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Molecular Genetics of Dyslexia: An Overview.
Published in:
Dyslexia (10769242), 2013, v. 19, n. 4, p. 214, doi. 10.1002/dys.1464
By:
- Carrion‐Castillo, Amaia;
- Franke, Barbara;
- Fisher, Simon E.
Publication type:
Article
Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort.
Published in:
Brain & Neuroscience Advances, 2020, p. 1, doi. 10.1177/2398212820961704
By:
- Henson, Richard N.;
- Suri, Sana;
- Knights, Ethan;
- Rowe, James B.;
- Kievit, Rogier A.;
- Lyall, Donald M.;
- Chan, Dennis;
- Eising, Else;
- Fisher, Simon E.
Publication type:
Article
Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort.
Published in:
Brain & Neuroscience Advances, 2020, v. 4, p. 1, doi. 10.1177/2398212820961704
By:
- Henson, Richard N.;
- Suri, Sana;
- Knights, Ethan;
- Rowe, James B.;
- Kievit, Rogier A.;
- Lyall, Donald M.;
- Chan, Dennis;
- Eising, Else;
- Fisher, Simon E.
Publication type:
Article
Patterns of Gray Matter Abnormalities in Schizophrenia Based on an International Mega-analysis.
Published in:
Schizophrenia Bulletin, 2015, v. 41, n. 5, p. 1133, doi. 10.1093/schbul/sbu177
By:
- Gupta, Cota Navin;
- Calhoun, Vince D.;
- Rachakonda, Srinivas;
- Jiayu Chen;
- Patel, Veena;
- Jingyu Liu;
- Segall, Judith;
- Franke, Barbara;
- Zwiers, Marcel P.;
- Arias-Vasquez, Alejandro;
- Buitelaar, Jan;
- Fisher, Simon E.;
- Fernandez, Guillen;
- van Erp, Theo G. M.;
- Potkin, Steven;
- Ford, Judith;
- Mathalon, Daniel;
- McEwen, Sarah;
- Hyo Jong Lee;
- Mueller, Bryon A.
Publication type:
Article
Developmental dyslexia: genetic dissection of a complex cognitive trait.
Published in:
Nature Reviews Neuroscience, 2002, v. 3, n. 10, p. 767, doi. 10.1038/nrn936
By:
- Fisher, Simon E.;
- DeFries, John C.
Publication type:
Article
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.
Published in:
Human Genetics, 2021, v. 140, n. 8, p. 1183, doi. 10.1007/s00439-021-02289-w
By:
- Carrion-Castillo, Amaia;
- Estruch, Sara B.;
- Maassen, Ben;
- Franke, Barbara;
- Francks, Clyde;
- Fisher, Simon E.
Publication type:
Article
High-precision spatial analysis of mouse courtship vocalization behavior reveals sex and strain differences.
Published in:
Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31554-3
By:
- Oliveira-Stahl, Gabriel;
- Farboud, Soha;
- Sterling, Max L.;
- Heckman, Jesse J.;
- van Raalte, Bram;
- Lenferink, Dionne;
- van der Stam, Amber;
- Smeets, Cleo J. L. M.;
- Fisher, Simon E.;
- Englitz, Bernhard
Publication type:
Article
The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults.
Published in:
2020
By:
- Doust, Catherine;
- Gordon, Scott D.;
- Garden, Natalie;
- Fisher, Simon E.;
- Martin, Nicholas G.;
- Bates, Timothy C.;
- Luciano, Michelle
Publication type:
journal article
Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 7, p. 555, doi. 10.1002/ajmg.b.32258
By:
- Brucato, Nicolas;
- DeLisi, Lynn E.;
- Fisher, Simon E.;
- Francks, Clyde
Publication type:
Article
Mapping brain asymmetry in health and disease through the ENIGMA consortium.
