Rebeqa Gunnarsson
Overview
Explore the profile of Rebeqa Gunnarsson including associated specialties, affiliations and a list of published articles.
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Articles
21
Citations
339
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Recent Articles
1.
Andersson J, Aydin E, Gunnarsson R, Lilljebjorn H, Fioretos T, Johansson B, et al.
Sci Rep
. 2024 Oct;
14(1):23181.
PMID: 39369032
Somatic copy number variations (CNVs), including abnormal chromosome numbers and structural changes leading to gain or loss of genetic material, play a crucial role in initiation and progression of cancer....
2.
Ragnarsson C, Yang M, Moura-Castro L, Aydin E, Gunnarsson R, Olsson-Arvidsson L, et al.
Genes Chromosomes Cancer
. 2024 May;
63(5):e23242.
PMID: 38738968
Constitutional polymorphisms in ARID5B are associated with an increased risk of developing high hyperdiploid (HeH; 51-67 chromosomes) pediatric B-cell precursor acute lymphoblastic leukemia (BCP ALL). Here, we investigated constitutional and...
3.
Yang M, Gunnarsson R, Duployez N, Zaliova M, Zuna J, Johansson B, et al.
Haematologica
. 2024 Feb;
109(6):1951-1955.
PMID: 38356456
No abstract available.
4.
Woodward E, Yang M, Moura-Castro L, van den Bos H, Gunnarsson R, Olsson-Arvidsson L, et al.
Nat Commun
. 2023 Mar;
14(1):1658.
PMID: 36966135
High hyperdiploid acute lymphoblastic leukemia (HeH ALL), one of the most common childhood malignancies, is driven by nonrandom aneuploidy (abnormal chromosome numbers) mainly comprising chromosomal gains. In this study, we...
5.
Gunnarsson R, Yang M, Biloglav A, Lazarevic V, Paulsson K, Johansson B
Leukemia
. 2022 Apr;
36(6):1681-1684.
PMID: 35365774
No abstract available.
6.
Gunnarsson R, Yang M, Olsson-Arvidsson L, Biloglav A, Behrendtz M, Castor A, et al.
Leukemia
. 2021 Apr;
35(5):1485-1489.
PMID: 33864028
No abstract available.
7.
Leeksma A, Baliakas P, Moysiadis T, Puiggros A, Plevova K, van der Kevie-Kersemaekers A, et al.
Haematologica
. 2020 Jan;
106(1):87-97.
PMID: 31974198
Complex karyotype (CK) identified by chromosome-banding analysis (CBA) has shown prognostic value in chronic lymphocytic leukemia (CLL). Genomic arrays offer high-resolution genome-wide detection of copy-number alterations (CNAs) and could therefore...
8.
Gunnarsson R, DiLorenzo S, Lundin-Strom K, Olsson L, Biloglav A, Lilljebjorn H, et al.
Leukemia
. 2018 Apr;
32(10):2117-2125.
PMID: 29626196
High-throughput sequencing was applied to investigate the mutation/methylation patterns on 1q and gene expression profiles in pediatric B-cell precursor acute lymphoblastic leukemia (BCP ALL) with/without (w/wo) dup(1q). Sequencing of the...
9.
Mansouri L, Sutton L, Ljungstrom V, Bondza S, Arngarden L, Bhoi S, et al.
J Exp Med
. 2015 May;
212(6):833-43.
PMID: 25987724
NF-κB is constitutively activated in chronic lymphocytic leukemia (CLL); however, the implicated molecular mechanisms remain largely unknown. Thus, we performed targeted deep sequencing of 18 core complex genes within the...
10.
Willander K, Dutta R, Ungerback J, Gunnarsson R, Juliusson G, Fredrikson M, et al.
BMC Cancer
. 2013 Jun;
13:274.
PMID: 23734977
Background: NOTCH1 PEST domain mutations in chronic lymphocytic leukemia have recently been shown to be of prognostic relevance. Both NOTCH1 and NOTCH2 are constitutively activated in B-cell CLL but not...