Browsing by Author "Fisher, S.E."

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Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity
Gunz, Philipp; Tilot, Amanda K.; Wittfeld, K.; Teumer, A.; Shapland, Chin Yang; van Erp, Theo G.M.; Dannemann, Michael; Vernot, Benjamin; Neubauer, Simon; Guadalupe, T.M. ; Fernandez, G.S.E. ; Brunner, H.G. ; Enard, Wolfgang; Fallon, James; Hosten, Norbert; Völker, Uwe; Profico, Antonio; Di Vincenzo, Fabio; Manzi, Giorgio; Kelso, Janet; St. Pourcain, Beate; Hublin, Jean-Jacques; Franke, B. ; Pääbo, Svante; Macciardi, Fabio; Grabe, H.J.; Fisher, S.E. et al. sine al.
2019, Article / Letter to editor (Current Biology, vol. 29, iss. 1, (2019), pp. 120-127.e5)
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Francks, C.; Fisher, Simon E. ; Mueller-Myhsok, Bertram; Schulte-Koerne, Gerd
2019, Article / Letter to editor (Translational Psychiatry, vol. 9, (2019), pp. 1-15, article 77)
Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila
Castells Nobau, A.; Eidhof, Ilse; Fenckova, M. ; Brenman-Suttner, Dova B.; Scheffer-de Gooyert, J.M. ; Christine, S.E. ; Fisher, Simon E. ; Simon, Anne F.; Schenck, A.
2019, Article / Letter to editor (PLoS One, vol. 14, iss. 2, (2019), article e0211652)
Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia
Morgan, A.; Haaften, L. van; Hulst, C.C. van ; Edley, Carol; Mei, C.; Tan, T.; Fisher, S.E. ; Koolen, D.A.
2018, Article / Letter to editor (European Journal of Human Genetics, vol. 26, iss. 1, (2018), pp. 75-84)
Mapping of Human FOXP2 Enhancers Reveals Complex Regulation
Becker, M; Devanna, Paolo; Fisher, Simon E. ; Vernes, S.C
2018, Article / Letter to editor (Frontiers in Molecular Neuroscience, vol. 11, (2018), pp. 1-15, article 47)
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder
Snijders Blok, L.; Hiatt, S.M.; Bowling, Kevin M.; Prokop, Jeremy W.; Engel, Krysta L.; Cochran, J.Nicholas; Pfundt, R.P. ; Brunner, H.G. ; Fisher, S.E. ; Kleefstra, T. ; Cooper, Gregory M. et al. sine al.
2018, Article / Letter to editor (Human Genetics, vol. 137, iss. 5, (2018), pp. 375-388)
Rare variants in axonogenesis genes connect three families with sound-color synesthesia
Tilot, Amanda K.; Kucera, Katerina S.; Vino, A.; Asher, J.E.; Baron-Cohen, Simon; Fisher, S.E.
2018, Article / Letter to editor (Proceedings of the National Academy of Science USA, vol. 115, iss. 12, (2018), pp. 3168-3173)
Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion
Xu, Shuqin; Liu, Pei; Chen, Yuanxing; Chen, Yi; Zhang, Wei; Zhao, Haixia; Fisher, S.E. ; Xia, Xuechun; Guo, Xizhi
2018, Article / Letter to editor (Proceedings of the National Academy of Science USA, vol. 115, iss. 35, (2018), pp. 8799-8804)
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion
Mei, C.; Fedorenko, E.; Amor, D.J.; Boys, A.; Hoeflin, Caitlyn; Carew, Peter; Fisher, Simon E. ; Morgan, A.
2018, Article / Letter to editor (European Journal of Human Genetics, vol. 26, iss. 5, (2018), pp. 676-686)
Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains
Kovel, C.G. de; Lisgo, S.; Fisher, Simon E. ; Francks, C.
2018, Article / Letter to editor (Scientific Reports, vol. 8, (2018), pp. 1-13, article 12606)
Functional characterization of TBR1 variants in neurodevelopmental disorder
Hoed, J. den; Sollis, E.; Venselaar, H. ; Estruch, S.B. ; Deriziotis, P.; Fisher, S.E.
