Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

Authors

Karen Oliver (ORCID: https://orcid.org/0000-0001-5188-6153)
Bronwyn E. Grinton (ORCID: https://orcid.org/0000-0003-4880-2486)
Colin A. Ellis (ORCID: https://orcid.org/0000-0003-2152-8106)
Ingrid Eileen Scheffer (ORCID: https://orcid.org/0000-0002-2311-2174)

Institutions

Walter and Eliza Hall Institute of Medical Research (AU)
Austin Hospital (AU)
Austin Health (AU)
University of Pennsylvania (US)

Publication Details

Journal: EBioMedicine
Published: 2024-10-31
DOI: https://doi.org/10.1016/j.ebiom.2024.105404
Citations: 21
Primary Topic: Genomics and Rare Diseases
Type: article
Field-Weighted Citation Impact: 11.56

Funders

Australian Government
State Government of Victoria
National Institutes of Health
Medical Research Council
National Health and Medical Research Council

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article

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

Karen Oliver, Bronwyn E. Grinton, Colin A. Ellis, Ingrid Eileen Scheffer

Oct 31, 2024

21 citations

EBioMedicine

Genomics and Rare Diseases

11.56

article

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

Karen Oliver, Bronwyn E. Grinton, Colin A. Ellis, Ingrid Eileen Scheffer

October 31, 2024article en

21 citations

Abstract

No abstract available for this paper.

EBioMedicineVol. 109

Walter and Eliza Hall Institute of Medical Research (AU), Austin Hospital (AU), Austin Health (AU), University of Pennsylvania (US)

Australian Government, State Government of Victoria, National Institutes of Health, Medical Research Council, National Health and Medical Research Council

Openalex Percentile: Top 1%

Genomics and Rare Diseases

11.56

DOI Open Access PDF OpenAlex

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