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Reproductive and Child Health
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| Endothelial nitric oxide synthase G894T, intron 4 VNTR, and T786C polymorphisms in retinopathy of prematurity. Journal of neonatal-perinatal medicine 2021 Sep . Tekke?in F, Yurdakok M, Gumus E, Babaoglu M O, Bozkurt A, Caliskan Kadayifcilar S, Eldem M B, Korkmaz A, Yigit S, Tekinalp |
| The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms. Ophthalmic genetics 2021 Aug 1-7. Ilguy Serdar, Cilingir Oguz, Bilgec Mustafa Deger, Ozalp Onur, Erzurumluoglu Gokalp Ebru, Arslan Serap, Tekin Neslihan, Aydemir Ozge, Erol Nazmiye, Colak Ertugrul, Gursoy Husey |
| Pro12Ala polymorphism of peroxisome proliferator activated receptor gamma 2 may be associated with adverse neurodevelopment in European preterm babies. Brain and behavior 2021 Jun . Victor Suresh, Chew Andrew, Falconer Sho |
| Association between perinatal factors, genetic susceptibility to obesity and age at adiposity rebound in children of the EDEN mother-child cohort. International journal of obesity (2005) 2021 May . Cissé Aminata Hallimat, Lioret Sandrine, de Lauzon-Guillain Blandine, Forhan Anne, Ong Ken K, Charles Marie Aline, Heude Barba |
| Therapy for Apnoea of Prematurity: A Retrospective Study on Effects of Standard Dose and Genetic Variability on Clinical Response to Caffeine Citrate in Chinese Preterm Infants. Advances in therapy 2020 Nov . He Xin, Qiu Jin-Chun, Lu Ke-Yu, Guo Hong-Li, Li Ling, Jia Wei-Wei, Ni Ming-Ming, Liu Yun, Xu Jing, Chen Feng, Cheng R |
| Developmental population pharmacokinetics of caffeine in Chinese premature infants with apnoea of prematurity: A post-marketing study to support paediatric labelling in China. British journal of clinical pharmacology 2020 Jul . Gao Xiang-Bo, Zheng Yi, Yang Fan, Wang Chen-Hong, Jiang Zhou-Hong, Wu Yue-E, Jacqz-Aigrain Evelyne, Ni Shao-Qing, Zhao W |
| Association of preeclampsia with infant APOL1 genotype in African Americans. BMC medical genetics 2020 May 21 (1): 110. Miller Anna K, Azhibekov Timur, O'Toole John F, Sedor John R, Williams Scott M, Redline Raymond W, Bruggeman Leslie |
| Interaction Between Prematurity and the MAOA Gene on Mental Development in Children: A Longitudinal View. Frontiers in pediatrics 2020 8 92. Yao Nai-Jia, Hsieh Wu-Shiun, Lin Chyi-Her, Tseng Ching-Ing, Lin Wan-Yu, Kuo Po-Hsiu, Yu Yen-Ting, Chen Wei J, Jeng Suh-Fa |
| Single nucleotide vitamin D receptor polymorphisms (FokI, BsmI, ApaI, and TaqI) in the pathogenesis of prematurity complications. Scientific reports 2020 12 10 (1): 21098. Kosik Katarzyna, Szpecht Dawid, Al-Saad Salwan R, Karbowski Lukasz M, Kurzawinska Grazyna, Szymankiewicz Marta, Drews Krzysztof, Wolski Hubert, Seremak-Mrozikiewicz Agniesz |
| An Updated and Comprehensive Meta-Analysis of Association between VEGA -634G?>?C, -460T?>?C, +405G?>?C and +936C?>?T Polymorphisms and Retinopathy of Prematurity Risk. Fetal and pediatric pathology 2019 Dec 1-17. Gohari Mohsen, Bahrami Reza, Dastgheib Seyed Alireza, Lookzadeh Mohamad Hosein, Noorishadkam Mahmood, Mirjalili Seyed Reza, Zare-Shehneh Masoud, Neamatzadeh Hosse |
| Association between vitamin D plasma concentrations and VDR gene variants and the risk of premature birth. BMC pregnancy and childbirth 2019 Dec 20 (1): 3. Dutra Letícia Veríssimo, Affonso-Kaufman Fernando Alves, Cafeo Fernanda Ramires, Kassai Milene Saori, Barbosa Caio Parente, Santos Figueiredo Francisco Winter, Suano-Souza Fabíola Isabel, Bianco Bian |
| Influence of single nucleotide polymorphisms (SNPs) in immunoregulatory genes in the morbidity of preterm newborns. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2019 Nov 1-6. Ribeiro de Andrade Ramos Bruna, Cosi Bento Giovana Fernanda, Navascues Bernardino Rômulo Augusto, Miot Hélio Amante, Guimarães da Silva Márc |
| Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. Scientific reports 2019 Feb 9 (1): 1976. Cullen Harriet, Krishnan Michelle L, Selzam Saskia, Ball Gareth, Visconti Alessia, Saxena Alka, Counsell Serena J, Hajnal Jo, Breen Gerome, Plomin Robert, Edwards A Dav |
| The relevance of IL-1ß and IL-1RN gene polymorphisms in the etiology of preterm delivery in the population of Polish women. Ginekologia polska 2019 90 (4): 212-216. Barlik Magdalena, Mrozikiewicz Aleksandra E, Drews-Piasecka Elzbieta, Kurzawinska Grazyna, Malewski Zbyszko, Drews Krzyszt |
| Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth. BMC genetics 2018 Oct 19 (1): 94. Hamvas Aaron, Feng Rui, Bi Yingtao, Wang Fan, Bhattacharya Soumyaroop, Mereness Jared, Kaushal Madhurima, Cotten C Michael, Ballard Philip L, Mariani Thomas J, |
| Genotype-phenotype correlations in pediatric patients with myotonic dystrophy type 1. Korean journal of pediatrics 2018 Sep . Kim Hyeong Jung, Na Ji-Hoon, Lee Young-Mo |
| Influence of MBL2 and NOS3 polymorphisms on spontaneous preterm birth in North East Brazil: genetics and preterm birth. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2018 Jun 1-231. Vasconcelos Carvalho da Silva Lícia, Javorski Natassia, Cavalcanti Brandão Lucas André, de Carvalho Lima Marília, Crovella Sergio, Eickmann Sophie Hele |
| Evidence of a gene-environment interaction of NODAL variants and inflammation in preterm birth. Journal of perinatology : official journal of the California Perinatal Association 2018 Feb . Starr Lisa M, Heba Taghreed, Dufort Dani |
| Genetic association of single nucleotide polymorphisms of FZD4 and BDNF genes with retinopathy of prematurity. Ophthalmic genetics 2018 Feb 1-6. Lasabova Zora, Stanclova Andrea, Grendar Marian, Mikolajcikova Silvia, Calkovska Andrea, Lenhartova Nina, Ziak Peter, Matasova Katarina, Caprnda Martin, Kruzliak Peter, Zibolen Mir |
| Influence of polymorphisms in VEGF, ACE, TNF and GST genes on the susceptibility to retinopathy of prematurity among Chinese infants. International journal of ophthalmology 2018 11 (9): 1451-1457. Lei Xiao-Jun, Zhao Yong-Xia, Qiao To |
| Mutation spectrum of NDP, FZD4 and TSPAN12 genes in Indian patients with retinopathy of prematurity. The British journal of ophthalmology 2017 Oct . Rathi Sonika, Jalali Subhadra, Musada Ganeswara Rao, Patnaik Satish, Balakrishnan Divya, Hussain Anjli, Kaur Inderje |
| Candidate gene analysis in pathogenesis of surgically and non-surgically treated necrotizing enterocolitis in preterm infants. Molecular and cellular biochemistry 2017 Aug . Szpecht Dawid, Neumann-Klimasi?ska Natalia, B?aszczy?ski Micha?, Seremak-Mrozikiewicz Agnieszka, Kurzawi?ska Gra?yna, Cygan Dorothy, Szymankiewicz Marta, Drews Krzysztof, Gadzinowski Janu |
| Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene. Scientific reports 2017 Aug 7 (1): 9271. Mahlman Mari, Karjalainen Minna K, Huusko Johanna M, Andersson Sture, Kari M Anneli, Tammela Outi K T, Sankilampi Ulla, Lehtonen Liisa, Marttila Riitta H, Bassler Dirk, Poets Christian F, Lacaze-Masmonteil Thierry, Danan Claude, Delacourt Christophe, Palotie Aarno, Muglia Louis J, Lavoie Pascal M, Hadchouel Alice, Rämet Mika, Hallman Mik |
| Is the C242T Polymorphism of the CYBA Gene Linked with Oxidative Stress-Associated Complications of Prematurity? Antioxidants & redox signaling 2017 Apr . Huizing Maurice J, Cavallaro Giacomo, Moonen Rob M, Gonzalez-Luis Gema E, Mosca Fabio, Vento Maximo, Villamor Eduar |
| An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2016 Sep . Robertson Catherine C, Gillies Christopher E, Putler Rosemary K B, Ng Derek, Reidy Kimberly J, Crawford Brendan, Sampson Matthew |
| Maternal Interleukin Genotypes Are Associated With NICU Outcomes Among Low-Birth-Weight Infants. Biological research for nursing 2016 Sep . Baumgartel Kelley L, Groer Maureen W, Cohen Susan M, Ren Dianxu, Spatz Diane L, Conley Yvette |
| Early Erythropoietin Administration does not Increase the Risk of Retinopathy in Preterm Infants. Pediatrics and neonatology 2016 Jun . Chou Hsin-Hsu, Chung Mei-Yung, Zhou Xiao-Guang, Lin Hung-Ch |
| The association between antioxidant enzyme polymorphisms and cerebral palsy after perinatal hypoxic-ischaemic encephalopathy. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2016 Jun . Esih Katarina, Gori?ar Katja, Dolžan Vita, Rener-Primec Zvon |
| Association between VEGF polymorphisms (-460 T/C and +936 C/T) and retinopathy of prematurity risk: A meta-analysis. Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society 0 30 (3): 157-162. Shukla Swati, Malik Manzoor Ahmad, Chandra Parijat, Kaur Jasb |
| Detection of FZD4, LRP5 and TSPAN12 Genes Variants in Malay Premature Babies with Retinopathy of Prematurity. Journal of ophthalmic & vision research 0 14 (2): 171-178. Mohd Khair Siti Zulaikha Nashwa, Ismail Abdul Salim, Embong Zunaina, Mohamed Yusoff Abdul Az |
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- Page last updated:Jan 27, 2023
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