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Circulating miRNAs in bone health and disease

Bone (New York, N.Y.), 2021-04, Vol.145, p.115787-115787, Article 115787

2021

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Altered MicroRNA Profile in Osteoporosis Caused by Impaired WNT Signaling

The journal of clinical endocrinology and metabolism, 2018-05, Vol.103 (5), p.1985-1996

2018

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Changes in occurrence and management of laryngeal fractures at the Helsinki University Hospital during 25 years

European archives of oto-rhino-laryngology, 2024-02, Vol.281 (2), p.915-924

2024

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New Insights Into Monogenic Causes of Osteoporosis

Frontiers in endocrinology (Lausanne), 2019, Vol.10, p.70-70

2019

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Osteoporosis related to WNT1 variants: a not infrequent cause of osteoporosis

Osteoporosis international, 2023-02, Vol.34 (2), p.405-411

2023

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Early‐Onset Osteoporosis: Rare Monogenic Forms Elucidate the Complexity of Disease Pathogenesis Beyond Type I Collagen

Journal of bone and mineral research, 2022-09, Vol.37 (9), p.1623-1641

2022

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Fibrous dysplasia of the head and neck in Southern Finland: a retrospective study on clinical characteristics, diagnostics, and treatment

European archives of oto-rhino-laryngology, 2024-06, Vol.281 (6), p.3189-3195

2024

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Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults

Journal of bone and mineral research, 2016-09, Vol.31 (9), p.1734-1742

2016

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Impaired WNT signaling and the spine—Heterozygous WNT1 mutation causes severe age-related spinal pathology

Bone (New York, N.Y.), 2017-08, Vol.101, p.3-9

2017

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Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23

Journal of bone and mineral research, 2020-05, Vol.35 (5), p.901-912

2020

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Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis

Frontiers in endocrinology (Lausanne), 2022-09, Vol.13, p.954730-954730

2022

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Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity

Frontiers in endocrinology (Lausanne), 2020-02, Vol.11, p.81-81

2020

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SGMS2 in primary osteoporosis with facial nerve palsy

Frontiers in endocrinology (Lausanne), 2023-10, Vol.14, p.1224318-1224318

2023

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Bone material properties and response to teriparatide in osteoporosis due to WNT1 and PLS3 mutations

Bone (New York, N.Y.), 2021-05, Vol.146, p.115900-115900, Article 115900

2021

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A Novel Osteochondrodysplasia With Empty Sella Associates With a TBX2 Variant

Frontiers in endocrinology (Lausanne), 2022-03, Vol.13, p.845889-845889

2022

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Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility

Frontiers in endocrinology (Lausanne), 2018-07, Vol.9, p.380-380

2018

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High bone mass due to novel LRP5 and AMER1 mutations

European journal of medical genetics, 2017-12, Vol.60 (12), p.675-679

2017

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PLS3 Mutations Cause Severe Age and Sex-Related Spinal Pathology

Frontiers in endocrinology (Lausanne), 2020-06, Vol.11, p.393-393

2020

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Osteocyte Protein Expression Is Altered in Low-Turnover Osteoporosis Caused by Mutations in WNT1 and PLS3

The journal of clinical endocrinology and metabolism, 2017-07, Vol.102 (7), p.2340-2348

2017

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A multi-omics study to characterize the transdifferentiation of human dermal fibroblasts to osteoblast-like cells

Frontiers in molecular biosciences, 2022-11, Vol.9, p.1032026-1032026

2022

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Recessive multiple epiphyseal dysplasia – Clinical characteristics caused by rare compound heterozygous SLC26A2 genotypes

European journal of medical genetics, 2019-11, Vol.62 (11), p.103573-103573, Article 103573

2019

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Abnormal Bone Tissue Organization and Osteocyte Lacunocanalicular Network in Early‐Onset Osteoporosis Due to SGMS2 Mutations

JBMR plus, 2021-11, Vol.5 (11), p.e10537-n/a

2021

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New Genetic Forms of Childhood-Onset Primary Osteoporosis

Hormone research in paediatrics, 2015-01, Vol.84 (6), p.361-369

2015

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Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility

Current osteoporosis reports, 2017-08, Vol.15 (4), p.303-310

2017

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Circulating miRNAs in bone health and disease

Altered MicroRNA Profile in Osteoporosis Caused by Impaired WNT Signaling

Changes in occurrence and management of laryngeal fractures at the Helsinki University Hospital during 25 years

New Insights Into Monogenic Causes of Osteoporosis

Osteoporosis related to WNT1 variants: a not infrequent cause of osteoporosis

Early‐Onset Osteoporosis: Rare Monogenic Forms Elucidate the Complexity of Disease Pathogenesis Beyond Type I Collagen

Fibrous dysplasia of the head and neck in Southern Finland: a retrospective study on clinical characteristics, diagnostics, and treatment

Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults

Impaired WNT signaling and the spine—Heterozygous WNT1 mutation causes severe age-related spinal pathology

Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23

Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis

Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity

SGMS2 in primary osteoporosis with facial nerve palsy

Bone material properties and response to teriparatide in osteoporosis due to WNT1 and PLS3 mutations

A Novel Osteochondrodysplasia With Empty Sella Associates With a TBX2 Variant

Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility

High bone mass due to novel LRP5 and AMER1 mutations

PLS3 Mutations Cause Severe Age and Sex-Related Spinal Pathology

Osteocyte Protein Expression Is Altered in Low-Turnover Osteoporosis Caused by Mutations in WNT1 and PLS3

A multi-omics study to characterize the transdifferentiation of human dermal fibroblasts to osteoblast-like cells

Recessive multiple epiphyseal dysplasia – Clinical characteristics caused by rare compound heterozygous SLC26A2 genotypes

Abnormal Bone Tissue Organization and Osteocyte Lacunocanalicular Network in Early‐Onset Osteoporosis Due to SGMS2 Mutations

New Genetic Forms of Childhood-Onset Primary Osteoporosis

Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2

Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility

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