Anna-Maija Sulonen
Overview
Explore the profile of Anna-Maija Sulonen including associated specialties, affiliations and a list of published articles.
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6
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1515
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Recent Articles
1.
Lehtonen J, Sulonen A, Almusa H, Lehtokari V, Johari M, Palva A, et al.
Sci Rep
. 2024 Feb;
14(1):4306.
PMID: 38383731
Rare or novel missense variants in large genes such as TTN and NEB are frequent in the general population, which hampers the interpretation of putative disease-causing biallelic variants in patients...
2.
Sulonen A, Ellonen P, Almusa H, Lepisto M, Eldfors S, Hannula S, et al.
Genome Biol
. 2011 Sep;
12(9):R94.
PMID: 21955854
Background: Techniques enabling targeted re-sequencing of the protein coding sequences of the human genome on next generation sequencing instruments are of great interest. We conducted a systematic comparison of the...
3.
Sawcer S, Hellenthal G, Pirinen M, Spencer C, Patsopoulos N, Moutsianas L, et al.
Nature
. 2011 Aug;
476(7359):214-9.
PMID: 21833088
Multiple sclerosis is a common disease of the central nervous system in which the interplay between inflammatory and neurodegenerative processes typically results in intermittent neurological disturbance followed by progressive accumulation...
4.
Jakkula E, Leppa V, Sulonen A, Varilo T, Kallio S, Kemppinen A, et al.
Am J Hum Genet
. 2010 Feb;
86(2):285-91.
PMID: 20159113
Genetic risk for multiple sclerosis (MS) is thought to involve both common and rare risk alleles. Recent GWAS and subsequent meta-analysis have established the critical role of the HLA locus...
5.
Sulonen A, Kallio S, Ellonen P, Suvela M, Elovaara I, Koivisto K, et al.
J Neuroimmunol
. 2008 Nov;
206(1-2):86-90.
PMID: 19019460
Loss-of-function mutations of DAP12 and TREM2 cause a recessively inherited disease PLOSL, manifesting in brain white matter. The genes of the DAP12-TREM2 signaling receptor are located on 19q13.12 and 6p21.1,...
6.
Yu X, Koczan D, Sulonen A, Akkad D, Kroner A, Comabella M, et al.
PLoS One
. 2008 Feb;
3(2):e1530.
PMID: 18270557
Background: Mitochondrial DNA (mtDNA) polymorphism is a possible factor contributing to the maternal parent-of-origin effect in multiple sclerosis (MS) susceptibility. Methods And Findings: In order to investigate the role of...