1. A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number‐dependent manner. Issue 4 (31st January 2020) Authors: Bertuzzi, Maria; Tang, Dave; Calligaris, Raffaella; Vlachouli, Christina; Finaurini, Sara; Sanges, Remo; Goldwurm, Stefano; Catalan, Mauro; Antonutti, Lucia; Manganotti, Paolo; Pizzolato, Gilberto; Pezzoli, Gianni; Persichetti, Francesca; Carninci, Piero; Gustincich, Stefano Journal: Human mutation Issue: Volume 41:Issue 4(2020) Page Start: 807 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population. (9th March 2021) Authors: Jamieson, Sarra E; Fakiola, Michaela; Tang, Dave; Scaman, Elizabeth; Syn, Genevieve; Francis, Richard W; Coates, Harvey L; Anderson, Denise; Lassmann, Timo; Cordell, Heather J; Blackwell, Jenefer M Journal: Clinical infectious diseases Issue: Volume 73:Number 10(2021) Page Start: 1860 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. High expression of insulin receptor on tumour‐associated blood vessels in invasive bladder cancer predicts poor overall and progression‐free survival. Issue 2 (3rd May 2017) Authors: Roudnicky, Filip; Dieterich, Lothar C; Poyet, Cedric; Buser, Lorenz; Wild, Peter; Tang, Dave; Camenzind, Peter; Ho, Chien Hsien; Otto, Vivianne I; Detmar, Michael Journal: Journal of pathology Issue: Volume 242:Issue 2(2017) Page Start: 193 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. PiRNAs Warrant Investigation in Rett Syndrome: An Omics Perspective. Issue 5 (21st May 2013) Authors: Saxena, Alka; Tang, Dave; Carninci, Piero Journal: Disease markers Issue: Volume 33:Issue 5(2012) Page Start: 261 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene. (December 2017) Authors: Abraham, Mary; Li, Dong; Tang, Dave; O'Connell, Susan; McKenzie, Fiona; Lim, Ee; Hakonarson, Hakon; Levine, Michael; Choong, Catherine Journal: International journal of pediatric endocrinology Issue: Volume 2017(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service. Issue 1 (December 2016) Authors: Baynam, Gareth; Pachter, Nicholas; McKenzie, Fiona; Townshend, Sharon; Slee, Jennie; Kiraly-Borri, Cathy; Vasudevan, Anand; Hawkins, Anne; Broley, Stephanie; Schofield, Lyn; Verhoef, Hedwig; Walker, Caroline; Molster, Caron; Blackwell, Jenefer; Jamieson, Sarra; Tang, Dave; Lassmann, Timo; Mina, K... Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