James Cranley

Wellcome/MRC Cambridge Stem Cell Institute

Also affiliated with University of Cambridge, Papworth 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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 5 papers. Top paper: “Spatially resolved multiomics of human cardiac niches”.

Spatially resolved multiomics of human cardiac niches

Nature(2023)10.1038/s41586-023-06311-1

N/A

5.6DataRank · unranked

405 citations

James Cranley, Daniele Muraro, Antonio M. A. Miranda, Siew Yen Ho, Anna Wilbrey-Clark +33 more

Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies

Science(2022)10.1126/science.abo1984

N/A

0.818DataRank · unranked

233 citations

Eric L. Lindberg, Henrike Maatz, Antonio M. A. Miranda, Anissa Viveiros, Nikolay Shvetsov +50 more

inVAE: Conditionally invariant representation learning for generating multivariate single-cell reference maps

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.12.06.627196

N/A

0.302DataRank · unranked

6 citations

Ferdinand Kapl, Duy Pham, Batuhan Cakir, Takahiro Jimba, James Cranley +7 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more