2002 - Fellow of the American Association for the Advancement of Science (AAAS)
2002 - William Allan Award, the American Society of Human Genetics
1997 - Member of the National Academy of Sciences
Member of the Association of American Physicians
Albert de la Chapelle mainly focuses on Genetics, Internal medicine, Colorectal cancer, Germline mutation and Microsatellite instability. His Internal medicine study incorporates themes from Endocrinology and Oncology. His work carried out in the field of Oncology brings together such families of science as BAALC and Myeloid leukemia, Immunology.
His research in Immunology intersects with topics in Survival rate, Blockade and Metastatic carcinoma. The Microsatellite instability study combines topics in areas such as MLH1, Loss of heterozygosity and Pathology. His studies deal with areas such as Immune checkpoint, Cancer research and Adenocarcinoma as well as DNA mismatch repair.
His main research concerns Genetics, Internal medicine, Cancer research, Gene and Molecular biology. Genetics is represented through his Locus, Genetic linkage, Haplotype, Gene mapping and Mutation research. He has included themes like Endocrinology and Oncology in his Internal medicine study.
In Oncology, Albert de la Chapelle works on issues like Myeloid leukemia, which are connected to BAALC. As a member of one scientific family, Albert de la Chapelle mostly works in the field of Cancer research, focusing on Thyroid carcinoma and, on occasion, Thyroid cancer. His study on Lynch syndrome also encompasses disciplines like
Albert de la Chapelle focuses on Internal medicine, Oncology, Cancer, Genome-wide association study and Colorectal cancer. His work in the fields of Internal medicine, such as Lynch syndrome, Myeloid leukemia, Cohort and Odds ratio, intersects with other areas such as Mendelian randomization. His Lynch syndrome study introduces a deeper knowledge of DNA mismatch repair.
The study incorporates disciplines such as Germline mutation, Genetic risk, Gene mutation, Penetrance and Leukemia in addition to Oncology. Albert de la Chapelle's looking at Genome-wide association study as part of his Genetics and Single-nucleotide polymorphism and Genome-wide association study study. While the research belongs to areas of Colorectal cancer, Albert de la Chapelle spends his time largely on the problem of Epidemiology, intersecting his research to questions surrounding Body mass index.
Internal medicine, Oncology, Genetics, Lynch syndrome and Cancer are his primary areas of study. His Internal medicine research includes elements of CHEK2 and Chromatin. His Oncology research incorporates elements of Myeloid, Colorectal cancer, Leukemia, Family history and Cohort.
Albert de la Chapelle works mostly in the field of Genetics, limiting it down to concerns involving Myeloid leukemia and, occasionally, Susceptibility locus. His research integrates issues of Germline mutation, MSH6 and Microsatellite instability in his study of Lynch syndrome. His research investigates the connection between DNA mismatch repair and topics such as Follicular thyroid cancer that intersect with problems in Cancer research.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
PD-1 Blockade in Tumors with Mismatch-Repair Deficiency
Dung T. Le;Jennifer N. Uram;Hao Wang;Bjarne R. Bartlett.
The New England Journal of Medicine (2015)
Clues to the pathogenesis of familial colorectal cancer
Lauri A. Aaltonen;Päivi Peltomäki;Fredrick S. Leach;Pertti Sistonen.
Science (1993)
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)
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
Fredrick S. Leach;Nicholas C. Nicolaides;Nickolas Papadopoulos;Bo Liu.
Cell (1993)
Hereditary Colorectal Cancer
Henry T. Lynch;Albert de la Chapelle.
Seminars in Oncology (1990)
Mutation of a mutL homolog in hereditary colon cancer
Nickolas Papadopoulos;Nicholas C. Nicolaides;Ying Fei Wei;Steven M. Ruben.
Science (1994)
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
Nicholas C. Nicolaides;Nickolas Papadopoulos;Bo Liu;Ying Fei Weit.
Nature (1994)
A serine/threonine kinase gene defective in Peutz–Jeghers syndrome
A Hemminki;D Markie;I Tomlinson;E Avizienyte.
Nature (1998)
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene
Renee Reijo;Tien-Yi Lee;Pia Salo;Raaji Alagappan.
Nature Genetics (1995)
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
Heikki J. Järvinen;Markku Aarnio;Harri Mustonen;Katja Aktan–Collan‡.
Gastroenterology (2000)
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