Lista de obras - Christina Therkildsen - Dominio Público Uruguay

An effect from anticipation also in hereditary nonpolyposis colorectal cancer families without identified mutations

artículo científico publicado en 2009

BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.

artículo científico publicado en 2016

Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.

artículo científico publicado en 2012

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

scientific article published on 24 July 2019

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

artículo científico publicado en 2020

Danish Lynch syndrome families

artículo científico publicado en 2008

Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2011

Distinct gene expression signatures in Lynch syndrome and familial colorectal cancer type X

article

Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

artículo científico publicado en 2013

Familial colorectal cancer type X: genetic profiles and phenotypic features.

artículo científico

Frequent mismatch-repair defects link prostate cancer to Lynch syndrome

artículo científico publicado en 2016

Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein

artículo científico publicado en 2014

Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.

artículo científico publicado en 2012

Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome

artículo científico publicado en 2015

Immunoprofiles of colorectal cancer from Lynch syndrome

artículo científico publicado en 2018

Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2.

artículo científico publicado en 2015

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

scientific article published on 28 February 2019

Renal cell cancer linked to Lynch syndrome: Increased incidence and loss of mismatch repair protein expression

artículo científico publicado en 2016

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2020

Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

artículo científico publicado en 2009

The predictive value of KRAS, NRAS, BRAF, PIK3CA and PTEN for anti-EGFR treatment in metastatic colorectal cancer: A systematic review and meta-analysis

artículo científico publicado en 2014

Towards gene- and gender-based risk estimates in Lynch syndrome; age-specific incidences for 13 extra-colorectal cancer types

artículo científico publicado en 2017

Urinary Tract Cancer in Lynch Syndrome; Increased Risk in Carriers of MSH2 Mutations.

artículo científico publicado en 2015

Lista de obras de Christina Therkildsen

An effect from anticipation also in hereditary nonpolyposis colorectal cancer families without identified mutations

BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.

Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Danish Lynch syndrome families

Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

Distinct gene expression signatures in Lynch syndrome and familial colorectal cancer type X

Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.

Familial colorectal cancer type X: genetic profiles and phenotypic features.

Frequent mismatch-repair defects link prostate cancer to Lynch syndrome

Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein

Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.

Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome

Immunoprofiles of colorectal cancer from Lynch syndrome

Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2.

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

Renal cell cancer linked to Lynch syndrome: Increased incidence and loss of mismatch repair protein expression

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

The predictive value of KRAS, NRAS, BRAF, PIK3CA and PTEN for anti-EGFR treatment in metastatic colorectal cancer: A systematic review and meta-analysis

Towards gene- and gender-based risk estimates in Lynch syndrome; age-specific incidences for 13 extra-colorectal cancer types

Urinary Tract Cancer in Lynch Syndrome; Increased Risk in Carriers of MSH2 Mutations.