-
1
-
-
0003564810
-
Centers for Disease Control and Prevention
-
Centers for Disease Control and Prevention. [http://www.cdc.gov].
-
-
-
-
2
-
-
34247851021
-
The epidemiology of obesity
-
10.1053/j.gastro.2007.03.052, 17498505
-
Ogden CL, Yanovski SZ, Carroll MD, Flegal KM. The epidemiology of obesity. Gastroenterology 2007, 132(6):2087-2102. 10.1053/j.gastro.2007.03.052, 17498505.
-
(2007)
Gastroenterology
, vol.132
, Issue.6
, pp. 2087-2102
-
-
Ogden, C.L.1
Yanovski, S.Z.2
Carroll, M.D.3
Flegal, K.M.4
-
3
-
-
84857883645
-
Obesity and cardiovascular disease
-
10.1161/CIRCULATIONAHA.111.022541, 3693443, 22392865
-
Apovian C, Gokce N. Obesity and cardiovascular disease. Circulation 2012, 125(9):1178-1182. 10.1161/CIRCULATIONAHA.111.022541, 3693443, 22392865.
-
(2012)
Circulation
, vol.125
, Issue.9
, pp. 1178-1182
-
-
Apovian, C.1
Gokce, N.2
-
4
-
-
84858702540
-
The worldwide epidemiology of type 2 diabetes mellitus-present and future perspectives
-
10.1038/nrendo.2011.183, 22064493
-
Chen L, Magliano D, Zimmet P. The worldwide epidemiology of type 2 diabetes mellitus-present and future perspectives. Nat Rev Endocrinol 2011, 8(4):228. 10.1038/nrendo.2011.183, 22064493.
-
(2011)
Nat Rev Endocrinol
, vol.8
, Issue.4
, pp. 228
-
-
Chen, L.1
Magliano, D.2
Zimmet, P.3
-
5
-
-
85027950107
-
Metabolic diseases and cancer risk
-
10.1097/CCO.0b013e32834e0582, 22123235
-
Faulds M, Dahlman Wright K. Metabolic diseases and cancer risk. Curr Opin Oncol 2012, 24(1):58-61. 10.1097/CCO.0b013e32834e0582, 22123235.
-
(2012)
Curr Opin Oncol
, vol.24
, Issue.1
, pp. 58-61
-
-
Faulds, M.1
Dahlman Wright, K.2
-
6
-
-
0030843960
-
Genetic and environmental factors in relative body weight and human adiposity
-
10.1023/A:1025635913927, 9519560
-
Maes HH, Neale MC, Eaves LJ. Genetic and environmental factors in relative body weight and human adiposity. Behav Genet 1997, 27(4):325-351. 10.1023/A:1025635913927, 9519560.
-
(1997)
Behav Genet
, vol.27
, Issue.4
, pp. 325-351
-
-
Maes, H.H.1
Neale, M.C.2
Eaves, L.J.3
-
7
-
-
70849120493
-
Recent progress in the genetics of common obesity
-
10.1111/j.1365-2125.2009.03523.x, 2810793, 20002076
-
Loos RJF. Recent progress in the genetics of common obesity. Br J Clin Pharmacol 2009, 68(6):811. 10.1111/j.1365-2125.2009.03523.x, 2810793, 20002076.
-
(2009)
Br J Clin Pharmacol
, vol.68
, Issue.6
, pp. 811
-
-
Loos, R.J.F.1
-
8
-
-
80155182174
-
Developments in obesity genetics in the era of genome-wide association studies
-
10.1159/000332158, 22056736
-
Day F, Loos RJF. Developments in obesity genetics in the era of genome-wide association studies. J Nutrigenet Nutrigenomics 2011, 4(4):222-238. 10.1159/000332158, 22056736.
-
(2011)
J Nutrigenet Nutrigenomics
, vol.4
, Issue.4
, pp. 222-238
-
-
Day, F.1
Loos, R.J.F.2
-
9
-
-
78049337953
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
-
10.1038/ng.686, 3014648, 20935630
-
Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Magi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segre AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpelainen TO, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 2010, 42(11):937. 10.1038/ng.686, 3014648, 20935630.
-
(2010)
Nat Genet
, vol.42
, Issue.11
, pp. 937
-
-
Speliotes, E.K.1
Willer, C.J.2
Berndt, S.I.3
Monda, K.L.4
Thorleifsson, G.5
Jackson, A.U.6
Lango Allen, H.7
Lindgren, C.M.8
Luan, J.9
Magi, R.10
Randall, J.C.11
Vedantam, S.12
Winkler, T.W.13
Qi, L.14
Workalemahu, T.15
Heid, I.M.16
Steinthorsdottir, V.17
Stringham, H.M.18
Weedon, M.N.19
Wheeler, E.20
Wood, A.R.21
Ferreira, T.22
Weyant, R.J.23
Segre, A.V.24
Estrada, K.25
Liang, L.26
Nemesh, J.27
Park, J.H.28
Gustafsson, S.29
Kilpelainen, T.O.30
more..
-
10
-
-
77954168060
-
Genome-wide association of anthropometric traits in African- and African-derived populations; Human molecular genetics
-
10.1093/hmg/ddq154, 2883343, 20400458
-
Kang SJ, Chiang CW, Palmer CD, Tayo BO, Lettre G, Butler JL, Hackett R, Adeyemo AA, Guiducci C, Berzins I, Nguyen TT, Feng T, Luke A, Shriner D, Ardlie K, Rotimi C, Wilks R, Forrester T, McKenzie CA, Lyon HN, Cooper RS, Zhu X, Hirschhorn JN. Genome-wide association of anthropometric traits in African- and African-derived populations; Human molecular genetics. Hum Mol Genet 2010, 19:2725-38. 10.1093/hmg/ddq154, 2883343, 20400458.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 2725-2738
-
-
Kang, S.J.1
Chiang, C.W.2
Palmer, C.D.3
Tayo, B.O.4
Lettre, G.5
Butler, J.L.6
Hackett, R.7
Adeyemo, A.A.8
Guiducci, C.9
Berzins, I.10
Nguyen, T.T.11
Feng, T.12
Luke, A.13
Shriner, D.14
Ardlie, K.15
Rotimi, C.16
Wilks, R.17
Forrester, T.18
McKenzie, C.A.19
Lyon, H.N.20
Cooper, R.S.21
Zhu, X.22
Hirschhorn, J.N.23
more..
-
11
-
-
84857685319
-
Genome-wide association of BMI in African Americans
-
10.1038/oby.2011.154, 3291470, 21701570
-
Ng MC, Hester JM, Wing MR, Li J, Xu J, Hicks PJ, Roh BH, Lu L, Divers J, Langefeld CD, Freedman BI, Palmer ND, Bowden DW. Genome-wide association of BMI in African Americans. Obesity (Silver Spring) 2012, 20(3):622-627. 10.1038/oby.2011.154, 3291470, 21701570.
-
(2012)
Obesity (Silver Spring)
, vol.20
, Issue.3
, pp. 622-627
-
-
Ng, M.C.1
Hester, J.M.2
Wing, M.R.3
Li, J.4
Xu, J.5
Hicks, P.J.6
Roh, B.H.7
Lu, L.8
Divers, J.9
Langefeld, C.D.10
Freedman, B.I.11
Palmer, N.D.12
Bowden, D.W.13
-
12
-
-
84858282155
-
Implication of European-derived adiposity loci in African Americans
-
Hester JM, Wing MR, Li J, Palmer ND, Xu J, Hicks PJ, Roh BH, Norris JM, Wagenknecht LE, Langefeld CD, Freedman BI, Bowden DW, Ng MCY. Implication of European-derived adiposity loci in African Americans. Int J Obes 2012, 36(3):465-473.
-
(2012)
Int J Obes
, vol.36
, Issue.3
, pp. 465-473
-
-
Hester, J.M.1
Wing, M.R.2
Li, J.3
Palmer, N.D.4
Xu, J.5
Hicks, P.J.6
Roh, B.H.7
Norris, J.M.8
Wagenknecht, L.E.9
Langefeld, C.D.10
Freedman, B.I.11
Bowden, D.W.12
Ng, M.C.Y.13
-
13
-
-
84873504695
-
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study
-
10.1371/journal.pgen.1003171, 3547789, 23341774
-
Peters U, North KE, Sethupathy P, Buyske S, Haessler J, Jiao S, Fesinmeyer MD, Jackson RD, Kuller LH, Rajkovic A, Lim U, Cheng I, Schumacher F, Wilkens L, Li R, Monda K, Ehret G, Nguyen KD, Cooper R, Lewis CE, Leppert M, Irvin MR, Gu CC, Houston D, Buzkova P, Ritchie M, Matise TC, Le Marchand L, Hindorff LA, Crawford DC, et al. A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. PLoS Genet 2013, 9(1):e1003171. 10.1371/journal.pgen.1003171, 3547789, 23341774.
-
(2013)
PLoS Genet
, vol.9
, Issue.1
-
-
Peters, U.1
North, K.E.2
Sethupathy, P.3
Buyske, S.4
Haessler, J.5
Jiao, S.6
Fesinmeyer, M.D.7
Jackson, R.D.8
Kuller, L.H.9
Rajkovic, A.10
Lim, U.11
Cheng, I.12
Schumacher, F.13
Wilkens, L.14
Li, R.15
Monda, K.16
Ehret, G.17
Nguyen, K.D.18
Cooper, R.19
Lewis, C.E.20
Leppert, M.21
Irvin, M.R.22
Gu, C.C.23
Houston, D.24
Buzkova, P.25
Ritchie, M.26
Matise, T.C.27
Le Marchand, L.28
Hindorff, L.A.29
Crawford, D.C.30
more..
-
14
-
-
84878720938
-
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
-
10.1038/ng.2608, 3694490, 23583978
-
Monda KL, Chen GK, Taylor KC, Palmer C, Edwards TL, Lange LA, Ng MCY, Adeyemo AA, Allison MA, Bielak LF, Chen G, Graff M, Irvin MR, Rhie SK, Li G, Liu Y, Liu Y, Lu Y, Nalls MA, Sun YV, Wojczynski MK, Yanek LR, Aldrich MC, Ademola A, Amos CI, Bandera EV, Bock CH, Britton A, Broeckel U, Cai Q, et al. A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Nat Genet 2013, 45(6):690-696. 10.1038/ng.2608, 3694490, 23583978.
-
(2013)
Nat Genet
, vol.45
, Issue.6
, pp. 690-696
-
-
Monda, K.L.1
Chen, G.K.2
Taylor, K.C.3
Palmer, C.4
Edwards, T.L.5
Lange, L.A.6
Ng, M.C.Y.7
Adeyemo, A.A.8
Allison, M.A.9
Bielak, L.F.10
Chen, G.11
Graff, M.12
Irvin, M.R.13
Rhie, S.K.14
Li, G.15
Liu, Y.16
Liu, Y.17
Lu, Y.18
Nalls, M.A.19
Sun, Y.V.20
Wojczynski, M.K.21
Yanek, L.R.22
Aldrich, M.C.23
Ademola, A.24
Amos, C.I.25
Bandera, E.V.26
Bock, C.H.27
Britton, A.28
Broeckel, U.29
Cai, Q.30
more..
-
15
-
-
79957588287
-
Genome partitioning of genetic variation for complex traits using common SNPs
-
10.1038/ng.823, 21552263
-
Yang J, Manolio T, Pasquale L, Boerwinkle E, Caporaso N, Cunningham J, De Andrade M, Feenstra B, Feingold E, Hayes MG, Hill W, Landi M, Alonso A, Lettre G, Lin P, Ling H, Lowe W, Mathias R, Melbye M, Pugh E, Cornelis M, Weir B, Goddard M, Visscher P. Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet 2011, 43(6):519-525. 10.1038/ng.823, 21552263.
-
(2011)
Nat Genet
, vol.43
, Issue.6
, pp. 519-525
-
-
Yang, J.1
Manolio, T.2
Pasquale, L.3
Boerwinkle, E.4
Caporaso, N.5
Cunningham, J.6
De Andrade, M.7
Feenstra, B.8
Feingold, E.9
Hayes, M.G.10
Hill, W.11
Landi, M.12
Alonso, A.13
Lettre, G.14
Lin, P.15
Ling, H.16
Lowe, W.17
Mathias, R.18
Melbye, M.19
Pugh, E.20
Cornelis, M.21
Weir, B.22
Goddard, M.23
Visscher, P.24
more..
-
16
-
-
34147154100
-
Medical sequencing at the extremes of human body mass
-
10.1086/513471, 1852707, 17357083
-
Ahituv N, Kavaslar N, Schackwitz W, Ustaszewska A, Martin J, Hebert S, Doelle H, Ersoy B, Kryukov G, Schmidt S, Yosef N, Ruppin E, Sharan R, Vaisse C, Sunyaev S, Dent R, Cohen J, McPherson R, Pennacchio L. Medical sequencing at the extremes of human body mass. Am J Hum Genet 2007, 80(4):779-791. 10.1086/513471, 1852707, 17357083.
