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Research Output 2001 2019

2019

Auditory frequency discrimination in developmental dyslexia: A meta‐analysis

Witton, C., Swoboda, K., Shapiro, L. R. & Talcott, J. B., 26 Dec 2019, In : Dyslexia.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
dyslexia
discrimination
Epidemiologic Effect Modifiers
moderator

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

Gialluisi, A., Andlauer, T. F. M., Mirza-schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K. U., Czamara, D., St Pourcain, B., Brandler, W., Honbolygó, F., Tóth, D., Csépe, V., Huguet, G., Morris, A. P., Hulslander, J., Willcutt, E. G., Defries, J. C., Olson, R. K., Smith, S. D. & 25 others, Pennington, B. F., Vaessen, A., Maurer, U., Lyytinen, H., Peyrard-janvid, M., Leppänen, P. H. T., Brandeis, D., Bonte, M., Stein, J. F., Talcott, J. B., Fauchereau, F., Wilcke, A., Francks, C., Bourgeron, T., Monaco, A. P., Ramus, F., Landerl, K., Kere, J., Scerri, T. S., Paracchini, S., Fisher, S. E., Schumacher, J., Nöthen, M. M., Müller-myhsok, B. & Schulte-körne, G., 11 Feb 2019, In : Translational psychiatry. 9, 1, p. 77 77.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
Genome-Wide Association Study
Attention Deficit Disorder with Hyperactivity
Reading
Genome

Long-term Effects of Cholestatic Liver Disease in Childhood on Neuropsychological Outcomes and Neurochemistry

Talcott, J. B., Patel, T., Griffiths, G., Kelly, D. & Beath, S. V., 1 Aug 2019, In : Journal of Pediatric Gastroenterology and Nutrition. 69, 2, p. 145-151 7 p.

Research output: Contribution to journalArticle

Neurochemistry
Liver Diseases
Transplantation
Acute Liver Failure
Aptitude

On the neural basis of word reading: A meta-analysis of fMRI evidence using activation likelihood estimation

Murphy, K., Talcott, J. B. & Jogia, J. R., 1 Feb 2019, In : Journal of Neurolinguistics. 49, p. 71-83 13 p.

Research output: Contribution to journalArticle

activation
Meta-Analysis
Reading
Magnetic Resonance Imaging
evidence
2018

From Subtypes to Taxons: Identifying Distinctive Profiles of Reading Development in Children

Burgess, A. P., Witton, C., Shapiro, L. & Talcott, J. B., 28 Jul 2018, Reading and Dyslexia. Springer, p. 207-227 Chapter 11. (Reading and Dyslexia; vol. 16).

Research output: Chapter in Book/Report/Conference proceedingChapter

dyslexia
grouping
candidacy
Group
evidence
2017

Common brain structure findings across children with varied reading disability profiles

Eckert, M. A., Vaden Jr., K. I., Maxwell, A. B., Cute, S. L., Gebregziabher, M., Berninger, V. W. & Wandell, B., 20 Jul 2017, In : Scientific Reports. 7, 10 p., 6009.

Research output: Contribution to journalArticle

Open Access
File
Reading
Dyslexia
Brain
Internal Capsule
Learning Disorders

Processing of structural neuroimaging data in young children: bridging the gap between current practice and state-of-the-art methods

Phan, T. V., Smeets, D., Talcott, J. B. & Vandermosten, M., 24 Aug 2017, In : Developmental Cognitive Neuroscience. Early online

Research output: Contribution to journalArticle

Open Access
File
Neuroimaging
Magnetic Resonance Imaging
Pediatrics
Brain
Atlases

Psychophysical measurements in children: challenges, pitfalls, and considerations

Witton, C., Talcott, J. B. & Henning, G. B., 11 May 2017, In : PeerJ. 2017, 5, 22 p., e3231.

