Elizabeth Fisher

Also affiliated with Royal Prince Alfred Hospital, The London College, National Hospital for Neurology and Neurosurgery, University College London, Vanderbilt University Medical Center

MedicineBiochemistry, 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

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 13 papers. Top paper: “Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain”.

Patient-specific Alzheimer-like pathology in trisomy 21 cerebral organoids reveals BACE2 as a gene dose-sensitive AD suppressor in human brain

Molecular Psychiatry(2020)10.1038/s41380-020-0806-5

N/A

2.9DataRank · unranked

124 citations

Pollyanna Goh, Aoife Murray, Erik Portelius, Eleni Gkanatsiou, Gillian Gough +41 more

FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation

Science Advances(2021)10.1126/sciadv.abf8660

N/A

0.631DataRank · unranked

66 citations

Agnieszka M. Ule, Maria Giovanna Garone, Brian Tsang, Francesca Mattedi, P. Andrew Chong +15 more

Common ALS/FTD risk variants in UNC13A exacerbate its cryptic splicing and loss upon TDP-43 mislocalization

Research Square(2021)10.21203/rs.3.rs-386600/v1

N/A

0.442DataRank · unranked

18 citations

Oscar G. Wilkins, Matthew J. Keuss, Sarah E. Hill, Matteo Zanovello, Weaverly Lee +18 more

Maternal iron deficiency perturbs embryonic cardiovascular development in mice

Nature Communications(2021)10.1038/s41467-021-23660-5

N/A

0DataRank · unranked

56 citations

Nikita Ved, Dorota Szumska, Jacob E. Munro, Michael Troup, Shelley Harris +17 more

A landmark-free morphometrics pipeline for high-resolution phenotyping: application to a mouse model of Down syndrome

Development(2021)10.1242/dev.188631

N/A

0DataRank · unranked

51 citations

Yushi Redhead, Marta Vidal‐García, Lucas Lo Vercio, Wei Liu, Elizabeth Fisher +5 more

Building the Future Therapies for Down Syndrome: The Third International Conference of the T21 Research Society

Molecular Syndromology(2021)10.1159/000514437

N/A

0DataRank · unranked

10 citations

Yann Hérault, Pablo Helguera, María Martínez de Lagrán, Anna Vazquez, Bradley T. Christian +29 more

Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia

Journal of Clinical Investigation(2020)10.1172/jci139741

N/A

0DataRank · unranked

258 citations

Jack Humphrey, Sarah Pickles, Anna‐Leigh Brown, Sarah E. Hill, Jennifer M. Kachergus +47 more

Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down Syndrome-related phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.11.430828

N/A

0DataRank · unranked

1 citations

Heather Cater, Sheona Watson-Scales, Simon Greenaway, Jennifer Müller, Dorota Gibbins +21 more

TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A

Nature(2022)10.1038/s41586-022-04436-3

N/A

0DataRank · unranked

525 citations

Oscar G. Wilkins, Matthew J. Keuss, Sarah E. Hill, Matteo Zanovello, Weaverly Colleen Lee +90 more

Creation of de novo cryptic splicing for ALS and FTD precision medicine

Science(2024)10.1126/science.adk2539

N/A

0DataRank · unranked

34 citations

Max Z. Y. J. Chien, Josette J Wlaschin, Simone Barattucci, Peter Harley, Francesca Mattedi +19 more

DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.10.03.616443

N/A

0DataRank · unranked

0 citations

Amy Southern, Pratik Vikhe, Eva Lana‐Elola, Sheona Watson-Scales, Dorota Gibbins +13 more

DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome

eLife(2025)10.7554/elife.101969

N/A

0DataRank · unranked

0 citations

Amy Southern, Pratik Vikhe, Eva Lana‐Elola, Sheona Watson-Scales, Dorota Gibbins +13 more

Interaction of sexual dimorphism and gene dosage imbalance in skeletal deficits associated with Down syndrome

Bone(2020)10.1016/j.bone.2020.115367

N/A

0DataRank · unranked

30 citations

Jonathan LaCombe, Rachel Long, Eva Lana‐Elola, Sheona Watson-Scales, Joseph M. Wallace +4 more