🧬BARANOVA MONACO ®
Where cutting-edge science meets personalised longevity and beauty
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A world-renowned expert's company
Founded by Professor Elena Baranova, a world-renowned expert in epigenomics and anti-ageing medicine, the BARANOVA MONACO ® concept combines science, innovation, and a premium approach to health and wellness.
Since 2002, Professor Baranova has pioneered personalised systems that integrate genetics, lifestyle, nutrition, and emotional health. In 2010, after being invited to live and work in Monaco for her outstanding achievements, she introduced an advanced molecular anti-ageing model — laying the foundation for what is today known as BARANOVA MONACO ®.
Transform the energy of your genes into the energy of your life!
Live in harmony with your Genes, Mind and Body.
The intelligence of the future, tailored to you
At the core of BARANOVA MONACO ® is a step-by-step personalised activation of your epigenetic potential — optimising DNA expression to unlock full physical, mental, and emotional resilience.
The result is a powerful anti-fatigue, anti-ageing, and metabolic optimisation effect that activates your body’s own regenerative intelligence.
A method particularly effective for individuals aged 40 and above.
It addresses various forms of fatigue, helps manage stress—including chronic stress and burnout syndrome—and supports the rebalancing of hormonal systems.
Additionally, it tackles what are often called the “syndromes of the 21st century,” such as Leaky Gut Syndrome, Metabolic Syndrome, and issues related to weight regulation.
Supplements to support your metabolic needs.
Each formula within the BARANOVA MONACO ® nutraceutical line is created with precision, based on over 20 years of scientific expertise and a fully personalised approach.
Designed to amplify your health program, these functional supplements support your individual epigenetic and metabolic needs—bringing visible and long-lasting results.
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Есть ли у некоторых женщин генетическая предрасположенность к эндометриозу? Исследование, опубликованное в журнале Molecular Human Reproduction, показывает, что вариация в гене GSTM1 — ключевом уча...
Может ли один-единственный вариант гена изменить риск развития эндометриоза у женщин? Исследование, опубликованное в журнале Molecular Human Reproduction, изучает, как нулевой генотип GSTM1 — деле...
Почему у одних женщин развивается эндометриоз, а у других нет? Знаковое исследование 1997 года показало, что нулевой генотип GSTM1 — генетическая делеция, которая отключает критически важный ферме...
