John Hopper
#78,015
Most Influential Person Now
Australian epidemiologist
John Hopper 's AcademicInfluence.com Rankings
John Hopper medical Degrees
Medical
#900
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#1161
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Epidemiology
#118
World Rank
#129
Historical Rank
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John Hopper 's Degrees
- Masters Epidemiology University of Melbourne
Why Is John Hopper Influential?
(Suggest an Edit or Addition)According to Wikipedia, John L. Hopper is an Australian genetic epidemiologist and professor at the University of Melbourne, where he is a Professorial Fellow and Director of the Centre for Epidemiology and Biostatistics in the School of Population Global Health. He is also a National Health and Medical Research Council Senior Principal Research Fellow, and was one of the first nine Australia Fellows chosen by the NHMRC in 2007. Since 1990, he has been the director of Twins Research Australia .
John Hopper 's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. (2003) (3543)
- Genome-wide association study identifies novel breast cancer susceptibility loci (2007) (2351)
- Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers (2017) (1644)
- Genetic determinants of bone mass in adults. A twin study. (1987) (1269)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk (2013) (1063)
- Association analysis identifies 65 new breast cancer risk loci (2017) (922)
- A Prospective Population‐Based Study of Menopausal Symptoms (2000) (874)
- Multiple newly identified loci associated with prostate cancer susceptibility (2008) (866)
- Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. (2002) (805)
- Alcohol, tobacco and breast cancer – collaborative reanalysis of individual data from 53 epidemiological studies, including 58 515 women with breast cancer and 95 067 women without the disease (2002) (781)
- Menarche, menopause, and breast cancer risk: individual participant meta-analysis, including 118 964 women with breast cancer from 117 epidemiological studies (2012) (745)
- Reduced bone mass in daughters of women with osteoporosis. (1989) (623)
- A common coding variant in CASP8 is associated with breast cancer risk (2007) (591)
- A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 (2008) (578)
- Mammographic breast density as an intermediate phenotype for breast cancer. (2005) (571)
- Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. (2005) (571)
- Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (2018) (559)
- MicroRNA Related Polymorphisms and Breast Cancer Risk (2014) (557)
- Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array (2012) (550)
- Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies. (2011) (536)
- Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer (2013) (534)
- Extensions to multivariate normal models for pedigree analysis (1982) (529)
- Iron-overload-related disease in HFE hereditary hemochromatosis. (2008) (519)
- The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations. (2008) (516)
- Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
- Genetics of asthma and hay fever in Australian twins. (1990) (510)
- Preoperative MRI predicts outcome of temporal lobectomy (1995) (509)
- Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2 (2009) (502)
- Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer (2015) (502)
- Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants (2015) (471)
- Heritability of mammographic density, a risk factor for breast cancer. (2002) (457)
- Identification of Lynch syndrome among patients with colorectal cancer. (2012) (456)
- Genome-wide association study identifies three loci associated with melanoma risk (2009) (444)
- A prospective longitudinal study of serum testosterone, dehydroepiandrosterone sulfate, and sex hormone-binding globulin levels through the menopause transition. (2000) (444)
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study (2009) (428)
- A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma (2011) (414)
- Genome-wide association studies identify four ER negative–specific breast cancer risk loci (2013) (411)
- The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions (2008) (403)
- Prospectively measured levels of serum follicle-stimulating hormone, estradiol, and the dimeric inhibins during the menopausal transition in a population-based cohort of women. (1999) (390)
- Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics (2008) (390)
- Epilepsies in twins: Genetics of the major epilepsy syndromes (1998) (387)
- Colon Cancer Family Registry: An International Resource for Studies of the Genetic Epidemiology of Colon Cancer (2007) (373)
- Cancer Risk in Relatives of Patients with Common Colorectal Cancer (1993) (371)
- Breast-cancer risk in families with mutations in PALB2. (2014) (367)
- RAD51B in Familial Breast Cancer (2016) (366)
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017) (359)
- A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population (2010) (357)
- Multiple loci with different cancer specificities within the 8q24 gene desert. (2008) (357)
- Type and timing of menopausal hormone therapy and breast cancer risk: individual participant meta-analysis of the worldwide epidemiological evidence (2019) (350)
- Risks of Lynch syndrome cancers for MSH6 mutation carriers. (2010) (346)
- The endocrinology of the menopausal transition: a cross-sectional study of a population-based sample. (1995) (338)
- Menopausal symptoms in Australian women (1993) (334)
- Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study. (2007) (321)
- Obesity and Outcomes in Premenopausal and Postmenopausal Breast Cancer (2005) (317)
- Multiple loci on 8q24 associated with prostate cancer susceptibility (2009) (316)
- Epileptic seizures in acute stroke. (1990) (316)
- The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer (2004) (309)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. (2013) (300)
- Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. (2012) (300)
- Childhood predictors of lung function trajectories and future COPD risk: a prospective cohort study from the first to the sixth decade of life. (2018) (298)
- Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study (2011) (295)
- Identification of IL6R and chromosome 11q13.5 as risk loci for asthma (2011) (294)
- Key concepts in genetic epidemiology (2005) (293)
- Bone turnover markers and bone density across the menopausal transition. (1996) (293)
- Genome-wide association analysis identifies three new breast cancer susceptibility loci (2012) (291)
- Should Older People in Residential Care Receive Vitamin D to Prevent Falls? Results of a Randomized Trial (2005) (290)
- Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (2019) (280)
- Discovery of common and rare genetic risk variants for colorectal cancer (2018) (279)
- Dominant negative ATM mutations in breast cancer families. (2002) (275)
- Factors in childhood as predictors of asthma in adult life (1994) (268)
- Antihypertensive Treatments Obscure Familial Contributions to Blood Pressure Variation (2003) (268)
- Mammographic density phenotypes and risk of breast cancer: a meta-analysis. (2014) (266)
- The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations (1998) (259)
- Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer (2016) (253)
- Genome-wide association study identifies three new melanoma susceptibility loci (2011) (252)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
- Stroke topography and outcome in relation to hyperglycaemia and diabetes. (1992) (249)
- Distinct molecular pathogeneses of early-onset breast cancers in BRCA1 and BRCA2 mutation carriers: a population-based study. (1999) (248)
- Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery (2010) (247)
- Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer (2017) (244)
- Genetic factors in bone turnover. (1991) (240)
- Common sequence variants on 20q11.22 confer melanoma susceptibility (2008) (238)
- Serum Vitamin D and Falls in Older Women in Residential Care in Australia (2003) (236)
- Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk (2012) (234)
- Familial temporal lobe epilepsy: A common disorder identified in twins (1996) (225)
- Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers. (2013) (225)
- Bone density determinants in elderly women: A twin study (1995) (220)
- Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk (2014) (218)
- Sunbed use during adolescence and early adulthood is associated with increased risk of early‐onset melanoma (2011) (215)
- Childhood allergic rhinitis predicts asthma incidence and persistence to middle age: a longitudinal study. (2007) (213)
- Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer. (2005) (212)
- Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers (2012) (210)
- Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome. (2012) (207)
- Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent (2016) (205)
- Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer (2011) (204)
- Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study. (2009) (202)
- Molecular Characterization of MSI-H Colorectal Cancer by MLHI Promoter Methylation, Immunohistochemistry, and Mismatch Repair Germline Mutation Screening (2008) (201)
- Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance. (2006) (201)
- Rare variants in the ATM gene and risk of breast cancer (2011) (200)
- Changes in axial bone density with age: A twin study (1993) (199)
- Meta-analysis of new genome-wide association studies of colorectal cancer risk (2012) (197)
- Determinants of bone mass in 10‐ to 26‐year‐old females: A twin study (1995) (196)
- Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families. (2019) (196)
- Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. (2011) (196)
- Sexuality, hormones and the menopausal transition. (1997) (196)
- Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction. (2010) (196)
- Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. (2014) (193)
- Circulating Steroid Hormones and the Risk of Prostate Cancer (2006) (193)
- Determining Risk of Colorectal Cancer and Starting Age of Screening Based on Lifestyle, Environmental, and Genetic Factors. (2018) (192)
- Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. (2011) (192)
- Red meat, chicken, and fish consumption and risk of colorectal cancer. (2004) (191)
- Twin study of genetic and environmental influences on adult body size, shape, and composition (2004) (190)
- HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG) (2012) (186)
- Identification of Novel Genetic Markers of Breast Cancer Survival (2015) (185)
- Familial risks, early-onset breast cancer, and BRCA1 and BRCA2 germline mutations. (2003) (184)
- Genome-wide association study identifies new prostate cancer susceptibility loci. (2011) (183)
- Case-control study of overweight, obesity, and colorectal cancer risk, overall and by tumor microsatellite instability status. (2010) (183)
- A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. (2012) (182)
- Risk of Colorectal Cancer in Monoallelic and Biallelic Carriers of MYH Mutations: A Population-Based Case-Family Study (2006) (181)
- Determinants of restenosis and lack of effect of dietary supplementation with eicosapentaenoic acid on the incidence of coronary artery restenosis after angioplasty. (1989) (178)
- PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS (2016) (174)
- Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer. (2009) (170)
- Multiple Novel Prostate Cancer Predisposition Loci Confirmed by an International Study: The PRACTICAL Consortium (2008) (169)
- Mammographic density—a review on the current understanding of its association with breast cancer (2014) (166)
- Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer. (2014) (165)
- CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer. (2012) (164)
- Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource (2006) (163)
- BRCA2 Mutation-associated Breast Cancers Exhibit a Distinguishing Phenotype Based on Morphology and Molecular Profiles From Tissue Microarrays (2007) (163)
- Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers. (2013) (163)
- Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study. (2006) (163)
- A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. (2005) (161)
- Mechanisms of Bone Loss Following Allogeneic and Autologous Hemopoietic Stem Cell Transplantation (1999) (160)
- Familial patterns of covariation for cardiovascular risk factors in adults: The Victorian Family Heart Study. (2000) (160)
- Evidence of Gene–Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors (2013) (159)
- Population-based family studies in genetic epidemiology (2005) (158)
- Body size and composition and colon cancer risk in men. (2004) (157)
- Hepatitis C virus infection among a cohort of Victorian injecting drug users (1993) (155)
- Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer (2010) (154)
- Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers. (2016) (154)
- Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations (2004) (154)
