Mone F - Search Results

1

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

Blayney GV, Laffan E, Jacob PA, Baptiste CD, Gabriel H, Sparks TN, Yaron Y, Norton ME, Diderich K, Wang Y, Chong K, Chitayat D, Saini N, Aggarwal S, Pauta M, Borrell A, Gilmore K, Chandler NJ, Allen S, Vora N, Noor A, Monaghan C, Kilby MD, Wapner RJ, Chitty LS, Mone F. Blayney GV, et al. Among authors: mone f. Prenat Diagn. 2024 Apr;44(4):422-431. doi: 10.1002/pd.6466. Epub 2023 Dec 6. Prenat Diagn. 2024. PMID: 38054560 Free PMC article.

2

Prenatal detection of structural cardiac defects and presence of associated anomalies: a retrospective observational study of 1262 fetal echocardiograms.

Mone F, Walsh C, Mulcahy C, McMahon CJ, Farrell S, MacTiernan A, Segurado R, Mahony R, Higgins S, Carroll S, McParland P, McAuliffe FM. Mone F, et al. Prenat Diagn. 2015 Jun;35(6):577-82. doi: 10.1002/pd.4575. Epub 2015 Mar 10. Prenat Diagn. 2015. PMID: 25663276

3

Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.

Mone F, Quinlan-Jones E, Kilby MD. Mone F, et al. Eur J Obstet Gynecol Reprod Biol. 2018 Dec;231:19-24. doi: 10.1016/j.ejogrb.2018.10.016. Epub 2018 Oct 6. Eur J Obstet Gynecol Reprod Biol. 2018. PMID: 30317140 Review.

4

Exome sequencing in the assessment of congenital malformations in the fetus and neonate.

Mone F, Quinlan-Jones E, Ewer AK, Kilby MD. Mone F, et al. Arch Dis Child Fetal Neonatal Ed. 2019 Jul;104(4):F452-F456. doi: 10.1136/archdischild-2018-316352. Epub 2019 Feb 1. Arch Dis Child Fetal Neonatal Ed. 2019. PMID: 30816854 Free article. Review.

5

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.

Chong HP, Hamilton S, Mone F, Cheung KW, Togneri FS, Morris RK, Quinlan-Jones E, Williams D, Allen S, McMullan DJ, Kilby MD. Chong HP, et al. Among authors: mone f. Prenat Diagn. 2019 Nov;39(12):1064-1069. doi: 10.1002/pd.5545. Epub 2019 Aug 22. Prenat Diagn. 2019. PMID: 31393021

6

Evolution of a prenatal genetic clinic-A 10-year cohort study.

Mone F, O'Connor C, Hamilton S, Quinlan-Jones E, Allen S, Marton T, Williams D, Kilby MD. Mone F, et al. Prenat Diagn. 2020 Apr;40(5):618-625. doi: 10.1002/pd.5661. Epub 2020 Feb 21. Prenat Diagn. 2020. PMID: 32037575

7

COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic review.

Mone F, Eberhardt RY, Morris RK, Hurles ME, McMullan DJ, Maher ER, Lord J, Chitty LS, Giordano JL, Wapner RJ, Kilby MD; CODE Study Collaborators. Mone F, et al. Ultrasound Obstet Gynecol. 2021 Jan;57(1):43-51. doi: 10.1002/uog.22072. Epub 2020 Dec 3. Ultrasound Obstet Gynecol. 2021. PMID: 32388881 Free article.

8

Diagnostic and perinatal outcomes in consanguineous couples with a structural fetal anomaly: A cohort study.

Mone F, Doyle S, Ahmad A, Abu Subieh H, Hamilton S, Allen S, Marton T, Williams D, Kilby MD. Mone F, et al. Acta Obstet Gynecol Scand. 2021 Mar;100(3):418-424. doi: 10.1111/aogs.14036. Epub 2020 Nov 27. Acta Obstet Gynecol Scand. 2021. PMID: 33128783 Free article.

9

The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort Study.

Mone F, Stott BK, Hamilton S, Seale AN, Quinlan-Jones E, Allen S, Hurles ME, McMullan DJ, Maher ER, Kilby MD. Mone F, et al. Fetal Diagn Ther. 2021 Feb 5:1-8. doi: 10.1159/000512488. Online ahead of print. Fetal Diagn Ther. 2021. PMID: 33550297

10

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021.

Mone F, McMullan DJ, Williams D, Chitty LS, Maher ER, Kilby MD; Fetal Genomics Steering Group of the British Society for Genetic Medicine; Royal College of Obstetricians and Gynaecologists. Mone F, et al. BJOG. 2021 Aug;128(9):e39-e50. doi: 10.1111/1471-0528.16616. Epub 2021 Feb 15. BJOG. 2021. PMID: 33590639 Review.

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