HuGE Literature Finder
Reproductive and Child Health
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| Association between monoamine oxidase A promoter polymorphism and the risk of sudden infant death syndrome: a meta-analysis. International journal of legal medicine 2021 Feb . Zhou Qiaoxia, Gong Daoyin, Zhang Yu, Huang Feij |
| Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS). International journal of legal medicine 2021 Feb . Kerz J, Schürmann P, Rothämel T, Dörk T, Klintschar |
| Aquaporin-1 and aquaporin-9 gene variations in sudden infant death syndrome. International journal of legal medicine 2021 Jan . Opdal Siri Hauge, Ferrante Linda, Rognum Torleiv Ole, Stray-Pedersen Ar |
| Polymorphisms in the myeloid differentiation primary response 88 pathway do not explain low expression levels in sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2019 Jul 108 (7): 1262-1266. Bjørnvall Christina Dybdrodt, Opdal Siri H, Rognum Torleiv O, Ferrante Lin |
| Association of SNPs in transferrin and transferrin receptor genes with blood iron levels in human. Legal medicine (Tokyo, Japan) 2018 Oct 36 17-20. Fujihara Junko, Yasuda Toshihiro, Kimura-Kataoka Kaori, Takeshita Har |
| Noncardiac genetic predisposition in sudden infant death syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Aug . Gray Belinda, Tester David J, Wong Leonie Ch, Chanana Pritha, Jaye Amie, Evans Jared M, Baruteau Alban-Elouen, Evans Margaret, Fleming Peter, Jeffrey Iona, Cohen Marta, Tfelt-Hansen Jacob, Simpson Michael A, Ackerman Michael J, Behr Elijah |
| Cardiac Genetic Predisposition in Sudden Infant Death Syndrome. Journal of the American College of Cardiology 2018 Mar 71 (11): 1217-1227. Tester David J, Wong Leonie C H, Chanana Pritha, Jaye Amie, Evans Jared M, FitzPatrick David R, Evans Margaret J, Fleming Peter, Jeffrey Iona, Cohen Marta C, Tfelt-Hansen Jacob, Simpson Michael A, Behr Elijah R, Ackerman Michael |
| Detoxification genes polymorphisms in SIDS exposed to tobacco smoke. Gene 2018 Jan . Filonzi Laura, Magnani Cinzia, Lavezzi Anna Maria, Vaghi Marina, Nosetti Luana, Marzano Francesco Nonn |
| Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome. The Journal of pediatrics 2018 12 203 423-428.e11. Tester David J, Wong Leonie C H, Chanana Pritha, Gray Belinda, Jaye Amie, Evans Jared M, Evans Margaret, Fleming Peter, Jeffrey Iona, Cohen Marta, Tfelt-Hansen Jacob, Simpson Michael A, Behr Elijah R, Ackerman Michael |
| The gene encoding the inwardly rectifying potassium channel Kir4.1 may be involved in sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2017 Sep 106 (9): 1474-1480. Opdal Siri H, Vege Åshild, Stray-Pedersen Arne, Rognum Torleiv |
| High serum serotonin in sudden infant death syndrome. Proceedings of the National Academy of Sciences of the United States of America 2017 Jul . Haynes Robin L, Frelinger Andrew L, Giles Emma K, Goldstein Richard D, Tran Hoa, Kozakewich Harry P, Haas Elisabeth A, Gerrits Anja J, Mena Othon J, Trachtenberg Felicia L, Paterson David S, Berry Gerard T, Adeli Khosrow, Kinney Hannah C, Michelson Alan |
| Influence of functional polymorphism in MIF promoter on sudden cardiac death in Chinese populations. Forensic sciences research 2017 2 (3): 152-157. Yin Zhixia, Zhang Qing, Zhou Wei, Wang Shouyu, Wang Chaoqun, He Yan, Li Lijuan, Gao Yuzh |
| Candidate gene variants of the immune system and sudden infant death syndrome. International journal of legal medicine 2016 Mar . Fard Delnaz, Läer Katharina, Rothämel Thomas, Schürmann Peter, Arnold Matthias, Cohen Marta, Vennemann Mechtild, Pfeiffer Heidi, Bajanowski Thomas, Pfeufer Arne, Dörk Thilo, Klintschar Micha |
| [High incidence of sudden cardiac death in one family with type-3 long QT syndrome: molecular genetics and electrophysiology mechanism analysis]. Zhonghua xin xue guan bing za zhi 2015 Dec 43 (12): 1046-50. Zhou Hui, Li Zhang, Ali Raza Ghani, Zhu Wengen, Zhou Qiongqiong, Shen Yang, Xie Jinyan, Cao Qing, Wan Rong, Hu Jinzhu, Hong K |
| Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases. European journal of human genetics : EJHG 2015 Sep . Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie |
| Polymorphisms in genes of respiratory control and sudden infant death syndrome. International journal of legal medicine 2015 Sep 129 (5): 977-84. Läer Katharina, Dörk Thilo, Vennemann Marielle, Rothämel Thomas, Klintschar Micha |
| That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS). International journal of legal medicine 2015 Sep 129 (5): 985-9. Poetsch Micaela, Todt Rebecca, Vennemann Mechtild, Bajanowski Thom |
| Increased prevalence of two mitochondrial DNA polymorphisms in functional disease: Are we describing different parts of an energy-depleted elephant? Mitochondrion 2015 Jul 23 1-6. Boles Richard G, Zaki Essam A, Kerr Jonathan R, Das Kingshuk, Biswas Sawona, Gardner A |
| Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland. Molecular and cellular probes 2015 Feb 29 (1): 31-4. Schubert Stephanie, Haas Cordula, Bartsch Christine, Mirshekarnejad Mandana, Kohrs Sarah, Roettinger Irene, Grosshennig Anika, Stuhrmann Manfred, Scholz Caroline, Schmidtke Jö |
| Genetic and Environmental Factors Affecting TNF-a Responses in Relation to Sudden Infant Death Syndrome. Frontiers in immunology 2015 6 374. Moscovis Sophia M, Gordon Ann E, Al Madani Osama M, Gleeson Maree, Scott Rodney J, Hall Sharron T, Burns Christine, Blackwell Caroli |
| Virus Infections and Sudden Death in Infancy: The Role of Interferon-?. Frontiers in immunology 2015 6 107. Moscovis Sophia M, Gordon Ann E, Al Madani Osama M, Gleeson Maree, Scott Rodney J, Hall Sharron T, Burns Christine, Blackwell Caroli |
| Sodium/proton exchanger 3 (NHE3) and sudden infant death syndrome (SIDS). International journal of legal medicine 2014 Nov 128 (6): 939-43. Studer Jacqueline, Bartsch Christine, Haas Cordu |
| Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians. Journal of forensic sciences 2014 Nov 59 (6): 1650-3. Studer Jacqueline, Bartsch Christine, Haas Cordu |
| The role of clinical, genetic and segregation evaluation in sudden infant death. Forensic science international 2014 Sep 242 9-15. Campuzano Oscar, Allegue Catarina, Sarquella-Brugada Georgia, Coll Monica, Mates Jesus, Alcalde Mireia, Ferrer-Costa Carles, Iglesias Anna, Brugada Josep, Brugada Ram |
| Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS). Pediatric research 2014 Jul 76 (1): 41-5. Studer Jacqueline, Bartsch Christine, Haas Cordu |
| Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases. Acta paediatrica (Oslo, Norway : 1992) 2014 Jul 103 (7): 775-9. Läer K, Vennemann M, Rothämel T, Klintschar |
| Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit. International journal of legal medicine 2014 Jan 128 (1): 43-9. Groß Maximilian, Bajanowski Thomas, Vennemann Mechtild, Poetsch Micae |
| Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2013 Dec 102 (12): e546-52. Barrett Karlene T, Rodikova Ekaterina, Weese-Mayer Debra E, Rand Casey M, Marazita Mary L, Cooper Margaret E, Berry-Kravis Elizabeth M, Bech-Hansen N Torben, Wilson Richard J |
| Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome. International journal of legal medicine 2013 Nov 127 (6): 1087-91. Läer Katharina, Vennemann Marielle, Rothämel Thomas, Klintschar Micha |
| Is prone sleeping dangerous for neonates? Polysomnographic characteristics and NDN gene analysis. Ci ji yi xue za zhi = Tzu-chi medical journal 0 31 (2): 113-117. Wong Shi-Bing, Zhao Lu-Lu, Chuang Shu-Hua, Tsai Wen-Hsin, Yu Chun-Hsien, Tsai Li-Pi |
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- Page last updated:Jun 28, 2022
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