Grants per year
Personal profile
Certifications and Licenses
Obstetrics & Gynecology | |
Clinical Genetics (MD) |
Training Experience
1991 | Residency, University of Virginia Hospitals |
1993 | Fellowship, University of Tennessee Medical Center |
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Education/Academic qualification
MD, Medicine, Creighton University
… → 1987
Research interests keywords
- Amniocentesis
- Chorionic Villi Sampling
- Ovarian Cancer Screening
- Preconception Genetics
- Prenatal Diagnosis
- Ultrasound
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Collaborations and top research areas from the last five years
Grants
- 12 Finished
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The VALUE Study: VAlidation of a Lower cost aneUploidy scrEen
Women & Infants Hospital of Rhode Island
10/22/17 → 10/22/22
Project: Research project
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Prot# VER-0007: Comparison of Aneuploidy Risk Evaluations (CARE) Performance of the Verinata Health Prenatal Aneuploidy Test Compared to Current Fetal Aneuploidy Screening Results and Pregnancy Outcomes in an 'All-Risk' Population
Dungan, J. S., Grobman, W. A., Shulman, L. P. & Stika, C. S.
SynteractHCR, Inc., Verinata Health, Inc.
6/21/12 → 6/21/15
Project: Research project
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Prot# SQNM-T21-107: Collection of Whole Blood Specimens from Pregnant Women at Increased Risk for Fetal Chromosomal Aneuploidy for use in Development of the SEQureDx™ Trisomy 21 Test in the Detection of the Relative Quantity of Chromosome 21 Circulating C
Dungan, J. S., Grobman, W. A. & Shulman, L. P.
1/5/12 → 1/5/18
Project: Research project
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A Qualitative Exploration of the Extended Decision Making Process in Pregnancy Termination for Fetal Indications
Simon, M. A., Cameron, K. A., Dungan, J. S., Hammond, C. & Kiley, J. W.
6/1/11 → 6/30/12
Project: Research project
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Prot# SQNM-RND-106: Collection of Whole Blood Specimens from Pregnant Subjects to Support Research and Development
Dungan, J. S., Grobman, W. A., Shulman, L. P. & Stika, C. S.
5/9/11 → 5/9/14
Project: Research project
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Erratum: Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG) (Genetics in Medicine (2023) 25(2), (S1098360022010048), (10.1016/j.gim.2022.11.004))
ACMG Board of Directors, Aug 2023, In: Genetics in Medicine. 25, 8, 100874.Research output: Contribution to journal › Comment/debate › peer-review
Open Access1 Scopus citations -
Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
ACMG Board of Directors, Feb 2023, In: Genetics in Medicine. 25, 2, 100336.Research output: Contribution to journal › Article › peer-review
29 Scopus citations -
Response to Prensky and Persson
Dungan, J. S. & Klugman, S., Sep 2023, In: Genetics in Medicine. 25, 9, 100873.Research output: Contribution to journal › Letter › peer-review
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Tamoxifen and the risk of breast cancer in women with a BRCA1 or BRCA2 mutation
and the Hereditary Breast Cancer Clinical Study Group, Sep 2023, In: Breast Cancer Research and Treatment. 201, 2, p. 257-264 8 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Bilateral Oophorectomy and the Risk of Breast Cancer in BRCA1 Mutation Carriers: A Reappraisal
the Hereditary Breast Cancer Clinical Study Group, Jul 2022, In: Cancer Epidemiology Biomarkers and Prevention. 31, 7, p. 1351-1358 8 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations