Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 110 Records) |
Query Trace: Bronchopulmonary Dysplasia[original query] |
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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 |
The significance of IL-1? +3953C>T, IL-6 -174G>C and -596G>A, TNF-? -308G>A gene polymorphisms and 86 bp variable number tandem repeat polymorphism of IL-1RN in bronchopulmonary dysplasia in infants born before 32 weeks of gestation. Central-European journal of immunology 2017 42 (3): 287-293. Szpecht Dawid, Gadzinowski Janusz, Nowak Irmina, Cygan Dorothy, Seremak-Mrozikiewicz Agnieszka, Kurzawi?ska Gra?yna, Madajczak Dariusz, Drews Krzysztof, Szymankiewicz Mar |
Association of cytokine gene polymorphisms with bronchopulmonary dysplasia in Han Chinese newborns. Pediatric pulmonology 2017 Nov . Chen Hui, Zheng W |
Using clinical and genetic data to predict pulmonary hypertension in bronchopulmonary dysplasia. Acta paediatrica (Oslo, Norway : 1992) 2018 Sep . Trittmann J K, Bartenschlag A, Zmuda E J, Frick J, Stewart W C L, Nelin L |
Ancestry and genetic associations with bronchopulmonary dysplasia in preterm infants.
American journal of physiology. Lung cellular and molecular physiology 2018 Nov 315 (5): L858-L869. Torgerson Dara G, Ballard Philip L, Keller Roberta L, Oh Sam S, Huntsman Scott, Hu Donglei, Eng Celeste, Burchard Esteban G, Ballard Roberta A, |
Genetic variation in CRHR1 is associated with short-term respiratory response to corticosteroids in preterm infants at risk for bronchopulmonary dysplasia. Pediatric research 2019 Apr 85 (5): 625-633. Lewis Tamorah, Truog William, Norberg Mike, Ballard Philip L, Torgerson Dara, |
Role of Genetic Susceptibility in the Development of Bronchopulmonary Dysplasia. The Journal of pediatrics 2018 Sep . Parad Richard B, Winston Abigail B, Kalish Leslie A, Gupta Munish, Thompson Ivana, Sheldon Yvonne, Morey Joann, Van Marter Linda |
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, |
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
Dual-specificity phosphatase (DUSP) genetic variants predict pulmonary hypertension in patients with bronchopulmonary dysplasia. Pediatric research 2019 Jul . Chen Lauren L, Zmuda Erik J, Talavera Maria M, Frick Jessica, Brock Guy N, Liu Yusen, Klebanoff Mark A, Trittmann Jennifer |
[The polymorphism of detoxification genes system genes in very preterm infants.]. Klinicheskaia laboratornaia diagnostika 2018 63 (10): 658-660. Mezhinskij S S, Shilova N A, Chasha T V, Fetisova I N, Kharlamova N V, Ratnikova S Yu, Fetisov N |
Exome sequencing of extreme phenotypes in bronchopulmonary dysplasia. European journal of pediatrics 2019 Dec . Hadchouel Alice, Decobert Fabrice, Besmond Claude, Delacourt Christop |
Diverging effects of premature birth and bronchopulmonary dysplasia on exercise capacity and physical activity - a case control study. Respiratory research 2019 11 20 (1): 260. Ruf Katharina, Thomas Wolfgang, Brunner Maximilian, Speer Christian P, Hebestreit Hel |
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 |
Neurodevelopmental outcomes in very preterm infants: The role of severity of Bronchopulmonary Dysplasia. Early human development 2020 11 152 105275. Gallini Francesca, Coppola Maria, De Rose Domenico Umberto, Maggio Luca, Arena Roberta, Romano Valerio, Cota Francesco, Ricci Daniela, Romeo Domenico Marco, Mercuri Eugenio Maria, Vento Giovan |
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 |
