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Items: 1 to 20 of 45

1.

A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy.

Fava VM, Manry J, Cobat A, Orlova M, Van Thuc N, Moraes MO, Sales-Marques C, Stefani MM, Latini AC, Belone AF, Thai VH, Abel L, Alcaïs A, Schurr E.

PLoS Genet. 2017 Feb 21;13(2):e1006637. doi: 10.1371/journal.pgen.1006637. eCollection 2017 Feb.

2.

Gene expression elucidates functional impact of polygenic risk for schizophrenia.

Fromer M, Roussos P, Sieberts SK, Johnson JS, Kavanagh DH, Perumal TM, Ruderfer DM, Oh EC, Topol A, Shah HR, Klei LL, Kramer R, Pinto D, Gümüş ZH, Cicek AE, Dang KK, Browne A, Lu C, Xie L, Readhead B, Stahl EA, Xiao J, Parvizi M, Hamamsy T, Fullard JF, Wang YC, Mahajan MC, Derry JM, Dudley JT, Hemby SE, Logsdon BA, Talbot K, Raj T, Bennett DA, De Jager PL, Zhu J, Zhang B, Sullivan PF, Chess A, Purcell SM, Shinobu LA, Mangravite LM, Toyoshiba H, Gur RE, Hahn CG, Lewis DA, Haroutunian V, Peters MA, Lipska BK, Buxbaum JD, Schadt EE, Hirai K, Roeder K, Brennand KJ, Katsanis N, Domenici E, Devlin B, Sklar P.

Nat Neurosci. 2016 Nov;19(11):1442-1453. doi: 10.1038/nn.4399. Epub 2016 Sep 26.

3.

Genetics ignite focus on microglial inflammation in Alzheimer's disease.

Malik M, Parikh I, Vasquez JB, Smith C, Tai L, Bu G, LaDu MJ, Fardo DW, Rebeck GW, Estus S.

Mol Neurodegener. 2015 Oct 5;10:52. doi: 10.1186/s13024-015-0048-1. Review.

4.

Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event.

Poirier JG, Faye LL, Dimitromanolakis A, Paterson AD, Sun L, Bull SB.

Genet Epidemiol. 2015 Nov;39(7):518-28. doi: 10.1002/gepi.21920. Epub 2015 Sep 28.

5.

Association of the Lipoprotein Receptor SCARB1 Common Missense Variant rs4238001 with Incident Coronary Heart Disease.

Manichaikul A, Wang XQ, Musani SK, Herrington DM, Post WS, Wilson JG, Rich SS, Rodriguez A.

PLoS One. 2015 May 20;10(5):e0125497. doi: 10.1371/journal.pone.0125497. eCollection 2015.

6.

The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration.

Logue MW, Amstadter AB, Baker DG, Duncan L, Koenen KC, Liberzon I, Miller MW, Morey RA, Nievergelt CM, Ressler KJ, Smith AK, Smoller JW, Stein MB, Sumner JA, Uddin M.

Neuropsychopharmacology. 2015 Sep;40(10):2287-97. doi: 10.1038/npp.2015.118. Epub 2015 Apr 23. Review.

7.

Prediction of treatment outcomes in psychiatry--where do we stand ?

McMahon FJ.

Dialogues Clin Neurosci. 2014 Dec;16(4):455-64. Review.

8.

G protein-coupled receptor kinase 5 gene polymorphisms are associated with postoperative atrial fibrillation after coronary artery bypass grafting in patients receiving β-blockers.

Kertai MD, Li YW, Li YJ, Shah SH, Kraus WE, Fontes ML, Stafford-Smith M, Newman MF, Podgoreanu MV, Mathew JP; Duke Perioperative Genetics and Safety Outcomes (PEGASUS) Investigative Team..

Circ Cardiovasc Genet. 2014 Oct;7(5):625-33. doi: 10.1161/CIRCGENETICS.113.000451. Epub 2014 Jul 21.

9.

Genome-wide association and functional studies identify a role for IGFBP3 in hip osteoarthritis.

Evans DS, Cailotto F, Parimi N, Valdes AM, Castaño-Betancourt MC, Liu Y, Kaplan RC, Bidlingmaier M, Vasan RS, Teumer A, Tranah GJ, Nevitt MC, Cummings SR, Orwoll ES, Barrett-Connor E, Renner JB, Jordan JM, Doherty M, Doherty SA, Uitterlinden AG, van Meurs JB, Spector TD, Lories RJ, Lane NE.

Ann Rheum Dis. 2015 Oct;74(10):1861-7. doi: 10.1136/annrheumdis-2013-205020. Epub 2014 Jun 13.

