE., Payne, AM., Bessant, DAR., Bhattacharya, SS. and Bird, AC. et al. (1999) 'Clinical features of codon 172 RDS macular dystrophy: Similar phenotype in 12 families'. Archives of Ophthalmology, 117 (10). pp. 1373 - 1383. ISSN: 0003-9950

Bessant, DAR., Anwar, K., Khaliq, S., Hameed, A., Ismail, M., Payne, AM., Mehdi, SQ. and Bhattacharya, SS. et al. (1999) 'Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32'. British Journal of Ophthalmology, 83 (8). pp. 919 - 922. ISSN: 0007-1161

Bessant, DA., Khaliq, S., Hameed, A., Anwar, K., Payne, AM., Mehdi, SQ. and Bhattacharya, SS. et al. (1999) 'Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online.'. Human mutation, 13 (1). pp. 83. ISSN: 1059-7794

Kučinskas, V., Payne, AM., Ambrasiene, D., Jurgelevičius, V., Steponavičiute, D., Arčiuliene, JV., Daktaravičiene, E. and Bhattacharya, S. et al. (1999) 'Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients'. Human Heredity, 49 (2). pp. 71 - 74. ISSN: 0001-5652

Bhattacharya, SS., Bessant, DAR., Payne, AM., Mitton, KP., Zack, DJ. and Swaroop, A. (1999) 'A mutation in the bZIP transcription factor NRL is associated with autosomal dominant retinitis pigmentosa in a family linked to a novel locus at 14q11'.ARVO 1999.  [unpublished]

Swaroop, A., Evans, A., Swain, PK., Wang, QL., Mitton, K., Wu, W., Cook, J., Xu, S., Bessant, DAR., Payne, AM., Chen, S., Zack, D., Sieving, PA. and Bhattacharya, SS. et al. (1999) 'Gene regulation and retinal diseases: Studies on NRL, CRX and associated transcription factors'. Investigative Ophthalmology and Visual Science, 40 (4). pp. 891 - 891. ISSN: 1552-5783

Payne, AM., Khaliq, S., Hameed, A., Ismail, M., Bessant, DAR., Mehdi, SQ. and Bhattacharya, SS. et al. (1999) 'Localisation of a gene for autosomal recessive cone-rod dystrophy to chromosome'. Investigative Ophthalmology and Visual Science, 40 (4). pp. 16624 - 16624. ISSN: 1552-5783

Hameed, A., Khaliq, S., Ismail, M., Ebenezer, ND., Jordan, T., Mehdi, SQ., Payne, AM. and Bhattacharya, SS. et al. (1999) 'A novel locus for Leber congential amaurosis (LCA) with anterior keratoconus mapping to chromosome'. American Journal of Human Genetics, 65 (4). pp. 1408 - 1408. ISSN: 1537-6605

Grammatopoulos, D., Dai, Y., Chen, J., Karteris, E., Papadopoulou, N., Easton, AJ. and Hillhouse, EW. et al. (1998) 'Human corticotropin-releasing hormone receptor: Differences in subtype expression between pregnant and nonpregnant myometria'. Journal of Clinical Endocrinology and Metabolism, 83 (7). pp. 2539 - 2544. ISSN: 0021-972X

Höfken, T., Linder, D., Kleene, R., Göke, B. and Wagner, ACC. (1998) 'Membrane dipeptidase and glutathione are major components of pig pancreatic zymogen granules'. Experimental Cell Research, 244 (2). pp. 481 - 490. ISSN: 0014-4827

Slijepcevic, P. (1998) 'Telomere length regulation - A view from the individual chromosome perspective'. Experimental Cell Research, 244 (1). pp. 268 - 274. ISSN: 0014-4827

Votruba, M., Payne, A., Moore, AT. and Bhattacharya, SS. (1998) 'Dominant optic atrophy: Exclusion and fine genetic mapping of the candidate gene, HRY'. Mammalian Genome, 9 (10). pp. 784 - 787. ISSN: 0938-8990

Kortenkamp, A. and Altenburger, R. (1998) 'Synergisms with mixtures of xenoestrogens: A reevaluation using the method of isoboles'. Science of the Total Environment, 221 (1). pp. 59 - 73. ISSN: 0048-9697

