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Items: 1 to 20 of 6458

1.

Association of a Genetic Risk Score With Body Mass Index Across Different Birth Cohorts.

Walter S, Mejía-Guevara I, Estrada K, Liu SY, Glymour MM.

JAMA. 2016 Jul 5;316(1):63-9. doi: 10.1001/jama.2016.8729.

PMID:
27380344
2.

Association Between CYP2C19 Loss-of-Function Allele Status and Efficacy of Clopidogrel for Risk Reduction Among Patients With Minor Stroke or Transient Ischemic Attack.

Wang Y, Zhao X, Lin J, Li H, Johnston SC, Lin Y, Pan Y, Liu L, Wang D, Wang C, Meng X, Xu J, Wang Y; CHANCE investigators.

JAMA. 2016 Jul 5;316(1):70-8. doi: 10.1001/jama.2016.8662.

PMID:
27348249
3.

[Association of genetic polymorphisms in HjV-BMPs-SMADs pathway of hepcidin regulation with the incidence of anemia in Chinese adolescent aged 12 -18 years old].

Piao W, Wang L, Zhang T, Wang Z, Shangguan Shaofang, Sun J, Huo J.

Wei Sheng Yan Jiu. 2016 Mar;45(2):173-8. Chinese.

PMID:
27301209
4.

Association of Polymorphisms (rs 1799782, rs25489 and rs25487) in XRCC1 and (rs 13181) XPD genes with Acute Coronary Artery Syndrome in Subjects from Multan, Pakistan.

Hameed H, Faryal M, Aslam MA, Akbar A, Saad AB, Pasha MB, Latif M, Rehan Sadiq Shaikh RR, Ali M, Iqbal F.

Pak J Pharm Sci. 2016 May;29(3):869-76.

PMID:
27166553
5.

Biology, Genetics, and Environment: Underlying Factors Influencing Alcohol Metabolism.

Wall TL, Luczak SE, Hiller-Sturmhöfel S.

Alcohol Res. 2016;38(1):59-68. Review.

6.

-1195 A/G promoter variants of the cyclooxygenase-2 gene increases the risk of pain occurrence in endometriotic women.

Wang H, Sun L, Jiang M, Liu L, Wang G.

Clin Exp Obstet Gynecol. 2016;43(2):254-7.

PMID:
27132422
7.

A Meta-Analysis of the Association between ESR1 Genetic Variants and the Risk of Breast Cancer.

Li T, Zhao J, Yang J, Ma X, Dai Q, Huang H, Wang L, Liu P.

PLoS One. 2016 Apr 12;11(4):e0153314. doi: 10.1371/journal.pone.0153314. eCollection 2016.

9.

[Effect of CD14 promoter variants on the susceptibility to laryngeal cancer].

Yang L, Wen S, Lin J, Zhang X.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Mar;51(3):197-202. doi: 10.3760/cma.j.issn.1673-0860.2016.03.008. Chinese.

PMID:
27033574
10.

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.

Tyrrell J, Richmond RC, Palmer TM, Feenstra B, Rangarajan J, Metrustry S, Cavadino A, Paternoster L, Armstrong LL, De Silva NM, Wood AR, Horikoshi M, Geller F, Myhre R, Bradfield JP, Kreiner-Møller E, Huikari V, Painter JN, Hottenga JJ, Allard C, Berry DJ, Bouchard L, Das S, Evans DM, Hakonarson H, Hayes MG, Heikkinen J, Hofman A, Knight B, Lind PA, McCarthy MI, McMahon G, Medland SE, Melbye M, Morris AP, Nodzenski M, Reichetzeder C, Ring SM, Sebert S, Sengpiel V, Sørensen TI, Willemsen G, de Geus EJ, Martin NG, Spector TD, Power C, Järvelin MR, Bisgaard H, Grant SF, Nohr EA, Jaddoe VW, Jacobsson B, Murray JC, Hocher B, Hattersley AT, Scholtens DM, Davey Smith G, Hivert MF, Felix JF, Hyppönen E, Lowe WL Jr, Frayling TM, Lawlor DA, Freathy RM; Early Growth Genetics (EGG) Consortium.

JAMA. 2016 Mar 15;315(11):1129-40. doi: 10.1001/jama.2016.1975. Erratum in: JAMA. 2016 Apr 19;315(15):1661.

PMID:
26978208
11.

Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.

