Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study (Q46969020)

27 December 2017

title

Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study (English)

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27 December 2017

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Cassandra Szoeke

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27 December 2017

Alice V. Stanton

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27 December 2017

Terence J O'Brien

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27 December 2017

Ley Sander

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27 December 2017

John S. Duncan

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27 December 2017

Samuel Berkovic

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27 December 2017

Nicholas W. Wood

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27 December 2017

Gianpiero L. Cavalleri

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Gianpiero L Cavalleri

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Rachel A Gibson

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Ingrid E Scheffer

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Michael Hanna

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Michael G Hanna

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27 December 2017

author name string

Kevin V Shianna

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27 December 2017

Rinki Singh

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27 December 2017

John M Lynch

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Bronwyn Grinton

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27 December 2017

Kevin Murphy

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27 December 2017

Peter Kinirons

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27 December 2017

Deirdre O'Rourke

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27 December 2017

Dongliang Ge

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27 December 2017

Chantal Depondt

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27 December 2017

Kristl G Claeys

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Massimo Pandolfo

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27 December 2017

Curtis Gumbs

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Nicole Walley

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27 December 2017

James McNamara

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27 December 2017

John C Mulley

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27 December 2017

Kristen N Linney

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Leslie J Sheffield

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27 December 2017

Rodney A Radtke

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27 December 2017

Sarah K Tate

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27 December 2017

Stephanie L Chissoe

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27 December 2017

David Hosford

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27 December 2017

Tracey D Graves

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27 December 2017

Kai Eriksson

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27 December 2017

Anne-Mari Kantanen

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27 December 2017

Reetta Kalviainen

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27 December 2017

Colin P Doherty

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27 December 2017

Norman Delanty

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27 December 2017

Sanjay M Sisodiya

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David B Goldstein

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publication date

1 November 2007

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27 December 2017

published in

Lancet Neurology

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volume

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issue

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27 December 2017

page(s)

970-980

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27 December 2017

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

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7 January 2021

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Sacred disease secrets revealed: the genetics of human epilepsy

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Family study of epilepsy in first degree relatives: data from the Italian Episcreen Study

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Genetic influences on myoclonic and absence seizures

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Familial clustering of seizure types within the idiopathic generalized epilepsies

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Exploration of the genetic architecture of idiopathic generalized epilepsies.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Genetic association studies in epilepsy: "the truth is out there".

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Understanding human diversity

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Twenty-four-hour ambulatory blood pressure in men and women aged 17 to 80 years: the Allied Irish Bank Study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Genetic and environmental factors in febrile seizures: a Danish population-based twin study

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Fever, genes, and epilepsy

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Combining probability from independent tests: the weighted Z-method is superior to Fisher's approach

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Trimming, weighting, and grouping SNPs in human case-control association studies

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies

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https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor ?4 subunit (CHRNA4) and IGE

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2807%2970247-8

7 January 2021

10.1016/S1474-4422(07)70247-8

Identifiers

DOI

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27 December 2017

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27 December 2017