The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age
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Timothy C. Bates | I. Deary | A. Gow | A. Pattie | M. Luciano | T. Bates
[1] Stefano Tamburin,et al. Neuropsychological Testing , 2021, Mastering Modern Psychological Testing.
[2] Stuart J. Ritchie,et al. A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence , 2018, Molecular Psychiatry.
[3] Joanna M. Wardlaw,et al. Brain grey and white matter predictors of verbal ability traits in older age: The Lothian Birth Cohort 1936 , 2017, NeuroImage.
[4] Timothy C. Bates,et al. Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes , 2017, Behavior Genetics.
[5] P. Khatri,et al. Gene annotation bias impedes biomedical research , 2017, bioRxiv.
[6] G. Gong,et al. ROBO1 polymorphisms, callosal connectivity, and reading skills , 2017, Human brain mapping.
[7] M. Varshney,et al. Genes, Gender, Environment, and Novel Functions of Estrogen Receptor Beta in the Susceptibility to Neurodevelopmental Disorders , 2017, Brain sciences.
[8] Peng-Xiang Zuo,et al. DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children , 2017, Neural regeneration research.
[9] F. Wang,et al. Modulatory effects of acupuncture on brain networks in mild cognitive impairment patients , 2017, Neural regeneration research.
[10] C. Francks,et al. Association analysis of dyslexia candidate genes in a Dutch longitudinal sample , 2017, European Journal of Human Genetics.
[11] Jiajia Zhang,et al. The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants , 2016, Molecular Neurobiology.
[12] A. Friederici,et al. Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort , 2016, Scientific Reports.
[13] Ruirui Jia,et al. Expression Patterns and Potential Biological Roles of Dip2a , 2015, PloS one.
[14] C. Wijmenga,et al. Population-specific genotype imputations using minimac or IMPUTE2 , 2015, Nature Protocols.
[15] M. Nöthen,et al. Polymorphisms in DCDC2 and S100B associate with developmental dyslexia , 2015, Journal of Human Genetics.
[16] Joris M. Mooij,et al. MAGMA: Generalized Gene-Set Analysis of GWAS Data , 2015, PLoS Comput. Biol..
[17] L. Field,et al. Association of the ROBO1 gene with reading disabilities in a family‐based analysis , 2014, Genes, brain, and behavior.
[18] R. Giorda,et al. KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia , 2014, Journal of Human Genetics.
[19] P. Padakannaya,et al. Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia. , 2013, Gene.
[20] A. Morris,et al. Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort , 2013, European Journal of Human Genetics.
[21] Dominika Dykiert,et al. Retrospective validation of WTAR and NART scores as estimators of prior cognitive ability using the Lothian Birth Cohort 1936 , 2014 .
[22] Timothy C. Bates,et al. A genome-wide association study for reading and language abilities in two population cohorts , 2013, Genes, brain, and behavior.
[23] Prakash Padakannaya,et al. Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population , 2013, Journal of Human Genetics.
[24] Carsten O. Daub,et al. Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins , 2013, Biological Psychiatry.
[25] Christopher Schatschneider,et al. Exploring how nature and nurture affect the development of reading: an analysis of the Florida Twin Project on reading. , 2013, Developmental psychology.
[26] T. Richards,et al. The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes , 2013, Front. Psychology.
[27] R. Todd Constable,et al. Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability , 2012, NeuroImage.
[28] Torkel Klingberg,et al. Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter Structure , 2012, Biological Psychiatry.
[29] Margit Burmeister,et al. Association of the DYX1C1 Dyslexia Susceptibility Gene with Orthography in the Chinese Population , 2012, PloS one.
[30] M. Nöthen,et al. The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language , 2012, Behavior genetics.
[31] Dorothy V.M. Bishop,et al. DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits , 2011, Biological Psychiatry.
[32] Lorna M. Lopez,et al. Genome-wide association studies establish that human intelligence is highly heritable and polygenic , 2011, Molecular Psychiatry.
[33] D. Bishop,et al. CNTNAP2 variants affect early language development in the general population , 2011, Genes, brain, and behavior.
[34] B. Franke,et al. A theoretical molecular network for dyslexia: integrating available genetic findings , 2011, Molecular Psychiatry.
[35] C. Pennell,et al. Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population , 2011, Genes, brain, and behavior.
[36] J. B. Talcott,et al. Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects , 2010, Behavior genetics.
[37] Timothy C. Bates,et al. Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation , 2010, Molecular Psychiatry.
[38] H. Hakonarson,et al. Analysing biological pathways in genome-wide association studies , 2010, Nature Reviews Genetics.
[39] T. Mimori,et al. DIP2 disco‐interacting protein 2 homolog A (Drosophila) is a candidate receptor for follistatin‐related protein/follistatin‐like 1 – analysis of their binding with TGF‐β superfamily proteins , 2010, The FEBS journal.
[40] R. Plomin,et al. Quantitative genetics in the era of molecular genetics: learning abilities and disabilities as an example. , 2010, Journal of the American Academy of Child and Adolescent Psychiatry.
[41] Yun Li,et al. METAL: fast and efficient meta-analysis of genomewide association scans , 2010, Bioinform..
[42] P. Visscher,et al. Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. , 2010, American journal of human genetics.
[43] R. Plomin,et al. Preschool speech, language skills, and reading at 7, 9, and 10 years: etiology of the relationship. , 2010, Journal of speech, language, and hearing research : JSLHR.
[44] R. Tannock,et al. Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319 , 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[45] G. Schulte-Körne,et al. Genetics of developmental dyslexia , 2010, European Child & Adolescent Psychiatry.
[46] Nicholas G Martin,et al. Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample , 2010, European Journal of Human Genetics.
