Sergi Castellví-Bel


Ontology type: schema:Person     


Person Info

NAME

Sergi

SURNAME

Castellví-Bel

Publications in SciGraph latest 50 shown

  • 2021-09-23 MCM9 is associated with germline predisposition to early-onset cancer—clinical evidence in NPJ GENOMIC MEDICINE
  • 2021-05-27 Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer in SCIENTIFIC REPORTS
  • 2021-04-10 A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancer in FAMILIAL CANCER
  • 2020-12-17 Adiposity, metabolites, and colorectal cancer risk: Mendelian randomization study in BMC MEDICINE
  • 2020-01-30 Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis in NATURE COMMUNICATIONS
  • 2018-12-03 Discovery of common and rare genetic risk variants for colorectal cancer in NATURE GENETICS
  • 2018-10-04 Colon-specific eQTL analysis to inform on functional SNPs in BRITISH JOURNAL OF CANCER
  • 2018-06-14 Mutational Signatures in Cancer (MuSiCa): a web application to implement mutational signatures analysis in cancer samples in BMC BIOINFORMATICS
  • 2017-10-12 Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia in BRITISH JOURNAL OF CANCER
  • 2017-07-25 Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia in BRITISH JOURNAL OF CANCER
  • 2016-11-25 Candidate predisposing germline copy number variants in early onset colorectal cancer patients in CLINICAL AND TRANSLATIONAL ONCOLOGY
  • 2016-05-11 The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-03-10 Correspondence: SEMA4A variation and risk of colorectal cancer in NATURE COMMUNICATIONS
  • 2015-12-01 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 in SCIENTIFIC REPORTS
  • 2015-11-10 Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer in SCIENTIFIC REPORTS
  • 2014-07-24 Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer in GENETICS IN MEDICINE
  • 2014-06-22 The transcription factor GATA6 enables self-renewal of colon adenoma stem cells by repressing BMP gene expression in NATURE CELL BIOLOGY
  • 2014-04-02 Pharmacogenomics of CRC treatments: putting bricks on the path to personalized medicine in BMC GENOMICS
  • 2013-11-12 A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer in HUMAN GENETICS
  • 2013-01-26 A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12 in BMC GENOMICS
  • 2012-02-07 Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration in THE PHARMACOGENOMICS JOURNAL
  • 2011-08-05 Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins in BMC CANCER
  • 2011-08-02 A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22 in BRITISH JOURNAL OF CANCER
  • 2011-01-12 Novel MLH1 duplication identified in Colombian families with Lynch syndrome in GENETICS IN MEDICINE
  • 2010-11-23 Serum matrilysin correlates with poor survival independently of KRAS and BRAF status in refractory advanced colorectal cancer patients treated with irinotecan plus cetuximab in TUMOR BIOLOGY
  • 2010-01-19 COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2009-11-17 COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2009-08-15 Association of MUTYH and MSH6 germline mutations in colorectal cancer patients in FAMILIAL CANCER
  • 2009-06-16 Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations? in BMC MEDICAL GENETICS
  • 2008-03-30 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 in NATURE GENETICS
  • 2008-01-31 Who requires genetic testing? in CURRENT COLORECTAL CANCER REPORTS
  • 2006-05-01 Clinical Performance of Original and Revised Bethesda Guidelines for the Identification of MSH2/MLH1 Gene Carriers in Patients with Newly Diagnosed Colorectal Cancer: Proposal of a New and Simpler Set of Recommendations in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2000-08-01 Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles in HUMAN GENETICS
  • 1997-09 Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation in HUMAN GENETICS
  • 1996-08 A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion in HUMAN GENETICS
  • 1994-10 Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families in HUMAN GENETICS
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