Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 30 (of 110 Records) |
| Query Trace: Sudden Infant Death Syndrome[original query] |
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| 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 |
| 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 |
| 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 |
| 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 |
| Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
| 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 |
| Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study. Lancet (London, England) 2018 4 391 (10129): 1483-1492. Männikkö Roope, Wong Leonie, Tester David J, Thor Michael G, Sud Richa, Kullmann Dimitri M, Sweeney Mary G, Leu Costin, Sisodiya Sanjay M, FitzPatrick David R, Evans Margaret J, Jeffrey Iona J M, Tfelt-Hansen Jacob, Cohen Marta C, Fleming Peter J, Jaye Amie, Simpson Michael A, Ackerman Michael J, Hanna Michael G, Behr Elijah R, Matthews Em |
| Multiple genetic variations in sodium channel subunits in a case of sudden infant death syndrome. Pacing and clinical electrophysiology : PACE 2018 3 41 (6): 620-626. Denti Federico, Bentzen Bo Hjorth, Wojciak Julianne, Thomsen Nancy Mutsaers, Scheinman Melvin, Schmitt Nico |
| 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 |
| 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 |
| 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 |
| Detoxification genes polymorphisms in SIDS exposed to tobacco smoke. Gene 2018 Jan . Filonzi Laura, Magnani Cinzia, Lavezzi Anna Maria, Vaghi Marina, Nosetti Luana, Nonnis Marzano Frances |
| Genetic Polymorphism of ?-Casein Gene in Polish Red Cattle-Preliminary Study of A1 and A2 Frequency in Genetic Conservation Herd. Animals : an open access journal from MDPI 2019 6 9 (6): . Cie?li?ska Anna, Fiedorowicz Ewa, Zwierzchowski Grzegorz, Kordulewska Natalia, Jarmo?owska Beata, Kostyra El?bie |
| Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts. European journal of human genetics : EJHG 2019 5 27 (9): 1427-1435. Paludan-Müller Christian, Ghouse Jonas, Vad Oliver B, Herfelt Cecilie B, Lundegaard Pia, Ahlberg Gustav, Schmitt Nicole, Svendsen Jesper H, Haunsø Stig, Bundgaard Henning, Hansen Torben, Kanters Jørgen K, Olesen Morten |
| 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 |
| Evidence for an association of interferon gene variants with sudden infant death syndrome. International journal of legal medicine 2019 1 133 (3): 863-869. Hafke Angelina, Schürmann Peter, Rothämel Thomas, Dörk Thilo, Klintschar Micha |
| Post-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases. International journal of legal medicine 2020 8 135 (1): 207-212. Köffer Jasmin, Scheiper-Welling Stefanie, Verhoff Marcel A, Bajanowski Thomas, Kauferstein Sil |
| 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 |
| 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 |
| Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation. Pediatric research 2021 11 92 (3): 694-699. Pfisterer Nina, Meyer-Bockenkamp Fiona, Qu Dong, Preuss Vanessa, Rothämel Thomas, Geisenberger Dorothee, Läer Katharina, Vennemann Benedikt, Albers Anne, Engelmann Theresa A, Frieling Helge, Rhein Mathias, Klintschar Micha |
| 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 |
| Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death. PloS one 2022 4 17 (4): e0267751. Ueda Atsushi, Osawa Motoki, Naito Haruaki, Ochiai Eriko, Kakimoto |
| Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edema. International journal of legal medicine 2022 4 136 (4): 1113-1120. Qu Dong, Schürmann Peter, Rothämel Thomas, Dörk Thilo, Klintschar Micha |
| Investigating genetic variants in microRNA regulators of Neurokinin-1 receptor in sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2022 Oct . Shaukat Zeeshan, Byard Roger W, Vink Robert, Hussain Rashid, Ricos Michael G, Dibbens Leanne |
| Polymorphisms of the hypothalamic-pituitary-adrenal axis may lead to an inadequate response to stress and contribute to sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2023 3 . Uzuntas Elanur, Schürmann Peter, Rothämel Thomas, Dörk Thilo, Klintschar Micha |
| Revisiting the association of sudden infant death syndrome (SIDS) with polymorphisms of NHE3 and IL13. International journal of legal medicine 2023 12 . Dong Qu, Peter Schürmann, Thomas Rothämel, Jessica Fleßner, Daniela Rehberg, Thilo Dörk, Michael Klintsch |
| Investigating cardiac genetic background in sudden infant death syndrome (SIDS). International journal of legal medicine 2024 6 . Francesca Cazzato, Mònica Coll, Simone Grassi, Anna Fernàndez-Falgueras, Laia Nogué-Navarro, Anna Iglesias, Josep Castellà, Antonio Oliva, Ramon Bruga |
- Page last reviewed:Feb 1, 2024
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