Joanna Poulton

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 3 papers. Top paper: “Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations”.

Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations

Human Molecular Genetics(2020)10.1093/hmg/ddaa077

N/A

0DataRank · unranked

78 citations

Xiaoping Huang, Diana Nguyen, Mario K. Shammas, Beverly P Wu, Eszter Dombi +5 more

Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease

Human Molecular Genetics(2022)10.1093/hmg/ddac002

N/A

0DataRank · unranked

13 citations

Jia Xin Tang, Kate Sergeant, Marco F Moedas, Charlotte M Zierz, David Moore +13 more

Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis

Heliyon(2024)10.1016/j.heliyon.2024.e24975

N/A

0DataRank · unranked

11 citations

Marcel Weinreich, James Lee, Allan C. Shaw, Laura Ferraiuolo, Heather Mortiboys +20 more