-
1
-
-
2642583283
-
Mapping complex disease loci in whole-genome association studies
-
Carlson CS, Eberle MA, Kruglyak L, Nickerson DA: Mapping complex disease loci in whole-genome association studies. Nature 2004;429:446-452.
-
(2004)
Nature
, vol.429
, pp. 446-452
-
-
Carlson, C.S.1
Eberle, M.A.2
Kruglyak, L.3
Nickerson, D.A.4
-
2
-
-
23944469845
-
Recent developments in genomewide association scans: A workshop summary and review
-
Thomas DC, Haile RW, Duggan D: Recent developments in genomewide association scans: A workshop summary and review. Am J Hum Genet 2005;77:337-345.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 337-345
-
-
Thomas, D.C.1
Haile, R.W.2
Duggan, D.3
-
3
-
-
13144265739
-
Genome-wide association studies: Theoretical and practical concerns
-
Wang WY, Barratt BJ, Clayton DG, Todd JA: Genome-wide association studies: Theoretical and practical concerns. Nat Rev Genet 2005;6:109-118.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 109-118
-
-
Wang, W.Y.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
4
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn JN, Daly MJ: Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 2005;6:95-108.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
5
-
-
33646234965
-
Are we ready for genome-wide association studies?
-
Thomas DC: Are we ready for genome-wide association studies? Cancer Epidemiol Biomarkers Prev 2006;15:595-598.
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 595-598
-
-
Thomas, D.C.1
-
6
-
-
16844366786
-
Genome-wide strategies for detecting multiple loci that influence complex diseases
-
Marchini J, Donnelly P, Cardon LR: Genome-wide strategies for detecting multiple loci that influence complex diseases. Nat Genet 2005;37:413-417.
-
(2005)
Nat Genet
, vol.37
, pp. 413-417
-
-
Marchini, J.1
Donnelly, P.2
Cardon, L.R.3
-
7
-
-
33646250184
-
Optimal two-stage genotyping designs for genome-wide association scans
-
Wang H, Thomas DC, Pe'er I, Stram DO: Optimal two-stage genotyping designs for genome-wide association scans. Genet Epidemiol 2006;30:356-368.
-
(2006)
Genet Epidemiol
, vol.30
, pp. 356-368
-
-
Wang, H.1
Thomas, D.C.2
Pe'er, I.3
Stram, D.O.4
-
8
-
-
10044277900
-
Twostage sampling designs for gene association studies
-
Thomas D, Xie R, Gebregziabher M: Twostage sampling designs for gene association studies. Genet Epidemiol 2004;27:401-414.
-
(2004)
Genet Epidemiol
, vol.27
, pp. 401-414
-
-
Thomas, D.1
Xie, R.2
Gebregziabher, M.3
-
9
-
-
33751296482
-
Optimum two-stage designs in case-control association studies using false discovery rate
-
Kuchiba A, Tanaka NY, Ohashi Y: Optimum two-stage designs in case-control association studies using false discovery rate. J Hum Genet 2006;51:1046-1054.
-
(2006)
J Hum Genet
, vol.51
, pp. 1046-1054
-
-
Kuchiba, A.1
Tanaka, N.Y.2
Ohashi, Y.3
-
10
-
-
31744435871
-
Joint analysis is more efficient than replication-based analysis for two-stage genomewide association studies
-
Skol AD, Scott LJ, Abecasis GR, Boehnke M: Joint analysis is more efficient than replication-based analysis for two-stage genomewide association studies. Nat Genet 2006;38:209-213.
-
(2006)
Nat Genet
, vol.38
, pp. 209-213
-
-
Skol, A.D.1
Scott, L.J.2
Abecasis, G.R.3
Boehnke, M.4
-
11
-
-
33745592507
-
Statistical false positive or true disease pathway?
-
Todd JA: Statistical false positive or true disease pathway? Nat Genet 2006;38:731-733.
-
(2006)
Nat Genet
, vol.38
, pp. 731-733
-
-
Todd, J.A.1
-
13
-
-
1642295096
-
Assessing the probability that a positive report is false: An approach for molecular epidemiology studies
-
Wacholder S, Chanock S, Garcia-Closas M, El Ghormli L, Rothman N: Assessing the probability that a positive report is false: An approach for molecular epidemiology studies. J Natl Cancer Inst 2004;96:434-442.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 434-442
-
-
Wacholder, S.1
Chanock, S.2
Garcia-Closas, M.3
El Ghormli, L.4
Rothman, N.5
-
14
-
-
0038813649
-
Genetic associations: False or true?
-
Ioannidis JP: Genetic associations: False or true? Trends Mol Med 2003;9:135-138.
