Browsing by Author "Fisher, S.E."

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Correction to 'Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits'
Tilot, A.K.; Vino, A.; Kucera, K.S.; Carmichael, D.A.; Heuvel, L.J.S. van den; Hoed, J. den; Sidoroff-Dorso, A.V.; Campbell, A.; Porteous, D.J.; St Pourcain, B.; Leeuwen, T.M. van ; Ward, J.; Rouw, R.; Simner, J.; Fisher, S.E. et al. sine al.
2020, Article / Letter to editor (Philosophical Transactions - Royal Society. Biological Sciences, vol. 375, iss. 1795, (2020), article 20190746)
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)
Genome sequencing for rightward hemispheric language dominance
Carrion-Castillo, A.; Haegen, L. Van der; Tzourio-Mazoyer, N.; Kavaklioglu, Tulya; Badillo, Solveig; Chavent, Marie; Fisher, Simon E. ; Mazoyer, B.; Francks, Clyde
2019, Article / Letter to editor (Genes, Brain and Behavior, vol. 18, iss. 5, (2019), pp. 1-12, article UNSP e12572)
Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila
Castells Nobau, A.; Eidhof, I.J.M.; Fenckova, M. ; Brenman-Suttner, Dova B.; Scheffer-de Gooyert, J.M. ; Christine, S.E. ; Schellevis, R.L.; Fisher, S.E. ; Simon, Anne F.; Schenck, A.
2019, Article / Letter to editor (PLoS One, vol. 14, iss. 2, (2019), pp. 1-37, article e0211652)
Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth
Truong, Dongnhu Thuy; Adams, Andrew Kenneth; Paniagua, Steven; Frijters, Jan C.; Boada, Richard; Hill, Dina E.; Francks, C.; Fisher, Simon E. ; Bosson-Heenan, Joan; Gruen, Jeffrey R.
2019, Article / Letter to editor (Journal of Medical Genetics, vol. 56, iss. 8, (2019), pp. 557-566)
Towards robust functional neuroimaging genetics of cognition
Uddén, J.U.; Hultén, A.H. ; Bendtz, K.; Mineroff, Z.; Kucera, K.S.; Vino, A.; Fedorenko, E.; Hagoort, P. ; Fisher, S.E.
2019, Article / Letter to editor (The Journal of Neuroscience, vol. 39, iss. 44, (2019), pp. 8778-8787)
Enhanced self-reported affect and prosocial behaviour without differential physiological responses in mirror-sensory synaesthesia
Ioumpa, K.; Graham, S.A.; Clausner, T.; Fisher, S.E. ; Lier, R.J. van ; Leeuwen, T.M. van
2019, Article / Letter to editor (Philosophical Transactions - Royal Society. Biological Sciences, vol. 374, iss. 1787, (2019), article 20190395)
Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits
Tilot, A.K.; Vino, A.; Kucera, K.S.; Carmichael, D.A.; Heuvel, L.J.S. van den; Hoed, J. den; Sidoroff-Dorso, A.V.; Campbell, A.; Porteous, D.J.; St Pourcain, B.; Leeuwen, T.M. van ; Ward, J.; Rouw, R.; Simner, J.; Fisher, S.E. et al. sine al.
2019, Article / Letter to editor (Philosophical Transactions - Royal Society. Biological Sciences, vol. 374, iss. 1787, (2019), article 20190026)
Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity
Gunz, Philipp; Tilot, A.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)
Bridging senses: novel insights from synaesthesia
Fisher, S.E. ; Tilot, A.K.
2019, Article / Letter to editor (Philosophical Transactions - Royal Society. Biological Sciences, vol. 374, (2019))
Genetic insights into the neurobiology of speech and language
Burenkova, O.V.; Fisher, S.E.
2019, Part of book or chapter of book (All About Language: Science, Theory, and Practice)
Key issues and future directions: Genes and language
Fisher, S.E.
2019, Part of book or chapter of book (Hagoort, P. (ed.), Human language: From genes and brain to behavior, pp. 527-532)
Human Genetics: The Evolving Story of FOXP2
Fisher, S.E.
2019, Article / Letter to editor (Current Biology, vol. 29, iss. 2, (2019), pp. R65-R67)
Enhanced self-reported affect and prosocial behaviour without differential physiological responses in mirror-sensory synesthesia
Ioumpa, K.; Graham, S.A.; Clausner, T.; Fisher, S.E. ; Lier, R.J. van ; Leeuwen, T.M. van
2019, Dataset
Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language
Verhoef, E.; Demontis, D.; Burgess, S.; Fisher, S.E. ; Borglum, A.D.; Pourcain, B. St
2019, Article / Letter to editor (Translational Psychiatry, vol. 9, (2019), article 35)
Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets
Postema, M.C. ; Rooij, D. van ; Anagnostou, Evdokia; Arango, Celso; Auzias, Guillaume; Behrmann, Marlene; Floris, Dorothea L. ; Hoekstra, L.; Fisher, S.E. ; Buitelaar, J.K. ; Francks, C. et al. sine al.
2019, Article / Letter to editor (Nature Communications, vol. 10, (2019), article 4958)
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition
Meer, D. van der ; Sonderby, I.E.; Fisher, S.E. ; Thompson, P.M.; Andreassen, O.A.
2019, Article / Letter to editor (JAMA Psychiatry, (2019), pp. 1-11)
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder
Snijders Blok, L.; Kleefstra, T. ; Venselaar, H. ; Maas, Saskia; Kroes, Hester Y.; Lachmeijer, Augusta M. A.; Gilissen, C. ; Pfundt, R.P. ; Brunner, H.G. ; Fisher, S.E.
2019, Article / Letter to editor (American Journal of Human Genetics, vol. 105, iss. 2, (2019), pp. 403-412)
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal, Claudia L.; Adams, H.; Hibar, Derrek P.; White, Charles C.; Knol, Maria J.; Stein, Jason L.; Arias Vasquez, A. ; Bralten, J.B. ; Becker, D.; Hoogman, M. ; Klein, M.; Marquand, A.F. ; Shumskaya, E. ; Rooij, D. van ; Wolfers, T. ; Zwiers, M.P. ; Bokhoven, H. van ; Brunner, H.G. ; Buitelaar, J.K. ; Fisher, S.E. ; Fernandez, G.S.E. ; Franke, B. ; Seshadri, Sudha; Arfan Ikram, M. et al. sine al.
2019, Article / Letter to editor (Nature Genetics, vol. 51, iss. 11, (2019), pp. 1624-1636)
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)
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)
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)
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))
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, (2018), article 14279)
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 Sciences USA, vol. 115, iss. 35, (2018), pp. 8799-8804)
Rare variants in axonogenesis genes connect three families with sound-color synesthesia
Tilot, Amanda K.; Kucera, K.S.; Vino, A.; Asher, J.E.; Baron-Cohen, Simon; Fisher, S.E.
2018, Article / Letter to editor (Proceedings of the National Academy of Sciences USA, vol. 115, iss. 12, (2018), pp. 3168-3173)
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)
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 Sciences 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)
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)
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)
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.; Zeeuw, C.I. de
2018, Article / Letter to editor (Molecular Psychiatry, vol. 24, (2018), pp. 447-462)
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)
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)
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)
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)
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)
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)

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