Human Genome Epidemiology Literature Finder
Reproductive and Child Health
Records 1 - 30 (of 184 Records) |
Query Trace: Prematurity[original query] |
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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 |
Population pharmacokinetic modeling of caffeine in preterm infants with apnea of prematurity: New findings from concomitant erythromycin and AHR genetic polymorphisms. Pharmacological research 2022 8 184 106416. Dai Hao-Ran, Liu Yun, Lu Ke-Yu, He Xin, Guo Hong-Li, Hu Ya-Hui, Xu Jing, Ding Xuan-Sheng, Chen Feng, Cheng Rui, Jiao Zhe |
Liver Cirrhosis Patients Homozygous for MTHFR C677T Develop Portal Vein Thrombosis 8 Years Earlier Than Wild Type. Digestive diseases and sciences 2022 Aug . Ames Paul R J, D'Andrea Giovanna, Arcaro Alessia, Marottoli Vincenzo, Iannaccone Luigi, Maraglione Maurizio, Gentile Fabriz |
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 |
Juvenile patients with the homozygous MTHFR C677T genotype develop ischemic stroke 5 years earlier than wild type. Journal of thrombosis and thrombolysis 2022 Aug 54 (2): 330-338. Ames Paul R J, D'Andrea Giovanna, Marottoli Vincenzo, Arcaro Alessia, Iannaccone Luigi, Gentile Fabrizio, Maraglione Mauriz |
Disparities in first evaluation of infants with cystic fibrosis since implementation of newborn screening. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2022 7 . McColley Susanna A, Martiniano Stacey L, Ren Clement L, Sontag Marci K, Rychlik Karen, Balmert Lauren, Elbert Alexander, Wu Runyu, Farrell Philip |
Outcome of Twin Pregnancies Complicated by a Single Intrauterine Death. Cureus 2022 7 14 (6): e26055. Al-Alaiyan Saleh, Abdulaziz Najlaa, Bukhari Hanifah, Hawari Amal, Alturki Amjad, Alghamdi Reem, Elsaidawi We |
Frequency of Leiden Mutation in Newborns with Birth Weight below 1500 g. Healthcare (Basel, Switzerland) 2022 5 10 (5): . Dusek Jiri, Nedvedova Lenka, Scheinost Ondrej, Hanzl Milan, Kantorova Eva, Fendrstatova Eva, Sram Radim J, Kotouckova Hana, Voracek J |
Pustular psoriasis of pregnancy: Clinical and genetic characteristics in a series of eight patients and review of the literature. Dermatologic therapy 2022 5 35 (8): e15593. Ennouri Mariem, Bahloul Emna, Sellami Khadija, Marrakchi Slaheddine, Fakhfakh Faiza, Turki Hamida, Bougacha-Elleuch Nou |
Earlier onset of peripheral arterial thrombosis in homozygous MTHFR C677T carriers than in other MTHFR genotypes: a cohort study. Clinical and experimental medicine 2022 4 . Ames Paul R J, D'Andrea Giovanna, Marottoli Vincenzo, Arcaro Alessia, Iannaccone Luigi, Maraglione Maurizio, Gentile Fabriz |
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this group. Pediatric diabetes 2022 3 23 (4): 457-461. Hewat Thomas I, Laver Thomas W, Houghton Jayne A L, Männistö Jonna M E, Alvi Sabah, Brearey Stephen P, Cody Declan, Dastamani Antonia, De Los Santos La Torre Miguel, Murphy Nuala, Rami-Merhar Birgit, Wefers Birgit, Huopio Hanna, Banerjee Indraneel, Johnson Matthew B, Flanagan Sarah |
Caffeine Therapy for Apnea of Prematurity: Role of the Circadian CLOCK Gene Polymorphism. Frontiers in pharmacology 2022 2 12 724145. Guo Hong-Li, Long Jia-Yi, Hu Ya-Hui, Liu Yun, He Xin, Li Ling, Xia Ying, Ding Xuan-Sheng, Chen Feng, Xu Jing, Cheng R |
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European journal of medical research 2022 12 27 (1): 286. Tabib Avisa, Talebi Taravat, Ghasemi Serwa, Pourirahim Maryam, Naderi Niloofar, Maleki Majid, Kalayinia Sami |
Etiology and prognosis of nephrocalcinosis according to gestational age in Korean children. BMC pediatrics 2023 9 23 (1): 451. Jinwoon Joung, Heeyeon C |
Association of the EPAS1 rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen. Diagnostics (Basel, Switzerland) 2023 8 13 (15): . Diana G Rogel-Ayala, José Esteban Muñoz-Medina, Valeria Dejanira Vicente-Juárez, Patricia Grether-González, Deneb Algedi Morales-Barquet, Alfonso de Jesús Martínez-García, María Olga Leticia Echaniz-Aviles, Rosalba Sevilla-Montoya, Alejandro Martínez-Juárez, Jazmin Artega-Vázquez, Javier Angeles-Martínez, Gilberto Vargas-Alarcón, Alberto Hidalgo-Bravo, Irma Eloisa Monroy-Muñ |
