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Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajmg.a.30048openalex-snapshot
Early hearing detection and intervention programs: Opportunities for genetic services
inferredcites →https://doi.org/10.1007/s00405-011-1910-6openalex-snapshot
Genetics of hearing loss: where are we standing now?
inferredcites →https://doi.org/10.1007/s10815-009-9335-5openalex-snapshot
Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy
inferredcites →https://doi.org/10.1007/s10815-014-0405-yopenalex-snapshot
Karyomapping—a comprehensive means of simultaneous monogenic and cytogenetic PGD: comparison with standard approaches in real time for Marfan syndrome
inferredcites →https://doi.org/10.1007/s10815-016-0760-yopenalex-snapshot
The clinical application of preimplantation genetic diagnosis for the patient affected by congenital contractural arachnodactyly and spinal and bulbar muscular atrophy
inferredcites →https://doi.org/10.1007/s11427-015-4936-yopenalex-snapshot
Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment
inferredcites →https://doi.org/10.1007/s12070-014-0711-9openalex-snapshot
Preimplantation Genetic Diagnosis: Its Role in Prevention of Deafness
inferredcites →https://doi.org/10.1007/s12522-015-0224-6openalex-snapshot
Preimplantation genetic diagnosis: an update on current technologies and ethical considerations
inferredcites →https://doi.org/10.1016/j.fertnstert.2012.12.018openalex-snapshot
Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease
inferredcites →https://doi.org/10.1016/j.ijporl.2011.01.016openalex-snapshot
Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns
inferredcites →https://doi.org/10.1016/j.ijporl.2014.08.009openalex-snapshot
A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome
inferredcites →https://doi.org/10.1016/j.jgg.2016.03.011openalex-snapshot
Clinical applications of MARSALA for preimplantation genetic diagnosis of spinal muscular atrophy
inferredcites →https://doi.org/10.1016/j.rbmo.2010.09.016openalex-snapshot
First successful application of preimplantation genetic diagnosis and haplotyping for congenital hyperinsulinism
inferredcites →https://doi.org/10.1016/j.rbmo.2014.07.007openalex-snapshot
Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders
inferredcites →https://doi.org/10.1016/j.rbmo.2015.05.018openalex-snapshot
Live births following Karyomapping of human blastocysts: experience from clinical application of the method
inferredcites →https://doi.org/10.1016/j.rbmo.2015.08.017openalex-snapshot
Karyomapping allows preimplantation genetic diagnosis of a de-novo deletion undetectable using conventional PGD technology
inferredcites →https://doi.org/10.1016/j.tig.2007.12.007openalex-snapshot
The impact of next-generation sequencing technology on genetics
inferredcites →https://doi.org/10.1016/s0015-0282(00)00518-5openalex-snapshot
Blastocyst score affects implantation and pregnancy outcome: towards a single blastocyst transfer
inferredcites →https://doi.org/10.1016/s0030-6657(11)70738-7openalex-snapshot
Diagnostyka preimplantacyjna w kierunku niedosłuchu wrodzonego z mutacją 35delG w genie GJB2 – doniesienie wstępne
inferredcites →https://doi.org/10.1016/s0140-6736(05)71047-3openalex-snapshot
Sensorineural hearing loss in children
inferredcites →https://doi.org/10.1017/s0022215106003471openalex-snapshot
Post-operative complications of cochlear implantation in adults and children: five years' experience in Maastricht
inferredcites →https://doi.org/10.1038/ejhg.2013.50openalex-snapshot
PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers
inferredcites →https://doi.org/10.1038/gim.2014.45openalex-snapshot
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro
inferredcites →https://doi.org/10.1055/s-0035-1558402openalex-snapshot
Healthy Baby Born to a Robertsonian Translocation Carrier following Next-Generation Sequencing-Based Preimplantation Genetic Diagnosis: A Case Report
inferredcites →https://doi.org/10.1093/humrep/dev316openalex-snapshot
Conventional ovarian stimulation and single embryo transfer for IVF/ICSI. How many oocytes do we need to maximize cumulative live birth rates after utilization of all fresh and frozen embryos?
