Jamie M. Ellingford

Also affiliated with St Mary's Hospital, Manchester University NHS Foundation Trust, St Mary's Hospital, Health Innovation Manchester, Genomics England, Genomics (United Kingdom)

Biochemistry, Genetics and Molecular Biology

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 10 papers. Top paper: “A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations”.

A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations

Science Advances(2022)10.1126/sciadv.abn2265

N/A

0.803DataRank · unranked

210 citations

Mychel Morais, Jamie M. Ellingford, Sandhya Srinivasan, Richard W. Naylor, Craig Lawless +16 more

MRSD: A quantitative approach for assessing suitability of RNA-seq in the investigation of mis-splicing in Mendelian disease

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2021.12.014

N/A

0.510DataRank · unranked

29 citations

Algy Taylor, Gillian I. Rice, Nicola Whiffin, Hildegard Nikki Hall, William G. Newman +8 more

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4

N/A

0.370DataRank · unranked

8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438

N/A

0.360DataRank · unranked

10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Systematic identification of disease-causing promoter and untranslated region variants in 8,040 undiagnosed individuals with rare disease

medRxiv(2023)10.1101/2023.09.12.23295416

N/A

0.292DataRank · unranked

6 citations

Alexander J. M. Blakes, Ruebena Dawes, Scott D. Findlay, Jenny Lord, Susan Walker +17 more

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

medRxiv(2024)10.1101/2024.08.19.24312079

N/A

0.165DataRank · unranked

2 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +35 more

MRSD: a novel quantitative approach for assessing suitability of RNA-seq in the clinical investigation of mis-splicing in Mendelian disease

medRxiv(2021)10.1101/2021.03.19.21253973

N/A

0DataRank · unranked

5 citations

Algy Taylor, Gillian I. Rice, Nicola Whiffin, Hildegard Nikki Hall, William G. Newman +9 more

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.007

N/A

0DataRank · unranked

7 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +34 more

A basement membrane discovery pipeline uncovers network complexity, new regulators, and human disease associations

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.25.465762

N/A

0DataRank · unranked

6 citations

Mychel Morais, Jamie M. Ellingford, Sandhya Srinivasan, Richard W. Naylor, Craig Lawless +16 more

Paired DNA and RNA sequencing uncovers common and rare genetic variants regulating gene expression in the human retina

medRxiv(2025)10.1101/2025.04.25.25326445

N/A

0DataRank · unranked

0 citations

Ayellet V. Segrè, Kinga M. Bujakowska, Steve Haynes, Diana Baralle, Siddharth Banka +4 more