Smith M - Search Results

1

Mitochondrial and ion channel gene alterations in autism.

Smith M, Flodman PL, Gargus JJ, Simon MT, Verrell K, Haas R, Reiner GE, Naviaux R, Osann K, Spence MA, Wallace DC. Smith M, et al. Biochim Biophys Acta. 2012 Oct;1817(10):1796-802. doi: 10.1016/j.bbabio.2012.04.004. Epub 2012 Apr 17. Biochim Biophys Acta. 2012. PMID: 22538295 Free PMC article. Clinical Trial.

2

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.

3

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.

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

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.

Ramanathan S, Woodroffe A, Flodman PL, Mays LZ, Hanouni M, Modahl CB, Steinberg-Epstein R, Bocian ME, Spence MA, Smith M. Ramanathan S, et al. Among authors: smith m. BMC Med Genet. 2004 Apr 16;5:10. doi: 10.1186/1471-2350-5-10. BMC Med Genet. 2004. PMID: 15090072 Free PMC article.

6

Mitochondrial dysfunction in autistic patients with 15q inverted duplication.

Filipek PA, Juranek J, Smith M, Mays LZ, Ramos ER, Bocian M, Masser-Frye D, Laulhere TM, Modahl C, Spence MA, Gargus JJ. Filipek PA, et al. Among authors: smith m. Ann Neurol. 2003 Jun;53(6):801-4. doi: 10.1002/ana.10596. Ann Neurol. 2003. PMID: 12783428 Free article.

7

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

8

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

9

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.

10

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

Smith M, Filipek PA, Wu C, Bocian M, Hakim S, Modahl C, Spence MA. Smith M, et al. Am J Med Genet. 2000 Dec 4;96(6):765-70. doi: 10.1002/1096-8628(20001204)96:6<765::aid-ajmg13>3.0.co;2-l. Am J Med Genet. 2000. PMID: 11121177

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