-
1
-
-
26244444318
-
A question of standards: What makes a good genetic association study?
-
Hattersley AT, McCarthy MI: A question of standards: what makes a good genetic association study? Lancet 366:1315-1323, 2005
-
(2005)
Lancet
, vol.366
, pp. 1315-1323
-
-
Hattersley, A.T.1
McCarthy, M.I.2
-
2
-
-
12344279952
-
Genetic factors in type 2 diabetes: The end of the beginning?
-
O'Rahilly S, Barroso I, Wareham NJ: Genetic factors in type 2 diabetes: the end of the beginning? Science 307:370-373, 2005
-
(2005)
Science
, vol.307
, pp. 370-373
-
-
O'Rahilly, S.1
Barroso, I.2
Wareham, N.J.3
-
3
-
-
3543008338
-
Candidate genes for type 2 diabetes
-
(Review)
-
Parikh H, Groop L: Candidate genes for type 2 diabetes (Review). Rev Endocr Metab Disord 5:151-176, 2004
-
(2004)
Rev Endocr Metab Disord
, vol.5
, pp. 151-176
-
-
Parikh, H.1
Groop, L.2
-
4
-
-
0033624575
-
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, Vohl MC, Nemesh J, Lane CR, Schaffner SF, Bolk S, Brewer C, Tuomi T, Gaudet D, Hudson TJ, Daly M, Groop L, Lander ES: The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 26:76-80, 2000
-
(2000)
Nat Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.C.5
Nemesh, J.6
Lane, C.R.7
Schaffner, S.F.8
Bolk, S.9
Brewer, C.10
Tuomi, T.11
Gaudet, D.12
Hudson, T.J.13
Daly, M.14
Groop, L.15
Lander, E.S.16
-
5
-
-
0037317981
-
ATP channel subunits Kir6.2 KCNJ11 and SUR1 (ABCC8) confirm that the (KCNJ11) E23K variant is associated with type 2 diabetes
-
ATP channel subunits Kir6.2 KCNJ11 and SUR1 (ABCC8) confirm that the (KCNJ11) E23K variant is associated with type 2 diabetes. Diabetes 52:568-572, 2003
-
(2003)
Diabetes
, vol.52
, pp. 568-572
-
-
Gloyn, A.L.1
Weedon, M.N.2
Owen, K.R.3
Turner, M.J.4
Knight, B.A.5
Hitman, G.A.6
Walker, M.7
Levy, J.C.8
Sampson, M.J.9
Halford, S.10
McCarthy, M.I.11
Hattersley, A.T.12
Frayling, T.M.13
-
6
-
-
32544451924
-
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
-
Grant SF, Thorleifsson G, Reynisdottir I, Benediktsson R, Manolescu A, Sainz J, Helgason A, Stefansson H, Emilsson V, Helgadottir A, Styrkarsdottir U, Magnusson KP, Walters GB, Palsdottir E, Jonsdottir T, Gudmundsdottir T, Gylfason A, Saemundsdottir J, Wilensky RL, Reilly MP, Rader DJ, Bagger Y, Christiansen C, Gudnason V, Sigurdsson G, Thorsteinsdottir U, Gulcher JR, Kong A, Stefansson K: Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat Genet 38:320-323, 2006
-
(2006)
Nat Genet
, vol.38
, pp. 320-323
-
-
Grant, S.F.1
Thorleifsson, G.2
Reynisdottir, I.3
Benediktsson, R.4
Manolescu, A.5
Sainz, J.6
Helgason, A.7
Stefansson, H.8
Emilsson, V.9
Helgadottir, A.10
Styrkarsdottir, U.11
Magnusson, K.P.12
Walters, G.B.13
Palsdottir, E.14
Jonsdottir, T.15
Gudmundsdottir, T.16
Gylfason, A.17
Saemundsdottir, J.18
Wilensky, R.L.19
Reilly, M.P.20
Rader, D.J.21
Bagger, Y.22
Christiansen, C.23
Gudnason, V.24
Sigurdsson, G.25
Thorsteinsdottir, U.26
Gulcher, J.R.27
Kong, A.28
Stefansson, K.29
more..
