Simon E. Fisher, D.Phil. - Publications

Affiliations: 
Wellcome Trust Centre for Human Genetics University of Oxford, Oxford, United Kingdom 
Area:
speech, language
Website:
http://www.well.ox.ac.uk/simon-e-fisher-homepage

146 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Postema MC, Carrion-Castillo A, Fisher SE, Vingerhoets G, Francks C. The genetics of situs inversus without primary ciliary dyskinesia. Scientific Reports. 10: 3677. PMID 32111882 DOI: 10.1038/s41598-020-60589-z  0.44
2019 Carrion-Castillo A, Pepe A, Kong XZ, Fisher SE, Mazoyer B, Tzourio-Mazoyer N, Crivello F, Francks C. Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 124: 137-153. PMID 31887566 DOI: 10.1016/j.cortex.2019.11.006  0.44
2019 Postema MC, van Rooij D, Anagnostou E, Arango C, Auzias G, Behrmann M, Filho GB, Calderoni S, Calvo R, Daly E, Deruelle C, Di Martino A, Dinstein I, Duran FLS, Durston S, ... ... Fisher SE, et al. Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets. Nature Communications. 10: 4958. PMID 31673008 DOI: 10.1038/s41467-019-13005-8  0.44
2019 Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV, Smith AV, Bis JC, Jian X, Luciano M, Hofer E, ... ... Fisher SE, et al. Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics. PMID 31636452 DOI: 10.1038/s41588-019-0511-y  0.44
2019 Truong DT, Adams AK, Paniagua S, Frijters JC, Boada R, Hill DE, Lovett MW, Mahone EM, Willcutt EG, Wolf M, Defries JC, Gialluisi A, Francks C, Fisher SE, Olson RK, et al. Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Journal of Medical Genetics. PMID 30995994 DOI: 10.1136/jmedgenet-2018-105874  0.44
2019 Carrion-Castillo A, Van der Haegen L, Tzourio-Mazoyer N, Kavaklioglu T, Badillo S, Chavent M, Saracco J, Brysbaert M, Fisher SE, Mazoyer B, Francks C. Genome sequencing for rightward hemispheric language dominance. Genes, Brain, and Behavior. e12572. PMID 30950222 DOI: 10.1111/gbb.12572  0.44
2019 Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, ... ... Fisher SE, et al. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry. 9: 77. PMID 30741946 DOI: 10.1038/s41398-019-0402-0  0.76
2018 van Rhijn JR, Fisher SE, Vernes SC, Nadif Kasri N. Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release. Brain Structure & Function. PMID 30187194 DOI: 10.1007/s00429-018-1746-6  0.52
2018 de Kovel CGF, Lisgo SN, Fisher SE, Francks C. Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains. Scientific Reports. 8: 12606. PMID 30181561 DOI: 10.1038/s41598-018-29496-2  0.44
2018 Kong XZ, Mathias SR, Guadalupe T, Glahn DC, Franke B, Crivello F, Tzourio-Mazoyer N, Fisher SE, Thompson PM, Francks C. Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium. Proceedings of the National Academy of Sciences of the United States of America. PMID 29764998 DOI: 10.1073/pnas.1718418115  0.44
2018 Becker M, Devanna P, Fisher SE, Vernes SC. Mapping of HumanEnhancers Reveals Complex Regulation. Frontiers in Molecular Neuroscience. 11: 47. PMID 29515369 DOI: 10.3389/fnmol.2018.00047  0.52
2018 Eising E, Carrion-Castillo A, Vino A, Strand EA, Jakielski KJ, Scerri TS, Hildebrand MS, Webster R, Ma A, Mazoyer B, Francks C, Bahlo M, Scheffer IE, Morgan AT, Shriberg LD, ... Fisher SE, et al. A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. Molecular Psychiatry. PMID 29463886 DOI: 10.1038/s41380-018-0020-x  0.44
2017 Chen XS, Reader RH, Hoischen A, Veltman JA, Simpson NH, Francks C, Newbury DF, Fisher SE. Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment. Scientific Reports. 7: 46105. PMID 28440294 DOI: 10.1038/srep46105  0.76
2017 de Kovel CG, Lisgo S, Karlebach G, Ju J, Cheng G, Fisher SE, Francks C. Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development. Biological Psychiatry. PMID 28267988 DOI: 10.1016/j.biopsych.2017.01.016  0.44
2017 Carrion-Castillo A, Maassen B, Franke B, Heister A, Naber M, van der Leij A, Francks C, Fisher SE. Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. European Journal of Human Genetics : Ejhg. PMID 28074887 DOI: 10.1038/ejhg.2016.194  0.44
2016 Guadalupe T, Mathias SR, vanErp TG, Whelan CD, Zwiers MP, Abe Y, Abramovic L, Agartz I, Andreassen OA, Arias-Vásquez A, Aribisala BS, Armstrong NJ, Arolt V, Artiges E, Ayesa-Arriola R, ... ... Fisher SE, et al. Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior. PMID 27738994 DOI: 10.1007/s11682-016-9629-z  0.44