inferredcites →https://doi.org/10.1111/bjd.13858openalex-snapshot
Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa
inferredcites →https://doi.org/10.1111/j.1749-6632.1991.tb19572.xopenalex-snapshot
Genetic Epidemiology of Hearing Impairment
inferredcites →https://doi.org/10.1136/jmg.2009.069971openalex-snapshot
Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes
inferredcites →https://doi.org/10.1146/annurev-genom-091212-153408openalex-snapshot
The Genetics of Microdeletion and Microduplication Syndromes: An Update
inferredcites →https://doi.org/10.1155/2011/210838openalex-snapshot
The Cost of Cochlear Implantation: A Review of Methodological Considerations
inferredcites →https://doi.org/10.1159/000284349openalex-snapshot
Preimplantation Genetic Diagnosis (Embryo Screening) for Enlarged Vestibular Aqueduct due to SLC26A4 Mutation
inferredcites →https://doi.org/10.1179/1467010013z.00000000080openalex-snapshot
Enter the dragon – China's journey to the hearing world
inferredcites →https://doi.org/10.1186/1471-2350-14-57openalex-snapshot
The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing age
inferredcites →https://doi.org/10.1196/annals.1345.028openalex-snapshot
Preimplantation Genetics: Improving Access to Stem Cell Therapy
inferredcites →https://doi.org/10.1515/jbcpp-2013-0063openalex-snapshot
Advances in genetic diagnostics for hereditary hearing loss
inferredcites →https://doi.org/10.5603/gp.2016.0037openalex-snapshot
Current methods for preimplantation genetic diagnosis
inferredcites →https://doi.org/10.5858/arpa.2015-0507-raopenalex-snapshot
Next-Generation Sequencing Informatics: Challenges and Strategies for Implementation in a Clinical Environment
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4144503openalex-extracted
Mitochondrial DNA Quantification Correlates with the Developmental Potential of Human Euploid Blastocysts but not with that of Mosaic Blastocysts
inferred← citeshttps://doi.org/10.1002/inm3.70041openalex-snapshot
Pregnancy Outcomes and Postnatal Health From Transferred Mosaic Embryos Following Preimplantation Genetic Testing for Aneuploidy
inferred← citeshttps://doi.org/10.1007/s10815-023-02753-8openalex-snapshot
Preimplantation genetic testing for hereditary hearing loss in Chinese population
inferred← citeshttps://doi.org/10.1007/s10815-025-03504-7openalex-snapshot
Clinical application of preimplantation genetic testing based on low-coverage next-generation sequencing with linkage analyses in hereditary hearing loss families
inferred← citeshttps://doi.org/10.1007/s10815-025-03630-2openalex-snapshot
Impact of repeated vitrification and biopsy on the developmental potential of blastocysts and clinical outcomes: A retrospective propensity-score-matched cohort study
inferred← citeshttps://doi.org/10.1007/s10815-025-03676-2openalex-snapshot
Assessing the efficacy of targeted enrichment protocol in PGT-M applications: a comprehensive analysis
inferred← citeshttps://doi.org/10.1007/s12041-021-01267-5openalex-snapshot
Application of single-sperm sequencing in a male with Marfan syndrome: a case report and a literature review
inferred← citeshttps://doi.org/10.1080/19396368.2019.1590479openalex-snapshot
Clinical application of NGS-based SNP haplotyping for the preimplantation genetic diagnosis of primary open angle glaucoma
inferred← citeshttps://doi.org/10.1080/19396368.2020.1832158openalex-snapshot
Successful four-factor preimplantation genetic testing: α- and β-thalassemia, human leukocyte antigen typing, and aneuploidy screening
inferred← citeshttps://doi.org/10.1097/jbr.0000000000000106openalex-snapshot
Preimplantation genetic diagnosis of hereditary hearing loss: a narrative review
inferred← citeshttps://doi.org/10.1186/s12884-023-05760-wopenalex-snapshot
Mitochondrial DNA quantification correlates with the developmental potential of human euploid blastocysts but not with that of mosaic blastocysts
inferred← citeshttps://doi.org/10.1186/s12920-024-01803-zopenalex-snapshot
Development of preimplantation genetic testing for monogenic reference materials using next-generation sequencing
inferred← citeshttps://doi.org/10.18314/cogo.v3i1.2068openalex-snapshot
Genetic, Prenatal, and Preimplantation Genetic Diagnosis of Glutaric Aciduria Type I
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2571158/v1openalex-snapshot
Mitochondrial DNA Quantification Correlates with the Developmental Potential of Human Euploid Blastocysts but not with that of Mosaic Blastocysts
inferred← citeshttps://doi.org/10.2174/1389450122666210806125919openalex-snapshot
Exploring AT2R and its Polymorphism in Different Diseases: An Approach to Develop AT2R as a Drug Target beyond Hypertension
inferred← citeshttps://doi.org/10.21926/obm.genet.1903084openalex-snapshot
Preimplantation Genetic Testing for HLA-matching: An Overview of Clinical Application and Utility
inferred← citeshttps://doi.org/10.3390/diagnostics11122395openalex-snapshot
Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment
inferred← citeshttps://doi.org/10.6084/m9.figshare.26597516openalex-snapshot
Additional file 1 of Mitochondrial DNA quantification correlates with the developmental potential of human euploid blastocysts but not with that of mosaic blastocysts
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