# Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/epilepsy-subtype-specific-copy-number-burden-observed-in-a-genome-wide-study-of/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Lisa‐Marie Niestroj,Eduardo Pérez‐Palma,Daniel P. Howrigan,Yadi Zhou,Feixiong Cheng,Elmo Saarentaus,Peter Nürnberg,Remi Stevelink,Mark J. Daly,Aarno Palotie,Dennis Lal,the Epi25 Collaborative,Yen‐Chen Anne Feng,Daniel P. Howrigan,Liam Abbott,Katherine Tashman,Felecia Cerrato,Dennis Lal,Claire Churchhouse,Namrata Gupta,Benjamin M. Neale,Samuel F. Berkovic,Holger Lerche,David B. Goldstein,Daniel H. Lowenstein,Gianpiero L. Cavalleri,Patrick Cossette,Chris Cotsapas,Peter De Jonghe,Tracy Dixon‐Salazar,Renzo Guerrini,Håkon Håkonarson,Erin L. Heinzen,Ingo Helbig,Patrick Kwan,Anthony G Marson,Slavé Petrovski,Sitharthan Kamalakaran,Sanjay M Sisodiya,Randy Stewart,Sarah Weckhuysen,Chantal Depondt,Dennis Dlugos,Ingrid E. Scheffer,Pasquale Striano,Catharine Freyer,Roland Krause,Patrick May,Kevin E. McKenna,Brigid M. Regan,Susannah T. Bellows,Costin Leu,Brigid M. Regan,Caitlin A. Bennett,Susannah T. Bellows,Esther C Johns,Alexandra MacDonald,Hannah Shilling,Rosemary Burgess,Dorien Weckhuysen,Melanie Bahlo,Terence J. O’Brien,Patrick Kwan,Slavé Petrovski,Marian Todaro,Sarah Weckhuysen,Hannah Stamberger,Peter De Jonghe,Chantal Depondt,Danielle M. Andrade,Tara Sadoway,Kelly Mo,Heinz Krestel,Sabina Gallati,Savvas Papacostas,Ioanna Kousiappa,George A. Tanteles,Katalin Štěrbová,Markéta Vlčková,Lucie Sedláčková,Petra Laššuthová,Karl Martin Klein,Felix Rosenow,Philipp S. Reif,Susanne Knake,Wolfram S. Kunz,Gábor Zsurka,Christian E. Elger,Jürgen Bauer,Michael Rademacher,Manuela Pendziwiat,Hiltrud Muhle,Annika Rademacher,Andreas van Baalen,Sarah von Spiczak,Ulrich Stephani,Zaid Afawi,Amos D. Korczyn,Moien Kanaan,Christina Canavati |
| Citations | 81 |
| DOI | 10.1093/brain/awaa171 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://academic.oup.com/brain/article-pdf/143/7/2106/33502843/awaa171.pdf |
| OpenAlex ID | https://openalex.org/W3036000905 |
| PMID | 32568404 |
| Type | article |
| Year | 2020 |

## Paper authors

- [Nerses Bebek](https://scholariq.org/researchers/nerses-bebek/)

## Paper journal

- [Brain](https://scholariq.org/journals/brain/)

## Paper primary topic

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

## Paper topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.