-
(2003)
Trends Mol Med
, vol.9
, pp. 135-138
-
-
Ioannidis, J.P.1
-
15
-
-
20244380171
-
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: Complement factor H polymorphism in age-related macular degeneration. Science 2005;308:385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
Tsai, J.Y.4
Sackler, R.S.5
Haynes, C.6
Henning, A.K.7
SanGiovanni, J.P.8
Mane, S.M.9
Mayne, S.T.10
Bracken, M.B.11
Ferris, F.L.12
Ott, J.13
Barnstable, C.14
Hoh, J.15
-
16
-
-
33645825830
-
A common genetic variant is associated with adult and childhood obesity
-
Herbert A, Gerry NP, McQueen MB, Heid IM, Pfeufer A, Illig T, Wichmann HE, Meitinger T, Hunter D, Hu FB, Colditz G, Hinney A, Hebebrand J, Koberwitz K, Zhu X, Cooper R, Ardlie K, Lyon H, Hirschhorn JN, Laird NM, Lenburg ME, Lange C, Christman MF: A common genetic variant is associated with adult and childhood obesity. Science 2006;312:279-283.
-
(2006)
Science
, vol.312
, pp. 279-283
-
-
Herbert, A.1
Gerry, N.P.2
McQueen, M.B.3
Heid, I.M.4
Pfeufer, A.5
Illig, T.6
Wichmann, H.E.7
Meitinger, T.8
Hunter, D.9
Hu, F.B.10
Colditz, G.11
Hinney, A.12
Hebebrand, J.13
Koberwitz, K.14
Zhu, X.15
Cooper, R.16
Ardlie, K.17
Lyon, H.18
Hirschhorn, J.N.19
Laird, N.M.20
Lenburg, M.E.21
Lange, C.22
Christman, M.F.23
more..
-
17
-
-
27244451809
-
-
Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG: High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 2005;77:685-693.
-
Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG: High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 2005;77:685-693.
-
-
-
-
18
-
-
18744407845
-
Functional SNPs in the lymphotoxin-gene that are associated with susceptibility to myocardial infarction
-
Ozaki K, Ohnishi Y, Iida A, Skine A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, et al: Functional SNPs in the lymphotoxin-gene that are associated with susceptibility to myocardial infarction. Nat Genet 2002;32:650-654.
-
(2002)
Nat Genet
, vol.32
, pp. 650-654
-
-
Ozaki, K.1
Ohnishi, Y.2
Iida, A.3
Skine, A.4
Yamada, R.5
Tsunoda, T.6
Sato, H.7
Sato, H.8
Hori, M.9
Nakamura, Y.10
-
19
-
-
33751004690
-
A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration
-
Yang Z, Camp NJ, Sun H, Tong Z, Gibbs D, Cameron DJ, Chen H, Zhao Y, Pearson E, Li X, Chien J, Dewan A, Harmon J, Bernstein PS, Shridhar V, Zabriskie NA, Hoh J, Howes K, Zhang K: A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration. Science 2006;314:992-993.
-
(2006)
Science
, vol.314
, pp. 992-993
-
-
Yang, Z.1
Camp, N.J.2
Sun, H.3
Tong, Z.4
Gibbs, D.5
Cameron, D.J.6
Chen, H.7
Zhao, Y.8
Pearson, E.9
Li, X.10
Chien, J.11
Dewan, A.12
Harmon, J.13
Bernstein, P.S.14
Shridhar, V.15
Zabriskie, N.A.16
Hoh, J.17
Howes, K.18
Zhang, K.19
-
20
-
-
33745237158
-
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
-
Arking DE, Pfeufer A, Post W, Kao WH, Newton-Cheh C, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Gieger C, Guo CY, Larson MG, Wichmann HE, Marban E, O'Donnell CJ, Hirschhorn JN, Kaab S, Spooner PM, Meitinger T, Chakravarti A: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet 2006;38:644-651.
-
(2006)
Nat Genet
, vol.38
, pp. 644-651
-
-
Arking, D.E.1
Pfeufer, A.2
Post, W.3
Kao, W.H.4
Newton-Cheh, C.5
Ikeda, M.6
West, K.7
Kashuk, C.8
Akyol, M.9
Perz, S.10
Jalilzadeh, S.11
Illig, T.12
Gieger, C.13
Guo, C.Y.14
Larson, M.G.15
Wichmann, H.E.16
Marban, E.17
O'Donnell, C.J.18
Hirschhorn, J.N.19
Kaab, S.20
Spooner, P.M.21
Meitinger, T.22
Chakravarti, A.23
more..
-
21
-
-
33845340501
-
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: A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 2006;314:1461-1463.
-
(2006)
Science
, vol.314
, pp. 1461-1463
-
-
Duerr, R.H.1
Taylor, K.D.2
Brant, S.R.3
Rioux, J.D.4
Silverberg, M.S.5
Daly, M.J.6
Steinhart, A.H.7
Abraham, C.8
Regueiro, M.9
Griffiths, A.10
Dassopoulos, T.11
Bitton, A.12
Yang, H.13
Targan, S.14
Datta, L.W.15
Kistner, E.O.16
Schumm, L.P.17
Lee, A.T.18
Gregersen, P.K.19
Barmada, M.M.20
Rotter, J.I.21
Nicolae, D.L.22
Cho, J.H.23
more..