2018, Article / Letter to editor (Scientific Reports, vol. 8, iss. 1, (2018), article 14279)
Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium
Kong, X.; Mathias, S.R.; Guadalupe, T.M. ; Glahn, D.C.; Franke, B. ; Crivello, F.; Batalla, A.; Arias Vasquez, A. ; Fernandez, G.S.E. ; Buitelaar, J.K. ; Luijten, M. ; Fisher, S.E. ; Thompson, P.M.; Francks, C. et al. sine al.
2018, Article / Letter to editor (Proceedings of the National Academy of Science USA, vol. 115, iss. 22, (2018), pp. E5154-E5163)
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Snijders Blok, C.; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, H. ; Pfundt, R.P. ; Jansen, S; Kleefstra, T. ; Brunner, H.G. ; Fisher, S.E. ; Campeau, Philippe M. et al. sine al.
2018, Article / Letter to editor (Nature Communications, vol. 9, (2018), article 4619)
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders
Estruch, S.B. ; Graham, S.A.; Quevedo, Marti; Vino, A.; Dekkers, Dick H. W.; Deriziotis, P.; Sollis, Elliot; Poot, R.A.; Fisher, Simon E.
2018, Article / Letter to editor (Human Molecular Genetics, vol. 27, iss. 7, (2018), pp. 1212-1227)
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release
Rhijn, J. van; Fisher, S.E. ; Vernes, S.C. ; Nadif Kasri, N.
2018, Article / Letter to editor (Brain Structure and Function, vol. 223, iss. 9, (2018), pp. 4211-4226)
Defining the biological bases of individual differences in musicality.
Gingras, B; Honing, H.J; Peretz, I.; Trainor, L.J.; Fisher, S.E.
2018, Book (monograph)
Molecular Genetic Methods
Kovel, C. de; Fisher, S.E.
2018, Part of book or chapter of book (Groot, M.B. de; Hagoort, P. (ed.), Research methods in psycholinguistics and the neurobiology of language: A practical guide, pp. 330-353)
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
Sonderby, I.E.; Gustafsson, O.; Doan, N.T.; Hibar, D.P.; Martin-Brevet, S.; Westlye, L.T.; Jacquemont, S.; Djurovic, S.; Stefansson, H.; Stefansson, K.; Thompson, P.M.; Andreassen, O.A.; Fisher, S.E. et al. sine al.
2018, Article / Letter to editor (Molecular Psychiatry, (2018), pp. 1-16)
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
van der Meer, Dennis; Rokicki, Jaroslav; Kaufmann, Tobias; Córdova-Palomera, Aldo; Moberget, Torgeir; Alnæs, Dag; Bettella, Francesco; Frei, Oleksandr; Doan, Nhat Trung; Sønderby, Ida E.; Smeland, Olav B.; Agartz, Ingrid; Bertolino, Alessandro; Bralten, Janita; Brandt, Christine L.; Buitelaar, J.K. ; Djurovic, Srdjan; van Donkelaar, Marjolein; Dørum, Erlend S.; Espeseth, Thomas; Faraone, S.V.; Fernández, Guillén; Fisher, S.E. ; Franke, B. ; Haatveit, Beathe; Hartman, C.A.; Hoekstra, P.J.; Håberg, Asta K.; Jönsson, Erik G.; Kolskår, Knut K.; Le Hellard, Stephanie; Lund, Martina J.; Lundervold, Astri J.; Lundervold, Arvid; Melle, Ingrid; Monereo Sánchez, Jennifer; Norbom, Linn C.; Nordvik, Jan E.; Nyberg, Lars; Oosterlaan, J.; Papalino, Marco; Papassotiropoulos, Andreas; Pergola, Giulio; de Quervain, Dominique J. F.; Richard, Geneviève; Sanders, Anne-Marthe; Selvaggi, Pierluigi; Shumskaya, A.N. ; Steen, Vidar M.; Tønnesen, Siren; Ulrichsen, Kristine M.; Zwiers, M.P. ; Andreassen, Ole A.; Westlye, Lars T.; et al. sine al.
2018, Article / Letter to editor (Molecular Psychiatry, (2018))
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Eising, E.; Carrion-Castillo, A.; Vino, A.; Francks, C.; Fisher, S.E. ; et al.
2018, Article / Letter to editor (Molecular Psychiatry, (2018), pp. 1-14)
Differential effects of Foxp2 disruption in distinct motor circuits
French, Catherine A.; Vinueza Veloz, María F.; Zhou, Kuikui; Peter, Saša; Fisher, S.E. ; Costa, Rui M.; De Zeeuw, Chris I.
