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Results: 1 to 20 of 275

Cited In for PubMed (Select 20647212)

1.

Influence of Feature Encoding and Choice of Classifier on Disease Risk Prediction in Genome-Wide Association Studies.

Mittag F, Römer M, Zell A.

PLoS One. 2015 Aug 18;10(8):e0135832. doi: 10.1371/journal.pone.0135832. eCollection 2015.

2.

Genetics of Human and Canine Dilated Cardiomyopathy.

Simpson S, Edwards J, Ferguson-Mignan TF, Cobb M, Mongan NP, Rutland CS.

Int J Genomics. 2015;2015:204823. doi: 10.1155/2015/204823. Epub 2015 Jul 22. Review.

3.

Association of the I264T Variant in the Sulfide Quinone Reductase-Like (SQRDL) Gene with Osteoporosis in Korean Postmenopausal Women.

Jin HS, Kim J, Park S, Park E, Kim BY, Choi VN, Yoo YH, Kim BT, Jeong SY.

PLoS One. 2015 Aug 10;10(8):e0135285. doi: 10.1371/journal.pone.0135285. eCollection 2015.

4.

Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals.

Chang S, Fang K, Zhang K, Wang J.

PLoS One. 2015 Jul 20;10(7):e0133404. doi: 10.1371/journal.pone.0133404. eCollection 2015.

5.

Evaluating the Association of Eight Polymorphisms with Cancer Susceptibility in a Han Chinese Population.

Dong Y, Chen J, Chen Z, Tian C, Lu H, Ruan J, Yang W.

PLoS One. 2015 Jul 15;10(7):e0132797. doi: 10.1371/journal.pone.0132797. eCollection 2015.

6.

Implications of pleiotropy: challenges and opportunities for mining Big Data in biomedicine.

Yang C, Li C, Wang Q, Chung D, Zhao H.

Front Genet. 2015 Jun 30;6:229. doi: 10.3389/fgene.2015.00229. eCollection 2015. Review.

7.

Characterization of the Interleukin-28B Gene rs12979860 C/T Polymorphism in Turkish Chronic Hepatitis C Patients and Healthy Individuals.

Taheri S, Aygen B, Korkmaz K, Yıldız O, Zararsız G, Canatan H.

Balkan Med J. 2015 Apr;32(2):147-55. doi: 10.5152/balkanmedj.2015.15156. Epub 2015 Apr 1.

8.
9.

PSCA s2294008 C>T and rs2976392 G>A polymorphisms contribute to cancer susceptibility: evidence from published studies.

Gu Y, Dai QS, Hua RX, Zhang B, Zhu JH, Huang JW, Xie BH, Xiong SQ, Tan GS, Li HP.

Genes Cancer. 2015 May;6(5-6):254-64.

10.

The genetic and environmental factors for keratoconus.

Gordon-Shaag A, Millodot M, Shneor E, Liu Y.

Biomed Res Int. 2015;2015:795738. doi: 10.1155/2015/795738. Epub 2015 May 17. Review.

11.

Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population.

Abu-Amero KK, Helwa I, Al-Muammar A, Strickland S, Hauser MA, Allingham RR, Liu Y.

J Negat Results Biomed. 2015 Jun 4;14:10. doi: 10.1186/s12952-015-0029-5.

12.

Genetic variants and risk of gastric cancer: a pathway analysis of a genome-wide association study.

Lee JH, Kim Y, Choi JW, Kim YS.

Springerplus. 2015 May 6;4:215. doi: 10.1186/s40064-015-1005-8. eCollection 2015.

13.

Approaches for the identification of genetic modifiers of nutrient dependent phenotypes: examples from folate.

Zinck JW, MacFarlane AJ.

Front Nutr. 2014 Jul 14;1:8. doi: 10.3389/fnut.2014.00008. eCollection 2014. Review.

14.

Extracting research-quality phenotypes from electronic health records to support precision medicine.

Wei WQ, Denny JC.

Genome Med. 2015 Apr 30;7(1):41. doi: 10.1186/s13073-015-0166-y. eCollection 2015.

15.

Long-range regulatory interactions at the 4q25 atrial fibrillation risk locus involve PITX2c and ENPEP.

Aguirre LA, Alonso ME, Badía-Careaga C, Rollán I, Arias C, Fernández-Miñán A, López-Jiménez E, Aránega A, Gómez-Skarmeta JL, Franco D, Manzanares M.

BMC Biol. 2015 Apr 17;13:26. doi: 10.1186/s12915-015-0138-0.

16.

A meta-analysis strategy for gene prioritization using gene expression, SNP genotype, and eQTL data.

Che J, Shin M.

Biomed Res Int. 2015;2015:576349. doi: 10.1155/2015/576349. Epub 2015 Mar 22.

17.

The study to understand the genetics of the acute response to metformin and glipizide in humans (SUGAR-MGH): design of a pharmacogenetic resource for type 2 diabetes.

Walford GA, Colomo N, Todd JN, Billings LK, Fernandez M, Chamarthi B, Warner AS, Davis J, Littleton KR, Hernandez AM, Fanelli RR, Lanier A, Barbato C, Ackerman RJ, Khan SQ, Bui R, Garber L, Stolerman ES, Moore AF, Huang C, Kaur V, Harden M, Taylor A, Chen L, Manning AK, Huang P, Wexler D, McCarthy RM, Lo J, Thomas MK, Grant RW, Goldfine A, Hudson MS, Florez JC.

PLoS One. 2015 Mar 26;10(3):e0121553. doi: 10.1371/journal.pone.0121553. eCollection 2015.

18.

Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.

Jia Z, Leslie EJ, Cooper ME, Butali A, Standley J, Rigdon J, Suzuki S, Gongorjav A, Shonkhuuz TE, Natsume N, Shi B, Marazita ML, Murray JC.

Am J Med Genet A. 2015 May;167A(5):1054-60. doi: 10.1002/ajmg.a.36912. Epub 2015 Mar 18.

19.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PMID:
25741868
20.

TGF-β1-Induced Epithelial-Mesenchymal Transition Promotes Monocyte/Macrophage Properties in Breast Cancer Cells.

Johansson J, Tabor V, Wikell A, Jalkanen S, Fuxe J.

Front Oncol. 2015 Jan 26;5:3. doi: 10.3389/fonc.2015.00003. eCollection 2015.

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