Editorial

Por Barash, Carol Isaacson, Pavlidis, Cristiana
Publicado no Appl Transl Genom (2015)

Nutrigenomics: A controversy

Por Pavlidis, Cristiana, Patrinos, George P., Katsila, Theodora
Publicado no Appl Transl Genom (2015)

Nutrigenomics 2.0: The Need for Ongoing and Independent Evaluation and Synthesis of Commercial Nutrigenomics Tests' Scientific Knowledge Base for Responsible Innovation

Por Pavlidis, Cristiana, Nebel, Jean-Christophe, Katsila, Theodora, Patrinos, George P.
Publicado no OMICS (2016)

Comparative study and meta-analysis of meta-analysis studies for the correlation of genomic markers with early cancer detection

Por Lanara, Zoi, Giannopoulou, Efstathia, Fullen, Marta, Kostantinopoulos, Evangelos, Nebel, Jean-Christophe, Kalofonos, Haralabos P, Patrinos, George P, Pavlidis, Cristiana
Publicado em 2013

Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies

Por Papadopoulos, Petros, Viennas, Emmanouil, Gkantouna, Vassiliki, Pavlidis, Cristiana, Bartsakoulia, Marina, Ioannou, Zafeiria-Marina, Ratbi, Ilham, Sefiani, Abdelaziz, Tsaknakis, John, Poulas, Konstantinos, Tzimas, Giannis, Patrinos, George P.
Publicado em 2014

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

Por Giardine, Belinda, Borg, Joseph, Viennas, Emmanouil, Pavlidis, Cristiana, Moradkhani, Kamran, Joly, Philippe, Bartsakoulia, Marina, Riemer, Cathy, Miller, Webb, Tzimas, Giannis, Wajcman, Henri, Hardison, Ross C., Patrinos, George P.
Publicado em 2014

Challenges and opportunities for ELSI early career researchers

Por Bell, Jessica, Ancillotti, Mirko, Coathup, Victoria, Coy, Sarah, Rigter, Tessel, Tatum, Travis, Grewal, Jasjote, Akcesme, Faruk Berat, Brkić, Jovana, Causevic-Ramosevac, Anida, Milovanovic, Goran, Nobile, Marianna, Pavlidis, Cristiana, Finlay, Teresa, Kaye, Jane
Publicado no BMC Med Ethics (2016)

Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies

Por Viennas, Emmanouil, Komianou, Angeliki, Mizzi, Clint, Stojiljkovic, Maja, Mitropoulou, Christina, Muilu, Juha, Vihinen, Mauno, Grypioti, Panagiota, Papadaki, Styliani, Pavlidis, Cristiana, Zukic, Branka, Katsila, Theodora, van der Spek, Peter J., Pavlovic, Sonja, Tzimas, Giannis, Patrinos, George P.
Publicado no Nucleic Acids Res (2017)

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Por Karageorgos, Ioannis, Mizzi, Clint, Giannopoulou, Efstathia, Pavlidis, Cristiana, Peters, Brock A., Zagoriti, Zoi, Stenson, Peter D., Mitropoulos, Konstantinos, Borg, Joseph, Kalofonos, Haralabos P., Drmanac, Radoje, Stubbs, Andrew, van der Spek, Peter, Cooper, David N., Katsila, Theodora, Patrinos, George P.
Publicado no Hum Genomics (2015)