-
(2007)
Am J Hum Genet
, vol.80
, Issue.4
, pp. 779-791
-
-
Ahituv, N.1
Kavaslar, N.2
Schackwitz, W.3
Ustaszewska, A.4
Martin, J.5
Hebert, S.6
Doelle, H.7
Ersoy, B.8
Kryukov, G.9
Schmidt, S.10
Yosef, N.11
Ruppin, E.12
Sharan, R.13
Vaisse, C.14
Sunyaev, S.15
Dent, R.16
Cohen, J.17
McPherson, R.18
Pennacchio, L.19
-
17
-
-
76249116215
-
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
-
10.1038/nature08727, 2880448, 20130649
-
Walters RG, Jacquemont S, Valsesia A, De Smith AJ, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa JS, Chèvre J, Lecoeur C, Vatin V, Bouquillon S, Buxton JL, Boute O, Holder-Espinasse M, Cuisset J, Lemaitre M, Ambresin A, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, et al. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. Nature 2010, 463(7281):671. 10.1038/nature08727, 2880448, 20130649.
-
(2010)
Nature
, vol.463
, Issue.7281
, pp. 671
-
-
Walters, R.G.1
Jacquemont, S.2
Valsesia, A.3
De Smith, A.J.4
Martinet, D.5
Andersson, J.6
Falchi, M.7
Chen, F.8
Andrieux, J.9
Lobbens, S.10
Delobel, B.11
Stutzmann, F.12
El-Sayed Moustafa, J.S.13
Chèvre, J.14
Lecoeur, C.15
Vatin, V.16
Bouquillon, S.17
Buxton, J.L.18
Boute, O.19
Holder-Espinasse, M.20
Cuisset, J.21
Lemaitre, M.22
Ambresin, A.23
Brioschi, A.24
Gaillard, M.25
Giusti, V.26
Fellmann, F.27
Ferrarini, A.28
Hadjikhani, N.29
Campion, D.30
more..
-
18
-
-
76349083132
-
Large, rare chromosomal deletions associated with severe early-onset obesity
-
10.1038/nature08689, 3108883, 19966786
-
Bochukova E, Huang N, Keogh J, Henning E, Purmann C, Blaszczyk K, Saeed S, Hamilton-Shield J, Clayton-Smith J, O'Rahilly S, Hurles M, Farooqi IS. Large, rare chromosomal deletions associated with severe early-onset obesity. Nature 2010, 463(7281):666. 10.1038/nature08689, 3108883, 19966786.
-
(2010)
Nature
, vol.463
, Issue.7281
, pp. 666
-
-
Bochukova, E.1
Huang, N.2
Keogh, J.3
Henning, E.4
Purmann, C.5
Blaszczyk, K.6
Saeed, S.7
Hamilton-Shield, J.8
Clayton-Smith, J.9
O'Rahilly, S.10
Hurles, M.11
Farooqi, I.S.12
-
19
-
-
77957606877
-
Large copy-number variations are enriched in cases with moderate to extreme obesity
-
10.2337/db10-0192, 3279563, 20622171
-
Wang K, Li W, Glessner J, Grant SFA, Hakonarson H, Price RA. Large copy-number variations are enriched in cases with moderate to extreme obesity. Diabetes 2010, 59(10):2690-2694. 10.2337/db10-0192, 3279563, 20622171.
-
(2010)
Diabetes
, vol.59
, Issue.10
, pp. 2690-2694
-
-
Wang, K.1
Li, W.2
Glessner, J.3
Grant, S.F.A.4
Hakonarson, H.5
Price, R.A.6
-
20
-
-
78049237730
-
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity
-
Bachmann Gagescu R, Mefford H, Cowan C, Glew G, Hing A, Wallace S, Bader P, Hamati A, Reitnauer P, Smith R, Stockton D, Muhle H, Helbig I, Eichler E, Ballif B, Rosenfeld J, Tsuchiya K. Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. Gen Med 2010, 12(10):641.
-
(2010)
Gen Med
, vol.12
, Issue.10
, pp. 641
-
-
Bachmann Gagescu, R.1
Mefford, H.2
Cowan, C.3
Glew, G.4
Hing, A.5
Wallace, S.6
Bader, P.7
Hamati, A.8
Reitnauer, P.9
Smith, R.10
Stockton, D.11
Muhle, H.12
Helbig, I.13
Eichler, E.14
Ballif, B.15
Rosenfeld, J.16
Tsuchiya, K.17
-
21
-
-
78249239776
-
A genome-wide study reveals copy number variants exclusive to childhood obesity cases
-
10.1016/j.ajhg.2010.09.014, 2978976, 20950786
-
Glessner J, Bradfield J, Wang K, Takahashi N, Zhang H, Sleiman P, Mentch F, Kim C, Hou C, Thomas K, Garris M, Deliard S, Frackelton E, Otieno FG, Zhao J, Chiavacci R, Li M, Buxbaum J, Berkowitz R, Hakonarson H, Grant SFA. A genome-wide study reveals copy number variants exclusive to childhood obesity cases. Am J Hum Genet 2010, 87(5):661. 10.1016/j.ajhg.2010.09.014, 2978976, 20950786.
-
(2010)
Am J Hum Genet
, vol.87
, Issue.5
, pp. 661
-
-
Glessner, J.1
Bradfield, J.2
Wang, K.3
Takahashi, N.4
Zhang, H.5
Sleiman, P.6
Mentch, F.7
Kim, C.8
Hou, C.9
Thomas, K.10
Garris, M.11
Deliard, S.12
Frackelton, E.13
Otieno, F.G.14
Zhao, J.15
Chiavacci, R.16
Li, M.17
Buxbaum, J.18
Berkowitz, R.19
Hakonarson, H.20
Grant, S.F.A.21
more..
-
22
-
-
79956223036
-
11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity
-
Shinawi M, Sahoo T, Maranda B, Skinner SA, Skinner C, Chinault C, Zascavage R, Peters S, Patel A, Stevenson R, Beaudet A. 11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity. Am J Med Genet A 2011, 155A(6):1272-1280.
