(Q48710057)

14 February 2018

title

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy (English)

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14 February 2018

author

Michael S. Hildebrand

4

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Stefan Herms

16

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Christian Gieger

17

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Ingrid Scheffer

31

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Samuel Berkovic

32

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Brigid M Regan

Brigid M Regan

6

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Fritz Zimprich

Fritz Zimprich

39

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Jacques S Beckmann

Jacques S Beckmann

33

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Alexandre Reymond

38

Alexandre Reymond

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14 February 2018

29

Peter Nürnberg

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Gabriel M Ronen

10

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Susanne Schoch

21

Susanne Schoch

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Heather C. Mefford

30

Heather Mefford

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14 February 2018

Andre Franke

19

Andre Franke

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14 February 2018

Per Hoffmann

15

Per Hoffmann

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14 February 2018

Mohammad Reza Toliat

25

Mohammad R Toliat

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14 February 2018

Michael Wittig

20

Michael Wittig

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14 February 2018

EPICURE Consortium

34

EPICURE Consortium

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14 February 2018

Dennis Lal

2

Dennis Lal

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14 February 2018

Eva Reinthaler

1

Eva M Reinthaler

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14 February 2018

D Edda Haberlandt

14

Edda Haberlandt

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14 February 2018

Martha Feucht

7

Martha Feucht

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14 February 2018

Hannelore Steinböck

8

Hannelore Steinböck

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Ursula Gruber-Sedlmayr

12

Ursula Gruber-Sedlmayr

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14 February 2018

Julia Geldner

13

Julia Geldner

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14 February 2018

Holger Lerche

28

Holger Lerche

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14 February 2018

Bernd Neubauer

40

Bernd A Neubauer

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14 February 2018

Melanie Waldenberger

18

Melanie Waldenberger

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14 February 2018

Birgit Neophytou

9

Birgit Neophytou

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14 February 2018

EuroEPINOMICS Consortium

35

EuroEPINOMICS Consortium

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14 February 2018

author name string

Sebastien Lebon

3

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14 February 2018

Hans-Henrik M Dahl

5

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14 February 2018

Laurian Roche

11

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Albert J Becker

22

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14 February 2018

Andreas Hahn

23

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14 February 2018

Katrin Männik

24

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14 February 2018

Georg Winterer

26

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16p11.2 European Consortium

27

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Thomas Sander

36

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Sebastien Jacquemont

37

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publication date

16 June 2014

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14 February 2018

published in

Human Molecular Genetics

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14 February 2018

volume

23

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14 February 2018

issue

22

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14 February 2018

page(s)

6069-6080

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14 February 2018

Prevalence and characteristics of epilepsy in children in northern Sweden

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Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).

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Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

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DEPDC5 mutations in genetic focal epilepsies of childhood.

21 January 2018

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Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

21 January 2018

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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

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Large recurrent microdeletions associated with schizophrenia

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDU306

21 January 2018

Identifiers

DOI

10.1093/HMG/DDU306

1 reference

14 February 2018

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14 February 2018