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Project Inclusive Genetics: Exploring the impact of patient-centered counseling training on physical disability bias in the prenatal setting

PloS one, 2021-08, Vol.16 (8), p.e0255722-e0255722

2021

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Non-invasive prenatal screening: Testing motivations and decision making in the low-risk population

Journal of genetic counseling, 2024-05

2024

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Utility of expanded carrier screening in pregnancies with ultrasound abnormalities

Prenatal diagnosis, 2022-01, Vol.42 (1), p.60-78

2022

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P801: Abortion preferences of patients with abnormal prenatal genetic diagnosis in an access-restricted state

Genetics in Medicine Open, 2024, Vol.2, p.101709, Article 101709

2024

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It takes two: uptake of carrier screening among male reproductive partners

Prenatal diagnosis, 2020-02, Vol.40 (3), p.311-316

2020

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Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors

Journal of genetic counseling, 2023-06, Vol.32 (3), p.540-557

2023

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Project Inclusive Genetics: Protecting reproductive autonomy from bias via prenatal patient-centered counseling

HGG advances, 2023-10, Vol.4 (4), p.100228-100228, Article 100228

2023

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Exploring the predicted yield of prenatal testing by evaluating a postnatal population with structural abnormalities using a novel mathematical model

Prenatal diagnosis, 2021-02, Vol.41 (3), p.354-361

2021

Volltextzugriff (PDF)

Impact of Emerging Technologies in Prenatal Genetic Counseling

Cold Spring Harbor perspectives in medicine, 2020-12, Vol.10 (12), p.a036517

Stevens, Blair

2020

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Genetic Counseling Overview for the Obstetrician-Gynecologist

Obstetrics and gynecology clinics of North America, 2018-03, Vol.45 (1), p.1-12

2018

Volltextzugriff (PDF)

Obesity and the Risk and Detection of Fetal Malformations

Seminars in perinatology, 2012-06, Vol.36 (3), p.213-221

2012

Volltextzugriff (PDF)

Characterization of a Complex Derivative Chromosome 18

Cancer genetics, 2016-05, Vol.209 (5), p.247-248

2016

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Patients with unexplained mismatch repair deficiency are interested in updated genetic testing

Hereditary cancer in clinical practice, 2020-09, Vol.18 (1), p.19-19, Article 19

2020

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Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications

Journal of genetic counseling, 2019-06, Vol.28 (3), p.692-699

2019

Volltextzugriff (PDF)

Finding Middle Ground in Constructing a Clinically Useful Expanded Carrier Screening Panel

Obstetrics and gynecology (New York. 1953), 2017-08, Vol.130 (2), p.279-284

2017

Volltextzugriff (PDF)

Patient Perception of Negative Noninvasive Prenatal Testing Results

American journal of perinatology reports, 2016-10, Vol.6 (4), p.e391-e406

2016

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Informed Consent for Routine Genetic Screening: Realistic or Idealistic?

American journal of obstetrics and gynecology, 2023-01, Vol.228 (1), p.S101-S102

2023

Volltextzugriff (PDF)

Effect of physical inactivity on major non-communicable diseases worldwide: an analysis of burden of disease and life expectancy

The Lancet (British edition), 2012-07, Vol.380 (9838), p.219-229

2012

Volltextzugriff (PDF)

The integration of health promotion and social marketing

Perspectives in public health, 2009-11, Vol.129 (6), p.268-271

2009

Volltextzugriff (PDF)

Global physical activity levels: surveillance progress, pitfalls, and prospects

The Lancet (British edition), 2012-07, Vol.380 (9838), p.247-257

2012

Volltextzugriff (PDF)

Correlates of physical activity: why are some people physically active and others not?

The Lancet (British edition), 2012-07, Vol.380 (9838), p.258-271

2012

Volltextzugriff (PDF)

The pandemic of physical inactivity: global action for public health

The Lancet (British edition), 2012-07, Vol.380 (9838), p.294-305

2012

Volltextzugriff (PDF)

Evidence-based intervention in physical activity: lessons from around the world

The Lancet (British edition), 2012-07, Vol.380 (9838), p.272-281

2012

Volltextzugriff (PDF)

1 Multicenter, prospective cohort of genome sequencing in 750 fetal structural anomalies

American journal of obstetrics and gynecology, 2024-01, Vol.230 (1), p.S2-S2

2024

Volltextzugriff (PDF)

Response to: Milosavljevic et al. “Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature”

American journal of medical genetics. Part A, 2017-07, Vol.173 (7), p.1992-1993

2017

Volltextzugriff (PDF)

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Project Inclusive Genetics: Exploring the impact of patient-centered counseling training on physical disability bias in the prenatal setting

Non-invasive prenatal screening: Testing motivations and decision making in the low-risk population

Utility of expanded carrier screening in pregnancies with ultrasound abnormalities

P801: Abortion preferences of patients with abnormal prenatal genetic diagnosis in an access-restricted state

It takes two: uptake of carrier screening among male reproductive partners

Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors

Project Inclusive Genetics: Protecting reproductive autonomy from bias via prenatal patient-centered counseling

Exploring the predicted yield of prenatal testing by evaluating a postnatal population with structural abnormalities using a novel mathematical model

Impact of Emerging Technologies in Prenatal Genetic Counseling

Genetic Counseling Overview for the Obstetrician-Gynecologist

Obesity and the Risk and Detection of Fetal Malformations

Characterization of a Complex Derivative Chromosome 18

Patients with unexplained mismatch repair deficiency are interested in updated genetic testing

Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications

Finding Middle Ground in Constructing a Clinically Useful Expanded Carrier Screening Panel

Patient Perception of Negative Noninvasive Prenatal Testing Results

Informed Consent for Routine Genetic Screening: Realistic or Idealistic?

Effect of physical inactivity on major non-communicable diseases worldwide: an analysis of burden of disease and life expectancy

The integration of health promotion and social marketing

Global physical activity levels: surveillance progress, pitfalls, and prospects

Correlates of physical activity: why are some people physically active and others not?

The pandemic of physical inactivity: global action for public health

Evidence-based intervention in physical activity: lessons from around the world

1 Multicenter, prospective cohort of genome sequencing in 750 fetal structural anomalies

Response to: Milosavljevic et al. “Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature”

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