Published in:
Human Brain Mapping, 2022, v. 43, n. 1, p. 167, doi. 10.1002/hbm.25033
By:
- Kong, Xiang‐Zhen;
- Postema, Merel C.;
- Guadalupe, Tulio;
- de Kovel, Carolien;
- Boedhoe, Premika S. W.;
- Hoogman, Martine;
- Mathias, Samuel R.;
- van Rooij, Daan;
- Schijven, Dick;
- Glahn, David C.;
- Medland, Sarah E.;
- Jahanshad, Neda;
- Thomopoulos, Sophia I.;
- Turner, Jessica A.;
- Buitelaar, Jan;
- van Erp, Theo G. M.;
- Franke, Barbara;
- Fisher, Simon E.;
- van den Heuvel, Odile A.;
- Schmaal, Lianne
Publication type:
Article
Early developmental gene enhancers affect subcortical volumes in the adult human brain.
Published in:
Human Brain Mapping, 2016, v. 37, n. 5, p. 1788, doi. 10.1002/hbm.23136
By:
- Becker, Martin;
- Guadalupe, Tulio;
- Franke, Barbara;
- Hibar, Derrek P.;
- Renteria, Miguel E.;
- Stein, Jason L.;
- Thompson, Paul M.;
- Francks, Clyde;
- Vernes, Sonja C.;
- Fisher, Simon E.
Publication type:
Article
G-protein genomic association with normal variation in gray matter density.
Published in:
Human Brain Mapping, 2015, v. 36, n. 11, p. 4272, doi. 10.1002/hbm.22916
By:
- Chen, Jiayu;
- Calhoun, Vince D.;
- Arias‐Vasquez, Alejandro;
- Zwiers, Marcel P.;
- van Hulzen, Kimm;
- Fernández, Guillén;
- Fisher, Simon E.;
- Franke, Barbara;
- Turner, Jessica A.;
- Liu, Jingyu
Publication type:
Article
Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets.
Published in:
Human Brain Mapping, 2014, v. 35, n. 7, p. 3277, doi. 10.1002/hbm.22401
By:
- Guadalupe, Tulio;
- Zwiers, Marcel P.;
- Teumer, Alexander;
- Wittfeld, Katharina;
- Vasquez, Alejandro Arias;
- Hoogman, Martine;
- Hagoort, Peter;
- Fernandez, Guillen;
- Buitelaar, Jan;
- Hegenscheid, Katrin;
- Völzke, Henry;
- Franke, Barbara;
- Fisher, Simon E.;
- Grabe, Hans J.;
- Francks, Clyde
Publication type:
Article
Mapping of Human FOXP2 Enhancers Reveals Complex Regulation.
Published in:
Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00047
By:
- Becker, Martin;
- Devanna, Paolo;
- Fisher, Simon E.;
- Vernes, Sonja C.
Publication type:
Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Published in:
2012
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
Publication type:
Correction Notice
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Published in:
Nature Genetics, 2011, v. 43, n. 6, p. 585, doi. 10.1038/ng.835
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.
Publication type:
Article
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Published in:
Nature Genetics, 2002, v. 30, n. 1, p. 86, doi. 10.1038/ng792
By:
- Fisher, Simon E.;
- Francks, Clyde;
- Marlow, Angela J.;
- MacPhie, I. Laurence;
- Newbury, Dianne F.;
- Cardon, Lon R.;
- Ishikawa-Brush, Yumiko;
- Richardson, Alex J.;
- Talcott, Joel B.;
- Gayán, Javier;
- Olson, Richard K.;
- Pennington, Bruce F.;
- Smith, Shelley D.;
- DeFries, John C.;
- Stein, John F.;
- Monaco, Anthony P.
Publication type:
Article
A major susceptibility locus for leprosy in India maps to chromosome 10p13.