Genetic Modulation of the Erythrocyte Phenotype Associated with Retinopathy of Prematurity-A Multicenter Portuguese Cohort Study. International journal of molecular sciences 2023 7 24 (14): . Mariza Fevereiro-Martins, Ana Carolina Santos, Carlos Marques-Neves, Hercília Guimarães, Manuel Bicho, On Behalf Of The GenE-Rop Study Gro |
Genome-wide association identifies novel ROP risk loci in a multi-ethnic cohort. Research square 2023 6 . Jerome Rotter, Xiaohui Li, Leah A Owen, Kent Taylor, Susan Ostmo, Yii-Der Ida Chen, Aaron Coyner, Kemal Sonmez, M Elizabeth Hartnett, Xiuqing Guo, Eli Ipp, Kathryn Roll, Pauline Genter, R V Paul Chan, Margaret DeAngelis, Michael Chiang, J Peter Campbe |
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 |
Hypoxia-Inducible Pathway Polymorphisms and Their Role in the Complications of Prematurity. Genes 2023 5 14 (5): . Ewa Strauss, Anna Gotz-Wi?ckowska, Alicja Sobaniec, Anna Chmielarz-Czarnoci?ska, Dawid Szpecht, Danuta Januszkiewicz-Lewandows |
Genetic Polymorphisms of Vascular Endothelial Growth Factor in Neonatal Pathologies: A Systematic Search and Narrative Synthesis of the Literature. Children (Basel, Switzerland) 2023 5 10 (4): . Monica G H??m??anu, Lucia M Procopciuc, Melinda Matyas, Gabriela I Zonda, Gabriela C Zahar |
SELENOP rs3877899 Variant Affects the Risk of Developing Advanced Stages of Retinopathy of Prematurity (ROP). International journal of molecular sciences 2023 4 24 (8): . Ewa Strauss, Danuta Januszkiewicz-Lewandowska, Alicja Sobaniec, Anna Gotz-Wi?ckows |
Developmental Trends in Postnatal Thyroid Hormones and Thyroid Dysfunction in Preterm Infants Born at less than 34 weeks Gestation. Fetal and pediatric pathology 2023 4 1-11. Chen Shaohong, Lu Xiaoyan, Yang Bicheng, Wu Jieru, Huang Hui, Zou Yang, Tang Wenyan, Xu Ping, Yang |
Predictors of whole exome sequencing in dystonic cerebral palsy and cerebral palsy-like disorders. Parkinsonism & related disorders 2023 3 105352. Pavelekova P, Necpal J, Jech R, Havrankova P, Svantnerova J, Jurkova V, Gdovinova Z, Lackova A, Han V, Winkelmann J, Zech M, Skorvanek |
Evaluation of Patients with Neonatal Thrombosis. Indian journal of pediatrics 2023 3 . Guzoglu Nilufer, Albayrak Meryem, Aliefendioglu Did |
Potential role of eNOS and EDN-1 gene polymorphisms in the development and progression of retinopathy of prematurity. BMC ophthalmology 2023 2 23 (1): 78. Chor?ziak-Michalak Aneta, Gotz-Wi?ckowska Anna, Chmielarz-Czarnoci?ska Anna, Seremak-Mrozikiewicz Agnieszka, Szpecht Daw |
Disseminated Disease After Candidemia in Children and Young Adults: Epidemiology, Diagnostic Evaluation and Risk Factors. The Pediatric infectious disease journal 2023 12 . Catherine R Murphy, Zheyi Teoh, Daniel Whitehurst, Caitlin Brammer, Kerrigan Perkins, Grant Paulsen, Hilary Miller-Handley, Lara Danziger-Isakov, William R Ot |
Comprehensive Analysis of the Role of Gene Variants in Matrix Metalloproteinases and Their Tissue Inhibitors in Retinopathy of Prematurity: A Study in the Polish Population. International journal of molecular sciences 2023 10 24 (20): . Aneta Chor?ziak-Michalak, Dawid Szpecht, Anna Chmielarz-Czarnoci?ska, Agnieszka Seremak-Mrozikiewicz, Krzysztof Drews, Gra?yna Kurzawi?ska, Ewa Strauss, Anna Gotz-Wi?ckows |
The role of vitamin D receptor gene polymorphism in the development of necrotizing enterocolitis. Pediatric research 2023 1 . Barut Dogan, Akisu Mete, Koroglu Ozge Altun, Terek Demet, Ergin Firat, Onay Huseyin, Yalaz Mehmet, Kultursay Nilg |
Genome-wide association identifies novel ROP risk loci in a multiethnic cohort. Communications biology 2024 1 7 (1): 107. Xiaohui Li, Leah A Owen, Kent D Taylor, Susan Ostmo, Yii-Der Ida Chen, Aaron S Coyner, Kemal Sonmez, M Elizabeth Hartnett, Xiuqing Guo, Eli Ipp, Kathryn Roll, Pauline Genter, R V Paul Chan, Margaret M DeAngelis, Michael F Chiang, J Peter Campbell, Jerome I Rotter, |
Genetic variants of the beta-adrenergic receptor pathways as both risk and protective factors for retinopathy of prematurity. American journal of ophthalmology 2024 1 . Hélène Paradis, Salem Werdyani, Guangju Zhai, Robert L Gendron, Reza Tabrizchi, Margaret McGovern, J Michael Jumper, Daniel Brinton, William V Go |
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- Page last updated:Apr 22, 2024
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