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Results: 1 to 20 of 100

1.

Effects of GWAS-Associated Genetic Variants on lncRNAs within IBD and T1D Candidate Loci.

Mirza AH, Kaur S, Brorsson CA, Pociot F.

PLoS One. 2014 Aug 21;9(8):e105723. doi: 10.1371/journal.pone.0105723. eCollection 2014.

PMID:
25144376
[PubMed - in process]
Free PMC Article
2.

Systematic Genetic Analysis Identifies Cis-eQTL Target Genes Associated with Glioblastoma Patient Survival.

Chen QR, Hu Y, Yan C, Buetow K, Meerzaman D.

PLoS One. 2014 Aug 18;9(8):e105393. doi: 10.1371/journal.pone.0105393. eCollection 2014.

PMID:
25133526
[PubMed - in process]
Free PMC Article
3.

Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.

Ng MC, Shriner D, Chen BH, Li J, Chen WM, Guo X, Liu J, Bielinski SJ, Yanek LR, Nalls MA, Comeau ME, Rasmussen-Torvik LJ, Jensen RA, Evans DS, Sun YV, An P, Patel SR, Lu Y, Long J, Armstrong LL, Wagenknecht L, Yang L, Snively BM, Palmer ND, Mudgal P, Langefeld CD, Keene KL, Freedman BI, Mychaleckyj JC, Nayak U, Raffel LJ, Goodarzi MO, Chen YD, Taylor HA Jr, Correa A, Sims M, Couper D, Pankow JS, Boerwinkle E, Adeyemo A, Doumatey A, Chen G, Mathias RA, Vaidya D, Singleton AB, Zonderman AB, Igo RP Jr, Sedor JR; FIND Consortium, Kabagambe EK, Siscovick DS, McKnight B, Rice K, Liu Y, Hsueh WC, Zhao W, Bielak LF, Kraja A, Province MA, Bottinger EP, Gottesman O, Cai Q, Zheng W, Blot WJ, Lowe WL, Pacheco JA, Crawford DC; eMERGE Consortium; DIAGRAM Consortium, Grundberg E; MuTHER Consortium, Rich SS, Hayes MG, Shu XO, Loos RJ, Borecki IB, Peyser PA, Cummings SR, Psaty BM, Fornage M, Iyengar SK, Evans MK, Becker DM, Kao WH, Wilson JG, Rotter JI, Sale MM, Liu S, Rotimi CN, Bowden DW; MEta-analysis of type 2 DIabetes in African Americans (MEDIA) Consortium.

PLoS Genet. 2014 Aug 7;10(8):e1004517. doi: 10.1371/journal.pgen.1004517. eCollection 2014 Aug.

PMID:
25102180
[PubMed - in process]
Free PMC Article
4.

A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach.

Traylor M, Mäkelä KM, Kilarski LL, Holliday EG, Devan WJ, Nalls MA, Wiggins KL, Zhao W, Cheng YC, Achterberg S, Malik R, Sudlow C, Bevan S, Raitoharju E; METASTROKE, International Stroke Genetics Consortium, Wellcome Trust Case Consortium 2 (WTCCC2), Oksala N, Thijs V, Lemmens R, Lindgren A, Slowik A, Maguire JM, Walters M, Algra A, Sharma P, Attia JR, Boncoraglio GB, Rothwell PM, de Bakker PI, Bis JC, Saleheen D, Kittner SJ, Mitchell BD, Rosand J, Meschia JF, Levi C, Dichgans M, Lehtimäki T, Lewis CM, Markus HS.

PLoS Genet. 2014 Jul 31;10(7):e1004469. doi: 10.1371/journal.pgen.1004469. eCollection 2014 Jul.

PMID:
25078452
[PubMed - in process]
Free PMC Article
5.

Non-coding polymorphisms in nucleotide binding domain 1 in ABCC1 gene associate with transcript level and survival of patients with breast cancer.

