Errata (DOI:10.1016/S1474-4422(07)70081-9);A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Lancet Neurology

Volumn 6, Issue 5, 2007, Pages 414-420

  Matarín, Mar ^a   Brown, W Mark ^f   Scholz, Sonja ^e   Simón Sánchez, Javier ^a,b   Fung, Hon Chung ^a,c,d   Hernandez, Dena ^a   Gibbs, J Raphael ^a,e   De Vrieze, Fabienne Wavrant ^a   Crews, Cynthia ^a   Britton, Angela ^a   Langefeld, Carl D ^f   Brott, Thomas G ^g   Brown Jr , Robert D ^h   Worrall, Bradford B ⁱ   Frankel, Michael ^j   Silliman, Scott ^k   Case, L Douglas ^f   Singleton, Andrew ^a   Hardy, John A ^a,e   Rich, Stephen S ^f   Meschia, James F ^g   more..

^a NATIONAL INSTITUTE ON AGING   (United States)

^b INSTITUTO DE BIOMEDICINA DE VALENCIA   (Spain)

^c CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

^f WAKE FOREST SCHOOL OF MEDICINE   (United States)

^g MAYO CLINIC   (United States)

^h MAYO CLINIC   (United States)

ⁱ UNIVERSITY OF VIRGINIA   (United States)

^j EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^k UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ALLELE; ARTICLE; CEREBROVASCULAR ACCIDENT; CONTROLLED STUDY; DEMOGRAPHY; FEMALE; GENE FREQUENCY; GENE LOCUS; GENETIC VARIABILITY; GENOME; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PRIORITY JOURNAL; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 34047274599     PISSN: 14744422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1474-4422(08)70129-7     Document Type: Erratum

References (46)

