| 1 | Menopausal hormone therapy: assessing associations with breast and colorectal cancers by familial risk | 2.9 | 0 | Citations (PDF) |
| 2 | Smart Nonuniformity for Calibrating Sequencing Depth of a Targeted Gene Panel to Simultaneously Detect Somatic and Germline Variants | 2.5 | 0 | Citations (PDF) |
| 3 | Genetic and Environmental Causes of Variation in an Automated Breast Cancer Risk Factor Based on Mammographic Textures | 1.1 | 1 | Citations (PDF) |
| 4 | Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes | 13.7 | 15 | Citations (PDF) |
| 5 | Self-rated health, epigenetic ageing, and long-term mortality in older Australians | 4.6 | 4 | Citations (PDF) |
| 6 | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel | 6.5 | 63 | Citations (PDF) |
| 7 | Pregnancy-Related Factors and Breast Cancer Risk for Women Across a Range of Familial Risk | 6.6 | 5 | Citations (PDF) |
| 8 | Dietary factors and DNA methylation-based markers of ageing in 5310 middle-aged and older Australian adults | 4.6 | 4 | Citations (PDF) |
| 9 | Region-Based Analyses of Existing Genome-Wide Association Studies Identifies Novel Potential Genetic Susceptibility Regions for Glioma | 2.8 | 1 | Citations (PDF) |
| 10 | Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men | 2.9 | 8 | Citations (PDF) |
| 11 | Epigenome-wide association study of short-term temperature fluctuations based on within-sibship analyses in Australian females | 10.2 | 5 | Citations (PDF) |
| 12 | Methylation scores for smoking, alcohol consumption and body mass index and risk of seven types of cancer | 4.3 | 15 | Citations (PDF) |
| 13 | The impact of coding germline variants on contralateral breast cancer risk and survival | 6.5 | 18 | Citations (PDF) |
| 14 | Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel | 3.8 | 3 | Citations (PDF) |
| 15 | Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants | 25.2 | 122 | Citations (PDF) |
| 16 | Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries | 4.9 | 59 | Citations (PDF) |
| 17 | Association of Markers of Inflammation, the Kynurenine Pathway and B Vitamins with Age and Mortality, and a Signature of Inflammaging | 3.5 | 44 | Citations (PDF) |
| 18 | Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants | 4.2 | 28 | Citations (PDF) |
| 19 | Value of the loss of heterozygosity to BRCA1 variant classification | 6.4 | 8 | Citations (PDF) |
| 20 | Independent evaluation of melanoma polygenic risk scores in
UK
and Australian prospective cohorts* | 1.7 | 19 | Citations (PDF) |
| 21 | Early life affects late-life health through determining DNA methylation across the lifespan: A twin study | 9.7 | 32 | Citations (PDF) |
| 22 | A Genome-Wide Gene-Based Gene–Environment Interaction Study of Breast Cancer in More than 90,000 Women | 2.8 | 10 | Citations (PDF) |
| 23 | Weight is More Informative than Body Mass Index for Predicting Postmenopausal Breast Cancer Risk: Prospective Family Study Cohort (ProF-SC) | 1.5 | 5 | Citations (PDF) |
| 24 | Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects | 25.2 | 327 | Citations (PDF) |
| 25 | Epigenetic mechanisms of lung carcinogenesis involve differentially methylated CpG sites beyond those associated with smoking | 5.3 | 9 | Citations (PDF) |
| 26 | Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies | 4.6 | 38 | Citations (PDF) |
| 27 | Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling | 1.7 | 1 | Citations (PDF) |
| 28 | Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium | 1.7 | 47 | Citations (PDF) |
| 29 | Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries | 25.2 | 194 | Citations (PDF) |
| 30 | Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer | 4.3 | 55 | Citations (PDF) |
