Samango-Sprouse CA - Search Results

1

Detection of maternal X chromosome abnormalities using single nucleotide polymorphism-based noninvasive prenatal testing.

Martin KA, Samango-Sprouse CA, Kantor V, Dhamankar R, Valenti E, Trefogli MT, Balosbalos I, Lagrave D, Lyons D, Kao C, Hakonarson H, Billings PR. Martin KA, et al. Among authors: samango sprouse ca. Am J Obstet Gynecol MFM. 2020 Aug;2(3):100152. doi: 10.1016/j.ajogmf.2020.100152. Epub 2020 Jun 25. Am J Obstet Gynecol MFM. 2020. PMID: 33345882 Free article.

2

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy.

Samango-Sprouse C, Banjevic M, Ryan A, Sigurjonsson S, Zimmermann B, Hill M, Hall MP, Westemeyer M, Saucier J, Demko Z, Rabinowitz M. Samango-Sprouse C, et al. Prenat Diagn. 2013 Jul;33(7):643-9. doi: 10.1002/pd.4159. Epub 2013 Jun 20. Prenat Diagn. 2013. PMID: 23712453 Free PMC article.

3

Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population.

Samango-Sprouse C, Kırkızlar E, Hall MP, Lawson P, Demko Z, Zneimer SM, Curnow KJ, Gross S, Gropman A. Samango-Sprouse C, et al. PLoS One. 2016 Aug 11;11(8):e0161045. doi: 10.1371/journal.pone.0161045. eCollection 2016. PLoS One. 2016. PMID: 27512996 Free PMC article.

4

Impact of early diagnosis and noninvasive prenatal testing (NIPT): Knowledge, attitudes, and experiences of parents of children with sex chromosome aneuploidies (SCAs).

Samango-Sprouse CA, Porter GF, Lasutschinkow PC, Tran SL, Sadeghin T, Gropman AL. Samango-Sprouse CA, et al. Prenat Diagn. 2020 Mar;40(4):470-480. doi: 10.1002/pd.5580. Epub 2019 Dec 4. Prenat Diagn. 2020. PMID: 31661555

5

Incidence of sex chromosome aneuploidy in a prenatal population: 27-year longitudinal study in Northern Italy.

Samango-Sprouse CA, Grati FR, Brooks M, Hamzik MP, Khaksari K, Gropman A, Taylor A, Malvestiti F, Grimi B, Liuti R, Milani S, Chinetti S, Trotta A, Agrati C, Repetti E, Martin KA. Samango-Sprouse CA, et al. Ultrasound Obstet Gynecol. 2023 Aug;62(2):266-272. doi: 10.1002/uog.26201. Ultrasound Obstet Gynecol. 2023. PMID: 36929222

6

Prenatal diagnosis and 47,XXY.

Simpson JL, Samango-Sprouse C. Simpson JL, et al. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):64-70. doi: 10.1002/ajmg.c.31356. Am J Med Genet C Semin Med Genet. 2013. PMID: 23359597 Review.

7

The benefits and limitations of cell-free DNA screening for 47, XXY (Klinefelter syndrome).

Samango-Sprouse C, Keen C, Sadeghin T, Gropman A. Samango-Sprouse C, et al. Prenat Diagn. 2017 May;37(5):497-501. doi: 10.1002/pd.5044. Epub 2017 Apr 17. Prenat Diagn. 2017. PMID: 28346690 Review.

8

A review of the intriguing interaction between testosterone and neurocognitive development in males with 47,XXY.

Samango-Sprouse CA, Yu C, Porter GF, Tipton ES, Lasutschinkow PC, Gropman AL. Samango-Sprouse CA, et al. Curr Opin Obstet Gynecol. 2020 Apr;32(2):140-146. doi: 10.1097/GCO.0000000000000612. Curr Opin Obstet Gynecol. 2020. PMID: 32004174 Review.

9

Neurodevelopmental outcome of prenatally diagnosed boys with 47,XXY (Klinefelter syndrome) and the potential influence of early hormonal therapy.

Samango-Sprouse CA, Tran SL, Lasutschinkow PC, Sadeghin T, Powell S, Mitchell FL, Gropman A. Samango-Sprouse CA, et al. Am J Med Genet A. 2020 Aug;182(8):1881-1889. doi: 10.1002/ajmg.a.61561. Epub 2020 Mar 27. Am J Med Genet A. 2020. PMID: 32220052

10

Speech and language development in children with 49,XXXXY syndrome.

Samango-Sprouse CA, Lasutschinkow PC, McLeod M, Porter GF, Powell S, St Laurent J, Sadeghin T, Gropman AL. Samango-Sprouse CA, et al. Am J Med Genet A. 2021 Dec;185(12):3567-3575. doi: 10.1002/ajmg.a.61767. Epub 2020 Jul 28. Am J Med Genet A. 2021. PMID: 32725750

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