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

Tekijä Erginel‐Unaltuna, Nihan, Akbas, Fahri
Julkaisussa J Clin Lab Anal (2004)

Role of simvastatin and RORa activity in the macrophage apoptotic pathway

Tekijä Çoban, Neslihan, Güleç, Çağrı, Selçuk, Bilge Özsait, Erginel-Ünaltuna, Nihan
Julkaisussa Anatol J Cardiol (2017)

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

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

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

Tekijä Lohmann, Ebba, Guerreiro, Rita J., Erginel-Unaltuna, Nihan, Gurunlian, Nicole, Bilgic, Basar, Gurvit, Hakan, Hanagasi, Hasmet A., Luu, Nga, Emre, Murat, Singleton, Andrew
Julkaisussa 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

Tekijä 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
Julkaisussa J Alzheimers Dis (2019)

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

Tekijä 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
Julkaisussa Neurobiol Aging (2017)

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

Tekijä 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
Julkaisussa PLoS One (2016)

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

Tekijä 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
Julkaisussa Am J Hum Genet (2016)