about
Correspondence: SEMA4A variation and risk of colorectal cancerRe: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesisA candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMSA colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis.Multiple sporadic colorectal cancers display a unique methylation phenotype.The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individualsGenetic Variants Associated with Colorectal Adenoma Susceptibility.Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerAssociation between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric studyNew genes emerging for colorectal cancer predisposition.Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC).The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.Modeling Respiratory Depression Induced by Remifentanil and Propofol during Sedation and Analgesia Using a Continuous Noninvasive Measurement of pCO2.Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancerPrevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer.The transcription factor GATA6 enables self-renewal of colon adenoma stem cells by repressing BMP gene expression.A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.Mutational Signatures in Cancer (MuSiCa): a web application to implement mutational signatures analysis in cancer samples.Integrated Analysis of Germline and Tumor DNA Identifies New Candidate Genes Involved in Familial Colorectal CancerUsing linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancerColorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility
P50
Q28602609-4D26BB6A-A3D1-4BB3-880F-6A79EA26C265Q28606428-EF178B85-3FE3-4DC0-AFB4-130BA7EFBF13Q28652720-E9647335-8B35-49BE-BF0A-84C032B788F4Q33825967-C7B823D5-24F7-48E6-A9C2-045136A94A31Q35124378-59C4C920-A204-4E9A-A578-166D6644B437Q35151813-5B281827-A09E-407F-84BF-16AC77283907Q35990039-37CBDAB8-6E61-4399-91D6-EBF302B01A6AQ36265886-1359B15E-1DAC-47D8-B085-BFDC1EDA33D7Q37499529-FF302EFF-F9FB-493D-B2A5-E50ED4A6A4DCQ37602721-55FD6FC6-5139-4B3C-94E3-0D98750D128BQ39730089-27A57835-1775-4E6A-B14E-917DC09856E2Q39778179-D500EA58-D2F0-4D53-86A4-4A07AC78521FQ40218663-6001A6CE-CDA4-4BCE-A330-A0318195AFD6Q42020935-EDA1BC2F-145B-4150-9BC6-DC414C847B1FQ42175718-823AF413-A50B-433B-B8AC-DA86CC3B65AEQ50468134-7E43976F-03F2-453F-9433-CA399E69B02BQ50483571-6F74579B-DA5A-4835-A26D-42655FCA5022Q55405659-320DD0D5-DE73-4918-A8A6-B5126069CCC0Q64097248-232D7D57-1BC9-471A-92B9-BD477B8B7B6BQ90123910-68F3754F-9C71-4960-9B82-5B4ED7197C9CQ90316005-FA55FAC1-6B8F-45FC-83FC-9D6DC253E0F0
P50
description
researcher
@en
researcher
@en-gb
wetenschapper
@nl
հետազոտող
@hy
name
Sergi Castellví-Bel
@ast
Sergi Castellví-Bel
@en
Sergi Castellví-Bel
@en-gb
Sergi Castellví-Bel
@es
Sergi Castellví-Bel
@nl
Sergi Castellví-Bel
@sl
type
label
Sergi Castellví-Bel
@ast
Sergi Castellví-Bel
@en
Sergi Castellví-Bel
@en-gb
Sergi Castellví-Bel
@es
Sergi Castellví-Bel
@nl
Sergi Castellví-Bel
@sl
prefLabel
Sergi Castellví-Bel
@ast
Sergi Castellví-Bel
@en
Sergi Castellví-Bel
@en-gb
Sergi Castellví-Bel
@es
Sergi Castellví-Bel
@nl
Sergi Castellví-Bel
@sl
P106
P108
P31
P496
0000-0003-1217-5097