| 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 | 714 | 2019 |
| 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 | 492 | 2012 |
| 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 | 432 | 2019 |
| 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 & Gynecology 124 (2 PART 1), 210-218, 2014 | 405 | 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 | 387 | 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 | 321 | 2014 |
| 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 | 257 | 2016 |
| 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 | 256 | 2013 |
| 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 | 239 | 2014 |
| 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, 2018 | 230 | 2018 |
| 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 | 227 | 2015 |
| Evidence of selection against complex mitotic-origin aneuploidy during preimplantation development RC McCoy, ZP Demko, A Ryan, M Banjevic, M Hill, S Sigurjonsson, ... PLoS genetics 11 (10), e1005601, 2015 | 221 | 2015 |
| SQL query generator utilizing matrix structures ÁS Egilsson, H Gudbjartsson, S Sigurjónsson US Patent 6,578,028, 2003 | 153 | 2003 |
| 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 | 152 | 2012 |
| Multiple user writing on dirty paper YH Kim, A Sutivong, S Sigurjonsson International Symposium onInformation Theory, 2004. ISIT 2004. Proceedings., 534, 2004 | 152 | 2004 |
| 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 | 138 | 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 | 136 | 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 | 123 | 2015 |
| 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 | 118 | 2013 |
| 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 | 103 | 2014 |
