2019 - Fellow of the Royal Society, United Kingdom
Fellow of The Academy of Medical Sciences, United Kingdom
Julian Peto focuses on Breast cancer, Cancer, Internal medicine, Genetics and Genome-wide association study. His research in Breast cancer intersects with topics in Relative risk, Penetrance, Family history and Genetic predisposition. His research brings together the fields of Risk factor and Cancer.
His work deals with themes such as Endocrinology, Oncology and Allele frequency, which intersect with Internal medicine. His work deals with themes such as BRCA mutation, Hereditary breast–ovarian cancer syndrome and Breast Cancer Genetics, which intersect with Endocrinology. His Genome-wide association study research includes elements of Genetic association and Locus.
His primary scientific interests are in Breast cancer, Internal medicine, Oncology, Genetics and Cancer. His Breast cancer study combines topics in areas such as Odds ratio, Genome-wide association study, Genotype, Single-nucleotide polymorphism and Case-control study. His Internal medicine study combines topics from a wide range of disciplines, such as Endocrinology and Gynecology.
His Gynecology research is multidisciplinary, relying on both Relative risk, Epidemiology, Cervical intraepithelial neoplasia and Cytology. The various areas that he examines in his Oncology study include Carcinoma, Pathology, Ovarian cancer, Prostate cancer and Family history. The Cancer study combines topics in areas such as CHEK2, Penetrance and Surgery.
Julian Peto mostly deals with Breast cancer, Genome-wide association study, Internal medicine, Genetics and Oncology. His Breast cancer research is multidisciplinary, incorporating perspectives in Odds ratio, Expression quantitative trait loci, Locus and Genotype. His Internal medicine research includes themes of Disease cluster, Placebo and Immunology.
In the subject of general Genetics, his work in Quantitative trait locus, Cancer, Allele and Endometrial cancer is often linked to B-Cell Childhood Acute Lymphoblastic Leukemia, thereby combining diverse domains of study. Menarche and Family history is closely connected to Bioinformatics in his research, which is encompassed under the umbrella topic of Cancer. His research in Oncology tackles topics such as Ovarian cancer which are related to areas like Endometriosis.
The scientist’s investigation covers issues in Breast cancer, Genome-wide association study, Genetics, Internal medicine and Oncology. His research on Breast cancer concerns the broader Cancer. In general Cancer study, his work on BRCA2 Protein often relates to the realm of Regional development, thereby connecting several areas of interest.
His work carried out in the field of Genome-wide association study brings together such families of science as Expression quantitative trait loci, Colorectal cancer, Genetic predisposition and Locus. Internal medicine is represented through his Odds ratio and Epidemiology research. His biological study spans a wide range of topics, including Case-control study, Gene mutation and Risk factor.
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Human papillomavirus is a necessary cause of invasive cervical cancer worldwide.
J. M. M. Walboomers;M. V. Jacobs;M. M. Manos;F. X. Bosch.
The Journal of Pathology (1999)
Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples.
R Peto;M C Pike;P Armitage;N E Breslow.
British Journal of Cancer (1977)
Asymptotically Efficient Rank Invariant Test Procedures
Richard Peto;Julian Peto.
Journal of the Royal Statistical Society: Series A (General) (1972)
Prevalence of Human Papillomavirus in Cervical Cancer: a Worldwide Perspective
F. Xavier Bosch;M. Michele Manos;Nubia Muñoz;Mark Sherman.
Journal of the National Cancer Institute (1995)
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
A Antoniou;Pdp Pharoah;S Narod;HA Risch.
American Journal of Human Genetics (2003)
Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
D Ford;D F Easton;M Stratton;S Narod.
American Journal of Human Genetics (1998)
Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52 705 women with breast cancer and 108 411 women without breast cancer
E. E. Calle;C. W. Heath;R. J. Coates;J. M. Liff.
The Lancet (1997)
Design and analysis of randomized clinical trials requiring prolonged observation of each patient. I. Introduction and design.
R. Peto;M. C. Pike;P. Armitage;N. E. Breslow.
British Journal of Cancer (1976)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton;Karen A. Pooley;Alison M. Dunning;Paul D. P. Pharoah.
Breast cancer and hormonal contraceptives : collaborative reanalysis of individual data on 53.297 women with breast cancer and 100.239 women without breast cancer from 54 epidemiological studies
E. E. Calle;C. W. Heath;H. L. Miracle-McMahill;R. J. Coates.
The Lancet (1996)
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