Search

Author/Creator Sharp, Sally I.

1. Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. (17th November 2017)

Authors:
Al Eissa, Mariam M.; Fiorentino, Alessia; Sharp, Sally I.; O'Brien, Niamh L.; Wolfe, Kate; Giaroli, Giovanni; Curtis, David; Bass, Nicholas J.; McQuillin, Andrew
Journal:
Annals of human genetics
Issue:
Volume 82:Number 2(2018:Mar.)
Page Start:
88
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome. Issue 4 (9th May 2014)

Authors:
Sharp, Sally I.; McQuillin, Andrew; Marks, Michael; Hunt, Stephen P.; Stanford, S. Clare; Lydall, Greg J.; Morgan, Marsha Y.; Asherson, Philip; Curtis, David; Gurling, Hugh M. D.
Journal:
American journal of medical genetics
Issue:
Volume 165:Issue 4(2014)
Page Start:
373
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. Issue 7 (18th July 2017)

Authors:
Leonenko, Ganna; Richards, Alexander L.; Walters, James T.; Pocklington, Andrew; Chambert, Kimberly; Al Eissa, Mariam M.; Sharp, Sally I.; O'Brien, Niamh L.; Curtis, David; Bass, Nicholas J.; McQuillin, Andrew; Hultman, Christina; Moran, Jennifer L.; McCarroll, Steven A.; Sklar, Pamela; Neale, Be...
Journal:
American journal of medical genetics
Issue:
Volume 174:Issue 7(2017)
Page Start:
724
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