Lista de obras - Lisa Hui - Dominio Público Uruguay

40 years of prenatal diagnosis in 2020

artículo científico publicado en 2020

A comparison of sample collection methods for quantifying cell-free fetal neurodevelopment transcripts in amniotic fluid

artículo científico publicado en 2016

A decade of non‐invasive prenatal screening in Australia: National impact on prenatal screening and diagnostic testing

scientific article published in 2022

A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort

artículo científico publicado en 2020

Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.

artículo científico publicado en 2016

Alobar holoprosencephaly detected in a 9-week embryo

scientific article published on 06 January 2019

Antenatal noninvasive DNA testing: clinical experience and impact

artículo científico

Assessing maternal clotting function with novel global coagulation assays: A prospective pilot study

artículo científico publicado en 2020

Assessing the fetal effects of maternal obesity via transcriptomic analysis of cord blood: a prospective case-control study

artículo científico publicado en 2016

Assessing the sensitivity of placental growth factor and soluble fms-like tyrosine kinase 1 at 36 weeks' gestation to predict small-for-gestational-age infants or late-onset preeclampsia: a prospective nested case-control study

artículo científico publicado en 2018

Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016

artículo científico publicado en 2019

Cell-free DNA testing for 22q11.2 deletion syndrome: appraising the viability, effectiveness and appropriateness of screening

scientific article published on 01 February 2016

Cell-free fetal nucleic acids in amniotic fluid

artículo científico publicado en 2010

Clinical implementation of cell-free DNA-based aneuploidy screening: perspectives from a national audit

artículo científico publicado en 2015

Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy

artículo científico publicado en 2017

Contemporary prenatal aneuploidy screening practice in Australia: Frequently asked questions in the cell-free DNA era.

artículo científico publicado en 2018

Cytomegalovirus (CMV) infection and pregnancy-potential for improvements in Australasian maternity health providers' knowledge.

artículo científico publicado en 2017

Declining invasive prenatal diagnostic procedures: A comparison of tertiary hospital and national data from 2012 to 2015.

artículo científico publicado en 2017

Early clinical experience of cell-free DNA-based aneuploidy screening: A survey of obstetric sonologists in Australia and New Zealand

artículo científico publicado en 2015

Effect of labor on postpartum clearance of cell-free fetal DNA from the maternal circulation

scientific article published on 01 April 2008

Emerging issues in invasive prenatal diagnosis: Safety and competency in the post-NIPT era.

artículo científico publicado en 2015

Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy

artículo científico publicado en 2022

Evolution of fetal acrania from 7 to 10 weeks gestation

artículo científico publicado en 2020

Feasibility of using self-reported ethnicity in pregnancy according to the gestation-related optimal weight classification: a cross-sectional study.

artículo científico publicado en 2017

Fetal fraction and noninvasive prenatal testing: What clinicians need to know

scientific article published on 10 December 2019

First and second trimester screening for fetal structural anomalies.

artículo científico publicado en 2017

Global gene expression analysis of amniotic fluid cell-free RNA from recipient twins with twin-twin transfusion syndrome

artículo científico publicado en 2013

How to safeguard competency and training in invasive prenatal diagnosis: 'the elephant in the room'

artículo científico publicado en 2016

Identification and management of congenital parvovirus B19 infection

artículo científico publicado en 2020

Maternal and perinatal outcomes for women with body mass index ≥50 kg/m2 in a non-tertiary hospital setting

scientific article published on 03 October 2019

Maternal obesity affects fetal neurodevelopmental and metabolic gene expression: a pilot study

artículo científico publicado en 2014

Maternity healthcare professionals' views and experiences of fetal genomic uncertainty: a review

artículo científico publicado en 2020

Measuring fetal brain and lung transcripts in amniotic fluid supernatant: a comparison of digital PCR and RT-qPCR methods.

