AveMariaLachiewiczMD

PubMed

• Best Practices in Fragile X Syndrome Treatment Development.
  Erickson, C. A.,Kaufmann, W. E.,Budimirovic, D. B.,Lachiewicz, A.,Haas-Givler, B.,Miller, R. M.,Weber, J. D.,Abbeduto, L.,Hessl, D.,Hagerman, R. J.,Berry-Kravis, E.> ;Brain Sci. 2018 Dec 19
• 70 citations
  Psychometric Study of the Aberrant Behavior Checklist in Fragile X Syndrome and Implications for Targeted Treatment
  Stephanie M. Sansone, Keith F. Widaman, Scott S. Hall, Allan L. Reiss, Amy A. Lightbody, Walter E. Kaufmann, Elizabeth Berry-Kravis, Ave M. Lachiewicz, Elaine C. Brown...> ;Journal of Autism and Developmental Disorders. 2012 Jul 1
• Indicators of anxiety and depression in women with the fragile X premutation: assessment of a clinical sample.
  Lachiewicz, A., Dawson, D., Spiridigliozzi, G., Cuccaro, M., Lachiewicz, M., McConkie-Rosell, A.> ;J Intellect Disabil Res. 2010 Jul
• Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.
  Markunas, C. A., Quinn, K. S., Collins, A. L., Garrett, M. E., Lachiewicz, A. M., Sommer, J. L., Morrissey-Kane, E., Kollins, S. H., Anastopoulos, A. D., Ashley-Koch, ...> ;Psychiatr Genet. 2010 Apr
• Effects of postnatal parental smoking on parent and teacher ratings of ADHD and oppositional symptoms.
  Kollins, S.H., Garrett, M.E., McClernon, F.J., Lachiewicz, A.M., Morrissey-Kane, E., FitzGerald, D., Collins, A.L., Anastopoulos, A.D., Ashley-Koch, A.E.> ;J Nerv Ment Dis. 2009 Jun 01
• Advances in the treatment of fragile X syndrome.
  Hagerman, R. J., Berry-Kravis, E., Kaufmann, W. E., Ono, M. Y., Tartaglia, N., Lachiewicz, A., Kronk, R., Delahunty, C., Hessl, D., Visootsak, J., Picker, J., Gane, L....> ;Pediatrics. 2009 Jan 01
• SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children an...
  Kollins, S. H., Anastopoulos, A. D., Lachiewicz, A. M., FitzGerald, D., Morrissey-Kane, E., Garrett, M. E., Keatts, S. L., Ashley-Koch, A. E.> ;Am J Med Genet B Neuropsychiatr Genet.
• Living with genetic risk: effect on adolescent self-concept.
  McConkie-Rosell, A., Spiridigliozzi, G. A., Melvin, E., Dawson, D. V., Lachiewicz, A. M.> ;Am J Med Genet C Semin Med Genet. 2008 Feb 15
• Arithmetic difficulties in females with the fragile X premutation.
  Lachiewicz, A. M., Dawson, D. V., Spiridigliozzi, G. A., McConkie-Rosell, A.> ;Am J Med Genet A. 2006 Apr 1
• Carrier testing in fragile X syndrome: when to tell and test.
  McConkie-Rosell, A., Spiridigliozzi, G. A., Sullivan, J. A., Dawson, D. V., Lachiewicz, A. M.> ;Am J Med Genet. 2002 Jun 1
• Longitudinal study of the carrier testing process for fragile X syndrome: perceptions and coping.
  McConkie-Rosell, A., Spiridigliozzi, G. A., Sullivan, J. A., Dawson, D. V., Lachiewicz, A. M.> ;Am J Med Genet. 2001 Jan 1
• Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.
  Tassone, F., Hagerman, R. J., Loesch, D. Z., Lachiewicz, A., Taylor, A. K., Hagerman, P. J.> ;Am J Med Genet. 2000 Sep 18
• Carrier testing in fragile X syndrome: effect on self-concept.
  McConkie-Rosell, A., Spiridigliozzi, G. A., Sullivan, J. A., Dawson, D. V., Lachiewicz, A. M.> ;Am J Med Genet. 2000 Jun 19
• Physical characteristics of young boys with fragile X syndrome: reasons for difficulties in making a diagnosis in young males.
  Lachiewicz, A. M., Dawson, D. V., Spiridigliozzi, G. A.> ;Am J Med Genet. 2000 Jun 5
• Parental attitudes regarding carrier testing in children at risk for fragile X syndrome.
  McConkie-Rosell, A., Spiridigliozzi, G. A., Rounds, K., Dawson, D. V., Sullivan, J. A., Burgess, D., Lachiewicz, A. M.> ;Am J Med Genet. 1999 Jan 29
• Ocular status of boys with fragile X syndrome: a prospective study.
  Hatton, D. D., Buckley, E., Lachiewicz, A., Roberts, J.> ;J AAPOS. 1998 Oct
• Carrier testing in the fragile X syndrome: attitudes and opinions of obligate carriers.
  McConkie-Rosell, A., Spiridigliozzi, G. A., Iafolla, T., Tarleton, J., Lachiewicz, A. M.> ;Am J Med Genet. 1997 Jan 10
• A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene.
  Lachiewicz, A. M., Spiridigliozzi, G. A., McConkie-Rosell, A., Burgess, D., Feng, Y., Warren, S. T., Tarleton, J.> ;Am J Med Genet. 1996 Aug 9
• Trajectories and profiles of adaptive behavior in males with fragile X syndrome: multicenter studies.
  Dykens, E., Ort, S., Cohen, I., Finucane, B., Spiridigliozzi, G., Lachiewicz, A., Reiss, A., Freund, L., Hagerman, R., O'Connor, R.> ;J Autism Dev Disord. 1996 Jun
• Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia.
  Van Hove, J. L., Kishnani, P., Muenzer, J., Wenstrup, R. J., Summar, M. L., Brummond, M. R., Lachiewicz, A. M., Millington, D. S., Kahler, S. G.> ;Am J Med Genet. 1995 Dec 4
• Fragile X phenotype in a patient with a large de novo deletion in Xq27-q28.
  Albright, S. G., Lachiewicz, A. M., Tarleton, J. C., Rao, K. W., Schwartz, C. E., Richie, R., Tennison, M. B., Aylsworth, A. S.> ;Am J Med Genet. 1994 Jul 15
• Behavior problems of young girls with fragile X syndrome: factor scores on the Conners' Parent's Questionnaire.
  Lachiewicz, A. M., Dawson, D. V.> ;Am J Med Genet. 1994 Jul 15
• Do young boys with fragile X syndrome have macroorchidism?
  Lachiewicz, A. M., Dawson, D. V.> ;Pediatrics. 1994 Jun
• Aberrant behaviors of young boys with fragile X syndrome.
  Lachiewicz, A. M., Spiridigliozzi, G. A., Gullion, C. M., Ransford, S. N., Rao, K.> ;Am J Ment Retard. 1994 Mar
• An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.
  Tarleton, J., Richie, R., Schwartz, C., Rao, K., Aylsworth, A. S., Lachiewicz, A.> ;Hum Mol Genet. 1993 Nov
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