Published in:
Nature Genetics, 2001, v. 27, n. 4, p. 439, doi. 10.1038/86958
By:
- Siddiqui, M. Ruby;
- Meisner, Sarah;
- Tosh, Kerrie;
- Balakrishnan, Karuppiah;
- Ghei, Satish;
- Fisher, Simon E.;
- Golding, Marina;
- Shanker Narayan, Nallakandy P.;
- Sitaraman, Thiagarajan;
- Sengupta, Utpal;
- Pitchappan, Ramasamy;
- Hill, Adrian V.S.
Publication type:
Article
Speech‐language profiles in the context of cognitive and adaptive functioning in SATB2‐associated syndrome.
Published in:
Genes, Brain & Behavior, 2021, v. 20, n. 7, p. 1, doi. 10.1111/gbb.12761
By:
- Snijders Blok, Lot;
- Goosen, Y. Max;
- van Haaften, Leenke;
- van Hulst, Karen;
- Fisher, Simon E.;
- Brunner, Han G.;
- Egger, Jos I. M.;
- Kleefstra, Tjitske
Publication type:
Article
Genome sequencing for rightward hemispheric language dominance.
Published in:
Genes, Brain & Behavior, 2019, v. 18, n. 5, p. N.PAG, doi. 10.1111/gbb.12572
By:
- Carrion‐Castillo, Amaia;
- Van der Haegen, Lise;
- Tzourio‐Mazoyer, Nathalie;
- Kavaklioglu, Tulya;
- Badillo, Solveig;
- Chavent, Marie;
- Saracco, Jérôme;
- Brysbaert, Marc;
- Fisher, Simon E.;
- Mazoyer, Bernard;
- Francks, Clyde
Publication type:
Article
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Published in:
Scientific Reports, 2017, p. 46105, doi. 10.1038/srep46105
By:
- Chen, Xiaowei Sylvia;
- Reader, Rose H.;
- Hoischen, Alexander;
- Veltman, Joris A.;
- Simpson, Nuala H.;
- Francks, Clyde;
- Newbury, Dianne F.;
- Fisher, Simon E.
Publication type:
Article
The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers.
Published in:
Scientific Reports, 2016, p. 20911, doi. 10.1038/srep20911
By:
- Estruch, Sara B.;
- Graham, Sarah A.;
- Deriziotis, Pelagia;
- Fisher, Simon E.
Publication type:
Article
Exome-wide analysis implicates rare protein-altering variants in human handedness.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46277-w
By:
- Schijven, Dick;
- Soheili-Nezhad, Sourena;
- Fisher, Simon E.;
- Francks, Clyde
Publication type:
Article
Structural models of genome-wide covariance identify multiple common dimensions in autism.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46128-8
By:
- de Hoyos, Lucía;
- Barendse, Maria T.;
- Schlag, Fenja;
- van Donkelaar, Marjolein M. J.;
- Verhoef, Ellen;
- Shapland, Chin Yang;
- Klassmann, Alexander;
- Buitelaar, Jan;
- Verhulst, Brad;
- Fisher, Simon E.;
- Rai, Dheeraj;
- St Pourcain, Beate
Publication type:
Article
A Pooled Genome-Wide Association Study of Asperger Syndrome.
Published in:
PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0131202
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
Publication type:
Article
The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21<sup>WAF1/CIP1</sup> in 143B Osteosarcoma Cell Growth Arrest.
Published in:
PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128513
By:
- Gascoyne, Duncan M.;
- Spearman, Hayley;
- Lyne, Linden;
- Puliyadi, Rathi;
- Perez-Alcantara, Marta;
- Coulton, Les;
- Fisher, Simon E.;
- Croucher, Peter I.;
- Banham, Alison H.
Publication type:
Article
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.
Published in:
PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0096374
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
Publication type:
Article
Foxp2 Mutations Impair Auditory-Motor Association Learning.
Published in:
PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033130
By:
- Kurt, Simone;
- Fisher, Simon E.;
- Ehret, Günter
Publication type:
Article
A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.
