Browsing by Author "Fisher, S.E."

Now showing items 1-50 of 132

Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults
Guadalupe, T.; Kong, X.Z.; Akkermans, S.E.A. ; Fisher, S.E.
2021, Article / Letter to editor (Brain Structure and Function, (2021))
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)
The genetics of situs inversus without primary ciliary dyskinesia
Postema, M.C. ; Carrion Castillo, A. ; Fisher, Simon E. ; Vingerhoets, G.; Francks, Clyde
2020, Article / Letter to editor (Scientific Reports, vol. 10, iss. 1, (2020), pp. 1-11, article 3677)
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment
Carrion-Castillo, A.; Pepe, A.; Kong, Xiang-Zhen; Fisher, Simon E. ; Mazoyer, B.; Tzourio-Mazoyer, N.; Crivello, Fabrice; Francks, C.
2020, Article / Letter to editor (Cortex, vol. 124, (2020), pp. 137-153)
Genetic pathways involved in human speech disorders
Hoed, J. den; Fisher, S.E.
2020, Article / Letter to editor (Current Opinion in Genetics & Development, vol. 65, (2020), pp. 103-111)
Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts
Urbanus, B.H.A.; Peter, S.; Fisher, S.E. ; Zeeuw, C.I. de
2020, Article / Letter to editor (Scientific Reports, vol. 10, (2020), article 21631)
Reproducibility in the absence of selective reporting: An illustration from large‐scale brain asymmetry research
Kong, X.Z.; Francks, C.; Mathias, S.R.; Guadalupe, T.M. ; Abé, C.; Agartz, I.; Buitelaar, J.K. ; Luijten, M. ; Fisher, S.E. ; Orhan, F.; Sellgren, C. et al. sine al.
2020, Article / Letter to editor (Human Brain Mapping, (2020))
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
Connaughton, D.M.; Dai, R.; Owen, D.J.; Marquez, J.; Mann, N.; Graham-Paquin, A.L.; Nakayama, M.; Coyaud, E.; Laurent, E.M.N.; St-Germain, J.R.; Snijders-Blok, L.; Vino, A.; Klämbt, V.; Deutsch, K.; Wu, C.H.W.; Kolvenbach, C.M.; Kause, F.; Ottlewski, I.; Schneider, R.; Kitzler, T.M.; Majmundar, A.J.; Buerger, F.; Onuchic-Whitford, A.C.; Youying, M.; Kolb, A.; Salmanullah, D.; Chen, E.; Ven, A.T. van der; Rao, J.; Ityel, H.; Seltzsam, S.; Rieke, J.M.; Chen, J.; Vivante, A.; Hwang, D.Y.; Kohl, S.; Dworschak, G.C.; Hermle, T.; Alders, M.; Bartolomaeus, T.; Bauer, S.T.; Baum, M.A.; Brilstra, E.H.; Challman, T.D.; Zyskind, J.; Costin, C.E.; Dipple, K.M.; Duijkers, F.A.; Ferguson, M.; Fitzpatrick, D.R.; Fick, R.; Glass, I.A.; Hulick, P.J.; Kline, A.D.; Krey, I.; Kumar, S.; Lu, W.; Marco, E.J.; Wentzensen, I.M.; Fisher, S.E. ; Bouchard, M.; Khokha, M.K.; Shril, S.; Hildebrandt, F. et al. sine al.
2020, Article / Letter to editor (American Journal of Human Genetics, vol. 107, iss. 4, (2020), pp. 727-742)
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation
Hildebrandt, M.S.; Jackson, V.E.; Scerri, T.S.; Reyk, O. van; Coleman, M.; Braden, R.O.; Turner, S.; Rigbye, K.A.; Boys, A.; Barton, S.; Webster, R.; Fahey, M.; Saunders, K.; Parry-Fielder, B.; Paxton, G.; Hayman, M.; Coman, D.; Goel, H.; Baxter, A.; Ma, A.; Davis, N.; Reilly, S.; Delatycki, M.; Liégeois, F.J.; Connelly, A.; Gecz, J.; Fisher, S.E. ; Amor, D.J.; Scheffer, I.E.; Bahlo, M.; Morgan, A.T. et al. sine al.
2020, Article / Letter to editor (Neurology, vol. 94, iss. 20, (2020), article e2148-e2167)
Gene expression correlates of the cortical network underlying sentence processing
Kong, X.Z.; Tzourio-Mazoyer, N.; Joliot, M.; Fedorenko, E.; Liu, J.; Fisher, S.E. ; Francks, C.
2020, Article / Letter to editor (Neurobiology of Language, vol. 1, iss. 1, (2020), pp. 77-103)
The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults
Doust, C.; Gordon, S.D.; Garden, N.; Fisher, S.E. ; Martin, N.G.; Bates, T.C.; Luciano, M.
2020, Article / Letter to editor (Twin Research and Human Genetics, vol. 23, iss. 1, (2020), pp. 22-32)
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities
Snijders Blok, C. ; Vino, A.; Hoed, J. den; Underhill, H.R.; Monteil, D.; Li, H.; Brunner, H.G. ; Kleefstra, T. ; Fisher, S.E.
2020, Article / Letter to editor (Genetics in Medicine, (2020))
