1. Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld‐Rieger Syndrome. Issue 2 (21st November 2016) Authors: Seifi, Morteza; Footz, Tim; Taylor, Sherry A. M.; Walter, Michael A. Journal: Human mutation Issue: Volume 38:Issue 2(2017) Page Start: 169 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cover Image, Volume 38, Issue 2. Issue 2 (February 2017) Authors: Seifi, Morteza; Footz, Tim; Taylor, Sherry A. M.; Walter, Michael A. Journal: Human mutation Issue: Volume 38:Issue 2(2017) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. FOXF2 is required for cochlear development in humans and mice. (17th December 2018) Authors: Bademci, Guney; Abad, Clemer; Incesulu, Armagan; Elian, Fahed; Reyahi, Azadeh; Diaz-Horta, Oscar; Cengiz, Filiz B; Sineni, Claire J; Seyhan, Serhat; Atli, Emine Ikbal; Basmak, Hikmet; Demir, Selma; Nik, Ali Moussavi; Footz, Tim; Guo, Shengru; Duman, Duygu; Fitoz, Suat; Gurkan, Hakan; Blanton, Sus... Journal: Human molecular genetics Issue: Volume 28:Number 8(2019) Page Start: 1286 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Hepatoma Derived Growth Factor Enhances Oligodendrocyte Genesis from Subventricular Zone Precursor Cells. (March 2022) Authors: Li, Yutong; Dittmann, Nicole Leanne; Watson, Adrianne Eve Scovil; de Almeida, Monique Marylin Alves; Footz, Tim; Voronova, Anastassia Journal: ASN neuro Issue: Volume 14(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma. (17th December 2018) Authors: Lahola-Chomiak, Adrian A; Footz, Tim; Nguyen-Phuoc, Kim; Neil, Gavin J; Fan, Baojian; Allen, Keri F; Greenfield, David S; Parrish, Richard K; Linkroum, Kevin; Pasquale, Louis R; Leonhardt, Ralf M; Ritch, Robert; Javadiyan, Shari; Craig, Jamie E; Allison, W T; Lehmann, Ordan J; Walter, Michael A; ... Journal: Human molecular genetics Issue: Volume 28:Number 8(2019) Page Start: 1298 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel PITX2 gene mutations in patients with Axenfeld‐Rieger syndrome. (24th March 2016) Authors: Seifi, Morteza; Footz, Tim; Taylor, Sherry A. M.; Elhady, Ghada M.; Abdalla, Ebtesam M.; Walter, Michael A. Journal: Acta ophthalmologica Issue: Volume 94:Number 7(2016) Page Start: e571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Regulation of CNS precursor function by neuronal chemokines. (10th January 2020) Authors: Watson, Adrianne Eve Scovil; Goodkey, Kara; Footz, Tim; Voronova, Anastassia Journal: Neuroscience letters Issue: Volume 715(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Regulation of NG2 glia by inhibitory neurons in the developing and regenerating brain. (September 2019) Authors: Voronova, Anastassia; Watson, Adrianne; Wang, Beatrix; Footz, Tim Journal: IBRO reports Issue: Volume 6(2019)Supplement Page Start: S33 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