-
(2011)
Am J Med Genet A
, vol.155 A
, Issue.6
, pp. 1272-1280
-
-
Shinawi, M.1
Sahoo, T.2
Maranda, B.3
Skinner, S.A.4
Skinner, C.5
Chinault, C.6
Zascavage, R.7
Peters, S.8
Patel, A.9
Stevenson, R.10
Beaudet, A.11
-
23
-
-
80053920983
-
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
-
10.1038/nature10406, 3637175, 21881559
-
Jacquemont S, Reymond A, Zufferey F, Harewood L, Walters RG, Kutalik Z, Martinet D, Shen Y, Valsesia A, Beckmann ND, Thorleifsson G, Belfiore M, Bouquillon S, Campion D, De Leeuw N, De Vries BBA, Esko T, Fernandez BA, Fernandez-Aranda F, Fernandez-Real JM, Gratacos M, Guilmatre A, Hoyer J, Jarvelin MR, Kooy FR, Kurg A, Le Caignec C, Mannik K, Platt OS, Sanlaville D, et al. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 2011, 478:97-102. 10.1038/nature10406, 3637175, 21881559.
-
(2011)
Nature
, vol.478
, pp. 97-102
-
-
Jacquemont, S.1
Reymond, A.2
Zufferey, F.3
Harewood, L.4
Walters, R.G.5
Kutalik, Z.6
Martinet, D.7
Shen, Y.8
Valsesia, A.9
Beckmann, N.D.10
Thorleifsson, G.11
Belfiore, M.12
Bouquillon, S.13
Campion, D.14
De Leeuw, N.15
De Vries, B.B.A.16
Esko, T.17
Fernandez, B.A.18
Fernandez-Aranda, F.19
Fernandez-Real, J.M.20
Gratacos, M.21
Guilmatre, A.22
Hoyer, J.23
Jarvelin, M.R.24
Kooy, F.R.25
Kurg, A.26
Le Caignec, C.27
Mannik, K.28
Platt, O.S.29
Sanlaville, D.30
more..
-
24
-
-
84355166559
-
A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene
-
10.1002/ajmg.a.34290, 22052655
-
Sofos E, Pescosolido MF, Quintos JB, Abuelo D, Gunn S, Hovanes K, Morrow EM, Shur N. A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene. Am J Med Genet A 2012, 158A(1):50-58. 10.1002/ajmg.a.34290, 22052655.
-
(2012)
Am J Med Genet A
, vol.158 A
, Issue.1
, pp. 50-58
-
-
Sofos, E.1
Pescosolido, M.F.2
Quintos, J.B.3
Abuelo, D.4
Gunn, S.5
Hovanes, K.6
Morrow, E.M.7
Shur, N.8
-
25
-
-
77950497675
-
A genome-wide association study of alcohol dependence
-
10.1073/pnas.0911109107, 2841942, 20202923
-
Bierut L, Agrawal A, Bucholz K, Doheny K, Laurie C, Pugh E, Fisher S, Fox L, Howells W, Bertelsen S, Hinrichs A, Almasy L, Breslau N, Culverhouse R, Dick D, Edenberg H, Foroud T, Grucza R, Hatsukami D, Hesselbrock V, Johnson E, Kramer J, Krueger R, Kuperman S, Lynskey M, Mann K, Neuman R, Nthen M, Nurnberger J, Porjesz B, et al. A genome-wide association study of alcohol dependence. Proc Natl Acad Sci U S A 2010, 107(11):5082-5087. 10.1073/pnas.0911109107, 2841942, 20202923.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, Issue.11
, pp. 5082-5087
-
-
Bierut, L.1
Agrawal, A.2
Bucholz, K.3
Doheny, K.4
Laurie, C.5
Pugh, E.6
Fisher, S.7
Fox, L.8
Howells, W.9
Bertelsen, S.10
Hinrichs, A.11
Almasy, L.12
Breslau, N.13
Culverhouse, R.14
Dick, D.15
Edenberg, H.16
Foroud, T.17
Grucza, R.18
Hatsukami, D.19
Hesselbrock, V.20
Johnson, E.21
Kramer, J.22
Krueger, R.23
Kuperman, S.24
Lynskey, M.25
Mann, K.26
Neuman, R.27
Nthen, M.28
Nurnberger, J.29
Porjesz, B.30
more..
-
26
-
-
0028202443
-
A new, semi-structured psychiatric interview for use in genetic linkage studies: a report on the reliability of the SSAGA
-
Bucholz KK, Cadoret R, Cloninger CR, Dinwiddie SH, Hesselbrock VM, Nurnberger JI, Reich T, Schmidt I, Schuckit MA. A new, semi-structured psychiatric interview for use in genetic linkage studies: a report on the reliability of the SSAGA. J Stud Alcohol 1994, 55(2):149-158.
-
(1994)
J Stud Alcohol
, vol.55
, Issue.2
, pp. 149-158
-
-
Bucholz, K.K.1
Cadoret, R.2
Cloninger, C.R.3
Dinwiddie, S.H.4
Hesselbrock, V.M.5
Nurnberger, J.I.6
Reich, T.7
Schmidt, I.8
Schuckit, M.A.9
-
27
-
-
0004235298
-
-
Washington, DC: American Psychiatric Association, American Psychiatric Association., American Psychiatric Association. Task Force on DSM-IV
-
American Psychiatric Association., American Psychiatric Association. Task Force on DSM-IV Diagnostic and Statistical Manual of Mental Disorders: DSM-IV-TR 2000, Washington, DC: American Psychiatric Association, American Psychiatric Association., American Psychiatric Association. Task Force on DSM-IV.
-
(2000)
Diagnostic and Statistical Manual of Mental Disorders: DSM-IV-TR
-
-
-
28
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
10.1371/journal.pgen.1000529, 2689936, 19543373
-
Howie B, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 2009, 5(6):e1000529-e1000529. 10.1371/journal.pgen.1000529, 2689936, 19543373.
-
(2009)
PLoS Genet
, vol.5
, Issue.6
-
-
Howie, B.1
Donnelly, P.2
Marchini, J.3
-
29
-
-
84863845193
-
Genotype imputation with thousands of genomes
-
2011, 3276165, 22384356
-
Howie B, Marchini J, Stephens M. Genotype imputation with thousands of genomes. G3 2011, 1(6):457-470. 2011, 3276165, 22384356.
-
(2011)
G3
, vol.1
, Issue.6
, pp. 457-470
-
-
Howie, B.1
Marchini, J.2
Stephens, M.3
-
30
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
10.1038/nature09534, 3042601, 20981092, 1000 Genomes Project Consortium
-
1000 Genomes Project Consortium A map of human genome variation from population-scale sequencing. Nature 2010, 467(7319):1061-1073. 10.1038/nature09534, 3042601, 20981092, 1000 Genomes Project Consortium.