| 31 | Methylation marks of prenatal exposure to maternal smoking and risk of cancer in adulthood | 4.9 | 25 | Citations (PDF) |
| 32 | Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort | 4.6 | 15 | Citations (PDF) |
| 33 | DNA Methylation in Peripheral Blood and Risk of Gastric Cancer: A Prospective Nested Case–control Study | 1.5 | 6 | Citations (PDF) |
| 34 | Alcohol consumption is associated with widespread changes in blood DNA methylation: Analysis of cross‐sectional and longitudinal data | 2.6 | 81 | Citations (PDF) |
| 35 | The EUS molecular evaluation of pancreatic cancer: A prospective multicenter cohort trial | 2.9 | 7 | Citations (PDF) |
| 36 | Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer | 3.9 | 18 | Citations (PDF) |
| 37 | Epigenetic Drift Association with Cancer Risk and Survival, and Modification by Sex | 3.8 | 11 | Citations (PDF) |
| 38 | Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects | 6.4 | 12 | Citations (PDF) |
| 39 | DNA Methylation Signatures and the Contribution of Age-Associated Methylomic Drift to Carcinogenesis in Early-Onset Colorectal Cancer | 3.8 | 29 | Citations (PDF) |
| 40 | Transcriptomic changes in peripheral blood mononuclear cells with weight loss: systematic literature review and primary data synthesis | 4.3 | 13 | Citations (PDF) |
| 41 | Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus | 2.9 | 32 | Citations (PDF) |
| 42 | Independent prognostic impact of plasma NCOA2 alterations in metastatic castration‐resistant prostate cancer | 2.1 | 8 | Citations (PDF) |
| 43 | Inflammation-Related Marker Profiling of Dietary Patterns and All-cause Mortality in the Melbourne Collaborative Cohort Study | 2.9 | 23 | Citations (PDF) |
| 44 | Surrounding Greenness and Biological Aging Based on DNA Methylation: A Twin and Family Study in Australia | 8.4 | 24 | Citations (PDF) |
| 45 | Androgens alter the heterogeneity of small extracellular vesicles and the small RNA cargo in prostate cancer | 12.6 | 35 | Citations (PDF) |
| 46 | Ambient temperature and genome-wide DNA methylation: A twin and family study in Australia | 7.7 | 18 | Citations (PDF) |
| 47 | Residential surrounding greenness and DNA methylation: An epigenome-wide association study | 10.2 | 31 | Citations (PDF) |
| 48 | Smoking Methylation Marks for Prediction of Urothelial Cancer Risk | 1.1 | 5 | Citations (PDF) |
| 49 | 1322A pilot study of faecal sample collection from prospective cohort study participants | 4.9 | 0 | Citations (PDF) |
| 50 | Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium | 1.1 | 35 | Citations (PDF) |
| 51 | Biological Aging Measures Based on Blood DNA Methylation and Risk of Cancer: A Prospective Study | 2.9 | 77 | Citations (PDF) |
| 52 | Prospective Evaluation over 15 Years of Six Breast Cancer Risk Models | 3.8 | 8 | Citations (PDF) |
| 53 | Repeatability of methylation measures using a QIAseq targeted methyl panel and comparison with the Illumina HumanMethylation450 assay | 1.5 | 4 | Citations (PDF) |
| 54 | Recreational Physical Activity and Outcomes After Breast Cancer in Women at High Familial Risk | 2.9 | 4 | Citations (PDF) |
| 55 | Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness | 3.8 | 48 | Citations (PDF) |
| 56 | Considerations When Using Breast Cancer Risk Models for Women with Negative BRCA1/BRCA2 Mutation Results | 4.6 | 1 | Citations (PDF) |
| 57 | 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 | 3.8 | 50 | Citations (PDF) |
| 58 | Smoking and blood DNA methylation: an epigenome-wide association study and assessment of reversibility | 3.0 | 81 | Citations (PDF) |
| 59 | Overall lack of replication of associations between dietary intake of folate and vitamin B-12 and DNA methylation in peripheral blood | 4.7 | 7 | Citations (PDF) |
