1. A further family of Stromme syndrome carrying CENPF mutation. Issue 6 (13th April 2017) Authors: Ozkinay, Ferda; Atik, Tahir; Isik, Esra; Gormez, Zeliha; Sagiroglu, Mahmut; Sahin, Ozlem Atan; Corduk, Nergul; Onay, Huseyin Journal: American journal of medical genetics Issue: Volume 173:Issue 6(2017) Page Start: 1668 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A further family of Stromme syndrome carrying CENPF mutation. Issue 6 (13th April 2017) Authors: Ozkinay, Ferda; Atik, Tahir; Isik, Esra; Gormez, Zeliha; Sagiroglu, Mahmut; Sahin, Ozlem Atan; Corduk, Nergul; Onay, Huseyin Journal: American journal of medical genetics Issue: Volume 173:Issue 6(2017) Page Start: 1668 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A new patient with LACHT syndrome (Mardini–Nyhan association). (8th December 2014) Authors: Atik, Tahir; Torun, Huseyin Ozan; Cogulu, Ozgur; Ozkinay, Ferda Journal: American journal of medical genetics Issue: Volume 167:Number 2(2015:Feb.) Page Start: 400 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A new type of familial partial lipodystrophy: distinctive fat distribution and proteinuria. (2nd October 2018) Authors: Yurekli, Banu; Ozdemir Kutbay, Nilufer; Altay, Canan; Unlu, Sadiye Mehtat; Sen, Sait; Onay, Huseyin; Atik, Tahir; Akinci, Baris Journal: Endocrine research Issue: Volume 43:Number 4(2018) Page Start: 258 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A rare cause of syndromic short stature: 3M syndrome in three families. Issue 2 (30th November 2020) Authors: Isik, Esra; Arican, Duygu; Atik, Tahir; Ooi, Joo Enn; Darcan, Sukran; Ozen, Samim; Simsek Kiper, Pelin Ozlem; Utine, Eda; Cogulu, Ozgur; Ozkinay, Ferda Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Clinical and molecular aspects of PTEN mutations in 10 pediatric patients. (12th March 2020) Authors: Isik, Esra; Simsir, Ozguc Semih; Solmaz, Asli Ece; Onay, Huseyin; Atik, Tahir; Aykut, Ayca; Durmaz, Asude; Cogulu, Ozgur; Ozkinay, Ferda Journal: Annals of human genetics Issue: Volume 84:Number 4(2020:Jul.) Page Start: 324 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Clinical and molecular findings in children and young adults with persistent low alkaline phosphatase concentrations. (July 2021) Authors: Araci, Mehmet Bilal; Akgun, Bilcag; Atik, Tahir; Isik, Esra; Ak, Gunes; Barutcuoglu, Burcu; Ozkinay, Ferda Journal: Annals of clinical biochemistry Issue: Volume 58:Number 4(2021) Page Start: 335 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Diffuse hypomyelination is not obligate for POLR3-related disorders. (26th April 2016) Authors: La Piana, Roberta; Cayami, Ferdy K.; Tran, Luan T.; Guerrero, Kether; van Spaendonk, Rosalina; Õunap, Katrin; Pajusalu, Sander; Haack, Tobias; Wassmer, Evangeline; Timmann, Dagmar; Mierzewska, Hanna; Poll-Thé, Bwee T.; Patel, Chirag; Cox, Helen; Atik, Tahir; Onay, Huseyin; Ozkınay, Ferda; Vanderv... Journal: Neurology Issue: Volume 86:Number 17(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Evaluation of social cognition, autistic traits, and dysmorphology in comorbid specific learning disorder and attention-deficit/hyperactivity disorder. (October 2022) Authors: Ozbaran, Nazli Burcu; Ozyasar, Senay Celenay; Dogan, Nurhak; Kafali, Helin Yilmaz; Isik, Esra; Satar, Aysegul; Kose, Sezen; Atik, Tahir; Cogulu, Ozgur Journal: Clinical child psychology and psychiatry Issue: Volume 27:Number 4(2022) Page Start: 991 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mannose binding lectin codon 54 polymorphism and susceptibility to recurrent respiratory tract infections in children: A meta-analysis. (February 2016) Authors: Atan, Ozlem; Kucukcelebi, Ahmet; Atik, Tahir; Ozkınay, Ferda Journal: International journal of pediatric otorhinolaryngology Issue: Volume 81(2016:Feb.) Page Start: 41 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