(Q57982315)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12366744%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

title

ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies (English)

1 reference

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13 December 2019

2

1 reference

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13 December 2019

Dick Lindhout

7

1 reference

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13 December 2019

Jeffrey L. Noebels

8

1 reference

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13 December 2019

Joan Bailey-Wilson

14

1 reference

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13 December 2019

ILAE Genetics Commission

22

object named as

ILAE Genetics Commission

1 reference

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13 December 2019

J Serratosa

11

0 references

Katrina Gwinn

object named as

K Gwinn-Hardy

17

0 references

author name string

E Anderson

1

1 reference

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13 December 2019

O Dulac

3

1 reference

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13 December 2019

M Gardiner

4

1 reference

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13 December 2019

S Jain

5

1 reference

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13 December 2019

M Laue Friis

6

1 reference

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13 December 2019

R Ottman

9

1 reference

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13 December 2019

A Scaramelli

10

1 reference

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13 December 2019

O Steinlein

12

1 reference

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13 December 2019

G Avanzini

13

1 reference

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13 December 2019

L Cardon

15

1 reference

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13 December 2019

R Fischbach

16

1 reference

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13 December 2019

M Leppert

18

1 reference

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13 December 2019

J Ott

19

1 reference

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13 December 2019

K Lindblad-Toh

20

1 reference

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13 December 2019

K Weiss

21

1 reference

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13 December 2019

publication date

1 October 2002

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13 December 2019

1 reference

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13 December 2019

volume

43

1 reference

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13 December 2019

issue

10

1 reference

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13 December 2019

page(s)

1262-1267

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12366744%20AND%20SRC:MED&resulttype=core&format=json

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

13 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Epilepsies in twins: genetics of the major epilepsy syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Are generalized and localization-related epilepsies genetically distinct?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Seizure risk in offspring of parents with generalized versus partial epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

21 January 2018

Targeting epilepsy genes

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Ion channels and epilepsy in man and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Identification of epilepsy genes in human and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Genome search for susceptibility loci of common idiopathic generalised epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Association study designs for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Mining for SNPs: putting the common variants--common disease hypothesis to the test

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Genomic control, a new approach to genetic-based association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Genetics of the epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Clinical Indicators of Genetic Susceptibility to Epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Linkage analysis in nuclear families. 2: Relationship between affected sib-pair tests and lod score analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

Family-based association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2002.29502.X

10.1046/J.1528-1157.2002.29502.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12366744%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

1 reference