Spence MA - Search Results

1

A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.

McPherson JD, Apostol B, Wagner-McPherson CB, Hakim S, Del Mastro RG, Aziz N, Baer E, Gonzales G, Krane MC, Markovich R, Masny P, Ortega M, Vu J, Vujicic M, Church DM, Segal A, Grady DL, Moyzis RK, Spence MA, Lovett M, Wasmuth JJ. McPherson JD, et al. Among authors: spence ma. Genome Res. 1997 Sep;7(9):897-909. doi: 10.1101/gr.7.9.897. Genome Res. 1997. PMID: 9314495 Free article.

2

The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.

Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, Grady DL, Ryder OA, Spence MA, Swanson JM, Moyzis RK. Wang E, et al. Among authors: spence ma. Am J Hum Genet. 2004 May;74(5):931-44. doi: 10.1086/420854. Epub 2004 Apr 9. Am J Hum Genet. 2004. PMID: 15077199 Free PMC article.

3

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. Among authors: spence ma. 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 Free article.

4

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: spence ma. Mol Psychiatry. 2003 May;8(5):536-45. doi: 10.1038/sj.mp.4001350. Mol Psychiatry. 2003. PMID: 12808433 Free article.

5

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: spence ma. 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.

6

Evidence of positive selection acting at the human dopamine receptor D4 gene locus.

Ding YC, Chi HC, Grady DL, Morishima A, Kidd JR, Kidd KK, Flodman P, Spence MA, Schuck S, Swanson JM, Zhang YP, Moyzis RK. Ding YC, et al. Among authors: spence ma. Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):309-14. doi: 10.1073/pnas.012464099. Epub 2001 Dec 26. Proc Natl Acad Sci U S A. 2002. PMID: 11756666 Free PMC article.

7

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

8

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: spence ma. 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.

9

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: spence ma. 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.

10

Bipolar disorder: dominant or recessive on chromosome 5?

Homer JP, Flodman PL, Spence MA. Homer JP, et al. Among authors: spence ma. 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

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