Accurate Gender Determination Using a Single-Nucleotide Polymorphism-based Non-invasive Prenatal Test
Susan J Gross , Kirsten J Curnow , Bernhard Zimmermann , Matthew Hill
Common variants spanning PLK4 are associated with mitotic-origin aneuploidy in human embryos.
R. C. McCoy , Z. Demko , A. Ryan , M. Banjevic
Science 348 ( 6231) 235 -238
78
2015
Single nucleotide polymorphism (SNP) based chromosome analysis of products of conception (POC) samples reveals uniparental disomy: cause for miscarriage or incidental finding?
D. Clark , M. Maisenbacher , S. Sigurjonsson , K. Paik
Fertility and Sterility 102 ( 3) e240
2014
Size matters: single nucleotide polymorphism (SNP) based chromosome analysis of products of conception (POC) samples identifies clinically significant deletions/duplications below karyotype resolution
M.K. Maisenbacher , K. Merrion , S. Sigurjonsson , K.G. Paik
Fertility and Sterility 104 ( 3)
2015
Informatics-based molecular karyotyping of products of conception (POC) with maternal cell contamination (MCC) detection: report on 344 consecutive analyses
R.B. Lathi , S. Sigurjonsson , J. Keller , M. Maisenbacher
Fertility and Sterility 96 ( 3)
1
2011
Parental Origin of Aneuploidy in First Trimester Miscarriages
R.B. Lathi , S. Sigurjonsson , J. Keller , Z. Demko
Fertility and Sterility 97 ( 3)
2012
High rate of microdeletions in miscarriage products of conception (POC) samples suggests role for preimplantation genetic diagnosis (PGD)
M. Rabinowitz , S. Sigurjonsson , J. Keller , M. Maisenbacher
Fertility and Sterility 98 ( 3) S54
2012
Informatics-based molecular karyotyping of products of conception (POC) preserved in paraffin with maternal cell contamination (MCC) detection: report on 46 consecutive analyses
R.B. Lathi , M. Maisenbacher , S. Sigurjonsson , J. Keller
Fertility and Sterility 98 ( 3)
2012
Triploidy detection via single nucleotide polymorphism (SNP)-based non-invasive prenatal testing (NIPT): two case studies
M. Hall , M. Hill , B. Zimmerman , S. Sigurjonsson
Fertility and Sterility 100 ( 3)
2013
Session 16: Innovations in reproductive genetics
J. Aizpurua , N. Szlarb , I. Moragues , B. Ramos
Human Reproduction 28
2
2013
Universal Minimax Discrete Denoising Under Channel Uncertainty
G.M. Gemelos , S. Sigurjonsson , T. Weissman
IEEE Transactions on Information Theory 52 ( 8) 3476 -3497
17
2006
Algorithms for discrete denoising under channel uncertainty
G.M. Gemelos , S. Sigurjonsson , T. Weissman
IEEE Transactions on Signal Processing 54 ( 6) 2263 -2276
16
2006
Universal minimax binary image denoising under channel uncertainty
G. Gemelos , S. Sigurjonsson , T. Weissman
international conference on image processing 2 997 -1000
8
2004
Right number of chromosomes, wrong parental source: the incidence of single uniparental disomy (UPD) in miscarriage and implications for causing loss
M.K. Maisenbacher , K. Merrion , M.J. Young , S. Sigurjonsson
Fertility and Sterility 108 ( 3) e291
2017
Products of conception (POC) testing - counseling and medical management considerations for the under 35 crowd
K. Merrion , M.K. Maisenbacher , M.J. Young , S. Sigurjonsson
Fertility and Sterility 108 ( 3) e291
2017
Detection of ubiquitous and heterogeneous mutations in cell-free DNA from patients with early-stage non-small-cell lung cancer
M. Jamal-Hanjani , G.A. Wilson , S. Horswell , R. Mitter
Annals of Oncology 27 ( 5) 862 -867
107
2016
Multiple user writing on dirty paper
Young-Han Kim , A. Sutivong , S. Sigurjonsson
international symposium on information theory 534 -534
124
2004
On multiple user channels with state information at the transmitters
S. Sigurjonsson , Young-Han Kim
international symposium on information theory 72 -76
70
2005
Targeted sequencing of SNPs results in highly accurate non-invasive detection of fetal aneuploidy of chromosomes 13, 18, 21, X, and Y: a validation study
B Levy , M Banjevic , M Hill , B Zimmermann
Human Reproduction 28 26 -27
1
2013
Single Nucleotide Polymorphism (SNP)-based Products of Conception (POC) chromosome analysis identifies molar pregnancy and terminal imbalances to guide medical management
MK Maisenbacher , K Merrion , D Clark , L Campbell
EUROPEAN JOURNAL OF HUMAN GENETICS 26 161 -161
2018