Lagrave D - 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: lagrave d. 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

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.

Rose NC, Barrie ES, Malinowski J, Jenkins GP, McClain MR, LaGrave D, Leung ML; ACMG Professional Practice and Guidelines Committee. Electronic address: documents@acmg.net. Rose NC, et al. Among authors: lagrave d. Genet Med. 2022 Jul;24(7):1379-1391. doi: 10.1016/j.gim.2022.03.019. Epub 2022 May 24. Genet Med. 2022. PMID: 35608568 Free article. Review.

3

A cost-effectiveness analysis of cell free DNA as a replacement for serum screening for Down syndrome.

Walker BS, Jackson BR, LaGrave D, Ashwood ER, Schmidt RL. Walker BS, et al. Among authors: lagrave d. Prenat Diagn. 2015 May;35(5):440-6. doi: 10.1002/pd.4511. Prenat Diagn. 2015. PMID: 25273838

4

The impact of utilization of early aneuploidy screening on amniocenteses available for training in obstetrics and fetal medicine.

Rose NC, Lagrave D, Hafen B, Jackson M. Rose NC, et al. Among authors: lagrave d. Prenat Diagn. 2013 Mar;33(3):242-4. doi: 10.1002/pd.4052. Epub 2013 Jan 27. Prenat Diagn. 2013. PMID: 23354826

5

Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder.

Bhat G, LaGrave D, Millson A, Herriges J, Lamb AN, Matalon R. Bhat G, et al. Among authors: lagrave d. Eur J Med Genet. 2016 Sep;59(9):470-3. doi: 10.1016/j.ejmg.2016.05.014. Epub 2016 May 27. Eur J Med Genet. 2016. PMID: 27238888

6

A tradeoff analysis of risk cutoffs for the quadruple serum screen for Down syndrome.

Walker B, Ashwood ER, Jackson BR, Lagrave D. Walker B, et al. Among authors: lagrave d. Prenat Diagn. 2013 Dec;33(12):1201-6. doi: 10.1002/pd.4225. Epub 2013 Sep 12. Prenat Diagn. 2013. PMID: 24027169

7

Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature.

Herriges JC, Arch EM, Burgio PA, Baldwin EE, LaGrave D, Lamb AN, Toydemir RM. Herriges JC, et al. Among authors: lagrave d. J Child Neurol. 2019 Feb;34(2):86-93. doi: 10.1177/0883073818811454. Epub 2018 Nov 21. J Child Neurol. 2019. PMID: 30458662

8

Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing.

Miller CE, Krautscheid P, Baldwin EE, Tvrdik T, Openshaw AS, Hart K, Lagrave D. Miller CE, et al. Among authors: lagrave d. Am J Med Genet A. 2014 May;164A(5):1094-101. doi: 10.1002/ajmg.a.36453. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24665052

9

Tobacco and Cannabis Use During Pregnancy.

Hunsaker JJH, La'ulu SL, LaGrave D, Murphy W, Reichman HA, Snow TM, McMillin GA, Johnson-Davis KL, Genzen JR. Hunsaker JJH, et al. Among authors: lagrave d. Am J Clin Pathol. 2022 Jan 6;157(1):146-152. doi: 10.1093/ajcp/aqab093. Am J Clin Pathol. 2022. PMID: 34508553

10

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.

Rose NC, Barrie ES, Malinowski J, Jenkins GP, McClain MR, LaGrave D, Leung ML; ACMG Professional Practice and Guidelines Committee. Rose NC, et al. Among authors: lagrave d. Genet Med. 2022 Sep;24(9):1992. doi: 10.1016/j.gim.2022.07.002. Genet Med. 2022. PMID: 36063164 Free article. No abstract available.

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