2016 Adams HH, Hibar DP, Chouraki V, Stein JL, Nyquist PA, Rentería ME, Trompet S, Arias-Vasquez A, Seshadri S, Desrivières S, Beecham AH, Jahanshad N, Wittfeld K, Van der Lee SJ, Abramovic L, ... ... Fisher SE, et al. Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience. PMID 27694991 DOI: 10.1038/nn.4398  0.56
2016 Kavaklioglu T, Guadalupe T, Zwiers M, Marquand AF, Onnink M, Shumskaya E, Brunner H, Fernandez G, Fisher SE, Francks C. Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness. Brain Structure & Function. PMID 27566607 DOI: 10.1007/s00429-016-1295-9  0.76
2016 Gialluisi A, Guadalupe T, Francks C, Fisher SE. Neuroimaging genetic analyses of novel candidate genes associated with reading and language. Brain and Language. PMID 27476042 DOI: 10.1016/j.bandl.2016.07.002  0.44
2016 Fisher SE. Evolution of language: Lessons from the genome. Psychonomic Bulletin & Review. PMID 27432000 DOI: 10.3758/s13423-016-1112-8  0.76
2016 Woo YJ, Wang T, Guadalupe T, Nebel RA, Vino A, Del Bene VA, Molholm S, Ross LA, Zwiers MP, Fisher SE, Foxe JJ, Abrahams BS. A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus. Plos One. 11: e0158036. PMID 27351196 DOI: 10.1371/journal.pone.0158036  0.76
2016 Li S, Morley M, Lu M, Zhou S, Stewart K, French CA, Tucker HO, Fisher SE, Morrisey EE. Foxp transcription factors suppress a non-pulmonary gene expression program to permit proper lung development. Developmental Biology. PMID 27341756 DOI: 10.1016/j.ydbio.2016.06.020  0.76
2016 Carrion-Castillo A, van Bergen E, Vino A, van Zuijen T, de Jong PF, Francks C, Fisher SE. Evaluation of results from genome-wide studies of language and reading in a novel independent dataset. Genes, Brain, and Behavior. PMID 27198479 DOI: 10.1111/gbb.12299  0.76
2016 Gialluisi A, Visconti A, Willcutt EG, Smith SD, Pennington BF, Falchi M, DeFries JC, Olson RK, Francks C, Fisher SE. Investigating the effects of copy number variants on reading and language performance. Journal of Neurodevelopmental Disorders. 8: 17. PMID 27186239 DOI: 10.1186/s11689-016-9147-8  0.44
2016 Uddén J, Snijders TM, Fisher SE, Hagoort P. A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus. Brain and Language. PMID 27059522 DOI: 10.1016/j.bandl.2016.02.003  0.76
2016 Becker M, Guadalupe T, Franke B, Hibar DP, Renteria ME, Stein JL, Thompson PM, Francks C, Vernes SC, Fisher SE. Early developmental gene enhancers affect subcortical volumes in the adult human brain. Human Brain Mapping. PMID 26890892 DOI: 10.1002/hbm.23136  0.76
2016 Estruch SB, Graham SA, Deriziotis P, Fisher SE. The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers. Scientific Reports. 6: 20911. PMID 26867680 DOI: 10.1038/srep20911  0.76
2015 Thompson PM, Andreassen OA, Arias-Vasquez A, Bearden CE, Boedhoe PS, Brouwer RM, Buckner RL, Buitelaar JK, Bulaeva KB, Cannon DM, Cohen RA, Conrod PJ, Dale AM, Deary IJ, Dennis EL, ... ... Fisher SE, et al. ENIGMA and the Individual: Predicting Factors that Affect the Brain in 35 Countries Worldwide. Neuroimage. PMID 26658930 DOI: 10.1016/j.neuroimage.2015.11.057  0.76
2015 Sollis E, Graham SA, Vino A, Froehlich H, Vreeburg M, Dimitropoulou D, Gilissen C, Pfundt R, Rappold GA, Brunner HG, Deriziotis P, Fisher SE. Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. Human Molecular Genetics. PMID 26647308 DOI: 10.1093/hmg/ddv495  0.76
2015 Gaub S, Fisher SE, Ehret G. Ultrasonic vocalizations of adult male Foxp2-mutant mice: behavioral contexts of arousal and emotion. Genes, Brain, and Behavior. PMID 26566793 DOI: 10.1111/gbb.12274  0.76
2015 Graham SA, Fisher SE. Understanding Language from a Genomic Perspective. Annual Review of Genetics. PMID 26442845 DOI: 10.1146/annurev-genet-120213-092236  0.76
2015 Becker M, Devanna P, Fisher SE, Vernes SC. A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer. Molecular Cytogenetics. 8: 69. PMID 26300977 DOI: 10.1186/s13039-015-0173-0  0.76
2015 Chen J, Calhoun VD, Arias-Vasquez A, Zwiers MP, van Hulzen K, Fernández G, Fisher SE, Franke B, Turner JA, Liu J. G-protein genomic association with normal variation in gray matter density. Human Brain Mapping. PMID 26248772 DOI: 10.1002/hbm.22916  0.76
