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Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders
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Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders

Kong, Sek Won ; Collins, Christin D ; Shimizu-Motohashi, Yuko ; Holm, Ingrid A ; Campbell, Malcolm G ; Lee, In-Hee ; Brewster, Stephanie J ; Hanson, Ellen ; Harris, Heather K ; Lowe, Kathryn R ; Saada, Adrianna ; Mora, Andrea ; Madison, Kimberly ; Hundley, Rachel ; Egan, Jessica ; McCarthy, Jillian ; Eran, Ally ; Galdzicki, Michal ; Rappaport, Leonard ; Kunkel, Louis M ; Kohane, Isaac S Esteban, Francisco José

PloS one, 2012-12, Vol.7 (12), p.e49475-e49475 [Periódico revisado por pares]

United States: Public Library of Science

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2
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk
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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

Salyakina, Daria ; Cukier, Holly N ; Lee, Joycelyn M ; Sacharow, Stephanie ; Nations, Laura D ; Ma, Deqiong ; Jaworski, James M ; Konidari, Ioanna ; Whitehead, Patrice L ; Wright, Harry H ; Abramson, Ruth K ; Williams, Scott M ; Menon, Ramkumar ; Haines, Jonathan L ; Gilbert, John R ; Cuccaro, Michael L ; Pericak-Vance, Margaret A Zwick, Michael Edward

PloS one, 2011-10, Vol.6 (10), p.e26049-e26049 [Periódico revisado por pares]

United States: Public Library of Science

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3
Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disorders
Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disorders
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Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disorders

Lin, Mingyan ; Hrabovsky, Anastasia ; Pedrosa, Erika ; Wang, Tao ; Zheng, Deyou ; Lachman, Herbert M de Erausquin, Gabriel Alejandro

PloS one, 2012-08, Vol.7 (8), p.e44017-e44017 [Periódico revisado por pares]

United States: Public Library of Science

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4
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders
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PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders

Paemka, Lily ; Mahajan, Vinit B ; Skeie, Jessica M ; Sowers, Levi P ; Ehaideb, Salleh N ; Gonzalez-Alegre, Pedro ; Sasaoka, Toshikuni ; Tao, Hirotaka ; Miyagi, Asuka ; Ueno, Naoto ; Takao, Keizo ; Miyakawa, Tsuyoshi ; Wu, Shu ; Darbro, Benjamin W ; Ferguson, Polly J ; Pieper, Andrew A ; Britt, Jeremiah K ; Wemmie, John A ; Rudd, Danielle S ; Wassink, Thomas ; El-Shanti, Hatem ; Mefford, Heather C ; Carvill, Gemma L ; Manak, J Robert ; Bassuk, Alexander G Hu, Valerie W.

PloS one, 2013-12, Vol.8 (12), p.e80737-e80737 [Periódico revisado por pares]

United States: Public Library of Science

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5
Dissociable genetic contributions to error processing: a multimodal neuroimaging study
Dissociable genetic contributions to error processing: a multimodal neuroimaging study
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Dissociable genetic contributions to error processing: a multimodal neuroimaging study

Agam, Yigal ; Vangel, Mark ; Roffman, Joshua L ; Gallagher, Patience J ; Chaponis, Jonathan ; Haddad, Stephen ; Goff, Donald C ; Greenberg, Jennifer L ; Wilhelm, Sabine ; Smoller, Jordan W ; Manoach, Dara S Rypma, Bart

PloS one, 2014-07, Vol.9 (7), p.e101784-e101784 [Periódico revisado por pares]

United States: Public Library of Science

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6
Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function
Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function
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Rare mutations of CACNB2 found in autism spectrum disease-affected families alter calcium channel function

Breitenkamp, Alexandra F S ; Matthes, Jan ; Nass, Robert Daniel ; Sinzig, Judith ; Lehmkuhl, Gerd ; Nürnberg, Peter ; Herzig, Stefan Zwick, Michael Edward

PloS one, 2014-04, Vol.9 (4), p.e95579-e95579 [Periódico revisado por pares]

United States: Public Library of Science

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7
A simple cell-based assay reveals that diverse neuropsychiatric risk genes converge on primary cilia
A simple cell-based assay reveals that diverse neuropsychiatric risk genes converge on primary cilia
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A simple cell-based assay reveals that diverse neuropsychiatric risk genes converge on primary cilia

Marley, Aaron ; von Zastrow, Mark Saudou, Frédéric

PloS one, 2012-10, Vol.7 (10), p.e46647-e46647 [Periódico revisado por pares]

United States: Public Library of Science

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8
Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes
Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes
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Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes

Bruining, Hilgo ; de Sonneville, Leo ; Swaab, Hanna ; de Jonge, Maretha ; Kas, Martien ; van Engeland, Herman ; Vorstman, Jacob Aziz, Syed A.

PloS one, 2010-05, Vol.5 (5), p.e10887-e10887 [Periódico revisado por pares]

United States: Public Library of Science

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9
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
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Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population

Chaste, Pauline ; Clement, Nathalie ; Mercati, Oriane ; Guillaume, Jean-Luc ; Delorme, Richard ; Botros, Hany Goubran ; Pagan, Cécile ; Périvier, Samuel ; Scheid, Isabelle ; Nygren, Gudrun ; Anckarsäter, Henrik ; Rastam, Maria ; Ståhlberg, Ola ; Gillberg, Carina ; Serrano, Emilie ; Lemière, Nathalie ; Launay, Jean Marie ; Mouren-Simeoni, Marie Christine ; Leboyer, Marion ; Gillberg, Christopher ; Jockers, Ralf ; Bourgeron, Thomas Linden, Rafael

PloS one, 2010-07, Vol.5 (7), p.e11495-e11495 [Periódico revisado por pares]

United States: Public Library of Science

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10
Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders
Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders
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Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders

Voineskos, Aristotle N ; Lett, Tristram A P ; Lerch, Jason P ; Tiwari, Arun K ; Ameis, Stephanie H ; Rajji, Tarek K ; Müller, Daniel J ; Mulsant, Benoit H ; Kennedy, James L Herzog, Michael H.

PloS one, 2011-06, Vol.6 (6), p.e20982-e20982 [Periódico revisado por pares]

United States: Public Library of Science

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