Literature DB >> 17562581

Cognitive characteristics of children with genetic syndromes.

Tony J Simon1.   

Abstract

This article presents the cognitive profile observed in children with one of several common genetic syndromes associated with "nonverbal learning disorders." It introduces the concept of a cognitive endophenotype to help explain the similar pattern of impairments across the syndromes. It explores the explanation of diverse impairments in higher-order visual, spatial, temporal, numerical, and executive cognitive competencies deriving from origins in more basic attentional and spatial cognitive dysfunctions. The importance of a developmental approach to understanding dysfunction is stressed.

Entities:  

Mesh：

Year:  2007        PMID： 17562581      PMCID： PMC2435488          DOI： 10.1016/j.chc.2007.03.002

Source DB:  PubMed          Journal:  Child Adolesc Psychiatr Clin N Am        ISSN： 1056-4993


  59 in total

1.  Single-trial classification of parallel pre-attentive and serial attentive processes using functional magnetic resonance imaging.

Authors:  Manuela Piazza; Eric Giacomini; Denis Le Bihan; Stanislas Dehaene
Journal:  Proc Biol Sci       Date:  2003-06-22       Impact factor: 5.349

2.  Brain anatomy in Turner syndrome: evidence for impaired social and spatial-numerical networks.

Authors:  N Molko; A Cachia; D Riviere; J F Mangin; M Bruandet; D LeBihan; L Cohen; S Dehaene
Journal:  Cereb Cortex       Date:  2004-03-28       Impact factor: 5.357

3.  Three parietal circuits for number processing.

Authors:  Stanislas Dehaene; Manuela Piazza; Philippe Pinel; Laurent Cohen
Journal:  Cogn Neuropsychol       Date:  2003-05-01       Impact factor: 2.468

4.  Edinburgh study of growth and development of children with sex chromosome abnormalities. IV.

Authors:  S G Ratcliffe; G E Butler; M Jones
Journal:  Birth Defects Orig Artic Ser       Date:  1990

5.  Sex chromosome aneuploidy: the Denver Prospective Study.

Authors:  A Robinson; B G Bender; M G Linden; J A Salbenblatt
Journal:  Birth Defects Orig Artic Ser       Date:  1990

6.  Cognitive modularity and genetic disorders.

Authors:  S J Paterson; J H Brown; M K Gsödl; M H Johnson; A Karmiloff-Smith
Journal:  Science       Date:  1999-12-17       Impact factor: 47.728

7.  Further delineation of the executive deficit in males with fragile-X syndrome.

Authors:  John Wilding; Kim Cornish; Fehmidah Munir
Journal:  Neuropsychologia       Date:  2002       Impact factor: 3.139

8.  A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.

Authors:  R J Shprintzen; R B Goldberg; M L Lewin; E J Sidoti; M D Berkman; R V Argamaso; D Young
Journal:  Cleft Palate J       Date:  1978-01

9.  Infants' metaphysics: the case of numerical identity.

Authors:  F Xu; S Carey
Journal:  Cogn Psychol       Date:  1996-04       Impact factor: 3.468

10.  Visuospatial executive function in Turner syndrome: functional MRI and neurocognitive findings.

Authors:  Sarah J Hart; Marsha L Davenport; Stephen R Hooper; Aysenil Belger
Journal:  Brain       Date:  2006-02-27       Impact factor: 13.501
View more
  10 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

2.  Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation.

Authors:  Michael R Hunsaker; Naomi J Goodrich-Hunsaker; Rob Willemsen; Robert F Berman
Journal:  Behav Brain Res       Date:  2010-05-15       Impact factor: 3.332

Review 3.  Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.

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

4.  Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications.

Authors:  David D Stephenson; Elliott A Beaton; Carl F Weems; Kathleen Angkustsiri; Tony J Simon
Journal:  Behav Brain Res       Date:  2014-06-03       Impact factor: 3.332

5.  Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments.

Authors:  Naomi J Goodrich-Hunsaker; Ling M Wong; Yingratana McLennan; Siddharth Srivastava; Flora Tassone; Danielle Harvey; Susan M Rivera; Tony J Simon
Journal:  Brain Cogn       Date:  2011-02-03       Impact factor: 2.310

6.  Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?

Authors:  Kathleen Angkustsiri; Beth Goodlin-Jones; Lesley Deprey; Khyati Brahmbhatt; Susan Harris; Tony J Simon
Journal:  J Autism Dev Disord       Date:  2014-04

7.  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

8.  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

9.  Multimodal MRI reveals structural connectivity differences in 22q11 deletion syndrome related to impaired spatial working memory.

Authors:  Erik O'Hanlon; Sarah Howley; Sarah Prasad; Jane McGrath; Alexander Leemans; Colm McDonald; Hugh Garavan; Kieran C Murphy
Journal:  Hum Brain Mapp       Date:  2016-08-11       Impact factor: 5.038

10.  Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome.

Authors:  Margarita H Cabaral; Elliott A Beaton; Joel Stoddard; Tony J Simon
Journal:  J Neurodev Disord       Date:  2012-04-12       Impact factor: 4.025
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.