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Items: 1 to 20 of 113

1.

Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies.

Workalemahu T, Enquobahrie DA, Gelaye B, Sanchez SE, Garcia PJ, Tekola-Ayele F, Hajat A, Thornton TA, Ananth CV, Williams MA.

Placenta. 2018 Jun;66:8-16. doi: 10.1016/j.placenta.2018.04.008. Epub 2018 Apr 16.

2.

Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption.

Denis M, Enquobahrie DA, Tadesse MG, Gelaye B, Sanchez SE, Salazar M, Ananth CV, Williams MA.

PLoS One. 2014 Dec 30;9(12):e116346. doi: 10.1371/journal.pone.0116346. eCollection 2014.

3.

Abruptio placentae risk and genetic variations in mitochondrial biogenesis and oxidative phosphorylation: replication of a candidate gene association study.

Workalemahu T, Enquobahrie DA, Gelaye B, Thornton TA, Tekola-Ayele F, Sanchez SE, Garcia PJ, Palomino HG, Hajat A, Romero R, Ananth CV, Williams MA.

Am J Obstet Gynecol. 2018 Dec;219(6):617.e1-617.e17. doi: 10.1016/j.ajog.2018.08.042. Epub 2018 Sep 5.

4.

A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.

Moore A, Enquobahrie DA, Sanchez SE, Ananth CV, Pacora PN, Williams MA.

Int J Mol Epidemiol Genet. 2012;3(4):305-13. Epub 2012 Nov 15.

5.

Genome-wide and candidate gene association studies of placental abruption.

Workalemahu T, Enquobahrie DA, Moore A, Sanchez SE, Ananth CV, Pacora PN, Liang L, Salazar M, Williams MA.

Int J Mol Epidemiol Genet. 2013 Sep 12;4(3):128-39. eCollection 2013.

6.

Genetic variations related to maternal whole blood mitochondrial DNA copy number: a genome-wide and candidate gene study.

Workalemahu T, Enquobahrie DA, Tadesse MG, Hevner K, Gelaye B, Sanchez SE, Williams MA.

J Matern Fetal Neonatal Med. 2017 Oct;30(20):2433-2439. doi: 10.1080/14767058.2016.1252747. Epub 2017 Apr 4.

7.

Circadian clock-related genetic risk scores and risk of placental abruption.

Qiu C, Gelaye B, Denis M, Tadesse MG, Luque Fernandez MA, Enquobahrie DA, Ananth CV, Sanchez SE, Williams MA.

Placenta. 2015 Dec;36(12):1480-6. doi: 10.1016/j.placenta.2015.10.005. Epub 2015 Oct 23.

8.

Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.

Asai Y, Eslami A, van Ginkel CD, Akhabir L, Wan M, Ellis G, Ben-Shoshan M, Martino D, Ferreira MA, Allen K, Mazer B, de Groot H, de Jong NW, Gerth van Wijk RN, Dubois AEJ, Chin R, Cheuk S, Hoffman J, Jorgensen E, Witte JS, Melles RB, Hong X, Wang X, Hui J, Musk AWB, Hunter M, James AL, Koppelman GH, Sandford AJ, Clarke AE, Daley D.

J Allergy Clin Immunol. 2018 Mar;141(3):991-1001. doi: 10.1016/j.jaci.2017.09.015. Epub 2017 Oct 10.

9.

Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.

NINDS Stroke Genetics Network (SiGN); International Stroke Genetics Consortium (ISGC).

Lancet Neurol. 2016 Feb;15(2):174-184. doi: 10.1016/S1474-4422(15)00338-5. Epub 2015 Dec 19. Erratum in: Lancet Neurol. 2016 Mar;15(3):241.

10.

Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.

Noth I, Zhang Y, Ma SF, Flores C, Barber M, Huang Y, Broderick SM, Wade MS, Hysi P, Scuirba J, Richards TJ, Juan-Guardela BM, Vij R, Han MK, Martinez FJ, Kossen K, Seiwert SD, Christie JD, Nicolae D, Kaminski N, Garcia JGN.

Lancet Respir Med. 2013 Jun;1(4):309-317. doi: 10.1016/S2213-2600(13)70045-6. Epub 2013 Apr 17.

11.

Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene.

Nievergelt CM, Maihofer AX, Mustapic M, Yurgil KA, Schork NJ, Miller MW, Logue MW, Geyer MA, Risbrough VB, O'Connor DT, Baker DG.

Psychoneuroendocrinology. 2015 Jan;51:459-71. doi: 10.1016/j.psyneuen.2014.10.017. Epub 2014 Oct 30.

