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Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

Michael R. Johnson, A. Uitterlinden, P. May, 2018, The Lancet Neurology.

E‐cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer

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A case of Churg-Strauss syndrome associated with antiphospholipid antibodies.

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22q13 deletion syndrome.

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D. Weisenberger, G. Casey, G. Cooper, 2021 .

Carbon emission savings and short‐term health care impacts from telemedicine: An evaluation in epilepsy

H. Fowler, S. Sisodiya, S. Blenkinsop, 2021, Epilepsia.

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

Josemir W Sander, I. Scheffer, A. Palotie, 2015, EBioMedicine.