Christopher E. Shaw

Also affiliated with King's College London, EIA University, UK Dementia Research Institute

MedicineNeuroscience

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 10 papers. Top paper: “Co-deposition of SOD1, TDP-43 and p62 proteinopathies in ALS: evidence for multifaceted pathways underlying neurodegeneration”.

Co-deposition of SOD1, TDP-43 and p62 proteinopathies in ALS: evidence for multifaceted pathways underlying neurodegeneration

Acta Neuropathologica Communications(2022)10.1186/s40478-022-01421-9

N/A

1.3DataRank · unranked

54 citations

Jennifer A. Fifita, Alison Hogan, Natalie Grima, Bradley Smith, Claire Troakes +6 more

Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS

PLoS ONE(2012)10.1371/journal.pone.0035333

N/A

0.606DataRank · unranked

56 citations

Christiaan G. J. Saris, Wouter van Rheenen, Lude Franke, Ritsert C. Jansen, Michael A. van Es +23 more

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

npj Genomic Medicine(2022)10.1038/s41525-021-00267-9

N/A

0.571DataRank · unranked

44 citations

Alfredo Iacoangeli, Joke J.F.A. van Vugt, Harry Bowles, Matthieu Moisse, Ramona A.J. Zwamborn +42 more

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

JAMA Neurology(2021)10.1001/jamaneurol.2021.2598

N/A

0DataRank · unranked

85 citations

Ruth Chia, Danny E. Miller, Rachel Li, Ravindran Kumaran, Yevgeniya Abramzon +87 more

Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

Neuron(2022)10.1016/j.neuron.2021.12.019

N/A

0DataRank · unranked

124 citations

Johnathan Cooper‐Knock, Annika K. Weimer, Minyi Shi, Tobias Moll, Jack N.G. Marshall +48 more

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Brain Communications(2020)10.1093/braincomms/fcaa064

N/A

0DataRank · unranked

56 citations

Steven Boeynaems, Mathias De Decker, Joke J.F.A. van Vugt, Lindy Kool, H. Stephan Goedee +81 more

The impact of age on genetic testing decisions in amyotrophic lateral sclerosis

Brain(2022)10.1093/brain/awac279

N/A

0DataRank · unranked

50 citations

Alfredo Iacoangeli, Sarah Opie-Martin, Joke J.F.A. van Vugt, Ahmad Al Khleifat, Andrea Bredin +29 more

U7 small nuclear RNA splice-switching therapeutics for STMN2 and UNC13A in Amyotrophic Lateral Sclerosis

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.11.26.690143

N/A

0DataRank · unranked

1 citations

Travis E. Solomon, Sarah Pickles, Peter Harley, Michela Barioglio, Christoph Schweingruber +16 more

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

UNC Libraries(2020)10.17615/pbds-w495

N/A

0DataRank · unranked

0 citations

David Craig, Liming Qu, Jonathan L. Haines, Taniesha Morgan, Mark A. Sager +95 more

CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis

Brain(2020)10.1093/brain/awaa039

N/A

0DataRank · unranked

87 citations

Marianne Hallupp, Hamideh Shahheydari, Audrey Ragagnin, Zac Chatterton, Francine Carew‐Jones +34 more