-
22
-
-
33750201885
-
CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and metaanalyses
-
Conley YP, Jakobsdottir J, Mah T, Weeks DE, Klein R, Kuller L, Ferrell RE, Gorin MB: CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and metaanalyses. Hum Mol Genet 2006;15:3206-3218.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3206-3218
-
-
Conley, Y.P.1
Jakobsdottir, J.2
Mah, T.3
Weeks, D.E.4
Klein, R.5
Kuller, L.6
Ferrell, R.E.7
Gorin, M.B.8
-
23
-
-
33746041795
-
Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration
-
Despriet DD, Klaver CC, Witteman JC, Bergen AA, Kardys I, de Maat MP, Boekhoorn SS, Vingerling JR, Hofman A, Oostra BA, Uitterlinden AG, Stijnen T, van Duijn CM, de Jong PT: Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration. JAMA 2006;296:301-309.
-
(2006)
JAMA
, vol.296
, pp. 301-309
-
-
Despriet, D.D.1
Klaver, C.C.2
Witteman, J.C.3
Bergen, A.A.4
Kardys, I.5
de Maat, M.P.6
Boekhoorn, S.S.7
Vingerling, J.R.8
Hofman, A.9
Oostra, B.A.10
Uitterlinden, A.G.11
Stijnen, T.12
van Duijn, C.M.13
de Jong, P.T.14
-
24
-
-
33845776114
-
No association of complement factor H gene polymorphism and age-related macular degeneration in the Japanese population
-
Uka J, Tamura H, Kobayashi T, Yamane K, Kawakami H, Minamoto A, Mishima HK: No association of complement factor H gene polymorphism and age-related macular degeneration in the Japanese population. Retina 2006;26:985-987.
-
(2006)
Retina
, vol.26
, pp. 985-987
-
-
Uka, J.1
Tamura, H.2
Kobayashi, T.3
Yamane, K.4
Kawakami, H.5
Minamoto, A.6
Mishima, H.K.7
-
25
-
-
33745728418
-
No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese
-
Gotoh N, Yamada R, Hiratani H, Renault V, Kuroiwa S, Monet M, Toyoda S, Chida S, Mandai M, Otani A, Yoshimura N, Matsuda F: No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese. Hum Genet 2006;120:139-143.
-
(2006)
Hum Genet
, vol.120
, pp. 139-143
-
-
Gotoh, N.1
Yamada, R.2
Hiratani, H.3
Renault, V.4
Kuroiwa, S.5
Monet, M.6
Toyoda, S.7
Chida, S.8
Mandai, M.9
Otani, A.10
Yoshimura, N.11
Matsuda, F.12
-
26
-
-
33846933276
-
-
Rosskopf D, Bornhorst A, Rimmbach C, Schwahn C, Kayser A, Kruger A, Tessmann G, Geissler I, Kroemer HK, Volzke H: Comment on 'A common genetic variant is associated with adult and childhood obesity'. Science 2007;315:187.
-
Rosskopf D, Bornhorst A, Rimmbach C, Schwahn C, Kayser A, Kruger A, Tessmann G, Geissler I, Kroemer HK, Volzke H: Comment on 'A common genetic variant is associated with adult and childhood obesity'. Science 2007;315:187.
-
-
-
-
27
-
-
33846936809
-
-
Loos RJ, Barroso I, O'rahilly S, Wareham NJ: Comment on 'A common genetic variant is associated with adult and childhood obesity'. Science 2007;315:187.
-
Loos RJ, Barroso I, O'rahilly S, Wareham NJ: Comment on 'A common genetic variant is associated with adult and childhood obesity'. Science 2007;315:187.
-
-
-
-
28
-
-
33846903056
-
-
Dina C, Meyre D, Samson C, Tichet J, Marre M, Jouret B, Charles MA, Balkau B, Froguel P: Comment on 'A common genetic variant is associated with adult and childhood obesity'. Science 2007;315:187.
-
Dina C, Meyre D, Samson C, Tichet J, Marre M, Jouret B, Charles MA, Balkau B, Froguel P: Comment on 'A common genetic variant is associated with adult and childhood obesity'. Science 2007;315:187.
-
-
-
-
29
-
-
33749667971
-
-
Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van Den Eeden SK, Wirdefeldt K, Zabetian CP, Dehem M, Montimurro JS, Southwick A, Myers RM, Trikalinos TA: Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study. Lancet Neurol 2006;5:917-923.
-
Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van Den Eeden SK, Wirdefeldt K, Zabetian CP, Dehem M, Montimurro JS, Southwick A, Myers RM, Trikalinos TA: Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study. Lancet Neurol 2006;5:917-923.
-
-
-
-
30
-
-
33746597102
-
Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study
-
Clarke R, Xu P, Bennett D, Lewington S, Zondervan K, Parish S, Palmer A, Clark S, Cardon L, Peto R, Lathrop M, Collins R: Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study. PLoS Genet 2006;2:e107.
-
(2006)
PLoS Genet
, vol.2
-
-
Clarke, R.1
Xu, P.2
Bennett, D.3
Lewington, S.4
Zondervan, K.5
Parish, S.6
Palmer, A.7
Clark, S.8
Cardon, L.9
Peto, R.10
Lathrop, M.11
Collins, R.12
-
31
-
-
0003505146
-
-
New York, Wiley
-
Sutton AJ, Abrams KR, Jones DR, Sheldon TA, Song F: Methods for Meta-Analysis in Medical Research. New York, Wiley, 2000, pp 205-228.