- Hot Flushes, Menstrual Status, and Hormone Levels in a Population‐Based Sample of Midlife Women (1996) (154)
- Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies (2005) (149)
- A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer (2018) (149)
- Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees (2000) (148)
- Constitutional Methylation of the BRCA1 Promoter Is Specifically Associated with BRCA1 Mutation-Associated Pathology in Early-Onset Breast Cancer (2010) (147)
- Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types. (2016) (146)
- Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 (2011) (146)
- A genome wide linkage search for breast cancer susceptibility genes (2006) (146)
- Reduced femoral neck bone density in the daughters of women with hip fractures: The role of low peak bone density in the pathogenesis of osteoporosis (1994) (145)
- The CYP3A4*1B polymorphism has no functional significance and is not associated with risk of breast or ovarian cancer. (2002) (143)
- Nature or nurture in low back pain? Results of a systematic review of studies based on twin samples (2013) (142)
- Breast cancer prognosis in BRCA1 and BRCA2 mutation carriers: an International Prospective Breast Cancer Family Registry population-based cohort study. (2012) (139)
- Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis. (2014) (139)
- HFE C282Y homozygotes are at increased risk of breast and colorectal cancer (2010) (139)
- Genome-wide association study of colorectal cancer identifies six new susceptibility loci (2015) (138)
- Evidence for BRAF mutation and variable levels of microsatellite instability in a syndrome of familial colorectal cancer. (2005) (137)
- Oral Contraceptive Use and Risk of Early-Onset Breast Cancer in Carriers and Noncarriers of BRCA1 and BRCA2 Mutations (2005) (135)
- Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features (2013) (135)
- Biological markers that predict clinical recurrence in ductal carcinoma in situ of the breast. (2003) (135)
- Parathyroid hormone-related protein localization in breast cancers predict improved prognosis. (2006) (133)
- Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals (2012) (133)
- Association analyses identify 31 new risk loci for colorectal cancer susceptibility (2019) (132)
- A Comparison of Adiposity Measures as Predictors of All‐cause Mortality: The Melbourne Collaborative Cohort Study (2007) (131)
- A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. (2013) (131)
- After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer. (2001) (130)
- Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype (2013) (129)
- Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women (2018) (128)
- Cancer Risks for PMS2-Associated Lynch Syndrome. (2018) (128)
- Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
- A Prospective Study of Bone Loss in Menopausal Australian-Born Women (1998) (127)
- Foods, nutrients and prostate cancer (2004) (127)
- Associations between Smoking, Alcohol Consumption, and Colorectal Cancer, Overall and by Tumor Microsatellite Instability Status (2009) (125)
- BRCA1 and BRCA2 Mutation Carriers, Oral Contraceptive Use, and Breast Cancer Before Age 50 (2006) (124)
- Body size and composition and prostate cancer risk. (2003) (124)
- Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. (2009) (124)
- Breast-feeding and atopic disease: a cohort study from childhood to middle age. (2007) (123)
- PIK3CA Activating Mutation in Colorectal Carcinoma: Associations with Molecular Features and Survival (2013) (123)
- Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 (2016) (122)
- The interplay between the effects of lifetime asthma, smoking, and atopy on fixed airflow obstruction in middle age. (2013) (122)
- Identification of nine new susceptibility loci for endometrial cancer (2018) (122)
- Circulating steroid hormone concentrations in postmenopausal women in relation to body size and composition (2009) (121)
- Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry. (2011) (121)
- A variant in FTO shows association with melanoma risk not due to BMI (2013) (120)
- Penetrance Analysis of the PALB2 c.1592delT Founder Mutation (2008) (120)
- Obesity, Diabetes, and Hyperlipidemia in a Central Australian Aboriginal Community With a Long History of Acculturation (1993) (119)
- Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study (2015) (119)
- BRAFV600E Immunohistochemistry Facilitates Universal Screening of Colorectal Cancers for Lynch Syndrome (2013) (118)
- A PALB2 mutation associated with high risk of breast cancer (2010) (118)
- Using longitudinal data to define the perimenopause by menstrual cycle characteristics. (1998) (117)
- A co-twin study of the effect of calcium supplementation on bone density during adolescence (2005) (117)
- Parathyroid hormone-related protein production by breast cancers, improved survival, and reduced bone metastases. (2001) (117)
- Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. (2009) (116)
- House dust mite sensitization in toddlers predicts current wheeze at age 12 years. (2011) (115)
- Early seizures after acute stroke. Risk of late seizures. (1992) (115)
- 19p13.1 is a triple-negative-specific breast cancer susceptibility locus. (2012) (115)
- Common variants in ZNF365 are associated with both mammographic density and breast cancer risk (2011) (114)
- HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis‐related morbidity (2009) (113)
- Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation (2014) (112)
- The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions (2008) (112)
- DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers (2014) (112)
- The value of the Hospital Anxiety and Depression Scale (HADS) for comparing women with early onset breast cancer with population-based reference women (2004) (112)
- Agreement between self-reported breast cancer treatment and medical records in a population-based Breast Cancer Family Registry. (2005) (112)
- DNA methylation‐based biological aging and cancer risk and survival: Pooled analysis of seven prospective studies (2018) (111)
- Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk (2014) (111)
- Mammographic density and ageing: A collaborative pooled analysis of cross-sectional data from 22 countries worldwide (2017) (111)
- A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer (2015) (111)
- Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses (2019) (110)
- Crossed cerebellar diaschisis and brain recovery after stroke. (1995) (110)
- Body size and composition and the risk of gastric and oesophageal adenocarcinoma (2006) (109)
- Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. (2013) (109)
- A genetic and environmental analysis of a twin family study of alcohol use, anxiety, and depression (1984) (109)
- Genetic, common environment, and individual specific components of variance for bone mineral density in 10- to 26-year-old females: a twin study. (1998) (109)
- Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study (2014) (108)
- Decreased Prostate Cancer-Specific Survival of Men with BRCA2 Mutations from Multiple Breast Cancer Families (2011) (108)
- Segregation analyses of 1,476 population-based Australian families affected by prostate cancer. (2001) (107)
- Common Breast Cancer Susceptibility Variants in LSP1 and RAD51L1 Are Associated with Mammographic Density Measures that Predict Breast Cancer Risk (2012) (107)
- Ethnicity and Risk for Colorectal Cancers Showing Somatic BRAF V600E Mutation or CpG Island Methylator Phenotype (2008) (107)
- Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization. (2015) (107)
- Cohort Profile: The Melbourne Collaborative Cohort Study (Health 2020). (2017) (106)
- Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium (2002) (106)
- Breast cancer in Australian women under the age of 40 (1998) (105)
- The Heritability of Mammographically Dense and Nondense Breast Tissue (2006) (104)
- Measures of familial aggregation depend on definition of family history: meta-analysis for colorectal cancer. (2006) (104)
- Genes and Family Environment Explain Correlations Between Blood Pressure and Body Mass Index (2002) (104)
- The treatment-seeking woman at menopause. (1994) (102)
- Novel Common Genetic Susceptibility Loci for Colorectal Cancer (2018) (102)
- Circulating Steroid Hormone Levels and Risk of Breast Cancer for Postmenopausal Women (2010) (102)
- Risk of Metachronous Colon Cancer Following Surgery for Rectal Cancer in Mismatch Repair Gene Mutation Carriers (2013) (102)
- Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript (2011) (102)
- Body size and composition and colon cancer risk in women (2006) (102)
- Changes in Body Composition as Determinants of Longitudinal Changes in Bone Mineral Measures in 8 to 26-year-old Female Twins (2001) (102)
- Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles (2013) (102)
- Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (2011) (101)
- Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry. (2007) (100)
- Factors influencing asthma remission: a longitudinal study from childhood to middle age (2011) (100)
- Kathleen Cuningham Foundation Consortium For Research Into Familial Breast Cancer (2008) (100)
- Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study (2010) (100)
- Mammographic density: a heritable risk factor for breast cancer. (2009) (99)
- Dietary carbohydrate, fibre, glycaemic index, glycaemic load and the risk of postmenopausal breast cancer (2006) (97)
- Does dietary folate intake modify effect of alcohol consumption on breast cancer risk? Prospective cohort study (2005) (96)
- Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts (2020) (96)
- Association of ESR1 gene tagging SNPs with breast cancer risk. (2009) (95)
- Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases. (2011) (95)
- 10-year performance of four models of breast cancer risk: a validation study. (2019) (95)
- Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome. (2013) (95)
- The role of genetic breast cancer susceptibility variants as prognostic factors. (2012) (95)
- Risk Prediction Models for Colorectal Cancer: A Review (2011) (95)
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer (2016) (95)
- Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts. (2017) (95)
- Abdominal obesity and age-related macular degeneration. (2011) (94)
- Circulating Insulin-Like Growth Factor-I and Binding Protein-3 and the Risk of Breast Cancer (2007) (93)
- Cancer Risks for Relatives of Patients With Serrated Polyposis (2012) (93)
- Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer (2011) (93)
- Double-Strand Break Repair Gene Polymorphisms and Risk of Breast or Ovarian Cancer (2005) (93)
- Degree of left hippocampal atrophy correlates with severity of neuropsychological deficits (1997) (93)
- Body size and composition and risk of postmenopausal breast cancer. (2004) (92)
- Population-based estimate of the contribution of TP53 mutations to subgroups of early-onset breast cancer: Australian Breast Cancer Family Study. (2010) (92)
- Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers (2012) (92)
- Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH (2016) (92)
- Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry (2010) (92)
- Androgenetic alopecia and prostate cancer: findings from an Australian case-control study. (2002) (91)
- Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study (2011) (91)
- Relationship of endogenous sex hormones to lipids and blood pressure in mid-aged women. (1998) (91)
- Self-reported ballet classes undertaken at age 10–12 years and hip bone mineral density in later life (1998) (91)
- Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants. (2015) (91)
- Population‐based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066–6T>G (IVS10–6T>G) from the Breast Cancer Family Registry (2006) (90)
- Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. (2016) (90)
- Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. (2011) (90)
- Second to fourth digit ratio (2D:4D) and concentrations of circulating sex hormones in adulthood (2011) (89)
- Do selected kinanthropometric and performance variables predict injuries in female netball players? (1995) (89)
- Genome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Cancer (2014) (89)
- Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancer (2014) (88)
- Phenotype and Polyp Landscape in Serrated Polyposis Syndrome: A Series of 100 Patients From Genetics Clinics (2012) (88)
- Bone Mineral Density and Bone Turnover in Asthmatics Treated with Long‐Term Inhaled or Oral Glucocorticoids (1998) (88)
- Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. (2016) (87)
- Fracture risk and height: An association partly accounted for by cortical porosity of relatively thinner cortices (2013) (87)
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- Loss of Heterozygosity at the BRCA2 Locus Detected by Multiplex Ligation-Dependent Probe Amplification is Common in Prostate Cancers from Men with a Germline BRCA2 Mutation (2008) (38)
