Hannah M. Mitchison

Also affiliated with Institute of Child Health, University College London

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 9 papers. Top paper: “An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes”.

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201

N/A

0.831DataRank · unranked

253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 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

Axonemal structures reveal mechanoregulatory and disease mechanisms

Nature(2023)10.1038/s41586-023-06140-2

N/A

0DataRank · unranked

169 citations

Miao Gui, Simona A. Velkova, Mahmoud R. Fassad, Robert A. Hirst, Eric G. Haarman +6 more

IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans

PLoS Genetics(2023)10.1371/journal.pgen.1010796

N/A

0DataRank · unranked

26 citations

Oscar A. Cabrera, Julia Hoefele, Dinu Antony, Kaman Wu, Michael W. Stuck +21 more

Mutations of DNAI1 in Primary Ciliary Dyskinesia: Evidence of Founder Effect in a Common Mutation

UNC Libraries(2020)10.17615/evkw-v287

N/A

0DataRank · unranked

0 citations

Heike Olbrich, Anne-Marie Bridoux, Franck Ceppa, Lucy C. Morgan, Michael R. Knowles +20 more

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

Science(2024)10.1126/science.adf5489

N/A

0DataRank · unranked

48 citations

Sabrina Méchaussier, Patricia L. Yeyati, Fraser McPhie, Jacob R. Anderson, Chen Jing Khoo +75 more

Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia

European Journal of Human Genetics(2024)10.1038/s41431-024-01599-7

N/A

0DataRank · unranked

13 citations

Miranda Galey, Lizi Briggs, Matthew Edwards, Claire Hogg, Shibu John +18 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

0DataRank · unranked

3 citations

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

DYX1C1 is required for axonemal dynein assembly and ciliary motility

UNC Libraries(2020)10.17615/z79a-w507

N/A

0DataRank · unranked

0 citations

Cecilia Lo, Hannah M. Mitchison, Michael R. Knowles, Maimoona A. Zariwala, Ronald Roepman +6 more