Adjunct Senior Lecturer

Dr Melody Camellia Caramins

medicine-health
School of Medical Sciences
Phone
(02) 9005 7000

Publications

  • Book Chapters | 2014
    Caramins MC, 2014, 'Approaches for classifying DNA variants found by Sanger sequencing in a medical genetics laboratory.', in Clinical Bioinformatics, Springer, pp. 227 - 250, http://dx.doi.org/10.1007/978-1-4939-0847-9_13
    Book Chapters | 2004
    Trent RJA; Yu B; Caramins M, 2004, 'Introduction of Molecular Genetics and Genomics Into Clinical Practice', in Encyclopedia of Medical Genomics and Proteomics, Informa Healthcare, pp. 676 - 681, http://dx.doi.org/10.3109/9780203997352.136
    Book Chapters | 2004
    Trent RJA; Caramins M; Yu B, 2004, 'Capillary Electrophoresis', in Encyclopedia of Medical Genomics and Proteomics, Informa Healthcare, pp. 210 - 215, http://dx.doi.org/10.3109/9780203997352.043
    Book Chapters |
    Trent RJA; Caramins M; Yu B, 'Capillary Electrophoresis', in Encyclopedia of Medical Genomics and Proteomics, pp. 210 - 215, http://dx.doi.org/10.1081/E-EMGP-120020709
    Book Chapters |
    Trent RJA; Yu B; Caramins M, 'Introduction of Molecular Genetics and Genomics Into Clinical Practice', in Encyclopedia of Medical Genomics and Proteomics, pp. 676 - 681, http://dx.doi.org/10.1081/E-EMGP-120025589
  • Journal articles | 2020
    Robson SJ; Caramins M; Saad M; Suthers G, 2020, 'Socioeconomic status and uptake of reproductive carrier screening in Australia', Australian and New Zealand Journal of Obstetrics and Gynaecology, vol. 60, pp. 976 - 979, http://dx.doi.org/10.1111/ajo.13206
    Journal articles | 2019
    Polasek T; Caramins M; Suthers G, 2019, 'Regulatory and other responses to the pharmaceutical opioid problem', Medical Journal of Australia, vol. 211, pp. 237 - 237.e1, http://dx.doi.org/10.5694/mja2.50297
    Journal articles | 2019
    Bickley L; Taylor P; Caramins M; Kennedy B, 2019, 'Expanded carrier screening identifies Iranian carrier couple', Pathology, vol. 51, pp. S119 - S119, http://dx.doi.org/10.1016/j.pathol.2018.12.340
    Journal articles | 2019
    Caramins M; Baddrick T; Carpenter K, 2019, 'Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems: results of a survey in over 50 countries', European Journal of Human Genetics, vol. 27, pp. 1761 - 1762, http://dx.doi.org/10.1038/s41431-019-0470-x
    Journal articles | 2018
    Kovalenko S; Crooks R; Provan P; de Fazio A; Taylor P; Kennedy B; Friedlander M; Caramins M, 2018, 'Tumour profiling for treatment of patients with ovarian cancers', Pathology, vol. 50, pp. S77 - S77, http://dx.doi.org/10.1016/j.pathol.2017.12.200
    Journal articles | 2017
    Cliffe S; Bagnall R; Ingles J; Bainbridge M; Caramins M; Semsarian C, 2017, 'Evaluation of illumina trusight cardiomyopathy panel testing for detection of diagnostically relevant abnormalities in hypertrophic cardiomyopathy', Pathology, vol. 49, pp. S104 - S104, http://dx.doi.org/10.1016/j.pathol.2016.12.298
    Journal articles | 2015
    Bennetts B; Caramins M; Hsu A; Lau C; Scott Mead R; Meldrum C; Suthers G; Taylor G; Tyrrell V, 2015, 'RCPA standards for clinical databases of genetic variants', Pathology, vol. 47, pp. S30 - S30, http://dx.doi.org/10.1097/01.pat.0000461412.19347.75
    Journal articles | 2015
    Caramins M; Chia N; Mulligan S, 2015, 'Evaluation of SNP microarray based chromosome testing for detection of prognostically relevant genomic abnormalities in chronic lymphocytic leukemia.', LEUKEMIA & LYMPHOMA, vol. 56, pp. 34 - 35, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000368710200042&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Journal articles | 2015
    Hamad N; Kliman D; Best OG; Caramins M; Hertzberg M; Lindeman R; Porter R; Mulligan SP, 2015, 'Chronic lymphocytic leukaemia, monoclonal B-lymphocytosis and pregnancy: Five cases, a literature review and discussion of management', British Journal of Haematology, vol. 168, pp. 350 - 360, http://dx.doi.org/10.1111/bjh.13134
    Journal articles | 2014
    Bauer DC; Gaff C; Dinger ME; Caramins M; Buske FA; Fenech M; Hansen D; Cobiac L, 2014, 'Genomics and personalised whole-of-life healthcare', Trends in molecular medicine, vol. 20, pp. 479 - 486, http://dx.doi.org/10.1016/j.molmed.2014.04.001
    Journal articles | 2014
    Kassahn KS; Scott HS; Caramins MC, 2014, 'Integrating Massively Parallel Sequencing into Diagnostic Workflows and Managing the Annotation and Clinical Interpretation Challenge', Human Mutation, vol. 35, pp. 413 - 423, http://dx.doi.org/10.1002/humu.22525
    Journal articles | 2014
    Hamad N; Kliman D; Best OG; Caramins M; Hertzberg M; Lindeman R; Porter R; Mulligan SP, 2014, 'Chronic lymphocytic leukaemia, monoclonal B-lymphocytosis and pregnancy: Five cases, a literature review and discussion of management', British Journal of Haematology, http://dx.doi.org/10.1111/bjh.13134
