Lista de obras -

3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.

artículo científico publicado en 2015

Allelic Imbalance at rs6983267 Suggests Selection of the Risk Allele in Somatic Colorectal Tumor Evolution

artículo científico publicado en 2008

Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors

artículo científico publicado en 2004

CTCF/cohesin-binding sites are frequently mutated in cancer

artículo científico publicado en 2015

Candidate driver genes in microsatellite-unstable colorectal cancer

artículo científico publicado en 2011

Causes of death of mutation carriers in Finnish Lynch syndrome families

artículo científico publicado en 2012

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2017

Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

artículo científico publicado en 2017

DNA hypermethylation appears early and shows increased frequency with dysplasia in Lynch syndrome-associated colorectal adenomas and carcinomas

artículo científico publicado en 2015

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

artículo científico publicado en 2006

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2003

Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma

artículo científico publicado en 2003

Eleven candidate susceptibility genes for common familial colorectal cancer

artículo científico publicado en 2013

Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients

artículo científico publicado en 2013

Exome sequencing reveals frequent inactivating mutations in ARID1A, ARID1B, ARID2 and ARID4A in microsatellite unstable colorectal cancer

artículo científico publicado en 2014

Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors

artículo científico

Gene-expression profiling predicts recurrence in Dukes' C colorectal cancer

artículo científico publicado en 2005

Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases

artículo científico publicado en 2003

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

artículo científico publicado en 2017

High frequency of TTK mutations in microsatellite-unstable colorectal cancer and evaluation of their effect on spindle assembly checkpoint.

artículo científico publicado en 2010

Identification of candidate oncogenes in human colorectal cancers with microsatellite instability

artículo científico publicado en 2013

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

article

Little evidence for involvement of MLH3 in colorectal cancer predisposition

artículo científico publicado en 2003

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

article

Low-level microsatellite instability in most colorectal carcinomas

scientific article published on 01 February 2002

Low-penetrance susceptibility variants in familial colorectal cancer

artículo científico publicado en 2010

Mutations in Exon 1 highlight the role of MED12 in uterine leiomyomas

artículo científico publicado en 2014

Mutations in the circadian gene CLOCK in colorectal cancer

artículo científico publicado en 2010

Mutations in two short noncoding mononucleotide repeats in most microsatellite-unstable colorectal cancers

artículo científico publicado en 2005

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

artículo científico publicado en 2018

No evidence for association of NOD2 R702W and G908R with colorectal cancer

artículo científico publicado en 2007

Preferential amplification ofAURKA 91A (Ile31) in familial colorectal cancers

article

Psychosocial consequences of predictive genetic testing for Lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study

artículo científico publicado en 2013

SMAD4 as a Prognostic Marker in Colorectal Cancer

artículo científico publicado en 2005

SMAD4 levels and response to 5-fluorouracil in colorectal cancer

artículo científico publicado en 2005

Somatic MED12 mutations in prostate cancer and uterine leiomyomas promote tumorigenesis through distinct mechanisms

artículo científico publicado en 2015

Somatic mutations and germline sequence variants in patients with familial colorectal cancer.

artículo científico publicado en 2010

Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.

artículo científico publicado en 2011

Systematic search for rare variants in Finnish early-onset colorectal cancer patients

artículo científico publicado en 2014

The Role of Chromosomal Instability and Epigenetics in Colorectal Cancers Lacking β-Catenin/TCF Regulated Transcription

artículo científico publicado en 2016

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

artículo científico publicado en 2009

Unregulated smooth-muscle myosin in human intestinal neoplasia

artículo científico publicado en 2008

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease

artículo científico publicado en 2016

p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome

artículo científico publicado en 2005

Lista de obras de

3'-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.

Allelic Imbalance at rs6983267 Suggests Selection of the Risk Allele in Somatic Colorectal Tumor Evolution

Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors

CTCF/cohesin-binding sites are frequently mutated in cancer

Candidate driver genes in microsatellite-unstable colorectal cancer

Causes of death of mutation carriers in Finnish Lynch syndrome families

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer

DNA hypermethylation appears early and shows increased frequency with dysplasia in Lynch syndrome-associated colorectal adenomas and carcinomas

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer

Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma

Eleven candidate susceptibility genes for common familial colorectal cancer

Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients

Exome sequencing reveals frequent inactivating mutations in ARID1A, ARID1B, ARID2 and ARID4A in microsatellite unstable colorectal cancer

Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors

Gene-expression profiling predicts recurrence in Dukes' C colorectal cancer

Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

High frequency of TTK mutations in microsatellite-unstable colorectal cancer and evaluation of their effect on spindle assembly checkpoint.

Identification of candidate oncogenes in human colorectal cancers with microsatellite instability

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

Little evidence for involvement of MLH3 in colorectal cancer predisposition

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

Low-level microsatellite instability in most colorectal carcinomas

Low-penetrance susceptibility variants in familial colorectal cancer

Mutations in Exon 1 highlight the role of MED12 in uterine leiomyomas

Mutations in the circadian gene CLOCK in colorectal cancer

Mutations in two short noncoding mononucleotide repeats in most microsatellite-unstable colorectal cancers

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

No evidence for association of NOD2 R702W and G908R with colorectal cancer

Preferential amplification ofAURKA 91A (Ile31) in familial colorectal cancers

Psychosocial consequences of predictive genetic testing for Lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study

SMAD4 as a Prognostic Marker in Colorectal Cancer

SMAD4 levels and response to 5-fluorouracil in colorectal cancer

Somatic MED12 mutations in prostate cancer and uterine leiomyomas promote tumorigenesis through distinct mechanisms

Somatic mutations and germline sequence variants in patients with familial colorectal cancer.

Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.

Systematic search for rare variants in Finnish early-onset colorectal cancer patients

The Role of Chromosomal Instability and Epigenetics in Colorectal Cancers Lacking β-Catenin/TCF Regulated Transcription

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

Unregulated smooth-muscle myosin in human intestinal neoplasia

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease

p53 Codon 72 and MDM2 SNP309 Polymorphisms and Age of Colorectal Cancer Onset in Lynch Syndrome