-
(2000)
Methods for Meta-Analysis in Medical Research
, pp. 205-228
-
-
Sutton, A.J.1
Abrams, K.R.2
Jones, D.R.3
Sheldon, T.A.4
Song, F.5
-
32
-
-
0035956651
-
Sifting the evidence-what's wrong with significance tests?
-
Sterne JA, Davey Smith G: Sifting the evidence-what's wrong with significance tests? BMJ 2001;322:226-231.
-
(2001)
BMJ
, vol.322
, pp. 226-231
-
-
Sterne, J.A.1
Davey Smith, G.2
-
35
-
-
33845336152
-
The balance between heritable and environmental aetiology of human disease
-
Hemminki K, Lorenzo Bermejo J, Forsti A: The balance between heritable and environmental aetiology of human disease. Nat Rev Genet 2006;7:958-965.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 958-965
-
-
Hemminki, K.1
Lorenzo Bermejo, J.2
Forsti, A.3
-
36
-
-
0142178215
-
New York Breast Cancer Study Group: Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
King MC, Marks JH, Mandell JB;New York Breast Cancer Study Group: Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 2003;302:643-646.
-
(2003)
Science
, vol.302
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
37
-
-
13744256264
-
Breast cancer risks for BRCA1/2 carriers
-
Easton DF, Hopper JL, Thomas DC, Antoniou A, Pharoah PD, Whittemore AS, Haile RW: Breast cancer risks for BRCA1/2 carriers. Science 2004;306:2187-2191.
-
(2004)
Science
, vol.306
, pp. 2187-2191
-
-
Easton, D.F.1
Hopper, J.L.2
Thomas, D.C.3
Antoniou, A.4
Pharoah, P.D.5
Whittemore, A.S.6
Haile, R.W.7
-
38
-
-
13744256264
-
Breast cancer risks for BRCA1/2 carriers
-
Wacholder S, Struewing JP, Hartge P, Greene MH, Tucker MA: Breast cancer risks for BRCA1/2 carriers. Science 2004;306:2187-2191.
-
(2004)
Science
, vol.306
, pp. 2187-2191
-
-
Wacholder, S.1
Struewing, J.P.2
Hartge, P.3
Greene, M.H.4
Tucker, M.A.5
-
39
-
-
33749571327
-
Commonly studied single-nucleotide polymorphisms and breast cancer: Results from the Breast Cancer Association Consortium
-
Breast Cancer Association Consortium
-
Breast Cancer Association Consortium. Commonly studied single-nucleotide polymorphisms and breast cancer: Results from the Breast Cancer Association Consortium. J Natl Cancer Inst 2006;98:1382-1396.
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1382-1396
-
-
-
40
-
-
33749570519
-
Common genetic variants for breast cancer: 32 largely refuted candidates and larger prospects
-
Ioannidis JP: Common genetic variants for breast cancer: 32 largely refuted candidates and larger prospects. J Natl Cancer Inst 2006;98:1350-1353.
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1350-1353
-
-
Ioannidis, J.P.1
-
41
-
-
33748680524
-
Genetic regulation of bone mass and susceptibility to osteoporosis
-
Ralston SH, de Crombrugghe B: Genetic regulation of bone mass and susceptibility to osteoporosis. Genes Dev 2006;20:2492-2506.
-
(2006)
Genes Dev
, vol.20
, pp. 2492-2506
-
-
Ralston, S.H.1
de Crombrugghe, B.2
-
42
-
-
33745279056
-
Evaluating coverage of genome-wide association studies
-
Barrett JC, Cardon LR: Evaluating coverage of genome-wide association studies. Nat Genet 2006;38:659-662.
-
(2006)
Nat Genet
, vol.38
, pp. 659-662
-
-
Barrett, J.C.1
Cardon, L.R.2
-
43
-
-
33646017447
-
Coverage and power in genomewide association studies
-
Jorgenson E, Witte JS: Coverage and power in genomewide association studies. Am J Hum Genet 2006;78:884-888.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 884-888
-
-
Jorgenson, E.1
Witte, J.S.2
-
44
-
-
33646375453
-
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies
-
Service S
-
Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, Varilo T, Peddle L, Rahman P, Piras G, Monne M, Murray S, Galver L, Peltonen L, Sabatti C, Collins A, Freimer N: Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nat Genet 2006;38:556-560.
-
(2006)
Nat Genet
, vol.38
, pp. 556-560
-
-
DeYoung, J.1
Karayiorgou, M.2
Roos, J.L.3
Pretorious, H.4
Bedoya, G.5
Ospina, J.6
Ruiz-Linares, A.7
Macedo, A.8
Palha, J.A.9
Heutink, P.10
Aulchenko, Y.11
Oostra, B.12
van Duijn, C.13
Jarvelin, M.R.14
Varilo, T.15
Peddle, L.16
Rahman, P.17
Piras, G.18
Monne, M.19
Murray, S.20
Galver, L.21
Peltonen, L.22
Sabatti, C.23
Collins, A.24
Freimer, N.25
more..