    Journal articles | 2014
    Bennetts B; Caramins M; Hsu A; Lau C; Mead S; Meldrum C; Smith TD; Suthers G; Taylor GR; Cotton RGH; Tyrrell V, 2014, 'Quality standards for DNA sequence variation databases to improve clinical management under development in Australia', Applied and Translational Genomics, vol. 3, pp. 54 - 57, http://dx.doi.org/10.1016/j.atg.2014.07.002
    Journal articles | 2014
    Tyrrell V; Caramins M, 2014, 'AN ALTERNATIVE MEDICAL SERVICES ADVISORY COMMITTEE (MSAC) ASSESSMENT MODEL: INHERITED CANCER AS AN EXEMPLAR', ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, vol. 10, pp. 207 - 207, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000345350900392&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Journal articles | 2014
    Bauer DC; Gaff C; Dinger ME; Caramins M; Buske FA; Fenech M; Hansen D; Cobiac L, 2014, 'Genomics and personalised whole-of-life healthcare', Trends in molecular medicine, vol. 20, pp. 479 - 486, http://dx.doi.org/10.1016/j.molmed.2014.04.001
    Journal articles | 2013
    Caramins M; Colebatch JG; Bainbridge MN; Scherer SS; Abrams CK; Hackett EL; Freidin MM; Jhangiani SN; Wang M; Wu Y; Muzny DM; Lindeman R; Gibbs RA, 2013, 'Exomesequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)', Human Molecular Genetics, vol. 22, pp. 4329 - 4338, http://dx.doi.org/10.1093/hmg/ddt282
    Journal articles | 2012
    Galea MA; Elakis G; Caramins MC, 2012, 'Validation and implementation of the amplidex fragile X test in an Australian diagnostic laboratory', Pathology, vol. 44, pp. S54 - S54, http://dx.doi.org/10.1016/s0031-3025(16)32729-5
    Journal articles | 2011
    Caramins MC; Saville T; Shakeshaft R; Mullan GL; Miller B; Yip MY; Buckley MF, 2011, 'A comparison of molecular and cytogenetic techniques for the diagnosis of pregnancy loss', Genetics in Medicine, vol. 13, pp. 46 - 51, http://dx.doi.org/10.1097/GIM.0b013e3181faa0d2
    Journal articles | 2011
    Rieubland C; Holmes AD; Caramins M; Roscioli T; Amor DJ, 2011, 'Lambdoid synostosis and craniofacial dysmorphism with normal intellect: A novel syndrome?', American Journal of Medical Genetics, Part A, vol. 155, pp. 233 - 234, http://dx.doi.org/10.1002/ajmg.a.33776
    Journal articles | 2011
    Galea MA; Mullan GL; Caramins M, 2011, 'Colouring within the lines: improving laboratory efficiency whilst maintaining compliance with quality standards', Pathology, vol. 43, pp. S68 - S68, http://dx.doi.org/10.1016/s0031-3025(16)33233-0
    Journal articles | 2010
    Galea MA; Walsh CC; Caramins M, 2010, 'Development of a prenatal quantitative fluorescent-PCR chromosome 15 aneuploidy screen', Pathology, vol. 42, pp. S62 - S62, http://dx.doi.org/10.1097/01268031-201042001-00125
    Journal articles | 2009
    James P; Culling B; Mullan GL; Jenkins MA; Elalkis G; Turners A; Mowat D; Wilson M; Anderson P; Savarirayan R; Cliffe ST; Caramins MC; Buckley MF; Tucker K; Roscioli T, 2009, 'Breast Cancer Risk Is Not Increased in Individuals with TWISTI Mutation Confirmed Saethre-Chotzen Syndrome: An Australian Multicenter Study', Genes Chromosomes and Cancer, vol. 48, pp. 533 - 538, http://dx.doi.org/10.1002/gcc.20661
    Journal articles | 2005
    Yu B; Sawyer NA; Caramins M; Yuan ZG; Saunderson RB; Pamphlett R; Richmond DR; Jeremy RW; Trent RJ, 2005, 'Denaturing high performance liquid chromatography: High throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease', Journal of Clinical Pathology, vol. 58, pp. 479 - 485, http://dx.doi.org/10.1136/jcp.2004.021642
    Journal articles | 2004
    Trent RJA; Yu B; Caramins M, 2004, 'Challenges for clinical genetic DNA testing', Expert Review of Molecular Diagnostics, vol. 4, pp. 201 - 208, http://dx.doi.org/10.1586/14737159.4.2.201
    Journal articles | 2003
    Caramins M; Halliday GM; McCusker E; Trent RJ, 2003, 'Genetically confirmed clinical Huntingdon`s disease with no observable cell loss', Journal of Neurology Neurosurgery and Psychiatry, vol. 74, pp. 968 - 970, http://dx.doi.org/10.1136/jnnp.74.7.968
  • Conference Papers | 2017
    Chia N; Caramins M, 2017, 'Deletion 13q characterised by SNP microarray profiling of a large cohort of CLL patients', in MOLECULAR CYTOGENETICS, BIOMED CENTRAL LTD, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000410864800031&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
    Conference Abstracts | 2016
    Caramins M; Chia N; Mulligan S, 2016, 'Evaluation of snp microarray based chromosome testing for detection of prognostically relevant genomic abnormalities in chronic lymphocytic leukaemia.', in Pathology, England, Vol. 48 Suppl 1, pp. S97 - S98, England, http://dx.doi.org/10.1016/j.pathol.2015.12.277
    Theses / Dissertations | 2010
    Caramins MC, 2010, Fine mapping studies of quantitative trait loci for baseline platelet count in mice and humans, University of New South Wales

Awards

Grants

Media