|Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci|
B Zimmermann, M Hill, G Gemelos, Z Demko, M Banjevic, J Baner, ...
Prenatal diagnosis 32 (13), 1233-1241, 2012
|Single-nucleotide polymorphism–based noninvasive prenatal screening in a high-risk and low-risk cohort|
E Pergament, H Cuckle, B Zimmermann, M Banjevic, S Sigurjonsson, ...
Obstetrics and gynecology 124 (2 0 1), 210, 2014
|Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes|
RJ Wapner, JE Babiarz, B Levy, M Stosic, B Zimmermann, S Sigurjonsson, ...
American journal of obstetrics and gynecology 212 (3), 332. e1-332. e9, 2015
|Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing|
KJ Curnow, SJ Gross, MP Hall, M Stosic, Z Demko, B Zimmermann, M Hill, ...
American journal of obstetrics and gynecology 211 (5), 527. e1-527. e17, 2014
|SNP‐based non‐invasive prenatal testing detects sex chromosome aneuploidies with high accuracy|
C Samango‐Sprouse, M Banjevic, A Ryan, S Sigurjonsson, ...
Prenatal Diagnosis 33 (7), 643-649, 2013
|Analysis of plasma cell-free DNA by ultradeep sequencing in patients with stages I to III colorectal cancer|
T Reinert, TV Henriksen, E Christensen, S Sharma, R Salari, H Sethi, ...
JAMA oncology 5 (8), 1124-1131, 2019
|Detection of ubiquitous and heterogeneous mutations in cell-free DNA from patients with early-stage non-small-cell lung cancer|
M Jamal-Hanjani, GA Wilson, S Horswell, R Mitter, O Sakarya, ...
Annals of Oncology 27 (5), 862-867, 2016
|Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism–based noninvasive prenatal test|
KJ Curnow, L Wilkins-Haug, A Ryan, E Kırkızlar, M Stosic, MP Hall, ...
American journal of obstetrics and gynecology 212 (1), 79. e1-79. e9, 2015
|Multiple user writing on dirty paper|
YH Kim, A Sutivong, S Sigurjonsson
International Symposium onInformation Theory, 2004. ISIT 2004. Proceedings., 534, 2004
|Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis|
B Levy, S Sigurjonsson, B Pettersen, MK Maisenbacher, MP Hall, ...
Obstetrics & Gynecology 124 (2 PART 1), 202-209, 2014
|Evidence of selection against complex mitotic-origin aneuploidy during preimplantation development|
RC McCoy, ZP Demko, A Ryan, M Banjevic, M Hill, S Sigurjonsson, ...
PLoS Genet 11 (10), e1005601, 2015
|Early detection of metastatic relapse and monitoring of therapeutic efficacy by ultra-deep sequencing of plasma cell-free DNA in patients with urothelial bladder carcinoma|
E Christensen, K Birkenkamp-Demtröder, H Sethi, S Shchegrova, R Salari, ...
Journal of Clinical Oncology 37 (18), 1547-1557, 2019
|Methods for Non-Invasive Prenatal Paternity Testing|
A Ryan, S Sigurjonsson, M Banjevic, G Gemelos, M Hill, J Baner, ...
US Patent App. 13/335,043, 2012
|Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryos|
RC McCoy, Z Demko, A Ryan, M Banjevic, M Hill, S Sigurjonsson, ...
Science 348 (6231), 235-238, 2015
|Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics|
RB Lathi, M Loring, JAM Massie, ZP Demko, D Johnson, S Sigurjonsson, ...
PloS one 7 (3), e31282, 2012
|Optimizing detection of kidney transplant injury by assessment of donor-derived cell-free DNA via massively multiplex PCR|
TK Sigdel, FA Archila, T Constantin, SA Prins, J Liberto, I Damm, ...
Journal of clinical medicine 8 (1), 19, 2019
|Detection of clonal and subclonal copy-number variants in cell-free DNA from patients with breast cancer using a massively multiplexed PCR methodology|
E Kirkizlar, B Zimmermann, T Constantin, R Swenerton, B Hoang, ...
Translational oncology 8 (5), 407-416, 2015
|Reliability of 46, XX results on miscarriage specimens: a review of 1,222 first-trimester miscarriage specimens|
RB Lathi, SLF Gustin, J Keller, MK Maisenbacher, S Sigurjonsson, R Tao, ...
Fertility and sterility 101 (1), 178-182, 2014
|Informatics-based, highly accurate, noninvasive prenatal paternity testing|
A Ryan, J Baner, Z Demko, M Hill, S Sigurjonsson, ML Baird, ...
Genetics in Medicine 15 (6), 473-477, 2013
|On multiple user channels with state information at the transmitters|
S Sigurjónsson, YH Kim
Proceedings. International Symposium on Information Theory, 2005. ISIT 2005 …, 2005