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- A Novel Polymorphism in a Forkhead Box A1 (FOXA1) Binding Site of the Human UDP Glucuronosyltransferase 2B17 Gene Modulates Promoter Activity and Is Associated with Altered Levels of Circulating Androstane-3α,17β-diol Glucuronide (2010) (36)
- Diet and exercise during growth have site-specific skeletal effects: a co-twin control study (2005) (36)
- A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6 q 14 and 20 q 11 (2012) (36)
- MC1R genotypes and risk of melanoma before age 40 years: A population‐based case‐control‐family study (2012) (36)
- Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort (2016) (36)
- Alcohol Consumption and Survival after a Breast Cancer Diagnosis: A Literature-Based Meta-analysis and Collaborative Analysis of Data for 29,239 Cases (2014) (36)
- Menopause‐Related Appendicular Bone Loss is Mainly Cortical and Results in Increased Cortical Porosity (2018) (36)
- Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study. (2012) (36)
- Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia (2013) (36)
- Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers (2020) (35)
- High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies (2015) (35)
- An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. (2016) (35)
- Practical Problems With Clinical Guidelines for Breast Cancer Prevention Based on Remaining Lifetime Risk (2015) (35)
- Investigation of gene‐environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors (2015) (35)
- Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease (2016) (35)
- Mother's smoking and complex lung function of offspring in middle age: A cohort study from childhood (2016) (35)
- Red Meat Intake, NAT2, and Risk of Colorectal Cancer: A Pooled Analysis of 11 Studies (2014) (35)
- Identification of a novel percent mammographic density locus at 12q24. (2012) (35)
- Alcohol use, smoking habits and the Junior Eysenck personality questionnaire in adolescent Australian twins (1992) (35)
- Dietary intake of B vitamins and methionine and prostate cancer incidence and mortality (2012) (35)
- Prediagnosis Reproductive Factors and All-Cause Mortality for Women with Breast Cancer in the Breast Cancer Family Registry (2009) (35)
- Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk (2020) (35)
- Alcohol consumption and prostate cancer risk: Results from the Melbourne collaborative cohort study (2006) (35)
- Genetic and Environmental Causes of Variation in the Difference Between Biological Age Based on DNA Methylation and Chronological Age for Middle-Aged Women (2015) (35)
- Alcohol Consumption and the Risk of Colorectal Cancer for Mismatch Repair Gene Mutation Carriers (2016) (35)
- RAD51 and Breast Cancer Susceptibility: No Evidence for Rare Variant Association in the Breast Cancer Family Registry Study (2012) (34)
- Inference about Causation from Examination of Familial Confounding: Application to Longitudinal Twin Data on Mammographic Density Measures that Predict Breast Cancer Risk (2012) (34)
- Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers? (2013) (34)
- Review of Fisher (1988) (34)
- CYP17 genetic polymorphism, breast cancer, and breast cancer risk factors: Australian Breast Cancer Family Study (2005) (34)
- Is Chronic Low Back Pain Associated with the Prevalence of Coronary Heart Disease when Genetic Susceptibility Is Considered? A Co-Twin Control Study of Spanish Twins (2016) (34)
- Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk (2014) (34)
- Macrophage Inhibitory Cytokine-1 H6D Polymorphism, Prostate Cancer Risk, and Survival (2006) (34)
- Prostate cancer segregation analyses using 4390 families from UK and Australian population‐based studies (2009) (34)
- Recreational physical activity is associated with reduced breast cancer risk in adult women at high risk for breast cancer: a cohort study of women selected for familial and genetic risk. (2019) (34)
- Population-Based Estimate of Prostate Cancer Risk for Carriers of the HOXB13 Missense Mutation G84E (2013) (34)
- Explaining Variance in the Cumulus Mammographic Measures That Predict Breast Cancer Risk: A Twins and Sisters Study (2013) (34)
- Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21 (2016) (33)
- Longitudinal Study of Mammographic Density Measures That Predict Breast Cancer Risk (2017) (33)
- Mammographic Density and Candidate Gene Variants: A Twins and Sisters Study (2007) (33)
- Australian Twin Registry: 30 Years of Progress (2012) (33)
- Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study (2019) (33)
- The Australian Twin Registry. (2002) (33)
- Low somatic K-ras mutation frequency in colorectal cancer diagnosed under the age of 45 years. (2006) (33)
- Identification of New Genetic Susceptibility Loci for Breast Cancer Through Consideration of Gene‐Environment Interactions (2014) (33)
- Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness. (2019) (33)
- Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer (2011) (33)
- Dietary intake of one-carbon metabolism nutrients and DNA methylation in peripheral blood. (2018) (33)
- Genetic and environmental influences on adult human height across birth cohorts from 1886 to 1994 (2016) (33)
- No evidence of MMTV-like env sequences in specimens from the Australian Breast Cancer Family Study (2010) (33)
- Genetic and environmental variation in Eysenck Personality Questionnaire scales measured on Australian adolescent twins (1994) (33)
- Blood-borne virus infections among Australian injecting drug users: Implications for spread of HIV (1994) (33)
- Predictors of the use of complementary and alternative medicine (CAM) by women at high risk for breast cancer. (2009) (32)
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- Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome (2013) (32)
- Economic Evaluation of Population-Based BRCA1/BRCA2 Mutation Testing across Multiple Countries and Health Systems (2020) (32)
- Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 (2015) (32)
- Is childhood immunisation associated with atopic disease from age 7 to 32 years? (2006) (32)
- A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1 (2015) (32)
- Magnetic Resonance Imaging and Late‐Onset Epilepsy (1991) (32)
- Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus (2016) (32)
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- Streptokinase increases luxury perfusion after stroke. (1996) (31)
- Microsatellite Instability Markers for Identifying Early-Onset Colorectal Cancers Caused by Germ-Line Mutations in DNA Mismatch Repair Genes (2007) (31)
- Cerebral Hypoperfusion in Stroke Prognosis and Brain Recovery (1993) (31)
- iPrevent®: a tailored, web-based, decision support tool for breast cancer risk assessment and management (2016) (31)
- Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study (2014) (31)
- Zygosity Differences in Height and Body Mass Index of Twins From Infancy to Old Age: A Study of the CODATwins Project (2015) (30)
- Mammographic density defined by higher than conventional brightness threshold better predicts breast cancer risk for full-field digital mammograms (2015) (30)
- Genetic Predictors of Circulating 25-Hydroxyvitamin D and Risk of Colorectal Cancer (2013) (30)
- Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case–control study (2016) (30)
- Genomic Characterization of Upper-Tract Urothelial Carcinoma in Patients With Lynch Syndrome (2018) (30)
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- Genome-wide average DNA methylation is determined in utero (2018) (30)
- Occupational exposure to pesticides are associated with fixed airflow obstruction in middle-age (2017) (30)
- Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome) (2010) (30)
- Common Polymorphisms in ERCC2 (Xeroderma pigmentosum D) are not Associated with Breast Cancer Risk (2005) (30)
- Contralateral risk-reducing mastectomy in BRCA1 and BRCA2 mutation carriers and other high-risk women in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab) (2010) (29)
- Hallux Valgus, By Nature or Nurture? A Twin Study (2017) (29)
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- Asthma, Asthma Medications, and Prostate Cancer Risk (2010) (29)
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- Aetiological overlap between obsessive–compulsive related and anxiety disorder symptoms: Multivariate twin study (2016) (28)
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- Variants in the Prostate-Specific Antigen (PSA) Gene and Prostate Cancer Risk, Survival, and Circulating PSA (2006) (28)
- The progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of breast cancer in Australian women. (2002) (28)
- Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA) (2009) (28)
- Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer. (2015) (28)
- Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22 (2012) (28)
- Covariation between family members as a function of cohabitation history (1983) (28)
- Interleukin‐6 promoter variants, prostate cancer risk, and survival (2012) (28)
- The AIB1 Polyglutamine Repeat Does Not Modify Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers (2006) (28)
- Lifetime alcohol intake is associated with an increased risk of KRAS+ and BRAF‐/KRAS‐ but not BRAF+ colorectal cancer (2016) (28)
- Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer. (2013) (28)
- A network analysis to identify mediators of germline-driven differences in breast cancer prognosis (2020) (27)
- Prohibitin 3′ untranslated region polymorphism and breast cancer risk in Australian women (2002) (27)
- Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease (2014) (27)
- Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) (2016) (27)
- Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk. (2020) (27)
- Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis (2009) (27)
- Healthy adults' performance on the Austin Maze (1992) (27)
- Genes involved with folate uptake and distribution and their association with colorectal cancer risk (2010) (27)
- Risk factors for metachronous colorectal cancer following a primary colorectal cancer: A prospective cohort study (2016) (27)
- Cohort Profile: Melbourne Atopy Cohort study (MACS). (2016) (27)
- Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry (2015) (27)
- The Association of Tumor Microsatellite Instability Phenotype with Family History of Colorectal Cancer (2009) (27)
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- Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study (2016) (26)
- Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses (2020) (26)
- Genome‐wide association study and meta‐analysis in Northern European populations replicate multiple colorectal cancer risk loci (2017) (26)
- Family History of Colorectal Cancer in BRAF p.V600E-Mutated Colorectal Cancer Cases (2013) (26)
- Family history of breast cancer and all-cause mortality after breast cancer diagnosis in the Breast Cancer Family Registry (2009) (26)
- The interaction between farming/rural environment and TLR2, TLR4, TLR6 and CD14 genetic polymorphisms in relation to early- and late-onset asthma (2017) (26)
- Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study (2018) (26)
- Genome‐wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK and sumLOD analyses (2010) (26)
- Familial and Genomic Analyses of Postural Changes in Systolic and Diastolic Blood Pressure (2004) (26)
- Mutation searching in colorectal cancer studies: experience with a denaturing high‐pressure liquid chromatography system for exon‐by‐exon scanning of tumour suppressor genes (2002) (26)
- Natural history of HFE simple heterozygosity for C282Y and H63D: A prospective 12‐year study (2014) (26)
- Screening Practices of Unaffected People at Familial Risk of Colorectal Cancer (2011) (26)
- Cost-effectiveness of family history-based colorectal cancer screening in Australia (2014) (26)
- Architecture of cortical bone determines in part its remodelling and structural decay. (2013) (26)
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- Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk (2015) (25)
- Mammographic density defined by higher than conventional brightness thresholds better predicts breast cancer risk (2016) (25)
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- Tumour morphology predicts PALB2 germline mutation status (2013) (25)
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- Macrophage Scavenger Receptor 1 999C>T (R293X) Mutation and Risk of Prostate Cancer (2005) (25)
- Breast Cancer Risk Associations with Digital Mammographic Density by Pixel Brightness Threshold and Mammographic System. (2017) (25)
- Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer? (2014) (24)
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- Preterm birth and low birth weight continue to increase the risk of asthma from age 7 to 43 (2017) (24)
- FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer (2011) (24)
- Multivitamin, calcium and folic acid supplements and the risk of colorectal cancer in Lynch syndrome. (2016) (24)
- Mammographic density and risk of breast cancer in Korean women (2014) (24)
- Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer (2016) (24)
