SCOPUS 정보 검색 플랫폼

Volumn 79, Issue 1, 2006, Pages 183-184

Reply to Bertram et al. [2]

(10) Grupe, Andrew a Li, Yonghong a Rowland, Charles a Hinrichs, Tony b Holmans, Peter c Hardy, John d O'Donovan, Michael c Owen, Michael J c Williams, Julie c Goate, Alison b,e

a CELERA (United States)

b WASHINGTON UNIVERSITY (United States)

c CARDIFF UNIVERSITY (United Kingdom)

d NATIONAL INSTITUTE ON AGING (United States)

e WASHINGTON UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN E;

ALLELE; ALZHEIMER DISEASE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC MARKER; GENETIC RISK; HUMAN; LETTER; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 33745263286 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/505033 Document Type: Letter

Times cited : (1)

References (5)

1
- 33745244298
- Single-nucleotide polymorphism rs498055 on chromosome 10q24 is not associated with Alzheimer disease in two independent family samples
- in this issue
- Bertram L, Hsiao M, Lange C, Blacker D, Tanzi RE (2006) Single-nucleotide polymorphism rs498055 on chromosome 10q24 is not associated with Alzheimer disease in two independent family samples. Am J Hum Genet 79:180-183 (in this issue)
- (2006) Am J Hum Genet , vol.79 , pp. 180-183
- Bertram, L.¹ Hsiao, M.² Lange, C.³ Blacker, D.⁴ Tanzi, R.E.⁵

2
- 29244448999
- A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease
- Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JSK, et al (2006) A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. Am J Hum Genet 78:78-88
- (2006) Am J Hum Genet , vol.78 , pp. 78-88
- Grupe, A.¹ Li, Y.² Rowland, C.³ Nowotny, P.⁴ Hinrichs, A.L.⁵ Smemo, S.⁶ Kauwe, J.S.K.⁷

3
- 20044362721
- Family-based association between Alzheimer's disease and variants in UBQLN1
- Bertram L, Hiltunen M, Parkinson M, Ingelsson M, Lange C, Ramasamy K, Mullin K, Menon R, Sampson AJ, Hsiao MY, Elliott KJ, Velicelebi G, Moscarillo T, Hyman BT, Wagner SL, Becker KD, Blacker D, Tanzi RE (2005) Family-based association between Alzheimer's disease and variants in UBQLN1. N Engl J Med 352:884-894
- (2005) N Engl J Med , vol.352 , pp. 884-894
- Bertram, L.¹ Hiltunen, M.² Parkinson, M.³ Ingelsson, M.⁴ Lange, C.⁵ Ramasamy, K.⁶ Mullin, K.⁷ Menon, R.⁸ Sampson, A.J.⁹ Hsiao, M.Y.¹⁰ Elliott, K.J.¹¹ Velicelebi, G.¹² Moscarillo, T.¹³ Hyman, B.T.¹⁴ Wagner, S.L.¹⁵ Becker, K.D.¹⁶ Blacker, D.¹⁷ Tanzi, R.E.¹⁸

4
- 0032427048
- The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases 1: DNA pooling
- Risch N, Teng J (1998) The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases 1: DNA pooling. Genome Res 8:1273-1288
- (1998) Genome Res , vol.8 , pp. 1273-1288
- Risch, N.¹ Teng, J.²

5
- 18244407351
- A full genome screen for Alzheimer's disease: Stage two analysis
- Myers A, Wavrant De Frieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, et al (2002) A full genome screen for Alzheimer's disease: stage two analysis. Neuropsychiatric Genetics 114:235-244
- (2002) Neuropsychiatric Genetics , vol.114 , pp. 235-244
- Myers, A.¹ Wavrant De Frieze, F.² Holmans, P.³ Hamshere, M.⁴ Crook, R.⁵ Compton, D.⁶ Marshall, H.⁷

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.