Andreas Kindmark
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Explore the profile of Andreas Kindmark including associated specialties, affiliations and a list of published articles.
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1261
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Recent Articles
1.
Johnsson M, Wall H, Lopes Pinto F, Fleming R, McCormack H, Benavides-Reyes C, et al.
G3 (Bethesda)
. 2022 Dec;
13(2).
PMID: 36453438
Osteoporosis and bone fractures are a severe problem for the welfare of laying hens, with genetics and environment, such as housing system, each making substantial contributions to bone strength. In...
2.
Freyschuss B, Svensson M, Cars T, Lindhagen L, Johansson H, Kindmark A
J Bone Miner Res
. 2022 Jan;
37(4):649-659.
PMID: 34984745
Results from real-world evidence (RWE) from the largest healthcare region in Sweden show low uptake of antiresorptive (AR) treatment, but beneficial effect in those receiving treatment, especially for the composite...
3.
Wu P, Westerberg P, Kindmark A, Tivesten A, Karlsson M, Mellstrom D, et al.
Sci Rep
. 2020 Jun;
10(1):10243.
PMID: 32581247
The Klotho (KL) gene is involved in phosphate homeostasis. Polymorphisms in this gene have been reported to be associated with the risk of cardiovascular disease. Here we used computational tools...
4.
Hughes D, Mikosch P, Belmatoug N, Carubbi F, Cox T, Goker-Alpan O, et al.
J Bone Miner Res
. 2019 Jun;
34(6):996-1013.
PMID: 31233632
Gaucher disease (GD) is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunction in multiple organs. Involvement of the skeleton is one of the most prevalent aspects of...
5.
Clewemar P, Hailer N, Hailer Y, Klar J, Kindmark A, Ljunggren O, et al.
Mol Genet Genomic Med
. 2019 May;
7(7):e00723.
PMID: 31099171
Background: Osteogenesis imperfecta (OI) is a clinical and genetic heterogeneous group of connective tissue disorders, characterized by bone fragility and a propensity to fracture. Methods: In this report we describe...
6.
Bjork A, Mellstrom D, Ohlsson C, Karlsson M, Mallmin H, Johansson G, et al.
PLoS One
. 2018 Dec;
13(12):e0209268.
PMID: 30576350
Objective: Polymorphisms in the CYP2R1 gene encoding Vitamin D 25-hydroxylase have been reported to correlate with circulating levels of 25-OH vitamin D3 (25(OH)D). It is unknown whether these variations also...
7.
Lindahl K, Astrom E, Dragomir A, Symoens S, Coucke P, Larsson S, et al.
Bone
. 2018 Jun;
114:268-277.
PMID: 29936144
Background: Mutations of the endoplasmic reticulum (ER)-stress transducer OASIS (encoded by CREB3L1), cause severe recessive osteogenesis imperfecta (OI) not compatible with surviving the neonatal period, as has been shown in...
8.
Andersson K, Dahllof G, Lindahl K, Kindmark A, Grigelioniene G, Astrom E, et al.
PLoS One
. 2017 May;
12(5):e0176466.
PMID: 28498836
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused mainly by mutations in the collagen I genes (COL1A1 and COL1A2). Dentinogenesis imperfecta (DGI) and other dental...
9.
Ohlsson C, Nethander M, Kindmark A, Ljunggren O, Lorentzon M, Rosengren B, et al.
J Bone Miner Res
. 2017 Mar;
32(8):1607-1614.
PMID: 28276592
The adrenal-derived hormones dehydroepiandrosterone (DHEA) and its sulfate (DHEAS) are the most abundant circulating hormones and their levels decline substantially with age. DHEAS is considered an inactive precursor, which is...
10.
Laxman N, Mallmin H, Nilsson O, Kindmark A
Genes (Basel)
. 2016 Dec;
8(1).
PMID: 28025541
MicroRNAs (miRNAs) are a family of small, non-coding RNAs (17-24 nucleotides), which regulate gene expression either by the degradation of the target mRNAs or inhibiting the translation of genes. Recent...