Thomas Rothamel

Carl Neuberg Str. 1
Hannover, NI 30625, Germany

Last Updated: 09/26/2026

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Found 15 publications

Genetic Association Study of Acetylcholinesterase (ACHE) and Butyrylcholinesterase (BCHE) Variants in Sudden Infant Death Syndrome (SIDS).

Genetic Association Study of Acetylcholinesterase (ACHE) and Butyrylcholinesterase (BCHE) Variants in Sudden Infant Death Syndrome (SIDS).

Journal: Genes

Published: November 18, 2024

Revisiting the association of sudden infant death syndrome (SIDS) with polymorphisms of NHE3 and IL13.

Revisiting the association of sudden infant death syndrome (SIDS) with polymorphisms of NHE3 and IL13.

Journal: International journal of legal medicine

Published: October 04, 2023

Polymorphisms of the hypothalamic-pituitary-adrenal axis may lead to an inadequate response to stress and contribute to sudden infant death syndrome.

Polymorphisms of the hypothalamic-pituitary-adrenal axis may lead to an inadequate response to stress and contribute to sudden infant death syndrome.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: September 07, 2022

Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edema.

Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edema.

Journal: International journal of legal medicine

Published: November 26, 2021

Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation.

Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation.

Journal: Pediatric research

Published: June 05, 2021

Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS).

Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS).

Journal: International journal of legal medicine

Published: July 14, 2020

Evidence for an association of interferon gene variants with sudden infant death syndrome.

Evidence for an association of interferon gene variants with sudden infant death syndrome.

Journal: International journal of legal medicine

Published: July 27, 2018

Candidate gene variants of the immune system and sudden infant death syndrome.

Candidate gene variants of the immune system and sudden infant death syndrome.

Journal: International journal of legal medicine

Published: November 18, 2015

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.

Journal: Translational psychiatry

Published: September 28, 2015

Molecular characterization of disseminated pilocytic astrocytomas.

Molecular characterization of disseminated pilocytic astrocytomas.

Journal: Neuropathology and applied neurobiology

Published: February 24, 2015

Polymorphisms in genes of respiratory control and sudden infant death syndrome.

Polymorphisms in genes of respiratory control and sudden infant death syndrome.

Journal: International journal of legal medicine

Published: January 16, 2015

Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases.

Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: July 16, 2014

Showing 1-12 of 15

Last Updated: 09/26/2026