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Assessment of a Polygenic Risk Score for Colorectal Cancer to Predict Risk of Lynch Syndrome Colorectal Cancer.
- Published in:
- JNCI Cancer Spectrum, 2021, v. 5, n. 2, p. 1, doi. 10.1093/jncics/pkab022
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- Publication type:
- Article
Prospective Evaluation of the Addition of Polygenic Risk Scores to Breast Cancer Risk Models.
- Published in:
- JNCI Cancer Spectrum, 2021, v. 5, n. 3, p. 1, doi. 10.1093/jncics/pkab021
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- Publication type:
- Article
The Impact of a Comprehensive Risk Prediction Model for Colorectal Cancer on a Population Screening Program.
- Published in:
- JNCI Cancer Spectrum, 2020, v. 4, n. 5, p. 1, doi. 10.1093/jncics/pkaa062
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- Publication type:
- Article
Genetic testing in dementia-A medical genetics perspective.
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- International Journal of Geriatric Psychiatry, 2021, v. 36, n. 8, p. 1158, doi. 10.1002/gps.5535
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- Publication type:
- Article
Prevalence of Germline Pathogenic Variants in Renal Cancer Predisposition Genes in a Population-Based Study of Renal Cell Carcinoma.
- Published in:
- Cancers, 2024, v. 16, n. 17, p. 2985, doi. 10.3390/cancers16172985
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- Publication type:
- Article
Prospective Evaluation over 15 Years of Six Breast Cancer Risk Models.
- Published in:
- Cancers, 2021, v. 13, n. 20, p. 5194, doi. 10.3390/cancers13205194
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- Publication type:
- Article
DNA Methylation Signatures and the Contribution of Age-Associated Methylomic Drift to Carcinogenesis in Early-Onset Colorectal Cancer.
- Published in:
- Cancers, 2021, v. 13, n. 11, p. 2589, doi. 10.3390/cancers13112589
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- Publication type:
- Article
Population-Based Estimates of the Age-Specific Cumulative Risk of Breast Cancer for Pathogenic Variants in CHEK2 : Findings from the Australian Breast Cancer Family Registry.
- Published in:
- Cancers, 2021, v. 13, n. 6, p. 1378, doi. 10.3390/cancers13061378
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- Publication type:
- Article
The Use of Optimal Treatment for DLBCL Is Improving in All Age Groups and Is a Key Factor in Overall Survival, but Non-Clinical Factors Influence Treatment.
- Published in:
- Cancers, 2019, v. 11, n. 7, p. 928, doi. 10.3390/cancers11070928
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- Publication type:
- Article
Piebaldism: an autonomous autosomal dominant entity.
- Published in:
- Clinical Genetics, 1991, v. 39, n. 5, p. 330, doi. 10.1111/j.1399-0004.1991.tb03039.x
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- Publication type:
- Article
Sotos syndrome - autosomal dominant inheritance substantiated.
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- Clinical Genetics, 1985, v. 28, n. 3, p. 243, doi. 10.1111/j.1399-0004.1985.tb00393.x
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- Publication type:
- Article
The utility of genetics in inherited cancer.
- Published in:
- 2013
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- Publication type:
- Opinion
A funding model for public-good clinical trials.
- Published in:
- 2013
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- Publication type:
- Opinion
The Australasian Colorectal Cancer Family Registry.
- Published in:
- Medical Journal of Australia, 2012, v. 197, n. 9, p. 480, doi. 10.5694/mja12.11395
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- Publication type:
- Article
Polymorphism in intron 1 of the interferon-gamma gene influences both serum immunoglobulin E levels and the risk for chronic hepatitis B virus infection in Polynesians.
- Published in:
- Immunogenetics, 2007, v. 59, n. 3, p. 187, doi. 10.1007/s00251-006-0184-4
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- Publication type:
- Article
Making community voices heard in a research–health service alliance, the evolving role of the Community Advisory Group: a case study from the members' perspective.
- Published in:
- 2021
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- Publication type:
- Editorial
Study protocol: the Australian genetics and life insurance moratorium-monitoring the effectiveness and response (A-GLIMMER) project.
- Published in:
- 2021
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- Publication type:
- journal article
False-positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 4, p. 302, doi. 10.1002/pd.587
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- Publication type:
- Article
Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.
- Published in:
- Nephrology Dialysis Transplantation, 2006, v. 21, n. 3, p. 665, doi. 10.1093/ndt/gfi312
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- Publication type:
- Article
Distress and unmet needs during treatment and quality of life in early cancer survivorship: A longitudinal study of haematological cancer patients.
- Published in:
- European Journal of Haematology, 2017, v. 99, n. 5, p. 423, doi. 10.1111/ejh.12941
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- Publication type:
- Article
Insights into sudden cardiac death: exploring the potential relevance of non-diagnostic autopsy findings.
- Published in:
- European Heart Journal, 2019, v. 40, n. 10, p. 831, doi. 10.1093/eurheartj/ehy654
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- Publication type:
- Article
Familial SDHA Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma.
