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Items: 1 to 20 of 231


Physician Assistant Genomic Competencies.

Goldgar C, Michaud E, Park N, Jenkins J.

J Physician Assist Educ. 2016 Sep;27(3):110-6. doi: 10.1097/JPA.0000000000000081.


Other side of the coin for personalised medicine and healthcare: content analysis of 'personalised' practices in the literature.

Cesuroglu T, Syurina E, Feron F, Krumeich A.

BMJ Open. 2016 Jul 13;6(7):e010243. doi: 10.1136/bmjopen-2015-010243.


Attitudes to incorporating genomic risk assessments into population screening programs: the importance of purpose, context and deliberation.

Nicholls SG, Etchegary H, Carroll JC, Castle D, Lemyre L, Potter BK, Craigie S, Wilson BJ; CIHR Emerging Team in Genomics and Screening.

BMC Med Genomics. 2016 May 23;9(1):25. doi: 10.1186/s12920-016-0186-5.


Integrated Genomics for Pinpointing Survival Loci within Arm-Level Somatic Copy Number Alterations.

Roy DM, Walsh LA, Desrichard A, Huse JT, Wu W, Gao J, Bose P, Lee W, Chan TA.

Cancer Cell. 2016 May 9;29(5):737-50. doi: 10.1016/j.ccell.2016.03.025.


rAAV-compatible MiniPromoters for restricted expression in the brain and eye.

de Leeuw CN, Korecki AJ, Berry GE, Hickmott JW, Lam SL, Lengyell TC, Bonaguro RJ, Borretta LJ, Chopra V, Chou AY, D'Souza CA, Kaspieva O, Laprise S, McInerny SC, Portales-Casamar E, Swanson-Newman MI, Wong K, Yang GS, Zhou M, Jones SJ, Holt RA, Asokan A, Goldowitz D, Wasserman WW, Simpson EM.

Mol Brain. 2016 May 10;9(1):52. doi: 10.1186/s13041-016-0232-4.


Mirror, mirror on the wall: which microbiomes will help heal them all?

Nayak RR, Turnbaugh PJ.

BMC Med. 2016 May 4;14:72. doi: 10.1186/s12916-016-0622-6.


Next-Generation Sequencing in the Genetics of Human Atrial Fibrillation.

Hsieh CS, Chuang EY, Juang JM, Hwang JJ, Tseng CD, Chiang FT, Lai LP, Lin JL, Tsai CT.

Acta Cardiol Sin. 2013 Jul;29(4):317-22. Review.


Interpretations of education about gene-environment influences on health in rural Ethiopia: the context of a neglected tropical disease.

Tora A, Ayode D, Tadele G, Farrell D, Davey G, McBride CM.

Int Health. 2016 Jul;8(4):253-60. doi: 10.1093/inthealth/ihw016. Epub 2016 Apr 24.


Challenges, Solutions, and Quality Metrics of Personal Genome Assembly in Advancing Precision Medicine.

Xiao W, Wu L, Yavas G, Simonyan V, Ning B, Hong H.

Pharmaceutics. 2016 Apr 22;8(2). pii: E15. doi: 10.3390/pharmaceutics8020015. Review.


Test-Retest Reliability of the Genetics and Genomics in Nursing Practice Survey Instrument.

Calzone KA, Culp S, Jenkins J, Caskey S, Edwards PB, Fuchs MA, Reints A, Stange B, Questad J, Badzek L.

J Nurs Meas. 2016;24(1):54-68. doi: 10.1891/1061-3749.24.1.54.


Antibody Therapeutics in Oncology.

Wold ED, Smider VV, Felding BH.

Immunotherapy (Los Angel). 2016 Mar;2(1). pii: 108. Epub 2016 Feb 1.


A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.

Mucaki EJ, Caminsky NG, Perri AM, Lu R, Laederach A, Halvorsen M, Knoll JH, Rogan PK.

BMC Med Genomics. 2016 Apr 11;9:19. doi: 10.1186/s12920-016-0178-5.


Guiding Oncology Patients Through the Maze of Precision Medicine.

Giuse NB, Kusnoor SV, Koonce TY, Naylor HM, Chen SC, Blasingame MN, Anderson IA, Micheel CM, Levy MA, Ye F, Lovly CM.

J Health Commun. 2016;21 Suppl 1:5-17. doi: 10.1080/10810730.2015.1131772.


Patients' perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project.

Lupo PJ, Robinson JO, Diamond PM, Jamal L, Danysh HE, Blumenthal-Barby J, Lehmann LS, Vassy JL, Christensen KD, Green RC, McGuire AL; MedSeq Project team.

Per Med. 2016 Jan 1;13(1):13-20. Epub 2016 Jan 8.


Experiences and attitudes of residents regarding a community-based genome cohort study in Japan: a population-based, cross-sectional study.

Miyamoto K, Iwakuma M, Nakayama T.

BMC Med Genomics. 2016 Mar 15;9:14. doi: 10.1186/s12920-016-0175-8.


The major histocompatibility complex in Old World camelids and low polymorphism of its class II genes.

Plasil M, Mohandesan E, Fitak RR, Musilova P, Kubickova S, Burger PA, Horin P.

BMC Genomics. 2016 Mar 1;17:167. doi: 10.1186/s12864-016-2500-1.


An open access pilot freely sharing cancer genomic data from participants in Texas.

Becnel LB, Pereira S, Drummond JA, Gingras MC, Covington KR, Kovar CL, Doddapaneni HV, Hu J, Muzny D, McGuire AL, Wheeler DA, Gibbs RA.

Sci Data. 2016 Feb 16;3:160010. doi: 10.1038/sdata.2016.10.


Practical Approaches for Detecting Selection in Microbial Genomes.

Hedge J, Wilson DJ.

PLoS Comput Biol. 2016 Feb 11;12(2):e1004739. doi: 10.1371/journal.pcbi.1004739. eCollection 2016 Feb.


Scenario drafting for early technology assessment of next generation sequencing in clinical oncology.

Joosten SE, Retèl VP, Coupé VM, van den Heuvel MM, van Harten WH.

BMC Cancer. 2016 Feb 6;16:66. doi: 10.1186/s12885-016-2100-0.

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