Laura Valle
Laura Valle
Hereditary Cancer Program, Catalan Institute of Oncology, IDIBELL
Verified email at idibell.cat - Homepage
Title
Cited by
Cited by
Year
Methyl‐CpG binding proteins identify novel sites of epigenetic inactivation in human cancer
E Ballestar, MF Paz, L Valle, S Wei, MF Fraga, J Espada, JC Cigudosa, ...
The EMBO journal 22 (23), 6335-6345, 2003
3892003
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and …
F Bellido, M Pineda, G Aiza, R Valdés-Mas, M Navarro, DA Puente, ...
Genetics in Medicine 18 (4), 325-332, 2016
1642016
Germline allele-specific expression of TGFBR1 confers an increased risk of colorectal cancer
L Valle, T Serena-Acedo, S Liyanarachchi, H Hampel, I Comeras, Z Li, ...
Science 321 (5894), 1361-1365, 2008
1352008
New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis
L Valle, E Hernández-Illán, F Bellido, G Aiza, A Castillejo, MI Castillejo, ...
Human molecular genetics 23 (13), 3506-3512, 2014
1302014
Germline mutations in FAN1 cause hereditary colorectal cancer by impairing DNA repair
N Seguí, LB Mina, C Lázaro, R Sanz-Pamplona, T Pons, M Navarro, ...
Gastroenterology 149 (3), 563-566, 2015
922015
A predictor based on the somatic genomic changes of the BRCA1/BRCA2 breast cancer tumors identifies the non-BRCA1/BRCA2 tumors with BRCA1 promoter hypermethylation
S Alvarez, R Diaz-Uriarte, A Osorio, A Barroso, L Melchor, MF Paz, ...
Clinical Cancer Research 11 (3), 1146-1153, 2005
892005
Genetic predisposition to colorectal cancer: where we stand and future perspectives
L Valle
World journal of gastroenterology: WJG 20 (29), 9828, 2014
882014
Clinicopathologic and pedigree differences in Amsterdam I–positive hereditary nonpolyposis colorectal cancer families according to tumor microsatellite instability status
L Valle, J Perea, P Carbonell, V Fernandez, AM Dotor, J Benitez, ...
Journal of clinical oncology 25 (7), 781-786, 2007
782007
MLH1 germline epimutations in selected patients with early‐onset non‐polyposis colorectal cancer
L Valle, P Carbonell, V Fernandez, AM Dotor, M Sanz, J Benitez, ...
Clinical genetics 71 (3), 232-237, 2007
692007
Recent discoveries in the genetics of familial colorectal cancer and polyposis
L Valle
Clinical Gastroenterology and Hepatology 15 (6), 809-819, 2017
622017
Tgfbr1 haploinsufficiency is a potent modifier of colorectal cancer development
Q Zeng, S Phukan, Y Xu, M Sadim, DS Rosman, M Pennison, J Liao, ...
Cancer research 69 (2), 678-686, 2009
622009
Malignant degeneration of presacral teratoma in the Currarino anomaly
M Urioste, M del Carmen Garcia‐Andrade, L Valle, M Robledo, ...
American Journal of Medical Genetics Part A 128 (3), 299-304, 2004
532004
Analysis of myelodysplastic syndromes with complex karyotypes by high‐resolution comparative genomic hybridization and subtelomeric CGH array
A Martínez‐Ramírez, M Urioste, L Melchor, D Blesa, L Valle, ...
Genes, Chromosomes and Cancer 42 (3), 287-298, 2005
472005
Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype
JE Grolleman, RM de Voer, FA Elsayed, M Nielsen, RDA Weren, C Palles, ...
Cancer cell 35 (2), 256-266. e5, 2019
462019
Exome sequencing reveals AMER1 as a frequently mutated gene in colorectal cancer
R Sanz-Pamplona, A Lopez-Doriga, L Paré-Brunet, K Lázaro, F Bellido, ...
Clinical Cancer Research 21 (20), 4709-4718, 2015
402015
Genetic predisposition to colorectal cancer: syndromes, genes, classification of genetic variants and implications for precision medicine
L Valle, E Vilar, SV Tavtigian, EM Stoffel
The Journal of pathology 247 (5), 574-588, 2019
382019
Update on genetic predisposition to colorectal cancer and polyposis
L Valle, RM de Voer, Y Goldberg, W Sjursen, A Försti, C Ruiz-Ponte, ...
Molecular Aspects of Medicine 69, 10-26, 2019
342019
Delineating the phenotypic spectrum of the NTHL1-associated polyposis
S Belhadj, P Mur, M Navarro, S González, V Moreno, G Capellá, L Valle
Clinical Gastroenterology and Hepatology 15 (3), 461-462, 2017
332017
A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency
K Wimmer, A Beilken, R Nustede, T Ripperger, B Lamottke, B Ure, ...
Familial cancer 16 (1), 67-71, 2017
322017
Molecular cytogenetic characterization of rhabdomyosarcoma cell lines
S Rodriguez-Perales, A Martı́nez-Ramı́rez, SA de Andrés, L Valle, ...
Cancer genetics and cytogenetics 148 (1), 35-43, 2004
302004
The system can't perform the operation now. Try again later.
Articles 1–20