Neurogenomics of speech and language disorders: the road ahead

by Deriziotis, Pelagia, Fisher, Simon E
Published 2013

Foxp2 Mutations Impair Auditory-Motor Association Learning

by Kurt, Simone, Fisher, Simon E., Ehret, Günter
Published 2012

A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer

by Becker, Martin, Devanna, Paolo, Fisher, Simon E., Vernes, Sonja C.
Published 2015

Assessing the effects of common variation in the FOXP2 gene on human brain structure

by Hoogman, Martine, Guadalupe, Tulio, Zwiers, Marcel P., Klarenbeek, Patricia, Francks, Clyde, Fisher, Simon E.
Published 2014

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

by Estruch, Sara B., Graham, Sarah A., Chinnappa, Swathi M., Deriziotis, Pelagia, Fisher, Simon E.
Published 2016

The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers

by Estruch, Sara B., Graham, Sarah A., Deriziotis, Pelagia, Fisher, Simon E.
Published 2016

Is synaesthesia more common in autism?

by Baron-Cohen, Simon, Johnson, Donielle, Asher, Julian, Wheelwright, Sally, Fisher, Simon E, Gregersen, Peter K, Allison, Carrie
Published 2013

A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice

by Chabout, Jonathan, Sarkar, Abhra, Patel, Sheel R., Radden, Taylor, Dunson, David B., Fisher, Simon E., Jarvis, Erich D.
Published 2016

No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure

by Cousijn, Helena, Eissing, Marc, Fernández, Guillén, Fisher, Simon E., Franke, Barbara, Zwiers, Marcel, Harrison, Paul J., Arias-Vásquez, Alejandro
Published 2014

Differences in cerebral cortical anatomy of left- and right-handers

by Guadalupe, Tulio, Willems, Roel M., Zwiers, Marcel P., Arias Vasquez, Alejandro, Hoogman, Martine, Hagoort, Peter, Fernandez, Guillen, Buitelaar, Jan, Franke, Barbara, Fisher, Simon E., Francks, Clyde
Published 2014

A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: A Preliminary Study

by Baron-Cohen, Simon, Murphy, Laura, Chakrabarti, Bhismadev, Craig, Ian, Mallya, Uma, Lakatošová, Silvia, Rehnstrom, Karola, Peltonen, Leena, Wheelwright, Sally, Allison, Carrie, Fisher, Simon E., Warrier, Varun
Published 2014

Investigating the effects of copy number variants on reading and language performance

by Gialluisi, Alessandro, Visconti, Alessia, Willcutt, Erik G., Smith, Shelley D., Pennington, Bruce F., Falchi, Mario, DeFries, John C., Olson, Richard K., Francks, Clyde, Fisher, Simon E.
Published 2016

A Pooled Genome-Wide Association Study of Asperger Syndrome

by Warrier, Varun, Chakrabarti, Bhismadev, Murphy, Laura, Chan, Allen, Craig, Ian, Mallya, Uma, Lakatošová, Silvia, Rehnstrom, Karola, Peltonen, Leena, Wheelwright, Sally, Allison, Carrie, Fisher, Simon E., Baron-Cohen, Simon
Published 2015

The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest

by Gascoyne, Duncan M., Spearman, Hayley, Lyne, Linden, Puliyadi, Rathi, Perez-Alcantara, Marta, Coulton, Les, Fisher, Simon E., Croucher, Peter I., Banham, Alison H.
Published 2015

Associations of HLA alleles with specific language impairment

by Nudel, Ron, Simpson, Nuala H, Baird, Gillian, O’Hare, Anne, Conti-Ramsden, Gina, Bolton, Patrick F, Hennessy, Elizabeth R, Monaco, Anthony P, Knight, Julian C, Winney, Bruce, Fisher, Simon E, Newbury, Dianne F
Published 2014

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

by Newbury, Dianne F, Mari, Francesca, Sadighi Akha, Elham, MacDermot, Kay D, Canitano, Roberto, Monaco, Anthony P, Taylor, Jenny C, Renieri, Alessandra, Fisher, Simon E, Knight, Samantha J L
Published 2013

Genome-wide analysis identifies a role for common copy number variants in specific language impairment

by Simpson, Nuala H, Ceroni, Fabiola, Reader, Rose H, Covill, Laura E, Knight, Julian C, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, O'Hare, Anne, Baird, Gillian, Fisher, Simon E, Newbury, Dianne F
Published 2015

A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus

by Woo, Young Jae, Wang, Tao, Guadalupe, Tulio, Nebel, Rebecca A., Vino, Arianna, Del Bene, Victor A., Molholm, Sophie, Ross, Lars A., Zwiers, Marcel P., Fisher, Simon E., Foxe, John J., Abrahams, Brett S.
Published 2016

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

by O’Roak, Brian J., Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J., Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P., Ng, Sarah B., Baker, Carl, Rieder, Mark J., Nickerson, Deborah A., Bernier, Raphael, Fisher, Simon E., Shendure, Jay, Eichler, Evan E.
Published 2011

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

by Vernes, Sonja C., Oliver, Peter L., Spiteri, Elizabeth, Lockstone, Helen E., Puliyadi, Rathi, Taylor, Jennifer M., Ho, Joses, Mombereau, Cedric, Brewer, Ariel, Lowy, Ernesto, Nicod, Jérôme, Groszer, Matthias, Baban, Dilair, Sahgal, Natasha, Cazier, Jean-Baptiste, Ragoussis, Jiannis, Davies, Kay E., Geschwind, Daniel H., Fisher, Simon E.
Published 2011