Pertteli Salmenpera
Overview
Explore the profile of Pertteli Salmenpera 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
24
Citations
397
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Helio K, Cicerchia M, Hathaway J, Tommiska J, Huusko J, Saarinen I, et al.
Front Cardiovasc Med
. 2023 Oct;
10:1254272.
PMID: 37795486
Background: Familial dilated cardiomyopathy (DCM) causes heart failure and may lead to heart transplantation. DCM is typically a monogenic disorder with autosomal dominant inheritance. Currently disease-causing variants have been reported...
2.
Tuupanen S, Gall K, Sistonen J, Saarinen I, Kampjarvi K, Wells K, et al.
Transl Vis Sci Technol
. 2022 Jan;
11(1):6.
PMID: 34985506
Purpose: Comprehensive genetic testing for inherited retinal dystrophy (IRD) is challenged by difficult-to-sequence genomic regions, which are often mutational hotspots, such as RPGR ORF15. The purpose of this study was...
3.
Helio K, Mayranpaa M, Saarinen I, Ahonen S, Junnila H, Tommiska J, et al.
Front Genet
. 2021 Dec;
12:786705.
PMID: 34899865
Familial dilated cardiomyopathy (DCM) is a monogenic disorder typically inherited in an autosomal dominant pattern. We have identified two Finnish families with familial cardiomyopathy that is not explained by a...
4.
Soderhall C, Reinius L, Salmenpera P, Gentile M, Acevedo N, Konradsen J, et al.
Clin Epigenetics
. 2021 May;
13(1):106.
PMID: 33971943
Background: Methylation of DNA at CpG sites is an epigenetic modification and a potential modifier of disease risk, possibly mediating environmental effects. Currently, DNA methylation is commonly assessed using specific...
5.
Hathaway J, Helio K, Saarinen I, Tallila J, Seppala E, Tuupanen S, et al.
BMC Cardiovasc Disord
. 2021 Mar;
21(1):126.
PMID: 33673806
Background: Genetic testing in hypertrophic cardiomyopathy (HCM) is a published guideline-based recommendation. The diagnostic yield of genetic testing and corresponding HCM-associated genes have been largely documented by single center studies...
6.
Koskenvuo J, Saarinen I, Ahonen S, Tommiska J, Weckstrom S, Seppala E, et al.
PLoS One
. 2021 Feb;
16(2):e0245681.
PMID: 33534821
Background: Familial dilated cardiomyopathy (DCM) is typically a monogenic disorder with dominant inheritance. Although over 40 genes have been linked to DCM, more than half of the patients undergoing comprehensive...
7.
Maes P, Alkhovsky S, Bao Y, Beer M, Birkhead M, Briese T, et al.
Arch Virol
. 2018 Apr;
163(8):2295-2310.
PMID: 29680923
In 2018, the family Arenaviridae was expanded by inclusion of 1 new genus and 5 novel species. At the same time, the recently established order Bunyavirales was expanded by 3...
8.
Salmenpera P, Karhemo P, Rasanen K, Laakkonen P, Vaheri A
Exp Cell Res
. 2016 May;
345(1):17-24.
PMID: 27177832
Stromal fibroblasts have an important role in regulating tumor progression. Normal and quiescent fibroblasts have been shown to restrict and control cancer cell growth, while cancer-associated, i. e. activated fibroblasts...
9.
Vattulainen S, Aho J, Salmenpera P, Bruce S, Tallila J, Gentile M, et al.
Mol Genet Genomic Med
. 2015 Aug;
3(4):354-62.
PMID: 26247051
The genetic basis of pulmonary arterial hypertension (PAH) among Finnish PAH patients is poorly understood. We adopted a novel-targeted next-generation sequencing (NGS) approach called Oligonucleotide-Selective Sequencing (OS-Seq) and developed a...
10.
Akinrinade O, Ollila L, Vattulainen S, Tallila J, Gentile M, Salmenpera P, et al.
Eur Heart J
. 2015 Jun;
36(34):2327-37.
PMID: 26084686
Aims: Despite our increased understanding of the genetic basis of dilated cardiomyopathy (DCM), the clinical utility and yield of clinically meaningful findings of comprehensive next-generation sequencing (NGS)-based genetic diagnostics in...