Michael D. Bonifacio
Level 3/321 Kent Street
Sydney, NSW 2000, Australia
Sydney, NSW 2000, Australia
Last Updated: 09/26/2026
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Found 8 publications
Concordance between genome-wide cfDNA screening and diagnostic test results for large copy-number variants: a multi-site study from the Global Expanded NIPT Consortium.
Journal: Frontiers in genetics
Published: November 11, 2025
Chromosomal, gestational, and neonatal outcomes of embryos classified as a mosaic by preimplantation genetic testing for aneuploidy.
Journal: Fertility and sterility
Published: January 01, 2023
Comparison of noninvasive prenatal screening with combined first-trimester screening as a frontline screening approach for common trisomies in a public hospital in Australia.
Journal: The Australian & New Zealand journal of obstetrics & gynaecology
Published: December 28, 2021
Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome.
Journal: European journal of human genetics : EJHG
Published: February 10, 2018
Rare autosomal trisomies: Important and not so rare.
Journal: Prenatal diagnosis
Published: January 17, 2018
Assessment of the Access AMH assay as an automated, high-performance replacement for the AMH Generation II manual ELISA.
Journal: Reproductive biology and endocrinology : RB&E
Published: December 28, 2015
The original Beckman Coulter Generation II assay significantly underestimates AMH levels compared with the revised protocol.
Journal: Journal of assisted reproduction and genetics
Published: August 06, 2015
Comment on "MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21".
Journal: Prenatal diagnosis
Published: April 05, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026