Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.

Molecular and cellular probes - 1 Feb 2015

Schubert Stephanie, Haas Cordula, Bartsch Christine, Mirshekarnejad Mandana, Kohrs Sarah, Roettinger Irene, Grosshennig Anika, Stuhrmann Manfred, Scholz Caroline, Schmidtke Jörg

Abstract excerpt

Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.4...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Association Studies
Share to Germany

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Nuclear Proteins

Share to Sudden Infant Death

Share to Switzerland

Share to White People

Source

Identifiers

PMID: 25449952
DOI: 10.1016/j.mcp.2014.10.006

Genes

TSPYL1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25449952-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.PMID 25449952Read ↗

Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.Semantic proximity Read ↗

Sudden infant death with dysgenesis of the testes syndrome in a non-Amish infant: A case report.Semantic proximity Read ↗

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of <i>TSPYL</i> loss of functionSemantic proximity Read ↗

Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants.Semantic proximity Read ↗

Aquaporin-1 and aquaporin-9 gene variations in sudden infant death syndrome.Semantic proximity Read ↗

Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis.Semantic proximity Read ↗

Unravelling the disease mechanism for TSPYL1 deficiency.Semantic proximity Read ↗

Genetics of the sudden infant death syndrome.Semantic proximity Read ↗

Gene variants predisposing to SIDS: current knowledge.Semantic proximity Read ↗

Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians.Semantic proximity Read ↗

Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation.Semantic proximity Read ↗

That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.