Foroud T - Search Results

1

Longitudinal personality changes among presymptomatic Huntington disease gene carriers.

Kirkwood SC, Siemers E, Viken R, Hodes ME, Conneally PM, Christian JC, Foroud T. Kirkwood SC, et al. Among authors: foroud t. Neuropsychiatry Neuropsychol Behav Neurol. 2002 Sep;15(3):192-7. Neuropsychiatry Neuropsychol Behav Neurol. 2002. PMID: 12218712

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

Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13.

Carn G, Koller DL, Peacock M, Hui SL, Evans WE, Conneally PM, Johnston CC Jr, Foroud T, Econs MJ. Carn G, et al. Among authors: foroud t. J Clin Endocrinol Metab. 2002 Aug;87(8):3819-24. doi: 10.1210/jcem.87.8.8740. J Clin Endocrinol Metab. 2002. PMID: 12161516

4

Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales.

Close Kirkwood S, Siemers E, Viken RJ, Hodes ME, Conneally PM, Christian JC, Foroud T. Close Kirkwood S, et al. Among authors: foroud t. J Psychiatr Res. 2002 Nov-Dec;36(6):377-82. doi: 10.1016/s0022-3956(02)00054-7. J Psychiatr Res. 2002. PMID: 12393306

5

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.

6

Defining alcohol-related phenotypes in humans. The Collaborative Study on the Genetics of Alcoholism.

Bierut LJ, Saccone NL, Rice JP, Goate A, Foroud T, Edenberg H, Almasy L, Conneally PM, Crowe R, Hesselbrock V, Li TK, Nurnberger J Jr, Porjesz B, Schuckit MA, Tischfield J, Begleiter H, Reich T. Bierut LJ, et al. Among authors: foroud t. Alcohol Res Health. 2002;26(3):208-13. Alcohol Res Health. 2002. PMID: 12875049 Free PMC article. Clinical Trial.

7

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

8

Visual function in Huntington's disease patients and presymptomatic gene carriers.

O'Donnell BF, Wilt MA, Hake AM, Stout JC, Kirkwood SC, Foroud T. O'Donnell BF, et al. Among authors: foroud t. Mov Disord. 2003 Sep;18(9):1027-34. doi: 10.1002/mds.10491. Mov Disord. 2003. PMID: 14502670

9

A genomic scan for habitual smoking in families of alcoholics: common and specific genetic factors in substance dependence.

Bierut LJ, Rice JP, Goate A, Hinrichs AL, Saccone NL, Foroud T, Edenberg HJ, Cloninger CR, Begleiter H, Conneally PM, Crowe RR, Hesselbrock V, Li TK, Nurnberger JI Jr, Porjesz B, Schuckit MA, Reich T. Bierut LJ, et al. Among authors: foroud t. Am J Med Genet A. 2004 Jan 1;124A(1):19-27. doi: 10.1002/ajmg.a.20329. Am J Med Genet A. 2004. PMID: 14679582

10

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.

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