artículo científico publicado en 2017

Minimal impact of maternal intravenous immunoglobulin infusion on cell-free DNA sequencing for fetal aneuploidy

artículo científico publicado en 2016

Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development

artículo científico publicado en 2018

Non-invasive prenatal testing for fetal aneuploidy: charting the course from clinical validity to clinical utility

scientific article published on 01 January 2013

Noninvasive Approaches to Prenatal Diagnosis: Historical Perspective and Future Directions

artículo científico publicado en 2019

Noninvasive Prenatal DNA Testing: The Vanguard of Genomic Medicine

artículo científico publicado en 2016

Noninvasive prenatal testing for aneuploidy using cell-free DNA - New implications for maternal health.

artículo científico publicado en 2016

Noninvasive prenatal testing for fetal aneuploidy and single gene disorders

artículo científico publicado en 2017

Novel neurodevelopmental information revealed in amniotic fluid supernatant transcripts from fetuses with trisomies 18 and 21.

artículo científico publicado en 2012

Opportunities and challenges for international societies in the COVID-19 era

artículo científico publicado en 2020

Perinatal management of hepatitis B virus: Clinical implementation of updated Australasian management guidelines.

artículo científico publicado en 2017

Perinatal outcome after maternal primary cytomegalovirus infection in the first trimester: a practical update and counseling aid.

artículo científico

Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy.

artículo científico publicado en 2017

Population-based trends in invasive prenatal diagnosis for ultrasound-based indications: two decades of change from 1994 to 2016

artículo científico publicado en 2019

Population-based trends in prenatal screening and diagnosis for aneuploidy: a retrospective analysis of 38 years of state-wide data.

artículo científico publicado en 2015

Population-based trends in the prenatal diagnosis of sex chromosome aneuploidy before and after non-invasive prenatal testing

artículo científico publicado en 2018

Pregnancy outcomes before and after institution of a specialised twins clinic: a retrospective cohort study.

artículo científico publicado en 2015

Prenatal and preimplantation genetic diagnosis for single gene disorders: A population-based study from 1977 to 2016

artículo científico publicado en 2018

Prenatal diagnosis and socioeconomic status in the non-invasive prenatal testing era: A population-based study

artículo científico publicado en 2018

Prenatal diagnostic testing and atypical chromosome abnormalities following combined first-trimester screening: implications for contingent models of non-invasive prenatal testing.

artículo científico publicado en 2017

Prenatal pharmacotherapy for fetal anomalies: a 2011 update.

artículo científico publicado en 2011

Prenatal screening for fetal and obstetric complications: New opportunities and challenges.

artículo científico publicado en 2018

Prospective longitudinal assessment of the fetal left modified Myocardial Performance Index

artículo científico publicado en 2017

RNA-Seq and expression microarray highlight different aspects of the fetal amniotic fluid transcriptome.

artículo científico publicado en 2014

Re: First-trimester risk assessment based on ultrasound and cell-free DNA vs combined screening: a randomized controlled trial. K. O. Kagan, R. Sroka, J. Sonek, H. Abele, K. Lüthgens, M. Schmid, P. Wagner, S. Brucker, D. Wallwiener and M. Hoopmann.

scientific article published on 01 April 2018

Re: Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. T. K. Lau, S. W. Cheung, P. S. S. Lo, A. N. Pursley, M. K. Cha

artículo científico publicado en 2014

Recent advances in the prenatal interrogation of the human fetal genome

artículo científico publicado en 2012

Reduced growth velocity across the third trimester is associated with placental insufficiency in fetuses born at a normal birthweight: a prospective cohort study.

artículo científico publicado en 2017

Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study

artículo científico publicado en 2021

Repeated failed non-invasive prenatal testing owing to low cell-free fetal DNA fraction and increased variance in a woman with severe autoimmune disease

artículo científico publicado en 2014

Right or wrong? Looking Through the Retrospectoscope to Analyse predictions made a decade ago in Prenatal Diagnosis and Fetal Surgery

artículo científico publicado en 2020

Should second trimester hypoplastic nasal bone be a sole indication for diagnostic testing with chromosomal microarray?

