PGD for a complex chromosomal rearrangement by array comparative genomic hybridization.

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Human Reproduction

• Publication date

  2011-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1093/humrep/der004PMID 21292638
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Comprehensive embryo analysis of advanced maternal age-related aneuploidies and mosaicism by short comparative genomic hybridization.

  2011cited by this paper
• Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays.

  2010cited by this paper
• Proliferation of aneuploid human cells is limited by a p53-dependent mechanism

  2010cited by this paper
• The use of endoscopy in fetal medicine

  2010cited by this paper
• Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocol

  2010cited by this paper
• What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate

  2009cited by this paper
• Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletions.

  2009cited by this paper
• Identification of small gains and losses in single cells after whole genome amplification on tiling oligo arrays

  2009cited by this paper
• Chromosome instability is common in human cleavage-stage embryos

  2009cited by this paper
• Preimplantation Genetic Diagnosis: Preimplantation genetic testing: normative reflections

  2009cited by this paper
• Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes

  2009cited by this paper
• Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening.

  2008cited by this paper
• Preimplantation genetic diagnosis for complex chromosome rearrangements

  2008cited by this paper
• Detection of Chromosomal Structural Alterations in Single Cells by SNP Arrays: A Systematic Survey of Amplification Bias and Optimized Workflow

  2007cited by this paper
• Checkpoint-apoptosis uncoupling in human and mouse embryonic stem cells: a source of karyotpic instability.

  2007cited by this paper
• Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.

  2007cited by this paper
• Single-cell chromosomal imbalances detection by array CGH

  2006cited by this paper
• High resolution array-CGH analysis of single cells

  2006cited by this paper
• The frequency of chromosomal abnormalities in patients with reproductive failure.

  2006cited by this paper
• Whole-genome multiple displacement amplification from single cells

  2006cited by this paper
• Preimplantation genetic diagnosis significantly improves the pregnancy outcome of translocation carriers with a history of recurrent miscarriage and unsuccessful pregnancies.

  2006cited by this paper
• Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy.

  2005cited by this paper
• Structural Chromosome Rearrangements

  2005influential reference
• Preimplantation genetic diagnosis and chromosome analysis of blastomeres using comparative genomic hybridization.

  2005cited by this paper
• Hormone therapy: new insights on the management of postmenopausal and premenopausal women

  2005cited by this paper
• Preimplantation genetic diagnosis for an insertional translocation carrier.

  2004cited by this paper
• Preimplantation genetic diagnosis.

  2003cited by this paper
• Preimplantation aneuploidy screening using comparative genomic hybridization or fluorescence in situ hybridization of embryos from patients with recurrent implantation failure.

  2003cited by this paper
• Cytogenetic analysis of human blastocysts

  2002cited by this paper
• Chromosome abnormalities identified by comparative genomic hybridization in embryos from women with repeated implantation failure.

  2002cited by this paper
• High rate of mixoploidy among human blastocysts cultured in vitro.

  2002cited by this paper
• Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

  2000cited by this paper
• Outcome of preimplantation genetic diagnosis of translocations.

  2000cited by this paper
• Improvements of preimplantation diagnosis of aneuploidy by using microwave hybridization, cell recycling and monocolour labelling of probes.

  2000cited by this paper
• Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization.

  2000cited by this paper
• Patient-Specific Probes for Preimplantation Genetic Diagnosis of Structural and Numerical Aberrations in Interphase Cells

  1999cited by this paper
• Management of transient ovarian failure: Pregnancy after in vitro fertilization and intracytoplasmic sperm injection—A case report

  1998cited by this paper
• Chromosomal Mosaicism in Cleavage-Stage Human Embryos and the Accuracy of Single-Cell Genetic Analysis

  1998cited by this paper
• Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis

  1998cited by this paper
• Structural chromosome rearrangements in couples with recurrent fetal wastage.

  1998cited by this paper
• Preimplantation genetic diagnosis of chromosome balance in embryos from a patient with a balanced reciprocal translocation.

  1998cited by this paper
• The origin of genetic defects in the human and their detection in the preimplantation embryo.

  1995cited by this paper
• Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer.

  1995cited by this paper
• Chromosome mosaicism in human embryos.

  1994cited by this paper

• Live birth rates with and without preimplantation genetic testing: a single-center retrospective study

  2025cites this paper
• Clinical outcomes of complex chromosomal rearrangement carriers and couples both harbouring chromosomal rearrangements who undergo preimplantation genetic testing.

