-
1
-
-
0032018755
-
Evaluation of neonates born with intrauterine growth retardation: review and practice guidelines
-
Alkalay AL, Graham JM, Pomerance JJ. Evaluation of neonates born with intrauterine growth retardation: review and practice guidelines. J Perinatol 1998, 18:142-151.
-
(1998)
J Perinatol
, vol.18
, pp. 142-151
-
-
Alkalay, A.L.1
Graham, J.M.2
Pomerance, J.J.3
-
2
-
-
0037974806
-
International Small for Gestational Age Advisory Board: International Small for Gestational Age Advisory Board consensus development conference statement: management of short children born small for gestational age, April 24 - October 1, 2001
-
International Small for Gestational Age Advisory Board
-
Lee PA, Chernausek SD, Hokken-Koelega AC, Czernichow P, . International Small for Gestational Age Advisory Board International Small for Gestational Age Advisory Board: International Small for Gestational Age Advisory Board consensus development conference statement: management of short children born small for gestational age, April 24 - October 1, 2001. Pediatrics 2001, 111:1253-1261. International Small for Gestational Age Advisory Board.
-
(2001)
Pediatrics
, vol.111
, pp. 1253-1261
-
-
Lee, P.A.1
Chernausek, S.D.2
Hokken-Koelega, A.C.3
Czernichow, P.4
-
3
-
-
0026008824
-
Fetal and infant growth and impaired glucose tolerance at age 64
-
10.1136/bmj.303.6809.1019, 1671766, 1954451
-
Hales CN, Barker DJ, Clark PM, Cox LJ, Fall C, Osmond C, Winter PD. Fetal and infant growth and impaired glucose tolerance at age 64. BMJ 1991, 303:1019-1022. 10.1136/bmj.303.6809.1019, 1671766, 1954451.
-
(1991)
BMJ
, vol.303
, pp. 1019-1022
-
-
Hales, C.N.1
Barker, D.J.2
Clark, P.M.3
Cox, L.J.4
Fall, C.5
Osmond, C.6
Winter, P.D.7
-
4
-
-
0027513981
-
Fetal nutrition and cardiovascular disease in adult life
-
10.1016/0140-6736(93)91224-A, 8096277
-
Barker DJ, Gluckman PD, Godfrey KM, Harding JE, Owens JA, Robinson JS. Fetal nutrition and cardiovascular disease in adult life. Lancet 1993, 341:938-941. 10.1016/0140-6736(93)91224-A, 8096277.
-
(1993)
Lancet
, vol.341
, pp. 938-941
-
-
Barker, D.J.1
Gluckman, P.D.2
Godfrey, K.M.3
Harding, J.E.4
Owens, J.A.5
Robinson, J.S.6
-
5
-
-
0027529974
-
Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth
-
10.1007/BF00399095, 8436255
-
Barker DJ, Hales CN, Fall CH, Osmond C, Phipps K, Clark PM. Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth. Diabetologia 1993, 36:62-67. 10.1007/BF00399095, 8436255.
-
(1993)
Diabetologia
, vol.36
, pp. 62-67
-
-
Barker, D.J.1
Hales, C.N.2
Fall, C.H.3
Osmond, C.4
Phipps, K.5
Clark, P.M.6
-
6
-
-
0035830040
-
Fetal and early life growth and body mass index from birth to early adulthood in 1958 British cohort: longitudinal study
-
10.1136/bmj.323.7325.1331, 60670, 11739217
-
Parsons TJ, Power C, Manor O. Fetal and early life growth and body mass index from birth to early adulthood in 1958 British cohort: longitudinal study. BMJ 2001, 323(7325):1331. 10.1136/bmj.323.7325.1331, 60670, 11739217.
-
(2001)
BMJ
, vol.323
, Issue.7325
, pp. 1331
-
-
Parsons, T.J.1
Power, C.2
Manor, O.3
-
7
-
-
0037369617
-
Programming of lean body mass: a link between birth weight, obesity, and cardiovascular disease?
-
Singhal A, Wells J, Cole TJ, Fewtrell M, Lucas A. Programming of lean body mass: a link between birth weight, obesity, and cardiovascular disease?. Am J Clin Nutr 2003, 77(3):726-30.
