Ruth Newbury‐Ecob

Also affiliated with St Michaels Hospital

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect”.

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect

Brain(2020)10.1093/brain/awaa176

N/A

0DataRank · unranked

49 citations

Emanuela Iovino, Luke Mansard, Christel Vaché, David Baux, Emma Bedoukian +15 more

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Human Molecular Genetics(2020)10.1093/hmg/ddaa050

N/A

0DataRank · unranked

42 citations

Athina Ververi, Ana Beleza‐Meireles, Weizhen Ji, Emily K. Mis, Quinten Patterson +25 more

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more

Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions

European Journal of Human Genetics(2025)10.1038/s41431-025-01916-8

N/A

0DataRank · unranked

2 citations

Xiaonan Zhao, Nichole Owen, Tom Evans, Muriel Holder‐Espinasse, Nayana Lahiri +28 more