1. Bonita R. Epidemiology of stroke. Lancet 339 (1992) 342-344
2. Rothwell P., Coull A., Giles M., et al. Change in stroke incidence, mortality, case-fatality, severity, and risk factors in Oxfordshire, UK from 1981 to 2004 (Oxford Vascular Study). Lancet 363 (2004) 1925-1933
3. Brown R., Whisnant J., Sicks J., O'Fallon W., and Wiebers D. Stroke incidence, prevalence, and survival: secular trends in Rochester, Minnesota, through 1989. Stroke 27 (1996) 373-380
4. Hassan A., and Markus H. Genetics and ischaemic stroke. Brain 123 (2000) 1784-1812
5. Joutel A., Corpechot C., Ducros A., et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383 (1996) 707-710
6. Tournier-Lasserve E. New players in the genetics of stroke. N Engl J Med 347 (2002) 1711-1712
7. Helgadottir A., Manolescu A., Thorleifsson G., et al. The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke. Nat Genet 36 (2004) 233-239
8. Gretarsdottir S., Thorleifsson G., Reynisdottir S., et al. The gene encoding phosphodiesterase 4D confers risk of ischaemic stroke. Nat Genet 35 (2003) 131-138
9. Gershon E., and Goldin L. Clinical methods in psychiatric genetics. I. Robustness of genetic marker investigative strategies. Acta Psychiatr Scand 74 (1986) 113-118
10. Risch N., and Merikangas K. The future of genetic studies of complex human diseases. Science 273 (1996) 1516-1517
11. Casas J., Hingorani A., Bautista L., and Sharma P. Meta-analysis of genetic studies in ischaemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch Neurol 61 (2004) 1652-1661
12. The International HapMap Project. Nature 426 (2003) 789-796
13. A haplotype map of the human genome. Nature 437 (2005) 1299-1320
14. Maraganore D., de Andrade M., Lesnick T., et al. High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 77 (2005) 685-693
15. Klein R., Zeiss C., Chew E., et al. Complement factor H polymorphism in age-related macular degeneration. Science 308 (2005) 385-389
16. Fung H., Scholz S., Matarin M., et al. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol 5 (2006) 911-916
17. Ozaki K., Ohnishi Y., Iida A., et al. Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction. Nat Genet 32 (2002) 650-654
18. Duerr R., Taylor K., Brant S., et al. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 314 (2006) 1461-1463
19. Folstein M., Folstein S., and McHugh P. Mini-mental state: a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 12 (1975) 189-198
20. Meschia J., Brott T., Brown Jr. R., et al. The Ischaemic Stroke Genetics Study (ISGS) Protocol. BMC Neurol 3 (2003) 4
21. Investigators WMPP. The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. J Clin Epidemiol 41 (1998) 105-114
22. Adams Jr. H., Bendixen B., Kappelle L., et al. Classification of subtype of acute ischaemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke 24 (1993) 35-41
23. Bamford J., Sandercock P., Dennis M., Burn J., and Warlow C. Classification and natural history of clinically identifiable subtypes of cerebral infarction. Lancet 337 (1991) 1521-1526
24. Johnson C., Kittner S., McCarter R., et al. Interrater reliability of an etiologic classification of ischemic stroke. Stroke 26 (1995) 46-51
25. Lyden P., Brott T., Tilley B., et al. Improved reliability of the NIH Stroke Scale using video training. NINDS TPA Stroke Study Group. Stroke 25 (1994) 2220-2226
26. Collin C., Wade D., Davies S., and Horne V. The Barthel ADL Index: a reliability study. Int Disabil Stud 10 (1988) 61-63
27. Bamford J., Sandercock P., Warlow C., and Slattery J. Interobserver agreement for the assessment of handicap in stroke patients. Stroke 30 (1989) 828
28. Jennett B., and Bond M. Assessment of outcome after severe brain damage. Lancet 305 (1975) 480-484
29. Miller G., Shope T., Lisco H., Stitt D., and Lipman M. Epstein-Barr virus: transformation, cytopathic changes, and viral antigens in squirrel monkey and marmoset leukocytes. Proc Natl Acad Sci USA 69 (1972) 383-387
30. Tumilowicz J., Gallick G., East J., Pathak S., Trentin J., and Arlinghaus R. Presence of retrovirus in the B95-8 Epstein-Barr virus-producing cell line from different sources. In Vitro 20 (1984) 486-492
31. Miller S., Dykes D., and Polesky H. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16 (1988) 1215
32. Simon-Sanchez J., Scholz S., Fung H., et al. Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. Hum Mol Genet 16 (2007) 1-14
33. Falush D., Stephens M., and Pritchard J. Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies. Genetics 164 (2003) 1567-1587
34. Wigginton J., Cutler D., and Abecasis G. A note on exact tests of Hardy-Weinberg equilibrium. Am J Hum Genet 76 (2005) 887-893
35. Zeger S., and Liang K. Longitudinal data analysis for discrete and continuous outcomes. Biometrics 42 (1986) 121-130
36. White H., Boden-Albala B., Wang C., et al. Ischaemic stroke subtype incidence among whites, blacks, and Hispanics: the Northern Manhattan Study. Circulation 111 (2005) 1327-1331
37. Casas J., Hingorani A., Bautista L., and Sharma P. Arch Neurol 61 (2004) 1652-1661
38. Holmqvist M., Cao J., Hernandez-Pineda R., et al. Elimination of fast inactivation in Kv4 A-type potassium channels by an auxiliary subunit domain. Proc Natl Acad Sci USA 99 (2002) 1035-1040
39. Pruunsild P., and Timmusk T. Structure, alternative splicing, and expression of the human and mouse KCNIP gene family. Genomics 86 (2005) 581-593
40. Morohashi Y., Hatano N., Ohya S., et al. Molecular cloning and characterization of CALP/KChIP4, a novel EF-hand protein interacting with presenilin 2 and voltage-gated potassium channel subunit Kv4. J Biol Chem 277 (2002) 14965-14975
41. Decher N., Maier M., Dittrich W., et al. Characterization of TASK-4, a novel member of the pH-sensitive, two-pore domain potassium channel family. FEBS Lett 492 (2001) 84-89
42. Lesage F., Reyes R., Fink M., Duprat F., Guillemare E., and Lazdunski M. Dimerization of TWIK-1 K+ channel subunits via a disulfide bridge. Embo J 15 (1996) 6400-6407
43. Kim Y., Bang H., and Kim D. TASK-3, a new member of the tandem pore K(+) channel family. J Biol Chem 275 (2000) 9340-9347
44. Hsieh C., Fukumoto S., Layne M., et al. Striated muscle preferentially expressed genes alpha and beta are two serine/threonine protein kinases derived from the same gene as the aortic preferentially expressed gene-1. J Biol Chem 275 (2000) 36966-36973
45. Skol A., Scott L., Abecasis G., and Boehnke M. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet 38 (2006) 209-213
46. Coon K., Myers A., Craig D., et al. A high-density whole-genome association study reveals that apoe is the major susceptibility gene for sporadic late-onset Alzheimer's disease. J Clin Psychiatry (2007) (in press).