Bunce KD - Search Results

1

High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions.

Chu T, Yeniterzi S, Yatsenko SA, Dunkel M, Shaw PA, Bunce KD, Peters DG. Chu T, et al. Among authors: bunce kd. PLoS One. 2016 Jun 1;11(6):e0153182. doi: 10.1371/journal.pone.0153182. eCollection 2016. PLoS One. 2016. PMID: 27249650 Free PMC article.

2

Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing.

Chu T, Shaw PA, Yeniterzi S, Dunkel M, Rajkovic A, Hogge WA, Bunce KD, Peters DG. Chu T, et al. Among authors: bunce kd. PLoS One. 2017 Mar 17;12(3):e0171882. doi: 10.1371/journal.pone.0171882. eCollection 2017. PLoS One. 2017. PMID: 28306738 Free PMC article.

3

Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease.

Chu T, Bunce K, Hogge WA, Peters DG. Chu T, et al. Bioinformatics. 2009 May 15;25(10):1244-50. doi: 10.1093/bioinformatics/btp156. Epub 2009 Mar 23. Bioinformatics. 2009. PMID: 19307238

4

Statistical considerations for digital approaches to non-invasive fetal genotyping.

Chu T, Bunce K, Hogge WA, Peters DG. Chu T, et al. Bioinformatics. 2010 Nov 15;26(22):2863-6. doi: 10.1093/bioinformatics/btq544. Epub 2010 Sep 23. Bioinformatics. 2010. PMID: 20870643

5

High resolution non-invasive detection of a fetal microdeletion using the GCREM algorithm.

Chu T, Yeniterzi S, Rajkovic A, Hogge WA, Dunkel M, Shaw P, Bunce K, Peters DG. Chu T, et al. Prenat Diagn. 2014 May;34(5):469-77. doi: 10.1002/pd.4331. Epub 2014 Feb 27. Prenat Diagn. 2014. PMID: 24452987 Free PMC article.

6

Correction: High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions.

Chu T, Yeniterzi S, Yatsenko SA, Dunkel M, Shaw PA, Bunce KD, Peters DG. Chu T, et al. Among authors: bunce kd. PLoS One. 2016 Sep 20;11(9):e0163578. doi: 10.1371/journal.pone.0163578. eCollection 2016. PLoS One. 2016. PMID: 27648843 Free PMC article.

7

A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease.

Chu T, Burke B, Bunce K, Surti U, Allen Hogge W, Peters DG. Chu T, et al. Prenat Diagn. 2009 Nov;29(11):1020-30. doi: 10.1002/pd.2335. Prenat Diagn. 2009. PMID: 19650061

8

Structural and regulatory characterization of the placental epigenome at its maternal interface.

Chu T, Handley D, Bunce K, Surti U, Hogge WA, Peters DG. Chu T, et al. PLoS One. 2011 Feb 23;6(2):e14723. doi: 10.1371/journal.pone.0014723. PLoS One. 2011. PMID: 21373191 Free PMC article.

9

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.

Peters D, Chu T, Yatsenko SA, Hendrix N, Hogge WA, Surti U, Bunce K, Dunkel M, Shaw P, Rajkovic A. Peters D, et al. N Engl J Med. 2011 Nov 10;365(19):1847-8. doi: 10.1056/NEJMc1106975. N Engl J Med. 2011. PMID: 22070496 Free PMC article. No abstract available.

10

Discovery of epigenetic biomarkers for the noninvasive diagnosis of fetal disease.

Bunce K, Chu T, Surti U, Hogge WA, Peters DG. Bunce K, et al. Prenat Diagn. 2012 Jun;32(6):542-9. doi: 10.1002/pd.3853. Epub 2012 Apr 11. Prenat Diagn. 2012. PMID: 22495992 Free PMC article.

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