The association between surfactant protein B gene variation and bronchopulmonary dysplasia in Chinese premature newborns. International journal of clinical and experimental pathology 2020 1 11 (7): 3753-3758. Zhang Feitong, Jia Chunhong, Lin Xiaojun, Su Zhiwen, Wu Fan, Li Ying, Lin Lili, Liu Guoshe |
Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genes. Pediatric research 2021 9 92 (1): 190-198. Blume Felix, Kirsten Holger, Ahnert Peter, Chakraborty Trinad, Gross Arnd, Horn Katrin, Toliat Mohammad Reza, Nürnberg Peter, Westenfelder Eva-Maria, Goepel Wolfgang, Scholz Mark |
Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information. Frontiers in genetics 2021 7 12 689071. Dai Dan, Chen Huiyao, Dong Xinran, Chen Jinglong, Mei Mei, Lu Yulan, Yang Lin, Wu Bingbing, Cao Yun, Wang Jin, Zhou Wenhao, Qian Lili |
Pulmonary Outcomes in Children Born Extremely and Very Preterm at 11 Years of Age. Frontiers in pediatrics 2021 6 9 635503. Di Filippo Paola, Giannini Cosimo, Attanasi Marina, Dodi Giulia, Scaparrotta Alessandra, Petrosino Marianna Immacolata, Di Pillo Sabrina, Chiarelli Frances |
Hedgehog signaling pathway gene variant influences bronchopulmonary dysplasia in extremely low birth weight infants. World journal of pediatrics : WJP 2021 Apr . Amatya Shaili, Rajbhandari Sharina, Pradhan Sandeep, Trinh Van, Paudel Umesh, Parton Lance |
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms. Pediatric research 2021 Dec . Akat Ayberk, Yilmaz Semerci Seda, Ugurel Osman Mutluhan, Erdemir Aysegul, Danhaive Olivier, Cetinkaya Merih, Turgut-Balik Dil |
Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants. Disease markers 2022 2022 2793846. Filonzi Laura, Perrone Serafina, Tataranno Maria Luisa, Magnani Cinzia, Dadomo Harold, Bottoni Anthea, Vaghi Marina, Nonnis Marzano Frances |
Genetic and Biochemical Predictors of Neonatal Bronchopulmonary Dysplasia. Journal of pediatric genetics 2022 8 11 (3): 173-178. Abdellatif May A K, Eyada Eman, Rabie Walaa, Abdelaziz Azza, Shahin Wal |
Polymorphisms of fibronectin-1 (rs3796123; rs1968510; rs10202709; rs6725958; and rs35343655) are not associated with bronchopulmonary dysplasia in preterm infants. Molecular and cellular biochemistry 2022 3 477 (6): 1645-1652. Kosik Katarzyna, Sowi?ska Anna, Seremak-Mrozikiewicz Agnieszka, Abu-Amara Jasmine A, Al-Saad Salwan R, Karbowski Lukasz M, Gryczka Katarzyna, Kurzawi?ska Gra?yna, Szymankiewicz-Br?borowicz Marta, Drews Krzysztof, Szpecht Daw |
Etiology and prognosis of nephrocalcinosis according to gestational age in Korean children. BMC pediatrics 2023 9 23 (1): 451. Jinwoon Joung, Heeyeon C |
Associations of VEGF Polymorphisms With Retinopathy of Prematurity. Investigative ophthalmology & visual science 2023 6 64 (7): 11. Xiao Chun Ling, Eugene Yu-Chuan Kang, Kuan-Jen Chen, Nan-Kai Wang, Laura Liu, Yen-Po Chen, Yih-Shiou Hwang, Chi-Chun Lai, Shun-Fa Yang, Wei-Chi |
Identification of genetic susceptibility in preterm newborns with bronchopulmonary dysplasia by whole-exome sequencing: BIVM gene may play a role. European journal of pediatrics 2023 2 . Luo Xi, Zhao Min, Chen Cheng, Lin Fengji, Li Xiaodong, Huang Haiyun, Dou Lei, Feng Jinxing, Xiao Shanqiu, Liu Dong, He Junli, Yu Jial |
Association between PER and CRY gene polymorphisms and the response to caffeine citrate treatment in infants with apnea of prematurity. Frontiers in pediatrics 2024 8 12 1414185. Jiang-Biao Xie, Wei Zhuang, Yao Zhu, Zhi Zheng, Yan-Ru Huang, Si-Min Ma, Xin-Zhu L |
- Page last reviewed:Feb 1, 2024
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