Research output: Contribution to journalArticle

Open Access
File
Measurement errors
shortenings

The DCDC2 deletion is not a risk factor for dyslexia

Scerri, T. S., Macpherson, E., Martinelli, A., Wa, W. C., Monaco, A. P., Stein, J., Zheng, M., Suk-Han Ho, C., McBride, C., Snowling, M., Hulme, C., Hayiou-Thomas, M. E., Waye, M. M. Y., Talcott, J. B. & Paracchini, S., 25 Jul 2017, In : Translational psychiatry. 7, e1182.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
Reading
Motion Perception
Visual Perception
Aptitude
2016

A case of bilateral perisylvian syndrome with reading disability

Eckert, M. A., Berninger, V. W., Hoeft, F. & Vaden Jr., K. I., Mar 2016, In : Cortex. 76, p. 121-124 4 p.

Research output: Contribution to journalArticle

Reading
Dyslexia
Agraphia
Language Development Disorders
Dysarthria

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

Pettigrew, K. A., Frinton, E., Nudel, R., Chan, M. T. M., Thompson, P., Hayiou-Thomas, M. E., Talcott, J. B., Stein, J., Monaco, A. P., Hulme, C., Snowling, M. J., Newbury, D. F. & Paracchini, S., 14 Jun 2016, In : Journal of Neurodevelopmental Disorders. 8, 8 p., 24.

Research output: Contribution to journalArticle

Open Access
File
Language
Phenotype
Reading
Genome-Wide Association Study
Child Language

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts

Shore, R., Covill, L., Pettigrew, K. A., Brandler, W. M., Diaz, R., Xu, Y., Tello, J. A., Talcott, J. B., Newbury, D. F., Stein, J., Monaco, A. P. & Paracchini, S., 1 May 2016, In : Human Molecular Genetics. 25, 9, p. 1771-1779 9 p.

Research output: Contribution to journalArticle

Open Access
File
Functional Laterality
Genome-Wide Association Study
Minisatellite Repeats
Long Noncoding RNA
Antisense RNA
2015
Open Access
File
Reading
stimulus
Linguistics
Structural Models
linguistics

Syndromes of collateral-reported psychopathology for ages 18-59 in 18 societies

Ivanova, M. Y., Achenbach, T. M., Rescorla, L. A., Turner, L. V., Árnadóttir, H. A., Au, A., Caldas, J. C., Chaalal, N., Chen, Y. C., da Rocha, M. M., Decoster, J., Fontaine, J. R. J., Funabiki, Y., Guðmundsson, H. S., Kim, Y. A., Leung, P., Liu, J., Malykh, S., Marković, J., Oh, K. J. & 10 others, Petot, J-M., Samaniego, V. C., Ferreira de Mattos Silvares, E., Šimulionienė, R., Šobot, V., Sokoli, E., Sun, G., Talcott, J. B., Vázquez, N. & Zasępa, E., Jan 2015, In : International Journal of Clinical and Health Psychology. 15, 1, p. 18-28 11 p.

Research output: Contribution to journalArticle

Open Access
File
Psychopathology
Social Problems
Checklist
Statistical Factor Analysis
Research Design

Syndromes of self-reported psychopathology for ages 18-59 in 29 societies

Ivanova, M. Y., Achenbach, T. M., Rescorla, L. A., Turner, L. V., Ahmeti-Pronaj, A., Au, A., Avila Maese, C., Bellina, M., Caldas, J. C., Chen, Y-C., Csemy, L., da Rocha, M. M., Decoster, J., Dobrean, A., Ezpeleta, L., Fontaine, J. R. J., Funabiki, Y., Guðmundsson, H. S., Harder, V. S., Leiner de la Cabada, M. & 20 others, Leung, P., Liu, J., Mahr, S., Malykh, S., Srdanovic Maras, J., Markovic, J., Ndetei, D. M., Oh, K. J., Petot, J-M., Riad, G., Sakarya, D., Samaniego, V. C., Sebre, S., Shahini, M., Silvares, E., Simulioniene, R., Sokoli, E., Talcott, J. B., Vázquez, N. & Zasępa, E., Jun 2015, In : Journal of Psychopathology and Behavioral Assessment. 37, 2, p. 171-183 13 p.