-
(2010)
Nature
, vol.467
, Issue.7319
, pp. 1061-1073
-
-
-
31
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
10.1038/ng1847, 16862161
-
Price A, Patterson N, Plenge R, Weinblatt M, Shadick N, Reich D. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006, 38(8):904. 10.1038/ng1847, 16862161.
-
(2006)
Nat Genet
, vol.38
, Issue.8
, pp. 904
-
-
Price, A.1
Patterson, N.2
Plenge, R.3
Weinblatt, M.4
Shadick, N.5
Reich, D.6
-
32
-
-
33846006923
-
Population structure and eigenanalysis
-
10.1371/journal.pgen.0020190, 1713260, 17194218
-
Patterson N, Price A, Reich D. Population structure and eigenanalysis. PLoS Genet 2006, 2(12):e190. 10.1371/journal.pgen.0020190, 1713260, 17194218.
-
(2006)
PLoS Genet
, vol.2
, Issue.12
-
-
Patterson, N.1
Price, A.2
Reich, D.3
-
33
-
-
80054804726
-
Investigating population stratification and admixture using eigenanalysis of dense genotypes
-
3128175,3128175, 21448230
-
Shriner D. Investigating population stratification and admixture using eigenanalysis of dense genotypes. Heredity 2011, 107(5):413-420. 3128175,3128175, 21448230.
-
(2011)
Heredity
, vol.107
, Issue.5
, pp. 413-420
-
-
Shriner, D.1
-
35
-
-
35948984173
-
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
10.1101/gr.6861907, 2045149, 17921354
-
Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA, Hakonarson H, Bucan M. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 2007, 17(11):1665-1674. 10.1101/gr.6861907, 2045149, 17921354.
-
(2007)
Genome Res
, vol.17
, Issue.11
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.A.6
Hakonarson, H.7
Bucan, M.8
-
36
-
-
34247877877
-
QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data
-
10.1093/nar/gkm076, 1874617, 17341461
-
Colella S, Yau C, Taylor J, Mirza G, Butler H, Clouston P, Bassett A, Seller A, Holmes C, Ragoussis J. QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Res 2007, 35(6):2013-2025. 10.1093/nar/gkm076, 1874617, 17341461.
-
(2007)
Nucleic Acids Res
, vol.35
, Issue.6
, pp. 2013-2025
-
-
Colella, S.1
Yau, C.2
Taylor, J.3
Mirza, G.4
Butler, H.5
Clouston, P.6
Bassett, A.7
Seller, A.8
Holmes, C.9
Ragoussis, J.10
-
37
-
-
56049110212
-
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
-
10.1093/nar/gkn556, 2577347, 18784189
-
Diskin S, Li M, Hou C, Yang S, Glessner J, Hakonarson H, Bucan M, Maris J, Wang K. Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. Nucleic Acids Res 2008, 36(19):e126-e126. 10.1093/nar/gkn556, 2577347, 18784189.
-
(2008)
Nucleic Acids Res
, vol.36
, Issue.19
-
-
Diskin, S.1
Li, M.2
Hou, C.3
Yang, S.4
Glessner, J.5
Hakonarson, H.6
Bucan, M.7
Maris, J.8
Wang, K.9
-
38
-
-
79960751640
-
Copy number variation accuracy in genome-wide association studies
-
10.1159/000324683, 3153341, 21778733
-
Lin P, Hartz S, Wang J, Krueger R, Foroud T, Edenberg H, Nurnberger J, Brooks A, Tischfield J, Almasy L, Webb B, Hesselbrock V, Porjesz B, Goate A, Bierut L, Rice J. Copy number variation accuracy in genome-wide association studies. Hum Hered 2011, 71(3):141-147. 10.1159/000324683, 3153341, 21778733.
-
(2011)
Hum Hered
, vol.71
, Issue.3
, pp. 141-147
-
-
Lin, P.1
Hartz, S.2
Wang, J.3
Krueger, R.4
Foroud, T.5
Edenberg, H.6
Nurnberger, J.7
Brooks, A.8
Tischfield, J.9
Almasy, L.10
Webb, B.11
Hesselbrock, V.12
Porjesz, B.13
Goate, A.14
Bierut, L.15
Rice, J.16
-
39
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
10.1016/j.neuron.2011.05.002, 3939065, 21658581
-
Sanders S, Ercan Sencicek AG, Hus V, Luo R, Murtha M, Moreno-De-Luca D, Chu S, Moreau M, Gupta A, Thomson S, Mason C, Bilguvar K, Celestino-Soper PBS, Choi M, Crawford E, Davis L, Wright NRD, Dhodapkar R, DiCola M, DiLullo N, Fernandez T, Fielding Singh V, Fishman D, Frahm S, Garagaloyan R, Goh G, Kammela S, Klei L, Lowe J, Lund S, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011, 70(5):863-885. 10.1016/j.neuron.2011.05.002, 3939065, 21658581.
-
(2011)
Neuron
, vol.70
, Issue.5
, pp. 863-885
-
-
Sanders, S.1
Ercan Sencicek, A.G.2
Hus, V.3
Luo, R.4
Murtha, M.5
Moreno-De-Luca, D.6
Chu, S.7
Moreau, M.8
Gupta, A.9
Thomson, S.10
Mason, C.11
Bilguvar, K.12
Celestino-Soper, P.B.S.13
Choi, M.14
Crawford, E.15
Davis, L.16
Wright, N.R.D.17
Dhodapkar, R.18
DiCola, M.19
DiLullo, N.20
Fernandez, T.21
Fielding Singh, V.22
Fishman, D.23
Frahm, S.24
Garagaloyan, R.25
Goh, G.26
Kammela, S.27
Klei, L.28
Lowe, J.29
Lund, S.30
more..
-
40
-
-
61449229353
-
A genome-wide investigation of SNPs and CNVs in schizophrenia
-
10.1371/journal.pgen.1000373, 2631150, 19197363
-
Need A, Ge D, Weale M, Maia J, Feng S, Heinzen E, Shianna K, Yoon W, Kasperaviciūte D, Gennarelli M, Strittmatter W, Bonvicini C, Rossi G, Jayathilake K, Cola P, McEvoy J, Keefe RSE, Fisher EMC, St Jean P, Giegling I, Hartmann A, Mller H, Ruppert A, Fraser G, Crombie C, Middleton L, St Clair D, Roses A, Muglia P, Francks C, et al. A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet 2009, 5(2):e1000373-e1000373. 10.1371/journal.pgen.1000373, 2631150, 19197363.
