1. A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation. (7th April 2014) Authors: Yariz, K.O.; Sakalar, Y.B.; Jin, X.; Hertz, J.; Sener, E.F.; Akay, H.; Özbek, M.N.; Farooq, A.; Goldberg, J.; Tekin, M. Journal: Clinical genetics Issue: Volume 87:Number 2(2015:Feb.) Page Start: 192 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Mayan founder mutation is a common cause of deafness in Guatemala. Issue 4 (6th October 2015) Authors: Carranza, C.; Menendez, I.; Herrera, M.; Castellanos, P.; Amado, C.; Maldonado, F.; Rosales, L.; Escobar, N.; Guerra, M.; Alvarez, D.; Foster, J.; Guo, S.; Blanton, S.H.; Bademci, G.; Tekin, M. Journal: Clinical genetics Issue: Volume 89:Issue 4(2016) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing. (6th December 2017) Authors: Lopategui, D. M.; Griswold, A. J.; Arora, H.; Clavijo, R. I.; Tekin, M.; Ramasamy, R. Journal: Andrology Issue: Volume 6:Number 1(2018) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss. (25th May 2022) Authors: Vona, B.; Schwartzbaum, D.A.; Rodriguez, A.A.; Lewis, S.S.; Toosi, M.B.; Radhakrishnan, P.; Bozan, N.; Akın, R.; Doosti, M.; Manju, R.; Duman, D.; Sineni, C.J.; Nampoothiri, S.; Karimiani, E.G.; Houlden, H.; Bademci, G.; Tekin, M.; Girisha, K.M.; Maroofian, R.; Douzgou, S. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 9(2022) Page Start: 1606 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Comprehensive genetic testing can save lives in hereditary hearing loss. (2nd April 2014) Authors: Tekin, D.; Tutar, E.; Ozturkmen Akay, H.; Blanton, S.; Foster, J.; Tekin, M. Journal: Clinical genetics Issue: Volume 87:Number 2(2015:Feb.) Page Start: 190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290. (31st October 2013) Authors: Ghaffari, S.R.; Rafati, M.; Ghaffari, G.; Morra, M.; Tekin, M. Journal: Clinical genetics Issue: Volume 86:Number 4(2014:Oct.) Page Start: 387 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. (27th December 2013) Authors: Foster, J.; Kapoor, S.; Diaz‐Horta, O.; Singh, A.; Abad, C.; Rastogi, A.; Moharana, R.; Tekeli, O.; Walz, K.; Tekin, M. Journal: Clinical genetics Issue: Volume 86:Number 6(2014:Dec.) Page Start: 589 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Protective effect of glucagon-like peptide-2 in experimental corrosive esophagitis. Issue 3 (1st April 2015) Authors: Tekin, M.; Topaloğlu, N.; Küçük, A.; Deniz, M.; Yıldırım, Ş.; Erdem, H. Journal: Diseases of the esophagus Issue: Volume 28:Issue 3(2015) Page Start: 258 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Protective effect of glucagon‐like peptide‐2 in experimental corrosive esophagitis. Issue 3 (18th March 2014) Authors: Tekin, M.; Topaloğlu, N.; Küçük, A.; Deniz, M.; Yıldırım, Ş.; Erdem, H. Journal: Diseases of the esophagus Issue: Volume 28:Issue 3(2015) Page Start: 258 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Relationship between periparturient diseases, metabolic markers and the dynamics of hair cortisol concentrations in dairy cows. (May 2023) Authors: Tekin, M.; Câmara, D.R.; Binz, T.M.; Bruckmaier, R.M.; Bollwein, H.; Wagener, K. Journal: Research in veterinary science Issue: Volume 158(2023) Page Start: 134 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