Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: FGR[original query] |
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The search for thrombophilic gene mutations in women with gestational hypertension does not help in predicting poor pregnancy outcome. Journal of hypertension 2003 Oct 21 (10): 1915-20. D'Aniello Gemma, Florio Pasquale, Sabatini Laura, Severi Filiberto M, Fineschi Daniela, Cito Giuseppe, Guidoni Claudio G, Petraglia Feli |
Polymorphism in maternal LRP8 gene is associated with fetal growth. American journal of human genetics 2006 May 78 (5): 770-7. Wang Lin, Wang Xiaobin, Laird Nan, Zuckerman Barry, Stubblefield Philip, Xu X |
Altered transmission of maternal angiotensin II receptor haplotypes in fetal growth restriction. Human mutation 2006 1 27 (2): 138-44. Tower Clare, Chappell Sally, Acharya Meera, Crane Richard, Szolin Stephanie, Symonds Lyneth, Chevins Helen, Kalsheker Noor, Baker Philip, Morgan Lin |
Polymorphism in the epidermal growth factor gene is associated with birthweight in Sinhalese and white Western Europeans. Molecular human reproduction 2007 Jun 13 (6): 425-9. Dissanayake V H W, Tower C, Broderick A, Stocker L J, Seneviratne H R, Jayasekara R W, Kalsheker N, Broughton Pipkin F, Morgan |
Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis. Journal of thrombosis and haemostasis : JTH 2008 Nov 6 (11): 1869-75. Dudding T, Heron J, Thakkinstian A, Nurk E, Golding J, Pembrey M, Ring S M, Attia J, Scott R |
Carriage of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism does not influence the first and second trimester uterine artery Doppler flow. European journal of obstetrics, gynecology, and reproductive biology 2008 Oct 140 (2): 178-82. Stonek Felix, Hafner Erich, Metzenbauer Martin, Stümpflen Ingrid, Philipp Ka |
Distinct association of genetic variations of vascular endothelial growth factor, transforming growth factor-beta, and fibroblast growth factor receptors with atopy and airway hyperresponsiveness. Allergy 2008 Apr 63 (4): 447-53. Park H-K, Park H W, Jeon S G, Shin E-S, Gho Y S, Cho S-H, Kim Y-Y, Kim Y |
Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and plasma concentrations of asymmetric dimethylarginine in Turkish pre-eclamptic women without fetal growth retardation. The journal of obstetrics and gynaecology research 2010 Jun 36 (3): 495-501. Turan Fahri, Ilhan Necip, Kaman Dilara, Ate? Kadir, Kafkasli Ay |
No correlation between androgen receptor CAG and GGN repeat length and the degree of genital virilization in females with 21-hydroxylase deficiency. The Journal of clinical endocrinology and metabolism 2010 May 95 (5): 2443-50. Welzel M, Schwarz H-P, Hedderich J, Dörr H G, Binder G, Brämswig J H, Krude H, Richter-Unruh A, Niedziela M, Gromoll J, Krone N, Riepe F G, Holterhus P |
Low molecular weight heparin treatment during subsequent pregnancies of women with inherited thrombophilia and previous severe pregnancy complications. 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 2011 1 24 (8): 1042-5. Kupferminc Michael J, Rimon Eli, Many Ariel, Sharon Maslovitz, Lessing Joseph B, Gamzu Ron |
A case control study of gene environmental interaction in fetal growth restriction with special reference to organochlorine pesticides. European journal of obstetrics, gynecology, and reproductive biology 2012 Apr 161 (2): 163-9. Sharma Esha, Mustafa Md, Pathak Rahul, Guleria Kiran, Ahmed Rafat S, Vaid N B, Banerjee B |
Nonsynonymous mutations in three anticoagulant genes in Japanese patients with adverse pregnancy outcomes. Thrombosis research 2014 May 133 (5): 914-8. Neki Reiko, Miyata Toshiyuki, Fujita Tomio, Kokame Koichi, Fujita Daisuke, Isaka Shigeyuki, Ikeda Tomoaki, Yoshimatsu J |
The Impact of Inherited Thrombophilia Types and Low Molecular Weight Heparin Treatment on Pregnancy Complications in Women with Previous Adverse Outcome. Yonsei medical journal 2016 Sep 57 (5): 1230-5. Aracic Nada, Roje Damir, Jakus Ivana Alujevic, Bakotin Marinela, Stefanovic Vedr |
