Choroidal vascular occlusion in a young male patient with sickle cell trait

od Kotoula, Maria, Papageorgiou, Eleni, Xanthou, Foteini, Kalampalikis, Sotirios, Androudi, Sofia, Tsironi, Evangelia E.
Wydane w Int J Ophthalmol (2018)

Spasm of the near reflex: a common diagnostic dilemma?

od Papageorgiou, Eleni, Kardaras, Dimitrios, Kapsalaki, Eftychia, Dardiotis, Efthymios, Mataftsi, Asimina, Tsironi, Evangelia E.
Wydane w Int J Ophthalmol (2021)

The Floppy Eyelid Syndrome: Evaluating Lid Laxity and Its Correlation to Sleep Apnea Syndrome and Body Mass Index

od Beis, Panagiotis G., Brozou, Catherine G., Gourgoulianis, Konstantinos I., Pastaka, Chaido, Chatzoulis, Dimitrios Z., Tsironi, Evangelia E.
Wydane 2012

Perimetric and retinal nerve fiber layer findings in patients with Parkinson’s disease

od Tsironi, Evangelia E, Dastiridou, Anna, Katsanos, Andreas, Dardiotis, Efthymios, Veliki, Stella, Patramani, Gianna, Zacharaki, Fani, Ralli, Stella, Hadjigeorgiou, Georgios M
Wydane 2012

European ST80 community-associated methicillin-resistant Staphylococcus aureus orbital cellulitis in a neonate

od Tsironi, Evangelia E, Zacharaki, Fani, Grivea, Ioanna N, Tachmitzi, Sophia V, Michoula, Aspasia N, Vlychou, Marianna, Petinaki, Efthimia, Syrogiannopoulos, George A
Wydane 2012

Clinical and imaging evaluation of the response to intravenous steroids in patients with Graves’ orbitopathy and analysis on who requires additional therapy

od Tsirouki, Theodora, Bargiota, Alexandra, Tigas, Stelios, Vasileiou, Agathi, Kapsalaki, Eftichia, Giotaki, Zoe, Asproudis, Ioannis, Tsatsoulis, Agathokles, Koukoulis, Georgios, Tsironi, Evangelia E
Wydane w Clin Ophthalmol (2016)

The Role of TOR1A Polymorphisms in Dystonia: A Systematic Review and Meta-Analysis

od Siokas, Vasileios, Dardiotis, Efthimios, Tsironi, Evangelia E., Tsivgoulis, Georgios, Rikos, Dimitrios, Sokratous, Maria, Koutsias, Stylianos, Paterakis, Konstantinos, Deretzi, Georgia, Hadjigeorgiou, Georgios M.
Wydane w PLoS One (2017)

Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma

od Tsironi, Evangelia E., Pefkianaki, Maria, Tsezou, Aspasia, Kotoula, Maria G., Dardiotis, Efthimios, Almpanidou, Pavlina, Papathanasiou, Afroditi A., Rodopoulou, Paraskevi, Chatzoulis, Dimitrios Z., Hadjigeorgiou, Georgios M.
Wydane 2009

Plasma homocysteine and genetic variants of homocysteine metabolism enzymes in patients from central Greece with primary open-angle glaucoma and pseudoexfoliation glaucoma

od Zacharaki, Fani, Hadjigeorgiou, Georgios M, Koliakos, Georgios G, Morrison, Margaux A, Tsezou, Aspasia, Chatzoulis, Dimitrios Z, Almpanidou, Pavlina, Topouridou, Konstantina, Karabatsas, Constantinos H, Pefkianaki, Maria, DeAngelis, Margaret M, Tsironi, Evangelia E
Wydane 2014

Influence of ROBO1 and RORA on Risk of Age-Related Macular Degeneration Reveals Genetically Distinct Phenotypes in Disease Pathophysiology

od Jun, Gyungah, Nicolaou, Michael, Morrison, Margaux A., Buros, Jacqueline, Morgan, Denise J., Radeke, Monte J., Yonekawa, Yoshihiro, Tsironi, Evangelia E., Kotoula, Maria G., Zacharaki, Fani, Mollema, Nissa, Yuan, Yang, Miller, Joan W., Haider, Neena B., Hageman, Gregory S., Kim, Ivana K., Schaumberg, Debra A., Farrer, Lindsay A., DeAngelis, Margaret M.
Wydane 2011