| 60 | Dysfunctional epigenetic aging of the normal colon and colorectal cancer risk | 3.9 | 66 | Citations (PDF) |
| 61 | Postmenopausal Hormone Therapy and Colorectal Cancer Risk by Molecularly Defined Subtypes and Tumor Location | 2.9 | 18 | Citations (PDF) |
| 62 | Stochastic Epigenetic Mutations Are Associated with Risk of Breast Cancer, Lung Cancer, and Mature B-cell Neoplasms | 1.1 | 28 | Citations (PDF) |
| 63 | Genetic and environmental causes of variation in epigenetic aging across the lifespan | 3.9 | 62 | Citations (PDF) |
| 64 | Characterization of the Cancer Spectrum in Men With GermlineBRCA1andBRCA2Pathogenic Variants | 14.4 | 61 | Citations (PDF) |
| 65 | Palm reading and water divining: A cross-sectional study of the accuracy of palmar hyperlinearity and transepidermal water loss to identify individuals with a filaggrin gene null mutation | 1.8 | 3 | Citations (PDF) |
| 66 | Novel Common Genetic Susceptibility Loci for Colorectal Cancer | 4.6 | 155 | Citations (PDF) |
| 67 | Accuracy of Risk Estimates from the iPrevent Breast Cancer Risk Assessment and Management Tool | 2.9 | 10 | Citations (PDF) |
| 68 | A Cost-effectiveness Analysis of Multigene Testing for All Patients With Breast Cancer | 14.4 | 121 | Citations (PDF) |
| 69 | Body size and dietary risk factors for aggressive prostate cancer: a case–control study | 1.7 | 3 | Citations (PDF) |
| 70 | 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 | 4.8 | 53 | Citations (PDF) |
| 71 | Epigenome-wide association study for lifetime estrogen exposure identifies an epigenetic signature associated with breast cancer risk | 3.9 | 26 | Citations (PDF) |
| 72 | Dietary Intake of Nutrients Involved in One-Carbon Metabolism and Risk of Gastric Cancer: A Prospective Study | 2.4 | 22 | Citations (PDF) |
| 73 | Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report | 3.8 | 41 | Citations (PDF) |
| 74 | Autologous platelet‐rich plasma for healing chronic venous leg ulcers: Clinical efficacy and potential mechanisms | 3.1 | 16 | Citations (PDF) |
| 75 | Benign breast disease increases breast cancer risk independent of underlying familial risk profile: Findings from a Prospective Family Study Cohort | 4.3 | 14 | Citations (PDF) |
| 76 | 10-year performance of four models of breast cancer risk: a validation study | 27.4 | 143 | Citations (PDF) |
| 77 | Physical Activity, Television Viewing Time, and DNA Methylation in Peripheral Blood | 0.8 | 19 | Citations (PDF) |
| 78 | Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC) | 4.8 | 46 | Citations (PDF) |
| 79 | Circulating concentrations of B group vitamins and urothelial cell carcinoma | 4.3 | 10 | Citations (PDF) |
| 80 | Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk | 4.6 | 38 | Citations (PDF) |
| 81 | Dietary intake of nutrients involved in one‐carbon metabolism and risk of urothelial cell carcinoma: A prospective cohort study | 4.3 | 14 | Citations (PDF) |
| 82 | Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases | 4.0 | 9 | Citations (PDF) |
| 83 | Association of DNA Methylation-Based Biological Age With Health Risk Factors and Overall and Cause-Specific Mortality | 3.3 | 136 | Citations (PDF) |
| 84 | Associations of alcohol intake, smoking, physical activity and obesity with survival following colorectal cancer diagnosis by stage, anatomic site and tumor molecular subtype | 4.3 | 96 | Citations (PDF) |
| 85 | DNA methylation‐based biological aging and cancer risk and survival: Pooled analysis of seven prospective studies | 4.3 | 208 | Citations (PDF) |
| 86 | Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 | 4.2 | 54 | Citations (PDF) |
| 87 | Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC) | 4.8 | 70 | Citations (PDF) |