Published in:
Frontiers in Behavioral Neuroscience, 2016, v. 10, p. 1, doi. 10.3389/fnbeh.2016.00197
By:
- Chabout, Jonathan;
- Sarkar, Abhra;
- Patel, Sheel R.;
- Radden, Taylor;
- Dunson, David B.;
- Fisher, Simon E.;
- Jarvis, Erich D.
Publication type:
Article
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Published in:
Developmental Medicine & Child Neurology, 2014, v. 56, n. 4, p. 346, doi. 10.1111/dmcn.12294
By:
- Simpson, Nuala H;
- Addis, Laura;
- Brandler, William M;
- Slonims, Vicky;
- Clark, Ann;
- Watson, Jocelynne;
- Scerri, Thomas S;
- Hennessy, Elizabeth R;
- Bolton, Patrick F;
- Conti‐Ramsden, Gina;
- Fairfax, Benjamin P;
- Knight, Julian C;
- Stein, John;
- Talcott, Joel B;
- O'Hare, Anne;
- Baird, Gillian;
- Paracchini, Silvia;
- Fisher, Simon E;
- Newbury, Dianne F;
- Consortium, SLI
Publication type:
Article
The developmental genetic architecture of vocabulary skills during the first three years of life: Capturing emerging associations with later-life reading and cognition.
Published in:
PLoS Genetics, 2021, v. 17, n. 2, p. 1, doi. 10.1371/journal.pgen.1009144
By:
- Verhoef, Ellen;
- Shapland, Chin Yang;
- Fisher, Simon E.;
- Dale, Philip S.;
- St Pourcain, Beate
Publication type:
Article
Molecular networks of the FOXP2 transcription factor in the brain.
Published in:
EMBO Reports, 2021, v. 22, n. 8, p. 1, doi. 10.15252/embr.202152803
By:
- den Hoed, Joery;
- Devaraju, Karthikeyan;
- Fisher, Simon E
Publication type:
Article
Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies.
Published in:
NPJ Science of Learning, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41539-021-00101-y
By:
- Shapland, Chin Yang;
- Verhoef, Ellen;
- Davey Smith, George;
- Fisher, Simon E.;
- Verhulst, Brad;
- Dale, Philip S.;
- St Pourcain, Beate
Publication type:
Article
The eloquent ape: genes, brains and the evolution of language.
Published in:
Nature Reviews Genetics, 2006, v. 7, n. 1, p. 9, doi. 10.1038/nrg1747
By:
- Fisher, Simon E.;
- Marcus, Gary F.
Publication type:
Article
Molecular Windows into Speech and Language Disorders.
Published in:
Folia Phoniatrica et Logopaedica, 2007, v. 59, n. 3, p. 130, doi. 10.1159/000101771
By:
- Simon E. Fisher
Publication type:
Article
Associations of HLA alleles with specific language impairment.
Published in:
Journal of Neurodevelopmental Disorders, 2014, v. 6, n. 1, p. 1
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.
Publication type:
Article
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1702, doi. 10.1038/ejhg.2015.66
By:
- Lozano, Reymundo;
- Vino, Arianna;
- Lozano, Cristina;
- Fisher, Simon E;
- Deriziotis, Pelagia
Publication type:
Article
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1370, doi. 10.1038/ejhg.2014.296
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
Publication type:
Article
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1113, doi. 10.1038/ejhg.2014.275
By:
- Ceroni, Fabiola;
- Simpson, Nuala H;
- Francks, Clyde;
- Baird, Gillian;
- Conti-Ramsden, Gina;
- Clark, Ann;
- Bolton, Patrick F;
- Hennessy, Elizabeth R;
- Donnelly, Peter;
- Bentley, David R;
- Martin, Hilary;
- Parr, Jeremy;
- Pagnamenta, Alistair T;
- Maestrini, Elena;
- Bacchelli, Elena;
- Fisher, Simon E;
- Newbury, Dianne F
Publication type:
Article
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
Published in:
European Journal of Human Genetics, 2014, v. 22, n. 10, p. 1165, doi. 10.1038/ejhg.2014.4
By:
- Ceroni, Fabiola;
- Simpson, Nuala H;
- Francks, Clyde;
- Baird, Gillian;
- Conti-Ramsden, Gina;
- Clark, Ann;
- Bolton, Patrick F;
- Hennessy, Elizabeth R;
- Donnelly, Peter;
- Bentley, David R;
- Martin, Hilary;
- Parr, Jeremy;
- Pagnamenta, Alistair T;
- Maestrini, Elena;
- Bacchelli, Elena;
- Fisher, Simon E;
- Newbury, Dianne F
Publication type:
Article
Persistence and transmission of recessive deafness and sign language: new insights from village sign languages.
