1. A novel homozygous RIPK4 variant in a family with severe Bartsocas‐Papas syndrome. Issue 6 (13th March 2021) Authors: Dinçer, Tuba; Gümüş, Evren; Toraman, Bayram; Er, İdris; Yildiz, Gokhan; Yüksel, Zafer; Kalay, Ersan Journal: American journal of medical genetics Issue: Volume 185:Issue 6(2021) Page Start: 1691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations. (11th March 2021) Authors: Toraman, Bayram; Bilginer, Samiye Çilem; Hesapçıoğlu, Selma Tural; Göker, Zeynep; Soykam, Hüseyin Okan; Ergüner, Bekir; Dinçer, Tuba; Yıldız, Gökhan; Ünsal, Serbülent; Kasap, Burak Kaan; Kandil, Sema; Kalay, Ersan Journal: Journal of gene medicine Issue: Volume 23:Number 4(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmia. Issue 6 (25th February 2014) Authors: Semerci, C Nur; Kalay, Ersan; Yıldırım, Cem; Dinçer, Tuba; Ölmez, Akgün; Toraman, Bayram; Koçyiğit, Ali; Bulgu, Yunus; Okur, Volkan; Şatıroğlu-Tufan, Lale; Akarsu, Nurten A Journal: British journal of ophthalmology Issue: Volume 98:Issue 6(2014) Page Start: 832 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. RIPK4 suppresses the TGF‐β1 signaling pathway in HaCaT cells. (19th December 2019) Authors: Dinçer, Tuba; Boz Er, Asiye Büşra; Er, İdris; Toraman, Bayram; Yildiz, Gokhan; Kalay, Ersan Journal: Cell biology international Issue: Volume 44:Number 3(2020) Page Start: 848 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