# Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/ultra-rare-genetic-variation-in-common-epilepsies-a-case-control-sequencing/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Andrew S. Allen,Susannah T. Bellows,Samuel F. Berkovic,Joshua Bridgers,Rosemary Burgess,Gianpiero L. Cavalleri,Seo‐Kyung Chung,Patrick Cossette,Norman Delanty,Dennis Dlugos,Michael P. Epstein,Catharine Freyer,David B. Goldstein,Erin L. Heinzen,Michael S. Hildebrand,Michael R. Johnson,Ruben Kuzniecky,Daniel H. Lowenstein,Anthony G Marson,Richard Mayeux,Caroline M. Mebane,Heather C. Mefford,Terence J. O’Brien,Ruth Ottman,Steven Petrou,Slavgé Petrovski,William Owen Pickrell,Annapurna Poduri,Rodney A. Radtke,Mark I. Rees,Brigid M. Regan,Zhong Ren,Ingrid E. Scheffer,Graeme J. Sills,Rhys H. Thomas,Quanli Wang,Bassel Abou‐Khalil,Brian K. Alldredge,Dina Amrom,Eva Andermann,Frédérick Andermann,Jocelyn F. Bautista,Samuel F. Berkovic,Judith Bluvstein,Alex Boro,Gregory D. Cascino,D. Consalvo,Patricia K. Crumrine,Orrin Devinsky,Dennis Dlugos,Michael P. Epstein,Miguel Fiol,Nathan B. Fountain,Jacqueline A. French,Catharine Freyer,Daniel J. Friedman,Eric B. Geller,Tracy A. Glauser,Simon Glynn,Kevin F. Haas,Sheryl R. Haut,Jean Hayward,Sandra L. Helmers,Sucheta M. Joshi,Andrés M. Kanner,Heidi E. Kirsch,Robert C. Knowlton,Eric H. Kossoff,Rachel Kuperman,Ruben Kuzniecky,Daniel H. Lowenstein,Paul Motika,Edward J. Novotny,Ruth Ottman,Juliann Paolicchi,Jack M. Parent,Kristen Park,Annapurna Poduri,Lynette G. Sadleir,Ingrid E. Scheffer,Renée A. Shellhaas,Elliott H. Sherr,Jerry J. Shih,Shlomo Shinnar,Rani K. Singh,Joseph Sirven,Michael C. Smith,Joseph Sullivan,Liu Lin Thio,Anu Venkat,Eileen P.G. Vining,Gretchen K. Von Allmen,Judith Weisenberg,Peter Widdess‐Walsh,Melodie R. Winawer |
| Citations | 234 |
| DOI | 10.1016/s1474-4422(16)30359-3 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.thelancet.com/article/S1474442216303593/pdf |
| OpenAlex ID | https://openalex.org/W2587877487 |
| PMID | 28102150 |
| Type | article |
| Year | 2017 |

## Paper authors

- [Ingrid E. Scheffer](https://scholariq.org/researchers/ingrid-e-scheffer/)
- [Joseph Sullivan](https://scholariq.org/researchers/joseph-sullivan/)
- [Ruben Kuzniecky](https://scholariq.org/researchers/ruben-kuzniecky/)
- [Orrin Devinsky](https://scholariq.org/researchers/orrin-devinsky/)
- [Tracy A. Glauser](https://scholariq.org/researchers/tracy-a-glauser/)

## Paper primary topic

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Paper topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)

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