Human Genome Epidemiology Literature Finder
Reproductive and Child Health
Records 1 - 30 (of 41 Records) |
Query Trace: Infant Mortality[original query] |
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Investigation of genetic risk factors for chronic adult diseases for association with preterm birth. Human genetics 2013 Jan 132 (1): 57-67. Falah Nadia, McElroy Jude, Snegovskikh Victoria, Lockwood Charles J, Norwitz Errol, Murray Jeffey C, Kuczynski Edward, Menon Ramkumar, Teramo Kari, Muglia Louis J, Morgan Thom |
Rare copy number variants contribute to congenital left-sided heart disease. PLoS genetics 2012 Sep 8 (9): e1002903. Hitz Marc-Phillip, Lemieux-Perreault Louis-Philippe, Marshall Christian, Feroz-Zada Yassamin, Davies Robbie, Yang Shi Wei, Lionel Anath Christopher, D'Amours Guylaine, Lemyre Emmanuelle, Cullum Rebecca, Bigras Jean-Luc, Thibeault Maryse, Chetaille Philippe, Montpetit Alexandre, Khairy Paul, Overduin Bert, Klaassen Sabine, Hoodless Pamela, Awadalla Philip, Hussin Julie, Idaghdour Youssef, Nemer Mona, Stewart Alexandre F R, Boerkoel Cornelius, Scherer Stephen W, Richter Andrea, Dubé Marie-Pierre, Andelfinger Greg |
GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect. Pediatric cardiology 2013 Mar 34 (3): 504-11. Wei Dong, Bao Han, Zhou Ning, Zheng Gui-Fen, Liu Xing-Yuan, Yang Yi-Qi |
High-resolution melting (HRM) analysis as a feasible method for detecting spinal muscular atrophy via dried blood spots. Clinica chimica acta; international journal of clinical chemistry 2012 Nov 413 (21-22): 1781-5. Er Tze-Kiong, Kan Tzu-Min, Su Yu-Fa, Liu Ta-Chih, Chang Jan-Gowth, Hung Shih-Ya, Jong Yuh-J |
Carnitine palmitoyltransferase I and sudden unexpected infant death in British Columbia First Nations. Pediatrics 2012 Oct . Sinclair GB, Collins S, Popescu O, McFadden D, Arbour L, Vallance HD |
A prospective newborn screening and treatment program for sickle cell anemia in Luanda, Angola. American journal of hematology 2013 Dec 88 (12): 984-9. McGann Patrick T, Ferris Margaret G, Ramamurthy Uma, Santos Brigida, de Oliveira Vysolela, Bernardino Luis, Ware Russell |
Toll-like receptor variants are associated with infant HIV-1 acquisition and peak plasma HIV-1 RNA level. AIDS (London, England) 2013 Sep 27 (15): 2431-9. Beima-Sofie Kristin M, Bigham Abigail W, Lingappa Jairam R, Wamalwa Dalton, Mackelprang Romel D, Bamshad Michael J, Maleche-Obimbo Elizabeth, Richardson Barbra A, John-Stewart Grace |
PITX2c loss-of-function mutations responsible for congenital atrial septal defects. International journal of medical sciences 2013 10 (10): 1422-9. Yuan Fang, Zhao Lan, Wang Juan, Zhang Wei, Li Xin, Qiu Xing-Biao, Li Ruo-Gu, Xu Ying-Jia, Xu Lei, Qu Xing-Kai, Fang Wei-Yi, Yang Yi-Qi |
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Nature genetics 2013 Jul 45 (7): 818-21. Hu Zhibin, Shi Yongyong, Mo Xuming, Xu Jing, Zhao Bijun, Lin Yuan, Yang Shiwei, Xu Zhengfeng, Dai Juncheng, Pan Shandong, Da Min, Wang Xiaowei, Qian Bo, Wen Yang, Wen Juan, Xing Jinliang, Guo Xuejiang, Xia Yankai, Ma Hongxia, Jin Guangfu, Yu Shiqiang, Liu Jiayin, Zhou Zuomin, Wang Xinru, Chen Yijiang, Sha Jiahao, Shen Hongbi |
Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight. Frontiers in genetics 2013 4 196. Zheng Xiaojing, Feingold Eleanor, Ryckman Kelli K, Shaffer John R, Boyd Heather A, Feenstra Bjarke, Melbye Mads, Marazita Mary L, Murray Jeffrey C, Cuenco Karen |
Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations. PloS one 2014 9 (9): e107411. Zhao Bijun, Lin Yuan, Xu Jing, Ni Bixian, Da Min, Ding Chenyue, Hu Yuanli, Zhang Kai, Yang Shiwei, Wang Xiaowei, Yu Shiqiang, Chen Yijiang, Mo Xuming, Liu Jiayin, Shen Hongbing, Sha Jiahao, Ma Hongx |
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease. International journal of molecular medicine 2014 May 33 (5): 1201-8. Wei Dong, Gong Xiao-Hui, Qiu Gang, Wang Juan, Yang Yi-Qi |
Spectrum and distribution of CFTR gene mutations in asthma and chronic pancreatitis cases of North Indian population. Gene 2014 Apr 539 (1): 125-31. Muthuswamy Srinivasan, Agarwal Sarita, Awasthi Shally, Singh Shweta, Dixit Pratibha, Maurya Nutan, Choudhuri Gourd |
Evidence for an association between infant mortality and homozygosity for the arctic variant of carnitine palmitoyltransferase 1A. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jan . Gessner Bradford D, Wood Thalia, Johnson Monique A, Richards Carolyn Sue, Koeller David |
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 |
Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth.
Nature communications 2017 Jun 8 15608. Hong Xiumei, Hao Ke, Ji Hongkai, Peng Shouneng, Sherwood Ben, Di Narzo Antonio, Tsai Hui-Ju, Liu Xin, Burd Irina, Wang Guoying, Ji Yuelong, Caruso Deanna, Mao Guangyun, Bartell Tami R, Zhang Zhongyang, Pearson Colleen, Heffner Linda, Cerda Sandra, Beaty Terri H, Fallin M Daniele, Lee-Parritz Aviva, Zuckerman Barry, Weeks Daniel E, Wang Xiaob |
Genetic Variants at the rs4720169 Locus of TBX20 and the rs12921862 Locus of AXIN1 May Increase the Risk of Congenital Heart Defects in the Mexican Population: A Pilot Study. Genetic testing and molecular biomarkers 2019 9 23 (9): 664-670. Hernández-Almaguer Maria Dolores, Calvo-Anguiano Geovana, Cerda-Flores Ricardo M, Salinas-Torres Víctor M, Orozco-Galicia Francisco, Glenn Eva, García-Guerra Jaime, Sánchez-Cortés Gerardo, Lugo-Trampe José, Martínez-Garza Laura |
MiRNA-146a polymorphism increases the odds of malaria in pregnancy. Malaria journal 2019 1 18 (1): 7. van Loon Welmoed, Gai Prabhanjan P, Hamann Lutz, Bedu-Addo George, Mockenhaupt Frank |
Association of Maternal Diabetes Mellitus and Polymorphisms of the NKX2.5 Gene in Children with Congenital Heart Disease: A Single Centre-Based Case-Control Study. Journal of diabetes research 2020 2020 3854630. Zhao Mingyi, Diao Jingyi, Huang Peng, Li Jinqi, Li Yihuan, Yang Yang, Luo Liu, Zhang Senmao, Chen Letao, Wang Tingting, Zhu Ping, Qin Jia |
Carrier frequency of SMN1-related spinal muscular atrophy in north Indian population: The need for population based screening program. American journal of medical genetics. Part A 2020 10 185 (1): 274-277. Nilay Mayank, Moirangthem Amita, Saxena Deepti, Mandal Kausik, Phadke Shubha |
Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach. Bioscience reports 2021 Aug . Gupta Juhi K, Care Angharad, Goodfellow Laura, Alfirevic Zarko, Lian Lu-Yun, Müller-Myhsok Bertram, Alfirevic Ana, Phelan Marie |
Association of the CPT1A p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in Nunavut. Frontiers in pediatrics 2021 7 9 678553. Collins Sorcha A, Edmunds Sharon, Akearok Gwen Healey, Thompson J Robert, Erickson Anders C, Hildes-Ripstein Elske, Miners Amber, Somerville Martin, Goldfarb David M, Rockman-Greenberg Cheryl, Arbour Lau |
Maternal LINE-1 DNA Methylation in Early Spontaneous Preterm Birth. Biological research for nursing 2021 11 24 (1): 85-93. Bariši? Anita, Stankovi? Aleksandra, Stojkovi? Ljiljana, Pereza Nina, Ostoji? Saša, Peterlin Ana, Peterlin Borut, Vranekovi? Jadran |
The Impact of PTPRK and ROS1 Polymorphisms on the Preeclampsia Risk in Han Chinese Women. International journal of hypertension 2021 2021 3275081. Li Huihui, Yan Xingyu, Yang Man, Liu Mei, Tian Shan, Yu Mengru, Li Wei-Ping, Zhang Co |
Neutrophil trafficking to the site of infection requires Cpt1a-dependent fatty acid ?-oxidation. Communications biology 2022 12 5 (1): 1366. Pham Ly, Komalavilas Padmini, Eddie Alex M, Thayer Timothy E, Greenwood Dalton L, Liu Ken H, Weinberg Jaclyn, Patterson Andrew, Fessel Joshua P, Boyd Kelli L, Schafer Jenny C, Kuck Jamie L, Shaver Aaron C, Flaherty David K, Matlock Brittany K, Wijers Christiaan D M, Serezani C Henrique, Jones Dean P, Brittain Evan L, Rathmell Jeffrey C, Noto Michael |
GWAS on birth year infant mortality rates provides evidence of recent natural selection.
Proceedings of the National Academy of Sciences of the United States of America 2022 3 119 (12): e2117312119. Wu Yuchang, Furuya Shiro, Wang Zihang, Nobles Jenna E, Fletcher Jason M, Lu Qiongs |
Gene Polymorphism, Microdeletion, and Gene Expression of PRM1, PRM2, AZFc in Infertile Males. Reports of biochemistry & molecular biology 2023 9 12 (1): 173-184. Nashwah Jabbar Kadhim, Narges Dastmalchi, Parisa Banamolaei, Reza Safaralizad |
Transplacental Therapeutic Drug Monitoring in Pregnant Women with Fetal Tachyarrhythmia Using HPLC-MS/MS. International journal of molecular sciences 2023 2 24 (3): . Starodubtseva Natalia, Kindysheva Svetlana, Potapova Alyona, Kukaev Evgenii, Khodzhaeva Zulfiya, Bockeria Ekaterina, Chagovets Vitaliy, Frankevich Vladimir, Sukhikh Genna |
Leptin and Leptin Receptor Polymorphisms in Infants and Their Parents: Correlation with Preterm Birth. Genes 2024 1 15 (1): . Francesco Savino, Allegra Sardo, Stefano Gambarino, Maddalena Dini, Anna Clemente, Anna Pau, Ilaria Galliano, Massimiliano Bergal |
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie 2024 1 . Manal Elidrissi Errahhali, Mounia Elidrissi Errahhali, Sara Ramdani, Saida Lhousni, Noufissa Benajiba, Maria Rkain, Abdeladim Babakhouya, Aziza Elouali, Ayad Ghanam, Rim Amrani, Sahar Messaoudi, Anass Ayyad, Bouchra Oneib, Ahmed Mimouni, Hanane Saadi, Sanae Allaoui, Meryem Ouarzane, Agnès Guichet, Majida Charif, Redouane Boulouiz, Mohammed Bellao |
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- Page last updated:Apr 22, 2024
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