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Author Details

Graeme Suthers
University of Adelaide
1977
109
42
PMIDPaper TitleJournal TitlePublished Year
36465032Using a bedside test to detect genetic susceptibility to aminoglycoside-induced hearing loss: Has the future arrived?J Paediatr Child Health2023
37270788Avoiding severe drug hypersensitivity reactions: a case for HLA genotyping for at-risk patients.Med J Aust2023
36465032Using a bedside test to detect genetic susceptibility to aminoglycoside-induced hearing loss: Has the future arrived?J Paediatr Child Health2023
37270788Avoiding severe drug hypersensitivity reactions: a case for HLA genotyping for at-risk patients.Med J Aust2023
32270606Pharmacogenetics of statin intolerance.Intern Med J2020
32270606Pharmacogenetics of statin intolerance.Intern Med J2020
32748403Socioeconomic status and uptake of reproductive carrier screening in Australia.Aust N Z J Obstet Gynaecol2020
32748403Socioeconomic status and uptake of reproductive carrier screening in Australia.Aust N Z J Obstet Gynaecol2020
30327542Carrier screening "within the panel".Genet Med2019
31588874Letter to the editor: reply to Bousman <i>et al.</i>Pharmacogenomics2019
30327542Carrier screening "within the panel".Genet Med2019
31389024Regulatory and other responses to the pharmaceutical opioid problem.Med J Aust2019
30895596Comparing the performance of gene expression assays in breast cancer.Int J Cancer2019
31256470Pharmacogenomics in general practice: The time has come.Aust J Gen Pract2019
31389024Regulatory and other responses to the pharmaceutical opioid problem.Med J Aust2019
31588874Letter to the editor: reply to Bousman <i>et al.</i>Pharmacogenomics2019
31256470Pharmacogenomics in general practice: The time has come.Aust J Gen Pract2019
30895596Comparing the performance of gene expression assays in breast cancer.Int J Cancer2019
28369759Diagnostic performance and costs of contingent screening models for trisomy 21 incorporating non-invasive prenatal testing.Aust N Z J Obstet Gynaecol2017
28369759Diagnostic performance and costs of contingent screening models for trisomy 21 incorporating non-invasive prenatal testing.Aust N Z J Obstet Gynaecol2017
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
26712909Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.Blood2016
26712909Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.Blood2016
25251195Rising incidence of early-onset colorectal cancer in Australia over two decades: report and review.J Gastroenterol Hepatol2015
26181641Mosaic Epigenetic Inheritance as a Cause of Early-Onset Colorectal Cancer.JAMA Oncol2015
25251195Rising incidence of early-onset colorectal cancer in Australia over two decades: report and review.J Gastroenterol Hepatol2015
26181641Mosaic Epigenetic Inheritance as a Cause of Early-Onset Colorectal Cancer.JAMA Oncol2015
27294016Quality standards for DNA sequence variation databases to improve clinical management under development in Australia.Appl Transl Genom2014
27294016Quality standards for DNA sequence variation databases to improve clinical management under development in Australia.Appl Transl Genom2014
23370770Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins.Mod Pathol2013
23250040Clarity against the odds: standards for describing DNA sequence variants.Pathology2013
23370770Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins.Mod Pathol2013
23250040Clarity against the odds: standards for describing DNA sequence variants.Pathology2013
21813476Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome.Gut2012
22525305Cancer risks for relatives of patients with serrated polyposis.Am J Gastroenterol2012
22322191Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry.Mod Pathol2012
22991212Disease-specific databases: why we need them and some recommendations from the Human Variome Project Meeting, May 28, 2011.Am J Med Genet A2012
21813476Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome.Gut2012
22259179Quality standards and samples in genetic testing.J Clin Pathol2012
22991212Disease-specific databases: why we need them and some recommendations from the Human Variome Project Meeting, May 28, 2011.Am J Med Genet A2012
22525305Cancer risks for relatives of patients with serrated polyposis.Am J Gastroenterol2012
22322191Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry.Mod Pathol2012
22259179Quality standards and samples in genetic testing.J Clin Pathol2012
20878485An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations.Fam Cancer2011
21165777Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).Fam Cancer2011
20840664Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study.BJU Int2011
21254855"For all my family's sake, I should go and find out": an Australian report on genetic counseling and testing uptake in individuals at high risk of breast and/or ovarian cancer.Genet Test Mol Biomarkers2011
20878485An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations.Fam Cancer2011
21495936Alerting genetic relatives to a risk of serious inherited disease without a patient's consent.Med J Aust2011
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Collaborators

Kerry Phillips
Royal Adelaide Hospital
Co-authored papers 12
Jack Goldblatt
King Edward Memorial Hospital for Women
Co-authored papers 11
Bettina Meiser
Co-authored papers 9
Judy Kirk
Co-authored papers 8
Georgia Chenevix-Trench
QIMR Berghofer Medical Research Institute
Co-authored papers 7
Noralane M Lindor
Mayo Clinic
Co-authored papers 5
Stephen N Thibodeau
Mayo Clinic
Co-authored papers 5
Steven Gallinger
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto
Co-authored papers 5
Clara Gaff
Murdoch Children's Research Institute
Co-authored papers 5
Scott Grist
Australia College of Medicine and Public Health, Flinders University
Co-authored papers 5
Albert de la Chapelle
The Ohio State University Comprehensive Cancer Center
Co-authored papers 4
John A Baron
University of North Carolina at Chapel Hill
Co-authored papers 4
Daniel L Worthley
South Australian Health and Medical Research Institute
Co-authored papers 4
Charles E Schwartz
Co-authored papers 4
Amanda B Spurdle
QIMR Berghofer Medical Research Institute
Co-authored papers 4
David E Goldgar
University of Utah
Co-authored papers 3
Nicola K Poplawski
Royal Adelaide Hospital
Co-authored papers 3
Robert W Haile
Co-authored papers 3
Kevin Sweet
College of Medicine, The Ohio State University
Co-authored papers 3
Robyn L Ward
University of Sydney
Co-authored papers 3
Wendy S Rubinstein
CancerLinQ LLC, American Society of Clinical Oncology
Co-authored papers 2
Graham G Giles
Co-authored papers 2
Anna L Brown
Adelaide Medical School, University of Adelaide
Co-authored papers 2
Nicola Wayte
The Queensland Institute of Medical Research
Co-authored papers 2
David G Huntsman
University of British Columbia
Co-authored papers 2
Nicholas J Hawkins
School of Public Health, Imperial College London
Co-authored papers 2
Loic Le Marchand
Co-authored papers 2
Nicola Waddell
QIMR Berghofer Medical Research Institute
Co-authored papers 2
Jacqueline Armstrong
SA Pathology at the Women's and Children's Hospital
Co-authored papers 2
F??tima Carneiro
Centro Hospitalar Universitario de Sao Joao.
Co-authored papers 2
Release 1.2