Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients.

Autor: Masson AL; Centre for Information-Based Medicine, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, 2305, Australia; School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, New South Wales, 2308, Australia., Talseth-Palmer BA; Centre for Information-Based Medicine, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, 2305, Australia; School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, New South Wales, 2308, Australia., Evans TJ; Centre for Information-Based Medicine, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, 2305, Australia; School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, New South Wales, 2308, Australia., McElduff P; Centre for Public Health, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, 2305, Australia; School of Medicine and Public Health, Faculty of Health and Medicine, University of Newcastle, New South Wales, 2308, Australia., Spigelman AD; Hunter Family Cancer Service, Hunter New England Area Health, Newcastle, New South Wales, 2305, Australia; University of NSW, St Vincent's Hospital Clinical School, Sydney, New South Wales, 2010, Australia; Hereditary Cancer Clinic, St Vincent's Hospital, The Kinghorn Cancer Centre, Sydney, New South Wales, 2010, Australia., Hannan GN; CSIRO Food and Nutrition Flagship, North Ryde, New South Wales, 2113, Australia., Scott RJ; Centre for Information-Based Medicine, Hunter Medical Research Institute, University of Newcastle, Newcastle, New South Wales, 2305, Australia; School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, New South Wales, 2308, Australia; Division of Molecular Medicine, Hunter Area Pathology Service, John Hunter Hospital, Newcastle, New South Wales, 2305, Australia.

Publikováno v: Meta gene [Meta Gene] 2015 Dec 24; Vol. 7, pp. 95-104. Date of Electronic Publication: 2015 Dec 24 (Print Publication: 2016).

Expanding the genetic basis of copy number variation in familial breast cancer.

Autor: Masson AL; Information Based Medicine Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, NSW 2305, Australia ; School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle, Newcastle, NSW 2308, Australia., Talseth-Palmer BA; Information Based Medicine Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, NSW 2305, Australia ; School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle, Newcastle, NSW 2308, Australia., Evans TJ; Information Based Medicine Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, NSW 2305, Australia ; School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle, Newcastle, NSW 2308, Australia., Grice DM; Information Based Medicine Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, NSW 2305, Australia ; CSIRO Preventative Health Flagship and Animal, CSIRO Food and Health Sciences Division, North Ryde, NSW 2113, Australia., Hannan GN; CSIRO Preventative Health Flagship and Animal, CSIRO Food and Health Sciences Division, North Ryde, NSW 2113, Australia., Scott RJ; Information Based Medicine Program, Hunter Medical Research Institute, University of Newcastle, Newcastle, NSW 2305, Australia ; Division of Molecular Medicine, Hunter Area Pathology Service, John Hunter Hospital, Newcastle, NSW 2305, Australia ; School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle, Newcastle, NSW 2308, Australia.

Publikováno v: Hereditary cancer in clinical practice [Hered Cancer Clin Pract] 2014 May 24; Vol. 12 (1), pp. 15. Date of Electronic Publication: 2014 May 24 (Print Publication: 2014).

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.

Autor: Talseth-Palmer BA; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, NSW, Australia. Bente.Talseth-Palmer@newcastle.edu.au, Holliday EG, Evans TJ, McEvoy M, Attia J, Grice DM, Masson AL, Meldrum C, Spigelman A, Scott RJ

Publikováno v: BMC medical genomics [BMC Med Genomics] 2013 Mar 26; Vol. 6, pp. 10. Date of Electronic Publication: 2013 Mar 26.

Increasing output and low publication rate of Brazilian studies presented at the American Society of Clinical Oncology Annual Meetings.

Autor: Saad ED, Pinheiro CM, Masson AL, Borghesi G, Hoff PM, Prisco FE

Publikováno v: Clinics (Sao Paulo, Brazil) [Clinics (Sao Paulo)] 2008 Jun; Vol. 63 (3), pp. 293-6.