Themis, M., Forbes, SJ., Chan, L., Cooper, RG., Etheridge, CJ., Miller, AD., Hodgson, HJ. and Coutelle, C. et al. (1998) 'Enhanced in vitro and in vivo gene delivery using cationic agent complexed retrovirus vectors'. Gene Therapy, 5 (9). pp. 1180 - 1186. ISSN: 0969-7128

Slijepcevic, P. (1998) 'Telomere length and telomere-centromere relationships?'.4th International Symposium on Chromosomal Aberrations. UNIV ESSEN, ESSEN, GERMANY. 3 - 29 August. Elsevier BV. pp. 215 - 220. ISSN: 0027-5107

Roberts, T., Chernova, O. and Cowell, JK. (1998) 'NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma'. Human Molecular Genetics, 7 (7). pp. 1169 - 1178. ISSN: 0964-6906

Kelsell, RE., Gregory-Evans, K., Payne, AM., Perrault, I., Kaplan, J., Yang, RB., Garbers, DL., Bird, AC., Moore, AT. and Hunt, DM. et al. (1998) 'Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy'. Human Molecular Genetics, 7 (7). pp. 1179 - 1184. ISSN: 0964-6906

King, JA., Bridger, JM., Löchelt, M., Lichter, P., Schulz, TF., Schirrmacher, V. and Khazaie, K. et al. (1998) 'Nucleocytoplasmic transport of HTLV-1 RNA is regulated by two independent LTR encoded nuclear retention elements'. Oncogene, 16 (25). pp. 3309 - 3316. ISSN: 0950-9232

Kortenkamp, A. (1998) 'Chromium biomonitoring - Achievements, problems, and future challenges'.2nd International Symposium on Metals and Genetics. TORONTO, CANADA. 26 - 29 May. KLUWER ACADEMIC/PLENUM PUBL. pp. 87 - 100.

Slijepcevic, P. (1998) 'Telomeres and mechanisms of Robertsonian fusion'. Chromosoma, 107 (2). pp. 136 - 140. ISSN: 0009-5915

Elliott, DJ., Oghene, K., Makarov, G., Makarova, O., Hargreave, TB., Chandley, AC., Eperon, IC. and Cooke, HJ. et al. (1998) 'Dynamic changes in the subnuclear organisation of pre-mRNA splicing proteins and RBM during human germ cell development'. Journal of Cell Science, 111 (9). pp. 1255 - 1265. ISSN: 0021-9533

Slijepcevic, P. and Bryant, PE. (1998) 'Chromosome healing, telomere capture and mechanisms of radiation- induced chromosome breakage'. International Journal of Radiation Biology, 73 (1). pp. 1 - 13. ISSN: 0955-3002

Höfken, T., Linder, D., Kleene, R., Göke, B. and Wagner, ACC. (1998) 'Regulation of pancreatic membrane dipeptidase mRNA expression and identification as zymogen granule membrane protein by peptide sequencing'. Elsevier BV. pp. A469 - A469. ISSN: 0016-5085

Karteris, E., Grammatopoulos, D., Dai, Y., Olah, KB., Ghobara, TB., Easton, A. and Hillhouse, EW. et al. (1998) 'The human placenta and fetal membranes express the corticotropin-releasing hormone receptor 1alpha (CRH-1alpha) and the CRH-C variant receptor.'. J Clin Endocrinol Metab, 83 (4). pp. 1376 - 1379. ISSN: 0021-972X

Wilmen, A., Strowski, M., Höfken, T., Prinz, H., Göke, B. and Wagner, ACC. (1998) 'Differential regulation of pancreatic genes during experimental pancreatitis, investigated by differential display analysis'. Elsevier BV. pp. A510 - A510. ISSN: 0016-5085

Papaioannou, M., Payne, AM., Rougas, C., Bessant, D., Loutradis-Anagnostou, A., Balassopoulou, A. and Bhattacharya, S. et al. (1998) 'Mutation screening in the photoreceptor-specific gene (CRX) in patients of Greek origin'. Investigative Ophthalmology and Visual Science, 39 (4). ISSN: 1552-5783

