Capellá G - Search Results

1

Comprehensive analysis and ACMG-based classification of CHEK2 variants in hereditary cancer patients.

Vargas-Parra G, Del Valle J, Rofes P, Gausachs M, Stradella A, Moreno-Cabrera JM, Velasco A, Tornero E, Menéndez M, Muñoz X, Iglesias S, López-Doriga A, Azuara D, Campos O, Cuesta R, Darder E, de Cid R, González S, Teulé A, Navarro M, Brunet J, Capellá G, Pineda M, Feliubadaló L, Lázaro C. Vargas-Parra G, et al. Among authors: capella g. Hum Mutat. 2020 Dec;41(12):2128-2142. doi: 10.1002/humu.24110. Epub 2020 Oct 14. Hum Mutat. 2020. PMID: 32906215

2

Standardized approach for microsatellite instability detection in colorectal carcinomas.

González-García I, Moreno V, Navarro M, Martí-Ragué J, Marcuello E, Benasco C, Campos O, Capellà G, Peinado MA. González-García I, et al. Among authors: capella g. J Natl Cancer Inst. 2000 Apr 5;92(7):544-9. doi: 10.1093/jnci/92.7.544. J Natl Cancer Inst. 2000. PMID: 10749909

3

Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis.

Alazzouzi H, Domingo E, González S, Blanco I, Armengol M, Espín E, Plaja A, Schwartz S, Capella G, Schwartz S Jr. Alazzouzi H, et al. Among authors: capella g. Hum Mol Genet. 2005 Jan 15;14(2):235-9. doi: 10.1093/hmg/ddi021. Epub 2004 Nov 24. Hum Mol Genet. 2005. PMID: 15563510

4

Founder mutation in familial adenomatous polyposis (FAP) in the Balearic Islands.

González S, Blanco I, Campos O, Julià M, Reyes J, Llompart A, Cabeza E, Germà JR, Obrador A, Capellá G. González S, et al. Among authors: capella g. Cancer Genet Cytogenet. 2005 Apr 1;158(1):70-4. doi: 10.1016/j.cancergencyto.2004.07.003. Cancer Genet Cytogenet. 2005. PMID: 15771908

5

Polymorphisms of the dopamine receptor gene DRD2 and colorectal cancer risk.

Gemignani F, Landi S, Moreno V, Gioia-Patricola L, Chabrier A, Guino E, Navarro M, Cambray M, Capellà G, Canzian F. Gemignani F, et al. Among authors: capella g. Cancer Epidemiol Biomarkers Prev. 2005 Jul;14(7):1633-8. doi: 10.1158/1055-9965.EPI-05-0057. Cancer Epidemiol Biomarkers Prev. 2005. PMID: 16030094

6

Tumor LOH analysis provides reliable linkage information for prenatal genetic testing of sporadic NF1 patients.

Serra E, Pros E, García C, López E, Gili ML, Gómez C, Ravella A, Capellá G, Blanco I, Lázaro C. Serra E, et al. Among authors: capella g. Genes Chromosomes Cancer. 2007 Sep;46(9):820-7. doi: 10.1002/gcc.20468. Genes Chromosomes Cancer. 2007. PMID: 17563086

7

Functional characterization of the novel APC N1026S variant associated with attenuated familial adenomatous polyposis.

Menéndez M, González S, Obrador-Hevia A, Domínguez A, Pujol MJ, Valls J, Canela N, Blanco I, Torres A, Pineda-Lucena A, Moreno V, Bachs O, Capellá G. Menéndez M, et al. Among authors: capella g. Gastroenterology. 2008 Jan;134(1):56-64. doi: 10.1053/j.gastro.2007.10.009. Epub 2007 Oct 10. Gastroenterology. 2008. PMID: 18166348

8

Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 gene.

Pineda M, Castellsagué E, Musulén E, Llort G, Frebourg T, Baert-Desurmont S, González S, Capellá G, Blanco I. Pineda M, et al. Among authors: capella g. Genes Chromosomes Cancer. 2008 Apr;47(4):326-32. doi: 10.1002/gcc.20536. Genes Chromosomes Cancer. 2008. PMID: 18181177

9

Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments.

Castellsagué E, González S, Nadal M, Campos O, Guinó E, Urioste M, Blanco I, Frebourg T, Capellá G. Castellsagué E, et al. Among authors: capella g. Clin Chem. 2008 Jul;54(7):1132-40. doi: 10.1373/clinchem.2007.101006. Epub 2008 May 16. Clin Chem. 2008. PMID: 18487285

10

Antisense therapeutics for neurofibromatosis type 1 caused by deep intronic mutations.

Pros E, Fernández-Rodríguez J, Canet B, Benito L, Sánchez A, Benavides A, Ramos FJ, López-Ariztegui MA, Capellá G, Blanco I, Serra E, Lázaro C. Pros E, et al. Among authors: capella g. Hum Mutat. 2009 Mar;30(3):454-62. doi: 10.1002/humu.20933. Hum Mutat. 2009. PMID: 19241459

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