1. A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41‐q42 deletion phenotype. Issue 7 (16th July 2018) Authors: Balak, Chris; Belnap, Newell; Ramsey, Keri; Joss, Shelagh; Devriendt, Koen; Naymik, Marcus; Jepsen, Wayne; Siniard, Ashley L.; Szelinger, Szabolcs; Parker, Mary E.; Richholt, Ryan; Izatt, Tyler; LaFleur, Madison; Terraf, Panieh; Llaci, Lorida; De Both, Matt; Piras, Ignazio S.; Rangasamy, Sampathk... Journal: American journal of medical genetics Issue: Volume 176:Issue 7(2018) Page Start: 1549 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chemokine ligand 20 (CCL20) expression increases with NAFLD stage and hepatic stellate cell activation and is regulated by miR-590-5p. (November 2019) Authors: Hanson, Amanda; Piras, Ignazio S.; Wilhelmsen, Danielle; Still, Christopher D.; Chu, Xin; Petrick, Anthony; Gerhard, Glenn S.; DiStefano, Johanna K. Journal: Cytokine Issue: Volume 123(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Dopaminergic gene methylation is associated with cognitive performance in a childhood monozygotic twin study. Issue 3 (4th March 2019) Authors: Lewis, Candace R.; Henderson-Smith, Adrienne; Breitenstein, Reagan S.; Sowards, Hayley A.; Piras, Ignazio S.; Huentelman, Matthew J.; Doane, Leah D.; Lemery-Chalfant, Kathryn Journal: Epigenetics Issue: Volume 14:Issue 3(2019) Page Start: 310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evaluating the Association Between Genetically Proxied Neurodevelopmental Language Phenotypes and the Risk of Primary Progressive Aphasia. (2nd May 2023) Authors: Nassan, Malik; Piras, Ignazio S.; Rogalski, Emily; Geula, Changiz; Mesulam, M. Marsel; Huentelman, Matt Journal: Neurology Issue: Volume 100:Number 18(2023) Page Start: e1922 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. MiR-135a Inhibits Cancer Stem Cell-Driven Medulloblastoma Development by Directly Repressing Arhgef6 Expression. (23rd April 2015) Authors: Hemmesi, Katayoun; Squadrito, Mario Leonardo; Mestdagh, Pieter; Conti, Valentina; Cominelli, Manuela; Piras, Ignazio S.; Sergi, Lucia Sergi; Piccinin, Sara; Maestro, Roberta; Poliani, Pietro L.; Speleman, Frank; De Palma, Michele; Galli, Rossella Journal: Stem cells Issue: Volume 33:Number 5(2015:May) Page Start: 1377 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. MiR‐135a Inhibits Cancer Stem Cell‐Driven Medulloblastoma Development by Directly Repressing Arhgef6 Expression. (23rd April 2015) Authors: Hemmesi, Katayoun; Squadrito, Mario Leonardo; Mestdagh, Pieter; Conti, Valentina; Cominelli, Manuela; Piras, Ignazio S.; Sergi, Lucia Sergi; Piccinin, Sara; Maestro, Roberta; Poliani, Pietro L.; Speleman, Frank; De Palma, Michele; Galli, Rossella Journal: Stem cells Issue: Volume 33:Number 5(2015:May) Page Start: 1377 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. MiR‐135a Inhibits Cancer Stem Cell‐Driven Medulloblastoma Development by Directly Repressing Arhgef6 Expression. (May 2015) Authors: Hemmesi, Katayoun; Squadrito, Mario Leonardo; Mestdagh, Pieter; Conti, Valentina; Cominelli, Manuela; Piras, Ignazio S.; Sergi, Lucia Sergi; Piccinin, Sara; Maestro, Roberta; Poliani, Pietro L.; Speleman, Frank; De Palma, Michele; Galli, Rossella Journal: Stem cells Issue: Volume 33:Number 5(2015:May) Page Start: 1377 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. MOBP and HIP1 in multiple system atrophy: New α‐synuclein partners in glial cytoplasmic inclusions implicated in the disease pathogenesis. (19th January 2021) Authors: Bettencourt, Conceição; Miki, Yasuo; Piras, Ignazio S.; de Silva, Rohan; Foti, Sandrine C.; Talboom, Joshua S.; Revesz, Tamas; Lashley, Tammaryn; Balazs, Robert; Viré, Emmanuelle; Warner, Thomas T.; Huentelman, Matt J.; Holton, Janice L. Journal: Neuropathology & applied neurobiology Issue: Volume 47:Number 5(2021) Page Start: 640 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Two additional males with X‐linked, syndromic mental retardation carry de novo mutations in HNRNPH2. Issue 2 (24th June 2019) Authors: Jepsen, Wayne M.; Ramsey, Keri; Szelinger, Szabolcs; Llaci, Lorida; Balak, Chris; Belnap, Newell; Bilagody, Cherae; De Both, Matthew; Gupta, Raj; Naymik, Marcus; Pandey, Richa; Piras, Ignazio S.; Sanchez‐Castillo, Meredith; Rangasamy, Sampathkumar; Narayanan, Vinodh; Huentelman, Matthew J. Journal: Clinical genetics Issue: Volume 96:Issue 2(2019) Page Start: 183 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