Stoll K - Search Results

1

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.

Edwards JG, Feldman G, Goldberg J, Gregg AR, Norton ME, Rose NC, Schneider A, Stoll K, Wapner R, Watson MS. Edwards JG, et al. Among authors: stoll k. Obstet Gynecol. 2015 Mar;125(3):653-662. doi: 10.1097/AOG.0000000000000666. Obstet Gynecol. 2015. PMID: 25730230

2

Optimizing use of existing prenatal genetic tests: Screening and diagnostic testing for aneuploidy.

Stoll K, Norton ME. Stoll K, et al. Semin Perinatol. 2018 Aug;42(5):296-302. doi: 10.1053/j.semperi.2018.07.014. Epub 2018 Jul 26. Semin Perinatol. 2018. PMID: 30209012 Review.

3

Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations.

Skotko BG, Allyse MA, Bajaj K, Best RG, Klugman S, Leach M, Meredith S, Michie M, Stoll K, Gregg AR. Skotko BG, et al. Among authors: stoll k. Genet Med. 2019 Oct;21(10):2285-2292. doi: 10.1038/s41436-019-0485-2. Epub 2019 Apr 3. Genet Med. 2019. PMID: 30940924 Free article.

4

Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.

Fonda Allen J, Stoll K, Bernhardt BA. Fonda Allen J, et al. Among authors: stoll k. Semin Perinatol. 2016 Feb;40(1):44-55. doi: 10.1053/j.semperi.2015.11.007. Epub 2015 Dec 21. Semin Perinatol. 2016. PMID: 26718445 Free PMC article. Review.

5

The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine.

Stoll K, Kubendran S, Cohen SA. Stoll K, et al. Am J Med Genet C Semin Med Genet. 2018 Mar;178(1):24-37. doi: 10.1002/ajmg.c.31602. Epub 2018 Mar 7. Am J Med Genet C Semin Med Genet. 2018. PMID: 29512888

6

Noninvasive prenatal testing: limitations and unanswered questions.

Lutgendorf MA, Stoll KA, Knutzen DM, Foglia LM. Lutgendorf MA, et al. Genet Med. 2014 Apr;16(4):281-5. doi: 10.1038/gim.2013.126. Epub 2013 Sep 5. Genet Med. 2014. PMID: 24009001 Free article.

7

Supporting Patient Autonomy and Informed Decision-Making in Prenatal Genetic Testing.

Stoll K, Jackson J. Stoll K, et al. Cold Spring Harb Perspect Med. 2020 Jun 1;10(6):a036509. doi: 10.1101/cshperspect.a036509. Cold Spring Harb Perspect Med. 2020. PMID: 31615869 Free PMC article. Review.

8

Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide.

Allyse M, Aypar U, Bonhomme N, Darilek S, Dougherty M, Farrell R, Grody W, Highsmith WE, Michie M, Nunes M, Otto L, Pabst R, Palomaki G, Runke C, Sharp RR, Skotko B, Stoll K, Wick M. Allyse M, et al. Among authors: stoll k. J Womens Health (Larchmt). 2017 Jul;26(7):755-761. doi: 10.1089/jwh.2016.6098. Epub 2017 Apr 7. J Womens Health (Larchmt). 2017. PMID: 28388340

9

Why 99% may not be as good as you think it is: limitations of screening for rare diseases.

Lutgendorf MA, Stoll KA. Lutgendorf MA, et al. J Matern Fetal Neonatal Med. 2016;29(7):1187-9. doi: 10.3109/14767058.2015.1039977. Epub 2015 Jul 16. J Matern Fetal Neonatal Med. 2016. PMID: 26181768 No abstract available.

10

Considering the cost of expanded carrier screening panels.

Stoll K, Resta R. Stoll K, et al. Genet Med. 2013 Apr;15(4):318-9. doi: 10.1038/gim.2013.18. Genet Med. 2013. PMID: 23552453 Free article. No abstract available.

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