1. A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma. Issue 2 (13th March 2014) Authors: Ceroni, Fabiola; Sagar, Angela; Simpson, Nuala H.; Gawthrope, Alex J.T.; Newbury, Dianne F.; Pinto, Dalila; Francis, Sunday M.; Tessman, Dorothy C.; Cook, Edwin H.; Monaco, Anthony P.; Maestrini, Elena; Pagnamenta, Alistair T.; Jacob, Suma Journal: Autism research Issue: Volume 7:Issue 2(2014:Apr.) Page Start: 254 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A survey of seizures and current treatments in 15q duplication syndrome. Issue 3 (6th February 2014) Authors: Conant, Kerry D.; Finucane, Brenda; Cleary, Nicole; Martin, Ashley; Muss, Candace; Delany, Mary; Murphy, Erin K.; Rabe, Olivia; Luchsinger, Kadi; Spence, Sarah J.; Schanen, Carolyn; Devinsky, Orrin; Cook, Edwin H.; LaSalle, Janine; Reiter, Lawrence T.; Thibert, Ronald L. Journal: Epilepsia Issue: Volume 55:Issue 3(2014:Mar.) Page Start: 396 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Association of the CHRNA4 Neuronal Nicotinic Receptor Subunit Gene with Frequency of Binge Drinking in Young Adults. (15th January 2014) Authors: Coon, Hilary; Piasecki, Thomas M.; Cook, Edwin H.; Dunn, Diane; Mermelstein, Robin J.; Weiss, Robert B.; Cannon, Dale S. Journal: Alcoholism Issue: Volume 38:Number 4(2014:Apr.) Page Start: 930 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials. Issue 1 (26th October 2019) Authors: DiStefano, Charlotte; Wilson, Rujuta B.; Hyde, Carly; Cook, Edwin H.; Thibert, Ronald L.; Reiter, Lawrence T.; Vogel‐Farley, Vanessa; Hipp, Joerg; Jeste, Shafali Journal: American journal of medical genetics Issue: Volume 182:Issue 1(2020) Page Start: 71 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical and neurocognitive issues associated with Bosch‐Boonstra‐Schaaf optic atrophy syndrome: A case study. Issue 1 (15th November 2019) Authors: Bojanek, Erin K.; Mosconi, Matthew W.; Guter, Stephen; Betancur, Catalina; Macmillan, Carol; Cook, Edwin H. Journal: American journal of medical genetics Issue: Volume 182:Issue 1(2020) Page Start: 213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cognitive mechanisms of inhibitory control deficits in autism spectrum disorder. (20th October 2017) Authors: Schmitt, Lauren M.; White, Stormi P.; Cook, Edwin H.; Sweeney, John A.; Mosconi, Matthew W. Journal: Journal of child psychology and psychiatry and allied disciplines Issue: Volume 59:Number 5(2018) Page Start: 586 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Co‐occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion12. Issue 4 (26th February 2013) Authors: Sagar, Angela; Bishop, Jeffrey R.; Tessman, D. Clare; Guter, Steve; Martin, Christa L.; Cook, Edwin H. Journal: American journal of medical genetics Issue: Volume 161:Issue 4(2013:Apr.) Page Start: 845 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome. Issue 6 (13th April 2017) Authors: Sagar, Angela; Pinto, Dalila; Najjar, Fedra; Guter, Stephen J.; Macmillan, Carol; Cook, Edwin H. Journal: American journal of medical genetics Issue: Volume 173:Issue 6(2017) Page Start: 1656 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Escitalopram pharmacogenetics. Issue 11 (November 2015) Authors: Bishop, Jeffrey R.; Najjar, Fedra; Rubin, Leah H.; Guter, Stephen J.; Owley, Thomas; Mosconi, Matthew W.; Jacob, Suma; Cook, Edwin H. Journal: Pharmaocogenetics and genomics Issue: Volume 25:Issue 11(2015:Nov.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Escitalopram pharmacogenetics: CYP2C19 relationships with dosing and clinical outcomes in autism spectrum disorder. Issue 11 (November 2015) Authors: Bishop, Jeffrey R.; Najjar, Fedra; Rubin, Leah H.; Guter, Stephen J.; Owley, Thomas; Mosconi, Matthew W.; Jacob, Suma; Cook, Edwin H. Journal: Pharmaocogenetics and genomics Issue: Volume 25:Issue 11(2015:Nov.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