Literature DB >> 19504726

A specific pathway can be identified between genetic characteristics and behaviour profiles in Prader-Willi syndrome via cognitive, environmental and physiological mechanisms.

K A Woodcock1, C Oliver, G W Humphreys.   

Abstract

BACKGROUND: Behavioural phenotypes associated with genetic syndromes have been extensively investigated in order to generate rich descriptions of phenomenology, determine the degree of specificity of behaviours for a particular syndrome, and examine potential interactions between genetic predispositions for behaviour and environmental influences. However, relationships between different aspects of behavioural phenotypes have been less frequently researched and although recent interest in potential cognitive phenotypes or endophenotypes has increased, these are frequently studied independently of the behavioural phenotypes.
METHOD: Taking Prader-Willi syndrome (PWS) as an example, we discuss evidence suggesting specific relationships between apparently distinct aspects of the PWS behavioural phenotype and relate these to specific endophenotypic characteristics.
RESULTS: The framework we describe progresses through biological, cognitive, physiological and behavioural levels to develop a pathway from genetic characteristics to behaviour with scope for interaction with the environment at any stage.
CONCLUSIONS: We propose this multilevel approach as useful in setting out hypotheses in order to structure research that can more rapidly advance theory.

Entities:  

Mesh:

Year:  2009        PMID: 19504726     DOI: 10.1111/j.1365-2788.2009.01167.x

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  12 in total

1.  Repetitive behavior in Rubinstein-Taybi syndrome: parallels with autism spectrum phenomenology.

Authors:  Jane Waite; Joanna Moss; Sarah R Beck; Caroline Richards; Lisa Nelson; Kate Arron; Cheryl Burbidge; Katy Berg; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2015-05

2.  Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance.

Authors:  Donna Reid; Jo Moss; Lisa Nelson; Laura Groves; Chris Oliver
Journal:  J Neurodev Disord       Date:  2017-08-15       Impact factor: 4.025

3.  The neuroanatomy of genetic subtype differences in Prader-Willi syndrome.

Authors:  Robyn A Honea; Laura M Holsen; Rebecca J Lepping; Rodrigo Perea; Merlin G Butler; William M Brooks; Cary R Savage
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2012-03       Impact factor: 3.568

Review 4.  Epigenetics and biomarkers in the staging of neuropsychiatric disorders.

Authors:  Trevor Archer; Richard J Beninger; Tomas Palomo; Richard M Kostrzewa
Journal:  Neurotox Res       Date:  2010-03-17       Impact factor: 3.911

5.  Delineation of behavioral phenotypes in genetic syndromes: characteristics of autism spectrum disorder, affect and hyperactivity.

Authors:  Chris Oliver; Katy Berg; Jo Moss; Kate Arron; Cheryl Burbidge
Journal:  J Autism Dev Disord       Date:  2011-08

6.  Establishing the transdiagnostic contextual pathways of emotional outbursts.

Authors:  Justin Cheuk Yin Chung; Carmel Mevorach; Kate Anne Woodcock
Journal:  Sci Rep       Date:  2022-05-06       Impact factor: 4.996

7.  Dissociation of Cross-Sectional Trajectories for Verbal and Visuo-Spatial Working Memory Development in Rubinstein-Taybi Syndrome.

Authors:  Jane Waite; Sarah R Beck; Mary Heald; Laurie Powis; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2016-06

8.  Improving the Health and Well-Being of Adults With Conditions of a Genetic Origin: Views from Professionals, Syndrome Support Groups and Parents.

Authors:  Marcus Redley; Merel Pannebakker; Anthony Holland
Journal:  J Appl Res Intellect Disabil       Date:  2016-10-24

Review 9.  Puzzle Pieces: Neural Structure and Function in Prader-Willi Syndrome.

Authors:  Katherine E Manning; Anthony J Holland
Journal:  Diseases       Date:  2015-12-17

10.  Social and emotional processing in Prader-Willi syndrome: genetic subtype differences.

Authors:  Alexandra P Key; Dorita Jones; Elisabeth M Dykens
Journal:  J Neurodev Disord       Date:  2013-03-27       Impact factor: 4.025

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