Lista de obras - Xavier Llor - Dominio Público Uruguay

AGA White Paper: Roadmap for the Future of Colorectal Cancer Screening in the United States

artículo científico publicado en 2020

Association of MUTYH and MSH6 germline mutations in colorectal cancer patients.

artículo científico publicado en 2009

Clinical features and cancer risk in families with pathogenic CDH1 variants irrespective of clinical criteria

scientific article published on 11 July 2019

Colorectal cancers with microsatellite instability display unique miRNA profiles.

artículo científico publicado en 2011

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

artículo científico publicado en 2011

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome

artículo científico publicado en 2011

Implication of DNA repair genes in Lynch-like syndrome

scientific article published on 01 July 2019

Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

artículo científico publicado en 2010

Multiple sporadic colorectal cancers display a unique methylation phenotype

artículo científico publicado en 2014

NCCN Guidelines Insights: Colorectal Cancer Screening, Version 1.2018

artículo científico publicado en 2018

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019

artículo científico publicado en 2019

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 3.2017.

artículo científico publicado en 2017

Phenotypic differences in Juvenile Polyposis Syndrome with or without a disease-causing SMAD4/BMPR1A variant

artículo científico publicado en 2020

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer.

artículo científico publicado en 2015

Prevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer

artículo científico publicado en 2014

Risk of cancer in cases of suspected lynch syndrome without germline mutation.

artículo científico publicado en 2013

Lista de obras de Xavier Llor

AGA White Paper: Roadmap for the Future of Colorectal Cancer Screening in the United States

Association of MUTYH and MSH6 germline mutations in colorectal cancer patients.

Clinical features and cancer risk in families with pathogenic CDH1 variants irrespective of clinical criteria

Colorectal cancers with microsatellite instability display unique miRNA profiles.

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome

Implication of DNA repair genes in Lynch-like syndrome

Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

Multiple sporadic colorectal cancers display a unique methylation phenotype

NCCN Guidelines Insights: Colorectal Cancer Screening, Version 1.2018

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 3.2017.

Phenotypic differences in Juvenile Polyposis Syndrome with or without a disease-causing SMAD4/BMPR1A variant

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer.

Prevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer

Risk of cancer in cases of suspected lynch syndrome without germline mutation.