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Results: 1 to 20 of 3574

1.

Weighted Interaction SNP Hub (WISH) network method for building genetic networks for complex diseases and traits using whole genome genotype data.

Kogelman LJ, Kadarmideen HN.

BMC Syst Biol. 2014 Mar 13;8 Suppl 2:S5. doi: 10.1186/1752-0509-8-S2-S5. Epub 2014 Mar 13.

PMID:
25032480
[PubMed - in process]
Free PMC Article
2.

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.

Ramirez A, van der Flier WM, Herold C, Ramonet D, Heilmann S, Lewczuk P, Popp J, Lacour A, Drichel D, Louwersheimer E, Kummer MP, Cruchaga C, Hoffmann P, Teunissen C, Holstege H, Kornhuber J, Peters O, Naj AC, Chouraki V, Bellenguez C, Gerrish A; International Genomics of Alzheimer's Project (IGAP); Alzheimer's Disease Neuroimaging Initiative (ADNI), Heun R, Frölich L, Hüll M, Buscemi L, Herms S, Kölsch H, Scheltens P, Breteler MM, Rüther E, Wiltfang J, Goate A, Jessen F, Maier W, Heneka MT, Becker T, Nöthen MM.

Hum Mol Genet. 2014 Jul 15. pii: ddu372. [Epub ahead of print]

PMID:
25027320
[PubMed - as supplied by publisher]
3.

Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study.

Akerblom A, Eriksson N, Wallentin L, Siegbahn A, Barratt BJ, Becker RC, Budaj A, Himmelmann A, Husted S, Storey RF, Johansson A, James SK; PLATO Investigators.

Am Heart J. 2014 Jul;168(1):96-102.e2. doi: 10.1016/j.ahj.2014.03.010. Epub 2014 Apr 4.

PMID:
24952865
[PubMed - in process]
4.

A polymorphism rs12325489C>T in the lincRNA-ENST00000515084 exon was found to modulate breast cancer risk via GWAS-based association analyses.

Li N, Zhou P, Zheng J, Deng J, Wu H, Li W, Li F, Li H, Lu J, Zhou Y, Zhang C.

PLoS One. 2014 May 30;9(5):e98251. doi: 10.1371/journal.pone.0098251. eCollection 2014.

PMID:
24879036
[PubMed - in process]
Free PMC Article
5.

A comprehensive resequence-analysis of 250 kb region of 8q24.21 in men of African ancestry.

Chung CC, Hsing AW, Edward Yeboah, Biritwum R, Tettey Y, Adjei A, Cook MB, De Marzo A, Netto G, Tay E, Boland JF, Yeager M, Chanock SJ.

Prostate. 2014 May;74(6):579-89.

PMID:
24783269
[PubMed - indexed for MEDLINE]
6.

Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies.

Rodriguez-Fontenla C, Calaza M, Evangelou E, Valdes AM, Arden N, Blanco FJ, Carr A, Chapman K, Deloukas P, Doherty M, Esko T, Garcés Aletá CM, Gomez-Reino Carnota JJ, Helgadottir H, Hofman A, Jonsdottir I, Kerkhof HJ, Kloppenburg M, McCaskie A, Ntzani EE, Ollier WE, Oreiro N, Panoutsopoulou K, Ralston SH, Ramos YF, Riancho JA, Rivadeneira F, Slagboom PE, Styrkarsdottir U, Thorsteinsdottir U, Thorleifsson G, Tsezou A, Uitterlinden AG, Wallis GA, Wilkinson JM, Zhai G, Zhu Y; arcOGEN Consortium, Felson DT, Ioannidis JP, Loughlin J, Metspalu A, Meulenbelt I, Stefansson K, van Meurs JB, Zeggini E, Spector TD, Gonzalez A.

Arthritis Rheumatol. 2014 Apr;66(4):940-9. doi: 10.1002/art.38300.

PMID:
24757145
[PubMed - indexed for MEDLINE]
7.

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.

Castellani CA, Melka MG, Wishart AE, Locke ME, Awamleh Z, O'Reilly RL, Singh SM.

BMC Bioinformatics. 2014 Apr 21;15:114. doi: 10.1186/1471-2105-15-114.

PMID:
24750645
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Statistical power and significance testing in large-scale genetic studies.

Sham PC, Purcell SM.

Nat Rev Genet. 2014 May;15(5):335-46. doi: 10.1038/nrg3706. Review.

PMID:
24739678
[PubMed - indexed for MEDLINE]
9.

Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder.

Hart AB, Gamazon ER, Engelhardt BE, Sklar P, Kähler AK, Hultman CM, Sullivan PF, Neale BM, Faraone SV; Psychiatric Genomics Consortium: ADHD Subgroup, de Wit H, Cox NJ, Palmer AA.

Proc Natl Acad Sci U S A. 2014 Apr 22;111(16):5968-73. doi: 10.1073/pnas.1318810111. Epub 2014 Apr 7.

PMID:
24711425
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Association between heme oxygenase 1 gene promoter polymorphisms and susceptibility to coronary artery disease: a HuGE review and meta-analysis.

Qiao H, Sai X, Gai L, Huang G, Chen X, Tu X, Ding Z.

Am J Epidemiol. 2014 May 1;179(9):1039-48. doi: 10.1093/aje/kwu024. Epub 2014 Mar 26. Review.

PMID:
24670375
[PubMed - indexed for MEDLINE]
11.

GeMes, clusters of DNA methylation under genetic control, can inform genetic and epigenetic analysis of disease.

Liu Y, Li X, Aryee MJ, Ekström TJ, Padyukov L, Klareskog L, Vandiver A, Moore AZ, Tanaka T, Ferrucci L, Fallin MD, Feinberg AP.

Am J Hum Genet. 2014 Apr 3;94(4):485-95. doi: 10.1016/j.ajhg.2014.02.011. Epub 2014 Mar 20.

PMID:
24656863
[PubMed - indexed for MEDLINE]
12.

BCRgt: a Bayesian cluster regression-based genotyping algorithm for the samples with copy number alterations.

Yang S, Cui X, Fang Z.

BMC Bioinformatics. 2014 Mar 15;15:74. doi: 10.1186/1471-2105-15-74.

PMID:
24629125
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Genetic variants reflecting higher vitamin e status in men are associated with reduced risk of prostate cancer.

Major JM, Yu K, Weinstein SJ, Berndt SI, Hyland PL, Yeager M, Chanock S, Albanes D.

J Nutr. 2014 May;144(5):729-33. doi: 10.3945/jn.113.189928. Epub 2014 Mar 12.

PMID:
24623848
[PubMed - indexed for MEDLINE]
14.

Polymorphic L1 retrotransposons are frequently in strong linkage disequilibrium with neighboring SNPs.

Higashino S, Ohno T, Ishiguro K, Aizawa Y.

Gene. 2014 May 10;541(1):55-9. doi: 10.1016/j.gene.2014.03.008. Epub 2014 Mar 10.

PMID:
24614499
[PubMed - indexed for MEDLINE]
15.

Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participants.

Laurie CC, Laurie CA, Smoley SA, Carlson EE, Flinn I, Fridley BL, Greisman HA, Gribben JG, Jelinek DF, Nelson SC, Paietta E, Schaid D, Sun Z, Tallman MS, Weinshilboum R, Kay NE, Shanafelt TD.

Cancer Genet. 2014 Jan-Feb;207(1-2):19-30. doi: 10.1016/j.cancergen.2014.01.004. Epub 2014 Jan 17.

PMID:
24613276
[PubMed - indexed for MEDLINE]
16.

Clinical effect of naturally random allocation to lower systolic blood pressure beginning before the development of hypertension.

Ference BA, Julius S, Mahajan N, Levy PD, Williams KA Sr, Flack JM.

Hypertension. 2014 Jun;63(6):1182-8. doi: 10.1161/HYPERTENSIONAHA.113.02734. Epub 2014 Mar 3.

PMID:
24591335
[PubMed - indexed for MEDLINE]
17.

Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder.

Jan WC, Yang SY, Chuang LC, Lu RB, Lu MK, Sun HS, Kuo PH.

J Affect Disord. 2014 Mar;157:80-6. doi: 10.1016/j.jad.2013.12.044. Epub 2014 Jan 8.

PMID:
24581832
[PubMed - indexed for MEDLINE]
18.

[Genome-wide association study of high-altitude pulmonary edema in Han Chinese].

Yang YZ, Wang YP, Ma L, Du Y, Ge RL.

Yi Chuan. 2013 Nov;35(11):1291-9. Chinese.

PMID:
24579312
[PubMed - indexed for MEDLINE]
19.

Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.

Huang J, Huffman JE, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët DA, Chen WM, Smith NL, Kleber ME, Shin SY, Becker DM, Tang W, Dehghan A, Johnson AD, Truong V, Folkersen L, Yang Q, Oudot-Mellkah T, Buckley BM, Moore JH, Williams FM, Campbell H, Silbernagel G, Vitart V, Rudan I, Tofler GH, Navis GJ, Destefano A, Wright AF, Chen MH, de Craen AJ, Worrall BB, Rudnicka AR, Rumley A, Bookman EB, Psaty BM, Chen F, Keene KL, Franco OH, Böhm BO, Uitterlinden AG, Carter AM, Jukema JW, Sattar N, Bis JC, Ikram MA; Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group, Sale MM, McKnight B, Fornage M, Ford I, Taylor K, Slagboom PE, McArdle WL, Hsu FC, Franco-Cereceda A, Goodall AH, Yanek LR, Furie KL, Cushman M, Hofman A, Witteman JC, Folsom AR, Basu S, Matijevic N, van Gilst WH, Wilson JF, Westendorp RG, Kathiresan S, Reilly MP; CARDIoGRAM Consortium, Tracy RP, Polasek O, Winkelmann BR, Grant PJ, Hillege HL, Cambien F, Stott DJ, Lowe GD, Spector TD, Meigs JB, Marz W, Eriksson P, Becker LC, Morange PE, Soranzo N, Williams SM, Hayward C, van der Harst P, Hamsten A, Lowenstein CJ, Strachan DP, O'Donnell CJ; CHARGE Consortium Hemostatic Factor Working Group.

Arterioscler Thromb Vasc Biol. 2014 May;34(5):1093-101. doi: 10.1161/ATVBAHA.113.302088. Epub 2014 Feb 27.

PMID:
24578379
[PubMed - indexed for MEDLINE]
20.

Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.

Opherk C, Gonik M, Duering M, Malik R, Jouvent E, Hervé D, Adib-Samii P, Bevan S, Pianese L, Silvestri S, Dotti MT, De Stefano N, Liem M, Boon EM, Pescini F, Pachai C, Bracoud L, Müller-Myhsok B, Meitinger T, Rost N, Pantoni L, Lesnik Oberstein S, Federico A, Ragno M, Markus HS, Tournier-Lasserve E, Rosand J, Chabriat H, Dichgans M.

Stroke. 2014 Apr;45(4):968-72. doi: 10.1161/STROKEAHA.113.004461. Epub 2014 Feb 27.

PMID:
24578207
[PubMed - indexed for MEDLINE]

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