Minna Pekkinen

10PUBLICATIONS
26CO-AUTHORS
Predictive and prognostic markersMolecular targetsGene and molecular therapyOrthodontics and dentofacial orthopaedicsInfant and child health
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Publications (10)

|Jul 30, 2026
Cumulative microscopy reveals cellular states in fibroblasts from patients with genetic disorders.

|Oct 27, 2025
Utilizing CRISPR-Cas13d-knockdown in zebrafish to study a rare monogenic bone fragility syndrome.

Kirsi Määttä, Yu-Chia Chen, Sandra Pihlström

|Sep 22, 2025
Transcriptomic and lipidomic profiling provide novel insight into the pathogenesis of monogenic SGMS2-related osteoporosis.

Sandra Pihlström, Ali Oghabian, Kirsi Määttä

|Jan 29, 2025
A deep intronic PHEX variant associated with X-linked hypophosphatemia in a Finnish family.

Laura Koponen, Minna Pekkinen, Jelmer Legebeke

|Jul 02, 2021
Phosphate Concentrations and Modifying Factors in Healthy Children From 12 to 24 Months of Age.

Laura Koljonen, Maria Enlund-Cerullo, Helena Hauta-Alus

|Oct 19, 2020
A new family with epiphyseal chondrodysplasia type Miura.

Vladimir Kenis, Eugeniy Melchenko, Ilya Mazunin

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Frequent Collaborators

8 joint publications

Outi Mäkitie

2 joint publications

Arne Lindqvist

2 joint publications

Laura Koponen

2 joint publications

Helena Hauta-Alus