Research output: Contribution to journalArticle

Open Access
File
Psychopathology
Statistical Factor Analysis
Political Systems
Social Problems
Religion
2014
Open Access
File
Dyslexia
Crowding
literacy
Aptitude
Visual Fields

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

Becker, J., Czamara, D., Scerri, T. S., Ramus, F., Csépe, V., Talcott, J. B., Stein, J., Morris, A., Ludwig, K. U., Hoffmann, P., Honbolygó, F., Tóth, D., Fauchereau, F., Bogliotti, C., Iannuzzi, S., Chaix, Y., Valdois, S., Billard, C., George, F., Soares-Boucaud, I. & 21 others, Gérard, C-L., van der Mark, S., Schulz, E., Vaessen, A., Maurer, U., Lohvansuu, K., Lyytinen, H., Zucchelli, M., Brandeis, D., Blomert, L., Leppänen, P. H. T., Bruder, J., Monaco, A. P., Müller-Myhsok, B., Kere, J., Landerl, K., Nöthen, M. M., Schulte-Körne, G., Paracchini, S., Peyrard-Janvid, M. & Schumacher, J., 1 May 2014, In : European Journal of Human Genetics. 22, 5, p. 675-680 6 p.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
Genetic Association Studies
Linguistics
Haplotypes
Sample Size

Genome-wide screening for DNA variants associated with reading and language traits

Gialluisi, A., Newbury, D. F., Wilcutt, E. G., Olson, R. K., DeFries, J. C., Brandler, W. M., Pennington, B. F., Smith, S. D., Scerri, T. S., Simpson, N. H., Luciano, M., Evans, D. M., Bates, T. C., Stein, J. F., Talcott, J. B., Monaco, A. P., Paracchini, S., Francks, C. & Fisher, S. E., Sep 2014, In : Genes, Brain and Behavior. 13, 7, p. 686–701 16 p.

Research output: Contribution to journalArticle

Open Access
File
Reading
Language
Genome
DNA
Aptitude

Moderate relationships between NAA and cognitive ability in healthy adults: implications for cognitive spectroscopy

Patel, T., Blyth, J. C., Griffiths, G., Kelly, D. & Talcott, J. B., 14 Feb 2014, In : Frontiers in Human Neuroscience. 8, 10 p., 39.

Research output: Contribution to journalArticle

Open Access
File
Neurochemistry
Aptitude
Spectrum Analysis
Frontal Lobe
Intelligence

Postural control is not systematically related to reading skills: implications for the assessment of balance as a risk factor for developmental dyslexia

Loras, H., Sigmundsson, H., Stensdotter, A-K. & Talcott, J. B., 3 Jun 2014, In : PLoS ONE. 9, 6, 8 p., e98224.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
Reading
risk factors
Aptitude
Pressure measurement
2013

Auditory frequency discrimination: a meta-analysis and moderator variable analysis

Swoboda, K., Witton, C., Talcott, J. & Shapiro, L., 2013, (Unpublished).

Research output: Contribution to conferencePoster

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

Brandler, W. M., Morris, A. P., Evans, D. M., Scerri, T. S., Kemp, J. P., Timpson, N. J., St Pourcain, B., Smith, G. D., Ring, S. M., Stein, J., Monaco, A. P., Talcott, J. B., Fisher, S. E., Webber, C. & Paracchini, S., Sep 2013, In : PLoS Genetics. 9, 9, 11 p., e1003751.

Research output: Contribution to journalArticle

Open Access
File
asymmetry
Functional Laterality
hands
Hand
Genome-Wide Association Study

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

Simpson, N. H., Addis, L., Brandler, W. M., Slonims, V., Clark, A., Watson, J., Scerri, T. S., Hennessy, E. R., Bolton, P. F., Conti-Ramsden, G., Fairfax, B. P., Knight, J. C., Stein, J. F., Talcott, J. B., O'Hare, A., Baird, G., Paracchini, S., Fisher, S. E. & Newbury, D. F., 2013, In : Developmental Medicine and Child Neurology. 56, 4, p. 346-353 8 p.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
Sex Chromosomes
Aneuploidy
Language
Klinefelter Syndrome

Probing the neurocognitive trajectories of children's reading skills

Talcott, J., Witton, C. & Stein, J., Feb 2013, In : Neuropsychologia. 51, 3, p. 472-481 10 p.