2018, Article / Letter to editor (Molecular Psychiatry, (2018), pp. 1-16)
Evolution of language: Lessons from the genome
Fisher, S.E.
2017, Article / Letter to editor (Psychonomic Bulletin & Review, vol. 24, iss. 1, (2017), pp. 34-40)
Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development
Stergiakouli, E.; Smith, G.D.; Martin, J.; Skuse, D.H.; Viechtbauer, W.; Ring, S.M.; Ronald, A.; Evans, D.E.; Fisher, S.E. ; Thapar, A.; St Pourcain, B. et al. sine al.
2017, Article / Letter to editor (Molecular Autism, vol. 8, iss. 18, (2017), pp. 1-13)
Left-right asymmetry of maturation rates in human embryonic neural development
de Kovel, C.G.F.; Lisgo, S.; Karlebach, G.; Ju, J.; Cheng, G.; Fisher, S.E. ; Francks, C.
2017, Article / Letter to editor (Biological Psychiatry, vol. 82, iss. 3, (2017), pp. 204-212)
Genes, brain, and language: A brief introduction to the special issue
De Zubicaray, G.I.; Fisher, S.E.
2017, Article / Letter to editor (Brain and Language, vol. 172, (2017), pp. 1-2)
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
Chen, X.S.; Reader, R.H.; Hoischen, A. ; Veltman, J.A. ; Simpson, N.H.; Francks, C.; Newbury, D.F.; Fisher, S.E.
2017, Article / Letter to editor (Scientific Reports, vol. 7, (2017), article 46105)
Association analysis of dyslexia candidate genes in a Dutch longitudinal sample
Carrion Castillo, A. ; Maassen, B.A.M. ; Franke, B. ; Heister, A. ; Naber, M.; Leij, A. van der; Francks, C.; Fisher, S.E.
2017, Article / Letter to editor (European Journal of Human Genetics, vol. 25, iss. 4, (2017), pp. 452-460)
A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus
Uddén, J.U.; Snijders, T.M. ; Fisher, S.E. ; Hagoort, P.
2017, Article / Letter to editor (Brain and Language, vol. 172, (2017), pp. 16-21)
Identification of genetic interactions involved in dyslexia pathogenesis
Karbalai, N.; Czamara, D.; Moll, K.; Ramus, F.; Malik, R.; Scerri, T.S.; Schumacher, J.; Morris, A.P.; Bourgeron, T.; Monaco, A.P.; Paracchini, S.; Fisher, S.E. ; Nothen, M.; Schulte-Korne, G.; Muller-Myhsok, B. et al. sine al.
2017, Article in monograph or in proceedings (23rd Annual World Congress of Psychiatric Genetics (WCPG), pp. S183-S184)
Speech and language: Translating the genome
Deriziotis, P.; Fisher, S.E.
2017, Article / Letter to editor (Trends in Genetics, vol. 33, iss. 9, (2017), pp. 642-656)
Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders
Sollis, E.; Deriziotis, P.; Saitsu, H.; Miyake, N.; Matsumoto, N.; Hoffer, M.J.V.; Ruivenkamp, C.A.L.; Alders, M.; Okamoto, N.; Bijlsma, E.K.; Plomp, A.S.; Fisher, S.E. et al. sine al.
2017, Article / Letter to editor (Human Mutation, vol. 38, iss. 11, (2017), pp. 1542-1554)
Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness
Kavaklioglu, T.K.; Guadalupe, T.M. ; Zwiers, M.P. ; Marquand, A.F. ; Onnink, M. ; Shumskaya, E. ; Brunner, H.G. ; Fernandez, G.S.E. ; Fisher, S.E. ; Francks, C.
2017, Article / Letter to editor (Brain Structure and Function, vol. 222, iss. 4, (2017), pp. 1611-1623)
Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex
Guadalupe, T.M. ; Erp, T.G. van; Whelan, C.D.; Zwiers, M.P. ; Arias Vasquez, A. ; Buitelaar, J.K. ; Fernandez, G.S.E. ; Flor, H.; Fouche, J.P.; Frouin, V.; Wolfers, T. ; Fisher, S.E. ; Francks, C. et al. sine al.
