Ahmadi KR - Search Results

1

A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease.

Healy DG, Abou-Sleiman PM, Ozawa T, Lees AJ, Bhatia K, Ahmadi KR, Wullner U, Berciano J, Moller JC, Kamm C, Burk K, Barone P, Tolosa E, Quinn N, Goldstein DB, Wood NW. Healy DG, et al. Among authors: ahmadi kr. Ann Neurol. 2004 Mar;55(3):443-6. doi: 10.1002/ana.20063. Ann Neurol. 2004. PMID: 14991826

2

Population genetic approaches to neurological disease: Parkinson's disease as an example.

Gandhi S, Abou-Sleiman PM, Healy DG, Weale M, Gilks W, Ahmadi K, Goldstein DB, Wood NW. Gandhi S, et al. Philos Trans R Soc Lond B Biol Sci. 2005 Aug 29;360(1460):1573-8. doi: 10.1098/rstb.2005.1687. Philos Trans R Soc Lond B Biol Sci. 2005. PMID: 16096106 Free PMC article. Review.

3

The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism.

Healy DG, Abou-Sleiman PM, Ahmadi KR, Muqit MM, Bhatia KP, Quinn NP, Lees AJ, Latchmann DS, Goldstein DB, Wood NW. Healy DG, et al. Among authors: ahmadi kr. Ann Neurol. 2004 Sep;56(3):329-35. doi: 10.1002/ana.20206. Ann Neurol. 2004. PMID: 15349859

4

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.

Healy DG, Abou-Sleiman PM, Quinn N, Ahmadi KR, Ozawa T, Kamm C, Wullner U, Oertel WH, Burk K, Dupont E, Pellecchia MT, Tolosa E, Gasser T, Holton JL, Revesz T, Goldstein DB, Lees AJ, Wood NW; European MSA Study Group. Healy DG, et al. Among authors: ahmadi kr. Mov Disord. 2005 Oct;20(10):1338-43. doi: 10.1002/mds.20575. Mov Disord. 2005. PMID: 16007636

5

UCHL-1 is not a Parkinson's disease susceptibility gene.

Healy DG, Abou-Sleiman PM, Casas JP, Ahmadi KR, Lynch T, Gandhi S, Muqit MM, Foltynie T, Barker R, Bhatia KP, Quinn NP, Lees AJ, Gibson JM, Holton JL, Revesz T, Goldstein DB, Wood NW. Healy DG, et al. Among authors: ahmadi kr. Ann Neurol. 2006 Apr;59(4):627-33. doi: 10.1002/ana.20757. Ann Neurol. 2006. PMID: 16450370

6

NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.

Healy DG, Abou-Sleiman PM, Ahmadi KR, Gandhi S, Muqit MM, Bhatia KP, Quinn NP, Lees AJ, Holton JL, Revesz T, Wood NW. Healy DG, et al. Among authors: ahmadi kr. Mov Disord. 2006 Nov;21(11):1960-3. doi: 10.1002/mds.21018. Mov Disord. 2006. PMID: 16977628

7

Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.

Healy DG, Abou-Sleiman PM, Jain S, Ahmadi KR, Wood NW. Healy DG, et al. Among authors: ahmadi kr. Neurology. 2004 Jun 22;62(12):2335. doi: 10.1212/wnl.62.12.2335-a. Neurology. 2004. PMID: 15210917 No abstract available.

8

Multifactorial diseases: asthma genetics point the way.

Ahmadi KR, Goldstein DB. Ahmadi KR, et al. Curr Biol. 2002 Oct 15;12(20):R702-4. doi: 10.1016/s0960-9822(02)01211-3. Curr Biol. 2002. PMID: 12401189 Free article.

9

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses.

Goldstein DB, Ahmadi KR, Weale ME, Wood NW. Goldstein DB, et al. Among authors: ahmadi kr. Trends Genet. 2003 Nov;19(11):615-22. doi: 10.1016/j.tig.2003.09.006. Trends Genet. 2003. PMID: 14585613 No abstract available.

10

No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approach.

Shah PR, Ahmad-Annuar A, Ahmadi KR, Russ C, Sapp PC, Horvitz HR, Brown RH Jr, Goldstein DB, Fisher EM. Shah PR, et al. Among authors: ahmadi kr. Amyotroph Lateral Scler. 2006 Mar;7(1):46-56. doi: 10.1080/14660820500397057. Amyotroph Lateral Scler. 2006. PMID: 16546759

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