The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Expanded Carrier Screening in Reproductive Medicine—Points to Consider: A Joint Statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine
Abstract
The Perinatal Quality Foundation and the American College of Medical Genetics and Genomics, in association with the American College of Obstetricians and Gynecologists, the Society for Maternal-Fetal Medicine, and the National Society of Genetic Counselors, have collaborated to provide education for clinicians and laboratories regarding the use of expanded genetic carrier screening in reproductive medicine. This statement does not replace current screening guidelines, which are published by individual organizations to direct the practice of their constituents. As organizations develop practice guidelines for expanded carrier screening, further direction is likely. The current statement demonstrates an approach for health care providers and laboratories who wish to or who are currently offering expanded carrier screening to their patients.
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Cites
5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE Review
Botto, L. D., & Yang, Q. (2000) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a010290 · Cited by 1,044
Watson, M. S., Cutting, G. R., Desnick, R. J., Driscoll, D. A., Klinger, K., Mennuti, M., Palomaki, G. E., Popovich, B. W., Pratt, V. M., Rohlfs, E. M., et al. (2004) · Genetics in Medicine · doi:10.1097/01.gim.0000139506.11694.7c · Cited by 470
Self-citationFragile X syndrome: Diagnostic and carrier testing
Sherman, S., Pletcher, B. A., & Driscoll, D. A. (2005) · Genetics in Medicine · doi:10.1097/01.gim.0000182468.22666.dd · Cited by 277
Carrier screening for spinal muscular atrophy
Prior, T. W. (2008) · Genetics in Medicine · doi:10.1097/gim.0b013e318188d069 · Cited by 270
Prevalence of C282Y and H63D Mutations in the Hemochromatosis (HFE) Gene in the United States
Steinberg, K. K., Cogswell, M. E., Chang, J. C., Caudill, S. P., McQuillan, G. M., Bowman, B. A., Grummer-Strawn, L. M., Sampson, E. J., Khoury, M. J., & Gallagher, M. L. (2001) · JAMA · doi:10.1001/jama.285.17.2216 · Cited by 230
Carrier screening in individuals of Ashkenazi Jewish descent
Gross, S. J., Pletcher, B. A., & Monaghan, K. G. (2008) · Genetics in Medicine · doi:10.1097/gim.0b013e31815f247c · Cited by 211
Whitlock, E. P., Garlitz, B. A., Harris, E. L., Beil, T. L., & Smith, P. R. (2006) · Annals of Internal Medicine · doi:10.7326/0003-4819-145-3-200608010-00009 · Cited by 200
American College of Medical Genetics Consensus Statement on Factor V Leiden Mutation Testing
Grody, W. W., Griffin, J. H., Taylor, A. K., Korf, B. R., & Heit, J. A. (2001) · Genetics in Medicine · doi:10.1097/00125817-200103000-00009 · Cited by 176
ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing
Hickey, S. E., Curry, C. J., & Toriello, H. V. (2013) · Genetics in Medicine · doi:10.1038/gim.2012.165 · Cited by 175
HFE-associated hereditary hemochromatosis
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Cited by
Gregg, A. R., Aarabi, M., Klugman, S., Leach, N. T., Bashford, M. T., Goldwaser, T., Chen, E., Sparks, T. N., Reddi, H. V., Rajkovic, A., et al. (2021) · Genetics in Medicine · doi:10.1038/s41436-021-01203-z · Cited by 367
Self-citationSchmitz, M. J., Aarabi, M., Bashar, A., Rajkovic, A., Gregg, A. R., & Yatsenko, S. A. (2022) · Clinical Genetics · doi:10.1111/cge.14148 · Cited by 18
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Metadata
- Authors
- Edwards, J. G., Feldman, G., Goldberg, J., Gregg, A. R., Norton, M. E., Rose, N. C., Schneider, A., Stoll, K., Wapner, R., & Watson, M. S.
- Venue
- Obstetrics & Gynecology
- Published
- 2015-03
- Volume
- 125
- Issue
- 3
- Pages
- 653-662
- ISSN
- 0029-7844 (ISSN-L)
- OpenAlex
- W2040406984
- Cited by
- 358
- References
- 18
- FWCI
- 36.79
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Expanded Carrier Screening in Reproductive Medicine—Points to Consider: A Joint Statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine. https://app.cochat.ai/papers/10.1097/aog.0000000000000666
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- Edwards, J. G., Feldman, G., Goldberg, J., Gregg, A. R., Norton, M. E., Rose, N. C., Schneider, A., Stoll, K., Wapner, R., & Watson, M. S. (2015). Expanded Carrier Screening in Reproductive Medicine—Points to Consider: A Joint Statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine. Obstetrics & Gynecology. https://doi.org/10.1097/aog.0000000000000666
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