Kunická T, Václavíková R, Hlaváč V, Vrána D, Pecha V, Rauš K, Trnková M, Kubáčková K, Ambruš M, Vodičková L, Vodička P, Souček P.

PLoS One. 2014 Jul 31;9(7):e101740. doi: 10.1371/journal.pone.0101740. eCollection 2014.

PMID:
25078270
[PubMed - in process]
Free PMC Article
6.

Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease.

Mäkinen VP, Civelek M, Meng Q, Zhang B, Zhu J, Levian C, Huan T, Segrè AV, Ghosh S, Vivar J, Nikpay M, Stewart AF, Nelson CP, Willenborg C, Erdmann J, Blakenberg S, O'Donnell CJ, März W, Laaksonen R, Epstein SE, Kathiresan S, Shah SH, Hazen SL, Reilly MP; Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium, Lusis AJ, Samani NJ, Schunkert H, Quertermous T, McPherson R, Yang X, Assimes TL.

PLoS Genet. 2014 Jul 17;10(7):e1004502. doi: 10.1371/journal.pgen.1004502. eCollection 2014 Jul.

PMID:
25033284
[PubMed - in process]
Free PMC Article
7.

Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients.

Kaur H, Jajodia A, Grover S, Baghel R, Gupta M, Jain S, Kukreti R.

PLoS One. 2014 Jul 15;9(7):e102556. doi: 10.1371/journal.pone.0102556. eCollection 2014.

PMID:
25025909
[PubMed - in process]
Free PMC Article
8.

Systematic fine-mapping of association with BMI and type 2 diabetes at the FTO locus by integrating results from multiple ethnic groups.

Akiyama K, Takeuchi F, Isono M, Chakrawarthy S, Nguyen QN, Wen W, Yamamoto K, Katsuya T, Kasturiratne A, Pham ST, Zheng W, Matsushita Y, Kishimoto M, Do LD, Shu XO, Wickremasinghe AR, Kajio H, Kato N.

PLoS One. 2014 Jun 30;9(6):e101329. doi: 10.1371/journal.pone.0101329. eCollection 2014.

PMID:
24978468
[PubMed - in process]
Free PMC Article
9.

Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs.

Zhang X, Gierman HJ, Levy D, Plump A, Dobrin R, Goring HH, Curran JE, Johnson MP, Blangero J, Kim SK, O'Donnell CJ, Emilsson V, Johnson AD.

BMC Genomics. 2014 Jun 27;15:532. doi: 10.1186/1471-2164-15-532.

PMID:
24973796
[PubMed - in process]
Free PMC Article
10.

Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium.

Bis JC, DeStefano A, Liu X, Brody JA, Choi SH, Verhaaren BF, Debette S, Ikram MA, Shahar E, Butler KR Jr, Gottesman RF, Muzny D, Kovar CL, Psaty BM, Hofman A, Lumley T, Gupta M, Wolf PA, van Duijn C, Gibbs RA, Mosley TH, Longstreth WT Jr, Boerwinkle E, Seshadri S, Fornage M.

PLoS One. 2014 Jun 24;9(6):e99798. doi: 10.1371/journal.pone.0099798. eCollection 2014.

PMID:
24959832
[PubMed - in process]
Free PMC Article
11.

Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants.

Narahara M, Higasa K, Nakamura S, Tabara Y, Kawaguchi T, Ishii M, Matsubara K, Matsuda F, Yamada R.

PLoS One. 2014 Jun 23;9(6):e100924. doi: 10.1371/journal.pone.0100924. eCollection 2014.

PMID:
24956270
[PubMed - in process]
Free PMC Article
12.

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.

Kemp JP, Medina-Gomez C, Estrada K, St Pourcain B, Heppe DH, Warrington NM, Oei L, Ring SM, Kruithof CJ, Timpson NJ, Wolber LE, Reppe S, Gautvik K, Grundberg E, Ge B, van der Eerden B, van de Peppel J, Hibbs MA, Ackert-Bicknell CL, Choi K, Koller DL, Econs MJ, Williams FM, Foroud T, Zillikens MC, Ohlsson C, Hofman A, Uitterlinden AG, Davey Smith G, Jaddoe VW, Tobias JH, Rivadeneira F, Evans DM.

