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D. Pinto,
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B. Abrahams,
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Gary D Bader,
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A. Battaglia,
T. Berney,
N. Bolshakova,
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P. Bolton,
T. Bourgeron,
Sean Brennan,
J. Brian,
S. Bryson,
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G. Casallo,
J. Casey,
B. Chung,
L. Cochrane,
Christina M. Corsello,
Emily L. Crawford,
Andrew Crossett,
C. Cytrynbaum,
G. Dawson,
M. Jonge,
R. Delorme,
Irene Drmic,
E. Duketis,
F. Duque,
A. Estes,
Penny Farrar,
B. Fernandez,
S. Folstein,
E. Fombonne,
C. Freitag,
J. Gilbert,
C. Gillberg,
J. Glessner,
J. Goldberg,
A. Green,
Jonathan Green,
Stephen J. Guter,
H. Hakonarson,
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M. Hill,
R. Holt,
J. Howe,
G. Hughes,
Vanessa Hus,
R. Igliozzi,
Cecilia Kim,
S. Klauck,
A. Kolevzon,
Olena Korvatska,
Vlad Kustanovich,
C. Lajonchere,
J. Lamb,
Magdalena Laskawiec,
M. Leboyer,
A. Couteur,
B. Leventhal,
A. C. Lionel,
Xiao-qing Liu,
C. Lord,
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Sabata C. Lund,
E. Maestrini,
W. Mahoney,
Carine Mantoulan,
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H. McConachie,
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J. McGrath,
W. McMahon,
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O. Migita,
N. Minshew,
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A. Noor,
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D. Posey,
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Aparna Prasad,
J. Ragoussis,
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B. Rogé,
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L. Bierut,
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K. Sansom,
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A. Thompson,
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H. Coon,
M. Cuccaro,
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D. Geschwind,
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Joachim Hallmayer,
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A. Monaco,
J. Nurnberger,
A. Paterson,
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
19 auth.
S. Jamain,
Hélène Quach,
C. Betancur,
M. Råstam,
C. Colineaux,
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Henrik Söderström,
B. Giros,
I. Gillberg,
M. Leboyer,
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Christopher Gillberg,
T. Bourgeron,
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N. Chabane,
M. Mouren-Siméoni,
P. L. Pearl
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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
23 auth.
C. Durand,
C. Betancur,
Tobias M. Boeckers,
Juergen Bockmann,
P. Chaste,
F. Fauchereau,
G. Nygren,
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I. Gillberg,
H. Anckarsäter,
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E. Sponheim,
Hany Goubran‐Botros,
R. Delorme,
N. Chabane,
M. Mouren-Siméoni,
P. de Mas,
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2007 |
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements
138 auth.
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Biochemical and molecular investigations in respiratory chain deficiencies.
7 auth.
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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
134 auth.
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A synaptic trek to autism
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A genome-wide scan for common alleles affecting risk for autism
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D. Pinto,
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C. Freitag,
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Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2
27 auth.
M. Schmeisser,
Elodie Ey,
Stephanie Wegener,
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A. V. Stempel,
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Androgen insensitivity syndrome.
170 auth.
H. Scharnagl,
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