-
45
-
-
33749013001
-
Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases
-
Ioannidis JP, Trikalinos TA, Khoury MJ: Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases. Am J Epidemiol 2006;164:609-614.
-
(2006)
Am J Epidemiol
, vol.164
, pp. 609-614
-
-
Ioannidis, J.P.1
Trikalinos, T.A.2
Khoury, M.J.3
-
46
-
-
0003531985
-
-
2nd Edition, Oxford University Press
-
Kelsey JL, Whittemore AS, Evans AS, Thompson WD: Methods in observational epidemiology, 2nd Edition, Oxford University Press, 1996.
-
(1996)
Methods in observational epidemiology
-
-
Kelsey, J.L.1
Whittemore, A.S.2
Evans, A.S.3
Thompson, W.D.4
-
47
-
-
34447120975
-
-
Welcome Trust Case Control Consortium. Accessible at
-
Welcome Trust Case Control Consortium. Accessible at: http://www.wtccc.org.uk/.
-
-
-
-
48
-
-
30044440451
-
Genotyping errors: Causes, consequences and solutions
-
Pompanon F, Bonin A, Bellemain E, Taberlet P: Genotyping errors: causes, consequences and solutions. Nat Rev Genet 2005;6:847-859.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 847-859
-
-
Pompanon, F.1
Bonin, A.2
Bellemain, E.3
Taberlet, P.4
-
49
-
-
19944421744
-
Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studies
-
Kang SJ, Finch SJ, Haynes C, Gordon D: Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studies. Hum Hered 2004;58:139-144.
-
(2004)
Hum Hered
, vol.58
, pp. 139-144
-
-
Kang, S.J.1
Finch, S.J.2
Haynes, C.3
Gordon, D.4
-
50
-
-
25444509248
-
Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies
-
Edwards BJ, Haynes C, Levenstien MA, Finch SJ, Gordon D: Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies. BMC Genet 2005;6:18.
-
(2005)
BMC Genet
, vol.6
, pp. 18
-
-
Edwards, B.J.1
Haynes, C.2
Levenstien, M.A.3
Finch, S.J.4
Gordon, D.5
-
51
-
-
15544374093
-
The impact of diagnostic error on testing genetic association in case-control studies
-
Zheng G, Tian X: The impact of diagnostic error on testing genetic association in case-control studies. Stat Med 2005;24:869-882.
-
(2005)
Stat Med
, vol.24
, pp. 869-882
-
-
Zheng, G.1
Tian, X.2
-
52
-
-
1542401054
-
Estimation of magnitude in gene-environment interactions in the presence of measurement error
-
Wong MY, Day NE, Luan JA, Wareham NJ: Estimation of magnitude in gene-environment interactions in the presence of measurement error. Stat Med 2004;23:987-998.
-
(2004)
Stat Med
, vol.23
, pp. 987-998
-
-
Wong, M.Y.1
Day, N.E.2
Luan, J.A.3
Wareham, N.J.4
-
53
-
-
10844235506
-
Effect of population stratification on case-control association studies. II. False-positive rates and their limiting behavior as number of subpopulations increases
-
Gorroochurn P, Hodge SE, Heiman G, Greenberg DA: Effect of population stratification on case-control association studies. II. False-positive rates and their limiting behavior as number of subpopulations increases. Hum Hered 2004;58:40-48.
-
(2004)
Hum Hered
, vol.58
, pp. 40-48
-
-
Gorroochurn, P.1
Hodge, S.E.2
Heiman, G.3
Greenberg, D.A.4
-
54
-
-
31344454230
-
Hidden population substructures in an apparently homogeneous population bias association studies
-
Berger M, Stassen HH, Kohler K, Krane V, Monks D, Wanner C, Hoffmann K, Hoffmann MM, Zimmer M, Bickeboller H, Lindner TH: Hidden population substructures in an apparently homogeneous population bias association studies. Eur J Hum Genet 2006;14:236-244.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 236-244
-
-
Berger, M.1
Stassen, H.H.2
Kohler, K.3
Krane, V.4
Monks, D.5
Wanner, C.6
Hoffmann, K.7
Hoffmann, M.M.8
Zimmer, M.9
Bickeboller, H.10
Lindner, T.H.11
-
55
-
-
2442585696
-
The effects of human population structure on large genetic association studies
-
Marchini J, Cardon LR, Phillips MS, Donnelly P: The effects of human population structure on large genetic association studies. Nat Genet 2004;36:512-517.
-
(2004)
Nat Genet
, vol.36
, pp. 512-517
-
-
Marchini, J.1
Cardon, L.R.2
Phillips, M.S.3
Donnelly, P.4
-
56
-
-
10844267270
-
Effect of population stratification on case-control association studies. I. Elevation in false positive rates and comparison to confounding risk ratios (a simulation study)
-
Heiman GA, Hodge SE, Gorroochurn P, Zhang J, Greenberg DA: Effect of population stratification on case-control association studies. I. Elevation in false positive rates and comparison to confounding risk ratios (a simulation study). Hum Hered 2004;58:30-39.