-
(2009)
PLoS Genet
, vol.5
, Issue.2
-
-
Need, A.1
Ge, D.2
Weale, M.3
Maia, J.4
Feng, S.5
Heinzen, E.6
Shianna, K.7
Yoon, W.8
Kasperaviciute, D.9
Gennarelli, M.10
Strittmatter, W.11
Bonvicini, C.12
Rossi, G.13
Jayathilake, K.14
Cola, P.15
McEvoy, J.16
Keefe, R.S.E.17
Fisher, E.M.C.18
St Jean, P.19
Giegling, I.20
Hartmann, A.21
Mller, H.22
Ruppert, A.23
Fraser, G.24
Crombie, C.25
Middleton, L.26
St Clair, D.27
Roses, A.28
Muglia, P.29
Francks, C.30
more..
-
41
-
-
57249114505
-
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
-
10.1093/bioinformatics/btn564, 2720775, 18974171
-
Johnson A, Handsaker R, Pulit S, Nizzari M, O'Donnell C, De Bakker PIW. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 2008, 24(24):2938. 10.1093/bioinformatics/btn564, 2720775, 18974171.
-
(2008)
Bioinformatics
, vol.24
, Issue.24
, pp. 2938
-
-
Johnson, A.1
Handsaker, R.2
Pulit, S.3
Nizzari, M.4
O'Donnell, C.5
De Bakker, P.I.W.6
-
42
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
10.1086/519795, 1950838, 17701901
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, Bender D, Maller J, Sklar P, De Bakker PIW, Daly M, Sham P. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007, 81(3):559. 10.1086/519795, 1950838, 17701901.
-
(2007)
Am J Hum Genet
, vol.81
, Issue.3
, pp. 559
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.W.9
Daly, M.10
Sham, P.11
-
44
-
-
78951478378
-
Genetic risk sum score comprised of common polygenic variation is associated with body mass index
-
10.1007/s00439-010-0917-1, 3403709, 21104096
-
Peterson R, Maes H, Holmans P, Sanders A, Levinson D, Shi J, Kendler K, Gejman P, Webb B. Genetic risk sum score comprised of common polygenic variation is associated with body mass index. Hum Genet 2011, 129(2):221-230. 10.1007/s00439-010-0917-1, 3403709, 21104096.
-
(2011)
Hum Genet
, vol.129
, Issue.2
, pp. 221-230
-
-
Peterson, R.1
Maes, H.2
Holmans, P.3
Sanders, A.4
Levinson, D.5
Shi, J.6
Kendler, K.7
Gejman, P.8
Webb, B.9
-
45
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
-
10.1016/j.ajhg.2008.06.024, 2842185, 18691683
-
Li B, Leal S. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am J Hum Genet 2008, 83(3):311-321. 10.1016/j.ajhg.2008.06.024, 2842185, 18691683.
-
(2008)
Am J Hum Genet
, vol.83
, Issue.3
, pp. 311-321
-
-
Li, B.1
Leal, S.2
-
46
-
-
77958102016
-
Statistical analysis strategies for association studies involving rare variants. Nature reviews
-
3743540, 20940738
-
Bansal V, Libiger O, Torkamani A, Schork N. Statistical analysis strategies for association studies involving rare variants. Nature reviews. Genetics 2010, 11(11):773-785. 3743540, 20940738.
-
(2010)
Genetics
, vol.11
, Issue.11
, pp. 773-785
-
-
Bansal, V.1
Libiger, O.2
Torkamani, A.3
Schork, N.4
-
47
-
-
46049119818
-
StAR: a simple tool for the statistical comparison of ROC curves
-
Vergara I, Norambuena T, Ferrada E, Slater A, Melo F. StAR: a simple tool for the statistical comparison of ROC curves. BMC Bioinforma 2008, 9:265-265.
-
(2008)
BMC Bioinforma
, vol.9
, pp. 265-265
-
-
Vergara, I.1
Norambuena, T.2
Ferrada, E.3
Slater, A.4
Melo, F.5
-
48
-
-
58149163142
-
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
-
10.1038/ng.287, 2695662, 19079261
-
Willer CJ, Speliotes EK, Loos RJ, Li S, Lindgren CM, Heid IM, Berndt SI, Elliott AL, Jackson AU, Lamina C, Lettre G, Lim N, Lyon HN, McCarroll SA, Papadakis K, Qi L, Randall JC, Roccasecca RM, Sanna S, Scheet P, Weedon MN, Wheeler E, Zhao JH, Jacobs LC, Prokopenko I, Soranzo N, Tanaka T, Timpson NJ, Almgren P, Bennett A, et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet 2009, 41(1):25-34. 10.1038/ng.287, 2695662, 19079261.
-
(2009)
Nat Genet
, vol.41
, Issue.1
, pp. 25-34
-
-
Willer, C.J.1
Speliotes, E.K.2
Loos, R.J.3
Li, S.4
Lindgren, C.M.5
Heid, I.M.6
Berndt, S.I.7
Elliott, A.L.8
Jackson, A.U.9
Lamina, C.10
Lettre, G.11
Lim, N.12
Lyon, H.N.13
McCarroll, S.A.14
Papadakis, K.15
Qi, L.16
Randall, J.C.17
Roccasecca, R.M.18
Sanna, S.19
Scheet, P.20
Weedon, M.N.21
Wheeler, E.22
Zhao, J.H.23
Jacobs, L.C.24
Prokopenko, I.25
Soranzo, N.26
Tanaka, T.27
Timpson, N.J.28
Almgren, P.29
Bennett, A.30
more..
-
49
-
-
78751700313
-
Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
-
10.1093/hmg/ddq518, 3024044, 21131291
-
Jarick I, Vogel CIG, Scherag S, Schfer H, Hebebrand J, Hinney A, Scherag A. Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis. Hum Mol Genet 2011, 20(4):840. 10.1093/hmg/ddq518, 3024044, 21131291.
-
(2011)
Hum Mol Genet
, vol.20
, Issue.4
, pp. 840
-
-
Jarick, I.1
Vogel, C.I.G.2
Scherag, S.3
Schfer, H.4
Hebebrand, J.5
Hinney, A.6
Scherag, A.7
-
50
-
-
84876918129
-
Polygenic risk and the developmental progression to heavy, persistent smoking and nicotine dependence: Evidence from a 4-decade longitudinal study
-
Belsky DW, Moffitt TE, Baker TB, Biddle AK, Evans JP, Harrington H, Houts R, Meier M, Sugden K, Williams B, Poulton R, Caspi A. Polygenic risk and the developmental progression to heavy, persistent smoking and nicotine dependence: Evidence from a 4-decade longitudinal study. JAMA Psychiatry 2013, 1-9.
