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Articles published in PLoS Genet

Retrieve available abstracts of 17 articles:
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Single Articles

    October 2017
  1. CAIRNS J, Ingle JN, Wickerham LD, Weinshilboum R, et al
    SNPs near the cysteine proteinase cathepsin O gene (CTSO) determine tamoxifen sensitivity in ERalpha-positive breast cancer through regulation of BRCA1.
    PLoS Genet. 2017;13:e1007031.
    PubMed     Text format     Abstract available

    September 2017
  2. GAO G, Pierce BL, Olopade OI, Im HK, et al
    Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer.
    PLoS Genet. 2017;13:e1006727.
    PubMed     Text format     Abstract available

  3. LIU Y, Walavalkar NM, Dozmorov MG, Rich SS, et al
    Identification of breast cancer associated variants that modulate transcription factor binding.
    PLoS Genet. 2017;13:e1006761.
    PubMed     Text format     Abstract available

  4. WANG W, Xu ZZ, Costanzo M, Boone C, et al
    Pathway-based discovery of genetic interactions in breast cancer.
    PLoS Genet. 2017;13:e1006973.
    PubMed     Text format     Abstract available

  5. MECHANIC LE, Lindstrom S, Daily KM, Sieberts SK, et al
    Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology.
    PLoS Genet. 2017;13:e1006945.
    PubMed     Text format    

    July 2017
  6. KLAR J, Piontek J, Milatz S, Tariq M, et al
    Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage.
    PLoS Genet. 2017;13:e1006897.
    PubMed     Text format     Abstract available

    June 2017
  7. KAWAZU M, Kojima S, Ueno T, Totoki Y, et al
    Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency.
    PLoS Genet. 2017;13:e1006853.
    PubMed     Text format     Abstract available

    March 2017
  8. HOFFMAN JD, Graff RE, Emami NC, Tai CG, et al
    Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk.
    PLoS Genet. 2017;13:e1006690.
    PubMed     Text format     Abstract available

  9. STRICKER TP, Brown CD, Bandlamudi C, McNerney M, et al
    Robust stratification of breast cancer subtypes using differential patterns of transcript isoform expression.
    PLoS Genet. 2017;13:e1006589.
    PubMed     Text format     Abstract available

    February 2017
  10. HAGENAARS SP, Hill WD, Harris SE, Ritchie SJ, et al
    Genetic prediction of male pattern baldness.
    PLoS Genet. 2017;13:e1006594.
    PubMed     Text format     Abstract available

  11. EVANS JM, Noorai RE, Tsai KL, Starr-Moss AN, et al
    Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci.
    PLoS Genet. 2017;13:e1006604.
    PubMed     Text format     Abstract available

    January 2017
  12. KASPAREK P, Ileninova Z, Zbodakova O, Kanchev I, et al
    KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.
    PLoS Genet. 2017;13:e1006566.
    PubMed     Text format     Abstract available

    September 2016
  13. MAIR B, Konopka T, Kerzendorfer C, Sleiman K, et al
    Gain- and Loss-of-Function Mutations in the Breast Cancer Gene GATA3 Result in Differential Drug Sensitivity.
    PLoS Genet. 2016;12:e1006279.
    PubMed     Text format     Abstract available

    August 2016
  14. RUMP A, Benet-Pages A, Schubert S, Kuhlmann JD, et al
    Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer.
    PLoS Genet. 2016;12:e1006248.
    PubMed     Text format     Abstract available

    June 2016
  15. THOUVENOT P, Ben Yamin B, Fourriere L, Lescure A, et al
    Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making.
    PLoS Genet. 2016;12:e1006096.
    PubMed     Text format     Abstract available

    January 2016
  16. MANTERE T, Winqvist R, Kauppila S, Grip M, et al
    Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
    PLoS Genet. 2016;12:e1005816.
    PubMed     Text format     Abstract available

  17. FARAJI F, Hu Y, Yang HH, Lee MP, et al
    Post-transcriptional Control of Tumor Cell Autonomous Metastatic Potential by CCR4-NOT Deadenylase CNOT7.
    PLoS Genet. 2016;12:e1005820.
    PubMed     Text format     Abstract available

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