Albert de la Chapelle
Albert de la Chapelle
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PD-1 blockade in tumors with mismatch-repair deficiency
DT Le, JN Uram, H Wang, BR Bartlett, H Kemberling, AD Eyring, ...
New England Journal of Medicine 372 (26), 2509-2520, 2015
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
A Umar, CR Boland, JP Terdiman, S Syngal, A Chapelle, J Rüschoff, ...
Journal of the National Cancer Institute 96 (4), 261-268, 2004
Clues to the pathogenesis of familial colorectal cancer
A LA, P Peltomaki, FS Leach, P Sistonen, L Pylkkanen, JP Mecklin, ...
Science 260, 812-816, 1993
Hereditary colorectal cancer
HT Lynch, A De la Chapelle
New England Journal of Medicine 348 (10), 919-932, 2003
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
FS Leach, NC Nicolaides, N Papadopoulos, B Liu, J Jen, R Parsons, ...
Cell 75 (6), 1215-1225, 1993
Mutation of a mutL homolog is associated with hereditary colon cancer
N Papadopoulos, NC Nicolaides, YF Wei, SM Ruben, KC Carter, ...
Science 263, 1625-1629, 1994
A serine/threonine kinase gene defective in Peutz–Jeghers syndrome
A Hemminki, D Markie, I Tomlinson, E Avizienyte, S Roth, A Loukola, ...
Nature 391 (6663), 184-187, 1998
Mutations of two P/WS homologues in hereditary nonpolyposis colon cancer
NC Nicolaides, N Papadopoulos, B Liu, YF Weit, KC Carter, SM Ruben, ...
Nature 371 (6492), 75-80, 1994
Cancer risk in mutation carriers of DNA‐mismatch‐repair genes
M Aarnio, R Sankila, E Pukkala, R Salovaara, LA Aaltonen, ...
International journal of cancer 81 (2), 214-218, 1999
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene
R Reijo, TY Lee, P Salo, R Alagappan, LG Brown, M Rosenberg, S Rozen, ...
Nature genetics 10 (4), 383-393, 1995
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
H Hampel, WL Frankel, E Martin, M Arnold, K Khanduja, P Kuebler, ...
New England Journal of Medicine 352 (18), 1851-1860, 2005
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
HJ Järvinen, M Aarnio, H Mustonen, K Aktan–Collan, LA Aaltonen, ...
Gastroenterology 118 (5), 829-834, 2000
The role of microRNA genes in papillary thyroid carcinoma
H He, K Jazdzewski, W Li, S Liyanarachchi, R Nagy, S Volinia, GA Calin, ...
Proceedings of the National Academy of Sciences 102 (52), 19075-19080, 2005
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
LA Aaltonen, R Salovaara, P Kristo, F Canzian, A Hemminki, P Peltomäki, ...
New England Journal of Medicine 338 (21), 1481-1487, 1998
Hypermutability and mismatch repair deficiency in RER+ tumor cells
R Parsons, GM Li, MJ Longley, W Fang, N Papadopoulos, J Jen, ...
Cell 75 (6), 1227-1236, 1993
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
M Koenig, AH Beggs, M Moyer, S Scherpf, K Heindrich, T Bettecken, ...
American journal of human genetics 45 (4), 498, 1989
Genetic mapping of a locus predisposing to human colorectal cancer
P Peltomaki, LA Aaltonen, P Sistonen, P L, M J-P, J H, G JS, JR Jass, ...
Science 260, 810-812, 1993
analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
B Liu, R Parsons, N papadopoulos, NC Nicolaides, HT Lynch, P Watson, ...
Nature Medicine 2, 169-174, 1996
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
K Aittomäki, JLD Lucena, P Pakarinen, P Sistonen, J Tapanainen, ...
Cell 82 (6), 959-968, 1995
Genetic susceptibility to non-polyposis colorectal cancer
HT Lynch, A De la Chapelle
Journal of medical genetics 36 (11), 801-818, 1999
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