-
(2004)
Hum Hered
, vol.58
, pp. 30-39
-
-
Heiman, G.A.1
Hodge, S.E.2
Gorroochurn, P.3
Zhang, J.4
Greenberg, D.A.5
-
58
-
-
27644546712
-
Population structure, differential bias and genomic control in a large-scale, case-control association study
-
Clayton DG, Walker NM, Smyth DJ, Pask R, Cooper JD, Maier LM, Smink LJ, Lam AC, Ovington NR, Stevens HE, Nutland S, Howson JM, Faham M, Moorhead M, Jones HB, Falkowski M, Hardenbol P, Willis TD, Todd JA: Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat Genet 2005;37:1243-1246.
-
(2005)
Nat Genet
, vol.37
, pp. 1243-1246
-
-
Clayton, D.G.1
Walker, N.M.2
Smyth, D.J.3
Pask, R.4
Cooper, J.D.5
Maier, L.M.6
Smink, L.J.7
Lam, A.C.8
Ovington, N.R.9
Stevens, H.E.10
Nutland, S.11
Howson, J.M.12
Faham, M.13
Moorhead, M.14
Jones, H.B.15
Falkowski, M.16
Hardenbol, P.17
Willis, T.D.18
Todd, J.A.19
-
59
-
-
0035528921
-
Genomic control, a new approach to genetic-based association studies
-
Devlin B, Roeder K, Wasserman L: Genomic control, a new approach to genetic-based association studies. Theor Popul Biol 2001;60:155-166.
-
(2001)
Theor Popul Biol
, vol.60
, pp. 155-166
-
-
Devlin, B.1
Roeder, K.2
Wasserman, L.3
-
60
-
-
33644824316
-
Case-control association tests correcting for population stratification
-
Kohler K, Bickeboller H: Case-control association tests correcting for population stratification. Ann Hum Genet 2006;70:98-115.
-
(2006)
Ann Hum Genet
, vol.70
, pp. 98-115
-
-
Kohler, K.1
Bickeboller, H.2
-
61
-
-
0842285687
-
Matching strategies for genetic association studies in structured populations
-
Hinds DA, Stokowski RP, Patil N, Konvicka K, Kershenobich D, Cox DR, Ballinger DG: Matching strategies for genetic association studies in structured populations. Am J Hum Genet 2004;74:317-325.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 317-325
-
-
Hinds, D.A.1
Stokowski, R.P.2
Patil, N.3
Konvicka, K.4
Kershenobich, D.5
Cox, D.R.6
Ballinger, D.G.7
-
62
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006;38:904-909.
-
(2006)
Nat Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
63
-
-
33846563409
-
Why most published research findings are false
-
Ioannidis JP: Why most published research findings are false. PLoS Med 2005;2:e124.
-
(2005)
PLoS Med
, vol.2
-
-
Ioannidis, J.P.1
-
64
-
-
0001677717
-
Controlling the false discovery rate - a practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y: Controlling the false discovery rate - a practical and powerful approach to multiple testing. J R Stat Soc B 1995;57:289-300.
-
(1995)
J R Stat Soc B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
65
-
-
4444294164
-
Improving false discovery rate estimation
-
Pounds S, Cheng C: Improving false discovery rate estimation. Bioinformatics 2004;20:1737-1745.
-
(2004)
Bioinformatics
, vol.20
, pp. 1737-1745
-
-
Pounds, S.1
Cheng, C.2
-
66
-
-
0141450364
-
False discoveries and models for gene discovery
-
van den Oord EJ, Sullivan PF: False discoveries and models for gene discovery. Trends Genet 2003;19:537-542.
-
(2003)
Trends Genet
, vol.19
, pp. 537-542
-
-
van den Oord, E.J.1
Sullivan, P.F.2
-
67
-
-
27544506863
-
Two-stage designs for experiments with a large number of hypotheses
-
Zehetmayer S, Bauer P, Posch M: Two-stage designs for experiments with a large number of hypotheses. Bioinformatics 2005;21:3771-3777.
-
(2005)
Bioinformatics
, vol.21
, pp. 3771-3777
-
-
Zehetmayer, S.1
Bauer, P.2
Posch, M.3
-
68
-
-
25144501575
-
Genetic association studies
-
Cordell HJ, Clayton DG: Genetic association studies. Lancet 2005;366:1121-1131.
-
(2005)
Lancet
, vol.366
, pp. 1121-1131
-
-
Cordell, H.J.1
Clayton, D.G.2
-
69
-
-
29444443206
-
-
Ioannidis JP, Gwinn M, Little J, Higgins JP, Bernstein JL, Boffetta P, Bondy M, Bray MS, Brenchley PE, Buffler PA, Casas JP, Chokkalingam A, Danesh J, Smith GD, Dolan S, Duncan R, Gruis NA, Hartge P, Hashibe M, Hunter DJ, Jarvelin MR, Malmer B, Maraganore DM, Newton-Bishop JA, O'Brien TR, Petersen G, Riboli E, Salanti G, Seminara D, Smeeth L, Taioli E, Timpson N, Uitterlinden AG, Vineis P, Wareham N, Winn DM, Zimmern R, Khoury MJ;Human Genome Epidemiology Network and the Network of Investigator Networks. A road map for efficient and reliable human genome epidemiology. Nat Genet 2006;38:3-5.