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- SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer (2016) (23)
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- The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations (2018) (23)
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- Breast cancer risk variants at 6 q 25 display different phenotype associations and regulate ESR 1 , RMND 1 and CCDC 170 (2016) (22)
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- International Network of Twin Registries (INTR): Building a Platform for International Collaboration (2014) (22)
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- Prospective study of breast cancer risk for mutation negative women from BRCA1 or BRCA2 mutation positive families (2011) (21)
- Mammographic densities during the menopausal transition: a longitudinal study of Australian-born women (2007) (21)
- Age at Menopause (2020) (21)
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- The rs743572 common variant in the promoter of CYP17A1 is not associated with prostate cancer risk or circulating hormonal levels (2007) (20)
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- A three-protein biomarker panel assessed in diagnostic tissue predicts death from prostate cancer for men with localized disease (2014) (20)
- Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty. (2013) (20)
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- Is this back pain killing me? All‐cause and cardiovascular‐specific mortality in older Danish twins with spinal pain (2017) (19)
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- Evidence that the 5 p 12 Variant rs 10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF 10 and MRPS 30 Regulation (15)
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- Loss of Heterozygosity at the BRCA 2 Locus Detected byMultiplex Ligation-Dependent ProbeAmplification is Common in Prostate Cancers fromMenwith a Germline BRCA 2 Mutation (2008) (6)
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- Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer (2013) (4)
- Analysis of the breast cancer methylome using formalin-fixed paraffin-embedded tumour (2016) (4)
- Ability of known colorectal cancer susceptibility SNPs to predict colorectal cancer risk: A cohort study within the UK Biobank (2021) (4)
- Prospective Evaluation over 15 Years of Six Breast Cancer Risk Models (2021) (4)
- Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci (2022) (4)
- ‘Next-generation’ genome wide association studies (2012) (4)
- Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk (2014) (4)
- Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer (2017) (4)
- Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study (2010) (4)
- Re: On the use of familial aggregation in population-based case probands for calculating penetrance. (2003) (4)
- Family-based association study of IGF1 microsatellites and height, weight, and body mass index (2010) (4)
- Early Results From the ‘Diggers to Veterans’ Longitudinal Study of Australian Men who Served in the First World War. Short- and Long-Term Mortality of Early Enlisters (2019) (4)
- Australian Twin Registry: A Nationally Funded Resource for Medical and Scientific Research, Incorporating match and WATCH (2006) (4)
- Twin children in volunteer registries: biases in parental participation and reporting. (1990) (4)
- Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) (2012) (4)
- RESPONSE: Re: Dominant Negative ATM Mutations in Breast Cancer Families (2002) (4)
- Association between birth weight and educational attainment: an individual-based pooled analysis of nine twin cohorts (2018) (4)
- Reasons for ongoing participation in a longitudinal cohort study (2012) (4)
- Overall lack of replication of associations between dietary intake of folate and vitamin B-12 and DNA methylation in peripheral blood. (2020) (4)
- Genetic variation at CYP 3 A is associated with age at menarche and breast cancer risk : a case-control study (2014) (4)
- Erratum: A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer (2015) (4)
- Childhood measles contributes to post‐bronchodilator airflow obstruction in middle‐aged adults: A cohort study (2018) (4)
- Publisher Correction: Shared heritability and functional enrichment across six solid cancers (2019) (4)
- A streamlined model for use in clinical breast cancer risk assessment maintains predictive power and is further improved with inclusion of a polygenic risk score (2021) (4)
- Common variants in ZNF 365 are associated with both mammographic density and breast cancer risk (2019) (4)
- Prostate screening uptake in Australian BRCA1 and BRCA2 carriers (2007) (4)
- Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH 2 B 3 and TSHZ 1 (2015) (4)
- Association of FOXO3 Blood DNA Methylation with Cancer Risk, Cancer Survival, and Mortality (2021) (4)
- A09 Lifestyle approach to management of the menopause (1996) (4)
- Limited influence of germline genetic variation on all-cause mortality in women with early onset breast cancer: evidence from gene-based tests, single-marker regression, and whole-genome prediction (2017) (4)
- Ambient temperature and genome-wide DNA methylation: A twin and family study in Australia. (2021) (4)
- Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes (2016) (4)
- Performance of BCRAT in high-risk patients with breast cancer - Authors' reply. (2019) (3)
- Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing (2021) (3)
- Estimates of familial risks from family data are biased when ascertainment of families is not independent of family history (2010) (3)
- Innovations in the statistical analysis of twin studies. (1987) (3)
- The Charles Perkins Centre's Twins Research Node (2016) (3)
- Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment (2021) (3)
- Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk (2020) (3)
- F158 A prospective study of bone loss in perimenopausal australian-born women (1996) (3)
- Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancer (2017) (3)
- Prognosis in BRCA1, BRCA2 associated breast cancer (BC): a prospective Breast Cancer Family Registry (BCFR) international population-based cohort study. (2009) (3)
- The effects of stress–tension on depression and anxiety symptoms: evidence from a novel twin modelling analysis (2017) (3)
- Early life affects late-life health through determining DNA methylation across the lifespan: A twin study (2022) (3)
- Debunking a myopic view of nature versus nurture (2019) (3)
- InforMD: a new initiative to raise public awareness about breast density (2018) (3)
- Assessing breast cancer risk in primary care: What can we learn from cardiovascular disease? (2013) (3)
- Distribution of family history of a disease as a function of mode of inheritance, genetic relative hazard, allele frequency and disease status of the proband, with application to female breast cancer. (2001) (3)
- Physical activity, body size and composition, (2010) (3)
- An independent external validation of melanoma risk prediction models using the Australian Melanoma Family Study (2020) (3)
- A range of simple summary genome‐wide statistics for detecting genetic linkage using high density marker data (2007) (3)
- 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 (2021) (3)
- Epigenetic Prospects in Epidemiology and Public Health (2018) (3)
- Bayesian Sparse Global-Local Shrinkage Regression for Grouped Variables (2017) (3)
- Mendelian randomisation study of smoking exposure in relation to breast cancer risk (2021) (3)
- Meanings of abortion in context: accounts of abortion in the lives of women diagnosed with breast cancer (2017) (3)
- Abstracts (2011) (3)
- ADMANI: Annotated Digital Mammograms and Associated Non-Image Datasets (2022) (3)
- Population-based prospective cohort study of psychosocial factors and survival of young Australian women with breast cancer (2008) (3)
- Genetic Correlations and Covariances (2005) (3)
- Cancer risk management practices of non-carriers within BRCA1/2 mutation positive families in the Kathleen Cunningham Consortium for Research into Familial Breast Cancer (kConFab). (2006) (3)
- Association of Birth Weight and Current Body Size to Blood Pressure in Female Twins (2001) (3)
- Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2019) (3)
- Correction: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 (2018) (3)
- Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study (2019) (3)
- Lifetime alcohol intake, drinking patterns over time and risk of stomach cancer: A pooled analysis of data from two prospective cohort studies (2021) (3)
- Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins (2013) (3)
- Breast Cancer Chemoprevention: Use and Views of Australian Women and Their Clinicians (2020) (3)
- Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers (2008) (3)
- Familial and Genetic Influences on the Common Pediatric Primary Pain Disorders: A Twin Family Study (2021) (3)
- 1028 Comparison of the Clinical Prediction Model Premm1,2,6 With Colorectal Cancer Molecular Tumor Testing for Lynch Syndrome in the Colon Cancer Family Registry (2010) (3)
- Prospective study of breast cancer risk in mutation-negative women from BRCA1 or BRCA2 mutation-positive families in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab). (2011) (3)
- The Utility of a Multivariate Normal Model for Studying Familial Patterns in Medical and Psychiatric Data (1983) (3)
- Homozygosity for the C282Y mutation in the HFE gene is associated with increased risk of colorectailand breast cancer in Australian population (2007) (3)
- Segregation analysis of 17,425 population-based breast cancer families: Evidence for genetic susceptibility and risk prediction (2022) (3)
- Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk (2016) (3)
- Childhood obesity predicts current incident asthma in adult women (2005) (3)
- Breast cancer risks for BRCA 1/2 carriers [2] (multiple letters) (2004) (3)
- Socio‐economic status and survival from breast cancer for young, Australian, urban women (2010) (3)
- Methylation scores for smoking, alcohol consumption, and body mass index and risk of seven types of cancer (2021) (2)
- of the Menopausal Transition: A Cross-Sectional Study of a Population-Based Sample* (1995) (2)
- Healthiron: a longitudinal population study defining the burden of disease in HFE-associated hereditary hemochromatosis (2007) (2)
- rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk (2016) (2)
- Body size and dietary risk factors for aggressive prostate cancer: a case–control study (2019) (2)
- Physical activity and risks of breast and colorectal cancer: A Mendelian randomization analysis (2019) (2)
- A novel polymorphism in a FOXA1 binding site of the human UDP glucuronosyltransferase 2B17 gene modulates promoter activity and is associated with altered levels of circulating androstane-3α, 17β- (2010) (2)
- Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility (2016) (2)
- Research Note: Twin studies and their value for physiotherapy research. (2019) (2)
- Sexual dimorphism in radial and longitudinal bone growth differ by tempo and magnitude: A study in male-female co-twins pairs (2007) (2)
- Oral Contraceptive Use and Parity Associations with Uncommon Breast Cancer Histologies in the Breast Cancer Family Registry: the Role of Family History (2011) (2)
- Rationale for, and approach to, studying modifiers of risk in persons with a genetic predisposition to colorectal cancer (2006) (2)
- TWIN FAMILY CASE-CONTROL STUDY ON ADOLESCENT NON-SPECIFIC LOW BACK PAIN : INVESTIGATING HERITABILITY AND COMORBIDITIES (2013) (2)
- Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything? (2013) (2)
- Are the Relationships of Lean Mass and Fat Mass With Bone Microarchitecture Causal or Due to Familial Confounders? A Novel Study of Adult Female Twin Pairs (2020) (2)
- Fine-mapping identi fi es two additional breast cancer susceptibility loci at 9 q 31 . 2 (2015) (2)
- Two truncating variants in FANCC and breast cancer risk (2019) (2)
- A Genome-Wide Gene-Based Gene–Environment Interaction Study of Breast Cancer in More than 90,000 Women (2022) (2)
- Is BRCA2 c.9079 G > A a predisposing variant for early onset breast cancer? (2008) (2)
- Factors associated with type I and type II endometrial cancers in women with a germ-line mutation in a mismatch repair gene. (2011) (2)
- RESPONSE LETTER TO DR. GAU ET AL. (2006) (2)
- Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation? (2020) (2)
- Early birth is a key factor in educational disadvantage of twins: A data linkage study (2020) (2)
- Considerations when using breast cancer risk models for women with negative BRCA1/BRCA2 mutation results. (2020) (2)
- Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22 (2012) (2)
- Towards risk‐stratified population breast cancer screening: more than mammographic density (2021) (2)
- Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC) (2019) (2)
- Abstract LB-282: Transethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A (2014) (2)
- Height and Colorectal and Endometrial Cancer Risk for Persons with Lynch Syndrome. (2020) (2)