2017, Article / Letter to editor (Brain Imaging and Behavior, vol. 5, (2017), pp. 1497-1514)
ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide
Thompson, P.M.; Andreassen, O.A.; Arias Vasquez, A. ; Bearden, C.E.; Boedhoe, P.S.; Brouwer, R.M.; Buckner, R.L.; Buitelaar, J.K. ; Bulaeva, K.B.; Cannon, D.M.; Cohen, R.A.; Conrod, P.J.; Dale, A.M.; Deary, I.J.; Dennis, E.L.; de Reus, M.A.; Desrivieres, S.; Dima, D.; Donohoe, G.; Fisher, S.E. ; Fouche, J.-P.; Francks, C.; Frangou, S.; Franke, B. ; Ganjgahi, H.; Garavan, H.; Glahn, D.C.; Grabe, H.J.; Guadalupe, T.M. ; Gutman, B.A.; Hashimoto, R.; Hibar, D.P.; Holland, D.; Hoogman, M. ; Pol, H.E.H.; Hosten, N.; Jahanshad, N.; Kelly, S.; Kochunov, P.; Kremen, W.S.; Lee, P.H.; Mackey, S.; Martin, N.G.; Mazoyer, B.; McDonald, C.; Medland, S.E.; Morey, R.A.; Nichols, T.E.; Paus, T.; Pausova, Z.; Schmaal, L.; Schumann, G.; Shen, L.; Sisodiya, S.M.; Smit, D.J.A.; Smoller, J.W.; Stein, D.J.; Stein, J.L.; Toro, R.; Turner, J.A.; van den Heuvel, M.; van den Heuvel, O.A.; van Erp, T.G.M.; Rooij, D. van ; Veltman, D.J.; Walter, H.; Wang, Y; Wardlaw, J.M.; Whelan, C.D.; Wright, M.J.; Ye, J. et al. sine al.
2017, Article / Letter to editor (NeuroImage, vol. 145, iss. Pt B, (2017), pp. 389-408)
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.
Devanna, P.; Chen, X.S.; Ho, J.; Gajewski, D.; Smith, S.D.; Gialluisi, A.; Francks, C.; Fisher, S.E. ; Newbury, D.F.; Vernes, S.C.
2017, Article / Letter to editor (Molecular Psychiatry, (2017), pp. 1-10)
Neuroimaging genetic analyses of novel candidate genes associated with reading and language
Gialluisi, A.; Guadalupe, T.M. ; Francks, C.; Fisher, S.E.
2017, Article / Letter to editor (Brain and Language, vol. 172, (2017), pp. 9-15)
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies
Acuna Hidalgo, R.; Deriziotis, P.; Steehouwer, M. ; Gilissen, C.F. ; Graham, S.A.; Dam, S van; Hoover-Fong, J.; Telegrafi, A.B.; Destree, A.; Smigiel, R.; Lambie, L.A.; Kayserili, H.; Altunoglu, U.; Lapi, E.; Uzielli, M.L.; Aracena, M.; Nur, B.G.; Mihci, E.; Moreira, L.M.; Borges Ferreira, V.; Horovitz, D.D.; Rocha, K.M.; Jezela-Stanek, A.; Brooks, A.S.; Reutter, H.; Cohen, J.S.; Fatemi, A.; Smitka, M.; Grebe, T.A.; Donato, N. Di; Deshpande, C.; Vandersteen, A.; Lourenco, C.; Dufke, A.; Rossier, E.; Andre, G.; Baumer, A.; Spencer, C.; McGaughran, J.; Franke, L.; Veltman, J.A. ; Vries, B.B. de ; Schinzel, A.; Fisher, S.E. ; Hoischen, A. ; Bon, B.W.M. van et al. sine al.
2017, Article / Letter to editor (Plos Genetics, vol. 13, iss. 3, (2017), article e1006683)
Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals.
Pourcain, B. St; Eaves, L.J.; Ring, S.M.; Fisher, S.E. ; Medland, S.; Evans, D.M.; Davey Smith, G.
2017, Article / Letter to editor (Biological Psychiatry, (2017), pp. 598-606)
Loss of intercalated cells (ITCs) in the mouse amygdala of Tshz1 mutants correlates with fear, depression and social interaction phenotypes.
Kuerbitz, J.; Arnett, M.G.; Ehrman, S.; Williams, M.T.; Vorhees, C.V.; Fisher, S.E. ; Garratt, A.N.; Muglia, L.J.; Waclaw, R.R.; Campbell, K.