2015 Warrier V, Chakrabarti B, Murphy L, Chan A, Craig I, Mallya U, Lakatošová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Baron-Cohen S. A Pooled Genome-Wide Association Study of Asperger Syndrome. Plos One. 10: e0131202. PMID 26176695 DOI: 10.1371/journal.pone.0131202  0.76
2015 Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Magdalena Echeverry M, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER, ... ... Fisher SE, et al. Correction: Exome Sequencing in an Admixed Isolated Population IndicatesNFXL1 Variants Confer a Risk for Specific Language Impairment. Plos Genetics. 11: e1005336. PMID 26114769 DOI: 10.1371/journal.pgen.1005336  0.76
2015 Gascoyne DM, Spearman H, Lyne L, Puliyadi R, Perez-Alcantara M, Coulton L, Fisher SE, Croucher PI, Banham AH. The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest. Plos One. 10: e0128513. PMID 26034982 DOI: 10.1371/journal.pone.0128513  0.76
2015 Spaeth JM, Hunter CS, Bonatakis L, Guo M, French CA, Slack I, Hara M, Fisher SE, Ferrer J, Morrisey EE, Stanger BZ, Stein R. The FOXP1, FOXP2 and FOXP4 transcription factors are required for islet alpha cell proliferation and function in mice. Diabetologia. PMID 26021489 DOI: 10.1007/s00125-015-3635-3  0.76
2015 Lozano R, Vino A, Lozano C, Fisher SE, Deriziotis P. A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment. European Journal of Human Genetics : Ejhg. PMID 25853299 DOI: 10.1038/ejhg.2015.66  0.76
2015 Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Echeverry MM, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER, ... ... Fisher SE, et al. Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. Plos Genetics. 11: e1004925. PMID 25781923 DOI: 10.1371/journal.pgen.1004925  0.76
2015 Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE, Whitehouse AJ, Snowling MJ, et al. Lack of replication for the myosin-18B association with mathematical ability in independent cohorts. Genes, Brain, and Behavior. 14: 369-76. PMID 25778778 DOI: 10.1111/gbb.12213  0.76
2015 Brucato N, Guadalupe T, Franke B, Fisher SE, Francks C. A schizophrenia-associated HLA locus affects thalamus volume and asymmetry. Brain, Behavior, and Immunity. 46: 311-8. PMID 25728236 DOI: 10.1016/j.bbi.2015.02.021  0.76
2015 Gingras B, Honing H, Peretz I, Trainor LJ, Fisher SE. Defining the biological bases of individual differences in musicality. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 370: 20140092. PMID 25646515 DOI: 10.1098/rstb.2014.0092  0.76
2015 Graham SA, Deriziotis P, Fisher SE. Insights into the genetic foundations of human communication. Neuropsychology Review. 25: 3-26. PMID 25597031 DOI: 10.1007/s11065-014-9277-2  0.76
2015 Simpson NH, Ceroni F, Reader RH, Covill LE, Knight JC, Hennessy ER, Bolton PF, Conti-Ramsden G, O'Hare A, Baird G, Fisher SE, Newbury DF. Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics : Ejhg. PMID 25585696 DOI: 10.1038/ejhg.2014.296  0.76
2015 Zhao H, Zhou W, Yao Z, Wan Y, Cao J, Zhang L, Zhao J, Li H, Zhou R, Li B, Wei G, Zhang Z, French CA, Dekker JD, Yang Y, ... Fisher SE, et al. Foxp1/2/4 regulate endochondral ossification as a suppresser complex. Developmental Biology. 398: 242-54. PMID 25527076 DOI: 10.1016/j.ydbio.2014.12.007  0.76
2015 Guadalupe T, Zwiers MP, Wittfeld K, Teumer A, Vasquez AA, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, van Bokhoven H, Hegenscheid K, Völzke H, Franke B, Fisher SE, Grabe HJ, et al. Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 62: 41-55. PMID 25239853 DOI: 10.1016/j.cortex.2014.07.015  0.76
2014 Gupta CN, Calhoun VD, Rachakonda S, Chen J, Patel V, Liu J, Segall J, Franke B, Zwiers MP, Arias-Vasquez A, Buitelaar J, Fisher SE, Fernandez G, van Erp TG, Potkin S, et al. Patterns of Gray Matter Abnormalities in Schizophrenia Based on an International Mega-analysis. Schizophrenia Bulletin. PMID 25548384 DOI: 10.1093/schbul/sbu177  0.76
2014 Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H, Parr J, ... ... Fisher SE, et al. Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' European Journal of Human Genetics : Ejhg. PMID 25537359 DOI: 10.1038/ejhg.2014.275  0.76
