Literature DB >> 16830328

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.

Casey M Rand1, Debra E Weese-Mayer, Lili Zhou, Brion S Maher, Margaret E Cooper, Mary L Marazita, Elizabeth M Berry-Kravis.   

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Year:  2006        PMID： 16830328     DOI： 10.1002/ajmg.a.31336

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  7 in total

Review 1.  Gene variants predisposing to SIDS: current knowledge.

Authors:  Siri H Opdal; Torleiv O Rognum
Journal:  Forensic Sci Med Pathol       Date:  2010-07-11       Impact factor: 2.007

2.  PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population.

Authors:  Germaine Liebrechts-Akkerman; Fan Liu; Oscar Lao; Ariadne H A G Ooms; Kate van Duijn; Mark Vermeulen; Vincent W Jaddoe; Albert Hofman; Adèle C Engelberts; Manfred Kayser
Journal:  Int J Legal Med       Date:  2014-01-18       Impact factor: 2.686

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

Authors:  Micaela Poetsch; Rebecca Todt; Mechtild Vennemann; Thomas Bajanowski
Journal:  Int J Legal Med       Date:  2015-06-24       Impact factor: 2.686

Review 4.  The role of serotonin in respiratory function and dysfunction.

Authors:  Gérard Hilaire; Nicolas Voituron; Clément Menuet; Ronaldo M Ichiyama; Hari H Subramanian; Mathias Dutschmann
Journal:  Respir Physiol Neurobiol       Date:  2010-08-27       Impact factor: 1.931

5.  Genomic risk factors in sudden infant death syndrome.

Authors:  David W Van Norstrand; Michael J Ackerman
Journal:  Genome Med       Date:  2010-11-30       Impact factor: 11.117

6.  Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death.

Authors:  Atsushi Ueda; Motoki Osawa; Haruaki Naito; Eriko Ochiai; Yu Kakimoto
Journal:  PLoS One       Date:  2022-04-29       Impact factor: 3.752

7.  A Common 3'UTR Variant of the PHOX2B Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian Population.

Authors:  Tiziana Bachetti; Simona Bagnasco; Raffaele Piumelli; Antonella Palmieri; Isabella Ceccherini
Journal:  Front Neurol       Date:  2021-03-19       Impact factor: 4.003
  7 in total

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