Foroud TM - Search Results

1

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.

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. 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. 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. 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. 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. 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. 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

Heterogeneity in hereditary pancreatitis.

Dasouki MJ, Cogan J, Summar ML, Neblitt W 3rd, Foroud T, Koller D, Phillips JA 3rd. Dasouki MJ, et al. Am J Med Genet. 1998 Apr 28;77(1):47-53. Am J Med Genet. 1998. PMID: 9557894

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

425 results

Search Page

Filters