2014 Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE. De novo TBR1 mutations in sporadic autism disrupt protein functions. Nature Communications. 5: 4954. PMID 25232744 DOI: 10.1038/ncomms5954  0.76
2014 Schreiweis C, Bornschein U, Burguière E, Kerimoglu C, Schreiter S, Dannemann M, Goyal S, Rea E, French CA, Puliyadi R, Groszer M, Fisher SE, Mundry R, Winter C, Hevers W, et al. Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance. Proceedings of the National Academy of Sciences of the United States of America. 111: 14253-8. PMID 25225386 DOI: 10.1073/pnas.1414542111  0.76
2014 Cousijn H, Eissing M, Fernández G, Fisher SE, Franke B, Zwiers M, Harrison PJ, Arias-Vásquez A. No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure. Schizophrenia Research. 159: 329-32. PMID 25217366 DOI: 10.1016/j.schres.2014.08.007  0.76
2014 Cai DC, Fonteijn H, Guadalupe T, Zwiers M, Wittfeld K, Teumer A, Hoogman M, Arias-Vásquez A, Yang Y, Buitelaar J, Fernández G, Brunner HG, van Bokhoven H, Franke B, Hegenscheid K, ... ... Fisher SE, et al. A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus. Genes, Brain, and Behavior. 13: 675-85. PMID 25130324 DOI: 10.1111/gbb.12157  0.76
2014 Brucato N, DeLisi LE, Fisher SE, Francks C. Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 555-63. PMID 25111784 DOI: 10.1002/ajmg.b.32258  0.76
2014 Gialluisi A, Newbury DF, Wilcutt EG, Olson RK, DeFries JC, Brandler WM, Pennington BF, Smith SD, Scerri TS, Simpson NH, Luciano M, Evans DM, Bates TC, Stein JF, ... ... Fisher SE, et al. Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain, and Behavior. 13: 686-701. PMID 25065397 DOI: 10.1111/gbb.12158  0.76
2014 French CA, Fisher SE. What can mice tell us about Foxp2 function? Current Opinion in Neurobiology. 28: 72-9. PMID 25048596 DOI: 10.1016/j.conb.2014.07.003  0.76
2014 Hoogman M, Guadalupe T, Zwiers MP, Klarenbeek P, Francks C, Fisher SE. Assessing the effects of common variation in the FOXP2 gene on human brain structure. Frontiers in Human Neuroscience. 8: 473. PMID 25013396 DOI: 10.3389/fnhum.2014.00473  0.76
2014 Deriziotis P, Graham SA, Estruch SB, Fisher SE. Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer. Journal of Visualized Experiments : Jove. PMID 24893771 DOI: 10.3791/51438  0.76
2014 Guadalupe T, Zwiers MP, Teumer A, Wittfeld K, Vasquez AA, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, Hegenscheid K, Völzke H, Franke B, Fisher SE, Grabe HJ, Francks C. Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets. Human Brain Mapping. 35: 3277-89. PMID 24827550 DOI: 10.1002/hbm.22401  0.76
2014 Baron-Cohen S, Murphy L, Chakrabarti B, Craig I, Mallya U, LakatoÅ¡ová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Warrier V. 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. Plos One. 9: e96374. PMID 24801482 DOI: 10.1371/journal.pone.0096374  0.76
2014 Guadalupe T, Willems RM, Zwiers MP, Arias Vasquez A, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, Franke B, Fisher SE, Francks C. Differences in cerebral cortical anatomy of left- and right-handers. Frontiers in Psychology. 5: 261. PMID 24734025 DOI: 10.3389/fpsyg.2014.00261  0.76
2014 Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Genes, Brain, and Behavior. 13: 418-29. PMID 24571439 DOI: 10.1111/gbb.12127  0.76
2014 Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H, Parr J, ... ... Fisher SE, et al. Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. European Journal of Human Genetics : Ejhg. 22: 1165-71. PMID 24518835 DOI: 10.1038/ejhg.2014.4  0.76
2014 Willems RM, Van der Haegen L, Fisher SE, Francks C. On the other hand: including left-handers in cognitive neuroscience and neurogenetics. Nature Reviews. Neuroscience. 15: 193-201. PMID 24518415 DOI: 10.1038/nrn3679  0.76
2014 Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF. Associations of HLA alleles with specific language impairment. Journal of Neurodevelopmental Disorders. 6: 1. PMID 24433325 DOI: 10.1186/1866-1955-6-1  0.76
2014 Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, ... ... Fisher SE, et al. Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine and Child Neurology. 56: 346-53. PMID 24117048 DOI: 10.1111/dmcn.12294  0.76
