Minna Kankuri-Tammilehto
Publications
- 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 )



