Dr Thomas Berney
Associate Clinical Lecturer

  • Brugha TS, McManus S, Smith J, Scott FJ, Meltzer H, Purdon S, Berney T, Tantam D, Robinson J, Radley J, Bankart J. Validating two survey methods for identifying cases of autism spectrum disorder among adults in the community. Psychological Medicine 2012, 42(3), 647-656.
  • Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of Medical Genetics 2011, 48(1), 48-54.
  • 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, Int Mol Genetic Study Autism Cons. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. American Journal of Human Genetics 2001, 69(3), 570-581.
  • 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, Intl Molecular Genetic Study Autis. Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Human Molecular Genetics 2001, 10(9), 973-982.
  • O'Brien G, Pearson J, Berney T, Barnard L. Measuring behaviour in developmental disability: A review of existing schedules. Developmental Medicine and Child Neurology 2001, 43(87), 1-72.
  • Tyrer SP, Margallo-Lana ML, Moore PD, Kay DW, Perry RH, Berney TP, Morris C. Factors associated with cognitive decline in Down syndrome. In: 11th World Congress of the International Association for the Scientific Study of Intellectual Disabilities (IASSID). 2000, Seattle, Washington, USA: John Wiley & Sons.
  • Berney TP, Ireland M, Burn J. Behavioural phenotype of Cornelia de Lange syndrome. Archives of Disease in Childhood 1999, 81(4), 333-336.
  • Aspray TJ, Francis RM, Thompson A, Quilliam SJ, Berney TP, Lana M, Tyrer SP. Response. BONE 1999, 24(5), 525-525.
  • Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP, International Molecular Genetic Study of Autism Consortium. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. American Journal of Medical Genetics 1999, 88(5), 492-496.