2013 Baron-Cohen S, Johnson D, Asher J, Wheelwright S, Fisher SE, Gregersen PK, Allison C. Is synaesthesia more common in autism? Molecular Autism. 4: 40. PMID 24252644 DOI: 10.1186/2040-2392-4-40  0.76
2013 Carrion-Castillo A, Franke B, Fisher SE. Molecular genetics of dyslexia: an overview. Dyslexia (Chichester, England). 19: 214-40. PMID 24133036 DOI: 10.1002/dys.1464  0.76
2013 Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S. Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. Plos Genetics. 9: e1003751. PMID 24068947 DOI: 10.1371/journal.pgen.1003751  0.76
2013 Fisher SE, Ridley M. Evolution. Culture, genes, and the human revolution. Science (New York, N.Y.). 340: 929-30. PMID 23704558 DOI: 10.1126/science.1236171  0.76
2013 Ayub Q, Yngvadottir B, Chen Y, Xue Y, Hu M, Vernes SC, Fisher SE, Tyler-Smith C. FOXP2 targets show evidence of positive selection in European populations. American Journal of Human Genetics. 92: 696-706. PMID 23602712 DOI: 10.1016/j.ajhg.2013.03.019  0.76
2013 Deriziotis P, Fisher SE. Neurogenomics of speech and language disorders: the road ahead. Genome Biology. 14: 204. PMID 23597266 DOI: 10.1186/gb-2013-14-4-204  0.76
2013 Gregersen PK, Kowalsky E, Lee A, Baron-Cohen S, Fisher SE, Asher JE, Ballard D, Freudenberg J, Li W. Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. Human Molecular Genetics. 22: 2097-104. PMID 23406871 DOI: 10.1093/hmg/ddt059  0.76
2013 Gialluisi A, Dediu D, Francks C, Fisher SE. Persistence and transmission of recessive deafness and sign language: new insights from village sign languages. European Journal of Human Genetics : Ejhg. 21: 894-6. PMID 23321624 DOI: 10.1038/ejhg.2012.292  0.76
2013 Graham SA, Fisher SE. Decoding the genetics of speech and language. Current Opinion in Neurobiology. 23: 43-51. PMID 23228431 DOI: 10.1016/j.conb.2012.11.006  0.76
2013 Newbury DF, Mari F, Sadighi Akha E, Macdermot KD, Canitano R, Monaco AP, Taylor JC, Renieri A, Fisher SE, Knight SJ. Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. European Journal of Human Genetics : Ejhg. 21: 361-5. PMID 22909776 DOI: 10.1038/ejhg.2012.166  0.76
2013 Vernes SC, Fisher SE. Genetic pathways implicated in speech and language Animal Models of Speech and Language Disorders. 13-40. DOI: 10.1007/978-1-4614-8400-4_2  0.76
2012 Walker RM, Hill AE, Newman AC, Hamilton G, Torrance HS, Anderson SM, Ogawa F, Derizioti P, Nicod J, Vernes SC, Fisher SE, Thomson PA, Porteous DJ, Evans KL. The DISC1 promoter: characterization and regulation by FOXP2. Human Molecular Genetics. 21: 2862-72. PMID 22434823 DOI: 10.1093/hmg/dds111  0.76
2012 Kurt S, Fisher SE, Ehret G. Foxp2 mutations impair auditory-motor association learning. Plos One. 7: e33130. PMID 22412993 DOI: 10.1371/journal.pone.0033130  0.76
2012 French CA, Jin X, Campbell TG, Gerfen E, Groszer M, Fisher SE, Costa RM. An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning. Molecular Psychiatry. 17: 1077-85. PMID 21876543 DOI: 10.1038/mp.2011.105  0.76
2012 O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, MacKenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, et al. Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)) Nature Genetics. 44: 471. DOI: 10.1038/ng0412-471  0.76
2011 Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, ... ... Fisher SE, et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. Plos Genetics. 7: e1002145. PMID 21765815 DOI: 10.1371/journal.pgen.1002145  0.76
2011 O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature Genetics. 43: 585-9. PMID 21572417 DOI: 10.1038/ng.835  0.76
2011 Whitehouse AJ, Bishop DV, Ang QW, Pennell CE, Fisher SE. CNTNAP2 variants affect early language development in the general population. Genes, Brain, and Behavior. 10: 451-6. PMID 21310003 DOI: 10.1111/j.1601-183X.2011.00684.x  0.76
2010 Roll P, Vernes SC, Bruneau N, Cillario J, Ponsole-Lenfant M, Massacrier A, Rudolf G, Khalife M, Hirsch E, Fisher SE, Szepetowski P. Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Human Molecular Genetics. 19: 4848-60. PMID 20858596 DOI: 10.1093/hmg/ddq415  0.76
2010 Newbury DF, Fisher SE, Monaco AP. Recent advances in the genetics of language impairment. Genome Medicine. 2: 6. PMID 20193051 DOI: 10.1186/gm127  0.76
