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ANGEL ALONSO
ANGEL ALONSO
Medical Genetics, Navarrabiomed, Universidad Pública de Navarra (UPNA), Complejo Hospitalario de
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Year
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
9542010
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
8412013
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
8312008
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
7512007
A randomized placebo-controlled prevention trial of aspirin and/or resistant starch in young people with familial adenomatous polyposis
J Burn, DT Bishop, PD Chapman, F Elliott, L Bertario, MG Dunlop, ...
Cancer prevention research 4 (5), 655-665, 2011
2512011
The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome
EJ Crosbie, NAJ Ryan, MJ Arends, T Bosse, J Burn, JM Cornes, ...
Genetics in Medicine 21 (10), 2390-2400, 2019
1932019
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe
HFA Vasen, G Möslein, A Alonso, S Aretz, I Bernstein, L Bertario, I Blanco, ...
Familial cancer 9, 109-115, 2010
1462010
Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds
EM Grindedal, L Renkonen-Sinisalo, H Vasen, G Evans, P Sala, I Blanco, ...
Journal of medical genetics 47 (2), 99-102, 2010
912010
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of lynch syndrome patients
HM Van Der Klift, CMJ Tops, EC Bik, MW Boogaard, AM Borgstein, ...
Human mutation 31 (5), 578-587, 2010
742010
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
AK Win, JG Dowty, JC Reece, G Lee, AS Templeton, JP Plazzer, ...
The Lancet Oncology 22 (7), 1014-1022, 2021
642021
Comparison of prediction models for Lynch syndrome among individuals with colorectal cancer
F Kastrinos, RP Ojha, C Leenen, C Alvero, RC Mercado, J Balmaña, ...
Journal of the National Cancer Institute 108 (2), djv308, 2016
572016
CSVS, a crowdsourcing database of the Spanish population genetic variability
M Peña-Chilet, G Roldán, J Perez-Florido, FM Ortuno, R Carmona, ...
Nucleic acids research 49 (D1), D1130-D1137, 2021
442021
Surgical management of the duodenal manifestations of familial adenomatous polyposis
Y Parc, JY Mabrut, C Shields
Journal of British Surgery 98 (4), 480-484, 2011
412011
MLH1 Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
E Borràs, M Pineda, I Blanco, EM Jewett, F Wang, À Teulé, T Caldes, ...
Cancer research 70 (19), 7379-7391, 2010
362010
Delineation of a duplication map of chromosome 3q: A new case confirms the exclusion of 3q25‐q26.2 from the duplication 3q syndrome critical region
P Rizzu, BR Haddad, I Vallcorba, A Alonso, MT Ferro, JM Garcia‐Sagredo, ...
American journal of medical genetics 68 (4), 428-432, 1997
361997
10th Anniversary of the european association for predictive, preventive and Personalised (3P) Medicine-EPMA World Congress Supplement 2020
O Golubnitschaja, O Topolcan, R Kucera, V Costigliola
EPMA Journal 11 (Suppl 1), 1-133, 2020
352020
Charcot–Marie–Tooth disease type 2J with MPZ Thr124Met mutation: clinico-electrophysiological and MRI study of a family
E Gallardo, A García, C Ramón, E Maraví, J Infante, I Gastón, Á Alonso, ...
Journal of neurology 256, 2061-2071, 2009
292009
Primary constitutional MLH1 epimutations: a focal epigenetic event
E Dámaso, A Castillejo, MM Arias, J Canet-Hermida, M Navarro, ...
British Journal of Cancer 119 (8), 978-987, 2018
282018
Genetic mechanisms in the hereditary predisposition to colorectal cancer
A Alonso, S Moreno, A Valiente, M Artigas, A Perez-Juana, R Arroyo
Anales del sistema sanitario de Navarra 29 (1), 59-76, 2006
28*2006
The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases
S Laurie, D Piscia, L Matalonga, A Corvó, M Fernández‐Callejo, ...
Human mutation 43 (6), 717-733, 2022
272022
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