- Published in:
- 2013
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- Publication type:
- Journal Article
Body Mass Index, sex, non-steroidal anti-inflammatory drug medications, smoking and alcohol are differentially associated with World Health Organisation criteria and colorectal cancer risk in people with Serrated Polyposis Syndrome: an Australian case-control study.
- Published in:
- 2022
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- Publication type:
- journal article
Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?
- Published in:
- 2018
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- Publication type:
- journal article
Family history-based colorectal cancer screening in Australia: A modelling study of the costs, benefits, and harms of different participation scenarios.
- Published in:
- 2018
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- Publication type:
- journal article
Re: Microsatellite Instability and BRAF Mutation Testing in Colorectal Cancer Prognostication.
- Published in:
- 2014
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- Publication type:
- Letter to the Editor
Risks of Colorectal and Other Cancers After Endometrial Cancer for Women With Lynch Syndrome.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2013, v. 105, n. 4, p. 274, doi. 10.1093/jnci/djs525
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- Publication type:
- Article
Risks of Primary Extracolonic Cancers Following Colorectal Cancer in Lynch Syndrome.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2012, v. 104, n. 18, p. 1363, doi. 10.1093/jnci/djs351
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- Publication type:
- Article
Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2010, v. 102, n. 3, p. 193, doi. 10.1093/jnci/djp473
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- Publication type:
- Article
Genetic Diversity and Linkage Disequilibrium in the Polynesian Population of Niue Island.
- Published in:
- Human Biology, 2006, v. 78, n. 2, p. 131, doi. 10.1353/hub.2006.0031
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- Publication type:
- Article
Tumor mutational signatures in sebaceous skin lesions from individuals with Lynch syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.781
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- Publication type:
- Article
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated "Big Bang" pathway to CRC in three of the four Lynch syndromes.
- Published in:
- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00279-3
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- Publication type:
- Article
Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement.
- Published in:
- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00263-3
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- Publication type:
- Article
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
- Published in:
- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00241-1
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- Publication type:
- Article
Heterogeneity in the psychosocial and behavioral responses associated with a diagnosis of suspected Lynch syndrome in women with endometrial cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00233-1
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- Publication type:
- Article
Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families.
- Published in:
- Breast Cancer Research, 2013, v. 15, n. 1, p. 1, doi. 10.1186/bcr3392
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- Publication type:
- Article
Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families.
- Published in:
- 2013
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- Publication type:
- journal article
A Genomic Test for Colorectal Cancer Risk: Is This Acceptable and Feasible in Primary Care?
- Published in:
- Public Health Genomics, 2020, v. 23, n. 3-4, p. 110, doi. 10.1159/000508963
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- Publication type:
- Article
Healthcare System-Funded Preventive Genomic Screening: Challenges for Australia and Other Single-Payer Systems.
- Published in:
- Public Health Genomics, 2019, v. 22, n. 3/4, p. 140, doi. 10.1159/000502917
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- Publication type:
- Article
The use of a risk assessment and decision support tool (CRISP) compared with usual care in general practice to increase risk-stratified colorectal cancer screening: study protocol for a randomised controlled trial.
- Published in:
- 2018
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- Publication type:
- journal article
Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome.
- Published in:
- 2019
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- Publication type:
- journal article
Interpretation of genomic variation and disease association: the great missense mutation challenge!
- Published in:
- 2015
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- Publication type:
- Letter
Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry.
- Published in:
- 2015
- By:
- Publication type:
- Report
The influence of unmet supportive care needs on anxiety and depression during cancer treatment and beyond: a longitudinal study of survivors of haematological cancers.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Genetic variant interpretation: a primer for clinicians.
- Published in:
- Internal Medicine Journal, 2021, v. 51, n. 9, p. 1401, doi. 10.1111/imj.15485
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- Publication type:
- Article
Mainstreaming genomics: training experience of hospital medical officers at the Royal Melbourne Hospital.
- Published in:
- Internal Medicine Journal, 2021, v. 51, n. 2, p. 268, doi. 10.1111/imj.15185
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- Publication type:
- Article
Utility of immunohistochemistry for mismatch repair proteins on colorectal polyps in the familial cancer clinic.
- Published in:
- Internal Medicine Journal, 2018, v. 48, n. 11, p. 1325, doi. 10.1111/imj.13953
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- Publication type:
- Article
Absence of renal phenotype in hereditary haemorrhagic telangiectasia.
- Published in:
- Internal Medicine Journal, 2018, v. 48, n. 10, p. 1255, doi. 10.1111/imj.14059
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- Publication type:
- Article
Rare disease registries: a call to action.
- Published in:
- Internal Medicine Journal, 2017, v. 47, n. 9, p. 1075, doi. 10.1111/imj.13528
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- Publication type:
- Article
Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment.
- Published in:
- Internal Medicine Journal, 2017, v. 47, n. 6, p. 664, doi. 10.1111/imj.13429
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- Publication type:
- Article