Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 45

1.

A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.

Coon KD, Myers AJ, Craig DW, Webster JA, Pearson JV, Lince DH, Zismann VL, Beach TG, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Walker DG, Ravid R, Heward CB, Rogers J, Papassotiropoulos A, Reiman EM, Hardy J, Stephan DA.

J Clin Psychiatry. 2007 Apr;68(4):613-8.

PMID:
17474819
2.

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.

Simon-Sanchez J, Scholz S, Fung HC, Matarin M, Hernandez D, Gibbs JR, Britton A, de Vrieze FW, Peckham E, Gwinn-Hardy K, Crawley A, Keen JC, Nash J, Borgaonkar D, Hardy J, Singleton A.

Hum Mol Genet. 2007 Jan 1;16(1):1-14. Epub 2006 Nov 20.

PMID:
17116639
3.

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

Duerr RH, Taylor KD, Brant SR, Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, Abraham C, Regueiro M, Griffiths A, Dassopoulos T, Bitton A, Yang H, Targan S, Datta LW, Kistner EO, Schumm LP, Lee AT, Gregersen PK, Barmada MM, Rotter JI, Nicolae DL, Cho JH.

Science. 2006 Dec 1;314(5804):1461-3. Epub 2006 Oct 26.

4.

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.

Fung HC, Scholz S, Matarin M, Simón-Sánchez J, Hernandez D, Britton A, Gibbs JR, Langefeld C, Stiegert ML, Schymick J, Okun MS, Mandel RJ, Fernandez HH, Foote KD, Rodríguez RL, Peckham E, De Vrieze FW, Gwinn-Hardy K, Hardy JA, Singleton A.

Lancet Neurol. 2006 Nov;5(11):911-6.

PMID:
17052657
5.

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies.

Skol AD, Scott LJ, Abecasis GR, Boehnke M.

Nat Genet. 2006 Feb;38(2):209-13. Epub 2006 Jan 15. Erratum in: Nat Genet. 2006 Mar;38(3):390.

PMID:
16415888
6.

A haplotype map of the human genome.

International HapMap Consortium..

Nature. 2005 Oct 27;437(7063):1299-320.

7.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

8.

Structure, alternative splicing, and expression of the human and mouse KCNIP gene family.

Pruunsild P, Timmusk T.

Genomics. 2005 Nov;86(5):581-93. Epub 2005 Aug 19.

PMID:
16112838
9.

A note on exact tests of Hardy-Weinberg equilibrium.

Wigginton JE, Cutler DJ, Abecasis GR.

Am J Hum Genet. 2005 May;76(5):887-93. Epub 2005 Mar 23.

10.

Ischemic stroke subtype incidence among whites, blacks, and Hispanics: the Northern Manhattan Study.

White H, Boden-Albala B, Wang C, Elkind MS, Rundek T, Wright CB, Sacco RL.

Circulation. 2005 Mar 15;111(10):1327-31.

11.

Complement factor H polymorphism in age-related macular degeneration.

Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J.

Science. 2005 Apr 15;308(5720):385-9. Epub 2005 Mar 10.

12.

Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls.

Casas JP, Hingorani AD, Bautista LE, Sharma P.

Arch Neurol. 2004 Nov;61(11):1652-61.

PMID:
15534175
13.

Change in stroke incidence, mortality, case-fatality, severity, and risk factors in Oxfordshire, UK from 1981 to 2004 (Oxford Vascular Study).

Rothwell PM, Coull AJ, Giles MF, Howard SC, Silver LE, Bull LM, Gutnikov SA, Edwards P, Mant D, Sackley CM, Farmer A, Sandercock PA, Dennis MS, Warlow CP, Bamford JM, Anslow P; Oxford Vascular Study..

Lancet. 2004 Jun 12;363(9425):1925-33.

PMID:
15194251
14.

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.

Helgadottir A, Manolescu A, Thorleifsson G, Gretarsdottir S, Jonsdottir H, Thorsteinsdottir U, Samani NJ, Gudmundsson G, Grant SF, Thorgeirsson G, Sveinbjornsdottir S, Valdimarsson EM, Matthiasson SE, Johannsson H, Gudmundsdottir O, Gurney ME, Sainz J, Thorhallsdottir M, Andresdottir M, Frigge ML, Topol EJ, Kong A, Gudnason V, Hakonarson H, Gulcher JR, Stefansson K.

Nat Genet. 2004 Mar;36(3):233-9. Epub 2004 Feb 8.

PMID:
14770184
15.

The International HapMap Project.

International HapMap Consortium..

Nature. 2003 Dec 18;426(6968):789-96.

PMID:
14685227
16.

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.

Gretarsdottir S, Thorleifsson G, Reynisdottir ST, Manolescu A, Jonsdottir S, Jonsdottir T, Gudmundsdottir T, Bjarnadottir SM, Einarsson OB, Gudjonsdottir HM, Hawkins M, Gudmundsson G, Gudmundsdottir H, Andrason H, Gudmundsdottir AS, Sigurdardottir M, Chou TT, Nahmias J, Goss S, Sveinbjörnsdottir S, Valdimarsson EM, Jakobsson F, Agnarsson U, Gudnason V, Thorgeirsson G, Fingerle J, Gurney M, Gudbjartsson D, Frigge ML, Kong A, Stefansson K, Gulcher JR.

Nat Genet. 2003 Oct;35(2):131-8. Epub 2003 Sep 21. Erratum in: Nat Genet. 2005 May;37(5):555.

17.
18.

The Ischemic Stroke Genetics Study (ISGS) Protocol.

Meschia JF, Brott TG, Brown RD Jr, Crook RJ, Frankel M, Hardy J, Merino JG, Rich SS, Silliman S, Worrall BB; Ischemic Stroke Genetics Study..

BMC Neurol. 2003 Jul 8;3:4. Epub 2003 Jul 8.

19.

New players in the genetics of stroke.

Tournier-Lasserve E.

N Engl J Med. 2002 Nov 21;347(21):1711-2. Review. No abstract available.

PMID:
12444190
20.

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.

Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T.

Nat Genet. 2002 Dec;32(4):650-4. Epub 2002 Nov 11. Erratum in: Nat Genet. 2003 Jan;33(1):107..

PMID:
12426569

Supplemental Content

Support Center