Grati FR - Search Results

1

Benn P, Ferreira J, Grati FR. Benn P, et al. Among authors: grati fr. Genet Med. 2020 Feb;22(2):444-445. doi: 10.1038/s41436-019-0665-0. Epub 2019 Oct 1. Genet Med. 2020. PMID: 31570803 Free article. No abstract available.

2

Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results.

Grati FR, Malvestiti F, Ferreira JC, Bajaj K, Gaetani E, Agrati C, Grimi B, Dulcetti F, Ruggeri AM, De Toffol S, Maggi F, Wapner R, Gross S, Simoni G. Grati FR, et al. Genet Med. 2014 Aug;16(8):620-4. doi: 10.1038/gim.2014.3. Epub 2014 Feb 13. Genet Med. 2014. PMID: 24525917 Free article.

3

Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.

Grati FR, Ferreira JC, Bajaj K. Grati FR, et al. Am J Obstet Gynecol. 2014 Dec;211(6):711-2. doi: 10.1016/j.ajog.2014.07.015. Epub 2014 Jul 12. Am J Obstet Gynecol. 2014. PMID: 25025943 No abstract available.

4

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.

Grati FR, Molina Gomes D, Ferreira JC, Dupont C, Alesi V, Gouas L, Horelli-Kuitunen N, Choy KW, García-Herrero S, de la Vega AG, Piotrowski K, Genesio R, Queipo G, Malvestiti B, Hervé B, Benzacken B, Novelli A, Vago P, Piippo K, Leung TY, Maggi F, Quibel T, Tabet AC, Simoni G, Vialard F. Grati FR, et al. Prenat Diagn. 2015 Aug;35(8):801-9. doi: 10.1002/pd.4613. Epub 2015 Jun 24. Prenat Diagn. 2015. PMID: 25962607

5

The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.

Grati FR, Bajaj K, Malvestiti F, Agrati C, Grimi B, Malvestiti B, Pompilii E, Maggi F, Gross S, Simoni G, Ferreira JC. Grati FR, et al. Prenat Diagn. 2015 Oct;35(10):994-8. doi: 10.1002/pd.4659. Epub 2015 Sep 11. Prenat Diagn. 2015. PMID: 26211640

6

Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications.

Ferreira JC, Grati FR, Bajaj K, Malvestiti F, Grimi MB, Trotta A, Liuti R, Milani S, Branca L, Hartman J, Maggi F, Simoni G, Gross SJ. Ferreira JC, et al. Among authors: grati fr. Prenat Diagn. 2016 Dec;36(12):1146-1155. doi: 10.1002/pd.4951. Epub 2016 Nov 18. Prenat Diagn. 2016. PMID: 27770451

7

Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.

Grati FR, Bajaj K, Zanatta V, Malvestiti F, Malvestiti B, Marcato L, Grimi B, Maggi F, Simoni G, Gross SJ, Ferreira J. Grati FR, et al. Prenat Diagn. 2017 Oct;37(10):1017-1027. doi: 10.1002/pd.5138. Epub 2017 Sep 6. Prenat Diagn. 2017. PMID: 28801976

8

Comment on "The clinical utility of genome-wide non invasive prenatal screening".

Grati FR, Benn P. Grati FR, et al. Prenat Diagn. 2017 Oct;37(10):1050-1052. doi: 10.1002/pd.5098. Prenat Diagn. 2017. PMID: 29057529 No abstract available.

9

Genome-wide non-invasive prenatal screening for all cytogenetically visible imbalances.

Benn P, Grati FR. Benn P, et al. Among authors: grati fr. Ultrasound Obstet Gynecol. 2018 Apr;51(4):429-433. doi: 10.1002/uog.19014. Ultrasound Obstet Gynecol. 2018. PMID: 29363829 Free article. No abstract available.

10

Rare autosomal trisomies: comparison of detection through cell-free DNA analysis and direct chromosome preparation of chorionic villus samples.

Benn P, Malvestiti F, Grimi B, Maggi F, Simoni G, Grati FR. Benn P, et al. Among authors: grati fr. Ultrasound Obstet Gynecol. 2019 Oct;54(4):458-467. doi: 10.1002/uog.20383. Epub 2019 Sep 3. Ultrasound Obstet Gynecol. 2019. PMID: 31237735 Free article.

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