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Review Article

Premature birth and diseases in premature infants: common genetic background?

Pages 21-24 | Received 28 Feb 2012, Accepted 28 Feb 2012, Published online: 02 Mar 2012

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Nuran Ustun, Nilnur Eyerci, Nilgun Karadag, Ahmet Yesilyurt, Aysegul Zenciroglu & Nurullah Okumus. (2020) Association of vitamin D receptor gene FokI and TaqI polymorphisms and risk of RDS. The Journal of Maternal-Fetal & Neonatal Medicine 33:21, pages 3640-3646.
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Neda Fatahi, Nikoo Niknafs, Majid Kalani, Hosein Dalili, Mamak Shariat, Elaheh Amini, Tahereh Esmaeilnia Shirvani, Amir Kamal Hardani, Roya Taheritafti, Nasrin Ghasemi-Fakhr, Mohsen Ghadami, Javad Tavakkoly-Bazzaz, Ramin Rashidi-Nezhad, Fatemeh Nayeri & Ali Rashidi-Nezhad. (2018) Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS. The Journal of Maternal-Fetal & Neonatal Medicine 31:22, pages 2965-2970.
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Neda Fatahi, Hosein Dalili, Majid Kalani, Nikoo Niknafs, Mamak Shariat, Javad Tavakkoly-Bazzaz, Elaheh Amini, Tahereh Esmaeilnia Shirvani, Amir kamal Hardani, Roya Taheritafti, Nasrin Ghasemi-Fakhr, Mohsen Ghadami, Fatemeh Nayeri & Ali Rashidi-Nezhad. (2017) Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS. The Journal of Maternal-Fetal & Neonatal Medicine 30:21, pages 2585-2589.
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Articles from other publishers (11)

Lauren S. Richardson, Nkechinyere Emezienna, Irina Burd, Brandie D. Taylor, Morgan R. Peltier, Arum Han & Ramkumar Menon. (2022) Adapting an organ‐on‐chip device to study the effect of fetal sex and maternal race/ethnicity on preterm birth related intraamniotic inflammation leading to fetal neuroinflammation. American Journal of Reproductive Immunology 88:6.
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Wei Shen, Penghao Kuang, Bin Wang, Qiyi Zeng, Chao Chen & Xinzhu Lin. (2020) Genetic Polymorphisms of LPCAT1, CHPT1 and PCYT1B and Risk of Neonatal Respiratory Distress Syndrome among a Chinese Han Population. Pediatrics & Neonatology 61:3, pages 318-324.
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Nai-Jia Yao, Wu-Shiun Hsieh, Chyi-Her Lin, Ching-Ing Tseng, Wan-Yu Lin, Po-Hsiu Kuo, Yen-Ting Yu, Wei J. Chen & Suh-Fang Jeng. (2020) Interaction Between Prematurity and the MAOA Gene on Mental Development in Children: A Longitudinal View. Frontiers in Pediatrics 8.
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Kristen Ferriero & Pamela Arn. 2020. Cerebral Palsy. Cerebral Palsy 37 44 .
Kristen Ferriero & Pamela Arn. 2019. Cerebral Palsy. Cerebral Palsy 1 8 .
N. S. ArtyomovaO. M. KovalovaV. I. PokhylkoS. M. TsvirenkoL. A. Zhuk. (2018) THE ROLE OF 4a4b POLYMORPHISM OF THE eNOS GENE IN THE DEVELOPMENT OF LETHAL OUTCOMES OF SEVERE INTRAVENTRICULAR HAEMORRHAGE IN PRETERM INFANTS. Bulletin of Problems Biology and Medicine 4.3:141, pages 95.
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Prakasham Rumajogee, Tatiana Bregman, Steven P. Miller, Jerome Y. Yager & Michael G. Fehlings. (2016) Rodent Hypoxia–Ischemia Models for Cerebral Palsy Research: A Systematic Review. Frontiers in Neurology 7.
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Laura R. Ment, Ulrika Ådén, Charles R. Bauer, Henrietta S. Bada, Waldemar A. Carlo, Jeffrey R. Kaiser, Aiping Lin, Charles Michael Cotten, Jeffrey Murray, Grier Page, Mikko Hallman, Richard P. Lifton & Heping Zhang. (2015) Genes and environment in neonatal intraventricular hemorrhage. Seminars in Perinatology 39:8, pages 592-603.
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Anne Korhonen & Mari Kangasniemi. (2014) Nurses' narratives on termination of primary nursing relationship with parents in neonatal intensive care. Scandinavian Journal of Caring Sciences 28:4, pages 716-723.
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Laura R. Ment, Ulrika Ådén, Aiping Lin, Soo Hyun Kwon, Murim Choi, Mikko Hallman, Richard P. Lifton, Heping Zhang & Charles R. Bauer. (2013) Gene–environment interactions in severe intraventricular hemorrhage of preterm neonates. Pediatric Research 75:1-2, pages 241-250.
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A. Fucic, J. Katic, E. Fthenou, M. Kogevinas, D. Plavec, J. Koppe, D. Batinic, G. Chalkiadaki, L. Chatzi, R. Lasan, J. Kleinjans & M. Kirsch-Volders. (2013) Increased frequency of micronuclei in mononucleated lymphocytes and cytome analysis in healthy newborns as an early warning biomarkers of possible future health risks. Reproductive Toxicology 42, pages 110-115.
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