|
๐
|
Common genetic variants on 5p14.1 associate with autism spectrum disorders
56 auth.
Kai Wang,
Haitao Zhang,
D. Ma,
M. Bucan,
J. Glessner,
B. Abrahams,
D. Salyakina,
M. Imieliลski,
J. Bradfield,
P. Sleiman,
Cecilia Kim,
C. Hou,
E. Frackelton,
R. Chiavacci,
N. Takahashi,
...
T. Sakurai,
E. Rappaport,
C. Lajonchere,
J. Munson,
A. Estes,
Olena Korvatska,
J. Piven,
L. Sonnenblick,
A. I. A. Retuerto,
Edward I. Herman,
Hongmei Dong,
T. Hutman,
M. Sigman,
S. Ozonoff,
A. Klin,
Thomas Owley,
J. Sweeney,
Camille W. Brune,
R. Cantor,
R. Bernier,
J. Gilbert,
M. Cuccaro,
W. McMahon,
Judith N. Miller,
M. State,
T. Wassink,
H. Coon,
S. Levy,
R. Schultz,
J. Nurnberger,
J. Haines,
J. Sutcliffe,
E. Cook,
N. Minshew,
J. Buxbaum,
G. Dawson,
S. Grant,
D. Geschwind,
M. Pericak-Vance,
G. Schellenberg,
H. Hakonarson
|
9 |
2009 |
9
๐
|
|
๐
|
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
17 auth.
O. Bozdagi,
T. Sakurai,
Danae Papapetrou,
Xiaobin Wang,
D. Dickstein,
N. Takahashi,
Y. Kajiwara,
Mu Yang,
Adam M. Katz,
M. Scattoni,
...
Mark J. Harris,
Roheeni Saxena,
J. Silverman,
J. Crawley,
Qiang Zhou,
P. Hof,
J. Buxbaum
|
9 |
2010 |
9
๐
|
|
๐
|
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
71 auth.
J. Elia,
J. Elia,
J. Glessner,
Kai Wang,
N. Takahashi,
Corina J Shtir,
D. Hadley,
P. Sleiman,
Haitao Zhang,
Cecilia Kim,
Reid J. Robison,
G. Lyon,
J. Flory,
J. Bradfield,
M. Imieliลski,
...
C. Hou,
E. Frackelton,
R. Chiavacci,
T. Sakurai,
C. Rabin,
F. Middleton,
Kelly Thomas,
M. Garris,
F. Mentch,
C. Freitag,
H. Steinhausen,
H. Steinhausen,
H. Steinhausen,
A. Todorov,
A. Reif,
A. Rothenberger,
B. Franke,
E. Mick,
H. Roeyers,
J. Buitelaar,
K. Lesch,
T. Banaschewski,
R. Ebstein,
F. Mulas,
R. Oades,
J. Sergeant,
E. Sonuga-Barke,
E. Sonuga-Barke,
E. Sonuga-Barke,
T. Renner,
M. Romanos,
J. Romanos,
A. Warnke,
S. Walitza,
S. Walitza,
Jobst Meyer,
H. Pรกlmason,
C. Seitz,
S. Loo,
S. Smalley,
J. Biederman,
L. Kent,
P. Asherson,
R. Anney,
J. Gaynor,
P. Shaw,
M. Devoto,
P. White,
S. Grant,
S. Grant,
J. Buxbaum,
J. Rapoport,
N. Williams,
S. Nelson,
S. Faraone,
H. Hakonarson
|
8 |
2011 |
8
๐
|
|
๐ฆ
|
Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia
N. Takahashi,
T. Sakurai,
K. Davis,
J. Buxbaum
|
8 |
2011 |
8
๐ฆ
|
|
๐
|
HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity
26 auth.
M. Kurita,
Terrell Holloway,
A. Garcรญa-Bea,
A. Garcรญa-Bea,
A. Kozlenkov,
Allyson K. Friedman,
J. Moreno,
M. Heshmati,
S. Golden,
P. Kennedy,
N. Takahashi,
D. Dietz,
G. Mocci,
A. Gabilondo,
James B. Hanks,
...
A. Umali,
L. Callado,
A. Gallitano,
R. Neve,
Li Shen,
J. Buxbaum,
Ming-Hu Han,
E. Nestler,
J. Meana,
S. Russo,
J. Gonzรกlez-Maeso
|
8 |
2012 |
8
๐
|
|
๐
|
Strong synaptic transmission impact by copy number variations in schizophrenia
28 auth.
J. Glessner,
M. Reilly,
Cecilia Kim,
N. Takahashi,
A. Albano,
C. Hou,
J. Bradfield,
Haitao Zhang,
P. Sleiman,
J. Flory,
M. Imieliลski,
E. Frackelton,
R. Chiavacci,
Kelly Thomas,
M. Garris,
...
F. Otieno,
M. Davidson,
M. Weiser,
A. Reichenberg,
K. Davis,
J. Friedman,
T. Cappola,
K. Margulies,
D. Rader,
S. Grant,
J. Buxbaum,
R. Gur,
H. Hakonarson
|
7 |
2010 |
7
๐
|
|
๐
|
Rare structural variation of synapse and neurotransmission genes in autism
19 auth.
Xiaowu Gai,
H. Xie,
J. Perin,
N. Takahashi,
K. Murphy,
Adam S Wenocur,
M. D'arcy,
R. O'Hara,
E. Goldmuntz,
E. Goldmuntz,
...
D. Grice,
T. Shaikh,
H. Hakonarson,
H. Hakonarson,
J. Buxbaum,
J. Elia,
J. Elia,
P. White,
Peter S. White
|
7 |
2011 |
7
๐
|
|
๐ฌ
|
Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions
T. Sakurai,
N. Dorr,
N. Takahashi,
L. A. McInnes,
G. Elder,
J. Buxbaum
|
6 |
2011 |
6
๐ฌ
|
|
๐
|
A genome-wide study reveals copy number variants exclusive to childhood obesity cases.
26 auth.
J. Glessner,
J. Bradfield,
Kai Wang,
N. Takahashi,
Haitao Zhang,
P. Sleiman,
F. Mentch,
Cecilia Kim,
C. Hou,
Kelly Thomas,
M. Garris,
Sandra Deliard,
E. Frackelton,
F. Otieno,
Jianhua Zhao,
...
R. Chiavacci,
Mingyao Li,
J. Buxbaum,
R. Berkowitz,
R. Berkowitz,
H. Hakonarson,
H. Hakonarson,
H. Hakonarson,
S. Grant,
S. Grant,
S. Grant
|
6 |
2010 |
6
๐
|
|
๐ฌ
|
Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice
O. Bozdagi,
T. Sakurai,
N. Dorr,
M. Pilorge,
N. Takahashi,
J. Buxbaum
|
6 |
2012 |
6
๐ฌ
|
|
๐
|
Pathway-based association analysis of genome-wide screening data suggest that genes associated with the &ggr;-aminobutyric acid receptor signaling pathway are involved in neuroleptic-induced, treatment-resistant tardive dyskinesia
9 auth.
T. Inada,
M. Koga,
H. Ishiguro,
Y. Horiuchi,
A. Syu,
Takashi Yoshio,
...
N. Takahashi,
N. Ozaki,
T. Arinami
|
6 |
2008 |
6
๐
|
