List of works - Taina T Nieminen

A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres

scientific article published on 01 February 2020

BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.

scientific article

Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases

scientific article

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

scientific article published on 10 December 2015

Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors

article

Distinct genetic and epigenetic signatures of colorectal cancers according to ethnic origin

scientific article

Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency

scientific article

Identification of Rare Variants Predisposing to Thyroid Cancer

scientific article published on 13 May 2019

LINE-1 hypomethylation in familial and sporadic cancer ⬇️

scientific article published on January 8, 2012

Loss of p15INK⁴b expression in colorectal cancer is linked to ethnic origin.

scientific article

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

article

Molecular Analysis of Endometrial Tumorigenesis: Importance of Complex Hyperplasia Regardless of Atypia

article

Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results

scientific article published on 09 July 2020

Promoter-specific alterations ofAPCare a rare cause for mutation-negative familial adenomatous polyposis

scientific article published on 20 June 2014

Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

scientific article

Reply

scientific article published on 22 November 2014

Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

scientific article published on 14 November 2017

List of works by Taina T Nieminen

A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres

BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.

Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors

Distinct genetic and epigenetic signatures of colorectal cancers according to ethnic origin

Germline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiency

Identification of Rare Variants Predisposing to Thyroid Cancer

LINE-1 hypomethylation in familial and sporadic cancer ⬇️

Loss of p15INK⁴b expression in colorectal cancer is linked to ethnic origin.

Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer

Molecular Analysis of Endometrial Tumorigenesis: Importance of Complex Hyperplasia Regardless of Atypia

Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results

Promoter-specific alterations ofAPCare a rare cause for mutation-negative familial adenomatous polyposis

Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis

Reply

Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations