Lista de obras - Neeta L. Vora - Dominio Público Uruguay

1123: Diet-induced obesity aggravates preeclampsia-like phenotypes in ASB4-null mice ⬇️

scholarly article

169 Curating the fetal genome: experience of the ClinGen prenatal gene curation expert panel (GCEP)

artículo científico publicado en 2024

551: Impact of prenatal exome-sequencing (ES) for fetal diagnosis on maternal psychological outcomes: a prospective cohort ⬇️

scholarly article

784: Novel sequencing-based framework for non-invasive fetal genotyping ⬇️

scholarly article

A multifactorial relationship exists between total circulating cell-free DNA levels and maternal BMI

artículo científico publicado en 2012

A single center's experience with noninvasive prenatal testing

artículo científico

Advances in genetic prenatal diagnosis and screening.

artículo científico

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening

scientific article published on 07 March 2019

An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

scientific article published on 24 January 2020

Attitudes and Knowledge of Maternal-Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing.

artículo científico

Cell free DNA testing-interpretation of results using an online calculator.

artículo científico publicado en 2015

Cell-Free DNA Screening: Complexities and Challenges of Clinical Implementation.

artículo científico publicado en 2016

Cell-free DNA testing in a trisomy 21 pregnancy with confined placental mosaicism for a cell line with trisomy for both chromosomes 18 and 21.

artículo científico publicado en 2015

Circulating cell-free DNA levels increase variably following chorionic villus sampling.

artículo científico publicado en 2010

Cornual placenta accreta managed by postpartum total laparoscopic hysterectomy

scientific article published on 23 May 2013

Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

scientific article published on 18 June 2020

Delivery of the growth restricted preterm fetus.

artículo científico publicado en 2015

Development, Implementation, and Assessment of a Genetics Curriculum Across Institutions

scientific article published on October 2016

Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease

artículo científico publicado en 2013

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

artículo científico publicado en 2022

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

scientific article published in 2023

Ethical and Counseling Challenges in Prenatal Exome Sequencing

artículo científico publicado en 2018

Fetal phenotypes emerge as genetic technologies become robust

scientific article published on 05 August 2019

Genetic considerations in the prenatal diagnosis of overgrowth syndromes

artículo científico publicado en 2009

Genetics for the Women's Health Trainee: A Five-Module Curriculum

article

Impact of prenatal exome sequencing for fetal genetic diagnosis on maternal psychological outcomes and decisional conflict in a prospective cohort

scientific article published on 20 November 2020

In reply

Increased death of adipose cells, a path to release cell-free DNA into systemic circulation of obese women

artículo científico publicado en 2012

Increasing the diagnostic yield of exome sequencing by copy number variant analysis

artículo científico publicado en 2018

International Society for Prenatal Diagnosis (ISPD) Position Statement: Cell free (cf)DNA screening for Down syndrome in multiple pregnancies

artículo científico publicado en 2020

Investigating the Role of Fetal Gene Expression in Preterm Birth.

artículo científico publicado en 2016

Look before you leap: genomic screening in obstetrics and gynecology

artículo científico publicado en 2015

Maternal Genetic Disorders in Pregnancy

artículo científico publicado en 2018

Maternal Malignancy Evaluation After Discordant Cell-Free DNA Results

artículo científico publicado en 2018

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

artículo científico publicado en 2014

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis

artículo científico publicado en 2023

More chorionic villi obtained at a single center compared to previously published reports

scientific article published on 09 April 2014

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

artículo científico publicado en 2018

Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies

artículo científico publicado en 2015

Noninvasive prenatal testing for microdeletion syndromes and expanded trisomies: proceed with caution

artículo científico publicado en 2014

Prenatal Diagnosis: Screening and Diagnostic Tools.

artículo científico publicado en 2017

Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges

artículo científico publicado en 2017

Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT)

scientific article published on 05 August 2019

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

artículo científico publicado en 2018

Promises, pitfalls and practicalities of prenatal whole exome sequencing

artículo científico publicado en 2017

RNA-Sequencing of Umbilical Cord Blood to Investigate Spontaneous Preterm Birth: A Pilot Study

artículo científico publicado en 2019

Relationships Between Cell-Free DNA and Serum Analytes in the First and Second Trimesters of Pregnancy ⬇️

artículo científico publicado el 1 de septiembre de 2010

Reproductive issues for adults with autosomal dominant polycystic kidney disease.

