Minna K. Tammilehto-Kankuri

Turku, 20520, Finland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

Rare Germline Variants in DNA Repair Genes Detected in BRCA-Negative Finnish Patients with Early-Onset Breast Cancer.

Rare Germline Variants in DNA Repair Genes Detected in BRCA-Negative Finnish Patients with Early-Onset Breast Cancer.

Journal: Cancers

Published: June 24, 2024

Severe Untreated Scoliosis and Early Onset Breast Cancer in a Patient with Neurofibromatosis Associated with a Nonsense Variant of NF1 Gene.

Severe Untreated Scoliosis and Early Onset Breast Cancer in a Patient with Neurofibromatosis Associated with a Nonsense Variant of NF1 Gene.

Journal: Orthopedic research and reviews

Published: April 05, 2023

Long-term Outcome With Prolonged Use of Interferon-alpha Administered Intermittently for Metastatic Renal Cell Carcinoma: A Phase II Study.

Long-term Outcome With Prolonged Use of Interferon-alpha Administered Intermittently for Metastatic Renal Cell Carcinoma: A Phase II Study.

Journal: Anticancer research

Published: February 26, 2023

New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742-2A>G.

New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742-2A>G.

Journal: Molecular genetics & genomic medicine

Published: December 01, 2022

ATM c.7570G>C is a high-risk allele for breast cancer.

ATM c.7570G>C is a high-risk allele for breast cancer.

Journal: International journal of cancer

Published: June 23, 2022

Neurocognitive follow-up in adult siblings with Phelan-McDermid syndrome due to a novel SHANK3 splicing site mutation.

Neurocognitive follow-up in adult siblings with Phelan-McDermid syndrome due to a novel SHANK3 splicing site mutation.

Journal: Molecular genetics & genomic medicine

Published: January 19, 2021

Genetic, clinic and histopathologic characterization of BRCA-associated hereditary breast and ovarian cancer in southwestern Finland.

Genetic, clinic and histopathologic characterization of BRCA-associated hereditary breast and ovarian cancer in southwestern Finland.

Journal: Scientific reports

Published: January 11, 2021

Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland.

Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland.

Journal: Human genetics

Published: December 12, 2020

Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families.

Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families.

Journal: BMC cancer

Published: August 30, 2016

A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome.

A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: February 02, 2016

Whole-exome sequencing of Finnish hereditary breast cancer families.

Whole-exome sequencing of Finnish hereditary breast cancer families.

Journal: European journal of human genetics : EJHG

Published: January 22, 2016

copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

Journal: PloS one

Published: March 13, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026