(Q44445843)

3 December 2017

title

Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome (English)

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3 December 2017

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Siri H Opdal

1

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3 December 2017

Åshild Vege

series ordinal

2

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3 December 2017

Torleiv O Rognum

series ordinal

3

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3 December 2017

language of work or name

English

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publication date

27 December 2013

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3 December 2017

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3 December 2017

volume

103

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3 December 2017

issue

4

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3 December 2017

page(s)

393-397

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The brainstem and serotonin in the sudden infant death syndrome

3 December 2017

cites work

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Medullary serotonin defects and respiratory dysfunction in sudden infant death syndrome

21 January 2018

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Brainstem serotonergic deficiency in sudden infant death syndrome

21 January 2018

1 reference

Serotonin transporter gene variation is a risk factor for sudden infant death syndrome in the Japanese population

21 January 2018

1 reference

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome

21 January 2018

1 reference

Serotonin transporter gene variation in sudden infant death syndrome

21 January 2018

1 reference

No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians

21 January 2018

1 reference

A relationship between serotonin transporter genotype and in vivo protein expression and alcohol neurotoxicity.

21 January 2018

1 reference

Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531.

21 January 2018

1 reference

A functional polymorphism in the monoamine oxidase A gene promoter

21 January 2018

1 reference

Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis

21 January 2018

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Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome

21 January 2018

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Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome

21 January 2018

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Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome.

21 January 2018

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Monoamine oxidase A gene polymorphism and the pathogenesis of sudden infant death syndrome

21 January 2018

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Monoamine oxidase A and sudden infant death syndrome

21 January 2018

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Serotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome

21 January 2018

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Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

21 January 2018

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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

21 January 2018

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Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life

21 January 2018

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X-inactivation profile reveals extensive variability in X-linked gene expression in females

21 January 2018

1 reference

Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors

21 January 2018

1 reference

Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance

21 January 2018

1 reference

Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures

21 January 2018

1 reference

Gene variants predisposing to SIDS: current knowledge

21 January 2018

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Biochemical and immunological studies in SIDS victims. Clues to understanding the death mechanism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/APA.12526

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3 December 2017

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