1. Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility. (5th February 2015) Authors: Bacchelli, Elena; Battaglia, Agatino; Cameli, Cinzia; Lomartire, Silvia; Tancredi, Raffaella; Thomson, Susanne; Sutcliffe, James S; Maestrini, Elena Journal: American journal of medical genetics Issue: Volume 167:Number 4(2015:Apr.) Page Start: 715 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Issue 1 (23rd October 2010) Authors: Pagnamenta, Alistair T; Khan, Hameed; Walker, Susan; Gerrelli, Dianne; Wing, Kirsty; Bonaglia, Maria Clara; Giorda, Roberto; Berney, Tom; Mani, Elisa; Molteni, Massimo; Pinto, Dalila; Le Couteur, Ann; Hallmayer, Joachim; Sutcliffe, James S; Szatmari, Peter; Paterson, Andrew D; Scherer, Stephen W;... Journal: Journal of medical genetics Issue: Volume 48:Issue 1(2011) Page Start: 48 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