Styrmir Sigurjonsson
Overview
Explore the profile of Styrmir Sigurjonsson including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
1491
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0
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Recent Articles
1.
Reinert T, Vesterman Henriksen T, Christensen E, Sharma S, Salari R, Sethi H, et al.
JAMA Oncol
. 2019 May;
5(8):1124-1131.
PMID: 31070691
Importance: Novel sensitive methods for detection and monitoring of residual disease can improve postoperative risk stratification with implications for patient selection for adjuvant chemotherapy (ACT), ACT duration, intensity of radiologic...
2.
Christensen E, Birkenkamp-Demtroder K, Sethi H, Shchegrova S, Salari R, Nordentoft I, et al.
J Clin Oncol
. 2019 May;
37(18):1547-1557.
PMID: 31059311
Purpose: Novel sensitive methods for early detection of relapse and for monitoring therapeutic efficacy may have a huge impact on risk stratification, treatment, and ultimately outcome for patients with bladder...
3.
Sigdel T, Archila F, Constantin T, Prins S, Liberto J, Damm I, et al.
J Clin Med
. 2018 Dec;
8(1).
PMID: 30583588
Standard noninvasive methods for detecting renal allograft rejection and injury have poor sensitivity and specificity. Plasma donor-derived cell-free DNA (dd-cfDNA) has been reported to accurately detect allograft rejection and injury...
4.
McCoy R, Newnham L, Ottolini C, Hoffmann E, Chatzimeletiou K, Cornejo O, et al.
Hum Mol Genet
. 2018 Apr;
27(14):2573-2585.
PMID: 29688390
Aneuploidy is prevalent in human embryos and is the leading cause of pregnancy loss. Many aneuploidies arise during oogenesis, increasing with maternal age. Superimposed on these meiotic aneuploidies are frequent...
5.
Maisenbacher M, Merrion K, Pettersen B, Young M, Paik K, Iyengar S, et al.
Mol Cytogenet
. 2017 Mar;
10:6.
PMID: 28293297
Background: The 22q11.2 deletion syndrome is the most common microdeletion syndrome in livebirths, but data regarding its incidence in other populations is limited and also include ascertainment bias. This study...
6.
Ryan A, Hunkapiller N, Banjevic M, Vankayalapati N, Fong N, Jinnett K, et al.
Fetal Diagn Ther
. 2016 Mar;
40(3):219-223.
PMID: 27028530
Objective: To validate an updated version (Version 2) of a single-nucleotide polymorphism (SNP)-based noninvasive prenatal test (NIPT) and to determine the likelihood of success when testing for fetal aneuploidies following...
7.
Kirkizlar E, Zimmermann B, Constantin T, Swenerton R, Hoang B, Wayham N, et al.
Transl Oncol
. 2015 Oct;
8(5):407-416.
PMID: 26500031
We demonstrate proof-of-concept for the use of massively multiplexed PCR and next-generation sequencing (mmPCR-NGS) to identify both clonal and subclonal copy-number variants (CNVs) in circulating tumor DNA. This is the...
8.
McCoy R, Demko Z, Ryan A, Banjevic M, Hill M, Sigurjonsson S, et al.
PLoS Genet
. 2015 Oct;
11(10):e1005601.
PMID: 26491874
Whole-chromosome imbalances affect over half of early human embryos and are the leading cause of pregnancy loss. While these errors frequently arise in oocyte meiosis, many such whole-chromosome abnormalities affecting...
9.
Flowers N, Kelley J, Sigurjonsson S, Bruno D, Pertile M
Prenat Diagn
. 2015 Jul;
35(10):986-9.
PMID: 26151667
No abstract available.
10.
Kumar A, Ryan A, Kitzman J, Wemmer N, Snyder M, Sigurjonsson S, et al.
Genome Med
. 2015 May;
7(1):35.
PMID: 26019723
Background: Preimplantation genetic diagnosis (PGD) enables profiling of embryos for genetic disorders prior to implantation. The majority of PGD testing is restricted in the scope of variants assayed or by...