Ludwig KU, Ahmed ST, Böhmer AC, Sangani NB, Varghese S, Klamt J, Schuenke H, Gültepe P, Hofmann A, Rubini M, Aldhorae KA, Steegers-Theunissen RP, Rojas-Martinez A, Reiter R, Borck G, Knapp M, Nakatomi M, Graf D, Mangold E, Peters H.

PLoS Genet. 2016 Mar 11;12(3):e1005914. doi: 10.1371/journal.pgen.1005914. eCollection 2016 Mar.

12.

Apolipoprotein E ε4 Allele was Associated With Nonlesional Mesial Temporal Lobe Epilepsy in Han Chinese Population.

Li Z, Ding C, Gong X, Wang X, Cui T.

Medicine (Baltimore). 2016 Mar;95(9):e2894. doi: 10.1097/MD.0000000000002894.

13.

Chromosome 15q25 (CHRNA3-CHRNB4) Variation Indirectly Impacts Lung Cancer Risk in Chinese Males.

Zhang Y, Jiang M, Li Q, Liang W, He Q, Chen W, He J.

PLoS One. 2016 Mar 4;11(3):e0149946. doi: 10.1371/journal.pone.0149946. eCollection 2016.

14.

Association of Complement C5 Gene Polymorphisms with Proliferative Diabetic Retinopathy of Type 2 Diabetes in a Chinese Han Population.

Xu D, Yi H, Yu S, Li X, Qiao Y, Deng W.

PLoS One. 2016 Mar 2;11(3):e0149704. doi: 10.1371/journal.pone.0149704. eCollection 2016.

15.

Genotype-Specific Interaction of Latent TGFβ Binding Protein 4 with TGFβ.

Lamar KM, Miller T, Dellefave-Castillo L, McNally EM.

PLoS One. 2016 Feb 26;11(2):e0150358. doi: 10.1371/journal.pone.0150358. eCollection 2016.

16.

The phenotypic legacy of admixture between modern humans and Neandertals.

Simonti CN, Vernot B, Bastarache L, Bottinger E, Carrell DS, Chisholm RL, Crosslin DR, Hebbring SJ, Jarvik GP, Kullo IJ, Li R, Pathak J, Ritchie MD, Roden DM, Verma SS, Tromp G, Prato JD, Bush WS, Akey JM, Denny JC, Capra JA.

Science. 2016 Feb 12;351(6274):737-41. doi: 10.1126/science.aad2149.

17.

F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association.

Pinto P, Ghosh K, Shetty S.

Mutat Res. 2016 Apr;786:27-33. doi: 10.1016/j.mrfmmm.2016.02.002. Epub 2016 Feb 10.

PMID:
26897466
18.

Genetic variants in multisynthetase complex genes are associated with DNA damage levels in Chinese populations.

Liu J, Zhu M, Chen W, Xie K, Shen W, Yuan J, Cheng Y, Geng L, Wang Y, Jin G, Dai J, Ma H, Du J, Wang M, Zhang Z, Hu Z, Wu T, Shen H.

Mutat Res. 2016 Apr;786:8-13. doi: 10.1016/j.mrfmmm.2016.01.006. Epub 2016 Jan 25.

PMID:
26871430
19.

A Non-Synonymous Single Nucleotide Polymorphism in the HJURP Gene Associated with Susceptibility to Hepatocellular Carcinoma among Chinese.

Huang W, Zhang H, Hao Y, Xu X, Zhai Y, Wang S, Li Y, Ma F, Li Y, Wang Z, Zhang Y, Zhang X, Liang R, Wei Z, Cui Y, Li Y, Yu X, Ji H, He F, Xie W, Zhou G.

PLoS One. 2016 Feb 10;11(2):e0148618. doi: 10.1371/journal.pone.0148618. eCollection 2016.

20.

Association of Interferon Regulatory Factor-4 Polymorphism rs12203592 With Divergent Melanoma Pathways.

Gibbs DC, Orlow I, Bramson JI, Kanetsky PA, Luo L, Kricker A, Armstrong BK, Anton-Culver H, Gruber SB, Marrett LD, Gallagher RP, Zanetti R, Rosso S, Dwyer T, Sharma A, La Pilla E, From L, Busam KJ, Cust AE, Ollila DW, Begg CB, Berwick M, Thomas NE; GEM Study Group.

J Natl Cancer Inst. 2016 Feb 8;108(7). pii: djw004. doi: 10.1093/jnci/djw004. Print 2016 Jul.

PMID:
26857527
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