-
7
-
-
0042666793
-
Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2
-
Reynisdottir I, Thorleifsson G, Benediktsson R, Sigurdsson G, Emilsson V, Einarsdottir AS, Hjorleifdottir EE, Orlygsdottir GT, Bjornsdottir GT, Saemundsdottir J, Halldorsson S, Hrafnkelsdottir S, Sigurjonsdottir SB, Steinsdottir S, Martin M, Kochan JP, Rhees BK, Grant SFA, Frigge ML, Kong A, Gudnason V, Stefansson K, Gulcher JR: Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. Am J Hum Genet 73:323-335, 2003
-
(2003)
Am J Hum Genet
, vol.73
, pp. 323-335
-
-
Reynisdottir, I.1
Thorleifsson, G.2
Benediktsson, R.3
Sigurdsson, G.4
Emilsson, V.5
Einarsdottir, A.S.6
Hjorleifdottir, E.E.7
Orlygsdottir, G.T.8
Bjornsdottir, G.T.9
Saemundsdottir, J.10
Halldorsson, S.11
Hrafnkelsdottir, S.12
Sigurjonsdottir, S.B.13
Steinsdottir, S.14
Martin, M.15
Kochan, J.P.16
Rhees, B.K.17
Grant, S.F.A.18
Frigge, M.L.19
Kong, A.20
Gudnason, V.21
Stefansson, K.22
Gulcher, J.R.23
more..
-
8
-
-
24944592012
-
Replication publication
-
(Editorial)
-
Patterson M, Cardon LR: Replication publication (Editorial). PLoS Biol 3:e327, 2005
-
(2005)
PLoS Biol
, vol.3
-
-
Patterson, M.1
Cardon, L.R.2
-
9
-
-
0142059667
-
"Are we there yet?" Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits
-
(Review)
-
Page GP, George V, Page PZ, Allison DB: "Are we there yet?" Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits (Review). Am J Hum Genet 73:711-719, 2003
-
(2003)
Am J Hum Genet
, vol.73
, pp. 711-719
-
-
Page, G.P.1
George, V.2
Page, P.Z.3
Allison, D.B.4
-
10
-
-
0036517472
-
A comprehensive review of genetic association studies
-
Hirschhorn JN, Lohmueller K, Byrne E, Hirschhorn K: A comprehensive review of genetic association studies. Genet Med 4:45-61, 2002
-
(2002)
Genet Med
, vol.4
, pp. 45-61
-
-
Hirschhorn, J.N.1
Lohmueller, K.2
Byrne, E.3
Hirschhorn, K.4
-
11
-
-
0034893106
-
A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): Analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q
-
Wiltshire S, Hattersley AT, Hitman GA, Walker M, Levy JC, Sampson M, O'Rahilly S, Frayling TM, Bell JI, Lathrop GM, Bennett A, Dhillon R, Fletcher C, Groves CJ, Jones E, Prestwich P, Simecek N, Rao PV, Wishart M, Foxon R, Bottazzo GF, Howell S, Smedley D, Cardon LR, Menzel S, McCarthy MI: A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q. Am J Hum Genet 69:553-569, 2001
-
(2001)
Am J Hum Genet
, vol.69
, pp. 553-569
-
-
Wiltshire, S.1
Hattersley, A.T.2
Hitman, G.A.3
Walker, M.4
Levy, J.C.5
Sampson, M.6
O'Rahilly, S.7
Frayling, T.M.8
Bell, J.I.9
Lathrop, G.M.10
Bennett, A.11
Dhillon, R.12
Fletcher, C.13
Groves, C.J.14
Jones, E.15
Prestwich, P.16
Simecek, N.17
Rao, P.V.18
Wishart, M.19
Foxon, R.20
Bottazzo, G.F.21
Howell, S.22
Smedley, D.23
Cardon, L.R.24
Menzel, S.25
McCarthy, M.I.26
more..
