Geschwind DH - Search Results

1

Gene expression study on peripheral blood identifies progranulin mutations.

Coppola G, Karydas A, Rademakers R, Wang Q, Baker M, Hutton M, Miller BL, Geschwind DH. Coppola G, et al. Among authors: geschwind dh. Ann Neurol. 2008 Jul;64(1):92-6. doi: 10.1002/ana.21397. Ann Neurol. 2008. PMID: 18551524 Free PMC article.

2

The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia.

Geschwind D, Karrim J, Nelson SF, Miller B. Geschwind D, et al. Ann Neurol. 1998 Jul;44(1):134-8. doi: 10.1002/ana.410440122. Ann Neurol. 1998. PMID: 9667603 Clinical Trial.

3

Commentary.

Wilhelmsen KC, Miller B, Geschwind D. Wilhelmsen KC, et al. Neurobiol Aging. 2001 Jan-Feb;22(1):119-21. doi: 10.1016/s0197-4580(00)00198-6. Neurobiol Aging. 2001. PMID: 11164284 No abstract available.

4

Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness.

Geschwind DH, Miller BL, DeCarli C, Carmelli D. Geschwind DH, et al. Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):3176-81. doi: 10.1073/pnas.052494999. Epub 2002 Feb 26. Proc Natl Acad Sci U S A. 2002. PMID: 11867730 Free PMC article.

5

Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia.

Sobrido MJ, Miller BL, Havlioglu N, Zhukareva V, Jiang Z, Nasreddine ZS, Lee VM, Chow TW, Wilhelmsen KC, Cummings JL, Wu JY, Geschwind DH. Sobrido MJ, et al. Among authors: geschwind dh. Arch Neurol. 2003 May;60(5):698-702. doi: 10.1001/archneur.60.5.698. Arch Neurol. 2003. PMID: 12756133 Free PMC article.

6

Association of the serotonin transporter and receptor gene polymorphisms in neuropsychiatric symptoms in Alzheimer disease.

Assal F, Alarcón M, Solomon EC, Masterman D, Geschwind DH, Cummings JL. Assal F, et al. Among authors: geschwind dh. Arch Neurol. 2004 Aug;61(8):1249-53. doi: 10.1001/archneur.61.8.1249. Arch Neurol. 2004. PMID: 15313842

7

Middle-aged children of Alzheimer parents, a pilot study: stable neurocognitive performance at 20-year follow-up.

Jarvik LF, La Rue A, Gokhman I, Harrison T, Holt L, Steh B, Harker J, Larson S, Yaralian P, Matsuyama S, Rasgon N, Geschwind D, Freimer N, Jimenez E, Schaeffer J. Jarvik LF, et al. J Geriatr Psychiatry Neurol. 2005 Dec;18(4):187-91. doi: 10.1177/0891988705281862. J Geriatr Psychiatry Neurol. 2005. PMID: 16306237

8

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.

Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J, Vernes SC, Fisher SE, Ren B, Geschwind DH. Spiteri E, et al. Among authors: geschwind dh. Am J Hum Genet. 2007 Dec;81(6):1144-57. doi: 10.1086/522237. Epub 2007 Oct 31. Am J Hum Genet. 2007. PMID: 17999357 Free PMC article.

9

Genomic profiles of damage and protection in human intracerebral hemorrhage.

Carmichael ST, Vespa PM, Saver JL, Coppola G, Geschwind DH, Starkman S, Miller CM, Kidwell CS, Liebeskind DS, Martin NA. Carmichael ST, et al. Among authors: geschwind dh. J Cereb Blood Flow Metab. 2008 Nov;28(11):1860-75. doi: 10.1038/jcbfm.2008.77. Epub 2008 Jul 16. J Cereb Blood Flow Metab. 2008. PMID: 18628781 Free PMC article.

10

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.

Rutherford NJ, Zhang YJ, Baker M, Gass JM, Finch NA, Xu YF, Stewart H, Kelley BJ, Kuntz K, Crook RJ, Sreedharan J, Vance C, Sorenson E, Lippa C, Bigio EH, Geschwind DH, Knopman DS, Mitsumoto H, Petersen RC, Cashman NR, Hutton M, Shaw CE, Boylan KB, Boeve B, Graff-Radford NR, Wszolek ZK, Caselli RJ, Dickson DW, Mackenzie IR, Petrucelli L, Rademakers R. Rutherford NJ, et al. Among authors: geschwind dh. PLoS Genet. 2008 Sep 19;4(9):e1000193. doi: 10.1371/journal.pgen.1000193. PLoS Genet. 2008. PMID: 18802454 Free PMC article.

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