Literature DB >> 21761998

Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders.

Tony J Simon1.   

Abstract

Several neurodevelopmental disorders of known genetic etiology generate phenotypes that share the characteristic of numerical and mathematical cognitive impairments. This article reviews some of the main findings that suggest a possible key role that spatial and temporal information processing impairments may play in the atypical development of numerical cognitive competence. The question of what neural substrate might underlie these impairments is also addressed, as are the challenges for interpreting neural structure/cognitive function mapping in atypically developing populations.

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Year:  2011        PMID： 21761998      PMCID： PMC3152315          DOI： 10.1080/87565641.2010.549879

Source DB:  PubMed          Journal:  Dev Neuropsychol        ISSN： 1532-6942            Impact factor:   2.253


  111 in total

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2.  Diffusion tensor MR imaging of the human brain.

Authors:  C Pierpaoli; P Jezzard; P J Basser; A Barnett; G Di Chiro
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3.  Developmental changes in mental arithmetic: evidence for increased functional specialization in the left inferior parietal cortex.

Authors:  S M Rivera; A L Reiss; M A Eckert; V Menon
Journal:  Cereb Cortex       Date:  2005-02-16       Impact factor: 5.357

4.  Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome.

Authors:  Joel P Bish; Renee Chiodo; Victoria Mattei; Tony J Simon
Journal:  Brain Cogn       Date:  2007-05-11       Impact factor: 2.310

5.  Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.

Authors:  T L Jernigan; U Bellugi
Journal:  Arch Neurol       Date:  1990-05

6.  Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

Authors:  Linda E Campbell; Eileen Daly; Fiona Toal; Angela Stevens; Rayna Azuma; Marco Catani; Virginia Ng; Therese van Amelsvoort; Xavier Chitnis; William Cutter; Declan G M Murphy; Kieran C Murphy
Journal:  Brain       Date:  2006-03-28       Impact factor: 13.501

7.  Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome.

Authors:  S Eliez; C M Blasey; L S Freund; T Hastie; A L Reiss
Journal:  Brain       Date:  2001-08       Impact factor: 13.501

8.  Differential impact of the FMR1 gene on visual processing in fragile X syndrome.

Authors:  Cary S Kogan; Isabelle Boutet; Kim Cornish; Shahin Zangenehpour; Kathy T Mullen; Jeanette J A Holden; Vazken M Der Kaloustian; Eva Andermann; Avi Chaudhuri
Journal:  Brain       Date:  2004-01-21       Impact factor: 13.501

Review 9.  Effects of development and enculturation on number representation in the brain.

Authors:  Daniel Ansari
Journal:  Nat Rev Neurosci       Date:  2008-04       Impact factor: 34.870

10.  Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome.

Authors:  Tony J Simon; Zhongle Wu; Brian Avants; Hui Zhang; James C Gee; Glenn T Stebbins
Journal:  Behav Brain Funct       Date:  2008-06-17       Impact factor: 3.759
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  8 in total

Review 1.  The importance of considering all attributes of memory in behavioral endophenotyping of mouse models of genetic disease.

Authors:  Michael R Hunsaker
Journal:  Behav Neurosci       Date:  2012-06       Impact factor: 1.912

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Authors:  Michael R Hunsaker
Journal:  Prog Neurobiol       Date:  2012-01-13       Impact factor: 11.685

3.  CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation.

Authors:  Michael R Hunsaker; Kyoungmi Kim; Rob Willemsen; Robert F Berman
Journal:  Hippocampus       Date:  2012-06-18       Impact factor: 3.899

4.  White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging.

Authors:  Julio Villalon-Reina; Neda Jahanshad; Elliott Beaton; Arthur W Toga; Paul M Thompson; Tony J Simon
Journal:  Neuroimage       Date:  2013-04-18       Impact factor: 6.556

5.  Spatiotemporal processing deficits in female CGG KI mice modeling the fragile X premutation.

Authors:  Rachel M Borthwell; Michael R Hunsaker; Rob Willemsen; Robert F Berman
Journal:  Behav Brain Res       Date:  2012-04-26       Impact factor: 3.332

6.  Cognitive and behavioral functioning in two neurogenetic disorders; how different are these aspects in Duchenne muscular dystrophy and Neurofibromatosis type 1?

Authors:  Danique M J Hellebrekers; Sandra A M van Abeelen; Coriene E Catsman; Sander M J van Kuijk; Annick M Laridon; Sylvia Klinkenberg; Jos G M Hendriksen; Johan S H Vles
Journal:  PLoS One       Date:  2022-10-10       Impact factor: 3.752

7.  Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes.

Authors:  Andrea I Quintero; Elliott A Beaton; Danielle J Harvey; Judith L Ross; Tony J Simon
Journal:  J Neurodev Disord       Date:  2014-03-14       Impact factor: 4.025

8.  Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome.

Authors:  Kathryn L McCabe; Abbie M Popa; Courtney Durdle; Michele Amato; Margarita H Cabaral; Joshua Cruz; Ling M Wong; Danielle Harvey; Nicole Tartaglia; Tony J Simon
Journal:  J Neurodev Disord       Date:  2019-12-20       Impact factor: 4.025
  8 in total

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