- The cohort description of collaborative project of development of anthropometrical measures in twins (CODATwins) to study macro-environmental variation in genetic and environmental effects on anthropometric traits (2015) (2)
- Should we offer multi-gene testing to all patients with breast cancer: a cost-effectiveness analysis (2019) (2)
- The biology of panic-genetic evidence. (1989) (2)
- DEPTH: A Novel Algorithm for Feature Ranking with Application to Genome-Wide Association Studies (2013) (2)
- Mathematical and statistical methods for genetic analysis. K. Lange, Springer, Berlin, 1997. No. of pages: 290. Price: £36.50. ISBN 0‐387‐94909‐7 (2000) (2)
- Abstract 4266: Double somatic mutations as a cause of tumor mismatch repair-deficiency in population-based colorectal and endometrial cancer with Lynch-like syndrome (2017) (2)
- Validation study of risk prediction models for female relatives of Australian women with breast cancer (2012) (2)
- Together Alone: Going Online during COVID-19 Is Changing Scientific Conferences (2022) (2)
- Colorectal cancer cases with de novo germ-line mutations in MLH1, MSH2, and MSH6 from the Colon Cancer Family Registry. (2011) (2)
- Obstetric Events as a Risk Factor for Febrile Seizures: A Community-Based Twin Study (2008) (2)
- Correction: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk (2015) (2)
- Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study (2022) (2)
- Motivators of Inappropriate Ovarian Cancer Screening: A Survey of Women and Their Clinicians (2020) (2)
- Investigating the genetic relationship between Alzheimer’s disease and cancer using GWAS summary statistics (2017) (2)
- PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients (2022) (2)
- Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits (2022) (2)
- Smoking Methylation Marks for Prediction of Urothelial Cancer Risk (2021) (2)
- Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study (2017) (2)
- GENETIC FACTORS ASSOCIATED WITH ALTERED SODIUM TRANSPORT IN HUMAN HYPERTENSION: A TWIN STUDY (1997) (2)
- Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 (2017) (2)
- Register4: an Australian web‐enabled resource created by the National Breast Cancer Foundation to facilitate and accelerate cancer research (2014) (2)
- Tetranucleotide and Low Microsatellite Instability Are Inversely Associated with the CpG Island Methylator Phenotype in Colorectal Cancer (2021) (2)
- Genetic and environmental causes of variation in epigenetic aging across the lifespan (2020) (1)
- Commentary: Age and frailty-not quite the same thing. (2015) (1)
- Development of a tailored, computerized, breast cancer risk assessment and decision support tool: What do clinicians want? (2013) (1)
- Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study (2021) (1)
- Iconographies supplémentaires de l'article : Polymorphisms affecting vitamin D–binding protein modify the relationship between serum vitamin D (25[OH]D 3 ) and food allergy (2016) (1)
- Fine-mapping of the HNF1Bmulticancer locus identifies candidate variants thatmediate endometrial cancer risk (2015) (1)
- Heritable DNA methylation marks associated with susceptibility to breast cancer (2018) (1)
- MC1Rgenotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study (2013) (1)
- Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies? (2021) (1)
- 027. Mapping novel breast cancer susceptibility genes by linkage analysis of Australian multiple case kindreds (2004) (1)
- Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry (2012) (1)
- Short Communication The HER2 I655V Polymorphism and Risk of Breast Cancer in Women Age 40 Years 1 (2003) (1)
- Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG) (2011) (1)
- P.4.f.010 Understanding hypochondriasis: a novel twin study model of potential causal relationships with anxiety and OC-related disorder symptoms (2016) (1)
- Determining the familial risk distribution of colorectal cancer: a data mining approach (2015) (1)
- Abstract P6-09-05: Value of adding single-nucleotide polymorphism panel markers to phenotypic algorithms of breast cancer risk (2015) (1)
- Incorporation of twins in the regressive logistic model for pedigree disease data. (1990) (1)
- Predicting interval and screen-detected breast cancers from mammographic density defined by different brightness thresholds (2018) (1)
- Tools for translational epigenetic studies involving formalin-fixed paraffin-embedded human tissue: applying the Infinium HumanMethyation450 Beadchip assay to large population-based studies (2015) (1)
- Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 (vol 20, pg 890, 2018) (2018) (1)
- Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families (2013) (1)
- Comment on: On the use of familial aggregation in population-based case probands for calculating penetrance. Authors' reply (2003) (1)
- Twin birth changes DNA methylation of subsequent siblings (2017) (1)
- Syddansk Universitet Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12 p 11 locus (2016) (1)
- Breast Cancer Risk and 6 q 22 . 33 : Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA 1 / 2 (2012) (1)
- Title : A comparison of different methods for including ' age at menopause ' in analyses of the association between hormone replacement therapy use and breast cancer (2006) (1)
- Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer. (2016) (1)
- Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk (2007) (1)
- Association of chronic musculoskeletal pain with mortality among UK adults: A population-based cohort study with mediation analysis (2021) (1)
- Risk factors for low back pain among twins- a web-based population survey (2011) (1)
- Association of contralateral breast cancer risk with mammographic density defined at higher‐than‐conventional intensity thresholds (2022) (1)
- Polygenic Risk Modelling for Prediction of Epithelial Ovarian Cancer Risk (2020) (1)
- Identification of nine new susceptibility loci for endometrial cancer (2018) (1)
- Letter in response to “Identifying Lynch syndrome” by de la Chapelle et al. (2010) (1)
- Abstract P4-09-02: Validation of iPrevent using the prospective family study cohort (ProF-SC) (2019) (1)
- Review of: Are breast density and bone mineral density independent risk factors for breast cancer? (2005) (1)
- Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer (2021) (1)
- Familial Aspects of Mammographic Density Measures Associated with Breast Cancer Risk (2022) (1)
- Dietary intake of B vitamins and methionine and breast cancer risk (2013) (1)
- IMPACT OF COMMON GENOMIC VARIANTS ON MELANOMA RISK PREDICTION (2014) (1)
- The Australian NHMRC Twin Registry: A Resource for Pediatric Research (1993) (1)
- Trialling a colorectal cancer risk tool within general practice; NHMRC "Centre for Research Excellence for Reducing the Burden of Colorectal Cancer by Optimising Screening” (2014) (1)
- Prediagnosis alcohol intake and metachronous cancer risk in cancer survivors: A prospective cohort study (2021) (1)
- A new colorectal cancer risk prediction model incorporating family history, personal and environmental factors (2019) (1)
- Rare germline copy number variants (CNVs) and breast cancer risk (2022) (1)
- Edinburgh Research Explorer Anti-Müllerian Hormone Serum Concentrations of Women with Germline BRCA1 or 2 BRCA2 Mutations (2016) (1)
- Genetic Aspects of Mammographic Density Measures Associated with Breast Cancer Risk (2022) (1)
- lifepool: A collaboration between Women and Researchers (2011) (1)
- A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1 (2015) (1)
- Predictors of Asthma in Middle Age: A Longitudinal Study over 37 Years (2006) (1)
- Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study (2022) (1)
- Erratum: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: An international prospective cohort of BRCA1 and BRCA2 mutation carriers (Breast Cancer Res (2020) 22 (8) DOI: 10.1186/s13058-020-1247-4) (2020) (1)
- Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts (2017) (1)
- Associations between environmental breast cancer risk factors and DNA methylation-based risk-predicting measures (2018) (1)
- Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts (2018) (1)
- Double the value: how researching twins benefits everyone (2012) (1)
- Strong familial risks associated with early-onset breast cancer are only partly BRCA1- or BRCA2-related. (2002) (1)
- Research Participation of Twins Enrolled with the National, Volunteer Australian Twin Registry (2007) (1)
- Abstract 4276: Oral contraceptive use and breast cancer risk: a cohort study ofBRCA1andBRCA2mutation carriers (2017) (1)
- Approximating Message Lengths of Hierarchical Bayesian Models Using Posterior Sampling (2016) (1)
- 872Novel approach to estimating sex differences unconfounded by familial factors from studying male-female twin pairs (2021) (1)
- Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort (2021) (1)
- RE: Chemopreventive Agents to Reduce Mammographic Breast Density in Premenopausal Women: A Systematic Review of Clinical Trials (2021) (1)
- Repeatability of methylation measures using a QIAseq targeted methyl panel and comparison with the Illumina HumanMethylation450 assay (2021) (1)
- Abstract 3357: Heritable methylation marks associated with breast cancer risk (2017) (1)
- Germline HOXB 13 p . Gly 84 Glu Mutation and Risk of Colorectal Cancer (2013) (1)
- Colorectal Cancer Linkage on Chromosomes 4 q 21 , 8 q 13 , 12 q 24 , and 15 q 22 (2012) (1)
- Genome-wide association study of germline variants and breast cancer-speci fi c mortality (2019) (1)
- Subject Index Vol. 6, 1996 (1996) (1)
- Bayesian Robust Regression with the Horseshoe+ Estimator (2016) (1)
- Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (1)
- Abstract B98: Parity, breastfeeding and oral contraceptive use and risk of estrogen- and progesterone-negative breast cancer in the Breast Cancer Family Registry (2012) (1)
- HIV-related Chronic Obstructive Pulmonary Disease (2014) (1)
- Risks to Relatives (2008) (1)
- Prostate carcinomas arising in Lynch Syndrome patients frequently show concordant mismatch repair deficiency (2013) (1)
- How to Determine If, and by How Much, Genetic Variation Influences Osteoporosis (2000) (1)
- The Colorectal Cancer Family Registry: An international resource for studying the genetic and molecular epidemiology of colorectal cancer (2006) (1)
- Germline and Tumor Whole Genome Sequencing as a Diagnostic Tool to Resolve Suspected Lynch Syndrome (2020) (1)
- Abstract 1098: Epistasis analysis of the PTHLH region in European subjects of the iCOGS breast cancer GWAS suggest multiple genes may be implicated in its role in breast cancer (2015) (1)
- DNA methylation changes specific to environmental exposures: The strengths of twin studies using cigarette smoking as an example (2021) (1)
- Dietary intake of B vitamins and methionine and prostate cancer incidence and mortality (2012) (1)
- A TWIN REGISTRY (1974) (1)
- Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk (2015) (1)
- Metachronous colorectal cancer risk for mismatch repair gene mutation carriers – the advantage of more extensive surgery (2010) (1)
- Estimating risks for variants of unknown significance according to their predicted pathogenicity classes with application to BRCA1 (2014) (1)
- Improved definition of growing pains: A common familial primary pain disorder of early childhood (2022) (1)
- High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies (2015) (1)
- Recreational Physical Activity and Outcomes After Breast Cancer in Women at High Familial Risk (2021) (1)
- P-236Screening practices of Australians at population and familial risk following the partial roll-out of the National Bowel Cancer Screening Program, 2009-2012 (2016) (1)
- Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history (2019) (1)
- BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts (2018) (1)
- Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk (2019) (1)
- Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas (2017) (1)
- Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes (2016) (1)
- Comparison of the association of mammographic density and clinical factors with ductal carcinoma in situ versus invasive ductal breast cancer in Korean women (2017) (1)
- Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium (2015) (1)
- Genetic predisposition to ductal carcinoma in situ of the breast (2016) (1)
- A network analysis to identify mediators of germline-driven differences in breast cancer prognosis (2020) (1)
- Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci (2022) (1)
- Dependence of cancer risk from environmental exposures on underlying genetic susceptibility: an illustration with polycyclic aromatic hydrocarbons and breast cancer (2017) (1)
- Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations? (2018) (1)
- Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancer (2017) (1)
- Epidemiological issues: the Australasian colorectal cancer family study (2000) (1)
- Cost-effectiveness of family history-based colorectal cancer screening in Australia (2014) (1)
- The Australian NHMRC Twin Registry: A resource for paediatric research (1993) (1)
