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Items: 1 to 20 of 86

1.

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.

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.

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.

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.

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.

6.

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.

7.

Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood.

Rye MS, Warrington NM, Scaman ES, Vijayasekaran S, Coates HL, Anderson D, Pennell CE, Blackwell JM, Jamieson SE.

PLoS One. 2012;7(10):e48215. doi: 10.1371/journal.pone.0048215. Epub 2012 Oct 25.

8.

SNP-based pathway enrichment analysis for genome-wide association studies.

Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.

BMC Bioinformatics. 2011 Apr 15;12:99. doi: 10.1186/1471-2105-12-99.

9.

Endometrial vezatin and its association with endometriosis risk.

Holdsworth-Carson SJ, Fung JN, Luong HT, Sapkota Y, Bowdler LM, Wallace L, Teh WT, Powell JE, Girling JE, Healey M, Montgomery GW, Rogers PA.

Hum Reprod. 2016 May;31(5):999-1013. doi: 10.1093/humrep/dew047. Epub 2016 Mar 22.

PMID:
27005890
10.

Pathway analysis for a genome-wide association study of pneumoconiosis.

Wang T, Yang J, Ji X, Chu M, Zhang R, Dai J, Jin G, Hu Z, Shen H, Ni C.

Toxicol Lett. 2015 Jan 5;232(1):284-92. doi: 10.1016/j.toxlet.2014.10.028. Epub 2014 Nov 4.

PMID:
25445010
11.

Genetic variation and human longevity.

Soerensen M.

Dan Med J. 2012 May;59(5):B4454.

PMID:
22549493
12.

Network-based analysis of genome wide association data provides novel candidate genes for lipid and lipoprotein traits.

Sharma A, Gulbahce N, Pevzner SJ, Menche J, Ladenvall C, Folkersen L, Eriksson P, Orho-Melander M, Barabási AL.

Mol Cell Proteomics. 2013 Nov;12(11):3398-408. doi: 10.1074/mcp.M112.024851. Epub 2013 Jul 23.

13.

Shared genetic factors for age at natural menopause in Iranian and European women.

Rahmani M, Earp MA, Ramezani Tehrani F, Ataee M, Wu J, Treml M, Nudischer R, P-Behnami S; ReproGen Consortium, Perry JR, Murabito JM, Azizi F, Brooks-Wilson A.

Hum Reprod. 2013 Jul;28(7):1987-94. doi: 10.1093/humrep/det106. Epub 2013 Apr 16.

PMID:
23592221
14.

Pathway analysis of a genome-wide association study in schizophrenia.

Lee YH, Kim JH, Song GG.

Gene. 2013 Aug 1;525(1):107-15. doi: 10.1016/j.gene.2013.04.014. Epub 2013 May 1.

PMID:
23644028
15.

Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

Liu X, Cheng R, Verbitsky M, Kisselev S, Browne A, Mejia-Sanatana H, Louis ED, Cote LJ, Andrews H, Waters C, Ford B, Frucht S, Fahn S, Marder K, Clark LN, Lee JH.

BMC Med Genet. 2011 Aug 3;12:104. doi: 10.1186/1471-2350-12-104.

16.

Shared genetic etiology underlying Alzheimer's disease and type 2 diabetes.

Hao K, Di Narzo AF, Ho L, Luo W, Li S, Chen R, Li T, Dubner L, Pasinetti GM.

Mol Aspects Med. 2015 Jun-Oct;43-44:66-76. doi: 10.1016/j.mam.2015.06.006. Epub 2015 Jun 23. Review.

PMID:
26116273
17.

Genome-wide association study of Alzheimer's disease.

Kamboh MI, Demirci FY, Wang X, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ; Alzheimer's Disease Neuroimaging Initiative, Jun G, Baldwin C, Logue MW, Buros J, Farrer L, Pericak-Vance MA, Haines JL, Sweet RA, Ganguli M, Feingold E, Dekosky ST, Lopez OL, Barmada MM.

Transl Psychiatry. 2012 May 15;2:e117. doi: 10.1038/tp.2012.45.

18.

Analyses of shared genetic factors between asthma and obesity in children.

Melén E, Himes BE, Brehm JM, Boutaoui N, Klanderman BJ, Sylvia JS, Lasky-Su J.

J Allergy Clin Immunol. 2010 Sep;126(3):631-7.e1-8. doi: 10.1016/j.jaci.2010.06.030.

19.

Gene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data.

Liu Y, Maxwell S, Feng T, Zhu X, Elston RC, Koyutürk M, Chance MR.

BMC Syst Biol. 2012;6 Suppl 3:S15. doi: 10.1186/1752-0509-6-S3-S15. Epub 2012 Dec 17.

20.

Snat: a SNP annotation tool for bovine by integrating various sources of genomic information.

Jiang J, Jiang L, Zhou B, Fu W, Liu JF, Zhang Q.

BMC Genet. 2011 Oct 7;12:85. doi: 10.1186/1471-2156-12-85.

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