T. Nieminen

发表

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

Huiling He, Wei Li, S. Liyanarachchi, 2021, Molecular genetics & genomic medicine.

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

P. Peltomaki, S. Eissa, T. Nieminen, 2014, Asian Pacific journal of cancer prevention : APJCP.

/RVVRIp15 INK4b ((SUHVVLRQLQ&RORUHFWDO&DQFHULV/LQNHGWR Ethnic Origin

P. Peltomäki, S. Eissa, T. Nieminen, 2014 .

Distinct Genetic and Epigenetic Signatures of Colorectal Cancers According to Ethnic Origin

P. Peltomäki, S. Eissa, T. Nieminen, 2011, Cancer Epidemiology, Biomarkers & Prevention.

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

K. Aittomäki, T. Kuopio, P. Peltomäki, 2012, Breast Cancer Research.

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

P. Peltomäki, J. Mecklin, H. Järvinen, 2009, Clinical Cancer Research.

Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents

A. Ristimäki, P. Peltomäki, H. García-Rivello, 2022, Frontiers in Oncology.

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

P. Peltomäki, T. Nieminen, J. Lotsari, 2015, Genes, chromosomes & cancer.

LINE-1 hypomethylation in familial and sporadic cancer

P. Peltomäki, T. Nieminen, W. Pavicic, 2012, Journal of Molecular Medicine.

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Å. Borg, A. Ristimäki, P. Peltomäki, 2018, Genetics in Medicine.

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

S. Scherer, A. Paterson, P. Peltomäki, 2014, Gastroenterology.

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

P. Peltomäki, J. Mecklin, H. Järvinen, 2008, Carcinogenesis.

Thyroid carcinomas that occur in familial adenomatous polyposis patients recurrently harbor somatic variants in APC, BRAF, and KTM2D.

A. de la Chapelle, J. Church, J. Arola, 2020, Thyroid : official journal of the American Thyroid Association.

Genetic and epigenetic mechanisms of tumor predisposition in hereditary non-polyposis colorectal carcinoma and sporadic cancers

T. Nieminen, 2011 .

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

P. Peltomäki, H. Järvinen, M. Kankainen, 2016, Oncotarget.

Promoter‐specific alterations of APC are a rare cause for mutation‐negative familial adenomatous polyposis

P. Peltomäki, H. Järvinen, A. Gyenesei, 2014, Genes, chromosomes & cancer.

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Å. Borg, A. Ristimäki, P. Peltomäki, 2018, Genetics in Medicine.

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

P. Peltomäki, J. Mecklin, S. Eldfors, 2020, Cancers.

Reply: To PMID 24941021.

P. Peltomäki, J. Mecklin, H. Järvinen, 2015, Gastroenterology.

Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations

P. Peltomäki, S. Eldfors, Satu Mäki-Nevala, 2017, Oncotarget.

Updates in the field of hereditary nonpolyposis colorectal cancer

P. Peltomäki, T. Nieminen, A. Olkinuora, 2020, Expert review of gastroenterology & hepatology.

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

K. Aittomäki, T. Kuopio, P. Peltomäki, 2012, Breast Cancer Research.

Clinical Diagnosis and Therapy of Colorectal Cancer

T. Nieminen, S. Valo, Noora Porkka, 2015 .

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

A. Ristimäki, P. Peltomäki, L. Renkonen-Sinisalo, 2016, Journal of surgical oncology.

Epigenetic mechanisms in Lynch Syndrome

P. Peltomäki, T. Nieminen, Anni Niskakoski, 2016 .

Response to Yang et al.

P. Peltomäki, T. Nieminen, M. Nordling, 2019, Genetics in Medicine.

Identification of Rare Variants Predisposing to Thyroid Cancer.

D. Koboldt, Huiling He, Wei Li, 2019, Thyroid : official journal of the American Thyroid Association.

A truncating germline mutation of TINF2 in individuals with thyroid cancer or melanoma results in longer telomeres.

Huiling He, Wei Li, S. Liyanarachchi, 2020, Thyroid : official journal of the American Thyroid Association.

p 15 INK 4 b Ethnic Origin

P. Peltomaki, S. Eissa, T. Nieminen, 2014 .

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

A. Ristimäki, P. Peltomäki, J. Mecklin, 2011, Gastroenterology.

Identification of DHX40 as a candidate susceptibility gene for colorectal and hematological neoplasia

O. Kilpivaara, H. Järvinen, P. Peltomäki, 2023, Leukemia.

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

P. Peltomäki, J. Mecklin, H. Järvinen, 2009, Clinical Cancer Research.

Lynch Suspected Cases with Negative

P. Peltomäki, J. Mecklin, S. Eldfors, 2022 .