Gregory M. Findlay

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 5 papers. Top paper: “Accurate classification of BRCA1 variants with saturation genome editing”.

Accurate classification of BRCA1 variants with saturation genome editing

Nature(2018)10.1038/s41586-018-0461-z

N/A

1.0DataRank · unranked

914 citations

Riza M. Daza, Beth Martin, Melissa D. Zhang, Anh P. Leith, Molly Gasperini +6 more

spinDrop: a droplet microfluidic platform to maximise single-cell sequencing information content

Nature Communications(2023)10.1038/s41467-023-40322-w

N/A

0DataRank · unranked

64 citations

Tomasz S. Kamiński, David B. Morse, Marcin Tabaka, Anna L. Ellermann, Timo N. Kohler +7 more

spinDrop: a droplet microfluidic platform to maximise single-cell sequencing information content

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.12.523500

N/A

0DataRank · unranked

2 citations

Tomasz S. Kamiński, David B. Morse, Marcin Tabaka, Anna L. Ellermann, Timo N. Kohler +7 more

Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders

medRxiv(2025)10.1101/2025.04.08.25325442

N/A

0DataRank · unranked

13 citations

Hyung Chul Kim, Ayanfeoluwa Adedeji, Elsa Leitão, Ruebena Dawes, Yuyang Chen +37 more

Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

medRxiv(2025)10.1101/2025.08.13.25333306

N/A

0DataRank · unranked

5 citations

Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe, Javeria Raza Alvi, Florence Amblard +69 more