Woodcock, SC., Raux, EC., Evans, A., Dalvin, ST., Payne, AM., Downes, SM., Bird, AC., Bhattacharya, SS., Hunt, DM. and Warren, MJ. et al. (1998) 'Characterization of the Y99C mutant of a guanylate cyclase activator protein 1 (GCAP1)'. Investigative Ophthalmology and Visual Science, 39 (4). ISSN: 1552-5783

Slijepcevic, P. and Bryant, PE. (1998) 'Reply to J. P. Murnane's Letter to the Editor'. Radiation Research, 149 (3). pp. 310 - 310. ISSN: 0033-7587

Tosi, S., Giudici, G., Mosna, G., Harbott, J., Specchia, G., Grosveld, G., Prìvitera, E., Kearney, L., Biondi, A. and Cazzaniga, G. et al. (1998) 'Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies'. Genes Chromosomes and Cancer, 21 (3). pp. 223 - 229. ISSN: 1045-2257

Slijepcevic, P., Natarajan, AT. and Bryant, PE. (1998) 'Telomeres and radiation-induced chromosome breakage'. Mutagenesis, 13 (1). pp. 45 - 49. ISSN: 0267-8357

Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Holder, GE., Warren, MJ., Bird, AC. and Bhattacharya, SS. et al. (1998) 'A mutation in guanylate cyclase activator 1A(GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1'. Human Molecular Genetics, 7 (2). pp. 273 - 277. ISSN: 0964-6906

Papaioannou, M., Bessant, D., Payne, A., Bellingham, J., Rougas, C., Loutradis-Anagnostou, A., Gregory-Evans, C., Balassopoulou, A. and Bhattacharya, S. et al. (1998) 'A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q'. Journal of Medical Genetics, 35 (5). pp. 429 - 431. ISSN: 0022-2593

Hopwood, P., Harvey, A., Davies, J., Stephens, RJ., Girling, DJ., Gibson, D., Parmar, MKB., Blechen, NM., Bolger, JJ., Clark, PI., Connolly, CK., Hasleton, PS., Hopwood, P., Macbeth, FR., Moghissi, K., Saunders, MI., Thatcher, N., White, RJ., Barren, A., Bomford, CK., Cottier, B., Coyle, D., Crellin, AM., Dawes, PJK., Dische, S., Drummond, MF., Gaffney, C., Galpine, A., Gibson, D., Henk, JM., Herrmann, T., Littbrand, B., Linier, J., Morgan, DAL., Newman, H., Robertson, AG., Robinson, MH., Rothwell, RI., Symonds, RP., Tobias, JS., Whipp, MJ. and Yosef, HMA. et al. (1998) 'Survey of the administration of quality of life (QL) questionnaires in three multicentre randomised trials in cancer'. European Journal of Cancer, 34 (1). pp. 49 - 57. ISSN: 0959-8049

Sokal, I., Li, N., Surgucheva, I., Warren, MJ., Payne, AM., Bhattacharya, SS., Baehr, W. and Palczewski, K. et al. (1998) 'GCAP1(Y99C) mutant is constitutively active in autosomal dominant cone dystrophy'. Molecular Cell, 2 (1). pp. 129 - 133. ISSN: 1097-2765

Payne, AM., Downes, SM., Bessant, DAR., Bird, AC. and Bhattacharya, SS. (1998) 'Founder effect, seen in the British population, of the 172 peripherin/RDS mutation- and further refinement of genetic positioning of the peripherin/RDS gene [2]'. American Journal of Human Genetics, 62 (1). pp. 192 - 195. ISSN: 0002-9297

Bessant, DAR., Payne, AM., Plant, C., Bird, AC. and Bhattacharya, SS. (1998) 'Further refinement of the Usher 2A locus at 1q41'. Journal of Medical Genetics, 35 (9). pp. 773 - 774. ISSN: 0022-2593

Bessant, DAR., Khaliq, S., Hameed, A., Anwar, K., Mehdi, SQ., Payne, AM. and Bhattacharya, SS. et al. (1998) 'A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32'. American Journal of Human Genetics, 62 (5). pp. 1113 - 1116. ISSN: 0002-9297

