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Items: 1 to 20 of 62

1.
2.

Comparative oncology: what dogs and other species can teach us about humans with cancer.

Schiffman JD, Breen M.

Philos Trans R Soc Lond B Biol Sci. 2015 Jul 19;370(1673). pii: 20140231. doi: 10.1098/rstb.2014.0231. Review.

PMID:
26056372
3.

Advances in genetics and genomics: use and limitations in achieving malaria elimination goals.

Gunawardena S, Karunaweera ND.

Pathog Glob Health. 2015 May;109(3):123-41. doi: 10.1179/2047773215Y.0000000015. Review.

4.

ConPADE: genome assembly ploidy estimation from next-generation sequencing data.

Margarido GR, Heckerman D.

PLoS Comput Biol. 2015 Apr 16;11(4):e1004229. doi: 10.1371/journal.pcbi.1004229. eCollection 2015 Apr.

5.

The genomic load of deleterious mutations: relevance to death in infancy and childhood.

Morris JA.

Front Immunol. 2015 Mar 16;6:105. doi: 10.3389/fimmu.2015.00105. eCollection 2015. Review.

6.

Applications of systems approaches in the study of rheumatic diseases.

Kim KJ, Lee S, Kim WU.

Korean J Intern Med. 2015 Mar;30(2):148-60. doi: 10.3904/kjim.2015.30.2.148. Epub 2015 Feb 27. Review.

7.

The emergence of human-evolutionary medical genomics.

Crespi BJ.

Evol Appl. 2011 Mar;4(2):292-314. doi: 10.1111/j.1752-4571.2010.00156.x. Epub 2010 Oct 12.

8.

The evolution and adaptive potential of transcriptional variation in sticklebacks--signatures of selection and widespread heritability.

Leder EH, McCairns RJ, Leinonen T, Cano JM, Viitaniemi HM, Nikinmaa M, Primmer CR, Merilä J.

Mol Biol Evol. 2015 Mar;32(3):674-89. doi: 10.1093/molbev/msu328. Epub 2014 Nov 25.

9.

Comprehensive identification of single nucleotide polymorphisms associated with beta-lactam resistance within pneumococcal mosaic genes.

Chewapreecha C, Marttinen P, Croucher NJ, Salter SJ, Harris SR, Mather AE, Hanage WP, Goldblatt D, Nosten FH, Turner C, Turner P, Bentley SD, Parkhill J.

PLoS Genet. 2014 Aug 7;10(8):e1004547. doi: 10.1371/journal.pgen.1004547. eCollection 2014 Aug.

10.

Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.

Lange K, Papp JC, Sinsheimer JS, Sobel EM.

Annu Rev Stat Appl. 2014 Jan 1;1(1):279-300.

11.

Discussing race-related limitations of genomic testing for colon cancer risk: implications for education and counseling.

Butrick MN, Vanhusen L, Leventhal KG, Hooker GW, Nusbaum R, Peshkin BN, Salehizadeh Y, Pavlick J, Schwartz MD, Graves KD.

Soc Sci Med. 2014 Aug;114:26-37. doi: 10.1016/j.socscimed.2014.05.014. Epub 2014 May 15.

12.

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease.

Beilina A, Rudenko IN, Kaganovich A, Civiero L, Chau H, Kalia SK, Kalia LV, Lobbestael E, Chia R, Ndukwe K, Ding J, Nalls MA; International Parkinson’s Disease Genomics Consortium; North American Brain Expression Consortium, Olszewski M, Hauser DN, Kumaran R, Lozano AM, Baekelandt V, Greene LE, Taymans JM, Greggio E, Cookson MR.

Proc Natl Acad Sci U S A. 2014 Feb 18;111(7):2626-31. doi: 10.1073/pnas.1318306111. Epub 2014 Feb 7.

13.

Testing gene-gene interactions in genome wide association studies.

Hu JK, Wang X, Wang P.

Genet Epidemiol. 2014 Feb;38(2):123-34. doi: 10.1002/gepi.21786. Epub 2014 Jan 15.

14.

The contribution of genetic and environmental factors to the duration of pregnancy.

York TP, Eaves LJ, Neale MC, Strauss JF 3rd.

Am J Obstet Gynecol. 2014 May;210(5):398-405. doi: 10.1016/j.ajog.2013.10.001. Epub 2013 Oct 2. Review.

15.
16.

Detecting rare variants in case-parents association studies.

Cheng KF, Chen JH.

PLoS One. 2013 Sep 26;8(9):e74310. doi: 10.1371/journal.pone.0074310. eCollection 2013.

17.

Whole genome sequencing in support of wellness and health maintenance.

Patel CJ, Sivadas A, Tabassum R, Preeprem T, Zhao J, Arafat D, Chen R, Morgan AA, Martin GS, Brigham KL, Butte AJ, Gibson G.

Genome Med. 2013 Jun 27;5(6):58. doi: 10.1186/gm462. eCollection 2013.

18.

Implications of genome-wide association studies in cancer therapeutics.

Patel JN, McLeod HL, Innocenti F.

Br J Clin Pharmacol. 2013 Sep;76(3):370-80. doi: 10.1111/bcp.12166. Review.

19.

Principal components methods for narrow-sense heritability in the analysis of multidimensional longitudinal cognitive phenotypes.

Fung WL, Naylor MG, Bennett DA, Lange C, Blacker D.

Am J Med Genet B Neuropsychiatr Genet. 2013 Oct;162B(7):770-8. doi: 10.1002/ajmg.b.32151. Epub 2013 May 6.

20.

Sherlock: detecting gene-disease associations by matching patterns of expression QTL and GWAS.

He X, Fuller CK, Song Y, Meng Q, Zhang B, Yang X, Li H.

Am J Hum Genet. 2013 May 2;92(5):667-80. doi: 10.1016/j.ajhg.2013.03.022.

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