Author

Lily Islam

Birmingham Women's Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam JacksoniD· 1 shared Adnan Yousaf Manzur· 1 shared Alan DonaldsoniD· 1 shared Alejandro SifrimiD· 1 shared Alex C. Magee· 1 shared Alexander J. M. BlakesiD· 1 shared Alison Hills· 1 shared Alison Ross· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam JacksonORCID

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2 papers

Recent·Most cited

Genetic Risk of Axonal Neuropathy Following Infection

J. Robert Harkness, John Henry McDermott, Shea Marsden, Peter Jamieson, Kay Metcalfe, Naz Khan, William L. Macken, Robert D. S. Pitceathly, Christopher J. Record, Reza Maroofian, Kloepa Kloepas, Ataf Hussain Sabir, Lily Islam, Saikat Santra, Enise Avcı Durmuşalioğlu, , William G. Newman

The paper identifies biallelic RCC1 variants causing an acute axonal neuropathy triggered by infection, with mechanistic overlap with ALS and GBS.

medRxiv · Oct 4, 2024 · PreprintGenetic & Genomic Medicine

The contribution of X-linked coding variation to severe developmental disorders

Hilary C. Martin, Eugene J. Gardner, Kaitlin E. Samocha, Joanna Kaplanis, Nadia A. Akawi, Alejandro Sifrim, Ruth Y. Eberhardt, Ana Lisa Taylor Tavares, Matthew D. C. Neville, Mari Niemi, Giuseppe Gallone, Jeremy F. McRae, Deciphering Developmental Disorders Study, Silvia Borras, Caroline Clark, , Therese Bradley

The paper analyzes X-linked coding variation in developmental disorders, finding similar rates in males and females and estimating pathogenicity of inherited variants.

Nature Communications · Jan 27, 2021Peer-reviewedGenetic & Genomic Medicine