(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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2

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27 December 2017

Cassandra Szoeke

7

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27 December 2017

Alice V. Stanton

26

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27 December 2017

Terence J O'Brien

32

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27 December 2017

Ley Sander

33

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27 December 2017

John S. Duncan

34

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27 December 2017

Samuel Berkovic

36

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27 December 2017

Nicholas W. Wood

37

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27 December 2017

Gianpiero L. Cavalleri

Gianpiero L Cavalleri

1

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Rachel A Gibson

Rachel A Gibson

24

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Ingrid Scheffer

35

Ingrid E Scheffer

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Michael Hanna

28

Michael G Hanna

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27 December 2017

author name string

Kevin V Shianna

3

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27 December 2017

Rinki Singh

4

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27 December 2017

John M Lynch

5

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27 December 2017

Bronwyn Grinton

6

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27 December 2017

Kevin Murphy

8

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27 December 2017

Peter Kinirons

9

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27 December 2017

Deirdre O'Rourke

10

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27 December 2017

Dongliang Ge

11

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27 December 2017

Chantal Depondt

12

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27 December 2017

Kristl G Claeys

13

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27 December 2017

Massimo Pandolfo

14

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27 December 2017

Curtis Gumbs

15

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27 December 2017

Nicole Walley

16

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27 December 2017

James McNamara

17

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27 December 2017

John C Mulley

18

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27 December 2017

Kristen N Linney

19

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27 December 2017

Leslie J Sheffield

20

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27 December 2017

Rodney A Radtke

21

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27 December 2017

Sarah K Tate

22

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27 December 2017

Stephanie L Chissoe

23

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27 December 2017

David Hosford

25

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27 December 2017

Tracey D Graves

27

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27 December 2017

Kai Eriksson

29

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27 December 2017

Anne-Mari Kantanen

30

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27 December 2017

Reetta Kalviainen

31

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27 December 2017

Colin P Doherty

38

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27 December 2017

Norman Delanty

39

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27 December 2017

Sanjay M Sisodiya

40

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27 December 2017

David B Goldstein

41

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27 December 2017

publication date

1 November 2007

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27 December 2017

published in

Lancet Neurology

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27 December 2017

volume

6

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27 December 2017

page(s)

970-980

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27 December 2017

issue

11

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27 December 2017

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

1 reference

7 January 2021

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

1 reference

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

7 January 2021

Sacred disease secrets revealed: the genetics of human epilepsy

1 reference

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

1 reference

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

7 January 2021

Genetic influences on myoclonic and absence seizures

1 reference

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

1 reference

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.

1 reference

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".

1 reference

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?

1 reference

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

1 reference

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

7 January 2021

Understanding human diversity

1 reference

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

1 reference

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

7 January 2021

Fever, genes, and epilepsy

1 reference

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

1 reference

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

1 reference

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

1 reference

27 December 2017

PubMed ID

17913586

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27 December 2017