Rare gene deletions in genetic generalized and Rolandic epilepsies

EuroEPINOMICS CoGIE Consortium

Tutkimustuotos: ArtikkelijulkaisuArtikkeliTieteellinenvertaisarvioitu

Alkuperäiskielienglanti
Artikkeli0202022
LehtiPLoS One
Vuosikerta13
Numero8
Sivumäärä23
ISSN1932-6203
DOI - pysyväislinkit
TilaJulkaistu - 27 elokuuta 2018
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu

Tieteenalat

  • 3111 Biolääketieteet
  • 3112 Neurotieteet
  • 3124 Neurologia ja psykiatria

Lainaa tätä

EuroEPINOMICS CoGIE Consortium. / Rare gene deletions in genetic generalized and Rolandic epilepsies. Julkaisussa: PLoS One. 2018 ; Vuosikerta 13, Nro 8.
@article{87cddad2665e406699db3f4a10c4bd55,
title = "Rare gene deletions in genetic generalized and Rolandic epilepsies",
keywords = "GENOME-WIDE ASSOCIATION, AUTISM CANDIDATE GENES, COPY NUMBER VARIATION, DE-NOVO MUTATIONS, STRUCTURAL VARIATION, DEVELOPMENTAL DELAY, PARKINSONS-DISEASE, RISK LOCI, VARIANTS, DISORDERS, 3111 Biomedicine, 3112 Neurosciences, 3124 Neurology and psychiatry",
author = "{EuroEPINOMICS CoGIE Consortium} and Kamel Jabbari and Bobbili, {Dheeraj R.} and Dennis Lal and Reinthaler, {Eva M.} and Julian Schubert and Stefan Wolking and Vishal Sinha and Susanne Motameny and Holger Thiele and Amit Kawalia and Janine Altmueller and Toliat, {Mohammad Reza} and Robert Kraaij and {van Rooij}, Jeroen and Uitterlinden, {Andre G.} and Ikram, {M. Arfan} and Federico Zara and Anna-Elina Lehesjoki and Roland Krause and Fritz Zimprich and Thomas Sander and Neubauer, {Bernd A.} and Patrick May and Holger Lerche and Peter Nuernberg",
year = "2018",
month = "8",
day = "27",
doi = "10.1371/journal.pone.0202022",
language = "English",
volume = "13",
journal = "PLoS One",
issn = "1932-6203",
publisher = "PUBLIC LIBRARY OF SCIENCE",
number = "8",

}

Rare gene deletions in genetic generalized and Rolandic epilepsies. / EuroEPINOMICS CoGIE Consortium.

julkaisussa: PLoS One, Vuosikerta 13, Nro 8, 0202022, 27.08.2018.

Tutkimustuotos: ArtikkelijulkaisuArtikkeliTieteellinenvertaisarvioitu

TY - JOUR

T1 - Rare gene deletions in genetic generalized and Rolandic epilepsies

AU - EuroEPINOMICS CoGIE Consortium

AU - Jabbari, Kamel

AU - Bobbili, Dheeraj R.

AU - Lal, Dennis

AU - Reinthaler, Eva M.

AU - Schubert, Julian

AU - Wolking, Stefan

AU - Sinha, Vishal

AU - Motameny, Susanne

AU - Thiele, Holger

AU - Kawalia, Amit

AU - Altmueller, Janine

AU - Toliat, Mohammad Reza

AU - Kraaij, Robert

AU - van Rooij, Jeroen

AU - Uitterlinden, Andre G.

AU - Ikram, M. Arfan

AU - Zara, Federico

AU - Lehesjoki, Anna-Elina

AU - Krause, Roland

AU - Zimprich, Fritz

AU - Sander, Thomas

AU - Neubauer, Bernd A.

AU - May, Patrick

AU - Lerche, Holger

AU - Nuernberg, Peter

PY - 2018/8/27

Y1 - 2018/8/27

KW - GENOME-WIDE ASSOCIATION

KW - AUTISM CANDIDATE GENES

KW - COPY NUMBER VARIATION

KW - DE-NOVO MUTATIONS

KW - STRUCTURAL VARIATION

KW - DEVELOPMENTAL DELAY

KW - PARKINSONS-DISEASE

KW - RISK LOCI

KW - VARIANTS

KW - DISORDERS

KW - 3111 Biomedicine

KW - 3112 Neurosciences

KW - 3124 Neurology and psychiatry

U2 - 10.1371/journal.pone.0202022

DO - 10.1371/journal.pone.0202022

M3 - Article

VL - 13

JO - PLoS One

JF - PLoS One

SN - 1932-6203

IS - 8

M1 - 0202022

ER -