artículo científico publicado en 2019

State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study

artículo científico publicado en 2019

State‐wide increase in prenatal diagnosis of klinefelter syndrome on amniocentesis and chorionic villus sampling: Impact of non‐invasive prenatal testing for sex chromosome conditions

scientific article published in 2022

The 2018 Malcolm Ferguson-Smith Young Investigator Award

artículo científico publicado en 2019

The amniotic fluid transcriptome: a source of novel information about human fetal development

artículo científico publicado en 2012

The cerebral-placental-uterine ratio as a novel predictor of late fetal growth restriction: a prospective cohort study

artículo científico publicado en 2019

The intimate connection between maternal health and fetal development

scientific article published on 29 June 2020

The pathway not taken: understanding 'omics data in the perinatal context

artículo científico publicado en 2015

The predicted clinical workload associated with early post-term surveillance and inductions of labour in south Asian women in a non-tertiary hospital setting

scientific article published on 02 November 2020

Variable effect of maternal oral glucose load on circulating cell-free placental mRNAs.

artículo científico publicado en 2016

What is the real "price" of more prenatal screening and fewer diagnostic procedures? Costs and trade-offs in the genomic era.

artículo científico publicado en 2018

Lista de obras de Lisa Hui

40 years of prenatal diagnosis in 2020

A comparison of sample collection methods for quantifying cell-free fetal neurodevelopment transcripts in amniotic fluid

A decade of non‐invasive prenatal screening in Australia: National impact on prenatal screening and diagnostic testing

A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort

Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.

Alobar holoprosencephaly detected in a 9-week embryo

Antenatal noninvasive DNA testing: clinical experience and impact

Assessing maternal clotting function with novel global coagulation assays: A prospective pilot study

Assessing the fetal effects of maternal obesity via transcriptomic analysis of cord blood: a prospective case-control study

Assessing the sensitivity of placental growth factor and soluble fms-like tyrosine kinase 1 at 36 weeks' gestation to predict small-for-gestational-age infants or late-onset preeclampsia: a prospective nested case-control study

Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016

Cell-free DNA testing for 22q11.2 deletion syndrome: appraising the viability, effectiveness and appropriateness of screening

Cell-free fetal nucleic acids in amniotic fluid

Clinical implementation of cell-free DNA-based aneuploidy screening: perspectives from a national audit

Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy

Contemporary prenatal aneuploidy screening practice in Australia: Frequently asked questions in the cell-free DNA era.

Cytomegalovirus (CMV) infection and pregnancy-potential for improvements in Australasian maternity health providers' knowledge.

Declining invasive prenatal diagnostic procedures: A comparison of tertiary hospital and national data from 2012 to 2015.

Early clinical experience of cell-free DNA-based aneuploidy screening: A survey of obstetric sonologists in Australia and New Zealand

Effect of labor on postpartum clearance of cell-free fetal DNA from the maternal circulation

Emerging issues in invasive prenatal diagnosis: Safety and competency in the post-NIPT era.

Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy

Evolution of fetal acrania from 7 to 10 weeks gestation

Feasibility of using self-reported ethnicity in pregnancy according to the gestation-related optimal weight classification: a cross-sectional study.

Fetal fraction and noninvasive prenatal testing: What clinicians need to know

First and second trimester screening for fetal structural anomalies.

Global gene expression analysis of amniotic fluid cell-free RNA from recipient twins with twin-twin transfusion syndrome

How to safeguard competency and training in invasive prenatal diagnosis: 'the elephant in the room'

Identification and management of congenital parvovirus B19 infection

Maternal and perinatal outcomes for women with body mass index ≥50 kg/m2 in a non-tertiary hospital setting

Maternal obesity affects fetal neurodevelopmental and metabolic gene expression: a pilot study

Maternity healthcare professionals' views and experiences of fetal genomic uncertainty: a review

Measuring fetal brain and lung transcripts in amniotic fluid supernatant: a comparison of digital PCR and RT-qPCR methods.

