Rhiannon Mellis

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

Jenny Lord, Dominic McMullan, Ruth Y. Eberhardt et al. · The Lancet · 2019 · 708 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Lord J, McMullan DJ, Eberhardt RY et al. · Yearbook of pediatric endocrinology · 2019 · 155 citations

Life Sciences, Genetics, Molecular Genetics +17

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

Elizabeth Scotchman, Natalie Chandler, Rhiannon Mellis et al. · Clinical Chemistry · 2019 · 90 citations · Full text

Medicine, Genetics, Obstetrics +15

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

Rhiannon Mellis, Eberhardt RY, SJ Hamilton et al. · BJOG An International Journal of Obstetrics & Gynaecology · 2021 · 67 citations · Full text

Medicine, Genetics, Obstetrics +17

Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges

Melissa Hill, Jennifer Hammond, Celine Lewis et al. · European Journal of Human Genetics · 2020 · 53 citations · Full text

Life Sciences, Genetics, Pediatrics +14