Petra Loid
Helsinki, Finland
Last Updated: 09/26/2026
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Found 22 publications
Pathogenic SGMS2 variants are not a common cause of early-onset osteoporosis among Finnish patients.
Pathogenic SGMS2 variants are not a common cause of early-onset osteoporosis among Finnish patients.
Journal: Frontiers in endocrinology
Published: October 06, 2025
Delayed diagnosis of skeletal dysplasia in a girl with cartilage-hair hypoplasia.
Journal: JCEM case reports
Published: September 03, 2025
Short Stature and Response to Growth Hormone Treatment in CUL3-Related Neurodevelopmental Disorder.
Journal: Hormone research in paediatrics
Published: May 27, 2025
Short stature, brachydactyly and joint contractures associated with novel FBN2 variants in two families.
Journal: Journal of medical genetics
Published: November 21, 2024
Germline mutations in a G protein identify signaling cross-talk in T cells.
Journal: Science (New York, N.Y.)
Published: September 19, 2024
Rare gene variants and weight loss at 10 years after sleeve gastrectomy and gastric bypass - a randomized clinical trial.
Journal: Surgery for obesity and related diseases : official journal of the American Society for Bariatric Surgery
Published: July 02, 2024
Novel Insights: A Novel PHIP Variant in a Family with Severe Early-Onset Obesity.
Journal: Hormone research in paediatrics
Published: June 03, 2024
A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome.
Journal: Bone reports
Published: May 03, 2024
Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy.
Journal: BMC musculoskeletal disorders
Published: March 27, 2023
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly.
Journal: Genes
Published: March 06, 2023
Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome.
Journal: Frontiers in pediatrics
Published: August 10, 2022
Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis.
Journal: Frontiers in endocrinology
Published: May 27, 2022
Last Updated: 09/26/2026