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Preimplantation genetic diagnosis: State of the ART 2011

Human genetics, 2012-02, Vol.131 (2), p.175-186

2012

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MicroRNA expression and its association with DNA repair in preimplantation embryos

Journal of Reproduction and Development, 2016, Vol.62(3), pp.225-234

2016

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Detection of aneuploidy by array comparative genomic hybridization using cell lines to mimic a mosaic trophectoderm biopsy

Fertility and sterility, 2012-04, Vol.97 (4), p.943-947

2012

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Next Generation Sequencing Detects Premeiotic Errors in Human Oocytes

International journal of molecular sciences, 2022-01, Vol.23 (2), p.665

2022

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Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays

Human reproduction (Oxford), 2009-10, Vol.24 (10), p.2649-2655

2009

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Differentially expressed microRNAs in aneuploid preimplantation blastocysts: a systematic review

Frontiers in reproductive health, 2024-03, Vol.6, p.1370341-1370341

2024

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How common is germinal mosaicism that leads to premeiotic aneuploidy in the female?

Journal of assisted reproduction and genetics, 2019-12, Vol.36 (12), p.2403-2418

2019

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Investigation of gene expression profiles before and after embryonic genome activation and assessment of functional pathways at the human metaphase II oocyte and blastocyst stage

Fertility and sterility, 2013-03, Vol.99 (3), p.803-814.e23

2013

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The impact of mosaicism in preimplantation genetic diagnosis (PGD): approaches to PGD for dominant disorders in couples without family history

Prenatal diagnosis, 2016-09, Vol.36 (9), p.864-870

2016

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Differential expression of parental alleles of BRCA1 in human preimplantation embryos

European journal of human genetics : EJHG, 2016-01, Vol.25 (1), p.37-42

2016

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The status of preimplantation genetic testing in the UK and USA

Human reproduction (Oxford), 2020-04, Vol.35 (4), p.986-998

2020

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Live birth rate is associated with oocyte yield and number of biopsied and suitable blastocysts to transfer in preimplantation genetic testing (PGT) cycles for monogenic disorders and chromosomal structural rearrangements

European journal of obstetrics & gynecology and reproductive biology: X, 2019-10, Vol.4, p.100055-100055, Article 100055

2019

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Functional assessment for elimination of mismatches in nuclear and whole cell extracts obtained from mouse and human blastocysts

Systems biology in reproductive medicine, 2016-11, Vol.62 (6), p.415-422

2016

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Telomere length in human blastocysts

Reproductive biomedicine online, 2014-05, Vol.28 (5), p.624-637

2014

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Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis

Fertility and sterility, 2010-10, Vol.94 (5), p.1674-1679

2010

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Preimplantation Genetic Diagnosis: State of the ART 2011

Obstetrical & gynecological survey, 2012-06, Vol.67 (6), p.347-348

2012

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Preimplantation genetic diagnosis: recent triumphs and remaining challenges

Expert review of molecular diagnostics, 2012-07, Vol.12 (6), p.585-592

2012

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Preimplantation genetic diagnosis for hereditary cancers

Advances in experimental medicine and biology, 2012, Vol.732, p.103

2012

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Investigation of the relationship between embryo ploidy, nuclear mitochondrial mismatch and embryo morphology

Reproductive biomedicine online, 2018-03, Vol.36, p.e25-e26

2018

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P-22 - Investigation of the relationship between embryo ploidy, nuclear mitochondrial mismatch and embryo morphology

Reproductive biomedicine online, 2018-03, Vol.36, p.e25-e26

2018

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Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK

Neuromuscular disorders : NMD, 2008-02, Vol.18 (2), p.131-136

2008

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The origin and significance of additional aneuploidy events in couples undergoing preimplantation genetic diagnosis for translocations by array comparative genomic hybridization

Reproductive biomedicine online, 2016-02, Vol.32 (2), p.178-189

2016

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Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants

Reproductive biomedicine online, 2018-03, Vol.36, p.e33

2018

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P-41 - Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants

Reproductive biomedicine online, 2018-03, Vol.36, p.e33-e33

2018

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DNA repair in mammalian embryos

Mutation research, 2007-01, Vol.635 (1), p.53-77

2007

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Preimplantation genetic diagnosis: State of the ART 2011

MicroRNA expression and its association with DNA repair in preimplantation embryos

Detection of aneuploidy by array comparative genomic hybridization using cell lines to mimic a mosaic trophectoderm biopsy

Next Generation Sequencing Detects Premeiotic Errors in Human Oocytes

Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays

Differentially expressed microRNAs in aneuploid preimplantation blastocysts: a systematic review

How common is germinal mosaicism that leads to premeiotic aneuploidy in the female?

Investigation of gene expression profiles before and after embryonic genome activation and assessment of functional pathways at the human metaphase II oocyte and blastocyst stage

The impact of mosaicism in preimplantation genetic diagnosis (PGD): approaches to PGD for dominant disorders in couples without family history

Differential expression of parental alleles of BRCA1 in human preimplantation embryos

The status of preimplantation genetic testing in the UK and USA

Live birth rate is associated with oocyte yield and number of biopsied and suitable blastocysts to transfer in preimplantation genetic testing (PGT) cycles for monogenic disorders and chromosomal structural rearrangements

Functional assessment for elimination of mismatches in nuclear and whole cell extracts obtained from mouse and human blastocysts

Telomere length in human blastocysts

Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis

Preimplantation Genetic Diagnosis: State of the ART 2011

Preimplantation genetic diagnosis: recent triumphs and remaining challenges

Preimplantation genetic diagnosis for hereditary cancers

Investigation of the relationship between embryo ploidy, nuclear mitochondrial mismatch and embryo morphology

P-22 - Investigation of the relationship between embryo ploidy, nuclear mitochondrial mismatch and embryo morphology

Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK

The origin and significance of additional aneuploidy events in couples undergoing preimplantation genetic diagnosis for translocations by array comparative genomic hybridization

Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants

P-41 - Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants

DNA repair in mammalian embryos

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