Henry T. Lynch focuses on Internal medicine, Cancer, Breast cancer, Oncology and Colorectal cancer. His research in Internal medicine intersects with topics in Gastroenterology and Surgery. His study in Cancer is interdisciplinary in nature, drawing from both Genetic counseling, Germline mutation and Carcinoma, Pathology.
His Breast cancer study integrates concerns from other disciplines, such as Oophorectomy, Prospective cohort study, Gynecology and Ovarian cancer. His Oncology research is multidisciplinary, incorporating elements of Retrospective cohort study, Epidemiology of cancer, Genotype, Age of onset and Penetrance. His studies in Lynch syndrome integrate themes in fields like Amsterdam criteria and Familial adenomatous polyposis.
Henry T. Lynch mainly focuses on Internal medicine, Cancer, Oncology, Breast cancer and Colorectal cancer. In most of his Internal medicine studies, his work intersects topics such as Gastroenterology. Henry T. Lynch has included themes like Genetic counseling, Germline mutation and Pathology in his Cancer study.
His Genetic counseling research is multidisciplinary, relying on both Family medicine and Genetic testing. His Oncology study combines topics from a wide range of disciplines, such as Lynch Syndrome II, Epidemiology of cancer, Genotype, Age of onset and Prospective cohort study. His work carried out in the field of Breast cancer brings together such families of science as Odds ratio, Cancer research, Gynecology and Risk factor.
Henry T. Lynch mostly deals with Internal medicine, Cancer, Oncology, Breast cancer and Lynch syndrome. His Internal medicine research incorporates elements of Gastroenterology and Oophorectomy. His Cancer research also works with subjects such as
His work is dedicated to discovering how Oncology, Cancer research are connected with Mutation and other disciplines. His Breast cancer research is multidisciplinary, incorporating perspectives in Prospective cohort study, Ovarian cancer, Gynecology and Hazard ratio. His Colorectal cancer research includes elements of Surgery and Pathology.
His primary areas of investigation include Internal medicine, Breast cancer, Cancer, Oncology and Lynch syndrome. His research investigates the link between Internal medicine and topics such as Surgery that cross with problems in Body mass index and Colectomy. The concepts of his Breast cancer study are interwoven with issues in Case-control study, Gynecology, Hazard ratio, Prospective cohort study and Cohort.
His Cancer research is multidisciplinary, incorporating perspectives in Oophorectomy, Bioinformatics and PALB2. His work deals with themes such as BRCA2 Protein, Germline mutation, Incidence, Survival rate and Mastectomy, which intersect with Oncology. The Lynch syndrome study combines topics in areas such as Cancer research, PMS2, Microsatellite instability, MSH2 and MSH6.
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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)
Revised Bethesda Guidelines for Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) and Microsatellite Instability
Asad Umar;C. Richard Boland;Jonathan P. Terdiman;Sapna Syngal.
Journal of the National Cancer Institute (2004)
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.
Hans F.A. Vasen;Patrice Watson;Jukka–Pekka Mecklin;Henry T. Lynch.
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC).
H. F. A. Vasen;J. P. Mecklin;P. Meera Khan;H. T. Lynch.
Diseases of The Colon & Rectum (1991)
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
Fredrick S. Leach;Nicholas C. Nicolaides;Nickolas Papadopoulos;Bo Liu.
HNPCC (Lynch Syndrome): Differential Diagnosis, Molecular Genetics and Management - a Review
Henry T Lynch;Jane F Lynch;Trudy G Shaw;Jan Lubiński.
Hereditary Cancer in Clinical Practice (2003)
Hereditary Colorectal Cancer
Henry T. Lynch;Albert de la Chapelle.
Seminars in Oncology (1990)
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
Richard Wooster;Susan L. Neuhausen;Jonathan Mangion;Yvette Quirk.
Mutation of a mutL homolog in hereditary colon cancer
Nickolas Papadopoulos;Nicholas C. Nicolaides;Ying Fei Wei;Steven M. Ruben.
Prophylactic Oophorectomy in Carriers of BRCA1 or BRCA2 Mutations
Timothy R. Rebbeck;Henry T. Lynch;Susan L. Neuhausen;Steven A. Narod.
The New England Journal of Medicine (2002)
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