Research output: Contribution to journalArticle

Reading
Aptitude
Reading Skills
Trajectory
Vision Disorders

What drives the prediction of early reading? An analysis of stimulus and response-type

Cunningham, A., Shapiro, L., Witton, C., Talcott, J., Burgess, A. & Swoboda, K., 2013, (Unpublished).

Research output: Contribution to conferencePaper

Reading
Drive
Structural Models
Language
2012

Interval timing in children: effects of auditory and visual pacing stimuli and relationships with reading and attention variables

Birkett, E. & Talcott, J., 10 Aug 2012, In : PLoS ONE. 7, 8, 9 p., e42820.

Research output: Contribution to journalArticle

Open Access
File
Aptitude
Reading
Dyslexia
Psychometrics
Fingers

Investigating phonological and auditory processing in Reception children at risk of reading difficulties

Swoboda, K., Shapiro, L., Witton, C., Talcott, J., Rochelle, K. & Burgess, A., 2012, (Unpublished).

Research output: Contribution to conferencePoster

Language against the odds, or rather not: the weak central coherence hypothesis and language

Vulchanova, M., Vulchanov, V., Talcott, J. B. & Stankova, M., Jan 2012, In : Journal of Neurolinguistics. 25, 1, p. 13-30 18 p.

Research output: Contribution to journalArticle

Language
Aptitude
language
Learning
Asperger Syndrome

Morphology in autism spectrum disorders: local processing bias and language

Vulchanova, M., Talcott, J. B., Vulchanov, V., Stankova, M. & Eshuis, H., 2012, In : Cognitive Neuropsychology. 29, 7-8, p. 584-600 17 p.

Research output: Contribution to journalArticle

Language
Asperger Syndrome
Aptitude
Linguistics
Autistic Disorder

Sensory thresholds obtained from MEG data: cortical psychometric functions

Witton, C., Patel, T., Furlong, P., Worthen, S., Henning, G. B. & Talcott, J., 15 Nov 2012, In : Neuroimage. 63, 3, p. 1249-1256 8 p.

Research output: Contribution to journalArticle

Sensory Thresholds
Psychophysics
Psychometrics
Auditory Evoked Potentials
Population

Speech and non-speech skills in the prediction of letter-knowledge: the influence of task

Cunningham, A., Shapiro, L., Witton, C., Talcott, J., Rochelle, K. & Burgess, A., 2012, (Unpublished).

Research output: Contribution to conferencePoster

File
Reading
Longitudinal Studies

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure

Scerri, T. S., Darki, F., Newbury, D. F., Whitehouse, A. J. O., Peyrard-Janvid, M., Matsson, H., Ang, Q. W., Pennell, C. E., Ring, S., Stein, J., Morris, A. P., Monaco, A. P., Kere, J., Talcott, J., Klingberg, T. & Paracchini, S., 28 Nov 2012, In : PLoS ONE. 7, 11, 8 p., e50321.

Research output: Contribution to journalArticle

File
Dyslexia
Aptitude
Language
Genes
loci

Timing continuous or discontinuous movements across effectors specified by different pacing modalities and intervals

Lorås, H., Sigmundsson, H., Talcott, J., Ohberg, F. & Stensdotter, A. K., Aug 2012, In : Experimental Brain Research. 220, 3-4, p. 335-347 13 p.

Research output: Contribution to journalArticle

Hand
2011
File
Dyslexia
Crowding
Cues
Reaction Time
Aptitude

Cognitive outcomes in paediatric liver transplant survivors

Patel, T., Talcott, J. B., Beath, S. V., Blyth, J. C., Sira, J., Mears, J., Griffiths, G., van Mourik, I. & Kelly, D., 1 Aug 2011, In : Pediatric Transplantation . 15, S1, p. 65 1 p., 93.

