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9 research outputs found
Bioinformatics Study of m.9053G>A Mutation at the ATP6
Author
Babizhayev MA
Dassault Systemes
+5Â more
Houštěk JPK
Maksum IP
Maksum IP
Maksum IP
Trott O
Publication venue
'SAGE Publications'
Publication date
Field of study
No full text
Crossref
Major Vault Protein, a Candidate Gene in 16p11.2 Microdeletion Syndrome, Is Required for the Homeostatic Regulation of Visual Cortical Plasticity
Author
Ip JPK
Li KJ
+4Â more
Nagakura I
Petravicz J
Sur M
Wiemer Erik
Publication venue
'Society for Neuroscience'
Publication date
01/01/2018
Field of study
No full text
EUR Research Repository
KCC2 expression levels are reduced in post mortem brain tissue of Rett syndrome patients
Author
A Banerjee
AP Abdala
+29Â more
AV Egorov
C Pellegrino
CA Hübner
CJ Dubois
D Armstrong
DD Armstrong
DD Armstrong
DP Southall
G d’Orsi
I Chamma
J Tornberg
J Tornberg
JPK Ip
K Kaila
K Kovács
MJ Hawrylycz
MR Kelley
P Uvarov
P Uvarov
R El-Khoury
RD Smrt
RG Gogliotti
S Ito
ST Duarte
W Renthal
X Tang
Y Ben-Ari
Y Ben-Ari
Y Ben-Ari
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients
Author
A Untergasser
AK Percy
+34Â more
B Bertelsen
B De Hoon
B. B. Lake
E Landucci
E Monrós
F Ehrhart
H Leonard
IB Van Den Veyver
J Liu
JH Gibson
JL Neul
JPK Ip
KC Hoffbuhr
KH Ørstavik
LS Weaving
LS Weaving
LS Weaving
M Vacca
M Wan
MA Mencarelli
MD Shahbazian
ML Gonzales
N Sirianni
P Clerc
Q Zhang
R Cutler Allen
RE Amir
RE Gale
RM Plenge
S Vidal
SB Peeters
SI Swierczek
T Koressaar
VRB Liyanage
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster
Author
A Blaker-Lee
A Deshpande
+68Â more
A Krishnan
A von Kriegsheim
AM Bolger
B Nijhof
BJ Thomas
BR Pober
C Betancur
C Ernst
C Gilissen
C Slack
CA Schneider
CL Gatto
CO Escamilla
CS Greene
D Hadjieconomou
D Kent
D Kim
D Pinto
D Warde-Farley
EA Lindsay
EK Bijlsma
EW Green
F Zufferey
G Dietzl
H He
H Huang
HC Mefford
I Blumenthal
I Iossifov
J Bilen
J Iyer
J Pucilowska
J Shorter
J Zhou
JN Crawley
JPK Ip
JR Daniele
K Kochinke
KC Epi
M Fromer
M Haller
M Imielinski
M Lek
MC Marchetto
MD Robinson
MF Wangler
MN Loviglio
O Bozdagi
O Durak
OV Bulgakov
P Fichelson
P Penzes
RA Kumar
RE Slager
RG Walters
S Anders
S Girirajan
S Girirajan
S Petrovski
SJ Grice
SN Ehaideb
SY Kim
T Andrews
TF Mackay
TP Neufeld
WB Grueber
X He
YG Liu
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
The DPYSL2 gene connects mTOR and schizophrenia
Author
A Efeyan
A Fukao
+60Â more
A Gururajan
AE Pulver
AE Pulver
C Trapnell
CL Beasley
D Avramopoulos
D Martins-de-Souza
D Martins-de-Souza
D Martins-de-Souza
D Martins-de-Souza
D St Clair
DA Guertin
DC Fingar
E Charrier
E Kringlen
ES Susser
G Shaw
GM Khandaker
Gottesman II
H Lee
H Mi
H Wesseling
HJ Okano
I Patursky-Polischuk
J Chen
J Jaworski
J Zhu
JA English
JJ Howell
JL Blouin
JPK Ip
K Hensley
K Pennington
KT Gagnon
L Crews
L Swiech
L Yang
M Laplante
MD Fallin
ME Harris-White
N Hay
N Inagaki
N Takei
N Yamashita
NL Johnston-Wilson
NM Sosanya
PF Edgar
R Miloslavski
R Tao
R Yamashita
RC Deo
S-Y Ho
Schizophrenia Working Group of the Psychiatric Genomics Consortium
T Mita
T Morita
T Yoshimura
TT Quach
X Zhao
Y Kawano
Y Liu
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
CRMPs Function in Neurons and Glial Cells: Potential Therapeutic Targets for Neurodegenerative Diseases and CNS Injury
Author
A Sakurai
A Tsutiya
+136Â more
AE Fournier
AR Cole
AR Cole
C Vuaillat
C-G Yu
CC Quinn
CGT Tahimic
CN Parkhurst
D Ricard
D Thumkeo
D Tian
DA Fletcher
E Beurel
E Charrier
E Niisato
E Niisato
