Déborah Morris-Rosendahl

Guy's and St Thomas' NHS Foundation Trust

Also affiliated with Royal Brompton & Harefield NHS Foundation Trust, Harefield Hospital, Imperial College London

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 4 papers. Top paper: “De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry”.

De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry

UNC Libraries(2020)10.17615/yfnk-1f57

N/A

0DataRank · unranked

6 citations

P. Pennekamp, M. Wöste, M.R. Knowles, J. Atkinson, S.K. Dutcher +25 more

BRAT1–related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients

European Journal of Human Genetics(2023)10.1038/s41431-023-01410-z

N/A

0DataRank · unranked

10 citations

Stéphanie Valence, Geoffroy Delplancq, Reza Maroofian, Andrea Accogli, Emanuele Agolini +85 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

Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta Syndrome

The Journal of Pediatrics(2025)10.1016/j.jpeds.2025.114499

N/A

0DataRank · unranked

5 citations

Eveline Y. Wu, Déborah Morris-Rosendahl, Kenneth N. Olivier, Sharon Dell, Scott D. Sagel +13 more