LINE-1 hypomethylation in familial and sporadic cancer

door Pavicic, Walter, Joensuu, Emmi I., Nieminen, Taina, Peltomäki, Päivi
Gepubliceerd in 2012

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

door Nieminen, Taina T., Pavicic, Walter, Porkka, Noora, Kankainen, Matti, Järvinen, Heikki J., Lepistö, Anna, Peltomäki, Päivi
Gepubliceerd in Oncotarget (2016)

Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

door Porkka, Noora, Valo, Satu, Nieminen, Taina T., Olkinuora, Alisa, Mäki-Nevala, Satu, Eldfors, Samuli, Peltomäki, Päivi
Gepubliceerd in Oncotarget (2017)

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

door Olkinuora, Alisa, Gylling, Annette, Almusa, Henrikki, Eldfors, Samuli, Lepistö, Anna, Mecklin, Jukka-Pekka, Nieminen, Taina Tuulikki, Peltomäki, Päivi
Gepubliceerd in Cancers (Basel) (2020)

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

door Olkinuora, Alisa, Nieminen, Taina T., Mårtensson, Emma, Rohlin, Anna, Ristimäki, Ari, Koskenvuo, Laura, Lepistö, Anna, Gebre-Medhin, Samuel, Nordling, Margareta, Peltomäki, Päivi
Gepubliceerd in Genet Med (2018)

A novel essential splice site variant in SPTB in a large hereditary spherocytosis family

door Nieminen, Taina T., Liyanarachchi, Sandya, Comiskey, Daniel F., Wang, Yanqiang, Li, Wei, Hendrickson, Isabella V., Brock, Pamela, de la Chapelle, Albert, He, Huiling
Gepubliceerd in Mol Genet Genomic Med (2021)

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

door He, Huiling, Li, Wei, Comiskey, Daniel F., Liyanarachchi, Sandya, Nieminen, Taina T., Wang, Yanqiang, DeLap, Katherine E., Brock, Pamela, de la Chapelle, Albert
Gepubliceerd in Thyroid (2020)

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

door Lotsari, Johanna E, Gylling, Annette, Abdel-Rahman, Wael M, Nieminen, Taina T, Aittomäki, Kristiina, Friman, Marjukka, Pitkänen, Reino, Aarnio, Markku, Järvinen, Heikki J, Mecklin, Jukka-Pekka, Kuopio, Teijo, Peltomäki, Päivi
Gepubliceerd in 2012

Identification of Rare Variants Predisposing to Thyroid Cancer

door Wang, Yanqiang, Liyanarachchi, Sandya, Miller, Katherine E., Nieminen, Taina T., Comiskey, Daniel F., Li, Wei, Brock, Pamela, Symer, David E., Akagi, Keiko, DeLap, Katherine E., He, Huiling, Koboldt, Daniel C., de la Chapelle, Albert
Gepubliceerd in Thyroid (2019)

Germline Mutation of RPS20, Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency

door Nieminen, Taina T., O’Donohue, Marie-Françoise, Wu, Yunpeng, Lohi, Hannes, Scherer, Stephen W., Paterson, Andrew D., Ellonen, Pekka, Abdel-Rahman, Wael M., Valo, Satu, Mecklin, Jukka-Pekka, Järvinen, Heikki J., Gleizes, Pierre-Emmanuel, Peltomäki, Päivi
Gepubliceerd in 2014

Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in APC, BRAF, and KTM2D

door Nieminen, Taina T., Walker, Christopher J., Olkinuora, Alisa, Genutis, Luke K., O'Malley, Margaret, Wakely, Paul E., LaGuardia, Lisa, Koskenvuo, Laura, Arola, Johanna, Lepistö, Anna H., Brock, Pamela, Yilmaz, Ayse Selen, Eisfeld, Ann-Kathrin, Church, James M., Peltomäki, Päivi, de la Chapelle, Albert
Gepubliceerd in Thyroid (2020)