-
(2003)
Am J Clin Nutr
, vol.77
, Issue.3
, pp. 726-730
-
-
Singhal, A.1
Wells, J.2
Cole, T.J.3
Fewtrell, M.4
Lucas, A.5
-
8
-
-
0033594787
-
The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease
-
10.1016/S0140-6736(98)07546-1, 10348008
-
Hattersley AT, Tooke JE. The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease. Lancet 1999, 353:1789-1792. 10.1016/S0140-6736(98)07546-1, 10348008.
-
(1999)
Lancet
, vol.353
, pp. 1789-1792
-
-
Hattersley, A.T.1
Tooke, J.E.2
-
9
-
-
0025081078
-
The fetal and infant origins of adult disease
-
10.1136/bmj.301.6761.1111, 1664286, 2252919
-
Barker DJ. The fetal and infant origins of adult disease. BMJ 1990, 301:1111. 10.1136/bmj.301.6761.1111, 1664286, 2252919.
-
(1990)
BMJ
, vol.301
, pp. 1111
-
-
Barker, D.J.1
-
11
-
-
0030771971
-
Maternal nutrition, fetal nutrition and diseases in later life
-
10.1016/S0899-9007(97)00193-7, 9290095
-
Barker DJP. Maternal nutrition, fetal nutrition and diseases in later life. Nutrition 1997, 13:807. 10.1016/S0899-9007(97)00193-7, 9290095.
-
(1997)
Nutrition
, vol.13
, pp. 807
-
-
Barker, D.J.P.1
-
12
-
-
2442479898
-
Early origins of cardiovascular disease: is there a unifying hypothesis?
-
10.1016/S0140-6736(04)16210-7, 15145640
-
Singhal A, Lucas A. Early origins of cardiovascular disease: is there a unifying hypothesis?. Lancet 2004, 363:1642-1645. 10.1016/S0140-6736(04)16210-7, 15145640.
-
(2004)
Lancet
, vol.363
, pp. 1642-1645
-
-
Singhal, A.1
Lucas, A.2
-
13
-
-
0023624397
-
Determinants of low birth weight: methodological assessment and meta analysis
-
2491072, 3322602
-
Kramer MS. Determinants of low birth weight: methodological assessment and meta analysis. Bull WHO 1987, 65:663-737. 2491072, 3322602.
-
(1987)
Bull WHO
, vol.65
, pp. 663-737
-
-
Kramer, M.S.1
-
14
-
-
0034889424
-
Risk factors for small-for-gestational-age babies: The Auckland birthweight collaborative study
-
10.1046/j.1440-1754.2001.00684.x, 11532057
-
Thompson JM, Clark PM, Robinson E, Becroft DM, Pattison NS, Glavish N, Pryor JE, Wild CJ, Rees K, Mitchell EA. Risk factors for small-for-gestational-age babies: The Auckland birthweight collaborative study. J Paediatr Child Health 2001, 37:369-375. 10.1046/j.1440-1754.2001.00684.x, 11532057.
-
(2001)
J Paediatr Child Health
, vol.37
, pp. 369-375
-
-
Thompson, J.M.1
Clark, P.M.2
Robinson, E.3
Becroft, D.M.4
Pattison, N.S.5
Glavish, N.6
Pryor, J.E.7
Wild, C.J.8
Rees, K.9
Mitchell, E.A.10
-
15
-
-
4444274882
-
Maternal nutritional risk factors for small for gestational age babies in a developed country: a case-control study
-
10.1136/adc.2003.036970, 1721755, 15321964
-
Mitchell EA, Robinson E, Clark PM, Becroft DM, Glavish N, Pattison NS, Pryor JE, Thompson JM, Wild CJ. Maternal nutritional risk factors for small for gestational age babies in a developed country: a case-control study. Arch Dis Child Fetal Neonatal Ed 2004, 89(5):F431-F435. 10.1136/adc.2003.036970, 1721755, 15321964.
-
(2004)
Arch Dis Child Fetal Neonatal Ed
, vol.89
, Issue.5
-
-
Mitchell, E.A.1
Robinson, E.2
Clark, P.M.3
Becroft, D.M.4
Glavish, N.5
Pattison, N.S.6
Pryor, J.E.7
Thompson, J.M.8
Wild, C.J.9
-
16
-
-
0029558981
-
Familial aggregation of low birth weight among whites and blacks in the United States
-
10.1056/NEJM199512283332606, 7491139
-
Wang X, Zuckerman B, Coffman GA, Corwin MJ. Familial aggregation of low birth weight among whites and blacks in the United States. N Engl J Med 1995, 333:1744-1749. 10.1056/NEJM199512283332606, 7491139.