artículo científico publicado en 2008

Screening for fetal chromosomal and subchromosomal disorders

artículo científico publicado en 2017

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders

artículo científico publicado en 2020

Targeted Multiplex Gene Expression Profiling to Measure High-Fat Diet and Metformin Effects on Fetal Gene Expression in a Mouse Model

article

Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic

scientific article published on 20 April 2020

Toxic metals in amniotic fluid and altered gene expression in cell-free fetal RNA.

artículo científico publicado en 2017

Triplet ultrasound growth parameters

artículo científico publicado en 2006

Trisomy 13-confined placental mosaicism: is there an increased risk of gestational hypertensive disorders?

artículo científico publicado en 2017

Ubiquitous identification of inorganic arsenic in a cohort of second trimester amniotic fluid in women with preterm and term births

artículo científico publicado en 2019

Use of a novel computerized decision aid for aneuploidy screening: a randomized controlled trial

scientific article published on 14 September 2018

Utility of ultrasound examination at 10-14 weeks prior to cell-free DNA screening for fetal aneuploidy.

artículo científico publicado en 2016

Lista de obras de Neeta L. Vora

1123: Diet-induced obesity aggravates preeclampsia-like phenotypes in ASB4-null mice ⬇️

169 Curating the fetal genome: experience of the ClinGen prenatal gene curation expert panel (GCEP)

551: Impact of prenatal exome-sequencing (ES) for fetal diagnosis on maternal psychological outcomes: a prospective cohort ⬇️

784: Novel sequencing-based framework for non-invasive fetal genotyping ⬇️

A multifactorial relationship exists between total circulating cell-free DNA levels and maternal BMI

A single center's experience with noninvasive prenatal testing

Advances in genetic prenatal diagnosis and screening.

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening

An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

Attitudes and Knowledge of Maternal-Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing.

Cell free DNA testing-interpretation of results using an online calculator.

Cell-Free DNA Screening: Complexities and Challenges of Clinical Implementation.

Cell-free DNA testing in a trisomy 21 pregnancy with confined placental mosaicism for a cell line with trisomy for both chromosomes 18 and 21.

Circulating cell-free DNA levels increase variably following chorionic villus sampling.

Cornual placenta accreta managed by postpartum total laparoscopic hysterectomy

Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

Delivery of the growth restricted preterm fetus.

Development, Implementation, and Assessment of a Genetics Curriculum Across Institutions

Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Ethical and Counseling Challenges in Prenatal Exome Sequencing

Fetal phenotypes emerge as genetic technologies become robust

Genetic considerations in the prenatal diagnosis of overgrowth syndromes

Genetics for the Women's Health Trainee: A Five-Module Curriculum

Impact of prenatal exome sequencing for fetal genetic diagnosis on maternal psychological outcomes and decisional conflict in a prospective cohort

In reply

Increased death of adipose cells, a path to release cell-free DNA into systemic circulation of obese women

Increasing the diagnostic yield of exome sequencing by copy number variant analysis

International Society for Prenatal Diagnosis (ISPD) Position Statement: Cell free (cf)DNA screening for Down syndrome in multiple pregnancies

Investigating the Role of Fetal Gene Expression in Preterm Birth.

Look before you leap: genomic screening in obstetrics and gynecology

Maternal Genetic Disorders in Pregnancy

Maternal Malignancy Evaluation After Discordant Cell-Free DNA Results

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

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis

More chorionic villi obtained at a single center compared to previously published reports

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

Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies

Noninvasive prenatal testing for microdeletion syndromes and expanded trisomies: proceed with caution

Prenatal Diagnosis: Screening and Diagnostic Tools.

Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges

Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT)

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

Promises, pitfalls and practicalities of prenatal whole exome sequencing

RNA-Sequencing of Umbilical Cord Blood to Investigate Spontaneous Preterm Birth: A Pilot Study

Relationships Between Cell-Free DNA and Serum Analytes in the First and Second Trimesters of Pregnancy ⬇️

Reproductive issues for adults with autosomal dominant polycystic kidney disease.

Screening for fetal chromosomal and subchromosomal disorders

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders

Targeted Multiplex Gene Expression Profiling to Measure High-Fat Diet and Metformin Effects on Fetal Gene Expression in a Mouse Model

Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic

Toxic metals in amniotic fluid and altered gene expression in cell-free fetal RNA.

Triplet ultrasound growth parameters

Trisomy 13-confined placental mosaicism: is there an increased risk of gestational hypertensive disorders?

Ubiquitous identification of inorganic arsenic in a cohort of second trimester amniotic fluid in women with preterm and term births

Use of a novel computerized decision aid for aneuploidy screening: a randomized controlled trial

Utility of ultrasound examination at 10-14 weeks prior to cell-free DNA screening for fetal aneuploidy.