TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome (Q35963550)

11 August 2017

TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome (English)

1 reference

11 August 2017

Elisabeth M Dykens

1

1 reference

PMC publication ID

3353323

11 August 2017

Elizabeth Roof

series ordinal

2

1 reference

PMC publication ID

3353323

11 August 2017

Douglas Bittel

series ordinal

3

1 reference

PMC publication ID

3353323

11 August 2017

Merlin G Butler

series ordinal

4

1 reference

11 August 2017

18 March 2011

1 reference

The Journal of Child Psychology and Psychiatry

11 August 2017

1 reference

11 August 2017

52

1 reference

11 August 2017

5

1 reference

11 August 2017

580-587

1 reference

Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Long-acting octreotide treatment causes a sustained decrease in ghrelin concentrations but does not affect weight, behaviour and appetite in subjects with Prader-Willi syndrome.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Assessment of hyperphagia in Prader-Willi syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Serotonergic drugs : effects on appetite expression and use for the treatment of obesity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

The hypothalamus, hormones, and hunger: alterations in human obesity and illness

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Amygdala responsiveness is modulated by tryptophan hydroxylase-2 gene variation.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Neurocognitive consequences of sleep deprivation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2).

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

A unique central tryptophan hydroxylase isoform

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

The epidemiology of major depressive disorder: results from the National Comorbidity Survey Replication (NCS-R)

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Psychiatric disorders in Prader-Willi syndrome: epidemiology and management

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome.

11 July 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

21 January 2018

Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Obsessions and compulsions in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Acute tryptophan depletion improves performance and modulates the BOLD response during a Stroop task in healthy females

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Support for the involvement of TPH2 gene in affective disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Association study of tryptophan hydroxylase 2 gene polymorphisms in panic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Effects of acute tryptophan depletion on memory, attention and executive functions: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

TPH2 gene variation and conflict processing in a cognitive and an emotional Stroop task

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Family-based association study of TPH1 and TPH2 polymorphisms in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

A functional variant of the tryptophan hydroxylase 2 gene impacts working memory: a genetic imaging study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Disorder in the serotonergic system due to tryptophan hydroxylation impairment: a cause of hypothalamic syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Genetic variation of serotonin function and cognitive control.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02365.X

Influence of functional tryptophan hydroxylase 2 gene variation and sex on the startle response in children, young adults, and older adults

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

A population-based association study of candidate genes for depression and sleep disturbance.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Characterizing sleep in children with autism spectrum disorders: a multidimensional approach

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

Severe sleep disturbance and daytime challenging behaviour in children with severe learning disabilities.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3353323

10.1111/J.1469-7610.2011.02365.X

24 September 2018

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7ip3lfisyngfnnx4rdrdhdmzie

30 July 2022

release_7ip3lfisyngfnnx4rdrdhdmzie

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7ip3lfisyngfnnx4rdrdhdmzie

30 July 2022

https://api.fatcat.wiki/v0/release/7ip3lfisyngfnnx4rdrdhdmzie

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/7ip3lfisyngfnnx4rdrdhdmzie

PubMed publication ID

1 reference

30 July 2022