| 88 | Predicting interval and screen-detected breast cancers from mammographic density defined by different brightness thresholds | 4.8 | 26 | Citations (PDF) |
| 89 | Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study | 2.9 | 42 | Citations (PDF) |
| 90 | sEst: Accurate Sex-Estimation and Abnormality Detection in Methylation Microarray Data | 4.4 | 8 | Citations (PDF) |
| 91 | Genome-wide average DNA methylation is determined in utero | 4.9 | 42 | Citations (PDF) |
| 92 | Heritable methylation marks associated with breast and prostate cancer risk | 2.1 | 21 | Citations (PDF) |
| 93 | FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine | 1.8 | 23 | Citations (PDF) |
| 94 | The utility of DNA extracted from saliva for genome-wide molecular research platforms | 1.5 | 31 | Citations (PDF) |
| 95 | Epigenetic supersimilarity of monozygotic twin pairs | 8.1 | 105 | Citations (PDF) |
| 96 | Dietary intake of one-carbon metabolism nutrients and DNA methylation in peripheral blood | 4.7 | 46 | Citations (PDF) |
| 97 | Inference about causation between body mass index and DNA methylation in blood from a twin family study | 3.0 | 54 | Citations (PDF) |
| 98 | Cohort Profile: The Tasmanian Longitudinal Health STUDY (TAHS) | 4.9 | 26 | Citations (PDF) |
| 99 | Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci | 5.5 | 26 | Citations (PDF) |
| 100 | Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study | 1.4 | 6 | Citations (PDF) |
| 101 | Genome‐Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case‐Control Study | 2.1 | 36 | Citations (PDF) |
| 102 | Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia | 13.7 | 96 | Citations (PDF) |
| 103 | Association between DNA methylation at SOCS3 gene and body mass index might be due to familial confounding | 3.0 | 17 | Citations (PDF) |
| 104 | Total and beverage-specific alcohol intake and the risk of aggressive prostate cancer: a case–control study | 4.0 | 11 | Citations (PDF) |
| 105 | Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers | 16.6 | 2,546 | Citations (PDF) |
| 106 | Ejaculatory frequency and the risk of aggressive prostate cancer: Findings from a case-control study | 1.8 | 19 | Citations (PDF) |
| 107 | Twin birth changes DNA methylation of subsequent siblings | 3.4 | 10 | Citations (PDF) |
| 108 | Causes of blood methylomic variation for middle-aged women measured by the HumanMethylation450 array | 3.0 | 14 | Citations (PDF) |
| 109 | Characterisation of microbial communities within aggressive prostate cancer tissues | 2.5 | 67 | Citations (PDF) |
| 110 | DNA methylation changes measured in pre‐diagnostic peripheral blood samples are associated with smoking and lung cancer risk | 4.3 | 127 | Citations (PDF) |
| 111 | Body mass index and breast cancer survival: a Mendelian randomization analysis | 4.9 | 53 | Citations (PDF) |
| 112 | Mammographic density and risk of breast cancer by tumor characteristics: a case-control study | 2.9 | 8 | Citations (PDF) |
| 113 | Novel associations between blood DNA methylation and body mass index in middle-aged and older adults | 3.0 | 76 | Citations (PDF) |
| 114 | DNA Methylation in Breast Tumor from High-risk Women in the Breast Cancer Family Registry | 1.1 | 9 | Citations (PDF) |
| 115 | Strategies for Integrated Analysis of Genetic, Epigenetic, and Gene Expression Variation in Cancer: Addressing the Challenges | 2.3 | 24 | Citations (PDF) |
| 116 | Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers | 2.3 | 12 | Citations (PDF) |
| 117 | Mould‐sensitized adults have lower Th2 cytokines and a higher prevalence of asthma than those sensitized to other aeroallergens | 6.8 | 5 | Citations (PDF) |
| 118 | Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study | 4.8 | 36 | Citations (PDF) |
