Cristiana Pavlidis

According to our database, Cristiana Pavlidis authored at least 3 papers between 2014 and 2017.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2017

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

Emmanouil Viennas, Angeliki Komianou, Clint Mizzi, Maja Stojiljkovic, Christina Mitropoulou, Juha Muilu, Mauno Vihinen, Panagiota Grypioti, Styliani Papadaki, Cristiana Pavlidis, Branka Zukic, Theodora Katsila, Peter J. van der Spek, Sonja Pavlovic, Giannis Tzimas, George P. Patrinos

Nucleic Acids Res., 2017

2014

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

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

Nucleic Acids Res., 2014

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

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

Nucleic Acids Res., 2014