Genetic markers for inherited thrombophilia are associated with fetal growth retardation in the population of Central Russia. The journal of obstetrics and gynaecology research 2017 Jul 43 (7): 1139-1144. Reshetnikov Evgeny, Zarudskaya Oksana, Polonikov Alexey, Bushueva Olga, Orlova Valentina, Krikun Evgeny, Dvornyk Volodymyr, Churnosov Mikha |
Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants. European journal of human genetics : EJHG 2021 7 29 (12): 1756-1761. Pham Aurélie, Sobrier Marie-Laure, Giabicani Eloïse, Le Jules Fernandes Marilyne, Mitanchez Delphine, Brioude Fréderic, Netchine Irè |
Pregnancy complications in G20210A mutation carriers associated with high prothrombin activity. Thrombosis journal 2021 6 19 (1): 41. Nikolaeva M G, Momot A P, Zainulina M S, Yasafova N N, Taranenko I |
[Impact of confined placental mosaicism on non-invasive prenatal testing and pregnancy outcomes]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 4 38 (4): 335-338. Wu Xiaoqing, Huang Hailong, Chen Xuemei, Chen Xiaolan, Shen Qingmei, He Deqin, Xu Liang |
Genomic imbalances in the placenta are associated with poor fetal growth. Molecular medicine (Cambridge, Mass.) 2021 1 27 (1): 3. Del Gobbo Giulia F, Yin Yue, Choufani Sanaa, Butcher Emma A, Wei John, Rajcan-Separovic Evica, Bos Hayley, von Dadelszen Peter, Weksberg Rosanna, Robinson Wendy P, Yuen Ryan K |
Population history and genome wide association studies of birth weight in a native high altitude Ladakhi population. PloS one 2022 9 17 (9): e0269671. Bhandari Sushil, Dolma Padma, Mukerji Mitali, Prasher Bhavana, Montgomery Hugh, Kular Dalvir, Jain Vandana, Dadhwal Vatsla, Williams David J, Bhattacharyaa Aniket, Gilbert Edmund, Cavalleri Gianpiero L, Hillman Sara |
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center. Journal of translational medicine 2022 4 20 (1): 168. Cai Meiying, Lin Na, Su Linjuan, Wu Xiaoqing, Xie Xiaorui, Xu Shiyi, Fu Xianguo, Xu Liangpu, Huang Hailo |
Rs868058 in the Homeobox Gene HLX Contributes to Early-Onset Fetal Growth Restriction. Biology 2022 3 11 (3): . Wujcicka Wioletta Izabela, Kacerovsky Marian, Krekora Micha?, Kaczmarek Piotr, Le?niczak Beata, Grzesiak Mariu |
Maternal polymorphic loci of rs1979277 serine hydroxymethyl transferase and rs1805087 5-methylenetetrahydrofolate are correlated with the development of fetal growth restriction: A case-control study. International journal of reproductive biomedicine 2021 Dec 19 (12): 1067-1074. Efremova Olesya, Ponomarenko Irina, Churnosov Mikha |
Associations between IGFBP1 gene polymorphisms and the risk of preeclampsia and fetal growth restriction. Hypertension research : official journal of the Japanese Society of Hypertension 2023 5 . Xianglan Peng, Dong He, Rui Peng, Jianyang Feng, Dunjin Chen, Hongkai Xie, Qixuan Li, Yitong Guo, Jiaxiong Zhou, Yang Chen, Hong |
Variants in PSMB9 and FGR differentially affect Parkinson's disease risk in GBA and LRRK2 mutation carriers. Parkinsonism & related disorders 2023 4 111 105398. Shachar Shani, Orly Goldstein, Mali Gana-Weisz, Anat Bar-Shira, Avner Thaler, Tanya Gurevich, Anat Mirelman, Nir Giladi, Roy N Alcalay, Avi Orr-Urtreg |
Bioinformatic analysis reveals the clinical value of SASH3 in survival prognosis and immune infiltration of acute myelocytic leukemia (AML). American journal of translational research 2024 1 15 (12): 6858-6866. Yufei Li, Lin Wang, Xueyuan Jia, Yanru Yang, Zhengqi Q |
Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting. Scientific reports 2024 1 14 (1): 238. Mengmeng Li, Na Hao, Yulin Jiang, Huili Xue, Yifang Dai, Mingming Wang, Junjie Bai, Yan Lv, Qingwei Qi, Xiya Zh |
Novel insights into the complex interplay of immune dysregulation and inflammatory biomarkers in preeclampsia and fetal growth restriction: A two-step Mendelian randomization analysis. Journal of translational autoimmunity 2024 1 8 100226. Chumei Zeng, Huiying Liu, Zilian Wang, Jingting |
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- Page last updated:Apr 22, 2024
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