Shamima Rahman

ORCID: 0000-0003-2088-730X

Also affiliated with Great Ormond Street Hospital for Children NHS Foundation Trust, Institute of Child Health, University College London

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: “OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases”.

OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases

Communications Biology(2023)10.1038/s42003-022-04303-x

N/A

0.749DataRank · unranked

146 citations

Kalpita R. Karan, Anna S. Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris +24 more

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w

N/A

0.515DataRank · unranked

18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Community Consensus Guidelines to Support FAIR Data Standards in Clinical Research Studies in Primary Mitochondrial Disease

Advanced Genetics(2021)10.1002/ggn2.202100047

N/A

0.208DataRank · unranked

3 citations

Laura E. MacMullen, John C. Campbell, John Christodoulou, Bruce H. Cohen, Thomas Klopstock +11 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294

N/A

0.208DataRank · unranked

3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Pantethine ameliorates dilated cardiomyopathy features in PPCS deficiency disorder in patients and cell line models

Communications Medicine(2025)10.1038/s43856-025-01017-z

N/A

0.104DataRank · unranked

1 citations

Tatjana Dorn, Barbara Gnutti, Yair Anikster, Sarah Kuebler, Rebecca C. Ahrens‐Nicklas +24 more

Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome Spectrum

Annals of Neurology(2023)10.1002/ana.26716

N/A

0DataRank · unranked

61 citations

Kierstin Keller, Julie P. Taylor, Alison J. Coffey, Li Shen, Danuta Krotoski +7 more

Safety of drug use in patients with a primary mitochondrial disease: An international Delphi‐based consensus

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12196

N/A

0DataRank · unranked

68 citations

David A. Brown, Mitchell E. Allen, Laurence A. Bindoff, Gráinne S. Gorman, Amel Karaa +12 more

Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities

Genetics in Medicine(2022)10.1016/j.gim.2022.11.001

N/A

0DataRank · unranked

30 citations

Madison Chilian, Ehsan Ghayoor Karimiani, Helga Progri, Daniela Buhaş, Melis Köse +17 more

An international classification of inherited metabolic disorders (ICIMD)

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12348

N/A

0DataRank · unranked

340 citations

Shamima Rahman, Markus A. Keller, Johannes Zschocke, ICIMD Advisory Group, Carlos R. Ferreira

Complex I deficiency remains the most frequent cause of Leigh syndrome spectrum

Brain Communications(2024)10.1093/braincomms/fcae470

N/A

0DataRank · unranked

6 citations

Shamima Rahman