List of works - Xavier Llor

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

scientific article published on 24 January 2013

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

scientific article published on 25 August 2011

Colorectal cancers with microsatellite instability display unique miRNA profiles.

scientific article

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

scientific article published in December 2017

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

scientific article

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

scientific article published on 29 December 2014

NCCN Guidelines Insights: Colorectal Cancer Screening, Version 1.2018

scientific article published on 01 August 2018

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

scientific article published on 23 April 2015

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

scientific article published on 15 August 2009

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

scientific article published on 01 September 2019

Multiple sporadic colorectal cancers display a unique methylation phenotype

scientific article

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

scientific article

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

scientific article published on 11 July 2019

Implication of DNA repair genes in Lynch-like syndrome

scientific article published on 01 July 2019

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

scientific article published on 23 October 2020

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

scientific article published on 04 July 2020

List of works by Xavier Llor

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

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

Colorectal cancers with microsatellite instability display unique miRNA profiles.

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

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

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

NCCN Guidelines Insights: Colorectal Cancer Screening, Version 1.2018

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

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

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

Multiple sporadic colorectal cancers display a unique methylation phenotype

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

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

Implication of DNA repair genes in Lynch-like syndrome

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

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