Identifying autism susceptibility genes. by Maestrini, E, Paul, A, Monaco, A, Bailey, A

Molecular genetic investigations of autism. by Maestrini, E, Marlow, A, Weeks, D, Monaco, A

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. by Blasi, F, Bacchelli, E, Carone, S, Toma, C, Monaco, A, Bailey, A, Maestrini, E

Analysis of nine candidate genes for autism on chromosome 2q. by Maestrini, E, Bacchelli, E, Blasi, F, Biondolillo, M, Bailey, A, Monaco, A, Study, IMG

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. by Bonora, E, Bacchelli, E, Levy, E, Blasi, F, Marlow, A, Monaco, A, Maestrini, E

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region by Bonora, E, Bacchelli, E, Levy, E, Blasi, F, Marlow, A, Monaco, A, Maestrini, E, Conso, I

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International... by Maestrini, E, Lai, C, Marlow, A, Matthews, N, Wallace, S, Bailey, A, Cook, E, Weeks, D, Monaco, A

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. by Fisher, S, Marlow, A, Lamb, J, Maestrini, E, Williams, D, Richardson, A, Weeks, D, Stein, J, Monaco, A

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. by Maestrini, E, Korge, B, Ocaña-Sierra, J, Calzolari, E, Cambiaghi, S, Scudder, P, Hovnanian, A, Monaco, A, Munro, C

A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12. by Asher, J, Lamb, J, Brocklebank, D, Cazier, J, Maestrini, E, Addis, L, Sen, M, Baron-Cohen, S, Monaco, A

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta 3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families by Maestrini, E, Lai, C, Marlow, A, Matthews, N, Wallace, S, Bailey, A, Cook, E, Weeks, D, Monaco, A, Consortium, IMGSA

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication i... by Newbury, D, Warburton, P, Wilson, N, Bacchelli, E, Carone, S, Lamb, J, Maestrini, E, Volpi, E, Mohammed, S, Baird, G, Monaco, A

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations. by Toma, C, Rossi, M, Sousa, I, Blasi, F, Bacchelli, E, Alen, R, Vanhala, R, Monaco, A, Järvelä, I, Maestrini, E

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. by Sykes, N, Toma, C, Wilson, N, Volpi, E, Sousa, I, Pagnamenta, A, Tancredi, R, Battaglia, A, Maestrini, E, Bailey, A, Monaco, A

A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. by Maestrini, E, Monaco, A, McGrath, J, Ishida-Yamamoto, A, Camisa, C, Hovnanian, A, Weeks, D, Lathrop, M, Uitto, J, Christiano, A

MET and autism susceptibility: family and case-control studies. by Sousa, I, Clark, T, Toma, C, Kobayashi, K, Choma, M, Holt, R, Sykes, N, Lamb, J, Bailey, A, Battaglia, A, Maestrini, E, Monaco, A

International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample by Lamb, J, Bonora, E, Barnby, G, Sykes, N, Maestrini, E, Blasi, F, Bacchelli, E, Beyer, K, Klauck, S, Poustka, A, Bailey, A, Monaco, A

High-density SNP association study of the autism susceptibility loci on chromosome 7q by Sykes, N, Lamb, J, Maestrini, E, Winchester, L, Morris, A, Butler, H, Bacchelli, E, Blasi, F, Barnby, G, Sousa, I, Bailey, A, Monaco, A

A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma by Ceroni, F, Sagar, A, Simpson, N, Gawthrope, A, Newbury, D, Pinto, D, Francis, S, Tessman, D, Cook, E, Monaco, A, Maestrini, E, Pagnamenta, A, Jacob, S

A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. by Ceroni, F, Sagar, A, Simpson, N, Gawthrope, A, Newbury, D, Pinto, D, Francis, S, Tessman, D, Cook, E, Monaco, A, Maestrini, E, Pagnamenta, A, Jacob, S