Haines JL - Search Results

1

Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.

Hedera P, Ma S, Blair MA, Taylor KA, Hamati A, Bradford Y, Abou-Khalil B, Haines JL. Hedera P, et al. Among authors: haines jl. Epilepsia. 2006 Oct;47(10):1622-8. doi: 10.1111/j.1528-1167.2006.00637.x. Epilepsia. 2006. PMID: 17054683 Free article.

2

Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26.

Kenealy SJ, Schmidt S, Agarwal A, Postel EA, De La Paz MA, Pericak-Vance MA, Haines JL. Kenealy SJ, et al. Among authors: haines jl. Mol Vis. 2004 Jan 26;10:57-61. Mol Vis. 2004. PMID: 14758336 Free article.

3

Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.

Hedera P, Abou-Khalil B, Crunk AE, Taylor KA, Haines JL, Sutcliffe JS. Hedera P, et al. Among authors: haines jl. Epilepsia. 2004 Mar;45(3):218-22. doi: 10.1111/j.0013-9580.2004.47203.x. Epilepsia. 2004. PMID: 15009222 Free article.

4

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.

Hedera P, Fenichel GM, Blair M, Haines JL. Hedera P, et al. Among authors: haines jl. Arch Neurol. 2004 Oct;61(10):1600-3. doi: 10.1001/archneur.61.10.1600. Arch Neurol. 2004. PMID: 15477516

5

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures.

Ma S, Abou-Khalil B, Sutcliffe JS, Haines JL, Hedera P. Ma S, et al. Among authors: haines jl. BMC Med Genet. 2005 Mar 30;6:13. doi: 10.1186/1471-2350-6-13. BMC Med Genet. 2005. PMID: 15799783 Free PMC article.

6

Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.

Ma S, Abou-Khalil B, Blair MA, Sutcliffe JS, Haines JL, Hedera P. Ma S, et al. Among authors: haines jl. Neurosci Lett. 2006 Feb 6;394(1):74-8. doi: 10.1016/j.neulet.2005.10.006. Epub 2005 Oct 25. Neurosci Lett. 2006. PMID: 16256272

7

A genome-wide linkage analysis of dementia in the Amish.

Hahs DW, McCauley JL, Crunk AE, McFarland LL, Gaskell PC, Jiang L, Slifer SH, Vance JM, Scott WK, Welsh-Bohmer KA, Johnson SR, Jackson CE, Pericak-Vance MA, Haines JL. Hahs DW, et al. Among authors: haines jl. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):160-6. doi: 10.1002/ajmg.b.30257. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16389594 Free PMC article.

8

Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?

Ma S, Davis TL, Blair MA, Fang JY, Bradford Y, Haines JL, Hedera P. Ma S, et al. Among authors: haines jl. Mov Disord. 2006 Sep;21(9):1368-74. doi: 10.1002/mds.20950. Mov Disord. 2006. PMID: 16721753

9

Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease.

Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: haines jl. Hum Mutat. 2007 Nov;28(11):1065-73. doi: 10.1002/humu.20567. Hum Mutat. 2007. PMID: 17573676

10

No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasets.

Liang X, Schnetz-Boutaud N, Bartlett J, Allen MJ, Gwirtsman H, Schmechel DE, Carney RM, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: haines jl. Ann Hum Genet. 2008 Jan;72(Pt 1):141-4. doi: 10.1111/j.1469-1809.2007.00394.x. Epub 2007 Aug 24. Ann Hum Genet. 2008. PMID: 17725684

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