Investigating differential miRNA expression profiling using serum and urine specimens for detecting potential biomarkers for early prostate cancer diagnosis von Hasanoglu, Sevde, Goncu, Beyza, Yucesan, Emrah, Atasoy, Sezen, Kayali, Yunus, Ozten Kandas, Nur

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Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span von Yücel-Yılmaz, Didem, Yücesan, Emrah, Yalnızoğlu, Dilek, Oğuz, Kader Karlı, Sağıroğlu, Mahmut Şamil, Özbek, Uğur, Serdaroğlu, Esra, Bilgiç, Başar, Erdem, Sevim, İşeri, Sibel Aylin Uğur, Hanağası, Haşmet, Gürvit, Hakan, Özgül, Rıza Köksal, Dursun, Ali

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The Importance of Cryopreserved Parathyroid Tissue Autotransplantation in the Hypoparathyroidism Treatment after Secondary Hyperparathyroidism Surgery von İdiz, Ufuk Oğuz, Yücesan, Emrah, Göncü, Beyza, Özdemir, Burcu, Aysan, Erhan, Gürol, Ali Osman

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Biallelic loss of TRAPPC9 function links vesicle trafficking pathway to autosomal recessive intellectual disability von Aslanger, Ayca Dilruba, Goncu, Beyza, Duzenli, Omer Faruk, Yucesan, Emrah, Sengenc, Esma, Yesil, Gozde

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Effects of Boric Acid on Ehrlich Ascites Tumor von Idiz, Ufuk Oguz, Firat, Yurdakul Deniz, Cakir, Coskun, Yucesan, Emrah, Aysan, Erhan

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Alteration of housekeeping genes and proteins through senescence of human skin fibroblast cells von Goncu, Beyza, Duzenli, Omer Faruk, Yucesan, Emrah

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Biallelic loss of EEF1D function links heat shock response pathway to autosomal recessive intellectual disability von Ugur Iseri, Sibel Aylin, Yucesan, Emrah, Tuncer, Feyza Nur, Calik, Mustafa, Kesim, Yesim, Altiokka Uzun, Gunes, Ozbek, Ugur

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Sıçanlarda immünsupresyonsuz xenotransplantasyon uygulamasının etkililiği von Kanımdan,Ebru, Yücesan,Emrah, Göncü,Beyza, Özdemir,Burcu, İdiz,Oğuz, Ersoy,Yeliz Emine, Akbaş,Fahri, Ayşan,Erhan

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The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey von Haryanyan, Garen, Ozdemir, Ozkan, Tutkavul, Kemal, Dervent, Aysin, Ayta, Semih, Ozkara, Cigdem, Salman, Baris, Yucesan, Emrah, Kesim, Yesim, Susgun, Seda, Ozbek, Ugur, Baykan, Betul, Ugur Iseri, Sibel A., Bebek, Nerses

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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture von Stevelink, Remi, Campbell, Ciarán, Chen, Siwei, Abou-Khalil, Bassel, Adesoji, Oluyomi M., Afawi, Zaid, Amadori, Elisabetta, Anderson, Alison, Anderson, Joseph, Andrade, Danielle M., Annesi, Grazia, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bast, Thomas, Baum, Larry, Baumgartner, Tobias, Baykan, Betül, Bebek, Nerses, Becker, Albert J., Becker, Felicitas, Bennett, Caitlin A., Berghuis, Bianca, Berkovic, Samuel F., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blatt, Ilan, Bobbili, Dheeraj R., Borggraefe, Ingo, Bosselmann, Christian, Braatz, Vera, Bradfield, Jonathan P., Brockmann, Knut, Brody, Lawrence C., Buono, Russell J., Busch, Robyn M., Caglayan, Hande, Campbell, Ellen, Canafoglia, Laura, Canavati, Christina, Cascino, Gregory D., Castellotti, Barbara, Catarino, Claudia B., Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherny, Stacey S., Cheung, Ching-Lung, Chinthapalli, Krishna, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Clark, Peggy O., Cole, Andrew J., Compston, Alastair, Coppola, Antonietta, Cosico, Mahgenn, Cossette, Patrick, Craig, John J., Cusick, Caroline, Daly, Mark J., Davis, Lea K., de Haan, Gerrit-Jan, Delanty, Norman, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Di Vito, Lidia, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Elger, Christian E., Ellis, Colin A., Eriksson, Johan G., Faucon, Annika, Feng, Yen-Chen A., Ferguson, Lisa, Ferraro, Thomas N., Ferri, Lorenzo, Feucht, Martha, Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, Franke, Andre, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Geller, Eric B., Giangregorio, Tania, Gjerstad, Leif

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Obstacles and expectations of rare disease patients and their families in Türkiye: ISTisNA project survey results von Hatirnaz Ng, Ozden, Sahin, Ilayda, Erbilgin, Yucel, Ozdemir, Ozkan, Yucesan, Emrah, Erturk, Nazli, Yemenici, Merve, Akgun Dogan, Ozlem, Ugur Iseri, Sibel Aylin, Satman, Ilhan, Alanay, Yasemin, Ozbek, Ugur

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The Effect of Intravenously Paratyroid Cell Xenotransplantation in Sheep: As an Animal Model von Yucesan, Emrah, Goncu, Beyza, Idiz, Oguz, Ucak, Ramazan, Ozdemir, Burcu, Kanimdan, Ebru, Ersoy, Yeliz Emine, Aysan, Erhan

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Pharmacogenetics: Role of Single Nucleotide Polymorphisms von Yucesan, Emrah, Ozten, Nur

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Periferik kan mononükleer hücrelerin primer paratiroit dokusu hücreleri ile ko-kültürünün verimliliği von Hasanoğlu, Sevda, Göncü, Beyza, Yücesan, Emrah

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Gene Hunting Approaches through the Combination of Linkage Analysis with Whole-Exome Sequencing in Mendelian Diseases: From Darwin to the Present Day von Susgun, Seda, Kasan, Koray, Yucesan, Emrah

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Psychedelic therapy in depression and substance use disorders von Korkmaz, Nur Damla, Cikrikcili, Ugur, Akan, Merve, Yucesan, Emrah

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Discharging a Patient Treated With Parathyroid Allotransplantation After Having Been Hospitalized for 3.5 Years With Permanent Hypoparathyroidism: A Case Report von Aysan, Erhan, Yucesan, Emrah, Idiz, Ufuk Oguz, Goncu, Beyza

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Mikroenkapsülasyon Sisteminin Aljinat-Hücre Süspansiyon Yoğunluğuna Bağlı Hızlarının Değerlendirilmesi von Düzenli, Ömer, Göncü, Beyza, Yücesan, Emrah, Salepçioğlu Kaya, Harika, Ersoy, Yeliz, Akçakaya, Adem

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Gene Teams are on the Field: Evaluation of Variants in Gene-Networks Using High Dimensional Modelling von Tuna, Suha, Gulec, Cagri, Yucesan, Emrah, Cirakoglu, Ayse, Arguden, Yelda Tarkan

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HLA-DR, -DP, -DQ expression status of parathyroid tissue as a potential parathyroid donor selection criteria and review of literature von Goncu, Beyza, Yucesan, Emrah, Ersoy, Yeliz Emine, Aysan, Mustafa Erhan, Ozten Kandas, Nur

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