Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression (Q46174250)

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scientific article published on 6 January 2009

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English	Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression	scientific article published on 6 January 2009

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scholarly article

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Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/19125159

Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression (English)

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20 December 2017

http://europepmc.org/abstract/MED/19125159

metabolic syndrome

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S Kloiber

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A Menke

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Florian Holsboer

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F Holsboer

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S Ripke

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Elisabeth Binder

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E B Binder

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M A Kohli

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T Brueckl

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M Ising

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M Uhr

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P G Unschuld

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S Horstmann

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D Salyakina

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B Muller-Myhsok

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S Lucae

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6 January 2009

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Molecular Psychiatry

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15

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736-747

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https://scigraph.springernature.com/pub.10.1038/mp.2008.142

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The metabolic syndrome: prevalence and associated risk factor findings in the US population from the Third National Health and Nutrition Examination Survey, 1988-1994.

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The metabolic syndrome: an emerging health epidemic in women

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The genetics of depression: a review

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The metabolic syndrome is associated with reduced central serotonergic responsivity in healthy community volunteers

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Obesity and depression: same disease, different names?

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Low central nervous system serotonergic responsivity is associated with the metabolic syndrome and physical inactivity

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Association of functional polymorphisms of the human tryptophan hydroxylase 2 gene with risk for bipolar disorder in Han Chinese

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Nested association between genetic variation in tryptophan hydroxylase II, bipolar affective disorder, and suicide attempts.

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Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population.

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

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Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations

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Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene in suicide victims

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Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder

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Polymorphisms in the neuronal isoform of tryptophan hydroxylase 2 are associated with bipolar disorder in French Canadian pedigrees.

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Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons

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7 January 2021

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The prevalence of the metabolic syndrome and type 2 diabetes mellitus in children and adolescents

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10.1038/MP.2008.142

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/19125159

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1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/19125159

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