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Next Steps in Prader-Willi Syndrome Research: On the Relationship between Genotype and Phenotype

International journal of molecular sciences, 2022-10, Vol.23 (20), p.12089

2022

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The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype

EBioMedicine, 2022-04, Vol.78, p.103952-103952, Article 103952

2022

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Evidence for the independence of positive and negative well-being: Implications for quality of life assessment

British journal of health psychology, 2003-02, Vol.8 (1), p.107-122

2003

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Disorders of hypothalamic function: Insights from Prader–Willi syndrome and the effects of craniopharyngioma

Handbook of Clinical Neurology, 2021, Vol.181, p.381-389

2021

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Defining Mental and Behavioural Disorders in Genetically Determined Neurodevelopmental Syndromes with Particular Reference to Prader-Willi Syndrome

Genes, 2019-12, Vol.10 (12), p.1025

2019

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Cognition in people with Prader-Willi syndrome: Insights into genetic influences on cognitive and social development

Neuroscience and biobehavioral reviews, 2017-01, Vol.72, p.153-167

2017

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Mechanistic insights into the genetics of affective psychosis from Prader-Willi syndrome

The Lancet. Psychiatry, 2018-04, Vol.5 (4), p.370-378

2018

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A review of psychiatric conceptions of mental and behavioural disorders in Prader-Willi syndrome

Neuroscience and biobehavioral reviews, 2018-12, Vol.95, p.396-405

2018

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Developing an understanding of skin picking in people with Prader-Willi syndrome: A structured literature review and re-analysis of existing data

Neuroscience and biobehavioral reviews, 2020-05, Vol.112, p.48-61

2020

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Changing rates of genetic subtypes of Prader-Willi syndrome in the UK

European journal of human genetics : EJHG, 2007-01, Vol.15 (1), p.127-130

2007

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The transition between the phenotypes of Prader‐Willi syndrome during infancy and early childhood

Developmental medicine and child neurology, 2010-06, Vol.52 (6), p.e88-e93

2010

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Neurobehavioral phenotype in Prader-Willi syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2010-11, Vol.154C (4), p.438-447

2010

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Behaviour and cognition in the imprinted gene disorder, Prader-Willi Syndrome (PWS)

Current opinion in behavioral sciences, 2019-02, Vol.25, p.89-95

2019

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Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter

Journal of human genetics, 2007-04, Vol.52 (4), p.297-307

2007

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Symptoms of psychological distress predict 7-year mortality

Psychological medicine, 1995-09, Vol.25 (5), p.1073-1086

1995

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Neurobehavioral Phenotype in Prader-Willi Syndrome: Behavioral Phenotypes in Neurogenetic Syndromes

American journal of medical genetics. Part C, Seminars in medical genetics, 2010, Vol.154 (4), p.438-447

2010

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Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy

The Lancet (British edition), 2002-01, Vol.359 (9301), p.135-136

2002

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Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome

Journal of intellectual disability research, 2004-02, Vol.48 (2), p.172-187

2004

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The paradox of Prader-Willi syndrome: a genetic model of starvation

The Lancet (British edition), 2003-09, Vol.362 (9388), p.989-991

2003

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Relationship between the IQ of people with Prader-Willi syndrome and that of their siblings: evidence for imprinted gene effects

Journal of intellectual disability research, 2009-05, Vol.53 (5), p.411-418

2009

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Prader-Willi syndrome: A study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders

European child & adolescent psychiatry, 2004-02, Vol.13 (1), p.42-50

2004

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In search of the psychosis gene in people with Prader-Willi syndrome

American journal of medical genetics. Part A, 2008-04, Vol.146A (7), p.843-853

2008

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Academic underachievement by people with Prader-Willi syndrome

Journal of intellectual disability research, 2004-02, Vol.48 (2), p.188-200

2004

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The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder

Journal of intellectual disability research, 2009-06, Vol.53 (6), p.538-547

2009

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Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader–Willi syndrome: an ERP study

Clinical neurophysiology, 2005-06, Vol.116 (6), p.1464-1470

2005

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Next Steps in Prader-Willi Syndrome Research: On the Relationship between Genotype and Phenotype

The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype

Evidence for the independence of positive and negative well-being: Implications for quality of life assessment

Disorders of hypothalamic function: Insights from Prader–Willi syndrome and the effects of craniopharyngioma

Defining Mental and Behavioural Disorders in Genetically Determined Neurodevelopmental Syndromes with Particular Reference to Prader-Willi Syndrome

Cognition in people with Prader-Willi syndrome: Insights into genetic influences on cognitive and social development

Mechanistic insights into the genetics of affective psychosis from Prader-Willi syndrome

A review of psychiatric conceptions of mental and behavioural disorders in Prader-Willi syndrome

Developing an understanding of skin picking in people with Prader-Willi syndrome: A structured literature review and re-analysis of existing data

Changing rates of genetic subtypes of Prader-Willi syndrome in the UK

The transition between the phenotypes of Prader‐Willi syndrome during infancy and early childhood

Neurobehavioral phenotype in Prader-Willi syndrome

Behaviour and cognition in the imprinted gene disorder, Prader-Willi Syndrome (PWS)

Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter

Symptoms of psychological distress predict 7-year mortality

Neurobehavioral Phenotype in Prader-Willi Syndrome: Behavioral Phenotypes in Neurogenetic Syndromes

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome

The paradox of Prader-Willi syndrome: a genetic model of starvation

Relationship between the IQ of people with Prader-Willi syndrome and that of their siblings: evidence for imprinted gene effects

Prader-Willi syndrome: A study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders

In search of the psychosis gene in people with Prader-Willi syndrome

Academic underachievement by people with Prader-Willi syndrome

The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder

Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader–Willi syndrome: an ERP study

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