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Uniparental disomy: Origin, frequency, and clinical significance

Prenatal diagnosis, 2021-04, Vol.41 (5), p.564-572

Benn, Peter

2021

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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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Posttest risk calculation following positive noninvasive prenatal screening using cell-free DNA in maternal plasma

American journal of obstetrics and gynecology, 2016-06, Vol.214 (6), p.676.e1-676.e7

Benn, Peter, PhD, DSc

2016

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Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

Prenatal diagnosis, 2015-08, Vol.35 (8), p.725-734

2015

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Cell-free DNA screening for fetal aneuploidy as a clinical service

Clinical biochemistry, 2015-10, Vol.48 (15), p.932-941

2015

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Correspondence on "Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions" by Hoskovec et al

Genetics in medicine, 2023-09, Vol.25 (9), p.100902-100902, Article 100902

Benn, Peter

2023

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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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Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

Prenatal diagnosis, 2013-07, Vol.33 (7), p.622-629

2013

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Rare autosomal trisomies detected by non-invasive prenatal testing

European journal of human genetics : EJHG, 2022-12, Vol.30 (12), p.1318-1319

Benn, Peter

2022

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Prenatal counseling and the detection of copy-number variants

Genetics in medicine, 2013-04, Vol.15 (4), p.316-317

Benn, Peter A.

2013

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An Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population

PloS one, 2015-07, Vol.10 (7), p.e0132313-e0132313

2015

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Ethical challenges in providing noninvasive prenatal diagnosis

Current opinion in obstetrics & gynecology, 2010-04, Vol.22 (2), p.128-134

2010

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Prenatal technologies and the sex ratio

Genetics in medicine, 2014-06, Vol.16 (6), p.433-434

Benn, Peter A.

2014

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Practical and ethical considerations of noninvasive prenatal diagnosis

JAMA : the journal of the American Medical Association, 2009-05, Vol.301 (20), p.2154

2009

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Non‐invasive prenatal testing in the management of twin pregnancies

Prenatal diagnosis, 2021-09, Vol.41 (10), p.1233-1240

2021

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Obituary: Lillian YF Hsu, MD, FFACMG

Prenatal diagnosis, 2020-10, Vol.40 (11), p.1351-1352

Benn, Peter

2020

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Chromosome segregation of human nonhomologous Robertsonian translocations: insights from preimplantation genetic testing

European journal of human genetics : EJHG, 2024-09

2024

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Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis

PloS one, 2017-12, Vol.12 (12), p.e0189235-e0189235

2017

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Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value

American journal of obstetrics and gynecology, 2015-08, Vol.213 (2), p.254-255

2015

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Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing

Prenatal diagnosis, 2014-02, Vol.34 (2), p.145-152

2014

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Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011

Prenatal diagnosis, 2012-01, Vol.32 (1), p.1-2

2012

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Overview of Noninvasive Prenatal Testing (NIPT) for the Detection of Fetal Chromosome Abnormalities; Differences in Laboratory Methods and Scope of Testing

Clinical obstetrics and gynecology, 2023-09, Vol.66 (3), p.536-556

2023

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Non-invasive prenatal screening: A 20-year experience in Italy

European journal of obstetrics & gynecology and reproductive biology: X, 2019-07, Vol.3, p.100050-100050, Article 100050

2019

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P681: Carrier screening with the ACMG 113: An early look and new insights

Genetics in Medicine Open, 2024, Vol.2, p.101585, Article 101585

2024

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Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities

American journal of obstetrics and gynecology, 2016-08, Vol.215 (2), p.252-253

2016

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Uniparental disomy: Origin, frequency, and clinical significance

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

Posttest risk calculation following positive noninvasive prenatal screening using cell-free DNA in maternal plasma

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

Cell-free DNA screening for fetal aneuploidy as a clinical service

Correspondence on "Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions" by Hoskovec et al

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

Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

Rare autosomal trisomies detected by non-invasive prenatal testing

Prenatal counseling and the detection of copy-number variants

An Economic Analysis of Cell-Free DNA Non-Invasive Prenatal Testing in the US General Pregnancy Population

Ethical challenges in providing noninvasive prenatal diagnosis

Prenatal technologies and the sex ratio

Practical and ethical considerations of noninvasive prenatal diagnosis

Non‐invasive prenatal testing in the management of twin pregnancies

Obituary: Lillian YF Hsu, MD, FFACMG

Chromosome segregation of human nonhomologous Robertsonian translocations: insights from preimplantation genetic testing

Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis

Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value

Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing

Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011

Overview of Noninvasive Prenatal Testing (NIPT) for the Detection of Fetal Chromosome Abnormalities; Differences in Laboratory Methods and Scope of Testing

Non-invasive prenatal screening: A 20-year experience in Italy

P681: Carrier screening with the ACMG 113: An early look and new insights

Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities

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