Published in:
European Journal of Human Genetics, 2013, v. 21, n. 9, p. 894, doi. 10.1038/ejhg.2012.292
By:
- Gialluisi, Alessandro;
- Dediu, Dan;
- Francks, Clyde;
- Fisher, Simon E
Publication type:
Article
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
Published in:
European Journal of Human Genetics, 2013, v. 21, n. 4, p. 361, doi. 10.1038/ejhg.2012.166
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
Publication type:
Article
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
Published in:
European Journal of Human Genetics, 2009, v. 17, n. 10, p. 1354, doi. 10.1038/ejhg.2009.43
By:
- Vernes, Sonja C.;
- MacDermot, Kay D.;
- Monaco, Anthony P.;
- Fisher, Simon E.
Publication type:
Article
Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults.
Published in:
Brain Structure & Function, 2022, v. 227, n. 2, p. 561, doi. 10.1007/s00429-021-02220-z
By:
- Guadalupe, Tulio;
- Kong, Xiang-Zhen;
- Akkermans, Sophie E. A.;
- Fisher, Simon E.;
- Francks, Clyde
Publication type:
Article
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release.
Published in:
Brain Structure & Function, 2018, v. 223, n. 9, p. 4211, doi. 10.1007/s00429-018-1746-6
By:
- van Rhijn, Jon-Ruben;
- Fisher, Simon E.;
- Vernes, Sonja C.;
- Nadif Kasri, Nael
Publication type:
Article
Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language.
Published in:
Journal of Neuroscience, 2006, v. 26, n. 41, p. 10376, doi. 10.1523/JNEUROSCI.3379-06.2006
By:
- White, Stephanie A.;
- Fisher, Simon E.;
- Geschwind, Daniel H.;
- Scharff, Constance;
- Holy, Timothy E.
Publication type:
Article
The genetics of situs inversus without primary ciliary dyskinesia.
Published in:
Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-60589-z
By:
- Postema, Merel C.;
- Carrion-Castillo, Amaia;
- Fisher, Simon E.;
- Vingerhoets, Guy;
- Francks, Clyde
Publication type:
Article
Is synaesthesia more common in autism?
Published in:
Molecular Autism, 2013, v. 4, n. 1, p. 2, doi. 10.1186/2040-2392-4-40
By:
- Baron-Cohen, Simon;
- Johnson, Donielle;
- Asher, Julian;
- Wheelwright, Sally;
- Fisher, Simon E.;
- Gregersen, Peter K.;
- Allison, Carrie
Publication type:
Article
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
Published in:
Brain: A Journal of Neurology, 2003, v. 126, n. 11, p. 2455, doi. 10.1093/brain/awg247
By:
- Cecilia S. L. Lai;
- Dianne Gerrelli;
- Anthony P. Monaco;
- Simon E. Fisher;
- Andrew J. Copp
Publication type:
Article
Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness.
Published in:
Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06890-3
By:
- Amelink, Jitse S.;
- Postema, Merel C.;
- Kong, Xiang-Zhen;
- Schijven, Dick;
- Carrión-Castillo, Amaia;
- Soheili-Nezhad, Sourena;
- Sha, Zhiqiang;
- Molz, Barbara;
- Joliot, Marc;
- Fisher, Simon E.;
- Francks, Clyde
Publication type:
Article

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