Minna Pekkinen

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 6

Top Topics

Top Venues

American journal of medical genetics. Part A

Scientific reports

The Journal of clinical endocrinology and metabolism

This page only lists publications with an associated author ORCID identifier.

Publications

Laura Koljonen, Maria Enlund-Cerullo, Helena Henrietta Hauta-Alus, Elisa Holmlund-Suila, Saara Valkama, Jenni Rosendahl, Sture Andersson, Minna Pekkinen, Outimaija Mäkitie
Phosphate Concentrations and Modifying Factors in Healthy Children From 12 to 24 Months of Age. The Journal of clinical endocrinology and metabolism 106 (10) (2021)
Vladimir M Kenis, Eugeniy Melchenko, Ilya Mazunin, Minna Pekkinen, Outimaija Mäkitie
A new family with epiphyseal chondrodysplasia type Miura. American journal of medical genetics. Part A 185 (1) (2020)
Svetlana Vakkilainen, Tiina Skoog, Elisabet Einarsdottir, Anna Middleton, Minna Pekkinen, Tiina Öhman, Shintaro Katayama, Kaarel Krjutškov, Panu E Kovanen, Markku Varjosalo, Arne Lindqvist, Juha Kere, Outi Mäkitie
The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2. Scientific reports 9 (1) (2019)
Anders Kämpe, Maria Enlund-Cerullo, Saara Valkama, Elisa Holmlund-Suila, Jenni Rosendahl, Helena Henrietta Hauta-Alus, Minna Pekkinen, Sture Andersson, Outimaija Mäkitie
Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. PLoS genetics 15 (12) (2019)
Petra Loid, Riikka Mäkitie, Alice Costantini, Heli Viljakainen, Minna Pekkinen, Outimaija Mäkitie
A novel MYT1L mutation in a patient with severe early-onset obesity and intellectual disability. American journal of medical genetics. Part A 176 (9) (2018)
Minna Pekkinen, Giedre Grigelioniene, Leyla Akin, Krati Shah, Kadri Karaer, Selim Kurtoğlu, Alka Ekbote, Zehra Aycan, Elif Sağsak, Sumita Danda, Eva Åström, Outi Mäkitie
Novel mutations in the LRP5 gene in patients with Osteoporosis-pseudoglioma syndrome. American journal of medical genetics. Part A 173 (12) (2017)