His work on Systemic therapy expands to the thematically related Internal medicine. His research on Cancer often connects related topics like Cancer treatment. The study of Gene is intertwined with the study of Gene mutation in a number of ways. Mutation is often connected to Gene mutation in his work. Genetics is often connected to Adenocarcinoma in his work. With his scientific publications, his incorporates both Adenocarcinoma and Cancer. Archaeology and Cornerstone are commonly linked in his work. His research on Cornerstone often connects related topics like Archaeology. Gabriel Capellá undertakes multidisciplinary studies into Surgery and Intensive care medicine in his work.
Gabriel Capellá performs multidisciplinary study in Cancer and Metastasis in his work. Gabriel Capellá regularly links together related areas like Adenocarcinoma in his Internal medicine studies. Gabriel Capellá incorporates Gene and Point mutation in his research. His Genetics study frequently draws connections to adjacent fields such as Carcinogenesis. He applies his multidisciplinary studies on Colorectal cancer and Familial adenomatous polyposis in his research. In his papers, he integrates diverse fields, such as Familial adenomatous polyposis and Colorectal cancer. In his work, he performs multidisciplinary research in Cancer research and Oncology. He performs multidisciplinary study on Oncology and Cancer research in his works. Gabriel Capellá integrates many fields, such as Pathology and Gastroenterology, in his works.
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Peutz–Jeghers syndrome: a systematic review and recommendations for management
A. D. Beggs;A. R. Latchford;H. F. A. Vasen;G. Moslein.
Gut (2010)
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Hans F A Vasen;Ignacio Blanco;Katja Aktan-Collan;Jessica P Gopie.
Gut (2013)
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
H. F. A Vasen;G. Moslein;A. Alonso;S. Aretz.
Gut (2008)
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)
Hans F.A. Vasen;Gabriele Möslein;Angel Alonso;Inge Bernstein.
Journal of Medical Genetics (2007)
Analysis of adenomatous polyposis coli promoter hypermethylation in human cancer.
Manel Esteller;Andrew Sparks;Minoru Toyota;Montserrat Sanchez-Cespedes.
Cancer Research (2000)
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
Albert Tenesa;Susan M Farrington;James G D Prendergast;Mary E Porteous.
Nature Genetics (2008)
Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to A mutations in K-ras in colorectal tumorigenesis.
Manel Esteller;Minoru Toyota;Montserrat Sanchez-Cespedes;Gabriel Capella.
Cancer Research (2000)
Hypermethylation-associated inactivation of p14(ARF) is independent of p16(INK4a) methylation and p53 mutational status.
Manel Esteller;Silvia Tortola;Minoru Toyota;Gabriel Capella.
Cancer Research (2000)
Gene Expression Signature to Improve Prognosis Prediction of Stage II and III Colorectal Cancer
Ramon Salazar;Paul Roepman;Gabriel Capella;Victor Moreno.
Journal of Clinical Oncology (2011)
DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis
Manel Esteller;Mario F. Fraga;Mingzhou Guo;Jesus Garcia-Foncillas.
Human Molecular Genetics (2001)
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