| 119 | Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus | 4.8 | 37 | Citations (PDF) |
| 120 | Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 | 4.8 | 96 | Citations (PDF) |
| 121 | Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case–control study | 5.5 | 40 | Citations (PDF) |
| 122 | Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women | 4.8 | 63 | Citations (PDF) |
| 123 | Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer | 13.7 | 103 | Citations (PDF) |
| 124 | Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia | 13.7 | 109 | Citations (PDF) |
| 125 | Reliability of DNA methylation measures from dried blood spots and mononuclear cells using the HumanMethylation450k BeadArray | 3.4 | 72 | Citations (PDF) |
| 126 | Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH | 4.3 | 138 | Citations (PDF) |
| 127 | Global Measures of Peripheral Blood-Derived DNA Methylation as a Risk Factor in the Development of Mature B-Cell Neoplasms | 2.2 | 37 | Citations (PDF) |
| 128 | Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients | 3.0 | 18 | Citations (PDF) |
| 129 | Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families | 3.8 | 72 | Citations (PDF) |
| 130 | Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 | 2.4 | 20 | Citations (PDF) |
| 131 | A prospective study of peripheral blood DNA methylation at RPTOR, MGRN1 and RAPSN and risk of breast cancer | 2.4 | 9 | Citations (PDF) |
| 132 | Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry | 2.4 | 33 | Citations (PDF) |
| 133 | Hypomethylation of smoking-related genes is associated with future lung cancer in four prospective cohorts | 13.7 | 215 | Citations (PDF) |
| 134 | Genome-Wide Association Study of Prostate Cancer–Specific Survival | 1.1 | 28 | Citations (PDF) |
| 135 | Hi-Plex targeted sequencing is effective using DNA derived from archival dried blood spots | 2.4 | 8 | Citations (PDF) |
| 136 | A Genome-Wide “Pleiotropy Scan” Does Not Identify New Susceptibility Loci for Estrogen Receptor Negative Breast Cancer | 2.3 | 8 | Citations (PDF) |
| 137 | Reproductive risk factors and oestrogen/progesterone receptor-negative breast cancer in the Breast Cancer Family Registry | 5.5 | 57 | Citations (PDF) |
| 138 | DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers | 3.2 | 55 | Citations (PDF) |
| 139 | Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia | 4.8 | 110 | Citations (PDF) |
| 140 | Breast-Cancer Risk in Families With Mutations in PALB2 | 0.5 | 1 | Citations (PDF) |
| 141 | DNA mismatch repair gene MSH6 implicated in determining age at natural menopause | 2.9 | 65 | Citations (PDF) |
| 142 | Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers | 4.8 | 63 | Citations (PDF) |
| 143 | Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer | 2.8 | 159 | Citations (PDF) |
| 144 | Associations of Mammographic Dense and Nondense Areas and Body Mass Index With Risk of Breast Cancer | 3.3 | 55 | Citations (PDF) |
| 145 | Should the grading of colorectal adenocarcinoma include microsatellite instability status? | 2.3 | 46 | Citations (PDF) |
| 146 | FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium | 5.5 | 22 | Citations (PDF) |
| 147 | Detection of infectious organisms in archival prostate cancer tissues | 2.9 | 33 | Citations (PDF) |
| 148 | A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer | 25.2 | 432 | Citations (PDF) |
| 149 | Comparison of mRNA Splicing Assay Protocols across Multiple Laboratories: Recommendations for Best Practice in Standardized Clinical Testing | 1.1 | 100 | Citations (PDF) |
| 150 | COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration | 4.8 | 39 | Citations (PDF) |
