Czech Centre for Phenogenomics (@CZphenogenomics) header
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We are a research infrastructure hosted by the Institute of Molecular Genetics of the Czech Academy of Sciences in BIOCEV campus.

Vestec, Czech Republic
Joined April 2017
Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)Photo by Czech Centre for Phenogenomics (@CZphenogenomics)
Toni Cathonen reports on off- target effects of CRISPR technologies at the EMBO workshop, Sorrento
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Maria Jasin explains how loss of heterozygozity induces cancer at EMBO workshop, Sorrento
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Matilde Vale from Lab18 & CCP is presenting prime editing correction of Diamond-Blackfan Anemia at the EMBO workshop, Sorrento.
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Guillermo Montoya introduces DSB-free genome editing at the EMBO workshop in Sorrento
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Giando Turchiano teaches us about side effects of gene editing - there might be some 😉
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Jiri Eitler explains how the NK cell therapies work at the BIOCEV conference
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Our guest Axel Schambach introduces tailored gene therapy at the Biocev days conference
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CCP team explains the portfolio of services at the ESGCT conference in Seville.
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This IICCC paper unifies standards & best practices for preclinical indirect calorimetry; published Nat Metab. 2025 Sep23;7(9):1765. Great effort!
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Radislav Sedlacek, director of the Czech Centre for Phenogenomics (IMG), received the Jan Evangelista Purkyňe Medal for merits in biomedical sciences.
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Steve Murray gives a closing lecture on rare disease program to in JAX👍👏
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Tomas Pavlicek explains the life with Ataxia telangiectasie, from patient family perspective
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Tim Yu on precision therapy on Ataxia telangiectasia👏
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Andrew Miner about the patient with rare disease YWHAG
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Helen Chen reports on research for YWHAG rare disease foundation
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Albert Carbonell explains patients’ needs
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Carole Linster explains how distortion of lysine catabolism impacts human health: Charlie project
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Jakub Sikora tells the story of Kleefstra syndrome and EHMT2
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Yonghwan Kim talks on fibrodysplasia & BMPR2 mutations
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Samuele Ferrari continues with VEXA syndrome & clonal hematopoiesis
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