2017, Article / Letter to editor (The Journal of Neuroscience, vol. 38, iss. 5, (2017), pp. 1160-1177)
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties
St Pourcain, B.; Robinson, E.; Anttila, V.; Sullivan, B.; Maller, J; Golding, J; Skuse, D; Ring, S.; Evans, D M; Zammit, S; Fisher, S.E. ; Neale, B.; Anney, R J L; Ripke, S.; Hollegaard, M V; Werge, T.; iPSYCH-SSI-Broad Autism Group, .; Ronald, A.; Grove, J; Hougaard, D M; Børglum, A.D.; Mortensen, P B; Daly, M J; Davey Smith, G. et al. sine al.
2017, Article / Letter to editor (Molecular Psychiatry, vol. 23, iss. 2, (2017), pp. 263-270)
Ultrasonic vocalizations of adult male Foxp2-mutant mice: behavioral contexts of arousal and emotion
Gaub, S.; Fisher, S.E. ; Ehret, G.
2016, Article / Letter to editor (Genes, Brain and Behavior, vol. 15, iss. 2, (2016), pp. 243-259)
A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
Fedorenko, E.; Morgan, A.; Murray, E.; Cardinaux, A.; Mei, C.; Tager-Flusberg, H.; Fisher, S.E. ; Kanwisher, N.
2016, Article / Letter to editor (European Journal of Human Genetics, vol. 24, iss. 2, (2016), pp. 302-306)
A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice
Chabout, J.; Sarkar, A.; Patel, S.R.; Padden, T.; Dunson, D.B.; Fisher, S.E. ; Jarvis, E.D.
2016, Article / Letter to editor (Frontiers in Behavioral Neuroscience, vol. 10, (2016), pp. 18-36)
Foxp transcription factors suppress a non-pulmonary gene expression program to permit proper lung development
Li, S.; Morley, M.; Lu, MinMin; Zhou, S.; Stewart, K.; French, C.A.; Tucker, H.O.; Fisher, S.E. ; Morrisey, E.E.
2016, Article / Letter to editor (Developmental Biology, vol. 416, iss. 2, (2016), pp. 338-346)
Chapter 2 - A Molecular Genetic Perspective on Speech and Language A2 - Hickok, Gregory
Fisher, S.E.
2016, Part of book or chapter of book (Small, S.L. (ed.), Neurobiology of Language, pp. 13-24)
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus
Woo, Y.J.; Wang, T.; Guadalupe, T.M. ; Nebel, R.A.; Vino, A.; Bene, V.A. Del; Molholm, S.; Ross, L.A.; Zwiers, M.P. ; Fisher, S.E. ; Foxe, J.J.; Abrahams, B.S. et al. sine al.
2016, Article / Letter to editor (PLoS One, vol. 11, iss. 6, (2016), article e0158036)
Early developmental gene enhancers affect subcortical volumes in the adult human brain
Becker, M. ; Guadalupe, T.M. ; Franke, B. ; Hibar, D.P.; Renteria, M.E.; Stein, J.L.; Thompson, P.M.; Francks, C.; Vernes, S.C. ; Fisher, S.E.
2016, Article / Letter to editor (Human Brain Mapping, vol. 37, iss. 5, (2016), pp. 1788-1800)
Evaluation of results from genome-wide studies of language and reading in a novel independent dataset
Carrion Castillo, A. ; van Bergen, E.; Vino, A.; van Zuijen, T.; de Jong, P.F.; Francks, C.; Fisher, S.E.
2016, Article / Letter to editor (Genes, Brain and Behavior, vol. 15, iss. 6, (2016), pp. 531-541)
Investigating the effects of copy number variants on reading and language performance
Gialluisi, A.; Visconti, A.; Willcutt, E.G.; Smith, S.D.; Pennington, B.F.; Falchi, M.; DeFries, J.C.; Olson, R.K.; Francks, C.; Fisher, S.E.
2016, Article / Letter to editor (Journal of Neurodevelopmental Disorders, vol. 8, iss. 17, (2016), pp. 15-30)
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
Sollis, E.; Graham, S.A.; Vino, A.; Froehlich, H.; Vreeburg, M.; Dimitropoulou, D.; Gilissen, C.F. ; Pfundt, R.P. ; Rappold, G.A.; Brunner, H.G. ; Deriziotis, P.; Fisher, S.E. et al. sine al.
2016, Article / Letter to editor (Human Molecular Genetics, vol. 25, iss. 3, (2016), pp. 546-557)

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