Author

Knight Sjl.

Centre for Human Genetics

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

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alistair T. PagnamentaiD· 1 shared Dimitris V. VavoulisiD· 1 shared Elizabeth Caruana GaliziaiD· 1 shared Jenny C. TayloriD· 1 shared M Armstrong· 1 shared Melissa M. PentonyiD· 1 shared Sanjay M. SisodiyaiD· 1 shared Simona BalestriniiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alistair T. PagnamentaORCID

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1 paper

Recent·Most cited

Whole genome sequencing identifies putative associations between genomic polymorphisms and clinical response to the antiepileptic drug levetiracetam

Dimitris V. Vavoulis, Alistair T. Pagnamenta, Knight Sjl., Melissa M. Pentony, M Armstrong, Elizabeth Caruana Galizia, Simona Balestrini, Sanjay M. Sisodiya, Jenny C. Taylor

This study uses whole genome sequencing to identify genomic variants associated with clinical response to levetiracetam in patients with epilepsy, finding common and rare variants in genes related to synaptic function and neurotransmission.

medRxiv · Sep 27, 2019 · PreprintGenetic & Genomic Medicine