On the other hand: including left-handers in cognitive neuroscience and neurogenetics
Willems, Roel M., der Haegen, Lise Van, Fisher, Simon E., Francks, Clyde
Published in Nature reviews. Neuroscience (01.03.2014)
Published in Nature reviews. Neuroscience (01.03.2014)
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Journal Article
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T., Shriberg, Lawrence D., Fisher, Simon E.
Published in Molecular psychiatry (01.07.2019)
Published in Molecular psychiatry (01.07.2019)
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Journal Article
Exome-wide analysis implicates rare protein-altering variants in human handedness
Schijven, Dick, Soheili-Nezhad, Sourena, Fisher, Simon E., Francks, Clyde
Published in Nature communications (02.04.2024)
Published in Nature communications (02.04.2024)
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Journal Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
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 in Nature genetics (01.06.2011)
Published in Nature genetics (01.06.2011)
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Journal Article
Left-right asymmetry of maturation rates in human embryonic neural development
de Kovel, Carolien G.F., PhD, Lisgo, Steven, PhD, Karlebach, Guy, PhD, Ju, Jia, Msc, Cheng, Gang, Bsc, Fisher, Simon E., DPhil, Francks, Clyde, DPhil
Published in Biological psychiatry (1969) (01.08.2017)
Published in Biological psychiatry (1969) (01.08.2017)
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Journal Article
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
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 in PLoS genetics (01.07.2011)
Published in PLoS genetics (01.07.2011)
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A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice
Chabout, Jonathan, Sarkar, Abhra, Patel, Sheel R, Radden, Taylor, Dunson, David B, Fisher, Simon E, Jarvis, Erich D
Published in Frontiers in behavioral neuroscience (20.10.2016)
Published in Frontiers in behavioral neuroscience (20.10.2016)
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Journal Article
Self‐reported impact of developmental stuttering across the lifespan
Boyce, Jessica O., Jackson, Victoria E., Reyk, Olivia, Parker, Richard, Vogel, Adam P., Eising, Else, Horton, Sarah E., Gillespie, Nathan A., Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie, Morgan, Angela T.
Published in Developmental medicine and child neurology (01.10.2022)
Published in Developmental medicine and child neurology (01.10.2022)
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Journal Article
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
Chen, Xiaowei Sylvia, Reader, Rose H., Hoischen, Alexander, Veltman, Joris A., Simpson, Nuala H., Francks, Clyde, Newbury, Dianne F., Fisher, Simon E.
Published in Scientific reports (25.04.2017)
Published in Scientific reports (25.04.2017)
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Journal Article
Molecular Genetics of Dyslexia: An Overview
Carrion-Castillo, Amaia, Franke, Barbara, Fisher, Simon E.
Published in Dyslexia (Chichester, England) (01.11.2013)
Published in Dyslexia (Chichester, England) (01.11.2013)
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Journal Article
Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance
Schreiweis, Christiane, Bornschein, Ulrich, Burguière, Eric, Kerimoglu, Cemil, Schreiter, Sven, Dannemann, Michael, Goyal, Shubhi, Rea, Ellis, French, Catherine A., Puliyadi, Rathi, Groszer, Matthias, Fisher, Simon E., Mundry, Roger, Winter, Christine, Hevers, Wulf, Pääbo, Svante, Enard, Wolfgang, Graybiel, Ann M.
Published in Proceedings of the National Academy of Sciences - PNAS (30.09.2014)
Published in Proceedings of the National Academy of Sciences - PNAS (30.09.2014)
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Journal Article
A Functional Genetic Link between Distinct Developmental Language Disorders
Vernes, Sonja C, Newbury, Dianne F, Abrahams, Brett S, Winchester, Laura, Nicod, Jérôme, Groszer, Matthias, Alarcón, Maricela, Oliver, Peter L, Davies, Kay E, Geschwind, Daniel H, Monaco, Anthony P, Fisher, Simon E
Published in The New England journal of medicine (27.11.2008)
Published in The New England journal of medicine (27.11.2008)
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Journal Article
Genetic variations within human gained enhancer elements affect human brain sulcal morphology
Lemaitre, Herve, Le Guen, Yann, Tilot, Amanda K., Stein, Jason L., Philippe, Cathy, Mangin, Jean-François, Fisher, Simon E., Frouin, Vincent
Published in NeuroImage (Orlando, Fla.) (01.01.2023)
Published in NeuroImage (Orlando, Fla.) (01.01.2023)
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Journal Article
De novo TBR1 mutations in sporadic autism disrupt protein functions
Deriziotis, Pelagia, O’Roak, Brian J., Graham, Sarah A., Estruch, Sara B., Dimitropoulou, Danai, Bernier, Raphael A., Gerdts, Jennifer, Shendure, Jay, Eichler, Evan E., Fisher, Simon E.
Published in Nature communications (18.09.2014)
Published in Nature communications (18.09.2014)
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Journal Article
The developmental genetic architecture of vocabulary skills during the first three years of life: Capturing emerging associations with later-life reading and cognition
Verhoef, Ellen, Shapland, Chin Yang, Fisher, Simon E, Dale, Philip S, St Pourcain, Beate
Published in PLoS genetics (01.02.2021)
Published in PLoS genetics (01.02.2021)
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