2010 Fisher SE. Genetic susceptibility to stuttering. The New England Journal of Medicine. 362: 750-2. PMID 20147708 DOI: 10.1056/NEJMe0912594  0.76
2010 Gaub S, Groszer M, Fisher SE, Ehret G. The structure of innate vocalizations in Foxp2-deficient mouse pups. Genes, Brain, and Behavior. 9: 390-401. PMID 20132318 DOI: 10.1111/j.1601-183X.2010.00570.x  0.76
2009 Vernes SC, Fisher SE. Unravelling neurogenetic networks implicated in developmental language disorders. Biochemical Society Transactions. 37: 1263-9. PMID 19909259 DOI: 10.1042/BST0371263  0.76
2009 Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, ... ... Fisher SE, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American Journal of Human Genetics. 85: 264-72. PMID 19646677 DOI: 10.1016/j.ajhg.2009.07.004  0.76
2009 Kurt S, Groszer M, Fisher SE, Ehret G. Modified sound-evoked brainstem potentials in Foxp2 mutant mice. Brain Research. 1289: 30-6. PMID 19596273 DOI: 10.1016/j.brainres.2009.06.092  0.76
2009 Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, Brückner MK, Schreiweis C, Winter C, Sohr R, Becker L, Wiebe V, Nickel B, Giger T, Müller U, ... ... Fisher SE, et al. A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell. 137: 961-71. PMID 19490899 DOI: 10.1016/j.cell.2009.03.041  0.76
2009 Vernes SC, MacDermot KD, Monaco AP, Fisher SE. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European Journal of Human Genetics : Ejhg. 17: 1354-8. PMID 19352412 DOI: 10.1038/ejhg.2009.43  0.76
2009 Fisher SE, Scharff C. FOXP2 as a molecular window into speech and language. Trends in Genetics : Tig. 25: 166-77. PMID 19304338 DOI: 10.1016/j.tig.2009.03.002  0.76
2008 Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. A functional genetic link between distinct developmental language disorders. The New England Journal of Medicine. 359: 2337-45. PMID 18987363 DOI: 10.1056/NEJMoa0802828  0.76
2008 Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, ... ... Fisher SE, et al. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Current Biology : Cb. 18: 354-62. PMID 18328704 DOI: 10.1016/j.cub.2008.01.060  0.76
2008 Falcaro M, Pickles A, Newbury DF, Addis L, Banfield E, Fisher SE, Monaco AP, Simkin Z, Conti-Ramsden G. Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment. Genes, Brain, and Behavior. 7: 393-402. PMID 18005161 DOI: 10.1111/j.1601-183X.2007.00364.x  0.76
2007 Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE. High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. American Journal of Human Genetics. 81: 1232-50. PMID 17999362 DOI: 10.1086/522238  0.76
2007 Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J, Vernes SC, Fisher SE, Ren B, Geschwind DH. Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. American Journal of Human Genetics. 81: 1144-57. PMID 17999357 DOI: 10.1086/522237  0.76
2007 Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Fisher SE, et al. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry. 12: 1129-39, 1057. PMID 17667961 DOI: 10.1038/sj.mp.4002053  0.76
2007 French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE. Generation of mice with a conditional Foxp2 null allele. Genesis (New York, N.Y. : 2000). 45: 440-6. PMID 17619227 DOI: 10.1002/dvg.20305  0.76
2007 Fisher SE. Molecular windows into speech and language disorders. Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (Ialp). 59: 130-40. PMID 17556856 DOI: 10.1159/000101771  0.76
2007 Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Fisher SE, et al. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells Molecular Psychiatry. 12: 1057. DOI: 10.1038/sj.mp.4002116  0.76
2006 White SA, Fisher SE, Geschwind DH, Scharff C, Holy TE. Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10376-9. PMID 17035521 DOI: 10.1523/JNEUROSCI.3379-06.2006  0.76
2006 Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM, Bird LE, Davies KE, Fisher SE. Functional genetic analysis of mutations implicated in a human speech and language disorder. Human Molecular Genetics. 15: 3154-67. PMID 16984964 DOI: 10.1093/hmg/ddl392  0.76
2006 Fisher SE. Tangled webs: tracing the connections between genes and cognition. Cognition. 101: 270-97. PMID 16764847 DOI: 10.1016/j.cognition.2006.04.004  0.76