[47] Mabel L. Rice,et al. Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment , 2009, Journal of Neurodevelopmental Disorders.
[48] Dorothy V.M. Bishop,et al. CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment , 2009, American journal of human genetics.
[49] B. Byrne,et al. Genetic and environmental influences on aspects of literacy and language in early childhood: Continuity and change from preschool to Grade 2 , 2009, Journal of Neurolinguistics.
[50] Bertram Müller-Myhsok,et al. Further evidence for DYX1C1 as a susceptibility factor for dyslexia , 2009, Psychiatric genetics.
[51] Richard Wade-Martins,et al. A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene , 2009, PLoS genetics.
[52] P. Ahnert,et al. The role of gene DCDC2 in German dyslexics , 2009, Annals of dyslexia.
[53] B. Franke,et al. Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion , 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[54] Jiannis Ragoussis,et al. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. , 2008, The American journal of psychiatry.
[55] R. Tannock,et al. The KIAA0319-Like (KIAA0319L) Gene on Chromosome 1p34 as a Candidate for Reading Disabilities , 2008, Journal of neurogenetics.
[56] D. Geschwind,et al. A functional genetic link between distinct developmental language disorders. , 2008, The New England journal of medicine.
[57] Qizhai Li,et al. Improved correction for population stratification in genome‐wide association studies by identifying hidden population structures , 2008, Genetic epidemiology.
[58] Margaret J. Wright,et al. A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability , 2007, Biological Psychiatry.
[59] Ellen M Wijsman,et al. Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[60] Heikki Lyytinen,et al. A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. , 2007, Human molecular genetics.
[61] G. D. Rosen,et al. DYX1C1 functions in neuronal migration in developing neocortex , 2006, Neuroscience.
[62] M C O'Donovan,et al. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia , 2006, Molecular Psychiatry.
[63] F. Ramus,et al. From genes to behavior in developmental dyslexia , 2006, Nature Neuroscience.
[64] C. Schatschneider,et al. Longitudinal Genetic Analysis of Early Reading: The Western Reserve Reading Project , 2006, Reading and writing.
[65] A. Galaburda. Dyslexia—A molecular disorder of neuronal migration , 2005 .
[66] P. Skudlarski,et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[67] B. Pennington,et al. TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort , 2005, Human Genetics.
[68] Peter Holmans,et al. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. , 2005, American journal of human genetics.
[69] Maria Luisa Lorusso,et al. A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia , 2005, European Journal of Human Genetics.
[70] E. Green,et al. No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia , 2005, Molecular Psychiatry.
[71] C. Francks,et al. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. , 2004, American journal of human genetics.
[72] M W Lovett,et al. Support for EKN1 as the susceptibility locus for dyslexia on 15q21 , 2004, Molecular Psychiatry.
[73] C. Francks,et al. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK , 2004, Journal of Medical Genetics.
[74] Timothy C. Bates,et al. Behaviour genetic analyses of reading and spelling: A component processes approach , 2004 .
[75] B. Pennington,et al. Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses , 2004, Human Genetics.
[76] D. Nyholt. A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. , 2004, American journal of human genetics.
[77] J. Fletcher,et al. Interventions Aimed at Improving Reading Success: An Evidence-Based Approach , 2003, Developmental neuropsychology.
[78] M. Barnes,et al. Early Brain Injury in Children: Development and Reorganization of Cognitive Function , 2003, Developmental neuropsychology.
[79] Heikki Lyytinen,et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[80] S. Fisher,et al. Developmental dyslexia: genetic dissection of a complex cognitive trait , 2002, Nature Reviews Neuroscience.
[81] J. Hewitt,et al. Stability of Genetic and Environmental Influences on Reading Performance at 7, 12, and 16 Years of Age in the Colorado Adoption Project , 2001, Behavior genetics.
[82] Ian J. Deary,et al. The Stability of Individual Differences in Mental Ability from Childhood to Old Age: Follow-up of the 1932 Scottish Mental Survey , 2000 .
[83] M. C. Smith,et al. Differences in adults' reading practices and literacy proficiencies , 1996 .
[84] S. Folstein,et al. “Mini-mental state”: A practical method for grading the cognitive state of patients for the clinician , 1975 .
[85] Cyril Burt,et al. THE TREND OF SCOTTISH INTELLIGENCE , 1950 .
[86] A. Hill,et al. Wechsler Test of Adult Reading , 2017 .
[87] Sarah E Medland,et al. Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits , 2011, Behavior genetics.
[88] G. Abecasis,et al. Genotype imputation. , 2009, Annual review of genomics and human genetics.
[89] Carmela Bravaccio,et al. No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy , 2007, Journal of Molecular Neuroscience.
[90] Andreas Ziegler,et al. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. , 2006, American journal of human genetics.
[91] Ian J Deary,et al. The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947. , 2004, Journal of personality and social psychology.
[92] Ingvar Lundberg,et al. A technique for group screening of dyslexia among adults , 2003 .
[93] J. Mcardle,et al. Comparative longitudinal structural analyses of the growth and decline of multiple intellectual abilities over the life span. , 2002, Developmental psychology.
[94] M Coltheart,et al. DRC: a dual route cascaded model of visual word recognition and reading aloud. , 2001, Psychological review.
[95] M. C. Smith,et al. Change in Reading Ability and Attitudes from Childhood to Adulthood: A Life Span Perspective , 1993 .
[96] B. Pennington,et al. Spelling errors and reading fluency in compensated adult dyslexics , 1991, Annals of dyslexia.
[97] J. Raven,et al. Manual for Raven's progressive matrices and vocabulary scales , 1962 .
[98] P. Donnelly,et al. Progress and promise in understanding the genetic basis of common diseases , 2015, Proceedings of the Royal Society B: Biological Sciences.