R01 NS37167/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2002	2
2003	4
2004	1
2005	1
2006	3
2007	3
2008	4
2009	7
2010	2
2011	1
2025	0

1

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

2

LRRK2: both a cause and a risk factor for Parkinson disease?

Foroud T. Foroud T. Neurology. 2005 Sep 13;65(5):664-5. doi: 10.1212/01.wnl.0000179342.58181.c9. Neurology. 2005. PMID: 16157895 No abstract available.

3

Genetics of Parkinson disease.

Pankratz N, Foroud T. Pankratz N, et al. Genet Med. 2007 Dec;9(12):801-11. doi: 10.1097/gim.0b013e31815bf97c. Genet Med. 2007. PMID: 18091429 Free article. Review.

4

Alpha-synuclein and familial Parkinson's disease.

Pankratz N, Nichols WC, Elsaesser VE, Pauciulo MW, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Pfeiffer RF, Foroud T; Parkinson Study Group - PROGENI Investigators. Pankratz N, et al. Mov Disord. 2009 Jun 15;24(8):1125-31. doi: 10.1002/mds.22524. Mov Disord. 2009. PMID: 19412953 Free PMC article.

5

Trends in American Board of Psychiatry and Neurology specialties and neurologic subspecialties.

Faulkner LR, Juul D, Pascuzzi RM, Aminoff MJ, Crumrine PK, Dekosky ST, Jozefowicz RF, Massey JM, Pirzada N, Tilton A. Faulkner LR, et al. Neurology. 2010 Sep 21;75(12):1110-7. doi: 10.1212/WNL.0b013e3181f39a41. Neurology. 2010. PMID: 20855855 Free PMC article.

6

Clinical correlates of depressive symptoms in familial Parkinson's disease.

Pankratz N, Marder KS, Halter CA, Rudolph A, Shults CW, Nichols WC, Foroud T; Parkinson's Study Group-PROGENI Investigators. Pankratz N, et al. Mov Disord. 2008 Nov 15;23(15):2216-23. doi: 10.1002/mds.22285. Mov Disord. 2008. PMID: 18785635 Free PMC article.

7

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.

Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T; Parkinson Study Group-PROGENI Investigators. Simon DK, et al. BMC Med Genet. 2010 Apr 1;11:53. doi: 10.1186/1471-2350-11-53. BMC Med Genet. 2010. PMID: 20356410 Free PMC article.

8

Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH; PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories. Pankratz N, et al. Hum Genet. 2009 Jan;124(6):593-605. doi: 10.1007/s00439-008-0582-9. Epub 2008 Nov 6. Hum Genet. 2009. PMID: 18985386 Free PMC article.

9

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. 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.

10

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.

Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T; PSG-Progeni GenePD Investigators, Coordinators, and Molecular Genetic Laboratories. Latourelle JC, et al. Mov Disord. 2011 Sep;26(11):2039-44. doi: 10.1002/mds.23781. Epub 2011 Jun 9. Mov Disord. 2011. PMID: 21661047 Free PMC article.

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