| 151 | FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets | 3.0 | 10 | Citations (PDF) |
| 152 | The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array | 2.9 | 72 | Citations (PDF) |
| 153 | Tumour morphology predicts PALB2 germline mutation status | 5.5 | 19 | Citations (PDF) |
| 154 | Confirmation of the reduction of hormone replacement therapy-related breast cancer risk for carriers of the HSD17B1_937_G variant | 2.4 | 10 | Citations (PDF) |
| 155 | Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2 | 1.7 | 15 | Citations (PDF) |
| 156 | Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre | 5.5 | 46 | Citations (PDF) |
| 157 | Cross-platform compatibility of Hi-Plex, a streamlined approach for targeted massively parallel sequencing | 2.4 | 11 | Citations (PDF) |
| 158 | Diagnostic Chest X-Rays and Breast Cancer Risk before Age 50 Years for BRCA1 and BRCA2 Mutation Carriers | 1.1 | 23 | Citations (PDF) |
| 159 | Evaluation of a 5-Tier Scheme Proposed for Classification of Sequence Variants Using Bioinformatic and Splicing Assay Data: Inter-Reviewer Variability and Promotion of Minimum Reporting Guidelines | 4.5 | 69 | Citations (PDF) |
| 160 | Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles | 2.3 | 100 | Citations (PDF) |
| 161 | Population-Based Estimate of Prostate Cancer Risk for Carriers of the HOXB13 Missense Mutation G84E | 2.3 | 32 | Citations (PDF) |
| 162 | A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers | 1.1 | 24 | Citations (PDF) |
| 163 | High and low mammographic density human breast tissues maintain histological differential in murine tissue engineering chambers | 2.4 | 13 | Citations (PDF) |
| 164 | Genome-wide association analysis identifies three new breast cancer susceptibility loci | 25.2 | 271 | Citations (PDF) |
| 165 | Interleukin‐6 promoter variants, prostate cancer risk, and survival | 2.1 | 22 | Citations (PDF) |
| 166 | Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers | 4.8 | 83 | Citations (PDF) |
| 167 | Ovarian cancer susceptibility alleles and risk of ovarian cancer inBRCA1andBRCA2mutation carriers | 4.5 | 35 | Citations (PDF) |
| 168 | Design Considerations for Massively Parallel Sequencing Studies of Complex Human Disease | 2.3 | 20 | Citations (PDF) |
| 169 | Image-guided sampling reveals increased stroma and lower glandular complexity in mammographically dense breast tissue | 2.4 | 56 | Citations (PDF) |
| 170 | Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer | 4.3 | 103 | Citations (PDF) |
| 171 | 7q21-rs6964587 and breast cancer risk: an extended case–control study by the Breast Cancer Association Consortium | 3.8 | 5 | Citations (PDF) |
| 172 | The rs12975333 variant in the miR-125a and breast cancer risk in Germany, Italy, Australia and Spain | 3.8 | 13 | Citations (PDF) |
| 173 | Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers | 2.9 | 37 | Citations (PDF) |
| 174 | Body Mass Index in Early Adulthood and Endometrial Cancer Risk for Mismatch Repair Gene Mutation Carriers | 1.9 | 25 | Citations (PDF) |
| 175 | Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk | 5.5 | 5 | Citations (PDF) |
| 176 | The postmenopausal hormone replacement therapy-related breast cancer risk is decreased in women carrying the CYP2C19*17 variant | 2.4 | 6 | Citations (PDF) |
| 177 | The 4q27 locus and prostate cancer risk | 2.9 | 8 | Citations (PDF) |
| 178 | Sibship analysis of associations between SNP haplotypes and a continuous trait with application to mammographic density | 3.1 | 10 | Citations (PDF) |
| 179 | Letter in response to “Identifying Lynch syndrome” by de la Chapelle et al. | 4.3 | 1 | Citations (PDF) |
| 180 | Plasma concentration of Propionibacterium acnes antibodies and prostate cancer risk: results from an Australian population-based case–control study | 5.5 | 25 | Citations (PDF) |