FLT1 Genetic Variation Predisposes to Neovascular AMD in Ethnically Diverse Populations and Alters Systemic FLT1 Expression

od Owen, Leah A., Morrison, Margaux A., Ahn, Jeeyun, Woo, Se Joon, Sato, Hajime, Robinson, Rosann, Morgan, Denise J., Zacharaki, Fani, Simeonova, Marina, Uehara, Hironori, Chakravarthy, Usha, Hogg, Ruth E., Ambati, Balamurali K., Kotoula, Maria, Baehr, Wolfgang, Haider, Neena B., Silvestri, Giuliana, Miller, Joan W., Tsironi, Evangelia E., Farrer, Lindsay A., Kim, Ivana K., Park, Kyu Hyung, DeAngelis, Margaret M.
Wydane 2014

Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world

od Morrison, Margaux A., Magalhaes, Tiago R., Ramke, Jacqueline, Smith, Silvia E., Ennis, Sean, Simpson, Claire L., Portas, Laura, Murgia, Federico, Ahn, Jeeyun, Dardenne, Caitlin, Mayne, Katie, Robinson, Rosann, Morgan, Denise J., Brian, Garry, Lee, Lucy, Woo, Se J., Zacharaki, Fani, Tsironi, Evangelia E., Miller, Joan W., Kim, Ivana K., Park, Kyu H., Bailey-Wilson, Joan E., Farrer, Lindsay A., Stambolian, Dwight, DeAngelis, Margaret M.
Wydane w Front Genet (2015)

Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration

od Morrison Margaux A, Silveira Alexandra C, Huynh Nancy, Jun Gyungah, Smith Silvia E, Zacharaki Fani, Sato Hajime, Loomis Stephanie, Andreoli Michael T, Adams Scott M, Radeke Monte J, Jelcick Austin S, Yuan Yang, Tsiloulis Aristoteles N, Chatzoulis Dimitrios Z, Silvestri Giuliana, Kotoula Maria G, Tsironi Evangelia E, Hollis Bruce W, Chen Rui, Haider Neena B, Miller Joan W, Farrer Lindsay A, Hageman Gregory S, Kim Ivana K, Schaumberg Debra A, DeAngelis Margaret M
Wydane 2011-10-01

Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration

od Morrison, Margaux A, Silveira, Alexandra C, Huynh, Nancy, Jun, Gyungah, Smith, Silvia E, Zacharaki, Fani, Sato, Hajime, Loomis, Stephanie, Andreoli, Michael T, Adams, Scott M, Radeke, Monte J, Jelcick, Austin S, Yuan, Yang, Tsiloulis, Aristoteles N, Chatzoulis, Dimitrios Z, Silvestri, Giuliana, Kotoula, Maria G, Tsironi, Evangelia E, Hollis, Bruce W, Chen, Rui, Haider, Neena B, Miller, Joan W, Farrer, Lindsay A, Hageman, Gregory S, Kim, Ivana K, Schaumberg, Debra A, DeAngelis, Margaret M
Wydane 2011

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

od Ratnapriya, Rinki, Zhan, Xiaowei, Fariss, Robert N., Branham, Kari E., Zipprer, David, Chakarova, Christina F., Sergeev, Yuri V., Campos, Maria M., Othman, Mohammad, Friedman, James S., Maminishkis, Arvydas, Waseem, Naushin H., Brooks, Matthew, Rajasimha, Harsha K., Edwards, Albert O., Lotery, Andrew, Klein, Barbara E., Truitt, Barbara J., Li, Bingshan, Schaumberg, Debra A., Morgan, Denise J., Morrison, Margaux A., Souied, Eric, Tsironi, Evangelia E., Grassmann, Felix, Fishman, Gerald A., Silvestri, Giuliana, Scholl, Hendrik P.N., Kim, Ivana K., Ramke, Jacqueline, Tuo, Jingsheng, Merriam, Joanna E., Merriam, John C., Park, Kyu Hyung, Olson, Lana M., Farrer, Lindsay A., Johnson, Matthew P., Peachey, Neal S., Lathrop, Mark, Baron, Robert V., Igo, Robert P., Klein, Ronald, Hagstrom, Stephanie A., Kamatani, Yoichiro, Martin, Tammy M., Jiang, Yingda, Conley, Yvette, Sahel, Jose-Alan, Zack, Donald J., Chan, Chi-Chao, Pericak-Vance, Margaret A., Jacobson, Samuel G., Gorin, Michael B., Klein, Michael L., Allikmets, Rando, Iyengar, Sudha K., Weber, Bernhard H., Haines, Jonathan L., Léveillard, Thierry, Deangelis, Margaret M., Stambolian, Dwight, Weeks, Daniel E., Bhattacharya, Shomi S., Chew, Emily Y., Heckenlively, John R., Abecasis, Gonçalo R., Swaroop, Anand
Wydane 2014