Minimal impact of maternal intravenous immunoglobulin infusion on cell-free DNA sequencing for fetal aneuploidy

Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development

Non-invasive prenatal testing for fetal aneuploidy: charting the course from clinical validity to clinical utility

Noninvasive Approaches to Prenatal Diagnosis: Historical Perspective and Future Directions

Noninvasive Prenatal DNA Testing: The Vanguard of Genomic Medicine

Noninvasive prenatal testing for aneuploidy using cell-free DNA - New implications for maternal health.

Noninvasive prenatal testing for fetal aneuploidy and single gene disorders

Novel neurodevelopmental information revealed in amniotic fluid supernatant transcripts from fetuses with trisomies 18 and 21.

Opportunities and challenges for international societies in the COVID-19 era

Perinatal management of hepatitis B virus: Clinical implementation of updated Australasian management guidelines.

Perinatal outcome after maternal primary cytomegalovirus infection in the first trimester: a practical update and counseling aid.

Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy.

Population-based trends in invasive prenatal diagnosis for ultrasound-based indications: two decades of change from 1994 to 2016

Population-based trends in prenatal screening and diagnosis for aneuploidy: a retrospective analysis of 38 years of state-wide data.

Population-based trends in the prenatal diagnosis of sex chromosome aneuploidy before and after non-invasive prenatal testing

Pregnancy outcomes before and after institution of a specialised twins clinic: a retrospective cohort study.

Prenatal and preimplantation genetic diagnosis for single gene disorders: A population-based study from 1977 to 2016

Prenatal diagnosis and socioeconomic status in the non-invasive prenatal testing era: A population-based study

Prenatal diagnostic testing and atypical chromosome abnormalities following combined first-trimester screening: implications for contingent models of non-invasive prenatal testing.

Prenatal pharmacotherapy for fetal anomalies: a 2011 update.

Prenatal screening for fetal and obstetric complications: New opportunities and challenges.

Prospective longitudinal assessment of the fetal left modified Myocardial Performance Index

RNA-Seq and expression microarray highlight different aspects of the fetal amniotic fluid transcriptome.

Re: First-trimester risk assessment based on ultrasound and cell-free DNA vs combined screening: a randomized controlled trial. K. O. Kagan, R. Sroka, J. Sonek, H. Abele, K. Lüthgens, M. Schmid, P. Wagner, S. Brucker, D. Wallwiener and M. Hoopmann.

Re: Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. T. K. Lau, S. W. Cheung, P. S. S. Lo, A. N. Pursley, M. K. Cha

Recent advances in the prenatal interrogation of the human fetal genome

Reduced growth velocity across the third trimester is associated with placental insufficiency in fetuses born at a normal birthweight: a prospective cohort study.

Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study

Repeated failed non-invasive prenatal testing owing to low cell-free fetal DNA fraction and increased variance in a woman with severe autoimmune disease

Right or wrong? Looking Through the Retrospectoscope to Analyse predictions made a decade ago in Prenatal Diagnosis and Fetal Surgery

Should second trimester hypoplastic nasal bone be a sole indication for diagnostic testing with chromosomal microarray?

State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study

State‐wide increase in prenatal diagnosis of klinefelter syndrome on amniocentesis and chorionic villus sampling: Impact of non‐invasive prenatal testing for sex chromosome conditions

The 2018 Malcolm Ferguson-Smith Young Investigator Award

The amniotic fluid transcriptome: a source of novel information about human fetal development

The cerebral-placental-uterine ratio as a novel predictor of late fetal growth restriction: a prospective cohort study

The intimate connection between maternal health and fetal development

The pathway not taken: understanding 'omics data in the perinatal context

The predicted clinical workload associated with early post-term surveillance and inductions of labour in south Asian women in a non-tertiary hospital setting

Variable effect of maternal oral glucose load on circulating cell-free placental mRNAs.

What is the real "price" of more prenatal screening and fewer diagnostic procedures? Costs and trade-offs in the genomic era.