PLoS Genet. 2014 Jun 19;10(6):e1004423. doi: 10.1371/journal.pgen.1004423. eCollection 2014 Jun.

PMID:
24945404
[PubMed - in process]
Free PMC Article
13.

On the identification of potential regulatory variants within genome wide association candidate SNP sets.

Chen CY, Chang IS, Hsiung CA, Wasserman WW.

BMC Med Genomics. 2014 Jun 11;7:34. doi: 10.1186/1755-8794-7-34.

PMID:
24920305
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genetic analysis of long-lived families reveals novel variants influencing high density-lipoprotein cholesterol.

Feitosa MF, Wojczynski MK, Straka R, Kammerer CM, Lee JH, Kraja AT, Christensen K, Newman AB, Province MA, Borecki IB.

Front Genet. 2014 Jun 3;5:159. doi: 10.3389/fgene.2014.00159. eCollection 2014.

PMID:
24917880
[PubMed]
Free PMC Article
15.

Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance.

Choudhury A, Hazelhurst S, Meintjes A, Achinike-Oduaran O, Aron S, Gamieldien J, Jalali Sefid Dashti M, Mulder N, Tiffin N, Ramsay M.

BMC Genomics. 2014 Jun 6;15:437. doi: 10.1186/1471-2164-15-437.

PMID:
24906912
[PubMed - in process]
Free PMC Article
16.

CLOCK 3111 T/C SNP interacts with emotional eating behavior for weight-loss in a Mediterranean population.

López-Guimerà G, Dashti HS, Smith CE, Sánchez-Carracedo D, Ordovas JM, Garaulet M.

PLoS One. 2014 Jun 6;9(6):e99152. doi: 10.1371/journal.pone.0099152. eCollection 2014.

PMID:
24905098
[PubMed - in process]
Free PMC Article
17.

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia.

Juraeva D, Haenisch B, Zapatka M, Frank J; GROUP Investigators; PSYCH-GEMS SCZ Working Group, Witt SH, Mühleisen TW, Treutlein J, Strohmaier J, Meier S, Degenhardt F, Giegling I, Ripke S, Leber M, Lange C, Schulze TG, Mössner R, Nenadic I, Sauer H, Rujescu D, Maier W, Børglum A, Ophoff R, Cichon S, Nöthen MM, Rietschel M, Mattheisen M, Brors B.

PLoS Genet. 2014 Jun 5;10(6):e1004345. doi: 10.1371/journal.pgen.1004345. eCollection 2014 Jun.

PMID:
24901509
[PubMed - in process]
Free PMC Article
18.

Allelic expression analysis of the osteoarthritis susceptibility locus that maps to chromosome 3p21 reveals cis-acting eQTLs at GNL3 and SPCS1.

Gee F, Clubbs CF, Raine EV, Reynard LN, Loughlin J.

BMC Med Genet. 2014 May 4;15:53. doi: 10.1186/1471-2350-15-53.

PMID:
24886551
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Functional annotation signatures of disease susceptibility loci improve SNP association analysis.

Iversen ES, Lipton G, Clyde MA, Monteiro AN.

BMC Genomics. 2014 May 24;15:398. doi: 10.1186/1471-2164-15-398.

PMID:
24886216
[PubMed - in process]
Free PMC Article
20.

Increased genetic diversity of ADME genes in African Americans compared with their putative ancestral source populations and implications for pharmacogenomics.

Li J, Lao X, Zhang C, Tian L, Lu D, Xu S.

BMC Genet. 2014 May 1;15:52. doi: 10.1186/1471-2156-15-52.

PMID:
24884825
[PubMed - in process]
Free PMC Article

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