-
Ioannidis JP, Gwinn M, Little J, Higgins JP, Bernstein JL, Boffetta P, Bondy M, Bray MS, Brenchley PE, Buffler PA, Casas JP, Chokkalingam A, Danesh J, Smith GD, Dolan S, Duncan R, Gruis NA, Hartge P, Hashibe M, Hunter DJ, Jarvelin MR, Malmer B, Maraganore DM, Newton-Bishop JA, O'Brien TR, Petersen G, Riboli E, Salanti G, Seminara D, Smeeth L, Taioli E, Timpson N, Uitterlinden AG, Vineis P, Wareham N, Winn DM, Zimmern R, Khoury MJ;Human Genome Epidemiology Network and the Network of Investigator Networks. A road map for efficient and reliable human genome epidemiology. Nat Genet 2006;38:3-5.
-
-
-
-
70
-
-
0037103172
-
Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations
-
Little J, Bradley L, Bray MS, Clyne M, Dorman J, Ellsworth DL, Hanson J, Khoury M, Lau J, O'Brien TR, Rothman N, Stroup D, Taioli E, Thomas D, Vainio H, Wacholder S, Weinberg C: Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations. Am J Epidemiol 2002;156:300-310.
-
(2002)
Am J Epidemiol
, vol.156
, pp. 300-310
-
-
Little, J.1
Bradley, L.2
Bray, M.S.3
Clyne, M.4
Dorman, J.5
Ellsworth, D.L.6
Hanson, J.7
Khoury, M.8
Lau, J.9
O'Brien, T.R.10
Rothman, N.11
Stroup, D.12
Taioli, E.13
Thomas, D.14
Vainio, H.15
Wacholder, S.16
Weinberg, C.17
-
71
-
-
21744448518
-
Hardy-Weinberg equilibrium in genetic association studies: An empirical evaluation of reporting, deviations, and power
-
Salanti G, Amountza G, Ntzani EE, Ioannidis JP: Hardy-Weinberg equilibrium in genetic association studies: An empirical evaluation of reporting, deviations, and power. Eur J Hum Genet 2005;13:840-848.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 840-848
-
-
Salanti, G.1
Amountza, G.2
Ntzani, E.E.3
Ioannidis, J.P.4
-
72
-
-
33746869343
-
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease
-
Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Kruger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G, Hattori N, Kawakami H, Lambert JC, Lynch T, Mellick GD, Papapetropoulos S, Parsian A, Quattrone A, Riess O, Tan EK, Van Broeckhoven C: Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA 2006;296:661-670.
-
(2006)
JAMA
, vol.296
, pp. 661-670
-
-
Maraganore, D.M.1
de Andrade, M.2
Elbaz, A.3
Farrer, M.J.4
Ioannidis, J.P.5
Kruger, R.6
Rocca, W.A.7
Schneider, N.K.8
Lesnick, T.G.9
Lincoln, S.J.10
Hulihan, M.M.11
Aasly, J.O.12
Ashizawa, T.13
Chartier-Harlin, M.C.14
Checkoway, H.15
Ferrarese, C.16
Hadjigeorgiou, G.17
Hattori, N.18
Kawakami, H.19
Lambert, J.C.20
Lynch, T.21
Mellick, G.D.22
Papapetropoulos, S.23
Parsian, A.24
Quattrone, A.25
Riess, O.26
Tan, E.K.27
Van Broeckhoven, C.28
more..
-
74
-
-
79959524146
-
A haplotype map of the human genome
-
International HapMap Consortium
-
International HapMap Consortium. A haplotype map of the human genome. Nature 2005;437:1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
75
-
-
13844313862
-
Whole-genome patterns of common DNA variation in three human populations
-
Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR: Whole-genome patterns of common DNA variation in three human populations. Science 2005;307:1072-1079.
-
(2005)
Science
, vol.307
, pp. 1072-1079
-
-
Hinds, D.A.1
Stuve, L.L.2
Nilsen, G.B.3
Halperin, E.4
Eskin, E.5
Ballinger, D.G.6
Frazer, K.A.7
Cox, D.R.8
-
76
-
-
15944383403
-
Gene-environment interactions in human diseases
-
Hunter DJ: Gene-environment interactions in human diseases. Nat Rev Genet 2005;6:287-298.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 287-298
-
-
Hunter, D.J.1
-
78
-
-
23844512858
-
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: Results from the Spanish Bladder Cancer Study and meta-analyses
-
Garcia-Closas M, Malats N, Silverman D, Dosemeci M, Kogevinas M, Hein DW, Tardon A, Serra C, Carrato A, Garcia-Closas R, Lloreta J, Castano-Vinyals G, Yeager M, Welch R, Chanock S, Chatterjee N, Wacholder S, Samanic C, Tora M, Fernandez F, Real FX, Rothman N: NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: Results from the Spanish Bladder Cancer Study and meta-analyses. Lancet. 2005;366:649-659.