| 181 | Increased cancer risks for relatives of very early-onset breast cancer cases with and without BRCA1 and BRCA2 mutations | 5.5 | 30 | Citations (PDF) |
| 182 | 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 | 25.2 | 317 | Citations (PDF) |
| 183 | Molecular characterization of breast cancer in young Brazilian women | 0.8 | 10 | Citations (PDF) |
| 184 | Family-based association study of IGF1 microsatellites and height, weight, and body mass index | 2.0 | 4 | Citations (PDF) |
| 185 | Association of ESR1 gene tagging SNPs with breast cancer risk | 2.9 | 87 | Citations (PDF) |
| 186 | Familial Correlations in Postmenopausal Serum Concentrations of Sex Steroid Hormones and Other Mitogens: A Twins and Sisters Study | 4.1 | 23 | Citations (PDF) |
| 187 | Family-based genetic association study of insulin-like growth factor I microsatellite markers and premenopausal breast cancer risk | 2.4 | 5 | Citations (PDF) |
| 188 | A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2 | 25.2 | 296 | Citations (PDF) |
| 189 | Are PALB2 mutations associated with increased risk of male breast cancer? | 2.4 | 20 | Citations (PDF) |
| 190 | The rs743572 common variant in the promoter of CYP17A1 is not associated with prostate cancer risk or circulating hormonal levels | 3.2 | 13 | Citations (PDF) |
| 191 | The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions | 5.5 | 490 | Citations (PDF) |
| 192 | Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers | 3.8 | 1 | Citations (PDF) |
| 193 | Multiple Novel Prostate Cancer Predisposition Loci Confirmed by an International Study: The PRACTICAL Consortium | 1.1 | 151 | Citations (PDF) |
| 194 | The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case–control and family analysis | 2.4 | 21 | Citations (PDF) |
| 195 | The Common Variant rs1447295 on Chromosome 8q24 and Prostate Cancer Risk: Results from an Australian Population-Based Case-Control Study | 1.1 | 64 | Citations (PDF) |
| 196 | Mammographic Density and Candidate Gene Variants: A Twins and Sisters Study | 1.1 | 31 | Citations (PDF) |
| 197 | 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia | 4.3 | 61 | Citations (PDF) |
| 198 | Medical radiation exposure and breast cancer risk: Findings from the Breast Cancer Family Registry | 4.3 | 63 | Citations (PDF) |
| 199 | A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data | 3.1 | 3 | Citations (PDF) |
| 200 | Genome-wide association study identifies novel breast cancer susceptibility loci | 37.9 | 2,211 | Citations (PDF) |
| 201 | Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies | 3.3 | 26 | Citations (PDF) |
| 202 | Is MSH2 a breast cancer susceptibility gene? | 1.4 | 6 | Citations (PDF) |
| 203 | BRCA1 and BRCA2 Mutation Carriers, Oral Contraceptive Use, and Breast Cancer Before Age 50 | 1.1 | 120 | Citations (PDF) |
| 204 | A genome wide linkage search for breast cancer susceptibility genes | 3.0 | 114 | Citations (PDF) |
| 205 | The AIB1 Polyglutamine Repeat Does Not Modify Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers | 1.1 | 26 | Citations (PDF) |
| 206 | Macrophage Inhibitory Cytokine-1 H6D Polymorphism, Prostate Cancer Risk, and Survival | 1.1 | 34 | Citations (PDF) |
| 207 | Prediction of BRCA1 and BRCA2 mutation status using post-irradiation assays of lymphoblastoid cell lines is compromised by inter-cell-line phenotypic variability | 2.4 | 8 | Citations (PDF) |
| 208 | TwoATM variants and breast cancer risk | 4.5 | 44 | Citations (PDF) |
| 209 | Double-Strand Break Repair Gene Polymorphisms and Risk of Breast or Ovarian Cancer | 1.1 | 78 | Citations (PDF) |
| 210 | The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia | 1.1 | 80 | Citations (PDF) |
