Roger L Milne

Author PubWeight™ 154.81‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 2007 29.23
2 Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet 2013 8.24
3 A common coding variant in CASP8 is associated with breast cancer risk. Nat Genet 2007 7.35
4 Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet 2009 7.30
5 Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. PLoS Genet 2008 6.22
6 Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies. J Natl Cancer Inst 2010 4.54
7 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Nat Genet 2013 4.35
8 Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat Genet 2013 3.81
9 Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. Am J Hum Genet 2008 3.41
10 Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat Genet 2012 3.20
11 Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. Hum Mol Genet 2011 2.72
12 Agreement between self-reported breast cancer treatment and medical records in a population-based Breast Cancer Family Registry. J Clin Oncol 2005 2.70
13 An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA). Breast Cancer Res 2007 2.46
14 Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers. Am J Hum Genet 2013 2.24
15 Obesity and outcomes in premenopausal and postmenopausal breast cancer. Cancer Epidemiol Biomarkers Prev 2005 2.14
16 Incidence of total knee and hip replacement for osteoarthritis in relation to circulating sex steroid hormone concentrations in women. Arthritis Rheumatol 2014 2.05
17 Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk. PLoS Genet 2013 1.88
18 19p13.1 is a triple-negative-specific breast cancer susceptibility locus. Cancer Res 2012 1.81
19 Breast cancer prognosis in BRCA1 and BRCA2 mutation carriers: an International Prospective Breast Cancer Family Registry population-based cohort study. J Clin Oncol 2011 1.78
20 Is benign rolandic epilepsy genetically determined? Ann Neurol 2004 1.68
21 Association of ESR1 gene tagging SNPs with breast cancer risk. Hum Mol Genet 2009 1.58
22 The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin Cancer Res 2009 1.58
23 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. Hum Mol Genet 2011 1.56
24 Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors. PLoS Genet 2013 1.56
25 Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. Am J Hum Genet 2013 1.39
26 Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers. J Clin Oncol 2013 1.29
27 Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Cancer Epidemiol Biomarkers Prev 2009 1.29
28 11q13 is a susceptibility locus for hormone receptor positive breast cancer. Hum Mutat 2012 1.26
29 The role of genetic breast cancer susceptibility variants as prognostic factors. Hum Mol Genet 2012 1.23
30 Prognosis of premenopausal breast cancer and childbirth prior to diagnosis. J Clin Oncol 2004 1.20
31 IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility. J Neurol 2007 1.18
32 Association between a germline OCA2 polymorphism at chromosome 15q13.1 and estrogen receptor-negative breast cancer survival. J Natl Cancer Inst 2010 1.17
33 Medical radiation exposure and breast cancer risk: findings from the Breast Cancer Family Registry. Int J Cancer 2007 1.17
34 Psychosocial factors and survival of young women with breast cancer: a population-based prospective cohort study. J Clin Oncol 2008 1.17
35 Past recreational physical activity, body size, and all-cause mortality following breast cancer diagnosis: results from the Breast Cancer Family Registry. Breast Cancer Res Treat 2010 1.14
36 Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC). PLoS One 2012 1.13
37 Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes. Hum Genet 2005 1.13
38 A role for XRCC2 gene polymorphisms in breast cancer risk and survival. J Med Genet 2011 1.10
39 BRCA1 and BRCA2 mutation carriers, oral contraceptive use, and breast cancer before age 50. Cancer Epidemiol Biomarkers Prev 2006 1.07
40 Pancreatic cancer risk and levels of trace elements. Gut 2011 1.06
41 Genetic analysis of the vitamin D receptor gene in two epithelial cancers: melanoma and breast cancer case-control studies. BMC Cancer 2008 1.06
42 Immunohistochemical expression of DNA repair proteins in familial breast cancer differentiate BRCA2-associated tumors. J Clin Oncol 2005 1.05
43 Pigmentation-related genes and their implication in malignant melanoma susceptibility. Exp Dermatol 2009 1.02
44 Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma. Cancer Res 2007 1.01
45 Prediagnosis reproductive factors and all-cause mortality for women with breast cancer in the breast cancer family registry. Cancer Epidemiol Biomarkers Prev 2009 1.00
