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Reproductive Biomedicine Online|September 19, 2015
Karyomapping identifies second polar body DNA persisting to the blastocyst stage: implications for embryo biopsyChristian S Ottolini, Shaun Rogers, Karen Sage, et al.
Biochemical Society Transactions|August 17, 2016
Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy childrenAlan Diot, Eszter Dombi, Tiffany Lodge, et al.
Reproductive Biomedicine Online|July 25, 2015
Live births following Karyomapping of human blastocysts: experience from clinical application of the methodMichalis Konstantinidis, Renata Prates, N-Neka Goodall, et al.
Reproductive Biomedicine Online|March 10, 2020
Aneuploidy and recombination in the human preimplantation embryo. Copy number variation analysis and genome-wide polymorphism genotypingMichalis Konstantinidis, Krithika Ravichandran, Zeynep Gunes, et al.
Reproductive Biomedicine Online|August 27, 2014
Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disordersSenthilkumar A Natesan, Alan H Handyside, Alan R Thornhill, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2021
Frequent loss of heterozygosity in CRISPR-Cas9-edited early human embryosGregorio Alanis-Lobato, Jasmin Zohren, Afshan McCarthy, et al.
Elife|April 30, 2020
Maternal spindle transfer overcomes embryo developmental arrest caused by ooplasmic defects in miceNuno Costa-Borges, Katharina Spath, Irene Miguel-Escalada, et al.
Prenatal Diagnosis|July 13, 2002
Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disordersJoyce C Harper, Dagan Wells, Wirawit Piyamongkol, et al.
Nature Communications|May 27, 2020
The BCL-2 pathway preserves mammalian genome integrity by eliminating recombination-defective oocytesElias ElInati, Agata P Zielinska, Afshan McCarthy, et al.
Human Reproduction (Oxford, England)|November 19, 2011
A maternally inherited autosomal point mutation in human phospholipase C zeta (PLCζ) leads to male infertilityJunaid Kashir, Michalis Konstantinidis, Celine Jones, et al.
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