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Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes

American journal of obstetrics and gynecology, 2015-03, Vol.212 (3), p.332.e1-332.e9

2015

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Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing

American journal of obstetrics and gynecology, 2014-11, Vol.211 (5), p.527.e1-527.e17

2014

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Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism–based noninvasive prenatal test

American journal of obstetrics and gynecology, 2015, Vol.212 (1), p.79.e1-79.e9

2015

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A streamlined model for use in clinical breast cancer risk assessment maintains predictive power and is further improved with inclusion of a polygenic risk score

PloS one, 2021-01, Vol.16 (1), p.e0245375-e0245375

2021

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First-Trimester or Second-Trimester Screening, or Both, for Down's Syndrome

The New England journal of medicine, 2005-11, Vol.353 (19), p.2001-2011

2005

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Implications of fetoplacental mosaicism on cell‐free DNA testing for sex chromosome aneuploidies

Prenatal diagnosis, 2017-10, Vol.37 (10), p.1017-1027

2017

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Preconceptional folate supplementation and the risk of spontaneous preterm birth: a cohort study

PLoS medicine, 2009-05, Vol.6 (5), p.e1000061-e1000061

2009

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Validation of an Enhanced Version of a Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies

Fetal diagnosis and therapy, 2016-01, Vol.40 (3), p.219-223

2016

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Late preterm antenatal corticosteroids in singleton and twin gestations: a retrospective cohort study

BMC pregnancy and childbirth, 2022-12, Vol.22 (1), p.904-904

2022

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Positive predictive values and false-positive results in noninvasive prenatal screening

American journal of obstetrics and gynecology, 2015-10, Vol.213 (4), p.595-596

2015

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Carrier testing for Ashkenazi Jewish disorders in the prenatal setting: navigating the genetic maze

American journal of obstetrics and gynecology, 2014-09, Vol.211 (3), p.197-204

2014

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Revisiting the challenges of training Maternal Fetal Medicine fellows in chorionic villus sampling

American journal of obstetrics and gynecology, 2016-12, Vol.215 (6), p.777.e1-777.e4

2016

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Noninvasive screening by cell‐free DNA for 22q11.2 deletion: Benefits, limitations, and challenges

Prenatal diagnosis, 2019-01, Vol.39 (2), p.70-80

2019

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Improving preeclampsia risk prediction by modeling pregnancy trajectories from routinely collected electronic medical record data

NPJ digital medicine, 2022-06, Vol.5 (1), p.68-68, Article 68

2022

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Threatened abortion: a risk factor for poor pregnancy outcome, a population-based screening study

American journal of obstetrics and gynecology, 2004-03, Vol.190 (3), p.745-750

2004

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The genetics of diabetic pregnancy

Best practice & research. Clinical obstetrics & gynaecology, 2015-01, Vol.29 (1), p.102-109

2015

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The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Neurology, 2013-04, Vol.80 (17), p.1606

2013

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Ashkenazi Jewish Screening in the Twenty-first Century

Obstetrics and gynecology clinics of North America, 2010-03, Vol.37 (1), p.37-46

2010

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Focus on more specific fetal testing

Nature (London), 2015-07, Vol.523 (7560), p.290-290

2015

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Prenatal screening: Focus on more specific fetal testing

Nature (London), 2015-07, Vol.523 (7560), p.290-290

2015

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Carrier screening in individuals of Ashkenazi Jewish descent

Genetics in medicine, 2008-01, Vol.10 (1), p.54-56

2008

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Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications

Prenatal diagnosis, 2016-12, Vol.36 (12), p.1146-1155

2016

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Screening for fetal aneuploidy and neural tube defects

Genetics in medicine, 2009-11, Vol.11 (11), p.818-821

2009

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Noninvasive Prenatal Screening by Next-Generation Sequencing

Annual review of genomics and human genetics, 2014-01, Vol.15 (1), p.327-347

2014

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Carrier Screening: Past, Present, and Future

Journal of clinical medicine, 2014-09, Vol.3 (3), p.1033-1042

2014

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Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes

Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing

Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism–based noninvasive prenatal test

A streamlined model for use in clinical breast cancer risk assessment maintains predictive power and is further improved with inclusion of a polygenic risk score

First-Trimester or Second-Trimester Screening, or Both, for Down's Syndrome

Implications of fetoplacental mosaicism on cell‐free DNA testing for sex chromosome aneuploidies

Preconceptional folate supplementation and the risk of spontaneous preterm birth: a cohort study

Validation of an Enhanced Version of a Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies

Late preterm antenatal corticosteroids in singleton and twin gestations: a retrospective cohort study

Positive predictive values and false-positive results in noninvasive prenatal screening

Carrier testing for Ashkenazi Jewish disorders in the prenatal setting: navigating the genetic maze

Revisiting the challenges of training Maternal Fetal Medicine fellows in chorionic villus sampling

Noninvasive screening by cell‐free DNA for 22q11.2 deletion: Benefits, limitations, and challenges

Improving preeclampsia risk prediction by modeling pregnancy trajectories from routinely collected electronic medical record data

Threatened abortion: a risk factor for poor pregnancy outcome, a population-based screening study

The genetics of diabetic pregnancy

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Ashkenazi Jewish Screening in the Twenty-first Century

Focus on more specific fetal testing

Prenatal screening: Focus on more specific fetal testing

Carrier screening in individuals of Ashkenazi Jewish descent

Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications

Screening for fetal aneuploidy and neural tube defects

Noninvasive Prenatal Screening by Next-Generation Sequencing

Carrier Screening: Past, Present, and Future

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