Foroud T - Search Results

1

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation.

Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH. Dumitriu A, et al. Among authors: foroud t. PLoS Genet. 2012 Jun;8(6):e1002794. doi: 10.1371/journal.pgen.1002794. Epub 2012 Jun 28. PLoS Genet. 2012. PMID: 22761592 Free PMC article.

2

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.

Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T; Parkinson Study Group. Pankratz N, et al. Among authors: foroud t. Am J Hum Genet. 2002 Jul;71(1):124-35. doi: 10.1086/341282. Epub 2002 Jun 7. Am J Hum Genet. 2002. PMID: 12058349 Free PMC article.

3

Significant linkage of Parkinson disease to chromosome 2q36-37.

Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T; Parkinson Study Group. Pankratz N, et al. Among authors: foroud t. Am J Hum Genet. 2003 Apr;72(4):1053-7. doi: 10.1086/374383. Epub 2003 Mar 13. Am J Hum Genet. 2003. PMID: 12638082 Free PMC article.

4

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.

Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T; Parkinson Study Group. Pankratz N, et al. Among authors: foroud t. Hum Mol Genet. 2003 Oct 15;12(20):2599-608. doi: 10.1093/hmg/ddg270. Epub 2003 Aug 12. Hum Mol Genet. 2003. PMID: 12925570

5

Identification of genes for complex disease using longitudinal phenotypes.

Pankratz N, Mukhopadhyay N, Huang S, Foroud T, Kirkwood SC. Pankratz N, et al. Among authors: foroud t. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S58. doi: 10.1186/1471-2156-4-S1-S58. BMC Genet. 2003. PMID: 14975126 Free PMC article.

6

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.

Nichols WC, Uniacke SK, Pankratz N, Reed T, Simon DK, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T; Parkinson Study Group. Nichols WC, et al. Among authors: foroud t. Mov Disord. 2004 Jun;19(6):649-55. doi: 10.1002/mds.20097. Mov Disord. 2004. PMID: 15197702

7

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

Nichols WC, Pankratz N, Hernandez D, Paisán-Ruíz C, Jain S, Halter CA, Michaels VE, Reed T, Rudolph A, Shults CW, Singleton A, Foroud T; Parkinson Study Group-PROGENI investigators. Nichols WC, et al. Among authors: foroud t. Lancet. 2005 Jan 29-Feb 4;365(9457):410-2. doi: 10.1016/S0140-6736(05)17828-3. Lancet. 2005. PMID: 15680455

8

Genetics of Parkinson disease.

Pankratz N, Foroud T. Pankratz N, et al. Among authors: foroud t. NeuroRx. 2004 Apr;1(2):235-42. doi: 10.1602/neurorx.1.2.235. NeuroRx. 2004. PMID: 15717024 Free PMC article. Review.

9

The Familial Intracranial Aneurysm (FIA) study protocol.

Broderick JP, Sauerbeck LR, Foroud T, Huston J 3rd, Pankratz N, Meissner I, Brown RD Jr. Broderick JP, et al. Among authors: foroud t. BMC Med Genet. 2005 Apr 26;6:17. doi: 10.1186/1471-2350-6-17. BMC Med Genet. 2005. PMID: 15854227 Free PMC article.

10

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.

Pankratz N, Byder L, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC. Pankratz N, et al. Among authors: foroud t. Mov Disord. 2006 Jan;21(1):45-9. doi: 10.1002/mds.20663. Mov Disord. 2006. PMID: 16116614

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