Mellis R - Search Results

Year	Number of Results
1969	1
1997	1
2018	1
2019	2
2020	4
2021	3
2022	7
2023	2
2024	1

1

Should we offer prenatal exome sequencing for intrauterine growth restriction or short long bones? A systematic review and meta-analysis.

Mone F, Mellis R, Gabriel H, Baptiste C, Giordano J, Wapner R, Chitty LS. Mone F, et al. Among authors: mellis r. Am J Obstet Gynecol. 2023 Apr;228(4):409-417.e4. doi: 10.1016/j.ajog.2022.09.045. Epub 2022 Oct 7. Am J Obstet Gynecol. 2023. PMID: 36209938 Free article. Review.

2

Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta-analysis.

Mellis R, Oprych K, Scotchman E, Hill M, Chitty LS. Mellis R, et al. Prenat Diagn. 2022 May;42(6):662-685. doi: 10.1002/pd.6115. Epub 2022 May 7. Prenat Diagn. 2022. PMID: 35170059 Free PMC article.

3

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.

Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Among authors: mellis r. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.

4

Next-generation sequencing and the impact on prenatal diagnosis.

Mellis R, Chandler N, Chitty LS. Mellis R, et al. Expert Rev Mol Diagn. 2018 Aug;18(8):689-699. doi: 10.1080/14737159.2018.1493924. Epub 2018 Jul 18. Expert Rev Mol Diagn. 2018. PMID: 29962246 Review.

5

Lessons learnt from prenatal exome sequencing.

Chandler NJ, Scotchman E, Mellis R, Ramachandran V, Roberts R, Chitty LS. Chandler NJ, et al. Among authors: mellis r. Prenat Diagn. 2022 Jun;42(7):831-844. doi: 10.1002/pd.6165. Epub 2022 May 7. Prenat Diagn. 2022. PMID: 35506549 Free PMC article.

6

Fetal central nervous system anomalies: When should we offer exome sequencing?

Baptiste C, Mellis R, Aggarwal V, Lord J, Eberhardt R, Kilby MD, Maher ER, Wapner R, Giordano J, Chitty L. Baptiste C, et al. Among authors: mellis r. Prenat Diagn. 2022 May;42(6):736-743. doi: 10.1002/pd.6145. Epub 2022 Apr 20. Prenat Diagn. 2022. PMID: 35411553 Review.

7

Update on the use of exome sequencing in the diagnosis of fetal abnormalities.

Ferretti L, Mellis R, Chitty LS. Ferretti L, et al. Among authors: mellis r. Eur J Med Genet. 2019 Aug;62(8):103663. doi: 10.1016/j.ejmg.2019.05.002. Epub 2019 May 11. Eur J Med Genet. 2019. PMID: 31085342 Review.

8

Implementing a rapid fetal exome sequencing service: What do parents and health professionals think?

Mellis R, Tapon D, Shannon N, Dempsey E, Pandya P, Chitty LS, Hill M. Mellis R, et al. Prenat Diagn. 2022 May;42(6):783-795. doi: 10.1002/pd.6140. Epub 2022 Apr 14. Prenat Diagn. 2022. PMID: 35383981 Free PMC article.

9

Noninvasive Prenatal Diagnosis of Single-Gene Diseases: The Next Frontier.

Scotchman E, Chandler NJ, Mellis R, Chitty LS. Scotchman E, et al. Among authors: mellis r. Clin Chem. 2020 Jan 1;66(1):53-60. doi: 10.1373/clinchem.2019.304238. Clin Chem. 2020. PMID: 31843868

10

Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?

Mellis R, Eberhardt RY, Hamilton SJ; PAGE Consortium; McMullan DJ, Kilby MD, Maher ER, Hurles ME, Giordano JL, Aggarwal V, Goldstein DB, Wapner RJ, Chitty LS. Mellis R, et al. BJOG. 2022 Jan;129(1):52-61. doi: 10.1111/1471-0528.16869. Epub 2021 Sep 14. BJOG. 2022. PMID: 34411415 Free PMC article.

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