Anders Kampe
Overview
Explore the profile of Anders Kampe including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
20
Citations
219
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Partanen J, Happola P, Kampe A, Ahola-Olli A, Hellsten A, Rask S, et al.
Am J Psychiatry
. 2024 Sep;
181(10):879-892.
PMID: 39262212
Objective: The authors used longitudinal biobank data with up to 25 years of follow-up on over 2,600 clozapine users to derive reliable estimates of the real-world burden of clozapine adverse...
2.
Knol M, Poot R, Evans T, Satizabal C, Mishra A, Sargurupremraj M, et al.
Cell Rep Med
. 2024 May;
5(5):101529.
PMID: 38703765
The size of the human head is highly heritable, but genetic drivers of its variation within the general population remain unmapped. We perform a genome-wide association study on head size...
3.
Kampe A, Suvisaari J, Lahteenvuo M, Singh T, Ahola-Olli A, Urpa L, et al.
Mol Psychiatry
. 2024 Mar;
29(9):2733-2741.
PMID: 38556557
Genetic factors contribute to the susceptibility of psychotic disorders, but less is known how they affect psychotic disease-course development. Utilizing polygenic scores (PGSs) in combination with longitudinal healthcare data with...
4.
Koch E, Kampe A, Alver M, Sigurdarson S, Einarsson G, Partanen J, et al.
Neuropsychopharmacology
. 2024 Jan;
49(7):1113-1119.
PMID: 38184734
Genomic prediction of antipsychotic dose and polypharmacy has been difficult, mainly due to limited access to large cohorts with genetic and drug prescription data. In this proof of principle study,...
5.
Nethander M, Moverare-Skrtic S, Kampe A, Coward E, Reimann E, Grahnemo L, et al.
Nat Genet
. 2023 Nov;
55(11):1820-1830.
PMID: 37919453
Osteoporotic fracture is among the most common and costly of diseases. While reasonably heritable, its genetic determinants have remained elusive. Forearm fractures are the most common clinically recognized osteoporotic fractures...
6.
Baliakas P, Munters A, Kampe A, Tesi B, Bondeson M, Ladenvall C, et al.
J Med Genet
. 2023 Aug;
61(2):150-154.
PMID: 37580114
Background: Low-impact genetic variants identified in population-based genetic studies are not routinely measured as part of clinical genetic testing in familial breast cancer (BC). We studied the consequences of integrating...
7.
Formosa M, Bergen D, Gregson C, Maurizi A, Kampe A, Garcia-Giralt N, et al.
Front Endocrinol (Lausanne)
. 2021 Sep;
12:709711.
PMID: 34539568
Genetic disorders of the skeleton encompass a diverse group of bone diseases differing in clinical characteristics, severity, incidence and molecular etiology. Of particular interest are the monogenic rare bone mass...
8.
Makitie R, Henning P, Jiu Y, Kampe A, Kogan K, Costantini A, et al.
JBMR Plus
. 2021 Jul;
5(7):e10509.
PMID: 34258505
Ras homologous guanosine triphosphatases (RhoGTPases) control several cellular functions, including cytoskeletal actin remodeling and cell migration. Their activities are downregulated by GTPase-activating proteins (GAPs). Although RhoGTPases are implicated in bone...
9.
Makitie R, Niinimaki T, Suo-Palosaari M, Kampe A, Costantini A, Toiviainen-Salo S, et al.
Front Endocrinol (Lausanne)
. 2020 Jul;
11:393.
PMID: 32655496
Mutations in the X-chromosomal gene, encoding Plastin 3, lead to severe early-onset osteoporosis, suggesting a major role for PLS3 in bone metabolism. However, the consequences of abnormal PLS3 function in...
10.
Makitie R, Hackl M, Weigl M, Frischer A, Kampe A, Costantini A, et al.
J Bone Miner Res
. 2020 May;
35(10):1962-1973.
PMID: 32453450
Plastin 3 (PLS3), encoded by PLS3, is a newly recognized regulator of bone metabolism, and mutations in the encoding gene result in severe childhood-onset osteoporosis. Because it is an X...