Foroud T - Search Results

1

Whole-Exome Sequencing in Familial Parkinson Disease.

Farlow JL, Robak LA, Hetrick K, Bowling K, Boerwinkle E, Coban-Akdemir ZH, Gambin T, Gibbs RA, Gu S, Jain P, Jankovic J, Jhangiani S, Kaw K, Lai D, Lin H, Ling H, Liu Y, Lupski JR, Muzny D, Porter P, Pugh E, White J, Doheny K, Myers RM, Shulman JM, Foroud T. Farlow JL, et al. Among authors: foroud t. JAMA Neurol. 2016 Jan;73(1):68-75. doi: 10.1001/jamaneurol.2015.3266. JAMA Neurol. 2016. PMID: 26595808 Free PMC article.

2

False positive rates in association studies as a function of degree of stratification.

Koller DL, Peacock M, Lai D, Foroud T, Econs MJ. Koller DL, et al. Among authors: foroud t. J Bone Miner Res. 2004 Aug;19(8):1291-5. doi: 10.1359/JBMR.040409. Epub 2004 Apr 19. J Bone Miner Res. 2004. PMID: 15231016 Free article.

3

Genetics of Parkinson disease.

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

4

Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men.

Peacock M, Koller DL, Fishburn T, Krishnan S, Lai D, Hui S, Johnston CC, Foroud T, Econs MJ. Peacock M, et al. Among authors: foroud t. J Clin Endocrinol Metab. 2005 May;90(5):3060-6. doi: 10.1210/jc.2004-2143. Epub 2005 Mar 1. J Clin Endocrinol Metab. 2005. PMID: 15741260

5

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men.

Peacock M, Koller DL, Lai D, Hui S, Foroud T, Econs MJ. Peacock M, et al. Among authors: foroud t. Bone. 2005 Oct;37(4):467-73. doi: 10.1016/j.bone.2005.05.005. Bone. 2005. PMID: 16046210 Free PMC article.

6

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes.

Chu K, Koller DL, Snyder R, Fishburn T, Lai D, Waguespack SG, Foroud T, Econs MJ. Chu K, et al. Among authors: foroud t. Bone. 2005 Nov;37(5):655-61. doi: 10.1016/j.bone.2005.06.003. Epub 2005 Aug 24. Bone. 2005. PMID: 16120485

7

Mutations in DJ-1 are rare in familial Parkinson disease.

Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Shults CW, Foroud T, Nichols WC; Parkinson Study Group - PROGENI Investigators. Pankratz N, et al. Among authors: foroud t. Neurosci Lett. 2006 Nov 20;408(3):209-13. doi: 10.1016/j.neulet.2006.09.003. Epub 2006 Sep 25. Neurosci Lett. 2006. PMID: 16997464 Free PMC article.

8

Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.

Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T, Nichols WC; Parkinson Study Group-PROGENI Investigators. Pankratz N, et al. Among authors: foroud t. Mov Disord. 2006 Dec;21(12):2257-60. doi: 10.1002/mds.21162. Mov Disord. 2006. PMID: 17078063

9

Specific psychiatric manifestations among preclinical Huntington disease mutation carriers.

Marshall J, White K, Weaver M, Flury Wetherill L, Hui S, Stout JC, Johnson SA, Beristain X, Gray J, Wojcieszek J, Foroud T. Marshall J, et al. Among authors: foroud t. Arch Neurol. 2007 Jan;64(1):116-21. doi: 10.1001/archneur.64.1.116. Arch Neurol. 2007. PMID: 17210818

10

Genetics of Parkinson disease.

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

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