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Found 35 results

2013
Marschik PB, Kaufmann WE, Sigafoos J, Wolin T, Zhang D, Bartl-Pokorny KD, Pini G, Zappella M, Tager-Flusberg H, Einspieler C et al..  2013.  Changing the perspective on early development of Rett syndrome.. Research in developmental disabilities. 34(4):1236-9. Abstract
2012
Fjell AM, Walhovd KB, Brown TT, Kuperman JM, Chung Y, Hagler DJ, Venkatraman V, Roddey CJ, Erhart M, McCabe C et al..  2012.  Multimodal imaging of the self-regulating developing brain.. Proceedings of the National Academy of Sciences of the United States of America. 109(48):19620-5. Abstract
Bakken TE, Roddey CJ, Djurovic S, Akshoomoff N, Amaral DG, Bloss CS, Casey BJ, Chang L, Ernst TM, Gruen JR et al..  2012.  Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.. Proceedings of the National Academy of Sciences of the United States of America. 109(10):3985-90. Abstract
Walhovd KB, Fjell AM, Brown TT, Kuperman JM, Chung Y, Hagler DJ, Roddey CJ, Erhart M, McCabe C, Akshoomoff N et al..  2012.  Long-term influence of normal variation in neonatal characteristics on human brain development.. Proceedings of the National Academy of Sciences of the United States of America. 109(49):20089-94. Abstract
2011
Blue ME, Kaufmann WE, Bressler J, Eyring C, O'Driscoll C, Naidu S, Johnston MV.  2011.  Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice.. Anatomical record (Hoboken, N.J. : 2007). 294(10):1624-34. Abstract
Daniels AM, Rosenberg RE, Law KJ, Lord C, Kaufmann WE, Law PA.  2011.  Stability of initial autism spectrum disorder diagnoses in community settings.. Journal of autism and developmental disorders. 41(1):110-21. Abstract
Barnett BP, Bressler J, Chen T, Hutchins GM, Crain BJ, Kaufmann WE.  2011.  αB-crystallin negative astrocytic inclusions.. Brain & development. 33(4):349-52. Abstract
2010
Boyle L, Kaufmann WE.  2010.  The behavioral phenotype of FMR1 mutations.. American journal of medical genetics. Part C, Seminars in medical genetics. 154C(4):469-76. Abstract
Rimrodt SL, Peterson DJ, Denckla MB, Kaufmann WE, Cutting LE.  2010.  White matter microstructural differences linked to left perisylvian language network in children with dyslexia.. Cortex; a journal devoted to the study of the nervous system and behavior. 46(6):739-49. Abstract
2009
Rosenberg RE, Law KJ, Yenokyan G, McGready J, Kaufmann WE, Law PA.  2009.  Characteristics and concordance of autism spectrum disorders among 277 twin pairs.. Archives of pediatrics & adolescent medicine. 163(10):907-14. Abstract
Ranta ME, Crocetti D, Clauss JA, Kraut MA, Mostofsky SH, Kaufmann WE.  2009.  Manual MRI parcellation of the frontal lobe.. Psychiatry research. 172(2):147-54. Abstract
Carter JC, Lanham DC, Cutting LE, Clements-Stephens AM, Chen X, Hadzipasic M, Kim J, Denckla MB, Kaufmann WE.  2009.  A dual DTI approach to analyzing white matter in children with dyslexia.. Psychiatry research. 172(3):215-9. Abstract
Hernandez NR, Feinberg RL, Vaurio R, Passanante NM, Thompson RE, Kaufmann WE.  2009.  Autism spectrum disorder in fragile X syndrome: a longitudinal evaluation.. American journal of medical genetics. Part A. 149A(6):1125-37. Abstract
Horská A, Farage L, Bibat G, Nagae LM, Kaufmann WE, Barker PB, Naidu S.  2009.  Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.. Annals of neurology. 65(1):90-7. Abstract
Rosenberg RE, Daniels AM, Law KJ, Law PA, Kaufmann WE.  2009.  Trends in autism spectrum disorder diagnoses: 1994-2007.. Journal of autism and developmental disorders. 39(8):1099-111. Abstract
2008
Carter JC, Capone GT, Kaufmann WE.  2008.  Neuroanatomic correlates of autism and stereotypy in children with Down syndrome.. Neuroreport. 19(6):653-6. Abstract
2007
Carter JC, Capone GT, Gray RM, Cox CS, Kaufmann WE.  2007.  Autistic-spectrum disorders in Down syndrome: further delineation and distinction from other behavioral abnormalities.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 144B(1):87-94. Abstract
2006
Budimirovic DB, Bukelis I, Cox C, Gray RM, Tierney E, Kaufmann WE.  2006.  Autism spectrum disorder in Fragile X syndrome: differential contribution of adaptive socialization and social withdrawal.. American journal of medical genetics. Part A. 140A(17):1814-26. Abstract
2005
Kaufmann WE, Johnston MV, Blue ME.  2005.  MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution.. Brain & development. 27 Suppl 1:S77-S87. Abstract
Capone GT, Grados MA, Kaufmann WE, Bernad-Ripoll S, Jewell A.  2005.  Down syndrome and comorbid autism-spectrum disorder: characterization using the aberrant behavior checklist.. American journal of medical genetics. Part A. 134(4):373-80. Abstract
Kaufmann WE, Jarrar MH, Wang JS, Lee Y-JM, Reddy S, Bibat G, Naidu S.  2005.  Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation.. Brain & development. 27(5):331-9. Abstract
2004
Kaufmann WE, Cortell R, Kau ASM, Bukelis I, Tierney E, Gray RM, Cox C, Capone GT, Stanard P.  2004.  Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.. American journal of medical genetics. Part A. 129A(3):225-34. Abstract
Nagae-Poetscher LM, Bonekamp D, Barker PB, Brant LJ, Kaufmann WE, Horská A.  2004.  Asymmetry and gender effect in functionally lateralized cortical regions: a proton MRS imaging study.. Journal of magnetic resonance imaging : JMRI. 19(1):27-33. Abstract
Kraut MA, Gerring JP, Cooper KL, Thompson RE, Denckla MB, Kaufmann WE.  2004.  Longitudinal evolution of unidentified bright objects in children with neurofibromatosis-1.. American journal of medical genetics. Part A. 129A(2):113-9. Abstract
Kau ASM, Tierney E, Bukelis I, Stump MH, Kates WR, Trescher WH, Kaufmann WE.  2004.  Social behavior profile in young males with fragile X syndrome: characteristics and specificity.. American journal of medical genetics. Part A. 126A(1):9-17. Abstract

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