Ahmadi KR - Search Results

1

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

2

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

3

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

4

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.

5

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.

6

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

7

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.

8

A single-nucleotide polymorphism tagging set for human drug metabolism and transport.

Ahmadi KR, Weale ME, Xue ZY, Soranzo N, Yarnall DP, Briley JD, Maruyama Y, Kobayashi M, Wood NW, Spurr NK, Burns DK, Roses AD, Saunders AM, Goldstein DB. Ahmadi KR, et al. Nat Genet. 2005 Jan;37(1):84-9. doi: 10.1038/ng1488. Epub 2004 Dec 19. Nat Genet. 2005. PMID: 15608640

9

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

10

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

Traylor M, Zhang CR, Adib-Samii P, Devan WJ, Parsons OE, Lanfranconi S, Gregory S, Cloonan L, Falcone GJ, Radmanesh F, Fitzpatrick K, Kanakis A, Barrick TR, Moynihan B, Lewis CM, Boncoraglio GB, Lemmens R, Thijs V, Sudlow C, Wardlaw J, Rothwell PM, Meschia JF, Worrall BB, Levi C, Bevan S, Furie KL, Dichgans M, Rosand J, Markus HS, Rost N; International Stroke Genetics Consortium. Traylor M, et al. Neurology. 2016 Jan 12;86(2):146-53. doi: 10.1212/WNL.0000000000002263. Epub 2015 Dec 16. Neurology. 2016. PMID: 26674333 Free PMC article.

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