Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

by Werling, Donna M, Lowe, Jennifer K, Luo, Rui, Cantor, Rita M, Geschwind, Daniel H
Published 2014

Modeling the functional genomics of autism using human neurons

by Konopka, Genevieve, Wexler, Eric, Rosen, Ezra, Mukamel, Zohar, Osborn, Gregory E., Chen, Leslie, Lu, Daning, Gao, Fuying, Gao, Kun, Lowe, Jennifer K., Geschwind, Daniel H.
Published 2011

Transcriptomic Analysis of Autistic Brain Reveals Convergent Molecular Pathology

by Voineagu, Irina, Wang, Xinchen, Johnston, Patrick, Lowe, Jennifer K., Tian, Yuan, Horvath, Steve, Mill, Jonathan, Cantor, Rita, Blencowe, Benjamin J., Geschwind, Daniel H.
Published 2011

Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders

by Correia, Catarina T, Conceição, Inês C, Oliveira, Bárbara, Coelho, Joana, Sousa, Inês, Sequeira, Ana F, Almeida, Joana, Café, Cátia, Duque, Frederico, Mouga, Susana, Roberts, Wendy, Gao, Kun, Lowe, Jennifer K, Thiruvahindrapuram, Bhooma, Walker, Susan, Marshall, Christian R, Pinto, Dalila, Nurnberger, John I, Scherer, Stephen W, Geschwind, Daniel H, Oliveira, Guiomar, Vicente, Astrid M
Published 2014

Common genetic variants, acting additively, are a major source of risk for autism

by Klei, Lambertus, Sanders, Stephan J, Murtha, Michael T, Hus, Vanessa, Lowe, Jennifer K, Willsey, A Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E, Ledbetter, David H, Lord, Catherine, Mane, Shrikant M, Martin, Christa Lese, Martin, Donna M, Morrow, Eric M, Walsh, Christopher A, Melhem, Nadine M, Chaste, Pauline, Sutcliffe, James S, State, Matthew W, Cook, Edwin H, Roeder, Kathryn, Devlin, Bernie
Published 2012