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Mapping autism risk loci using genetic linkage and chromosomal rearrangements
138 auth.
P. Szatmari,
A. Paterson,
L. Zwaigenbaum,
W. Roberts,
J. Brian,
Xiao-qing Liu,
J. Vincent,
J. Skaug,
A. Thompson,
Lili Senman,
L. Feuk,
Cheng Qian,
S. Bryson,
Marshall B. Jones,
C. Marshall,
...
S. Scherer,
V. Vieland,
Christopher Bartlett,
L. Mangin,
R. Goedken,
Alberto Maria Segre,
M. Pericak-Vance,
M. Cuccaro,
J. Gilbert,
H. Wright,
R. Abramson,
C. Betancur,
T. Bourgeron,
C. Gillberg,
M. Leboyer,
J. Buxbaum,
K. Davis,
E. Hollander,
J. Silverman,
Joachim Hallmayer,
L. Lotspeich,
J. Sutcliffe,
J. Haines,
S. Folstein,
J. Piven,
T. Wassink,
V. Sheffield,
D. Geschwind,
M. Bucan,
W. Brown,
R. Cantor,
J. Constantino,
T. Gilliam,
M. Herbert,
C. Lajonchere,
D. Ledbetter,
Christa Lese-Martin,
Janet Miller,
S. Nelson,
C. Samango-Sprouse,
S. Spence,
M. State,
R. Tanzi,
H. Coon,
G. Dawson,
B. Devlin,
A. Estes,
P. Flodman,
L. Klei,
W. McMahon,
N. Minshew,
J. Munson,
E. Korvatska,
P. Rodier,
G. Schellenberg,
Moyra J. Smith,
M. Spence,
C. Stodgell,
P. Tepper,
E. Wijsman,
Chang-En Yu,
B. Rogé,
Carine Mantoulan,
Kerstin Wittemeyer,
A. Poustka,
B. Felder,
S. Klauck,
C. Schuster,
F. Poustka,
S. Bölte,
Sabine Feineis-Matthews,
Evelyn Herbrecht,
G. Schmötzer,
J. Tsiantis,
K. Papanikolaou,
E. Maestrini,
E. Bacchelli,
F. Blasi,
Simona Carone,
Claudio Toma,
H. van Engeland,
M. D. de Jonge,
C. Kemner,
F. Koop,
M. Langemeijer,
Channa T. Hijmans,
W. Staal,
G. Baird,
P. Bolton,
M. Rutter,
E. Weisblatt,
Jonathan Green,
C. Aldred,
J. Wilkinson,
A. Pickles,
A. Le Couteur,
T. Berney,
H. McConachie,
A. Bailey,
Kostas Francis,
Gemma Honeyman,
A. Hutchinson,
J. Parr,
S. Wallace,
A. Monaco,
G. Barnby,
Kazuhiro Kobayashi,
J. Lamb,
I. Sousa,
N. Sykes,
E. Cook,
Stephen J. Guter,
B. Leventhal,
Jeff Salt,
C. Lord,
Christina M. Corsello,
Vanessa Hus,
D. Weeks,
F. Volkmar,
M. Tauber,
E. Fombonne,
A. Shih,
Kacie J. Meyer
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10 |
2007 |
10 🐜
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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
J. Vorstman,
W. Staal,
E. Daalen,
H. Engeland,
P. Hochstenbach,
L. Franke
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8 |
2006 |
8 🐬
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🐢
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The neurobiology of repetitive behavior: …and men
M. Langen,
S. Durston,
M. Kas,
H. Engeland,
W. Staal
|
8 |
2011 |
8 🐢
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🦁
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Structural brain abnormalities in patients with schizophrenia and their healthy siblings.
W. Staal,
H. Pol,
H. Schnack,
M. Hoogendoorn,
Korn纯 Jellema,
Renç. Kahn
|
7 |
2000 |
7 🦁
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🐬
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Genetics of autistic disorders: review and clinical implications
C. Freitag,
W. Staal,
S. Klauck,
E. Duketis,
Regina Waltes
|
7 |
2009 |
7 🐬
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Volume changes in gray matter in patients with schizophrenia.
8 auth.
H. H. Hulshoff Pol,
H. Schnack,
M. Bertens,
N. V. van Haren,
I. van der Tweel,
W. Staal,
...
W. Baaré,
R. Kahn
|
7 |
2002 |
7 🐜
|
🐬
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The neurobiology of repetitive behavior: Of mice…
M. Langen,
M. Kas,
W. Staal,
H. Engeland,
S. Durston
|
7 |
2011 |
7 🐬
|
🐬
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Caudate Nucleus Is Enlarged in High-Functioning Medication-Naive Subjects with Autism
M. Langen,
S. Durston,
W. Staal,
S. Palmen,
H. Engeland
|
7 |
2007 |
7 🐬
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🐢
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Medical comorbidities in children and adolescents with autism spectrum disorders and attention deficit hyperactivity disorders: a systematic review
J. Muskens,
F. Velders,
W. Staal
|
7 |
2017 |
7 🐢
|
🦁
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Partial volume decrease of the thalamus in relatives of patients with schizophrenia.
W. Staal,
H. Pol,
H. Schnack,
A. V. D. Schot,
R. Kahn
|
7 |
1998 |
7 🦁
|
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Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
27 auth.
A. Pagnamenta,
E. Bacchelli,
M. D. de Jonge,
G. Mirza,
T. Scerri,
Fiorella Minopoli,
A. Chiocchetti,
K. Ludwig,
P. Hoffmann,
S. Paracchini,
E. Lowy,
D. Harold,
J. Chapman,
S. Klauck,
F. Poustka,
...
Renske H. Houben,
W. Staal,
R. Ophoff,
M. O’Donovan,
Julie Williams,
M. Nöthen,
G. Schulte-Körne,
P. Deloukas,
J. Ragoussis,
A. Bailey,
E. Maestrini,
A. Monaco
|
7 |
2010 |
7 🐜
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