2006 Fisher SE, Francks C. Genes, cognition and dyslexia: learning to read the genome. Trends in Cognitive Sciences. 10: 250-7. PMID 16675285 DOI: 10.1016/j.tics.2006.04.003  0.76
2006 Fisher SE, Marcus GF. The eloquent ape: genes, brains and the evolution of language. Nature Reviews. Genetics. 7: 9-20. PMID 16369568 DOI: 10.1038/nrg1747  0.76
2006 Ogdie MN, Bakker SC, Fisher SE, Francks C, Yang MH, Cantor RM, Loo SK, van der Meulen E, Pearson P, Buitelaar J, Monaco A, Nelson SF, Sinke RJ, Smalley SL. Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13. Molecular Psychiatry. 11: 5-8. PMID 16205734 DOI: 10.1038/sj.mp.4001760  0.76
2005 Fisher SE. On genes, speech, and language. The New England Journal of Medicine. 353: 1655-7. PMID 16236736 DOI: 10.1056/NEJMp058207  0.76
2005 Gayán J, Willcutt EG, Fisher SE, Francks C, Cardon LR, Olson RK, Pennington BF, Smith SD, Monaco AP, DeFries JC. Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 46: 1045-56. PMID 16178928 DOI: 10.1111/j.1469-7610.2005.01447.x  0.76
2005 MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American Journal of Human Genetics. 76: 1074-80. PMID 15877281 DOI: 10.1086/430841  0.76
2005 Fisher SE. Dissection of molecular mechanisms underlying speech and language disorders Applied Psycholinguistics. 26: 111-128. DOI: 10.1017.S0142716405050095  0.76
2004 Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. Journal of Medical Genetics. 41: 853-7. PMID 15520411 DOI: 10.1136/jmg.2004.018341  0.76
2004 Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American Journal of Human Genetics. 75: 1046-58. PMID 15514892 DOI: 10.1086/426404  0.76
2004 Ogdie MN, Fisher SE, Yang M, Ishii J, Francks C, Loo SK, Cantor RM, McCracken JT, McGough JJ, Smalley SL, Nelson SF. Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. American Journal of Human Genetics. 75: 661-8. PMID 15297934 DOI: 10.1086/424387  0.76
2004 Loo SK, Fisher SE, Francks C, Ogdie MN, MacPhie IL, Yang M, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects. Molecular Psychiatry. 9: 485-93. PMID 14625563 DOI: 10.1038/sj.mp.4001450  0.76
2003 Francks C, Fisher SE, Marlow AJ, MacPhie IL, Taylor KE, Richardson AJ, Stein JF, Monaco AP. Familial and genetic effects on motor coordination, laterality, and reading-related cognition. The American Journal of Psychiatry. 160: 1970-7. PMID 14594743 DOI: 10.1176/appi.ajp.160.11.1970  0.76
2003 Francks C, DeLisi LE, Shaw SH, Fisher SE, Richardson AJ, Stein JF, Monaco AP. Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human Molecular Genetics. 12: 3225-30. PMID 14583442 DOI: 10.1093/hmg/ddg362  0.76
2003 Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain : a Journal of Neurology. 126: 2455-62. PMID 12876151 DOI: 10.1093/brain/awg247  0.76
2003 Marcus GF, Fisher SE. FOXP2 in focus: what can genes tell us about speech and language? Trends in Cognitive Sciences. 7: 257-262. PMID 12804692 DOI: 10.1016/S1364-6613(03)00104-9  0.76
2003 Ogdie MN, Macphie IL, Minassian SL, Yang M, Fisher SE, Francks C, Cantor RM, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. American Journal of Human Genetics. 72: 1268-79. PMID 12687500 DOI: 10.1086/375139  0.76
2003 Francks C, DeLisi LE, Fisher SE, Laval SH, Rue JE, Stein JF, Monaco AP. Confirmatory evidence for linkage of relative hand skill to 2p12-q11. American Journal of Human Genetics. 72: 499-502. PMID 12596796 DOI: 10.1086/367548  0.76
2003 Marlow AJ, Fisher SE, Francks C, MacPhie IL, Cherny SS, Richardson AJ, Talcott JB, Stein JF, Monaco AP, Cardon LR. Use of multivariate linkage analysis for dissection of a complex cognitive trait. American Journal of Human Genetics. 72: 561-70. PMID 12587094 DOI: 10.1086/368201  0.76
2003 Fisher SE, Lai CS, Monaco AP. Deciphering the genetic basis of speech and language disorders. Annual Review of Neuroscience. 26: 57-80. PMID 12524432 DOI: 10.1146/annurev.neuro.26.041002.131144  0.76
2002 Fisher SE, DeFries JC. Developmental dyslexia: genetic dissection of a complex cognitive trait. Nature Reviews. Neuroscience. 3: 767-80. PMID 12360321 DOI: 10.1038/nrn936  0.76
2002 Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature. 418: 869-72. PMID 12192408 DOI: 10.1038/nature01025  0.76