- Common Polymorphisms in ERCC 2 ( Xeroderma pigmentosum D ) are not Associated with Breast Cancer Risk (2005) (1)
- Causal effect of smoking on DNA methylation in peripheral blood: a twin and family study (2018) (1)
- Childhood ‘bronchitis’ and respiratory outcomes in middle-age: a prospective cohort study from age 7 to 53 years (2022) (1)
- Prediction and clinical utility of a contralateral breast cancer risk model (2019) (1)
- Evaluating multiple next-generation sequencing derived tumor features to accurately predict DNA mismatch repair status (2022) (1)
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer (2016) (1)
- Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants (2018) (1)
- A competing risks model with binary time varying covariates for estimation of breast cancer risks in BRCA1 families (2021) (1)
- Epigenetic supersimilarity of monozygotic twin pairs (2018) (1)
- Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM (2022) (1)
- Serrated pathway colorectal carcinoma without microsatellite instability demonstrates Aggressive features and is associated with poor overall survival (2013) (1)
- 350 HFE C282Y HOMOZYGOSITY IS ASSOCIATED WITH AN INCREASED RISK OF TOTAL HIP REPLACEMENT FOR OSTEOARTHRITIS IN MEN BUT NOT WOMEN (2011) (1)
- Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis (2020) (1)
- Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2 (2013) (1)
- Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study (2014) (1)
- Blood DNA methylation score predicts breast cancer risk: applying OPERA in molecular, environmental, genetic and analytic epidemiology (2021) (1)
- Polygenic risk scores for cardiovascular diseases and type 2 diabetes (2022) (1)
- Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC) (2018) (1)
- Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer (2018) (1)
- Rare key functional domain missense substitutions in MRE11A, RAD50, and NBNcontribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study (2014) (1)
- Lynch syndrome-associated breast cancers: clinicopathological characteristics of a case series from the colon CFR (2010) (1)
- Current asthma contributes as much as smoking to chronic bronchitis in middle age: a prospective population-based study [Corrigendum] (2017) (1)
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study (2017) (1)
- Interaction Between Genetic and Nutritional Factors (1998) (1)
- Associations of Height With the Risks of Colorectal and Endometrial Cancer in Persons With Lynch Syndrome (2020) (1)
- Enhancing Value and Uptake for Whole-Population Cohorts of Children and Parents: Methods to Integrate Registries into the Generation Victoria Cohort (2021) (1)
- A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density (2015) (1)
- Genetic regulation of DNA methylation yields novel discoveries in GWAS of colorectal cancer. (2022) (1)
- Selected abstracts submitted to the Third International Symposium on Hereditary Breast and Ovarian Cancer (2009) (1)
- Risk of uterine cancer in BRCA1 and BRCA2 mutation carriers. (2016) (1)
- Selected abstracts submitted to the Third International Symposium on Hereditary Breast and Ovarian Cancer (2009) (1)
- Adenomas in lynch syndrome : Diagnostically useful? (2010) (1)
- Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- Acceptability and usability of iPrevent, a web-based decision support tool for assessment and management of breast cancer risk (2018) (0)
- Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- Novel mammogram-based measures improve breast cancer risk prediction beyond an established measure of mammographic density (2020) (0)
- Is breast cancer risk associated with alcohol intake before first full-term pregnancy? (2016) (0)
- RiskofPancreaticCancerinBreastCancerFamiliesfromthe Breast Cancer Family Registry (2013) (0)
- Back Pain without Disease or Substantial Injury in Children and Adolescents: A Twin Family Study Investigating Genetic Influence and Associations (2023) (0)
- Risks for Relatives (2017) (0)
- Development of a new method to calculate individuals’ melanoma risk (2020) (0)
- Oral Contraceptives and the Risk of Breast Cancer in BRCA 1 and BRCA 2 Mutation Carriers (2003) (0)
- OP-JNCI200057 329..337 (2021) (0)
- Repeatability of methylation measures using a QIAseq targeted methyl panel and comparison with the Illumina HumanMethylation450 assay (2021) (0)
- The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer (2019) (0)
- Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study (2016) (0)
- Abstract 165: Predicting risk of colorectal cancer depending on tumor pathology features for first-degree relatives of persons with colorectal cancer. (2013) (0)
- the Breast Cancer Association Consortium Five Polymorphisms and Breast Cancer Risk : Results from Updated (2009) (0)
- Genome-Wide LinkageAnalysis of 1 , 233 Prostate Cancer Pedigrees Fromthe International Consortium for ProstateCancerGeneticsUsingNovel sumLINKandsumLODAnalyses (2010) (0)
- Abstract A130: Effect of high-dose estrogen exposure in adolescence on mammographic density in adulthood. (2008) (0)
- 10 Global economic evaluation of population-based BRCA1/BRCA2 mutation testing (2019) (0)
- Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry (2016) (0)
- Abstract 3314: Heritable methylation marks associated with prostate and breast cancer risk (2018) (0)
- Association between Early Lung Health and Death in Adulthood (2006) (0)
- P-0184 Screening Practices of Australian Men and Women Categorised As “At or Slightly Above Average Risk” of Colorectal Cancer (2012) (0)
- The effect of ageing on intact PTH and bone density in women (1990) (0)
- A comparison ofrheumatoid arthritis inAustralia and (1986) (0)
- Antihypertensive medication use and breast cancer risk Reply (2017) (0)
- Mo1607 Role of Environmental Risk Factors on Early-Onset Colorectal Cancer Risk (2012) (0)
- Abstracts From the ISTS Satellite Meeting June 20, 2016, Brisbane (2016) (0)
- RADIFUSION: A multi-radiomics deep learning based breast cancer risk prediction model using sequential mammographic images with image attention and bilateral asymmetry refinement (2023) (0)
- Abstract PD6-05: Withdrawn (2019) (0)
- Implications of generating genetic test results for colon cancer in the international, population-based colon cancer family registry. (2012) (0)
- Do women with BRCA1 or BRCA2 mutations have reduced ovarian reserve (2015) (0)
- Familial aggregation of esophageal cancer. (2023) (0)
- Lifetime alcohol consumption and upper aero-digestive tract cancer risk in the Melbourne Collaborative Cohort Study (2014) (0)
- A Twin Study of Genetic Influences on Epilepsy Outcome (2003) (0)
- Association between Mammographic Density and IGF-1 Haplotypes (2006) (0)
- Su1851 Family History and Pathology Features in Early-Onset Colorectal Cancer Cases With a BRAF P.V600e Mutation (2012) (0)
- Risk Factors for Uncommon Breast Cancer Histologic Types (2012) (0)
- Abstract A1-10: The iCOGS breast cancer GWAS reveals 4 unique signals in the PTHLH region in patients of European origin (2015) (0)
- Bone's structural design determines its own decay (2010) (0)
- Cost-effectiveness of systematic population based screening for BRCA1, BRCA2, RAD51C, RAD51D and BRIP1 gene mutations in unselected general population women (2016) (0)
- Association of rs12662670 with breast cancer in Asian ER (2012) (0)
- Abstract PR07: Comparison of risk model recommendations for women at high-risk of breast cancer based on clinical thresholds using the Prospective Family Study Cohort (ProF-SC) (2017) (0)
- Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer (2013) (0)
- F201 The menopausal transition and cardiovascular risk factors (1996) (0)
- Abstract B132: Risk factors for uncommon histologically defined subgroups of breast cancer using the Breast Cancer Family Registry (2010) (0)
- Efficacy of a digital cognitive behavioral therapy for insomnia in people with low back pain: a feasibility randomized co-twin and singleton-controlled trial (2022) (0)
- Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis (2021) (0)
- Interpreting Between- and Within-pair Regression Coefficients in Models for Twin Data (2007) (0)
- Southern Europeans are at reduced risk of BRAF or CpG island methylator phenotype-related colorectal cancer. (2006) (0)
- Authors' reply [11] (2007) (0)
- Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk. (2013) (0)
- Session 2 Onco-genetics and cancer prevention — Defining risk groups: S2. Application of genetics to the prevention of colorectal cancer (2004) (0)
- P213 The natural history of the menopausal transition in australian born women: An update from the melbourne women's midlife health project (1996) (0)
- Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple‐Case Breast Cancer Families (2014) (0)
- Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease (2013) (0)
- Abstract P4-11-02: Acceptability and usability of iPrevent, a web-based decision support tool for assessment and management of breast cancer risk (2018) (0)
- 11-16-JFPRHC Jan 07 (2006) (0)
- Age Dependence of Risk Ratio as an Important Signature of Genetic Effects (2006) (0)
- Effects of Genetic Susceptibility on Dose-Response Curves Potential Relevance to Low-dose Radiation (2006) (0)
- Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia (2014) (0)
- under the age of 40 (1998) (0)
- Bone geometry and surfaces determine differences in structural decay produced by age and menopause: A co-twin control study (2009) (0)
- How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry (2013) (0)
- Assessing patient readiness for personalized genomic medicine (2018) (0)
- Explorer A new GWAS and meta-analysis with 1000 Genomes imputation identifies novel risk variants for colorectal cancer (2017) (0)
- The impact of obesity on outcomes in a population-based cohort of women with early-onset breast cancer. (2004) (0)
- 915Inference on Causation from Examining Changes in Regression coefficients and Innovative STatistical AnaLyses (ICE CRISTAL) (2021) (0)
- Modification of the effect of Flg on allergic disease risk by maternal smoking and siblings (2012) (0)
- Beyond the hype of the human genome (2001) (0)
- Abstract 630: Smoking is associated with risks of molecular subtypes of colorectal cancer (2019) (0)
- population based studies 6174delT mutations: a combined analysis of 22 BRCA1 5382insC and 185delAG and BRCA2 Breast and ovarian cancer risks to carriers of the (2006) (0)
- Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education (2020) (0)
- Abstract PR10: Development of a comprehensive colorectal cancer risk prediction tool (CRiPT) incorporating known and unknown major genes and polygenes (2017) (0)
- F004 The relative contribution of change in paid work status to change in health outcomes in midlife (1996) (0)
- Abstract PS7-04: Population-based estimates of breast cancer risk for germline pathogenic variants identified by gene-panel testing: An Australian perspective (2021) (0)
- Do differences in nutrient intake predict differences in bone mass in boys: A co-twin control study (2001) (0)
- From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes (2012) (0)
- Variance components models for ordinal family data: Baldness and the androgen receptor gene (2005) (0)
- THE AUSTRALIAN NHMRC TWIN REGISTRY: A RESOURCE FOR PEDIATRIC RESEARCH (1993) (0)
- Risks of cancers for carriers of monoallelic MUTYH mutation with a family history of colorectal cancer (2011) (0)
- McCormack-2015-International Consortium on Mam1 (2016) (0)
- rs 2735383 , located at a microRNA binding site in the 3 ’ UTR of NBS 1 , is not associated with breast cancer risk (2016) (0)
- Null Results in Brief No Association between Common Chemokine and Chemokine Receptor Gene Variants and Prostate Cancer Risk (2008) (0)
- Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival (2023) (0)
- Educational attainment of same-sex and opposite-sex dizygotic twins: An individual-level pooled study of 19 twin cohorts (2021) (0)
- Genome-wide association study of germline variants and breast cancer-specific mortality (2019) (0)
- THE AUSTRALIAN BRAIN HEALTH REGISTRY-HEALTHY BRAIN INITIATIVE (2019) (0)
- Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (2021) (0)
- SNP rs2180341 per-allele hazard ratios (HRs) and 95% confidence intervals (CIs) among Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) in A. BRCA1 mutation carriers B. BRCA2 mutation carriers. (2012) (0)
- Mammographic density assessed on paired raw and processed digital images and on paired screen-film and digital images across three mammography systems (2016) (0)
- Homologous recombination DNA repair defects in PALB2-associated breast cancers (2019) (0)
- sense Variants in ATM in 26 , 101 Breast Cancer B & P es and 29 , 842 Controls (2010) (0)
- Match (Mothers and Twin Children): A Prenatally Recruited Volunteer Register of Twins (2007) (0)
- Abstract 4842: Hazard ratio for colorectal cancer risk in Lynch syndrome is inversely associated with age. (2013) (0)
- P156 Sexuality, hormones and the menopausal transition (1996) (0)
- In reply [6] (2006) (0)
- Precision Medicine: Dawn of Supercomputing in ‘omics Research (2011) (0)
