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184 related items for PubMed ID: 30177054
1. Atrial fibrillation associated genetic variation near PITX2 gene increases the risk of preeclampsia. Rani U, Praveen Kumar KS, Munisamaiah M, Rajesh D, Balakrishna S. Pregnancy Hypertens; 2018 Jul; 13():214-217. PubMed ID: 30177054 [Abstract] [Full Text] [Related]
2. Novel association of SNP rs479200 in EGLN1 gene with predisposition to preeclampsia. Kumar K S P, Arcot M, Munisamaiah M, Balakrishna S. Gene; 2019 Jul 15; 705():1-4. PubMed ID: 31009679 [Abstract] [Full Text] [Related]
3. Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation. Shen Han Y, Ahmed AM, Chao Z, Jun W, Xiaochen Y. Anatol J Cardiol; 2023 Mar 15; 27(3):160-166. PubMed ID: 36856594 [Abstract] [Full Text] [Related]
4. Association between tumor necrosis factor (TNF)-alpha G-308A gene polymorphism and preeclampsia complicated by severe fetal growth restriction. Molvarec A, Jermendy A, Nagy B, Kovács M, Várkonyi T, Hupuczi P, Prohászka Z, Rigó J. Clin Chim Acta; 2008 Jun 15; 392(1-2):52-7. PubMed ID: 18396154 [Abstract] [Full Text] [Related]
5. Association between rs2200733 and rs7193343 genetic variants and atrial fibrillation in a Spanish population, and meta-analysis of previous studies. Ferrán A, Alegret JM, Subirana I, Aragonès G, Lluis-Ganella C, Romero-Menor C, Planas F, Joven J, Elosua R. Rev Esp Cardiol (Engl Ed); 2014 Oct 15; 67(10):822-9. PubMed ID: 25262128 [Abstract] [Full Text] [Related]
6. Fetal Val108/158Met catechol-O-methyltransferase (COMT) polymorphism and placental COMT activity are associated with the development of preeclampsia. Pertegal M, Fenoy FJ, Hernández M, Mendiola J, Delgado JL, Bonacasa B, Corno A, López B, Bosch V, Hernández I. Fertil Steril; 2016 Jan 15; 105(1):134-43.e1-3. PubMed ID: 26450530 [Abstract] [Full Text] [Related]
7. Transforming growth factor beta 1 related gene polymorphisms in gestational hypertension and preeclampsia: A case-control candidate gene association study. Li X, Tan H, Chen M, Zhou S. Pregnancy Hypertens; 2018 Apr 15; 12():155-160. PubMed ID: 29183791 [Abstract] [Full Text] [Related]
8. Incidence of dementia in relation to genetic variants at PITX2, ZFHX3, and ApoE ε4 in atrial fibrillation patients. Rollo J, Knight S, May HT, Anderson JL, Muhlestein JB, Bunch TJ, Carlquist J. Pacing Clin Electrophysiol; 2015 Feb 15; 38(2):171-7. PubMed ID: 25494715 [Abstract] [Full Text] [Related]
10. The association of single nucleotide polymorphisms of the maternal cystathionine-β-synthase gene with early-onset preeclampsia. Holwerda KM, Weedon-Fekjær MS, Staff AC, Nolte IM, van Goor H, Lely AT, Faas MM. Pregnancy Hypertens; 2016 Jan 15; 6(1):60-5. PubMed ID: 26955774 [Abstract] [Full Text] [Related]
11. Association Between rs2200733 Polymorphism on Chromosome 4q25 and Atrial Fibrillation in a Greek Population. Kalinderi K, Fragakis N, Koskinas KC, Katritsis D, Letsas K, Efremidis M, Korantzopoulos P, Rossios K, Pagourelias E, Giannakopoulou P, Mavroudi M, Kyriakou P, Skeberis V, Geleris P, Vassilikos V, Fidani L. Hellenic J Cardiol; 2015 Jan 15; 56(3):224-9. PubMed ID: 26021244 [Abstract] [Full Text] [Related]