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Sønderby, I.E.; Gústafsson, Ó.; Doan, N.T.; Hibar, D.P.; Martin-Brevet, S.; Abdellaoui, A.; Ames, D.; Amunts, K.; Andersson, M.; Armstrong, N.J.; Bernard, M.; Blackburn, N.; Blangero, J.; Boomsma, D.I. ; Bralten, J.B. ; Brattbak, H.R.; Brodaty, H.; Brouwer, R.M.; Bülow, R.; Calhoun, V.; Caspers, S.; Cavalleri, G.; Chen, Chih-Wei; Cichon, S.; Ciufolini, S.; Corvin, A.; Crespo-Facorro, B.; Curran, J.E.; Dale, A.M.; Dalvie, S.; Dazzan, P.; Geus, E.J. de; Zubicaray, G.I. de; Zwarte, S.M.C. de; Delanty, N.; Braber, A.; Desrivières, S.; Donohoe, G.; Draganski, B.; Ehrlich, S.; Espeseth, T.; Fisher, S.E. ; Franke, B. ; Frouin, V.; Fukunaga, M.; Gareau, T.; Glahn, D.C.; Grabe, H.; Groenewold, N.A.; Haavik, J.; Håberg, A.; Hashimoto, R.; Hehir-Kwa, J.Y.; Heinz, A.; Hillegers, M.H.; Hoffmann, P.; Holleran, L.; Hottenga, J.J.; Hulshoff, H.E.; Ikeda, M.; Jahanshad, N.; Jernigan, T.; Jockwitz, C.; Johansson, S.; Jonsdottir, G.A.; Jönsson, E.G.; Kahn, R.; Kaufmann, T.; Kelly, S.; Kikuchi, M.; Knowles, E.E.; Kolskår, K.K.; Kwok, J.B.; Hellard, S.L.; Leu, C.; Liu, J.; Lundervold, A.J.; Martin, N.G.; Mather, K.; Mathias, S.R.; McCormack, M.; McMahon, K.L.; McRae, A.; Milaneschi, Y.; Moreau, C.; Morris, D.; Mothersill, D.; Mühleisen, T.W.; Murray, R.; Nordvik, J.E.; Nyberg, L.; Loohuis, L.M.; Ophoff, R.; Paus, T.; Pausova, Z.; Penninx, B.; Peralta, J.M.; Pike, B.; Prieto, C.; Thompson, P.; Andreassen, O.A. et al. sine al.
2020, Article / Letter to editor (Molecular Psychiatry, vol. 25, iss. 3, (2020), pp. 584-602)
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
Meer, D. van der ; 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, I.; Bertolino, Alessandro; Bralten, J.B. ; Brandt, Christine L.; Buitelaar, J.K. ; Djurovic, Srdjan; Donkelaar, M.M.J. van ; Dørum, Erlend S.; Espeseth, Thomas; Faraone, S.V.; Fernandez, G. ; 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, O.A.; Westlye, Lars T. et al. sine al.
2020, Article / Letter to editor (Molecular Psychiatry, vol. 25, iss. 11, (2020), pp. 3053-3065)
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries.
Thompson, P.M.; Jahanshad, N.; Ching, C.R.K.; Salminen, L.E.; Thomopoulos, S.I.; Bright, J.; Baune, B.T.; Bralten, J.B. ; Klein, M. ; Kovel, C.G.F. de; Fisher, S.E. ; Francks, C.; Kong, Xiang-Zhen; Buitelaar, J.K. ; Franke, B. ; Rooij, D. van ; Zarei, M.; Zelman, V. et al. sine al.
2020, Article / Letter to editor (Translational Psychiatry, vol. 10, iss. 1, (2020), article 100)
Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort
Henson, R.N.; Suri, S.; Knights, E.; Rowe, J.B.; Kievit, R.; Lyall, D.M.; Chan, D.; Eising, E.; Fisher, S.E.
2020, Article / Letter to editor (Brain and Neuroscience Advances, vol. 4, (2020), article 2398212820961704)
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)
Toward robust functional neuroimaging genetics of cognition
Uddén, J.; 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)
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)
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)
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)
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)
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)
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)
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Gialluisi, Alessandro; Andlauer, Till F.M.; Mirza-Schreiber, Nazanin; Moll, K.; 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)
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)
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)
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)
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)
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)
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, B.; 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)
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)
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)
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)
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.; Zeeuw, C.I. de
2018, Article / Letter to editor (Molecular Psychiatry, vol. 24, (2018), pp. 447-462)
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)
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 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)

Now showing items 1-50 of 132

Radboud Repository

Browsing by Author "Fisher, S.E."

Search Repository

Browse

All of Repository