- Colorectal cancer in hyperplastic polyposis syndrome: In search of the polyp of origin (2011) (0)
- Short Communication Prediagnosis Reproductive Factors and All-Cause Mortality for Women with Breast Cancer in the Breast Cancer Family Registry (2009) (0)
- 3. Mathematical and statistical methods for genetic analysis (2nd edn). Kenneth Lange, Springer, Berlin, 2002. No. of pages: 361. Price: £52.50. ISBN: 0‐387‐95389‐2 (2004) (0)
- Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects (2021) (0)
- THORAXJNL146845 508..513 (0)
- Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2023) (0)
- Assessment Of Interaction Between Smoking And The LOC387715 (ARMS2)/HTRA1 Genes In Risk Of Age-related Macular Degeneration (AMD) (2012) (0)
- Issue Information (2018) (0)
- Cross-cancer genome-wide association analysis of lung, ovary, breast, prostate and colon cancer identifies a novel cancer locus at 1q22 (2015) (0)
- Does genetic predisposition modify the effect of lifestyle-related factors on DNA methylation? (2021) (0)
- Abstract P5-08-05: Prospective family cohort analyses of gene-environment interactions in breast cancer: Body mass index (2017) (0)
- CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers (2021) (0)
- 720 Rare Variants in CRC Susceptibility Genes Do Not Predispose to Serrated Polyposis Syndrome (2014) (0)
- 1205 POSTER Physical activity, body size and composition, and risk of ovarian cancer (2007) (0)
- Bivariate mixture models for the joint distribution of repeated serum ferritin and transferrin saturation measured 12 years apart in a cohort of healthy middle-aged Australians (2019) (0)
- The Australian NHMRC Twin Registry: A Resource for Pediatric Research (1993) (0)
- Co-twin control study of the effect of smoking on bone mass in women (1990) (0)
- 71 Rare, evolutionary unlikely missense substitutions in CHEK2 confer increased risk of breast cancer (2010) (0)
- Common germline polymorphisms associated with breast cancer-specific survival (2015) (0)
- Tamoxifen and risk of contralateral breast cancer for \textitBRCA1 and \textitBRCA2 mutation carriers (2013) (0)
- The NHMRC twin registry (1990) (0)
- Association Between Mammographic Breast Density and a Chromosome 7p Marker is Confounded by Allele Frequency Variation Across Populations (2010) (0)
- The impact of coding germline variants on contralateral breast cancer risk and survival (2023) (0)
- Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry (2023) (0)
- Volume 65 Part 6 November 2001. Power of regression and maximum likelihood methods to map QTL from sib‐pair and DZ twin data (2002) (0)
- Genetic Predictors of Circulating 25-Hydroxyvitamin D and Prognosis after Colorectal Cancer (2020) (0)
- The association between onset and persistence of Eczema and the risk of other allergic diseases (2011) (0)
- AI integration improves breast cancer screening in a real-world, retrospective cohort study (2022) (0)
- Can Twin Studies Be Used to Infer Causation (2007) (0)
- Alcohol and tobacco use and risk of multiple myeloma: A case‐control study (2021) (0)
- HFE-COMPOUND HETEROZYGOTES WITH SERUM FERRITIN < 1000 UG/L AT AGE 65 ARE NOT AT INCREASED RISK OF HEMOCHROMATOSIS COMPARED TO HFE WILD-TYPE CONTROLS (2008) (0)
- Null Results in Brief Dietary Patterns and Prostate Cancer Risk (2009) (0)
- University of Groningen DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers Osorio, (2014) (0)
- Null Results in Brief No Evidence of Gene – Calcium Interactions from Genome-Wide Analysis of Colorectal Cancer Risk (2014) (0)
- Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation? (2020) (0)
- Abstract P2-06-01: Non-genetic risk factors improve accuracy of breast cancer risk assessment for women at high familial risk: Comparison of risk estimation models using the prospective family study cohort (ProF-SC) (2017) (0)
- Using DEPendency of association on the number of Top Hits (DEPTH) as a complementary tool to identify novel risk loci in colorectal cancer (2022) (0)
- Lifetime alcohol intake and pancreatic cancer incidence and survival: findings from the Melbourne Collaborative Cohort Study (2019) (0)
- Heritability as a contributor for the prevalence of chronic low back pain: the Australian twin low back pain (AUTBACK) study [proceedings] (2014) (0)
- Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome (2019) (0)
- Do Genetic Factors Contribute to Variation in Insulin and Glucose Levels (2001) (0)
- Abstract P5-08-09: Use of oral contraceptives and risk of breast cancer inBRCA1andBRCA2mutation carriers: An international prospective cohort study; for the studies of EMBRACE, GENEPSO, HEBON, kConFab and BCFR (2017) (0)
- Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene (2015) (0)
- Contribution Abdominal Obesity and Age-related Macular Degeneration (2011) (0)
- SPARK: An Open-Source Knowledge Discovery Platform That Leverages Non-Relational Databases and Massively Parallel Computational Power for Heterogeneous Genomic Datasets (2016) (0)
- The healthiron study: A longitudinal study of environmental modifiers of hereditary hemochromatosis (2006) (0)
- EARLY AGE AT NATURAL MENOPAUSE IS ASSOCIATED WITH REDUCED LUNG FUNCTION IN THE TASMANIAN LONGITUDINAL HEALTH STUDY (2019) (0)
- Birthweight, gestational age and familial confounding in sex differences in infant mortality: a matched co-twin control study of Brazilian male-female twin pairs identified by population data linkage (2021) (0)
- Twin Study of Mammographic Breast Density for Age as a Risk Factor for Breast Cancer (2001) (0)
- Reply to a rejoinders informal voting and the A.L.P. (1982) (0)
- Sex differences in epigenetic profiles: The value of twin studies (2021) (0)
- PIK3CA activating mutation in colorectal carcinoma: a stratified analysis in a prospective cohort (2013) (0)
- Preface (2021) (0)
- Different, not biased. (1996) (0)
- Lifestyle factors in chronic low back pain: results from the Australian twin low back pain (AUTBACK) study [proceedings] (2014) (0)
- 150 Do genetic factors explain variations in blood pressure after adjusting for body composition? A study in adolescent and perimenopausal female twins (1993) (0)
- Value of twin and family study designs for epigenetic research (2021) (0)
- 821Surrounding greenness is associated with slower biological ageing based on epigenetics (2021) (0)
- Genetic variation in the immunosuppression pathway genes and breast cancer: a pooled analysis of 42,510 cases and 40,577 controls from the Breast (2015) (0)
- Mammographic Density and Circulating Sex Hormones: a Cross-Sectional Study in Postmenopausal Korean Women (2018) (0)
- 673Is weight more informative than body mass index for breast cancer risk (2021) (0)
- Suggested actions from the Melbourne HVP Information Seminar (2008) (0)
- Risk management practices of Australasian BRCA1 and BRCA2 mutation carriers (2006) (0)
- Heritability of Clinical Features of Age–Related Macular Degeneration – A Twin Study (2005) (0)
- Abstract 1975: The 3D chromatin structure of the PTHLH region comprises a dynamic hierarchical looping complex that approximates the protein-coding genes and facilitates promoter and enhancer promiscuity (2016) (0)
- Comment: On “The partisan component of the informal vote” (1979) (0)
- Reply to PA Dugué et (2019) (0)
- Bivariate Mixture Models of Serum Ferritin and Transferrin Saturation Predict Stable Components Measured 12 Years Apart in a Healthy Australian Population (2011) (0)
- 66 Should we offer multi-gene testing to all patients with breast cancer: a cost-effectiveness analysis (2019) (0)
- Breastfeeding, Atopic Disease and Lung Function: A Cohort Study from Childhood to Middle-age (2006) (0)
- Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer (2020) (0)
- CHILDHOOD BALLET CLASSES, NOT ADULT BALLET TRAINING, PREDICT ADULT HIP BONE DENSITY IN FORMER DANCERS 341 (1997) (0)
- Contribution Apolipoprotein E Gene Associations in Age-related Macular Degeneration The Melbourne Collaborative Cohort Study (2012) (0)
- Chemoprevention for breast cancer: A survey of the views of Australian women and clinicians (2020) (0)
- Haemochromatosis (HFE) Gene and Risk of Colorectal, Breast and Prostate Cancer (2006) (0)
- Are obestity and body fat distribution assoctiated with low back pain in women? A population-based study of 703 Spanish twins [proceedings] (2014) (0)
- Is birthweight related to blood pressure in female twins (2000) (0)
- Molecular and Cellular Pathobiology 19 p 13 . 1 Is a Triple-Negative – Speci fi c Breast Cancer Susceptibility Locus (2012) (0)
- Early life symptoms predict chronic bronchitis in middle-age: longitudinal study from age 7 to 44 years (2006) (0)
- Comparison of Chronic Health Conditions and Health Behaviors in Long-Term Young Adult Hodgkin Lymphoma (YAHL) Survivors to That of Their Unaffected Co-Twin Controls (2022) (0)
- Presenting a new methodology to investigate the influence of heritability and risk factors for low back pain: a twin-controlled study [Award for outstanding research abstract] (2013) (0)
- a novel candidate breast cancer susceptibility locus on (2017) (0)
- MENOPAUSAL BONE LOSS IS MAINLY CORTICAL, NOT TRABECULAR, AND DOES NOT ATTENUATE THE HERITABLE COMPONENT OF VARIANCE IN THIS MICROARCHITECTURE: A PROSPECTIVE STUDY OF TWINS (2016) (0)
- DNA methylation and breast cancer risk: value of twin and family studies (2021) (0)
- Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses (2020) (0)
- Mammographic texture features associated with contralateral breast cancer in the WECARE Study (2021) (0)
- Predictions of asthma in middle age: a longitudinal study over 35 years (2006) (0)
- Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry (2017) (0)
- Epigenome-wide association study of short-term temperature fluctuations based on within-sibship analyses in Australian females. (2022) (0)
- Advances in modeling of the bovine estrous cycle: Synchronization with PGF2 (2022) (0)
- Gastrointestinal Cancer (2010) (0)
- 595ICE FALCON: a causation assessment method analogous to, but more powerful than, Mendelian Randomisation (2021) (0)
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study (2017) (0)
- Fatness and Fitness: The Impact of Fitness on the Genetic Variation of Total and Abdominal Fat - Session: Poster (2004) (0)
- A validation of models for prediction of pathogenic variants in mismatch repair genes. (2022) (0)
- Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes (2020) (0)
- Low Birth Weight and the Development of Asthma (2006) (0)
- High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry (2014) (0)
- GWASeq: targeted re-sequencing follow up to GWAS (2016) (0)
- Prospective cohort study alcohol consumption on breast cancer risk? Does dietary folate intake modify effect of (2007) (0)
- The Effect of Pregnancy on the Epilepsies: A Study of 37 Pregnancies (1994) (0)
- Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes (2020) (0)
- 751 Identification of a Common Variant With Potential Pleiotropic Effect on Risk of Inflammatory Bowel Disease and Colorectal Cancer (2013) (0)
- An Autoradiographic Study of the Developing Parietal Cell Population In Neonatal Pigs (1988) (0)
- Mammographic density defined by higher than conventional brightness threshold better predicts breast cancer risk for full-field digital mammograms (2015) (0)
- Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer (2019) (0)
- A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer (2018) (0)
- Childhood cancers in families with and without Lynch syndrome (2015) (0)
- University of Southern Denmark Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age (2016) (0)
- What if the age at which a woman started regular mammographic screening depended on her risk, not age? (2022) (0)
- Common variants in breast cancer risk loci predispose to distinct tumor subtypes (2022) (0)
- External validation of CAPRA Score amongst radical prostatectomy patients from the Prostate Cancer Clinical Outcomes Database (2010) (0)
- A genetic effect on rates of change in bone density with aging: A twin study (1992) (0)
- Tu1602 Pathological and Clinical Features of Familial Colorectal Cancer Type X (2013) (0)
- Abstract B1-52: Analysis of the iCOGS breast cancer GWAS reveals 4 unique signals in the PTHLH region in patients of European origin (2015) (0)
- Abstract 798: Adenomas in Lynch syndrome: Diagnostically useful (2010) (0)
- The Relative Importance of Genetic and Environmental Factors on Variation in Fat Percent - the Impact of Fitness (2001) (0)
- complementary roles in the hemodynamic evaluation of the acute stroke patient, and it does appear that the two techniques have additive value in acute stroke prognosis. 3 - 4 (1994) (0)
- Addressing gaps in care for patients with rare cancers and blood disorders: The impact of a collaborative digital education initiative. (2021) (0)
- The association of age at menarche and adult height with mammographic density in the International Consortium of Mammographic Density (2022) (0)
- Sex Differences in Infant Mortality: A Population Data Linkage Study of Brazilian Male-Female Twin Pairs (2020) (0)
- Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26. (2022) (0)
