Foroud T - Search Results

1

Variation in GIGYF2 is not associated with Parkinson disease.

Nichols WC, Kissell DK, Pankratz N, Pauciulo MW, Elsaesser VE, Clark KA, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T; Parkinson Study Group-PROGENI Investigators. Nichols WC, et al. Among authors: foroud t. Neurology. 2009 Jun 2;72(22):1886-92. doi: 10.1212/01.wnl.0000346517.98982.1b. Epub 2009 Mar 11. Neurology. 2009. PMID: 19279319 Free PMC article.

2

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.

Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B. Dlouhy SR, et al. Among authors: foroud t. Nat Genet. 1992 Apr;1(1):64-7. doi: 10.1038/ng0492-64. Nat Genet. 1992. PMID: 1363809

3

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

Young K, Foroud T, Williams P, Jackson CE, Beckmann JS, Cohen D, Conneally PM, Tischfield J, Hodes ME. Young K, et al. Among authors: foroud t. Genomics. 1992 Aug;13(4):1370-1. doi: 10.1016/0888-7543(92)90074-3. Genomics. 1992. PMID: 1505977 No abstract available.

4

Cognitive scores in carriers of Huntington's disease gene compared to noncarriers.

Foroud T, Siemers E, Kleindorfer D, Bill DJ, Hodes ME, Norton JA, Conneally PM, Christian JC. Foroud T, et al. Ann Neurol. 1995 May;37(5):657-64. doi: 10.1002/ana.410370516. Ann Neurol. 1995. PMID: 7755361

5

Possible localization of a major gene for cleft lip and palate to 4q.

Beiraghi S, Foroud T, Diouhy S, Bixler D, Conneally PM, Delozier-Blanchet D, Hodes ME. Beiraghi S, et al. Among authors: foroud t. Clin Genet. 1994 Sep;46(3):255-6. doi: 10.1111/j.1399-0004.1994.tb04236.x. Clin Genet. 1994. PMID: 7820940 No abstract available.

6

Motor changes in presymptomatic Huntington disease gene carriers.

Siemers E, Foroud T, Bill DJ, Sorbel J, Norton JA Jr, Hodes ME, Niebler G, Conneally PM, Christian JC. Siemers E, et al. Among authors: foroud t. Arch Neurol. 1996 Jun;53(6):487-92. doi: 10.1001/archneur.1996.00550060029011. Arch Neurol. 1996. PMID: 8660148

7

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.

Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA 3rd, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Nichols WC, et al. Among authors: foroud t. Nat Genet. 1997 Mar;15(3):277-80. doi: 10.1038/ng0397-277. Nat Genet. 1997. PMID: 9054941

8

Differences in duration of Huntington's disease based on age at onset.

Foroud T, Gray J, Ivashina J, Conneally PM. Foroud T, et al. J Neurol Neurosurg Psychiatry. 1999 Jan;66(1):52-6. doi: 10.1136/jnnp.66.1.52. J Neurol Neurosurg Psychiatry. 1999. PMID: 9886451 Free PMC article.

9

Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers.

Kirkwood SC, Siemers E, Stout JC, Hodes ME, Conneally PM, Christian JC, Foroud T. Kirkwood SC, et al. Among authors: foroud t. Arch Neurol. 1999 May;56(5):563-8. doi: 10.1001/archneur.56.5.563. Arch Neurol. 1999. PMID: 10328251

10

Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus.

Takacs I, Koller DL, Peacock M, Christian JC, Hui SL, Conneally PM, Johnston CC Jr, Foroud T, Econs MJ. Takacs I, et al. Among authors: foroud t. J Clin Endocrinol Metab. 1999 Dec;84(12):4467-71. doi: 10.1210/jcem.84.12.6179. J Clin Endocrinol Metab. 1999. PMID: 10599704

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