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  Autoimmune Disorders

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Articles published in PLoS Genet

Retrieve available abstracts of 10 articles:
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Single Articles


    October 2019
  1. BARSH GS, Cooper GM, Copenhaver GP, Sirugo G, et al
    Evaluating the strength of genetic results: Risks and responsibilities.
    PLoS Genet. 2019;15:e1008437.
    PubMed    


    June 2019
  2. MATTNER J, Mohammed JP, Fusakio ME, Giessler C, et al
    Genetic and functional data identifying Cd101 as a type 1 diabetes (T1D) susceptibility gene in nonobese diabetic (NOD) mice.
    PLoS Genet. 2019;15:e1008178.
    PubMed     Abstract available


  3. VILARINO-GUELL C, Zimprich A, Martinelli-Boneschi F, Herculano B, et al
    Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
    PLoS Genet. 2019;15:e1008180.
    PubMed     Abstract available


    May 2019
  4. DEASY SK, Uehara R, Vodnala SK, Yang HH, et al
    Aicardi-Goutieres syndrome gene Rnaseh2c is a metastasis susceptibility gene in breast cancer.
    PLoS Genet. 2019;15:e1008020.
    PubMed     Abstract available


    April 2019
  5. MOLINEROS JE, Looger LL, Kim K, Okada Y, et al
    Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians.
    PLoS Genet. 2019;15:e1008092.
    PubMed     Abstract available


    February 2019
  6. HECKER M, Boxberger N, Illner N, Fitzner B, et al
    A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene.
    PLoS Genet. 2019;15:e1007961.
    PubMed     Abstract available


    January 2019
  7. CHI C, Shao X, Rhead B, Gonzales E, et al
    Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry.
    PLoS Genet. 2019;15:e1007808.
    PubMed     Abstract available


    October 2017
  8. ODHAMS CA, Cunninghame Graham DS, Vyse TJ
    Profiling RNA-Seq at multiple resolutions markedly increases the number of causal eQTLs in autoimmune disease.
    PLoS Genet. 2017;13:e1007071.
    PubMed     Abstract available


    February 2017
  9. KIRYLUK K, Li Y, Moldoveanu Z, Suzuki H, et al
    GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway.
    PLoS Genet. 2017;13:e1006609.
    PubMed     Abstract available


    July 2016
  10. KASSEM S, Gaud G, Bernard I, Benamar M, et al
    A Natural Variant of the T Cell Receptor-Signaling Molecule Vav1 Reduces Both Effector T Cell Functions and Susceptibility to Neuroinflammation.
    PLoS Genet. 2016;12:e1006185.
    PubMed     Abstract available


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