- 1574P The cognitive, affective, social and environmental drivers of inappropriate ovarian cancer screening: A survey of women and their clinicians using the theoretical domains framework (2020) (0)
- CYP17 promotor polymorphism and breast cancer in women under the age of forty (2000) (0)
- The effect of age and breast density on the sensitivity of mammography (2004) (0)
- Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2018) (0)
- Cancer Risks for PMS2-Associated Lynch Syndrome (vol 29, pg 2961, 2018) (2019) (0)
- 1032 Prevalence of Germline TP53 Mutations in 510 Population and Clinic-Based Cases of Colorectal Cancer Diagnosed Under Age 40 (2010) (0)
- The Structure of Negative Mood States: Evidence from a Novel Twin Study Analysis (2014) (0)
- 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 (2022) (0)
- Abstract P6-02-04: Screen detected and interval cancers; genomic analysis points to different molecular etiology? (2016) (0)
- Abstract 224: Evidence for a shared genetic basis between breast cancer and mammographic density phenotypes (2018) (0)
- A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome (2023) (0)
- Association analyses identify 31 new risk loci for colorectal cancer susceptibility (2019) (0)
- Alcohol Drinking Patterns and Cardiovascular Mortality Accounting for Possible Misclassification of Intake: Results from the Melbourne Collaborative Cohort Study (2007) (0)
- Abstract 2782: Risk loci for a breast-colon cancer phenotype: results from a genome-wide association study (2015) (0)
- Serum Th2 cytokine profiles in mould sensitised adults from a large population-based cohort (2015) (0)
- Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers (2020) (0)
- How do average woman think about breast cancer risk and prevention? 'A huge hot air balloon' (2016) (0)
- Seizures After Stroke-Reply (1991) (0)
- University of Dundee Interaction between polymorphisms in aspirin metabolic pathways , regular aspirin use and colorectal cancer (2018) (0)
- Dual role of TGFBR1 as a modifier of colorectal cancer risk. (2015) (0)
- 822a Metachronous Colorectal Cancer Risk Following Surgery for First Rectal Cancer in Mismatch Repair Gene Mutation Carriers (2012) (0)
- RE: Heterozygous BRCA1/BRCA2 and mismatch repair gene pathogenic variants in children and adolescents with cancer. (2023) (0)
- University of Southern Denmark Zygosity Differences in Height and Body Mass Index of Twins From Infancy to Old Age (2015) (0)
- Power of regression and maximum likelihood methods to map QTL from sib-pair and DZ twin data. (2001) (0)
- Disclosing genetic research results: experiences of the Colon Cancer Family Registry (2011) (0)
- CORTICAL EXCEEDS TRABECULAR BONE LOSS BEFORE MENOPAUSE BUT NET BONE LOSS IS MODEST BECAUSE PERIOSTEAL APPOSITION OCCURS (2013) (0)
- Genome-wide asociation study and meta-analysis in Northrn European populations replicate multiple colorectal cancer risk (2017) (0)
- International Symposium on Signal Transduction in Health and Disease on Neuroendocrinology: Basic and Clinical Aspects (2008) (0)
- Abstract P3-08-04: Aspirin and breast cancer risk for BRCA1 and BRCA2 mutation carriers (2015) (0)
- Cumulative impact of 10 common genetic variants on colorectal cancer risk in 42,333 individuals from eight populations (2013) (0)
- Wildfire-related PM2.5 and DNA methylation: An Australian twin and family study. (2022) (0)
- S1677 Over-Expression of the Chromosome 11 Mucins is Associated With CIMP and BRAF Mutation in Colorectal Cancer (2010) (0)
- Genetic factors in alcohol use-a genetic epidemiological perspective. (1994) (0)
- Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers (2020) (0)
- Are symptoms of depression associated with low back pain when genetics is considered? A population-based study of spanich twins [proceedings] (2014) (0)
- POD-02.07: BRCA2 Mutation Confers an Increased Risk of Aggressive Prostate Cancer in Australia and New Zealand (2009) (0)
- Abstract P6-09-04: Benign breast disease and breast cancer risk across the spectrum of familial risk using a prospective family study cohort (ProF-SC) (2018) (0)
- Meta-analysis of new genome-wide association studies of colorectal cancer risk (2011) (0)
- Role of tumor molecular and pathology features to estimate colorectal cancer risk for first-degree relatives (2014) (0)
- Accuracy of Self-Reported Nevus and Pigmentation Phenotype Compared with Clinical AssessmentinaPopulation-BasedStudyofYoung (2015) (0)
- THE ASSOCIATION OF LOBULAR BREAST CANCER WITH GERMLINE MUTATIONS OF CDH1 (2008) (0)
- Assessing the ProMCol classifier as a prognostic marker for non-metastatic colorectal cancer within the Melbourne Collaborative Cohort Study (2018) (0)
- Mammographic density and risk of breast cancer by tumor characteristics: a case-control study (2017) (0)
- Erratum: Phenotypic diversity in patients with multiple serrated polyps: A genetics clinic study (International Journal of Colorectal Disease (2010) 25 (1513-1515)) (2010) (0)
- Abstract 3862: Identification of a novel genetic variant in theKLK3gene which predisposes to prostate cancer (2010) (0)
- Screening practices of Australian men and women categorized as “at or slightly above average risk” of colorectal cancer (2012) (0)
- Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM (2022) (0)
- OP-IJEJ190194 1..15 (2019) (0)
- Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts (2022) (0)
- Abstract P3-02-03: Breast cancer screening by women fromBRCA1&BRCA2mutation positive families: (2015) (0)
- 2079 Risk factors for metachronous colorectal cancer following a primary colorectal cancer: A prospective cohort study (2015) (0)
- Mendelian randomization study of age at menarche and age at 1 menopause and the risk of colorectal cancer (2018) (0)
- [Title page i] (2019) (0)
- Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis (2013) (0)
- Performance of BCRAT in high-risk patients with breast cancer reply (2019) (0)
- OP-JNCI180212 331..334 (2019) (0)
- Heritable methylation marks associated with prostate and breast cancer risk (2018) (0)
- Genome disorder and breast cancer susceptibility (2014) (0)
- P155 Premenstrual syndrome and perimenopausal experiences: Is there a relationship (1996) (0)
- Australian NHMRC twin registry: A resource for pediatric research (1995) (0)
- The taller they are, the more porous the skeleton to fall harder upon (2012) (0)
- Validation of a breast cancer risk prediction model based on the key risk factors: family history, mammographic density and polygenic risk (2023) (0)
- q 31 . 2 and in ZNF 365 are associated with breast cancer risk for BRCA 1 and / or BRCA 2 mutation carriers (2012) (0)
- Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus (2016) (0)
- Contribution Associations of Mammographic Dense andNondenseAreas andBodyMass Index With Risk of Breast Cancer (2014) (0)
- P075 A comparison of the levels of immunoreactive inhibin and dimeric inhibin a in perimenopausal women (1996) (0)
- Breast-Cancer Risk in Families With Mutations in PALB2 EDITORIAL COMMENT (2014) (0)
- ASCIA 2011 Poster Abstract (2011) (0)
- Molecular and genetic epidemiology of breast cancer (2000) (0)
- Abstract P6-09-01: Risk-reducing oophorectomy and breast cancer risk across the spectrum of familial risk using a prospective family study cohort (ProF-SC) (2018) (0)
- Bone turnover indices in twins: Evidence for a genetic effect on bone formation but not resorption in women (1990) (0)
- Two ATM variants, IVS10-6T>G and 1420L>F, and breast cancer risk (2005) (0)
- OCCUPATIONAL EXPOSURE TO SOLVENTS AND METALS AND FIXED AIRFLOW OBSTRUCTION IN WOMEN (2017) (0)
- Reply (2005) (0)
- Obituary: Professor Roger Valentine Short, 31 July 1930–6 August 2021 (2021) (0)
- Abstract 3530: The parathyroid hormone-related peptide region likely features seven discrete breast cancer susceptibility loci (2014) (0)
- Mendelian Randomization Causal Analysis Mendelian randomization study of height and risk of colorectal cancer (2015) (0)
- 1057Addressing challenges in life-course epidemiology: established and novel approaches using big data and twin/family studies (2021) (0)
- Use of a novel non-parametric version of DEPTH to identify genomic regions associated with prostate cancer risk (2016) (0)
- Rare copy number variants (CNVs) and breast cancer risk (2021) (0)
- A Competing Risks Model with Time Varying Covariates for Estimation of Breast Cancer Risks in BRCA1 Families (2020) (0)
- DNA mismatch repair deficiency in breast cancers arising in breast/colon families (2008) (0)
- The association of global gene expression in human colon tumors with germline variation at rs6983267 on 8q24 suggests that this SNP is an eQTL hotspot (2009) (0)
- Weight is More Informative than Body Mass Index for Predicting Postmenopausal Breast Cancer Risk: Prospective Family Study Cohort (ProF-SC) (2021) (0)
- Issue Information (2021) (0)
- Abstract B06: Utah familial colorectal cancer risk model (2017) (0)
- Title Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes (2018) (0)
- Genome-wide association study of germline variants and breast cancer-speci fi c mortality (2019) (0)
- Identifying the early-onset cases of breast and colorectal cancers most likely to carry a germline mutation in a "high-risk" cancer predisposition gene (2008) (0)
- Early life tobacco smoke exposure is associated with asthma and lung function deficits in adolescents (2014) (0)
- Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling (2022) (0)
- Abstract 1322: A meta-analysis of genome-wide association studies identifies novel loci that influence breast cancer prognosis (2017) (0)
- Reply: Genetic influence on rolandic epilepsy (2005) (0)
- Breast cancer genetics in perspective: Results from population-based studies (2008) (0)
- A Simple Regression Approach to Decomposing the Genetic and Environmental Determinants of Associations Between Traits Using Twin and Family Data (2006) (0)
- Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium (2020) (0)
- Erratum: Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers (Breast cancer research : BCR (2020) 22 1 (8)) (2020) (0)
- This Provisional PDF corresponds to the article as it appeared upon acceptance. Copyedited and fully formatted PDF and full text (HTML) versions will be made available soon. (2010) (0)
- Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- Polygenic risk modeling for prediction of epithelial ovarian cancer risk (2022) (0)
- The association of age at menarche and adult height with mammographic density in the International Consortium of Mammographic Density (2022) (0)
- Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients (2022) (0)
- Residential surrounding greenness and DNA methylation: an epigenome-wide association study (2021) (0)
- InSiGHT, pedigree, familial aspects of cancer and the Human Variome Project in conjunction with the COSA familial cancer group (2013) (0)
- Spotlight on gynecologyMenopausal symptoms (2001) (0)
- Association of calcium and vitamin D intakes with mammographic density in twins. (2006) (0)
- Reply to V. Fallet et al. (2022) (0)
- TITLE: Mendelian randomization of circulating polyunsaturated fatty acids and colorectal cancer risk (2020) (0)
- Smoking, alcohol consumption, body fatness, and risk of myelodysplastic syndromes: A prospective study. (2021) (0)
- 888Discriminating between risk discriminators: OPERA, AUC, and polygenic variance (2021) (0)
- 14th Annual Meeting of the Collaborative Group of the Americas on Inherited Colorectal Cancer Dallas, TX, USA. 12-13 October 2010. Abstracts. (2011) (0)
- Genetic contributions to body composition and muscle strength: A twin study (1992) (0)
- 783Lifetime alcohol intake and stomach cancer risk: a pooled analysis of two prospective cohort studies (2021) (0)
- Penetrance of CDKN2A mutations estimated using population-based Australian families (2009) (0)
- Genetic Variants in the Regulatory T cell–Related Pathway and Colorectal Cancer Prognosis (2020) (0)
- Alcohol Drinking Patterns and Cardiovascular Mortality in a Cohort of Melbourne Men and Women (2006) (0)
- Abstract 2930: Novel colorectal cancer loci in multiplex-proficient mismatch repair families (2012) (0)
- INCREASED BONE TURNOVER IN ATHLETES WITH STRESS FRACTURES 31 (1996) (0)
- Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women (2017) (0)
- Abstract 4623: External validation of the BOADICEA model for predicting ovarian cancer risk: The Breast Cancer Family Registry (2020) (0)
- Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (2019) (0)
- Shared heritability and functional enrichment across six solid cancers (2019) (0)
- PP01 International pooling project of mammographic density - insights of a marker of breast cancer risk from 22 diverse countries (2015) (0)
- Uptake of Offer to Receive Genetic Information about Genetic Mutations in the Victorian Colorectal Cancer Family Study (2006) (0)
- Validation of an Abridged Breast Cancer Risk Prediction Model for the General Population (2023) (0)
- Precision breast and prostate cancer risk management: evidence-based translation of epigenetic testing (2018) (0)
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