Foroud T - Search Results

1

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

2

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.

3

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension.

Loyd JE, Butler MG, Foroud TM, Conneally PM, Phillips JA 3rd, Newman JH. Loyd JE, et al. Among authors: foroud tm. Am J Respir Crit Care Med. 1995 Jul;152(1):93-7. doi: 10.1164/ajrccm.152.1.7599869. Am J Respir Crit Care Med. 1995. PMID: 7599869 Free PMC article.

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

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22.

Edenberg HJ, Foroud T, Conneally PM, Sorbel JJ, Carr K, Crose C, Willig C, Zhao J, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Rice JP, Goate A, Reich T, Stine OC, McMahon F, DePaulo JR, Meyers D, Detera-Wadleigh SD, Goldin LR, Gershon ES, Blehar MC, Nurnberger JI Jr. Edenberg HJ, et al. Among authors: foroud t. Am J Med Genet. 1997 May 31;74(3):238-46. Am J Med Genet. 1997. PMID: 9184305

9

The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion.

Loyd JE, Slovis B, Phillips JA 3rd, Butler MG, Foroud TM, Conneally PM, Newman JH. Loyd JE, et al. Among authors: foroud tm. Chest. 1997 Jun;111(6 Suppl):82S-83S. doi: 10.1378/chest.111.6_supplement.82s. Chest. 1997. PMID: 9184540 Free PMC article. No abstract available.

10

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Murrell JR, et al. Among authors: foroud t. Am J Hum Genet. 1997 Nov;61(5):1131-8. doi: 10.1086/301594. Am J Hum Genet. 1997. PMID: 9345089 Free PMC article.

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