PMID:
25456346
12.

Reduced folate carrier 80A-->G polymorphism, plasma folate, and risk of placental abruption.

Ananth CV, Peltier MR, Moore DF, Kinzler WL, Leclerc D, Rozen RR; New Jersey-Placental Abruption Study Investigators.

Hum Genet. 2008 Sep;124(2):137-45. doi: 10.1007/s00439-008-0531-7. Epub 2008 Jul 16.

13.

Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study.

Carty CL, Spencer KL, Setiawan VW, Fernandez-Rhodes L, Malinowski J, Buyske S, Young A, Jorgensen NW, Cheng I, Carlson CS, Brown-Gentry K, Goodloe R, Park A, Parikh NI, Henderson B, Le Marchand L, Wactawski-Wende J, Fornage M, Matise TC, Hindorff LA, Arnold AM, Haiman CA, Franceschini N, Peters U, Crawford DC.

Hum Reprod. 2013 Jun;28(6):1695-706. doi: 10.1093/humrep/det071. Epub 2013 Mar 18.

14.

Associations between 2 polymorphisms in the methylenetetrahydrofolate reductase gene and placental abruption.

Ananth CV, Peltier MR, De Marco C, Elsasser DA, Getahun D, Rozen R, Smulian JC; New Jersey-Placental Abruption Study Investigators.

Am J Obstet Gynecol. 2007 Oct;197(4):385.e1-7.

15.

Association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with preterm delivery and placental abruption: a systematic review and meta-analysis.

Chen J, Chen L, Zhu LH, Zhang ST, Wu YL.

Acta Obstet Gynecol Scand. 2016 Feb;95(2):157-65. doi: 10.1111/aogs.12789. Epub 2015 Nov 6. Review.

PMID:
26439908
16.

Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis.

Zhao L, Li B, Dian K, Ying B, Lu X, Hu X, An Q, Chen C, Huang C, Tan B, Qin L.

PLoS One. 2015 Apr 13;10(4):e0123959. doi: 10.1371/journal.pone.0123959. eCollection 2015.

17.

Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.

Joshi AD, Andersson C, Buch S, Stender S, Noordam R, Weng LC, Weeke PE, Auer PL, Boehm B, Chen C, Choi H, Curhan G, Denny JC, De Vivo I, Eicher JD, Ellinghaus D, Folsom AR, Fuchs C, Gala M, Haessler J, Hofman A, Hu F, Hunter DJ, Janssen HL, Kang JH, Kooperberg C, Kraft P, Kratzer W, Lieb W, Lutsey PL, Darwish Murad S, Nordestgaard BG, Pasquale LR, Reiner AP, Ridker PM, Rimm E, Rose LM, Shaffer CM, Schafmayer C, Tamimi RM, Uitterlinden AG, Völker U, Völzke H, Wakabayashi Y, Wiggs JL, Zhu J, Roden DM, Stricker BH, Tang W, Teumer A, Hampe J, Tybjærg-Hansen A, Chasman DI, Chan AT, Johnson AD.

Gastroenterology. 2016 Aug;151(2):351-363.e28. doi: 10.1053/j.gastro.2016.04.007. Epub 2016 Apr 16.

18.

A variant on chromosome 2p13.3 is associated with atopic dermatitis in Chinese Han population.

Cai XY, Zheng XD, Fang L, Zhou FS, Sheng YJ, Wu YY, Yu CX, Zhu J, Xiao FL.

Gene. 2017 Sep 10;628:281-285. doi: 10.1016/j.gene.2017.07.059. Epub 2017 Jul 21.

PMID:
28739399
19.

Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.

Yang SK, Hong M, Zhao W, Jung Y, Baek J, Tayebi N, Kim KM, Ye BD, Kim KJ, Park SH, Lee I, Lee EJ, Kim WH, Cheon JH, Kim YH, Jang BI, Kim HS, Choi JH, Koo JS, Lee JH, Jung SA, Lee YJ, Jang JY, Shin HD, Kang D, Youn HS, Liu J, Song K.

Gut. 2014 Jan;63(1):80-7. doi: 10.1136/gutjnl-2013-305193. Epub 2013 Jul 14.

PMID:
23850713
20.

Placental genetic variations in circadian clock-related genes increase the risk of placental abruption.

Qiu C, Gelaye B, Denis M, Tadesse MG, Enquobahrie DA, Ananth CV, Pacora PN, Salazar M, Sanchez SE, Williams MA.

Int J Mol Epidemiol Genet. 2016 Mar 23;7(1):32-40. eCollection 2016.

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