Authors: Palferman, S Matthews, N Turner, H Moore, J Hervas, A Aubin, A Wallace, S Michelotti, J Wainhouse, C Paul, A Thompson, E Murin, M Gupta, R Garner, C Pickles, A Rutter, M Bailey, A Lamb, JA Marlow, A Scudder, P Barnby, G Monaco, AP Baird, G Cox, A Docherty, Z Warburton, P Green, EP Abbs, SJ Le Couteur, A McConachie, HR Berney, T Kelly, TP De Vries, PJ Bolton, P Green, J Gilchrist, A Whittacker, J Bolton, B Packer, R Maestrini, E Van Engeland, H De Jonge, MV Kemner, C Klauck, SM Beyer, KS Epp, S Poustka, A Benner, A Poustka, F Ruhl, D Schmotzer, G Bolte, S Feineis-Matthews, S Fombonne, E Roge, B Fremolle-Kruck, J Pienkowski, C Tauber, MT Pedersen, L Brondum-Nielsen, K Eriksen, G Haracopos, D Cotterill, RMJ Tsiantis, J Papanikolaou, K Lord, C Corsello, C Guter, S Leventhal, B Cook, E Smalley, S Bailey, J Liu, A Dedricks, M Chrzanowski, L Levitt, J Pauls, D Volkmar, F Weeks, DE

Citation: S. Palferman et al., Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q, HUM MOL GEN, 10(9), 2001, pp. 973-982

Authors: Palferman, S Matthews, N Turner, M Moore, J Hervas, A Aubin, A Wallace, S Michelotti, J Wainhouse, C Paul, A Thompson, E Gupta, R Garner, C Murin, M Freitag, C Ryder, N Cottington, E Parr, J Pickles, A Rutter, M Bailey, A Barnby, G Lamb, JA Marlow, A Scudder, P Monaco, AP Baird, G Cox, A Docherty, Z Warburton, P Green, EP Abbs, SJ Le Couteur, A McConachie, HR Berney, T Kelly, TP De Vries, PJ Bolton, PF Green, J Gilchrist, A Whittacker, J Bolton, B Packer, R Maestrini, E Blasi, F Van Engeland, H De Jonge, MV Kemner, C Klauck, SM Beyer, KS Epp, S Poustka, A Benner, A Goethe, JW Poustka, F Ruhl, D Schmotzer, G Boolte, S Feineis-Matthews, S Fombonne, E Rogee, B Fremolle-Kruck, J Pienkowski, C Tauber, MT Pedersen, L Nielsen, KB Eriksen, G Haracopos, D Cotterill, RMJ Tsiantis, J Papanikolaou, K Lord, C Corsello, C Guter, S Leventhal, B Cook, E Smalley, SL Bailey, J McGough, J Levitt, J Pauls, D Volkmar, F Weeks, DE

Citation: S. Palferman et al., A genomewide screen for autism: Strong evidence for linkage to chromosomes2q, 7q, and 16p, AM J HU GEN, 69(3), 2001, pp. 570-581

Authors: Maestrini, E Paul, A Monaco, AP Bailey, A

Citation: E. Maestrini et al., Identifying autism susceptibility genes, NEURON, 28(1), 2000, pp. 19-24

Authors: Maestrini, E Korge, BP Ocana-Sierra, J Calzolari, E Cambiaghi, S Scudder, PM Hovnanian, A Monaco, AP Munro, CS

Citation: E. Maestrini et al., A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families, HUM MOL GEN, 8(7), 1999, pp. 1237-1243

Authors: Maestrini, E Lai, C Marlow, A Matthews, N Wallace, S Bailey, A Cook, EH Weeks, DE Monaco, AP

Citation: E. Maestrini et al., Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunitbeta 3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families, AM J MED G, 88(5), 1999, pp. 492-496

Authors: Fisher, SE Marlow, AJ Lamb, J Maestrini, E Williams, DF Richardson, AJ Weeks, DE Stein, JF Monaco, AP

Citation: Se. Fisher et al., A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia, AM J HU GEN, 64(1), 1999, pp. 146-156