-
(2013)
JAMA Psychiatry
, pp. 1-9
-
-
Belsky, D.W.1
Moffitt, T.E.2
Baker, T.B.3
Biddle, A.K.4
Evans, J.P.5
Harrington, H.6
Houts, R.7
Meier, M.8
Sugden, K.9
Williams, B.10
Poulton, R.11
Caspi, A.12
-
51
-
-
84874898385
-
Rare genomic structural variants in complex disease: lessons from the Replication of Associations with Obesity
-
10.1371/journal.pone.0058048, 3595275, 23554873
-
Walters RG, Coin LJM, Ruokonen A, De Smith AJ, El-Sayed Moustafa JS, Jacquemont S, Elliott P, Esko T, Hartikainen A, Laitinen J, Männik K, Martinet D, Meyre D, Nauck M, Schurmann C, Sladek R, Thorleifsson G, Thorsteinsdóttir U, Valsesia A, Waeber G, Zufferey F, Balkau B, Pattou F, Metspalu A, Völzke H, Vollenweider P, Stefansson K, Järvelin M, Beckmann JS, Froguel P, et al. Rare genomic structural variants in complex disease: lessons from the Replication of Associations with Obesity. PLoS One 2013, 8(3):e58048. 10.1371/journal.pone.0058048, 3595275, 23554873.
-
(2013)
PLoS One
, vol.8
, Issue.3
-
-
Walters, R.G.1
Coin, L.J.M.2
Ruokonen, A.3
De Smith, A.J.4
El-Sayed Moustafa, J.S.5
Jacquemont, S.6
Elliott, P.7
Esko, T.8
Hartikainen, A.9
Laitinen, J.10
Männik, K.11
Martinet, D.12
Meyre, D.13
Nauck, M.14
Schurmann, C.15
Sladek, R.16
Thorleifsson, G.17
Thorsteinsdóttir, U.18
Valsesia, A.19
Waeber, G.20
Zufferey, F.21
Balkau, B.22
Pattou, F.23
Metspalu, A.24
Völzke, H.25
Vollenweider, P.26
Stefansson, K.27
Järvelin, M.28
Beckmann, J.S.29
Froguel, P.30
more..
-
52
-
-
64549158008
-
Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden
-
10.1093/hmg/ddp041, 2664142, 19164386
-
Renström F, Payne F, Nordström A, Brito E, Rolandsson O, Hallmans G, Barroso I, Nordstrm P, Franks P. Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden. Hum Mol Genet 2009, 18(8):1489. 10.1093/hmg/ddp041, 2664142, 19164386.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.8
, pp. 1489
-
-
Renström, F.1
Payne, F.2
Nordström, A.3
Brito, E.4
Rolandsson, O.5
Hallmans, G.6
Barroso, I.7
Nordstrm, P.8
Franks, P.9
-
53
-
-
74049138315
-
Cumulative effects and predictive value of common obesity-susceptibility variants identified by genome-wide association studies
-
10.3945/ajcn.2009.28403, 19812171
-
Li S, Zhao J, Luan J, Luben R, Rodwell S, Khaw K, Ong K, Wareham N, Loos RJF. Cumulative effects and predictive value of common obesity-susceptibility variants identified by genome-wide association studies. Am J Clin Nutr 2010, 91(1):184. 10.3945/ajcn.2009.28403, 19812171.
-
(2010)
Am J Clin Nutr
, vol.91
, Issue.1
, pp. 184
-
-
Li, S.1
Zhao, J.2
Luan, J.3
Luben, R.4
Rodwell, S.5
Khaw, K.6
Ong, K.7
Wareham, N.8
Loos, R.J.F.9
-
54
-
-
77749233777
-
Obesity Susceptibility Genetic Variants Identified from Recent Genome-Wide Association Studies: implications in a Chinese population
-
10.1210/jc.2009-1465, 20061430
-
Cheung CY, Tso AW, Cheung BM, Xu A, Ong KL, Fong CH, Wat NM, Janus ED, Sham PC, Lam KS. Obesity Susceptibility Genetic Variants Identified from Recent Genome-Wide Association Studies: implications in a Chinese population. J Clin Endocrinol Metab 2010, 95(3):1395-1403. 10.1210/jc.2009-1465, 20061430.
-
(2010)
J Clin Endocrinol Metab
, vol.95
, Issue.3
, pp. 1395-1403
-
-
Cheung, C.Y.1
Tso, A.W.2
Cheung, B.M.3
Xu, A.4
Ong, K.L.5
Fong, C.H.6
Wat, N.M.7
Janus, E.D.8
Sham, P.C.9
Lam, K.S.10
-
55
-
-
42249094741
-
Consequences of smoking for body weight, body fat distribution, and insulin resistance
-
Chiolero A, Faeh D, Paccaud F, Cornuz J. Consequences of smoking for body weight, body fat distribution, and insulin resistance. Am J Clin Nutr 2008, 87(4):801.
-
(2008)
Am J Clin Nutr
, vol.87
, Issue.4
, pp. 801
-
-
Chiolero, A.1
Faeh, D.2
Paccaud, F.3
Cornuz, J.4
-
56
-
-
84863722959
-
The effect of current and lifetime alcohol consumption on overall and central obesity
-
10.1038/ejcn.2012.20, 22378229
-
Lourenço S, Oliveira A, Lopes C. The effect of current and lifetime alcohol consumption on overall and central obesity. Eur J Clin Nutr 2012, 66(7):813. 10.1038/ejcn.2012.20, 22378229.
-
(2012)
Eur J Clin Nutr
, vol.66
, Issue.7
, pp. 813
-
-
Lourenço, S.1
Oliveira, A.2
Lopes, C.3
-
57
-
-
78049349396
-
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
-
10.1038/ng.685, 3000924,3000924, 20935629
-
Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Magi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpelainen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet 2010, 42(11):949-960. 10.1038/ng.685, 3000924,3000924, 20935629.
-
(2010)
Nat Genet
, vol.42
, Issue.11
, pp. 949-960
-
-
Heid, I.M.1
Jackson, A.U.2
Randall, J.C.3
Winkler, T.W.4
Qi, L.5
Steinthorsdottir, V.6
Thorleifsson, G.7
Zillikens, M.C.8
Speliotes, E.K.9
Magi, R.10
Workalemahu, T.11
White, C.C.12
Bouatia-Naji, N.13
Harris, T.B.14
Berndt, S.I.15
Ingelsson, E.16
Willer, C.J.17
Weedon, M.N.18
Luan, J.19
Vedantam, S.20
Esko, T.21
Kilpelainen, T.O.22
Kutalik, Z.23
Li, S.24
Monda, K.L.25
Dixon, A.L.26
Holmes, C.C.27
Kaplan, L.M.28
Liang, L.29
Min, J.L.30
more..