Roberts, T., Chernova, O. and Cowell, JK. (1998) 'Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)'. Cancer Genetics and Cytogenetics, 100 (1). pp. 10 - 20. ISSN: 0165-4608

Bridger, JM., Herrmann, H., Muenkel, C. and Lichter, P. (1998) 'Identification of an interchromosomal compartment by polymerization of nuclear-targeted vimentin'. Journal of Cell Science, 111 (9). pp. 1241 - 1253. ISSN: 0021-9533 Open Access Link

Weber, RG., Bridger, JM., Benner, A., Weisenberger, D., Ehemann, V., Reifenberger, G. and Lichter, P. et al. (1998) 'Centrosome amplification as a possible mechanism for numerical chromosome aberrations in cerebral primitive neuroectodermal tumors with TP53 mutations'. Cytogenet Cell Genetics, 83 (3-4). pp. 266 - 269. ISSN: 0301-0171 Open Access Link

King, JA., Bridger, JM., Gounari, F., Lichter, P., Schulz, TF., Schirrmacher, V. and Khazaie, K. et al. (1998) 'The extended packaging sequence of MoMLV contains a constitutive mRNA nuclear export function'. FEBS Letters, 434 (3). pp. 367 - 371. ISSN: 0014-5793

Bridger, JM., Kill, IR. and Lichter, P. (1998) 'Association of pKi-67 with satellite DNA of the human genome in early G(1) cells'. Chromosome Research, 6 (1). pp. 13 - 24. ISSN: 0967-3849

Forbes, SJ., Themis, M., Alison, MR., Selden, C., Coutelle, C. and Hodgson, HJF. (1998) 'Retroviral gene transfer to the liver in vivo during tri-iodothyronine induced hyperplasia'. Gene Therapy, 5 (4). pp. 552 - 555. ISSN: 0969-7128

Bridger, JM. and Bickmore, WA. (1998) 'Putting the genome on the map'. Trends in Genetics, 14 (10). pp. 403 - 409. ISSN: 0168-9525 Open Access Link

Slijepcevic, P., Hande, MP., Bouffler, SD., Lansdorp, P. and Bryant, PE. (1997) 'Telomere length, chromatin structure and chromosome fusigenic potential'. Chromosoma, 106 (7). pp. 413 - 421. ISSN: 0009-5915

Tosi, S., Scherer, SW., Biondi, A., Giudici, G. and Kearney, L. (1997) 'Cryptic deletion in 7q22 associated with a t(7;7) defines a new commonly deleted segment in myeloid malignancies'. Blood, 90 (10). pp. 292 - 292. ISSN: 0006-4971

Tosi, S., Scherer, SW., Biondi, A., Giudici, G. and Kearney, L. (1997) 'Cryptic deletion in 7q22 associated with a t(7;7) defines a new commonly deleted segment in myeloid malignancies. (Abstract)'. W B Saunders co. pp. 292 - 292. ISSN: 0006-4971

Kortenkamp, A., Jones, C. and Baker, J. (1997) 'Genotypic selection of mutated DNA sequences using mismatch cleavage analysis, a possible basis for novel mutation assays'. Mutagenesis, 12 (5). pp. 335 - 338. ISSN: 0267-8357

Lampel, S., Bridger, JM., Zirbel, R., Mathieu, U. and Lichter, P. (1997) 'Nuclear RNA accumulations represent released transcripts and exhibit specific distributions with respect to Sm antigens domains'. DNA and Cell Biology, 16 (10). pp. 1133 - 1142. ISSN: 1044-5498 Open Access Link

Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Fitzke, FW., Holder, G., Bird, AC. and Bhattacharya, S. et al. (1997) 'New locus for autosomal dominant cone dystrophy mapping to 6p21.1.'. CELL PRESS. pp. A290 - A290. ISSN: 0002-9297

Wilmen, A., Strowski, M., Hofken, T., Fuller, P., Printz, H., Goke, B. and Wagner, ACC. et al. (1997) 'Differential display analysis reveals differential regulation of pancreatic genes during experimental pancreatitis'. GUT. pp. A75 - A75. ISSN: 0017-5749