Minna Kankuri-Tammilehto
Publications 
1 of 2
- Kansallinen suositus auttaa tunnistamaan perinnöllisen haimasyöpäalttiuden (2024)
- Lääkärilehti
(D1 Article in a professional journal) - Perinnöllinen haimasyöpäalttius – kansallinen seurantasuositus (2024)
- Lääkärilehti
(A2 Refereed review article in a scientific journal ) - Rare Germline Variants in DNA Repair Genes Detected in BRCA-Negative Finnish Patients with Early-Onset Breast Cancer (2024)
- Cancers
(A1 Refereed original research article in a scientific journal) - Uudet menetelmät lääketietieteen koulutuksessa : esimerkkeinä mikro-oppiminen, pelillistäminen ja laajennettu todellisuus (2024)
- Duodecim
(A2 Refereed review article in a scientific journal ) - ATM c.7570G>C is a high-risk allele for breast cancer (2023)
- International Journal of Cancer
(A1 Refereed original research article in a scientific journal) - BRCA-geenivirhe löytyy kymmenesosasta rinta- ja munasarjasyöpäsuvuista Tyksin erva-alueella (2023)
- Lääkärilehti
(A1 Refereed original research article in a scientific journal) - Long-term Outcome With Prolonged Use of Interferon-alpha Administered Intermittently for Metastatic Renal Cell Carcinoma: A Phase II Study (2023)
- Anticancer Research
(A1 Refereed original research article in a scientific journal) - New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742-2A & gt;G (2023)
- Molecular Genetics and Genomic Medicine
(A1 Refereed original research article in a scientific journal) - Pelit oppimisprosessin rikastajina – kolme esimerkkiä (2023)
- Lääkärilehti
(A2 Refereed review article in a scientific journal ) - Severe Untreated Scoliosis and Early Onset Breast Cancer in a Patient with Neurofibromatosis Associated with a Nonsense Variant of NF1 Gene (2023)
- Orthopedic Research and Reviews
(A1 Refereed original research article in a scientific journal) - Suuren riskin rintasyöpäalttiuden seuranta on geenikohtaista (2023)
- Lääkärilehti
(A2 Refereed review article in a scientific journal ) - Genetic, clinic and histopathologic characterization of BRCA-associated hereditary breast and ovarian cancer in southwestern Finland (2022)
- Scientific Reports
(A1 Refereed original research article in a scientific journal) - Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland (2021)
- Human Genetics
(A1 Refereed original research article in a scientific journal) - Geeniohjatun syövän hoidon työryhmä hoitopäätösten apuna : Läntisen syöpäkeskuksen kokemus (2021)
- Duodecim
(D1 Article in a professional journal) - Genetic Susceptibility due to Moderate Breast Cancer Risk Gene CHEK2: a case report (2021)
- Journal of Clinical Oncology and Research
(B1 Non-refereed article in a scientific journal) - Genetic Susceptibility to Epithelial Ovarian and Endometrial Cancer (2021)
- Journal of Clinical Oncology and Research
(B1 Non-refereed article in a scientific journal) - Neurocognitive follow-up in adult siblings with Phelan-McDermid syndrome due to a novel SHANK3 splicing site mutation (2021)
- Molecular Genetics and Genomic Medicine
(A1 Refereed original research article in a scientific journal) - Novel Germline Variant in Tumor Suppressor SMAD3 Gene Associates with Familial Thoracic Aortic Aneurysm and Dissection Syndrome (2021)
- Journal of Clinical Oncology and Research
(B1 Non-refereed article in a scientific journal) - Perinnöllisyyslääkärin osuus syövän geenidiagnostiikassa - kokemukset Tyksistä ja muualta (2021)
- Duodecim
(A2 Refereed review article in a scientific journal ) - Tumor Profile and Neuropsychological Symptoms of a Family with Novel Pathogenic Variant in NF1 Found by an RNA-Based Analysis (2021)
- Journal of Clinical Oncology and Research
(B1 Non-refereed article in a scientific journal)
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