46 Mammographic densities during the menopausal transition: a longitudinal study of Australian-born women. Menopause 2007 0.99
47 Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia. Breast Cancer Res 2014 0.99
48 Immunohistochemical classification of non-BRCA1/2 tumors identifies different groups that demonstrate the heterogeneity of BRCAX families. Mod Pathol 2007 0.98
49 Are we overestimating the penetrance of mutations in SDHB? Hum Mutat 2010 0.97
50 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium. Cancer Epidemiol Biomarkers Prev 2012 0.95
51 No increased risk of breast cancer associated with alcohol consumption among carriers of BRCA1 and BRCA2 mutations ages <50 years. Cancer Epidemiol Biomarkers Prev 2006 0.93
52 Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration. Epilepsia 2006 0.93
53 Risk of pancreatic cancer in breast cancer families from the breast cancer family registry. Cancer Epidemiol Biomarkers Prev 2013 0.91
54 Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls. Cancer Epidemiol Biomarkers Prev 2010 0.91
55 The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis. J Neuroimmunol 2008 0.91
56 Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors. Int J Cancer 2014 0.90
57 BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers. J Natl Cancer Inst 2015 0.90
58 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). Breast Cancer Res Treat 2009 0.88
59 Family history of breast cancer and all-cause mortality after breast cancer diagnosis in the Breast Cancer Family Registry. Breast Cancer Res Treat 2008 0.88
60 An inverse association between ovarian cysts and breast cancer in the breast cancer family registry. Int J Cancer 2006 0.88
61 The HER2 I655V polymorphism and risk of breast cancer in women < age 40 years. Cancer Epidemiol Biomarkers Prev 2003 0.88
62 A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer. Breast Cancer Res Treat 2009 0.88
63 Preventing breast and ovarian cancers in high-risk BRCA1 and BRCA2 mutation carriers. Med J Aust 2013 0.87
64 Do BRCA1 and BRCA2 mutation carriers have earlier natural menopause than their noncarrier relatives? Results from the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer. J Clin Oncol 2013 0.87
65 Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions. Genet Epidemiol 2013 0.86
66 A twin study of genetic influences on epilepsy outcome. Twin Res 2003 0.85
67 Risk factors for uncommon histologic subtypes of breast cancer using centralized pathology review in the Breast Cancer Family Registry. Breast Cancer Res Treat 2012 0.84
68 Haplotype patterns in cancer-related genes with long-range linkage disequilibrium: no evidence of association with breast cancer or positive selection. Eur J Hum Genet 2007 0.83
69 Succinate dehydrogenase D variants do not constitute a risk factor for developing C cell hyperplasia or sporadic medullary thyroid carcinoma. J Clin Endocrinol Metab 2004 0.82
70 Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study. Gynecol Oncol 2008 0.82
71 Diagnostic chest X-rays and breast cancer risk before age 50 years for BRCA1 and BRCA2 mutation carriers. Cancer Epidemiol Biomarkers Prev 2013 0.81
72 Bone Morphogenetic Proteins in Spinal Surgery: What Is the Fusion Rate and Do They Cause Cancer? Spine (Phila Pa 1976) 2015 0.81
73 A protein-truncating mutation in CYP17A1 in three sisters with early-onset breast cancer. Hum Mutat 2005 0.81
74 Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2. PLoS One 2012 0.80
75 Polymorphisms in TRAIL receptor genes and risk of breast cancer in Spanish women. Cancer Biomark 2007 0.80
76 CYP17 genetic polymorphism, breast cancer, and breast cancer risk factors: Australian Breast Cancer Family Study. Breast Cancer Res 2005 0.79
77 Socio-economic status and survival from breast cancer for young, Australian, urban women. Aust N Z J Public Health 2010 0.75
78 The 'Pokemon' (ZBTB7) Gene: No Evidence of Association with Sporadic Breast Cancer. Clin Med Oncol 2008 0.75
79 Reply: To PMID 24692288. Arthritis Rheumatol 2015 0.75
80 Association of DNA Methylation-Based Biological Age with Health Risk Factors, and Overall and Cause-Specific Mortality. Am J Epidemiol 2017 0.75
81 Blood pressure and risk of breast cancer, overall and by subtypes: a prospective cohort study. J Hypertens 2017 0.75
82 Reply. J Hypertens 2017 0.75
83 Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer. Am J Epidemiol 2017 0.75
84 Human beta-defensins (HBD1 and HBD3) and malignant melanoma susceptibility. Melanoma Res 2009 0.75
85 Obstetric events as a risk factor for febrile seizures: a community-based twin study. Twin Res Hum Genet 2008 0.75