Search Results - "Nava, Tiago"

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    The analysis of GSTA1 promoter genetic and functional diversity of human populations by Mlakar, Vid, Curtis, Patricia Huezo-Diaz, Armengol, Marc, Ythier, Victor, Dupanloup, Isabelle, Hassine, Khalil Ben, Lesne, Laurence, Murr, Rabih, Mlakar, Simona Jurkovic, Nava, Tiago, Ansari, Marc

    Published in Scientific reports (03-03-2021)
    “…GSTA1 encodes a member of a family of enzymes that function to add glutathione to target electrophilic compounds, including carcinogens, therapeutic drugs,…”
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    Journal Article
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    A novel integrative multi-omics approach to unravel the genetic determinants of rare diseases with application in sinusoidal obstruction syndrome by Waespe, Nicolas, Mlakar, Simona Jurkovic, Dupanloup, Isabelle, Rezgui, Mohamed Aziz, Bittencourt, Henrique, Krajinovic, Maja, Kuehni, Claudia E, Nava, Tiago, Ansari, Marc

    Published in PloS one (05-04-2023)
    “…Genotype-phenotype analyses of rare diseases often suffer from a lack of power, due to small sample size, which makes identifying significant associations…”
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    Journal Article
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    Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary? by Nava, Tiago, Rivard, Georges-Etienne, Bonnefoy, Arnaud

    Published in Platelets (Edinburgh) (17-02-2018)
    “…Inherited platelet function disorders (IPFD) have been assessed for more than 50 years by aggregation- and secretion-based tests. Several decision trees are…”
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    Journal Article
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    The Biological and Clinical Relevance of G Protein-Coupled Receptors to the Outcomes of Hematopoietic Stem Cell Transplantation: A Systematized Review by Golay, Hadrien, Jurkovic Mlakar, Simona, Mlakar, Vid, Nava, Tiago, Ansari, Marc

    “…Hematopoietic stem cell transplantation (HSCT) remains the only curative treatment for several malignant and non-malignant diseases at the cost of serious…”
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    Predictors for participation in DNA self-sampling of childhood cancer survivors in Switzerland by Waespe, Nicolas, Strebel, Sven, Marino, Denis, Mattiello, Veneranda, Muet, Fanny, Nava, Tiago, Schindera, Christina, Belle, Fabien N, Mader, Luzius, Spoerri, Adrian, Kuehni, Claudia E, Ansari, Marc

    Published in BMC medical research methodology (30-10-2021)
    “…Abstract Background Research on germline genetic variants relies on enough eligible participants which is difficult to achieve for rare diseases such as…”
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    Journal Article
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