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De novo mutations revealed by whole-exome sequencing are strongly associated with autismSANDERS, Stephan J; MURTHA, Michael T; WALKER, Michael F et al.Nature (London). 2012, Vol 485, Num 7397, pp 237-241, issn 0028-0836, 5 p.Article

Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous TraitCHASTE, Pauline; KLEI, Lambertus; GESCHWIND, Daniel et al.Biological psychiatry (1969). 2013, Vol 74, Num 8, pp 576-584, issn 0006-3223, 9 p.Article

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHECELESTINO-SOPER, Patricia B. S; SHAW, Chad A; ZHISHUO OU et al.Human molecular genetics (Print). 2011, Vol 20, Num 22, pp 4360-4370, issn 0964-6906, 11 p.Article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseBARRETT, Jeffrey C; HANSOUL, Sarah; BITTON, Alain et al.Nature genetics. 2008, Vol 40, Num 8, pp 955-962, issn 1061-4036, 8 p.Article

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