Literature DB >> 23158400

Recent advances in the prenatal interrogation of the human fetal genome.

Lisa Hui1, Diana W Bianchi.   

Abstract

The amount of genetic and genomic information obtainable from the human fetus during pregnancy is accelerating at an unprecedented rate. Two themes have dominated recent technological advances in prenatal diagnosis: interrogation of the fetal genome in increasingly high resolution and the development of non-invasive methods of fetal testing using cell-free DNA in maternal plasma. These two areas of advancement have now converged with several recent reports of non-invasive assessment of the entire fetal genome from maternal blood. However, technological progress is outpacing the ability of the healthcare providers and patients to incorporate these new tests into existing clinical care, and further complicates many of the economic and ethical dilemmas in prenatal diagnosis. This review summarizes recent work in this field and discusses the integration of these new technologies into the clinic and society.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23158400      PMCID: PMC4378900          DOI: 10.1016/j.tig.2012.10.013

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  60 in total

1.  First and second trimester antenatal screening for Down's syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS).

Authors:  N J Wald; C Rodeck; A K Hackshaw; J Walters; L Chitty; A M Mackinson
Journal:  Health Technol Assess       Date:  2003       Impact factor: 4.014

2.  Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection.

Authors:  Jessica M E van den Oever; Sahila Balkassmi; E Joanne Verweij; Maarten van Iterson; Phebe N Adama van Scheltema; Dick Oepkes; Jan M M van Lith; Mariëtte J V Hoffer; Johan T den Dunnen; Egbert Bakker; Elles M J Boon
Journal:  Clin Chem       Date:  2012-01-25       Impact factor: 8.327

3.  Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

Authors:  Andrew B Sparks; Craig A Struble; Eric T Wang; Ken Song; Arnold Oliphant
Journal:  Am J Obstet Gynecol       Date:  2012-01-26       Impact factor: 8.661

4.  Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18.

Authors:  Ghalia Ashoor; Argyro Syngelaki; Marion Wagner; Cahit Birdir; Kypros H Nicolaides
Journal:  Am J Obstet Gynecol       Date:  2012-01-24       Impact factor: 8.661

Review 5.  Genomic microarrays: a technology overview.

Authors:  Paul D Brady; Joris R Vermeesch
Journal:  Prenat Diagn       Date:  2012-04       Impact factor: 3.050

6.  Intrauterine diagnosis and management of genetic defects.

Authors:  C B Jacobson; R H Barter
Journal:  Am J Obstet Gynecol       Date:  1967-11-15       Impact factor: 8.661

7.  Chromosome analysis of human amniotic-fluid cells.

Authors:  M W Steele; W R Breg
Journal:  Lancet       Date:  1966-02-19       Impact factor: 79.321

8.  Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service.

Authors:  K M Finning; P G Martin; P W Soothill; N D Avent
Journal:  Transfusion       Date:  2002-08       Impact factor: 3.157

9.  Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.

Authors:  Ronald J Wapner; Deborah A Driscoll; Joe Leigh Simpson
Journal:  Prenat Diagn       Date:  2012-04       Impact factor: 3.050

10.  Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study.

Authors:  D W Bianchi; J L Simpson; L G Jackson; S Elias; W Holzgreve; M I Evans; K A Dukes; L M Sullivan; K W Klinger; F Z Bischoff; S Hahn; K L Johnson; D Lewis; R J Wapner; F de la Cruz
Journal:  Prenat Diagn       Date:  2002-07       Impact factor: 3.050

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  10 in total

1.  Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testing.

Authors:  Xiang-Yin Liu; Hong-Guo Zhang; Rui-Xue Wang; Shuang Chen; Xiao-Wei Yu; Rui-Zhi Liu
Journal:  J Assist Reprod Genet       Date:  2014-02-05       Impact factor: 3.412

Review 2.  Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.

Authors:  Ignatia B van den Veyver; Christine M Eng
Journal:  Cold Spring Harb Perspect Med       Date:  2015-08-07       Impact factor: 6.915

3.  Cellular fetal microchimerism in preeclampsia.

Authors:  Hilary S Gammill; Tessa M Aydelotte; Katherine A Guthrie; Evangelyn C Nkwopara; J Lee Nelson
Journal:  Hypertension       Date:  2013-10-07       Impact factor: 10.190

4.  Transcriptomic Analysis of Cell-free Fetal RNA in the Amniotic Fluid of Vervet Monkeys (Chlorocebus sabaeus).

Authors:  Anna J Jasinska; Dalar Rostamian; Ashley T Davis; Kylie Kavanagh
Journal:  Comp Med       Date:  2020-01-22       Impact factor: 0.982

Review 5.  Tay-Sachs disease: current perspectives from Australia.

Authors:  Raelia M Lew; Leslie Burnett; Anné L Proos; Martin B Delatycki
Journal:  Appl Clin Genet       Date:  2015-01-21

6.  Pre-analytical conditions in non-invasive prenatal testing of cell-free fetal RHD.

Authors:  Frederik Banch Clausen; Tanja Roien Jakobsen; Klaus Rieneck; Grethe Risum Krog; Leif Kofoed Nielsen; Ann Tabor; Morten Hanefeld Dziegiel
Journal:  PLoS One       Date:  2013-10-18       Impact factor: 3.240

Review 7.  Recent advances in prenatal genetic screening and testing.

Authors:  Ignatia B Van den Veyver
Journal:  F1000Res       Date:  2016-10-28

8.  Maternal obesity alters methylation level of cytosine in CpG island for epigenetic inheritance in fetal umbilical cord blood.

Authors:  Zhuoyao Ma; Yingjin Wang; Yanmei Quan; Zhijie Wang; Yue Liu; Zhide Ding
Journal:  Hum Genomics       Date:  2022-08-31       Impact factor: 6.481

Review 9.  Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis.

Authors:  Lauren Westerfield; Sandra Darilek; Ignatia B van den Veyver
Journal:  J Clin Med       Date:  2014-09-12       Impact factor: 4.241

Review 10.  Genomic sequencing in clinical practice: applications, challenges, and opportunities.

Authors:  Joel B Krier; Sarah S Kalia; Robert C Green
Journal:  Dialogues Clin Neurosci       Date:  2016-09       Impact factor: 5.986

  10 in total

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