2002 Smalley SL, Kustanovich V, Minassian SL, Stone JL, Ogdie MN, McGough JJ, McCracken JT, MacPhie IL, Francks C, Fisher SE, Cantor RM, Monaco AP, Nelson SF. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American Journal of Human Genetics. 71: 959-63. PMID 12187510 DOI: 10.1086/342732  0.76
2002 Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. American Journal of Human Genetics. 70: 1183-96. PMID 11923911 DOI: 10.1086/340112  0.76
2002 Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco AP. Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric Genetics. 12: 35-41. PMID 11901358 DOI: 10.1097/00041444-200203000-00005  0.76
2002 Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP. FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics. 70: 1318-27. PMID 11894222 DOI: 10.1086/339931  0.76
2002 Francks C, Fisher SE, MacPhie IL, Richardson AJ, Marlow AJ, Stein JF, Monaco AP. A genomewide linkage screen for relative hand skill in sibling pairs. American Journal of Human Genetics. 70: 800-5. PMID 11774074 DOI: 10.1086/339249  0.76
2002 Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature Genetics. 30: 86-91. PMID 11743577 DOI: 10.1038/ng792  0.76
2001 Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 413: 519-23. PMID 11586359 DOI: 10.1038/35097076  0.76
2001 Marlow AJ, Fisher SE, Richardson AJ, Francks C, Talcott JB, Monaco AP, Stein JF, Cardon LR. Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behavior Genetics. 31: 219-30. PMID 11545538 DOI: 10.1023/A:1010209629021  0.76
2001 Siddiqui MR, Meisner S, Tosh K, Balakrishnan K, Ghei S, Fisher SE, Golding M, Shanker Narayan NP, Sitaraman T, Sengupta U, Pitchappan R, Hill AV. A major susceptibility locus for leprosy in India maps to chromosome 10p13. Nature Genetics. 27: 439-41. PMID 11279529 DOI: 10.1038/86958  0.76
2000 Francks C, Fisher SE, Marlow AJ, Richardson AJ, Stein JF, Monaco AP. A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability. Prostaglandins, Leukotrienes, and Essential Fatty Acids. 63: 27-31. PMID 10970709 DOI: 10.1054/plef.2000.0187  0.76
2000 Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. American Journal of Human Genetics. 67: 357-68. PMID 10880297 DOI: 10.1086/303011  0.76
1999 Fisher SE, Stein JF, Monaco AP. A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia). European Child & Adolescent Psychiatry. 8: 47-51. PMID 10638370  0.76
1999 Tanaka K, Fisher SE, Craig IW. Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis. Genomics. 58: 281-92. PMID 10373326 DOI: 10.1006/geno.1999.5839  0.76
1999 Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ, Weeks DE, Stein JF, Monaco AP. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. American Journal of Human Genetics. 64: 146-56. PMID 9915953 DOI: 10.1086/302190  0.76
1998 Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME. Localisation of a gene implicated in a severe speech and language disorder. Nature Genetics. 18: 168-70. PMID 9462748 DOI: 10.1038/ng0298-168  0.76
1997 Lloyd SE, Gunther W, Pearce SH, Thomson A, Bianchi ML, Bosio M, Craig IW, Fisher SE, Scheinman SJ, Wrong O, Jentsch TJ, Thakker RV. Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. Human Molecular Genetics. 6: 1233-9. PMID 9259268 DOI: 10.1093/hmg/6.8.1233  0.76
1996 Lloyd SE, Pearce SH, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SP, Wrong O, Jentsch TJ, Craig IW, Thakker RV. A common molecular basis for three inherited kidney stone diseases. Nature. 379: 445-9. PMID 8559248 DOI: 10.1038/379445a0  0.76
1995 Fisher SE, Hatchwell E, Chand A, Ockenden N, Monaco AP, Craig IW. Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146. Genomics. 29: 496-502. PMID 8666400 DOI: 10.1006/geno.1995.9976  0.76
1995 Fisher SE, van Bakel I, Lloyd SE, Pearce SH, Thakker RV, Craig IW. Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). Genomics. 29: 598-606. PMID 8575751 DOI: 10.1006/geno.1995.9960  0.76
1994 Fisher SE, Black GC, Lloyd SE, Hatchwell E, Wrong O, Thakker RV, Craig IW. Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). Human Molecular Genetics. 3: 2053-9. PMID 7874126  0.76
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