2011

• Dale, R., Grattan-Smith, P., Fung, V., Peters, G. (2011), Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletion. Neurology. 77(14), 1401-2. [Abstract]
• Dale, R., Nasti, J., Peters, G. (2011), Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis. Movement disorders : official journal of the Movement Disorder Society. , 1774-5. [Abstract]
• Ho, G., Yonezawa, A., Masuda, S., Inui, K., Sim, K., Carpenter, K., Olsen, R., Mitchell, J., Rhead, W., Peters, G., Christodoulou, J. (2011), Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B. Human mutation. 32(1), E1976-84. [Abstract]

2010

• van Bon, B., Koolen, D., Brueton, L., McMullan, D., Lichtenbelt, K., Adès, L., Peters, G., Gibson, K., Moloney, S., Novara, F., Pramparo, T., Dalla Bernardina, B., Zoccante, L., Balottin, U., Piazza, F., Pecile, V., Gasparini, P., Guerci, V., Kets, M., Pfundt, R., de Brouwer, A., Veltman, J., de Leeuw, N., Wilson, M., Antony, J., Reitano, S., Luciano, D., Fichera, M., Romano, C., Brunner, H., Zuffardi, O., de Vries, B. (2010), The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype. European Journal of Human Genetics. 18(2), 163-170. [Abstract]
• Balasubramaniam, S., Rudduck, C., Bennetts, B., Peters, G., Wilcken, B., Ellaway, C. (2010), Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency. Molecular genetics and metabolism. 99(1), 34-41. [Abstract]
• Mahajan, H., Sharma, R., Darmanian, A., Peters, G. (2010), Fibrosarcomatous variant of dermatofibrosarcoma protuberans showing COL1A1-PDGFB gene fusion, detected using a novel and disease-specific RT-PCR protocol. Pathology. 42(5), 488-491. [Abstract]

2009

• Tan, T., Aftimos, S., Worgan, L., Susman, R., Wilson, M., Ghedia, S., Kirk, E., Love, D., Ronan, A., Darmanian, A., Slavotinek, A., Hogue, J., Moeschler, J., Ozmore, J., Widmer, R., Savarirayan, R., Peters, G. (2009), Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome. Journal of Medical Genetics. , 480-489. [Abstract]

2008

• Mihelec, M., St Heaps, L., Flaherty, M., Billson, F., Rudduck, C., Tam, P., Grigg, J., Peters, G., Jamieson, R. (2008), Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma. Twin Research and Human Genetics. 11(4), 412-421. [Abstract]
• Gabbett, M., Peters, G., Carmichael, J., Darmanian, A., Collins, F. (2008), Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region. Clinical genetics. 73(4), 353-359. [Abstract]
• Wilson, M., Peters, G., Bennetts, B., McGillivray, G., Wu, Z., Poon, C., Algar, E. (2008), The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: Two new reports. American journal of medical genetics. Part A. 146A, 137-48. [Abstract]
• Daniel, A., St Heaps, L., Sylvester, D., Diaz, S., Peters, G. (2008), Two mosaic terminal inverted duplications arising post-zygotically: Evidence for possible formation of neo-telomeres. Cell & chromosome. 7, 1. [Abstract]
• Bonaglia, M., Giorda, R., Beri, S., Peters, G., Kirk, E., Hung, D., Ciccone, R., Gottardi, G., Zuffardi, O. (2008), Concurrent transposition of distal 6p and 20q to the 22q telomere: A recurrent benign chromosomal variant. European Journal of Medical Genetics. 51(2), 148-155. [Abstract]

2007

• Daniel, A., Darmanian, A., Peters, G., Goodwin, L., Hort, J. (2007), An innocuous duplication of 11.2 Mb at 13q21 is gene poor: Sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies. American journal of medical genetics. Part A. 143A(20), 2452-9. [Abstract]
• Algar, E., St Heaps, L., Darmanian, A., Dagar, V., Prawitt, D., Peters, G., Collins, F. (2007), Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis. Cancer research. 67(5), 2360-2365. [Abstract]

2006

• Mahjoubi, F., Hill, R., Peters, G. (2006), Chromosome microdissection identifies genomic amplifications associated with drug resistance in a leukemia cell line: an approach to understanding drug resistance in cancer. Chromosome Research. 14(3), 263-276. [Abstract]