-
(2005)
Lancet
, vol.366
, pp. 649-659
-
-
Garcia-Closas, M.1
Malats, N.2
Silverman, D.3
Dosemeci, M.4
Kogevinas, M.5
Hein, D.W.6
Tardon, A.7
Serra, C.8
Carrato, A.9
Garcia-Closas, R.10
Lloreta, J.11
Castano-Vinyals, G.12
Yeager, M.13
Welch, R.14
Chanock, S.15
Chatterjee, N.16
Wacholder, S.17
Samanic, C.18
Tora, M.19
Fernandez, F.20
Real, F.X.21
Rothman, N.22
more..
-
79
-
-
33644864549
-
Genome-wide prediction of C. elegans genetic interactions
-
Zhong W, Sternberg PW: Genome-wide prediction of C. elegans genetic interactions. Science 2006;311:1481-1484.
-
(2006)
Science
, vol.311
, pp. 1481-1484
-
-
Zhong, W.1
Sternberg, P.W.2
-
80
-
-
0034662061
-
Heterogeneity and statistical significance in meta-analysis: An empirical study of 125 meta-analyses
-
Engels EA, Schmid CH, Terrin N, Olkin I, Lau J: Heterogeneity and statistical significance in meta-analysis: an empirical study of 125 meta-analyses. Stat Med 2000;19:1707-1728.
-
(2000)
Stat Med
, vol.19
, pp. 1707-1728
-
-
Engels, E.A.1
Schmid, C.H.2
Terrin, N.3
Olkin, I.4
Lau, J.5
-
81
-
-
0020963636
-
Tests for interaction in epidemiologic studies: A review and a study of power
-
Greenland S: Tests for interaction in epidemiologic studies: A review and a study of power. Stat Med 1983;2:243-251.
-
(1983)
Stat Med
, vol.2
, pp. 243-251
-
-
Greenland, S.1
-
82
-
-
33746910265
-
Concordance among gene-expression-based predictors for breast cancer
-
Fan C, Oh DS, Wessels L, Weigelt B, Nuyten DS, Nobel AB, van't Veer LJ, Perou CM: Concordance among gene-expression-based predictors for breast cancer. N Engl J Med 2006;355:560-569.
-
(2006)
N Engl J Med
, vol.355
, pp. 560-569
-
-
Fan, C.1
Oh, D.S.2
Wessels, L.3
Weigelt, B.4
Nuyten, D.S.5
Nobel, A.B.6
van't Veer, L.J.7
Perou, C.M.8
-
83
-
-
29644447778
-
Local literature bias in genetic epidemiology: An empirical evaluation of the Chinese literature
-
Pan Z, Trikalinos TA, Kavvoura FK, Lau J, Ioannidis JP: Local literature bias in genetic epidemiology: An empirical evaluation of the Chinese literature. PLoS Med 2005;2:e334.
-
(2005)
PLoS Med
, vol.2
-
-
Pan, Z.1
Trikalinos, T.A.2
Kavvoura, F.K.3
Lau, J.4
Ioannidis, J.P.5
-
84
-
-
33750699026
-
The publication process itself was the major cause of publication bias in genetic epidemiology
-
Calnan M, Smith GD, Sterne JA: The publication process itself was the major cause of publication bias in genetic epidemiology. J Clin Epidemiol 2006;59:1312-1318.
-
(2006)
J Clin Epidemiol
, vol.59
, pp. 1312-1318
-
-
Calnan, M.1
Smith, G.D.2
Sterne, J.A.3
-
85
-
-
33947647431
-
Selection in reported epidemiological risks: An empirical assessment
-
Kavvoura FK, Liberopoulos G, Ioannidis JP: Selection in reported epidemiological risks: An empirical assessment. PLoS Med 2007;4:e79.
-
(2007)
PLoS Med
, vol.4
-
-
Kavvoura, F.K.1
Liberopoulos, G.2
Ioannidis, J.P.3
-
86
-
-
33645504222
-
Journals should publish all 'null' results and should sparingly publish 'positive' results
-
Ioannidis JP: Journals should publish all 'null' results and should sparingly publish 'positive' results. Cancer Epidemiol Biomarkers Prev 2006;15:186.
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 186
-
-
Ioannidis, J.P.1
-
87
-
-
34347364119
-
Meta-analysis in genome-wide association datasets: Strategies and application in Parkinson disease
-
Feb 7;
-
Evangelou E, Maraganore DM, Ioannidis JP: Meta-analysis in genome-wide association datasets: Strategies and application in Parkinson disease. PLoS ONE. 2007 Feb 7;2:e196.
-
(2007)
PLoS ONE
, vol.2
-
-
Evangelou, E.1
Maraganore, D.M.2
Ioannidis, J.P.3
|