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Pekkinen, Minna
130
results:
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Online (130)
Mediatypes
Articles (Online) (46)
OpenAccess-fulltext (84)
Languages
english (110)
finnish (1)
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?
1
A de novo PRPF8 Pathogenic Variant in Transient Severe Hypo..:
Koljonen, Laura
;
Salonen, Pia
;
Rusanen, Salla
...
Hormone Research in Paediatrics. , 2024
Link:
https://doi.org/10.1159/..
?
2
SGMS2 in primary osteoporosis with facial nerve palsy:
Pihlström, Sandra
;
Richardt, Sampo
;
Määttä, Kirsi
...
Frontiers in Endocrinology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Variation in the fibroblast growth factor 23 (FGF23) gene a..:
Enlund-Cerullo, Maria
;
Holmlund-Suila, Elisa
;
Valkama, Saara
...
Frontiers in Genetics. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
A multi-omics study to characterize the transdifferentiatio..:
Pihlström, Sandra
;
Määttä, Kirsi
;
Öhman, Tiina
...
Frontiers in Molecular Biosciences. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
5
Targeted Exome Sequencing of Genes Involved in Rare CNVs in..:
Loid, Petra
;
Pekkinen, Minna
;
Mustila, Taina
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
6
Osteogenically differentiated human fibroblasts – an altern..:
Pihlström, Sandra
;
Määttä, Kirsi
;
Mäkitie, Riikka
...
Bone Reports. 16 (2022) - p. 101391 , 2022
Link:
https://doi.org/10.1016/..
?
7
Abnormal Bone Tissue Organization and Osteocyte Lacunocanal..:
Mäkitie, Riikka E.
;
Blouin, Stéphane
;
Välimäki, Ville‐Valtteri
...
JBMR Plus. 5 (2021) 11 - p. , 2021
Link:
https://doi.org/10.1002/..
?
8
A novel IFITM5 variant associates with phenotype of osteopo..:
Mäkitie, Riikka
;
Pekkinen, Minna
;
Morisada, Naoya
...
Bone Reports. 14 (2021) - p. 100850 , 2021
Link:
https://doi.org/10.1016/..
?
9
AnARHGAP25variant links aberrantRac1function to early‐onset..:
Mäkitie, Riikka E.
;
Henning, Petra
;
Jiu, Yaming
...
JBMR Plus. 5 (2021) 7 - p. , 2021
Link:
https://doi.org/10.1002/..
?
10
Phosphate Concentrations and Modifying Factors in Healthy C..:
Koljonen, Laura
;
Enlund-Cerullo, Maria
;
Hauta-alus, Helena
...
The Journal of Clinical Endocrinology & Metabolism. 106 (2021) 10 - p. 2865-2875 , 2021
Link:
https://doi.org/10.1210/..
?
11
Rare Variants in Genes Linked to Appetite Control and Hypot..:
Loid, Petra
;
Mustila, Taina
;
Mäkitie, Riikka E.
...
Frontiers in Endocrinology. 11 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
12
GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Cha..:
Loid, Petra
;
Pekkinen, Minna
;
Reyes, Monica
...
Frontiers in Pediatrics. 8 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
13
Biallelic KIF24 Variants Are Responsible for a Spectrum of ..:
Reilly, Madeline Louise
;
Ain, Noor ul
;
Muurinen, Mari
...
Journal of Bone and Mineral Research. 37 (2020) 9 - p. 1642-1652 , 2020
Link:
https://doi.org/10.1002/..
?
14
Severe Phenotype of APECED (APS1) Increases Risk for Struct..:
Laakso, Saila
;
Borchers, Joonatan
;
Toiviainen-Salo, Sanna
..
Frontiers in Endocrinology. 11 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
15
A new family with epiphyseal chondrodysplasia type Miura:
Kenis, Vladimir
;
Melchenko, Eugeniy
;
Mazunin, Ilya
..
American Journal of Medical Genetics Part A. 185 (2020) 1 - p. 112-118 , 2020
Link:
https://doi.org/10.1002/..
1-15