Author

Jacqueline de Belleroche

Imperial College LondonORCID 0000-0002-0689-9577Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alex G. Morris· 1 shared Alexandra Rother· 1 shared Bradley N. SmithiD· 1 shared Christopher E. ShawiD· 1 shared Intan Barul Akma Bakhtiar· 1 shared Midhat SalmaniD· 1 shared Simon D. ToppiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

7 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alex G. Morris

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1 paper

Recent·Most cited

Identification of co-segregating RUBCN and KANK1 mutations in a UK amyotrophic lateral sclerosis kindred

Midhat Salman, Intan Barul Akma Bakhtiar, Alex G. Morris, Alexandra Rother, Simon D. Topp, Christopher E. Shaw, Bradley N. Smith, Jacqueline de Belleroche

The paper identifies co-segregating RUBCN and KANK1 mutations in a UK ALS family, showing their association with disease and functional impact on cellular processes.

medRxiv · Jul 23, 2025 · PreprintGenetic & Genomic Medicine