Smith M - Search Results

1

High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.

Grady DL, Chi HC, Ding YC, Smith M, Wang E, Schuck S, Flodman P, Spence MA, Swanson JM, Moyzis RK. Grady DL, et al. Among authors: smith m. Mol Psychiatry. 2003 May;8(5):536-45. doi: 10.1038/sj.mp.4001350. Mol Psychiatry. 2003. PMID: 12808433

2

Dopamine genes and ADHD.

Swanson JM, Flodman P, Kennedy J, Spence MA, Moyzis R, Schuck S, Murias M, Moriarity J, Barr C, Smith M, Posner M. Swanson JM, et al. Among authors: smith m. Neurosci Biobehav Rev. 2000 Jan;24(1):21-5. doi: 10.1016/s0149-7634(99)00062-7. Neurosci Biobehav Rev. 2000. PMID: 10654656 Free article. Clinical Trial.

3

Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention.

Swanson J, Oosterlaan J, Murias M, Schuck S, Flodman P, Spence MA, Wasdell M, Ding Y, Chi HC, Smith M, Mann M, Carlson C, Kennedy JL, Sergeant JA, Leung P, Zhang YP, Sadeh A, Chen C, Whalen CK, Babb KA, Moyzis R, Posner MI. Swanson J, et al. Among authors: smith m. Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4754-9. doi: 10.1073/pnas.080070897. Proc Natl Acad Sci U S A. 2000. PMID: 10781080 Free PMC article.

4

Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific.

Grady DL, Harxhi A, Smith M, Flodman P, Spence MA, Swanson JM, Moyzis RK. Grady DL, et al. Among authors: smith m. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):33-5. doi: 10.1002/ajmg.b.30182. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15892149 Free article.

5

Nuclear and mitochondrial genome defects in autisms.

Smith M, Spence MA, Flodman P. Smith M, et al. Ann N Y Acad Sci. 2009 Jan;1151:102-32. doi: 10.1111/j.1749-6632.2008.03571.x. Ann N Y Acad Sci. 2009. PMID: 19154520 Review.

6

Expanded Insights Into Mechanisms of Gene Expression and Disease Related Disruptions.

Smith M, Flodman PL. Smith M, et al. Front Mol Biosci. 2018 Nov 27;5:101. doi: 10.3389/fmolb.2018.00101. eCollection 2018. Front Mol Biosci. 2018. PMID: 30542652 Free PMC article. Review.

7

Evidence for multiple loci from a genome scan of autism kindreds.

Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM. Schellenberg GD, et al. Among authors: smith m. Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. doi: 10.1038/sj.mp.4001874. Epub 2006 Aug 1. Mol Psychiatry. 2006. PMID: 16880825 Free article.

8

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

Smith M, Escamilla JR, Filipek P, Bocian ME, Modahl C, Flodman P, Spence MA. Smith M, et al. Cytogenet Cell Genet. 2001;94(1-2):15-22. doi: 10.1159/000048775. Cytogenet Cell Genet. 2001. PMID: 11701947

9

Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits.

Smith M, Woodroffe A, Smith R, Holguin S, Martinez J, Filipek PA, Modahl C, Moore B, Bocian ME, Mays L, Laulhere T, Flodman P, Spence MA. Smith M, et al. Among authors: smith r. Cytogenet Genome Res. 2002;98(4):233-9. doi: 10.1159/000071040. Cytogenet Genome Res. 2002. PMID: 12826745

10

Autism and the serotonin transporter: the long and short of it.

Devlin B, Cook EH Jr, Coon H, Dawson G, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD; CPEA Genetics Network. Devlin B, et al. Among authors: smith m. Mol Psychiatry. 2005 Dec;10(12):1110-6. doi: 10.1038/sj.mp.4001724. Mol Psychiatry. 2005. PMID: 16103890 Clinical Trial.

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