Improved method for molecular diagnosis of myotonic dystrophy type 1 (DM1)

od Erginel‐Unaltuna, Nihan, Akbas, Fahri
Wydane w J Clin Lab Anal (2004)

Role of simvastatin and RORa activity in the macrophage apoptotic pathway

od Çoban, Neslihan, Güleç, Çağrı, Selçuk, Bilge Özsait, Erginel-Ünaltuna, Nihan
Wydane w Anatol J Cardiol (2017)

Sex-specific associations of TCF7L2 variants with fasting glucose, type 2 diabetes and coronary heart disease among Turkish adults

od Yüzbaşıoğulları, Ayşe Berna, Kömürcü-Bayrak, Evrim, Onat, Altan, Can, Günay, Mononen, Nina, Laaksonen, Reijo, Kähönen, Mika, Lehtimäki, Terho, Erginel-Ünaltuna, Nihan
Wydane w Anatol J Cardiol (2020)

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

od Lohmann, Ebba, Guerreiro, Rita J., Erginel-Unaltuna, Nihan, Gurunlian, Nicole, Bilgic, Basar, Gurvit, Hakan, Hanagasi, Hasmet A., Luu, Nga, Emre, Murat, Singleton, Andrew
Wydane w Neurobiol Aging (2012)

Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia

od Guven, Gamze, Bilgic, Başar, Tufekcioglu, Zeynep, Erginel Unaltuna, Nihan, Hanagasi, Hasmet, Gurvit, Hakan, Singleton, Andrew, Hardy, John, Emre, Murat, Gulec, Cagri, Bras, Jose, Guerreiro, Rita, Lohmann, Ebba
Wydane w J Alzheimers Dis (2019)

Mutations in TYROBP are not a common cause of dementia in a Turkish cohort

od Darwent, Lee, Carmona, Susana, Lohmann, Ebba, Guven, Gamze, Kun-Rodrigues, Celia, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Erginel-Unaltuna, Nihan, Pak, Meltem, Hardy, John, Singleton, Andrew, Brás, Jose, Guerreiro, Rita
Wydane w Neurobiol Aging (2017)

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients

od Guven, Gamze, Lohmann, Ebba, Bras, Jose, Gibbs, J. Raphael, Gurvit, Hakan, Bilgic, Basar, Hanagasi, Hasmet, Rizzu, Patrizia, Heutink, Peter, Emre, Murat, Erginel-Unaltuna, Nihan, Just, Walter, Hardy, John, Singleton, Andrew, Guerreiro, Rita
Wydane w PLoS One (2016)

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

od Lesage, Suzanne, Drouet, Valérie, Majounie, Elisa, Deramecourt, Vincent, Jacoupy, Maxime, Nicolas, Aude, Cormier-Dequaire, Florence, Hassoun, Sidi Mohamed, Pujol, Claire, Ciura, Sorana, Erpapazoglou, Zoi, Usenko, Tatiana, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Ding, Jinhui, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Vidailhet, Marie, Corvol, Jean-Christophe, Krack, Paul, Leutenegger, Anne-Louise, Nalls, Michael A., Hernandez, Dena G., Heutink, Peter, Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Gasser, Thomas, Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Kabashi, Edor, Singleton, Andrew, Corti, Olga, Brice, Alexis
Wydane w Am J Hum Genet (2016)