Flodman PL - Search Results

1

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: flodman pl. BMC Med Genet. 2004 Apr 16;5:10. doi: 10.1186/1471-2350-5-10. BMC Med Genet. 2004. PMID: 15090072 Free PMC article.

2

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

3

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. Cytogenet Genome Res. 2002;98(4):233-9. doi: 10.1159/000071040. Cytogenet Genome Res. 2002. PMID: 12826745

4

Language and other regression: assessment and timing.

Goldberg WA, Osann K, Filipek PA, Laulhere T, Jarvis K, Modahl C, Flodman P, Spence MA. Goldberg WA, et al. J Autism Dev Disord. 2003 Dec;33(6):607-16. doi: 10.1023/b:jadd.0000005998.47370.ef. J Autism Dev Disord. 2003. PMID: 14714930

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

Bipolar disorder: dominant or recessive on chromosome 5?

Homer JP, Flodman PL, Spence MA. Homer JP, et al. Among authors: flodman pl. Genet Epidemiol. 1997;14(6):647-51. doi: 10.1002/(SICI)1098-2272(1997)14:6<647::AID-GEPI16>3.0.CO;2-Q. Genet Epidemiol. 1997. PMID: 9433557

7

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. 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.

8

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. Among authors: flodman pl. 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.

9

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

Smith M, Flodman PL. Smith M, et al. Among authors: flodman pl. 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.

10

Bipolar disorder: evidence for a major locus.

Spence MA, Flodman PL, Sadovnick AD, Bailey-Wilson JE, Ameli H, Remick RA. Spence MA, et al. Among authors: flodman pl. Am J Med Genet. 1995 Oct 9;60(5):370-6. doi: 10.1002/ajmg.1320600505. Am J Med Genet. 1995. PMID: 8546148

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