E Preston
EJ Bradbury
EM Hol
F Hellal
F Mimura
F Nakamura
F Renault-Mihara
F Tan
G Yiu
H Tanaka
H Tanaka
H Witte
J Dill
J Manivannan
J Nagai
J Nagai
J Niewoehner
J Ruschel
J Silver
J Yuasa-Kawada
J-P Camdessanché
JE Herrmann
JE Minturn
JM Brittain
JM Brittain
JPK Ip
JPK Ip
Jun Nagai
K Hensley
K Hensley
K Hensley
K Liu
K MacAulay
K Taghian
K Yamauchi
K-Y Su
L Duplan
L Zhang
L-Q Zhu
LC Kapitein
LH Wang
LH Wang
M Balastik
M Stiess
M Tan
M Taniguchi
M Varrin-Doyer
M Varrin-Doyer
MA Liz
MI Romero
MP Kurnellas
MR Khazaei
MT Fitch
MV Astle
N Arimura
N Arimura
N Arimura
N Inagaki
N Mita
N Yamashita
N Yamashita
N Yamashita
N Yamashita
N Yamashita
N Yamashita
OS Kim
P Caroni
P Dergham
P Prashar
P Stenmark
P Vincent
P-C Lin
PR Williams
R Bhat
R Inatome
R Khanna
R Morimura
RC Deo
Rina Baba
S Bretin
S Brot
S Gögel
S Kaneko
S Lim
S Petratos
S Thuret
S Wakatsuki
SM Wilson
SM Wilson
SS Kang
SY Jang
T Byk
T Byk
T Mishiba
T Nishimura
T Ohshima
T Ohshima
T Yoshimura
Toshio Ohshima
TT Quach
TT Quach
TT Quach
TT Quach
V Rosslenbroich
W Li
W Liu
XKL Fink
XX Chi
Y Fukata
Y Goshima
Y Kawano
Y Sun
Y Suzuki
Y Uchida
Y Uchida
YR Na
YZ Alabed
YZ Alabed
Z Yu
Z Zhang
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
Author
A Ganna
A Gregor
+87Â more
A Matsuya
A Å ali
AA Boucard
AC Reichelt
Aleksic Branko
American Psychiatric Association
Ayako Imai
B Ullrich
BJ O'Roak
C Lowther
C O'Donnell
C Pak
C Zweier
CF Wright
CP Schaaf
CR Marshall
D Araç
D Malhotra
D Rujescu
Daisuke Mori
DF Wyss
DM Werling
E Rees
F Chen
F Varoqueaux
G Bekker
GI Elmer
H Berman
H Stefansson
Hiroki Kimura
Hisashi Mori
HM Grayton
I Dudanova
Itaru Kushima
J Gauthier
J Liu
JH Foss-Feig
JL Rapoport
JPK Ip
Jun Egawa
JY Joo
K Tabuchi
Kanako Ishizuka
L Duong
L Zeng
LM Iakoucheva
M Missler
Mako Morikawa
Masahide Usami
Masashi Ikeda
MJ Owen
MP Dabell
MR Etherton
MT Miller
N Craddock
Nakao Iwata
Norio Ozaki
P Szatmari
PH Lee
R Guerois
S De Rubeis
S Purcell
S Richards
S Teng
SH Jones
SM Purcell
T Bourgeron
T Bourgeron
T Kawabata
T Kawabata
T Kawabata
T Uemura
T Yoshida
Takashi Okada
Takeshi Kawabata
TC Südhof
TC Südhof
The UniProt Consortium
Tomoyuki Yoshida
Toshiya Inada
Toshiyuki Someya
V Den Bossche
V Harrison
Y Bourne
Y Yang
YA Ushkaryov
Yuko Okahisa
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref
Vascular contributions to 16p11.2 deletion autism syndrome modeled in mice
Author
A Dobin
A Miyazaki-Akita
+90Â more
A Needles
AB Tchagang
AW Anderson
B Lacoste
B Lacoste
B Ma
BA Travencolo
Baptiste Lacoste
BJ Andreone
BR Chen
C Reynell
Cameron J. Morse
CC Angelakos
Cesar H. Comin
Christopher J. Bergin
Christopher R. Kennedy
D Attwell
D Tian
DH Ebert
DR Zerbino
Duncan J. Stewart
Dylan Burger
E Flygare Wallen
EB Robinson
EC Azmitia
EH Cook Jr
EM Hillman
ER Sigmon
G Horev
GS Zode
HH Tsai
HK Mannell
JA Alva
JA Ospina
Jean-François Thibodeau
JF Thibodeau
JI Berman
JJ Walsh
JP Owen
JPK Ip
Julie Ouellette
JW Lovelace
K Blackmon
K Fischer
K Jann
K Kisler
L Hippolyte
L Pinto
LA Weiss
LR Dutton
Luciano da F. Costa
M Segarra
M Shin
M Tata
M Yang
Marie-Ève Tremblay
MarÃa Lacalle-Aurioles
MB Woodworth
MD Sweeney
Melissa Yin
MG Kozberg
MI Love
Micael Carrier
Mirabelle Ho
Moises Freitas-Andrade
NM Grissom
NM Munoz
Peter Van Dyken
Qing Yan Liu
R Harb
R Tatsumi
RC Gur
S Mitola
S Steinberg
S Yadav
SA Goldman
SJ Tunster
Sonia Leclerc
Sylvain Baillet
T Lindeberg
T Portmann
TH Wen
VY Cao
William L. Stanford
X Zheng
Xavier Toussay
XK Tong
Yannick D. Benoit
Youlian Pan
Ziying Liu
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
Crossref