  2025cites this paper
• Preimplantation genetic testing for complex chromosomal rearrangements: clinical outcomes and potential risk factors

  2024cites this paper
• Case report: Optical genome mapping revealed double rearrangements in a male undergoing preimplantation genetic testing

  2023cites this paper
• Preimplantation Genetic Testing for Genetic Diseases: Limits and Review of Current Literature

  2023cites this paper
• An Incidental Detection of a Cryptic Complex Chromosome Rearrangement Found During NGS Based PGT-SR: A Case Report

  2022cites this paper
• Aneuploid abortion correlates positively with MAD1 overexpression and miR-125b down-regulation

  2021cites this paper
• D-karyo—A New Prenatal Rapid Screening Test Detecting Submicroscopic CNVs and Mosaicism

  2021cites this paper
• Discrepancy of Karyotype and CMA /NGS in PGD Patient with Cryptical Complex Chromosomal Rearrangement

  2021cites this paper
• Aneuploid Abortion Positively Correlate With MAD1 Overexpression and mir125b Depression

  2020cites this paper
• Pathologies des hélicases et vieillissement précoce : modèle d’étude par dérivation de cellules souches pluripotentes induites

  2019cites this paper
• The evolving role of genetic tests in reproductive medicine

  2019cites this paper
• The influence of balanced complex chromosomal rearrangements on preimplantation embryonic development potential and molecular karyotype

  2019cites this paper
• Preimplantation genetic testing for balanced complex chromosomal rearrangement carriers by comprehensive chromosome screening

  2019cites this paper
• Preimplantation genetic testing for complex chromosomal rearrangement carriers by next-generation sequencing.

  2018cites this paper
• Clinical outcomes in carriers of complex chromosomal rearrangements: a retrospective analysis of comprehensive chromosome screening results in seven cases.

  2018cites this paper
• Detection of segmental aneuploidy and mosaicism in the human preimplantation embryo: technical considerations and limitations.

  2017cites this paper
• The Non-Human Primate Model for Early Human Development

  2017cites this paper
• Growth, progression and chromosome instability of Neuroblastoma: a new scenario of tumorigenesis?

  2017cites this paper
• Simple and Easy to Perform Preimplantation Genetic Diagnosis for β-thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction

  2017cites this paper
• Novel technologies emerging for preimplantation genetic diagnosis and preimplantation genetic testing for aneuploidy

  2017influential citation
• Pre-implantation Genetic Testing

  2017cites this paper
• Preimplantation genetic diagnosis for chromosomal rearrangements with the use of array comparative genomic hybridization at the blastocyst stage.

  2017cites this paper
• Advances in Preimplantation Genetic Testing for Monogenic Disease and Aneuploidy.

  2017cites this paper
• Cytoskeletal Functions, Defects, and Dysfunctions Affecting Human Fertilization and Embryo Development

  2016cites this paper
• Embryo signals for successful implantation

  2016cites this paper
• Prenatal and preimplantation genetic diagnosis

  2016cites this paper
• SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts

  2016cites this paper
• Prenatal and pre-implantation genetic diagnosis

  2016cites this paper
• Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification.

  2015cites this paper
• Chromosome constitution of human embryos generated after in vitro maturation including 3-isobutyl-1-methylxanthine in the oocyte collection medium.

  2015cites this paper
• Development of a reliable single-cell aCGH suitable for clinical samples

  2015cites this paper
• Is preimplantation genetic diagnosis the ideal embryo selection method in aneuploidy

  2014cites this paper
• Is preimplantation genetic diagnosis the ideal embryo selection method in aneuploidy screening?

  2014cites this paper
• Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review.

  2014cites this paper
• Detection of monogenic disorders and chromosome aberrations by preimplantation genetic diagnosis.

  2014cites this paper
• Walking the Edge with Controversial Use of Preimplantation Genetic Diagnosis (PGD): Opinions and Attitudes of Genetic Counselors

  2014cites this paper
• Un paradigme pour l'étude de l'instabilité

  2014cites this paper
• LOODUS- JA TEHNOLOOGIATEADUSKOND MOLEKULAAR- JA RAKUBIOLOOGIA INSTITUUT BIOTEHNOLOOGIA ÕPPETOOL

  2014cites this paper
• [Complex chromosomal rearrangements: a paradigm for the study of chromosomal instability].

  2014cites this paper
• Preimplantation genetic diagnosis guided by single-cell genomics

  2013cites this paper
• Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains

  2013cites this paper
• Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD

  2013cites this paper
• [Cytogenetic analysis of 105 new human abnormal karyotypes].

  2013influential citation
• Single-cell paired-end genome sequencing reveals structural variation per cell cycle

  2013cites this paper
• A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization.

  2013cites this paper
• Improving embryo quality in assisted reproduction

  2013cites this paper
• Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.

  2013cites this paper
• In Vitro Fertilization - Innovative Clinical and Laboratory Aspects

  2012cites this paper
• Preimplantation testing: Transition from genetic to genomic diagnosis

  2012cites this paper
• Genome-Wide Analysis of Human Preimplantation Aneuploidy

  2012cites this paper
• SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

  2012cites this paper
• Human pre-implantation embryo development

  2012cites this paper
• Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development

  2012cites this paper
• Viability Assessment for Artificial Gametes: The Need for Biomarkers of Functional Competency1

  2012cites this paper
• Preimplantation Genetic Testing: Current Status and Future Prospects

  2012cites this paper
• New Array Approaches to Explore Single Cells Genomes

  2011cites this paper
• Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies

  2011cites this paper
• Oligonucleotide microarrays in constitutional genetic diagnosis

  2011cites this paper
• Human preimplantation embryo development

  year unknowncites this paper