关注
Hans FA Vasen
Hans FA Vasen
其他姓名HF Vasen
Professor Hereditary Cancer, Leiden University Medical Center, Leiden, The Netherlands
在 stoet.nl 的电子邮件经过验证
标题
引用次数
引用次数
年份
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
D Ford, DF Easton, M Stratton, S Narod, D Goldgar, P Devilee, DT Bishop, ...
The American Journal of Human Genetics 62 (3), 676-689, 1998
39221998
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
38642004
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
HFA Vasen, P Watson, JP Mecklin, HT Lynch
Gastroenterology 116 (6), 1453-1456, 1999
32361999
The international collaborative group on hereditary non-polyposis colorectal cancer (ICG-HNPCC)
HFA Vasen, JP Mecklin, PM Khan, HT Lynch
Diseases of the Colon & Rectum 34 (5), 424-425, 1991
26751991
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
J Burn, AM Gerdes, F Macrae, JP Mecklin, G Moeslein, S Olschwang, ...
The Lancet 378 (9809), 2081-2087, 2011
11452011
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis
HF Vasen, JT Wijnen, FH Menko, JH Kleibeuker, BG Taal, G Griffioen, ...
Gastroenterology 110 (4), 1020-1027, 1996
10771996
Peutz–Jeghers syndrome: a systematic review and recommendations for management
AD Beggs, AR Latchford, HFA Vasen, G Moslein, A Alonso, S Aretz, ...
Gut 59 (7), 975-986, 2010
9842010
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
HFA Vasen, I Blanco, K Aktan-Collan, JP Gopie, A Alonso, S Aretz, ...
Gut 62 (6), 812-823, 2013
8562013
International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer
MI Canto, F Harinck, RH Hruban, GJ Offerhaus, JW Poley, I Kamel, Y Nio, ...
Gut 62 (3), 339-347, 2013
8562013
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
HFA Vasen, G Moeslein, A Alonso, S Aretz, I Bernstein, L Bertario, ...
Gut 57 (5), 704-713, 2008
8492008
Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary …
P Peltomaki, HF Vasen
Gastroenterology 113 (4), 1146-1158, 1997
8421997
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)
HFA Vasen, G Möslein, A Alonso, I Bernstein, L Bertario, I Blanco, J Burn, ...
Journal of medical genetics 44 (6), 353-362, 2007
7682007
The risk of extra‐colonic, extra‐endometrial cancer in the Lynch syndrome
P Watson, HFA Vasen, JP Mecklin, I Bernstein, M Aarnio, HJ Järvinen, ...
International journal of cancer 123 (2), 444-449, 2008
7242008
Mutations associated with HNPCC predisposition--Update of ICG-HNPCC/INSiGHT mutation database
P Peltomäki, H Vasen
Disease markers 20 (4-5), 269-276, 2004
5832004
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
P Møller, TT Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 67 (7), 1306-1316, 2018
5722018
Duodenal adenomatosis in familial adenomatous polyposis
S Bülow, J Björk, IJ Christensen, O Fausa, H Järvinen, F Moesgaard, ...
Journal of Medical Genetics 41 (5), 341-341, 2004
570*2004
Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases
MR Stratton
The Lancet 349 (9064), 1505-1510, 1997
5701997
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (3), 464-472, 2017
5622017
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
5352020
Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16‐Leiden)
HFA Vasen, NA Gruis, RR Frants, PA van Der Velden, ETM Hille, ...
International journal of cancer 87 (6), 809-811, 2000
5222000
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