10.

Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.

Garg P, Ludwig KU, Böhmer AC, Rubini M, Steegers-Theunissen R, Mossey PA, Mangold E, Sharp AJ.

Eur J Hum Genet. 2014 Jun;22(6):822-30. doi: 10.1038/ejhg.2013.235. Epub 2013 Oct 30.

11.

Genome-wide association studies in Alzheimer's disease: a review.

Tosto G, Reitz C.

Curr Neurol Neurosci Rep. 2013 Oct;13(10):381. doi: 10.1007/s11910-013-0381-0. Review.

12.

Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification.

Faye LL, Machiela MJ, Kraft P, Bull SB, Sun L.

PLoS Genet. 2013;9(8):e1003609. doi: 10.1371/journal.pgen.1003609. Epub 2013 Aug 8.

13.

Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry.

Ahmad S, Rukh G, Varga TV, Ali A, Kurbasic A, Shungin D, Ericson U, Koivula RW, Chu AY, Rose LM, Ganna A, Qi Q, Stančáková A, Sandholt CH, Elks CE, Curhan G, Jensen MK, Tamimi RM, Allin KH, Jørgensen T, Brage S, Langenberg C, Aadahl M, Grarup N, Linneberg A, Paré G; InterAct Consortium.; DIRECT Consortium., Magnusson PK, Pedersen NL, Boehnke M, Hamsten A, Mohlke KL, Pasquale LT, Pedersen O, Scott RA, Ridker PM, Ingelsson E, Laakso M, Hansen T, Qi L, Wareham NJ, Chasman DI, Hallmans G, Hu FB, Renström F, Orho-Melander M, Franks PW.

PLoS Genet. 2013;9(7):e1003607. doi: 10.1371/journal.pgen.1003607. Epub 2013 Jul 25.

14.

Association of a cystatin C gene variant with cystatin C levels, CKD, and risk of incident cardiovascular disease and mortality.

O'Seaghdha CM, Tin A, Yang Q, Katz R, Liu Y, Harris T, Astor B, Coresh J, Fox CS, Kao WH, Shlipak MG.

Am J Kidney Dis. 2014 Jan;63(1):16-22. doi: 10.1053/j.ajkd.2013.06.015. Epub 2013 Aug 7.

15.

Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans.

Wang H, Haiman CA, Burnett T, Fortini BK, Kolonel LN, Henderson BE, Signorello LB, Blot WJ, Keku TO, Berndt SI, Newcomb PA, Pande M, Amos CI, West DW, Casey G, Sandler RS, Haile R, Stram DO, Le Marchand L.

Hum Mol Genet. 2013 Dec 15;22(24):5048-55. doi: 10.1093/hmg/ddt337. Epub 2013 Jul 12.

16.

Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.

Jeff JM, Ritchie MD, Denny JC, Kho AN, Ramirez AH, Crosslin D, Armstrong L, Basford MA, Wolf WA, Pacheco JA, Chisholm RL, Roden DM, Hayes MG, Crawford DC.

Ann Hum Genet. 2013 Jul;77(4):321-32. doi: 10.1111/ahg.12023. Epub 2013 Mar 28.

17.

Evaluating reported candidate gene associations with polycystic ovary syndrome.

Pau C, Saxena R, Welt CK.

Fertil Steril. 2013 May;99(6):1774-8. doi: 10.1016/j.fertnstert.2012.12.033. Epub 2013 Jan 30.

18.

Genetic variants and associations of 25-hydroxyvitamin D concentrations with major clinical outcomes.

Levin GP, Robinson-Cohen C, de Boer IH, Houston DK, Lohman K, Liu Y, Kritchevsky SB, Cauley JA, Tanaka T, Ferrucci L, Bandinelli S, Patel KV, Hagström E, Michaëlsson K, Melhus H, Wang T, Wolf M, Psaty BM, Siscovick D, Kestenbaum B.

JAMA. 2012 Nov 14;308(18):1898-905. doi: 10.1001/jama.2012.17304.

19.

Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations.

Liu DJ, Leal SM.

Am J Hum Genet. 2012 Oct 5;91(4):585-96. doi: 10.1016/j.ajhg.2012.08.008. Epub 2012 Sep 27.

20.

Empirical Bayes correction for the Winner's Curse in genetic association studies.

Ferguson JP, Cho JH, Yang C, Zhao H.

Genet Epidemiol. 2013 Jan;37(1):60-8. doi: 10.1002/gepi.21683. Epub 2012 Sep 25.

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