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

od Fritsche, Lars G., Igl, Wilmar, Cooke Bailey, Jessica N., Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L., Burdon, Kathryn P., Hebbring, Scott J., Wen, Cindy, Gorski, Mathias, Kim, Ivana K., Cho, David, Zack, Donald, Souied, Eric, Scholl, Hendrik P. N., Bala, Elisa, Lee, Kristine E., Hunter, David J., Sardell, Rebecca J., Mitchell, Paul, Merriam, Joanna E., Cipriani, Valentina, Hoffman, Joshua D., Schick, Tina, Lechanteur, Yara T. E., Guymer, Robyn H., Johnson, Matthew P., Jiang, Yingda, Stanton, Chloe M., Buitendijk, Gabriëlle H. S., Zhan, Xiaowei, Kwong, Alan M., Boleda, Alexis, Brooks, Matthew, Gieser, Linn, Ratnapriya, Rinki, Branham, Kari E., Foerster, Johanna R., Heckenlively, John R., Othman, Mohammad I., Vote, Brendan J., Liang, Helena Hai, Souzeau, Emmanuelle, McAllister, Ian L., Isaacs, Timothy, Hall, Janette, Lake, Stewart, Mackey, David A., Constable, Ian J., Craig, Jamie E., Kitchner, Terrie E., Yang, Zhenglin, Su, Zhiguang, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Flagg, Ken, Lin, Danni, Mao, Guanping, Ferreyra, Henry, Stark, Klaus, von Strachwitz, Claudia N., Wolf, Armin, Brandl, Caroline, Rudolph, Guenther, Olden, Matthias, Morrison, Margaux A., Morgan, Denise J., Schu, Matthew, Ahn, Jeeyun, Silvestri, Giuliana, Tsironi, Evangelia E., Park, Kyu Hyung, Farrer, Lindsay A., Orlin, Anton, Brucker, Alexander, Li, Mingyao, Curcio, Christine, Mohand-Saïd, Saddek, Sahel, José-Alain, Audo, Isabelle, Benchaboune, Mustapha, Cree, Angela J., Rennie, Christina A., Goverdhan, Srinivas V., Grunin, Michelle, Hagbi-Levi, Shira, Campochiaro, Peter, Katsanis, Nicholas, Holz, Frank G., Blond, Frédéric, Blanché, Hélène, Deleuze, Jean-François, Igo, Robert P., Truitt, Barbara, Peachey, Neal S., Meuer, Stacy M., Myers, Chelsea E., Moore, Emily L., Klein, Ronald, Hauser, Michael A., Postel, Eric A., Courtenay, Monique D., Schwartz, Stephen G., Kovach, Jaclyn L., Scott, William K., Liew, Gerald, Tƒan, Ava G., Gopinath, Bamini, Merriam, John C., Smith, R. Theodore, Khan, Jane C., Shahid, Humma, Moore, Anthony T., McGrath, J. Allie, Laux, Reneé, Brantley, Milam A., Agarwal, Anita, Ersoy, Lebriz, Caramoy, Albert, Langmann, Thomas, Saksens, Nicole T. M., de Jong, Eiko K., Hoyng, Carel B., Cain, Melinda S., Richardson, Andrea J., Martin, Tammy M., Blangero, John, Weeks, Daniel E., Dhillon, Bal, van Duijn, Cornelia M., Doheny, Kimberly F., Romm, Jane, Klaver, Caroline C. W., Hayward, Caroline, Gorin, Michael B., Klein, Michael L., Baird, Paul N., den Hollander, Anneke I., Fauser, Sascha, Yates, John R. W., Allikmets, Rando, Wang, Jie Jin, Schaumberg, Debra A., Klein, Barbara E. K., Hagstrom, Stephanie A., Chowers, Itay, Lotery, Andrew J., Léveillard, Thierry, Zhang, Kang, Brilliant, Murray H., Hewitt, Alex W., Swaroop, Anand, Chew, Emily Y., Pericak-Vance, Margaret A., DeAngelis, Margaret, Stambolian, Dwight, Haines, Jonathan L., Iyengar, Sudha K., Weber, Bernhard H. F., Abecasis, Gonçalo R., Heid, Iris M.
Wydane w Nat Genet (2015)