Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses
Authors
Keywords
-
Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 112, Issue 52, Pages 15964-15969
Publisher
Proceedings of the National Academy of Sciences
Online
2015-12-29
DOI
10.1073/pnas.1523297113
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Single-Cell Whole-Genome Amplification and Sequencing: Methodology and Applications
- (2015) Lei Huang et al. Annual Review of Genomics and Human Genetics
- First systematic experience of preimplantation genetic diagnosis for single-gene disorders, and/or preimplantation human leukocyte antigen typing, combined with 24-chromosome aneuploidy testing
- (2015) Svetlana Rechitsky et al. FERTILITY AND STERILITY
- Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
- (2015) Brock A. Peters et al. GENOME RESEARCH
- Karyomapping—a comprehensive means of simultaneous monogenic and cytogenetic PGD: comparison with standard approaches in real time for Marfan syndrome
- (2015) Alan R. Thornhill et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Live births following Karyomapping of human blastocysts: experience from clinical application of the method
- (2015) Michalis Konstantinidis et al. REPRODUCTIVE BIOMEDICINE ONLINE
- Live births following karyomapping – a “key” milestone in the development of preimplantation genetic diagnosis
- (2015) Alan H. Handyside REPRODUCTIVE BIOMEDICINE ONLINE
- Validation of Copy Number Variation Sequencing for Detecting Chromosome Imbalances in Human Preimplantation Embryos1
- (2014) Li Wang et al. BIOLOGY OF REPRODUCTION
- Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro
- (2014) Senthilkumar A. Natesan et al. GENETICS IN MEDICINE
- Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates
- (2014) Kyle J. Tobler et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
- (2014) Dagan Wells et al. JOURNAL OF MEDICAL GENETICS
- Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders
- (2014) Senthilkumar A. Natesan et al. REPRODUCTIVE BIOMEDICINE ONLINE
- Advances in preimplantation genetic diagnosis/screening
- (2014) LiYing Yan et al. Science China-Life Sciences
- Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts1
- (2013) XuYang Yin et al. BIOLOGY OF REPRODUCTION
- Genome Analyses of Single Human Oocytes
- (2013) Yu Hou et al. CELL
- Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study
- (2013) Jos Dreesen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease
- (2013) Nathan R. Treff et al. FERTILITY AND STERILITY
- Use of array comparative genomic hybridization (array-CGH) for embryo assessment: clinical results
- (2013) Carmen Rubio et al. FERTILITY AND STERILITY
- Rare-disease genetics in the era of next-generation sequencing: discovery to translation
- (2013) Kym M. Boycott et al. NATURE REVIEWS GENETICS
- Successful PGD for late infantile neuronal ceroid lipofuscinosis achieved by combined chromosome and TPP1 gene analysis
- (2013) Jiandong Shen et al. REPRODUCTIVE BIOMEDICINE ONLINE
- First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening
- (2012) G Daina et al. CLINICAL GENETICS
- Development and validation of an accurate quantitative real-time polymerase chain reaction–based assay for human blastocyst comprehensive chromosomal aneuploidy screening
- (2012) Nathan R. Treff et al. FERTILITY AND STERILITY
- Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell
- (2012) C. Zong et al. SCIENCE
- Probing Meiotic Recombination and Aneuploidy of Single Sperm Cells by Whole-Genome Sequencing
- (2012) S. Lu et al. SCIENCE
- Molecular Genetic Analysis of Single Cells
- (2012) Francesco Fiorentino SEMINARS IN REPRODUCTIVE MEDICINE
- Polar body-based preimplantation genetic diagnosis for Mendelian disorders
- (2011) A. Kuliev et al. MOLECULAR HUMAN REPRODUCTION
- Tumour evolution inferred by single-cell sequencing
- (2011) Nicholas Navin et al. NATURE
- The causes of misdiagnosis and adverse outcomes in PGD
- (2009) L. Wilton et al. HUMAN REPRODUCTION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation