Rhiannon Mellis (R Mellis, Mellis R)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 10

Top Topics

High Throughput Sequencing

Preterm Infants

Top Venues

Prenatal diagnosis

NIHR open research

BJOG : an international journal of obstetrics and gynaecology

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Natalie Jane Chandler, Brace P, Roberts R, Rhiannon Mellis
Likely pathogenic variant in the BICD2 gene in fetus presenting with non-immune hydrops. Prenatal diagnosis (2023)
Natalie Jane Chandler, Poppy Brace, Rowenna Roberts, Rhiannon Mellis
Likely pathogenic variant in the BICD2 gene in fetus presenting with non-immune hydrops. Prenatal diagnosis (2023)
Rhiannon Mellis, Dagmar Tapon, Nora Shannon, Esther Dempsey, Pranav Pandya, Lyn S Chitty, Melissa Hill
Implementing a rapid fetal exome sequencing service: What do parents and health professionals think? Prenatal diagnosis 42 (6) (2022)
Caitlin D Baptiste, Rhiannon Mellis, Vimla Aggarwal, Jenny Lord, Ruth Eberhardt, Mark D Kilby, Eamonn R Maher, Ronald Wapner, Jessica L Giordano, Lyn S Chitty
Fetal central nervous system anomalies: When should we offer exome sequencing? Prenatal diagnosis 42 (6) (2022)
Melissa Hill, Sian Ellard, Jane Fisher, Naomi Fulop, Marian Knight, Mark Kroese, Jean Ledger, Kerry Leeson-Beevers, Alec McEwan, Dominic McMullan, Rhiannon Mellis, Stephen Morris, Michael J Parker, Dagmar Tapon, Emma Baple, Laura Blackburn, Asya Choudry, Caroline Lafarge, Hannah McInnes-Dean, Michelle Peter, Rema Ramakrishnan, Lauren Roberts, Beverly Searle, Emma Smith, Holly Walton, Sarah L Wynn, Wing Han Wu, Lyn S Chitty
Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service. NIHR open research 2 (2022)
Natalie Jane Chandler, Elizabeth Scotchman, Rhiannon Mellis, Vijaya Ramachandran, Rowenna Roberts, Lyn S Chitty
Lessons learnt from prenatal exome sequencing. Prenatal diagnosis 42 (7) (2022)
Rhiannon Mellis, Kathryn Oprych, Elizabeth Scotchman, Melissa Hill, Lyn S Chitty
Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta-analysis. Prenatal diagnosis 42 (6) (2022)
Silvia Martin-Almedina, Kazim Ogmen, Ege Ozkan, Dionysios Grigoriadis, Christina Karapouliou, Noeline Nadarajah, Cathrine Ebbing, Jenny Lord, Rhiannon Mellis, Fanny Kortuem, Mary Beth Dinulos, Cassandra Polun, Sherri Bale, Giles Atton, Alexandra Robinson, Hallvard Reigstad, Gunnar Houge, Axel von der Wense, Wolf-Henning Becker, Steve Jeffery, Peter S Mortimer, Kristiana Gordon, Katherine S Josephs, Sarah Robart, Mark David Kilby, Stephanie Vallee, Jerome L Gorski, Maja Hempel, Siren Berland, Shehla Mohammed, Pia Ostergaard
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes. Genetics in medicine : official journal of the American College of Medical Genetics 23 (7) (2021)
Rhiannon Mellis, R Y Eberhardt, S J Hamilton, null null, D J McMullan, Mark David Kilby, E R Maher, M E Hurles, J L Giordano, V Aggarwal, D B Goldstein, R J Wapner, L S Chitty
Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it? BJOG : an international journal of obstetrics and gynaecology (2021)
Rhiannon Mellis, Natalie Chandler, Lucy Jenkins, Lyn S Chitty
The role of sonographic phenotyping in delivering an efficient noninvasive prenatal diagnosis service for FGFR3-related skeletal dysplasias. Prenatal diagnosis 40 (7) (2020)