Minna Kankuri-Tammilehto
Overview
Explore the profile of Minna Kankuri-Tammilehto including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
13
Citations
70
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Kurkilahti V, Rathinakannan V, Nynas E, Goel N, Aittomaki K, Nevanlinna H, et al.
Cancers (Basel)
. 2024 Sep;
16(17).
PMID: 39272813
Background: Breast cancer is the most common malignancy, with a mean age of onset of approximately 60 years. Only a minority of breast cancer patients present with an early onset...
2.
Reinhold V, Saarinen A, Suominen E, Syrjanen S, Kankuri-Tammilehto M
Orthop Res Rev
. 2023 Oct;
15:183-189.
PMID: 37791039
Background: Neurofibromatosis 1 (NF1) is a relatively common genetic disorder linked to skeletal abnormalities and elevated risk of cancer. Early onset scoliosis is common in patients with NF1 although severe...
3.
Reinhold V, Syrjanen S, Kankuri-Tammilehto M
Mol Genet Genomic Med
. 2023 Sep;
11(12):e2275.
PMID: 37665136
Background: Ectodermal dysplasias are inherited disorders, which are characterized by congenital defects in two or more ectodermal structures such as skin, sweat glands, hair, nails, teeth, and mucous membranes. Method:...
4.
Kankuri-Tammilehto M, Perasto L, Pyrhonen S, Salminen E
Anticancer Res
. 2023 May;
43(6):2645-2657.
PMID: 37247917
Background/aim: Interferon-alpha (IFN-alpha) has shown survival benefits in metastatic renal cell carcinoma (mRCC), but the knowledge about long-term outcome is sparse. Additional knowledge is beneficial because IFN-alpha usage in combination...
5.
Kankuri-Tammilehto M, Tervasmaki A, Kraatari-Tiri M, Rahikkala E, Pylkas K, Kuismin O
Int J Cancer
. 2022 Sep;
152(3):429-435.
PMID: 36161273
ATM is generally described as a moderate-risk breast cancer susceptibility gene. However, some of ATM variants might encounter higher risk. ATM c.7570G>C, p.Ala2524Pro, (rs769142993) is a pathogenic Finnish founder variant...
6.
Kankuri-Tammilehto M, Sauna-Aho O, Arvio M
Mol Genet Genomic Med
. 2021 Aug;
9(12):e1780.
PMID: 34369668
Background: Phelan-McDermid syndrome (PMD) is usually not only caused by 22q13.3 deletion but also pathogenic variants (mutations) of SHANK3 gene. PMD is characterized by global intellectual disability, severely delayed or...
7.
Jarvela I, Maatta T, Acharya A, Leppala J, Jhangiani S, Arvio M, et al.
Hum Genet
. 2021 Mar;
140(7):1011-1029.
PMID: 33710394
The genetics of autosomal recessive intellectual disability (ARID) has mainly been studied in consanguineous families, however, founder populations may also be of interest to study intellectual disability (ID) and the...
8.
Maatta K, Nurminen R, Kankuri-Tammilehto M, Kallioniemi A, Laasanen S, Schleutker J
BMC Cancer
. 2017 Jul;
17(1):496.
PMID: 28738860
Background: BRCA1 and BRCA2 mutations explain approximately one-fifth of the inherited susceptibility in high-risk Finnish hereditary breast and ovarian cancer (HBOC) families. EMSY is located in the breast cancer-associated chromosomal...
9.
Maatta K, Rantapero T, Lindstrom A, Nykter M, Kankuri-Tammilehto M, Laasanen S, et al.
Eur J Hum Genet
. 2016 Oct;
25(1):85-93.
PMID: 27782108
A remarkable proportion of factors causing genetic predisposition to breast cancer (BC) are unknown in non-BRCA1/2 families. Exome sequencing was performed for 13 high-risk Finnish hereditary breast and/or ovarian cancer...
10.
Raivio V, Jonasson J, Myllykangas L, Ala-Mello S, Kankuri-Tammilehto M, Kiuru-Enari S, et al.
Amyloid
. 2016 Feb;
23(1):46-50.
PMID: 26828956
Objective: We describe a novel TTR mutation with vitreous opacities and carpal tunnel syndrome. Materials And Methods: A 78 year-old woman with vitreous opacities, her daughter with dry eye syndrome,...