Research output: Contribution to journalMeeting abstract

Survivors
Liver Diseases
Pediatrics
Transplants
Liver

Evaluation of brain development using 1H-MRS-Detectable metabolites as biomarkers in children with liver desease

Patel, T., Kelly, D., Beath, S. V., Blyth, J. C., Thai, J. N., Sira, J., Griffiths, G. & Talcott, J. B., 1 Aug 2011, In : Pediatric Transplantation . 15, S1, p. 121 1 p., 330.

Research output: Contribution to journalMeeting abstract

Biomarkers
Liver
Brain
Liver Diseases
Transplants

Introduction to volume 17 of Dyslexia

Talcott, J., Feb 2011, In : Dyslexia. 17, 1, p. 1 1 p.

Research output: Contribution to journalEditorial

Dyslexia
dyslexia

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects

Newbury, D. F., Paracchini, S., Scerri, T. S., Winchester, L., Addis, L., Richardson, A. J., Walter, J., Stein, J. F., Talcott, J. B. & Monaco, A. P., Jan 2011, In : Behavior Genetics. 41, 1, p. 90-104 15 p.

Research output: Contribution to journalArticle

Open Access
File
Dyslexia
Reading
Language
etiology
mouth

PCSK6 is associated with handedness in individuals with dyslexia

Scerri, T. S., Brandler, W. M., Paracchini, S., Morris, A. P., Ring, S. M., Richardson, A. J., Talcott, J. B., Stein, J. F. & Monaco, A. P., 1 Feb 2011, In : Human Molecular Genetics. 20, 3, p. 608-614 7 p., ddq475.

Research output: Contribution to journalArticle

Open Access
File
Functional Laterality
Dyslexia
Reading
Hand
Alleles

Polyunsaturated fatty acids and cognitive outcomes in paediatric liver disease

Griffiths, G., Talcott, J. B., Blyth, J., Sira, J., Mears, J., van Mourik, I., McKiernan, P., Beath, S. V. & Kelly, D., 1 Aug 2011, In : Pediatric Transplantation . 15, S1, p. 65 1 p., 94.

Research output: Contribution to journalMeeting abstract

Unsaturated Fatty Acids
Liver Diseases
Pediatrics
Omega-6 Fatty Acids
Automatic Data Processing
2010

Are poor mathematics skills associated with visual deficits in temporal processing?

Sigmundsson, H., Anholt, S. K. & Talcott, J. B., 22 Jan 2010, In : Neuroscience Letters. 469, 2, p. 248-250 3 p.

Research output: Contribution to journalArticle

Mathematics
Dyslexia
Dyscalculia
Forms and Records Control
Developmental Disabilities

Editorial

Talcott, J. B., Feb 2010, In : Dyslexia. 16, 1

Research output: Contribution to journalEditorial

Identification of candidate genes for dyslexia susceptibility on chromosome 18

Scerri, T. S., Paracchini, S., Morris, A., MacPhie, I. L., Talcott, J. B., Stein, J. F., Smith, S. D., Pennington, B. F., Olson, R. K., DeFries, J. C., Monaco, A. P. & Richardson, A. J., 28 Oct 2010, In : PLoS ONE. 5, 10, 8 p., e13712.

Research output: Contribution to journalArticle

Open Access
File
Chromosomes, Human, Pair 18
Dyslexia
Genetic Association Studies
Chromosomes
linkage (genetics)
2009

A snapshot of dyslexia from a research perspective

Talcott, J. B., 2009, Employment and Dyslexia Handbook 2009. McLoughlin, D. & Leather, C. (eds.). Bracknell (UK): The British Dyslexia Association, p. 31-39 9 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Considerations for pediatric neuroimaging at the translational coalface

Thai, N. J. & Talcott, J. B., 1 Jan 2009, In : American Journal of Bioethics. 9, 1, p. 18-20 3 p.

Research output: Contribution to journalArticle

Dyslexia from a cognitive neuroscience perspective: making links and moving forward

Talcott, J. B. & Birkett, E. E., 2009, The Dyslexia Handbook 2009/10. Brunswick, N. (ed.). Bracknell (UK): The British Dyslexia Association, p. 151-160 10 p.

Research output: Chapter in Book/Report/Conference proceedingChapter