-
12
-
-
7044229728
-
Common variants of the hepatocyte nuclear factor-4{alpha} P2 promoter are associated with type 2 diabetes in the U.K. population
-
Weedon MN, Owen KR, Shields B, Hitman G, Walker M, McCarthy MI, Love-Gregory LD, Permutt MA, Hattersley AT, Frayling TM: Common variants of the hepatocyte nuclear factor-4{alpha} P2 promoter are associated with type 2 diabetes in the U.K. population. Diabetes 53:3002-3006, 2004
-
(2004)
Diabetes
, vol.53
, pp. 3002-3006
-
-
Weedon, M.N.1
Owen, K.R.2
Shields, B.3
Hitman, G.4
Walker, M.5
McCarthy, M.I.6
Love-Gregory, L.D.7
Permutt, M.A.8
Hattersley, A.T.9
Frayling, T.M.10
-
13
-
-
0033499355
-
Parent-offspring trios: A resource to facilitate the identification of type 2 diabetes genes
-
Frayling T, Walker M, McCarthy M, Evans J, Allen L, Lynn S, Ayres S, Millauer B, Turner C, Turner R, Sampson M, Hitman G, Ellard S, Hattersley A: Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes. Diabetes 48:2475-2479, 1999
-
(1999)
Diabetes
, vol.48
, pp. 2475-2479
-
-
Frayling, T.1
Walker, M.2
McCarthy, M.3
Evans, J.4
Allen, L.5
Lynn, S.6
Ayres, S.7
Millauer, B.8
Turner, C.9
Turner, R.10
Sampson, M.11
Hitman, G.12
Ellard, S.13
Hattersley, A.14
-
14
-
-
0036227462
-
Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations
-
Minton JA, Hattersley AT, Owen K, McCarthy MI, Walker M, Latif F, Barrett T, Frayling TM: Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations. Diabetes 51:1287-1290, 2002
-
(2002)
Diabetes
, vol.51
, pp. 1287-1290
-
-
Minton, J.A.1
Hattersley, A.T.2
Owen, K.3
McCarthy, M.I.4
Walker, M.5
Latif, F.6
Barrett, T.7
Frayling, T.M.8
-
15
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F: Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 25:115-121, 2003
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
17
-
-
1542374068
-
Assessing whether an allele can account in part for a linkage signal: The Genotype-IBD Sharing Test (GIST)
-
Li C, Scott LJ, Boehnke M: Assessing whether an allele can account in part for a linkage signal: the Genotype-IBD Sharing Test (GIST). Am J Hum Genet 74:418-431, 2004
-
(2004)
Am J Hum Genet
, vol.74
, pp. 418-431
-
-
Li, C.1
Scott, L.J.2
Boehnke, M.3
-
18
-
-
1842526874
-
Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification
-
(Review)
-
McCarthy MI: Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification (Review). Hum Mol Genet 13:R33-R41, 2004
-
(2004)
Hum Mol Genet
, vol.13
-
-
McCarthy, M.I.1
-
19
-
-
2342633204
-
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
-
Gloyn AL, Pearson ER, Antcliff JF, Proks P, Bruining GJ, Slingerland AS, Howard N, Srinivasan S, Silva JM, Molnes J, Edghill EL, Frayling TM, Temple IK, Mackay D, Shield JP, Sumnik Z, van Rhijn A, Wales JK, Clark P, Gorman S, Aisenberg J, Ellard S, Njolstad PR, Ashcroft FM, Hattersley AT: Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 350:1838-1849, 2004
-
(2004)
N Engl J Med
, vol.350
, pp. 1838-1849
-
-
Gloyn, A.L.1
Pearson, E.R.2
Antcliff, J.F.3
Proks, P.4
Bruining, G.J.5
Slingerland, A.S.6
Howard, N.7
Srinivasan, S.8
Silva, J.M.9
Molnes, J.10
Edghill, E.L.11
Frayling, T.M.12
Temple, I.K.13
Mackay, D.14
Shield, J.P.15
Sumnik, Z.16
Van Rhijn, A.17
Wales, J.K.18
Clark, P.19
Gorman, S.20
Aisenberg, J.21
Ellard, S.22
Njolstad, P.R.23
Ashcroft, F.M.24
Hattersley, A.T.25
more..
-
20
-
-
33748333167
-
HLA genotyping supports a nonautoimmune aetiology in patients diagnosed with diabetes under the age of 6 months
-
Edghill EL, Dix RJ, Flanagan SE, Bingley PJ, Hattersley AT, Ellard S, Gillespie KM: HLA genotyping supports a nonautoimmune aetiology in patients diagnosed with diabetes under the age of 6 months. Diabetes 55:1895-1898, 2006
-
(2006)
Diabetes
, vol.55
, pp. 1895-1898
-
-
Edghill, E.L.1
Dix, R.J.2
Flanagan, S.E.3
Bingley, P.J.4
Hattersley, A.T.5
Ellard, S.6
Gillespie, K.M.7
-
21
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN: Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet 33:177-182, 2003
-
(2003)
Nat Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
22
-
-
27544432314
-
How many genes underlie the occurrence of common complex diseases in the population?
-
Yang Q, Khoury MJ, Friedman JM, Little J, Flanders WD: How many genes underlie the occurrence of common complex diseases in the population? Int J Epidemiol 34:1129-1137, 2005
-
(2005)
Int J Epidemiol
, vol.34
, pp. 1129-1137
-
-
Yang, Q.1
Khoury, M.J.2
Friedman, J.M.3
Little, J.4
Flanders, W.D.5
-
23
-
-
0032427048
-
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. I. DNA pooling
-
Risch N, Teng J: The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. I. DNA pooling. Genome Res 8:1273-1288, 1998
-
(1998)
Genome Res
, vol.8
, pp. 1273-1288
-
-
Risch, N.1
Teng, J.2
-
24
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K: The future of genetic studies of complex human diseases. Science 273:1516-1517, 1996
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
|