-
58
-
-
67651236725
-
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
-
10.1371/journal.pgen.1000508, 2695778, 19557161
-
Lindgren CM, Heid IM, Randall JC, Lamina C, Steinthorsdottir V, Qi L, Speliotes EK, Thorleifsson G, Willer CJ, Herrera BM, Jackson AU, Lim N, Scheet P, Soranzo N, Amin N, Aulchenko YS, Chambers JC, Drong A, Luan J, Lyon HN, Rivadeneira F, Sanna S, Timpson NJ, Zillikens MC, Zhao JH, Almgren P, Bandinelli S, Bennett AJ, Bergman RN, Bonnycastle LL, et al. Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet 2009, 5(6):e1000508. 10.1371/journal.pgen.1000508, 2695778, 19557161.
-
(2009)
PLoS Genet
, vol.5
, Issue.6
-
-
Lindgren, C.M.1
Heid, I.M.2
Randall, J.C.3
Lamina, C.4
Steinthorsdottir, V.5
Qi, L.6
Speliotes, E.K.7
Thorleifsson, G.8
Willer, C.J.9
Herrera, B.M.10
Jackson, A.U.11
Lim, N.12
Scheet, P.13
Soranzo, N.14
Amin, N.15
Aulchenko, Y.S.16
Chambers, J.C.17
Drong, A.18
Luan, J.19
Lyon, H.N.20
Rivadeneira, F.21
Sanna, S.22
Timpson, N.J.23
Zillikens, M.C.24
Zhao, J.H.25
Almgren, P.26
Bandinelli, S.27
Bennett, A.J.28
Bergman, R.N.29
Bonnycastle, L.L.30
more..
-
59
-
-
84878594902
-
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
-
10.1038/ng.2606, 3973018, 23563607
-
Berndt SI, Gustafsson S, Magi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka D, Day FR, Esko T, Fall T, Ferreira T, Gentilini D, Jackson AU, Luan J, Randall JC, Vedantam S, Willer CJ, Winkler TW, Wood AR, Workalemahu T, Hu Y, Lee SH, Liang L, Lin D, Min JL, Neale BM, Thorleifsson G, Yang J, et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet 2013, 45(5):501-512. 10.1038/ng.2606, 3973018, 23563607.
-
(2013)
Nat Genet
, vol.45
, Issue.5
, pp. 501-512
-
-
Berndt, S.I.1
Gustafsson, S.2
Magi, R.3
Ganna, A.4
Wheeler, E.5
Feitosa, M.F.6
Justice, A.E.7
Monda, K.L.8
Croteau-Chonka, D.9
Day, F.R.10
Esko, T.11
Fall, T.12
Ferreira, T.13
Gentilini, D.14
Jackson, A.U.15
Luan, J.16
Randall, J.C.17
Vedantam, S.18
Willer, C.J.19
Winkler, T.W.20
Wood, A.R.21
Workalemahu, T.22
Hu, Y.23
Lee, S.H.24
Liang, L.25
Lin, D.26
Min, J.L.27
Neale, B.M.28
Thorleifsson, G.29
Yang, J.30
more..
-
60
-
-
51649099799
-
Physical activity and the association of common FTO gene variants with body mass index and obesity
-
10.1001/archinte.168.16.1791, 3635949, 18779467
-
Rampersaud E, Mitchell B, Pollin T, Fu M, Shen H, O'Connell J, Ducharme J, Hines S, Sack P, Naglieri R, Shuldiner A, Snitker S. Physical activity and the association of common FTO gene variants with body mass index and obesity. Arch Intern Med 2008, 168(16):1791. 10.1001/archinte.168.16.1791, 3635949, 18779467.
-
(2008)
Arch Intern Med
, vol.168
, Issue.16
, pp. 1791
-
-
Rampersaud, E.1
Mitchell, B.2
Pollin, T.3
Fu, M.4
Shen, H.5
O'Connell, J.6
Ducharme, J.7
Hines, S.8
Sack, P.9
Naglieri, R.10
Shuldiner, A.11
Snitker, S.12
-
61
-
-
54949113309
-
The common obesity variant near MC4R gene is associated with higher intakes of total energy and dietary fat, weight change and diabetes risk in women
-
10.1093/hmg/ddn242, 2572696, 18697794
-
Qi L, Kraft P, Hunter D, Hu F. The common obesity variant near MC4R gene is associated with higher intakes of total energy and dietary fat, weight change and diabetes risk in women. Hum Mol Genet 2008, 17(22):3502. 10.1093/hmg/ddn242, 2572696, 18697794.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.22
, pp. 3502
-
-
Qi, L.1
Kraft, P.2
Hunter, D.3
Hu, F.4
-
62
-
-
82455175773
-
Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children
-
10.1371/journal.pmed.1001116, 3206047, 22069379
-
Kilpeläinen TO, Qi L, Brage S, Sharp SJ, Sonestedt E, Demerath E, Ahmad T, Mora S, Kaakinen M, Sandholt CH, Holzapfel C, Autenrieth CS, Hyppönen E, Cauchi S, He M, Kutalik Z, Kumari M, Stančáková A, Meidtner K, Balkau B, Tan JT, Mangino M, Timpson NJ, Song Y, Zillikens MC, Jablonski KA, Garcia ME, Johansson S, Bragg-Gresham JL, Wu Y, et al. Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children. PLoS Med 2011, 8(11):e1001116. 10.1371/journal.pmed.1001116, 3206047, 22069379.
-
(2011)
PLoS Med
, vol.8
, Issue.11
-
-
Kilpeläinen, T.O.1
Qi, L.2
Brage, S.3
Sharp, S.J.4
Sonestedt, E.5
Demerath, E.6
Ahmad, T.7
Mora, S.8
Kaakinen, M.9
Sandholt, C.H.10
Holzapfel, C.11
Autenrieth, C.S.12
Hyppönen, E.13
Cauchi, S.14
He, M.15
Kutalik, Z.16
Kumari, M.17
Stančáková, A.18
Meidtner, K.19
Balkau, B.20
Tan, J.T.21
Mangino, M.22
Timpson, N.J.23
Song, Y.24
Zillikens, M.C.25
Jablonski, K.A.26
Garcia, M.E.27
Johansson, S.28
Bragg-Gresham, J.L.29
Wu, Y.30
more..
|