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Vladimir Jojic

Researcher at University of North Carolina at Chapel Hill

Publications -  74
Citations -  5599

Vladimir Jojic is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Population & Immune system. The author has an hindex of 25, co-authored 70 publications receiving 4426 citations. Previous affiliations of Vladimir Jojic include Stanford University & University of Toronto.

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Variation in the Human Immune System Is Largely Driven by Non-Heritable Influences

TL;DR: A systems-level analysis of 210 healthy twins between 8 and 82 years of age found that 77% of parameters, including cell population frequencies, cytokine responses, and serum proteins, are dominated by non-heritable influences, and in MZ twins discordant for cytomegalovirus infection, more than half of all parameters are affected.
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Systems analysis of sex differences reveals an immunosuppressive role for testosterone in the response to influenza vaccination

TL;DR: A system analysis of the neutralizing antibody response to a trivalent inactivated seasonal influenza vaccine and a large number of immune system components finds a strong association between androgens and genes involved in lipid metabolism, suggesting that these could be important drivers of the differences in immune responses between males and females.
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Conservation and divergence in the transcriptional programs of the human and mouse immune systems

TL;DR: Two large compendia of transcriptional profiles of human and mouse immune cell types are compared, finding that global transcription profiles are conserved between corresponding cell lineages but to a lower degree, suggesting that distinct regulation may underlie some of the conserved transcriptional responses.
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Expression of specific inflammasome gene modules stratifies older individuals into two extreme clinical and immunological states

TL;DR: It is found that the expression of specific inflammasome gene modules stratifies older individuals into two extremes: those with constitutive expression of IL-1β, nucleotide metabolism dysfunction, elevated oxidative stress, high rates of hypertension and arterial stiffness; and those without constitutive expresses IL- 1β, who lack these characteristics.