| 211 | Genetic Variants in the Vitamin D Receptor Gene and Prostate Cancer Risk | 1.1 | 34 | Citations (PDF) |
| 212 | Macrophage Scavenger Receptor 1 999C>T (R293X) Mutation and Risk of Prostate Cancer | 1.1 | 21 | Citations (PDF) |
| 213 | Title is missing! | 4.8 | 46 | Citations (PDF) |
| 214 | Cytomegalovirus, Epstein–Barr virus and risk of breast cancer before age 40 years: a case–control study | 5.5 | 45 | Citations (PDF) |
| 215 | Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics | 2.9 | 44 | Citations (PDF) |
| 216 | A specific GFP expression assay, penetrance estimate, and histological assessment for a putative splice site mutation inBRCA1 | 4.5 | 10 | Citations (PDF) |
| 217 | Risk factors for breast cancer in young women by oestrogen receptor and progesterone receptor status | 5.5 | 37 | Citations (PDF) |
| 218 | Molecular Pathologic Analysis Enhances the Diagnosis and Management of Muir-Torre Syndrome and Gives Insight Into Its Underlying Molecular Pathogenesis | 3.5 | 45 | Citations (PDF) |
| 219 | Novel DNA sequence variants in the hHR21 DNA repair gene in radiosensitive cancer patients | 1.5 | 61 | Citations (PDF) |
| 220 | Mutation analysis of BRCA1 and BRCA2 cancer predisposition genes in radiation hypersensitive cancer patients | 1.5 | 63 | Citations (PDF) |
| 221 | HRAS1 Rare Minisatellite Alleles and Breast Cancer in Australian Women Under Age Forty Years | 4.6 | 18 | Citations (PDF) |
| 222 | De Novo BRCA1 Mutation in a Patient with Breast Cancer and an Inherited BRCA2 Mutation | 6.5 | 59 | Citations (PDF) |
| 223 | CFTR ΔF508 carrier status, risk of breast cancer before the age of 40 and histological grading in a population-based case-control study 1998, 79, 487-489 | | 20 | Citations (PDF) |
| 224 | BRCA1 mutations and other sequence variants in a population-based sample of Australian women with breast cancer | 5.5 | 73 | Citations (PDF) |
| 225 | Coexistent T-Cell Lymphoblastic Lymphoma and an Atypical Myeloproliferative Disorder Associated with t(8;13)(p21;q14) | 1.0 | 9 | Citations (PDF) |
| 226 | Chromosomal Localization of the Human P2y6Purinoceptor Gene and Phylogenetic Analysis of the P2y Purinoceptor Family | 2.8 | 13 | Citations (PDF) |
| 227 | COEXISTENT T-CELL LYMPHOBLASTIC LYMPHOMA AND AN ATYPICAL MYELOPROLIFERATIVE DISORDER ASSOCIATED WITH t(8;13)(p21;q14) | 1.0 | 8 | Citations (PDF) |
| 228 | Spatiotemporally Exact cDNA Libraries from Quail Embryos: A Resource for Studying Neural Crest Development and Neurocristopathies | 2.8 | 4 | Citations (PDF) |
| 229 | Molecular Analysis in the Diagnosis of Pediatric Lymphomas | 1.0 | 8 | Citations (PDF) |
| 230 | Molecular cloning and sequencing of a novel human P2 nucleotide receptor | 3.4 | 14 | Citations (PDF) |
| 231 | EWS/FLI-1 Fusion Transcript Detection and MIC2 Immunohistochemical Staining in the Diagnosis of Ewing's Sarcoma | 1.0 | 15 | Citations (PDF) |
| 232 | Primary Cutaneous Ewing??s Sarcoma/Peripheral Primitive Neuroectodermal Tumors in Childhood | 1.4 | 59 | Citations (PDF) |
| 233 | Active tyrosine phosphatase in immunoprecipitates of multiple isoforms of Ly-5 | 3.5 | 0 | Citations (PDF) |
| 234 | Cohort Profile: Melbourne Atopy Cohort study (MACS) | 4.9 | 22 | Citations (PDF) |
| 235 | Genetically determined body mass index is associated with diffuse large B‐cell lymphoma in polygenic and Mendelian randomization analyses | 4.3 | 0 | Citations (PDF) |
| 236 | Different diabetes types and pancreatic ductal adenocarcinoma: a Mendelian randomization and pathway/gene-set analysis | 4.6 | 0 | Citations (PDF) |
| 237 | Climate-related disasters and biological aging based on DNA methylation: a twin and family study in Australian women | 4.9 | 1 | Citations (PDF) |