-
(1995)
N Engl J Med
, vol.333
, pp. 1744-1749
-
-
Wang, X.1
Zuckerman, B.2
Coffman, G.A.3
Corwin, M.J.4
-
17
-
-
0030633333
-
Birth weight of relatives by maternal tendency to repeat small-for-gestational-age (SGA) births in successive pregnancies
-
Magnus P, Bakketeig LS, Hoffman H. Birth weight of relatives by maternal tendency to repeat small-for-gestational-age (SGA) births in successive pregnancies. Acta Obstet Gynecol Scand Suppl 1997, 165:35-38.
-
(1997)
Acta Obstet Gynecol Scand Suppl
, vol.165
, pp. 35-38
-
-
Magnus, P.1
Bakketeig, L.S.2
Hoffman, H.3
-
18
-
-
34548359380
-
Studying genetic predisposition among small-for-gestational-age newborns
-
10.1053/j.semperi.2007.05.001, 17825675
-
Infante-Rivard C. Studying genetic predisposition among small-for-gestational-age newborns. Semin Perinatol 2007, 31(4):213-218. 10.1053/j.semperi.2007.05.001, 17825675.
-
(2007)
Semin Perinatol
, vol.31
, Issue.4
, pp. 213-218
-
-
Infante-Rivard, C.1
-
19
-
-
14644435132
-
A systematic review of the association between factor V Leiden or prothrombin gene variant and intrauterine growth restriction
-
10.1016/j.ajog.2004.09.011, 15746660
-
Howley EA, Walker M, Rodger MA. A systematic review of the association between factor V Leiden or prothrombin gene variant and intrauterine growth restriction. Am J Obstet Gynecol 2005, 192:694-708. 10.1016/j.ajog.2004.09.011, 15746660.
-
(2005)
Am J Obstet Gynecol
, vol.192
, pp. 694-708
-
-
Howley, E.A.1
Walker, M.2
Rodger, M.A.3
-
20
-
-
17844375459
-
Thrombophilic polymorphisms and intrauterine growth restriction
-
10.1097/01.ede.0000158199.64871.b9, 15824541
-
Infante-Rivard C, Rivard GE, Guiguet M, Gauthier R. Thrombophilic polymorphisms and intrauterine growth restriction. Epidemiology 2005, 16:281-287. 10.1097/01.ede.0000158199.64871.b9, 15824541.
-
(2005)
Epidemiology
, vol.16
, pp. 281-287
-
-
Infante-Rivard, C.1
Rivard, G.E.2
Guiguet, M.3
Gauthier, R.4
-
21
-
-
0037045438
-
Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight
-
10.1001/jama.287.2.195, 11779261
-
Wang X, Zuckerman B, Pearson C, Kaufman G, Chen C, Wang G, Niu T, Wise PH, Bauchner H, Xu X. Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight. JAMA 2002, 287:195-202. 10.1001/jama.287.2.195, 11779261.
-
(2002)
JAMA
, vol.287
, pp. 195-202
-
-
Wang, X.1
Zuckerman, B.2
Pearson, C.3
Kaufman, G.4
Chen, C.5
Wang, G.6
Niu, T.7
Wise, P.H.8
Bauchner, H.9
Xu, X.10
-
22
-
-
33644878092
-
Xenobiotic-metabolizing genes and small-for-gestational-age births: interaction with maternal smoking
-
10.1097/01.ede.0000187669.34003.b1, 16357593
-
Infante-Rivard C, Weinberg CR, Guiguet M. Xenobiotic-metabolizing genes and small-for-gestational-age births: interaction with maternal smoking. Epidemiology 2006, 17:38-46. 10.1097/01.ede.0000187669.34003.b1, 16357593.
-
(2006)
Epidemiology
, vol.17
, pp. 38-46
-
-
Infante-Rivard, C.1
Weinberg, C.R.2
Guiguet, M.3
-
23
-
-
0042327819
-
Small babies receive the cardiovascular protective apolipoprotein 2 allele less frequently than expected
-
10.1136/jmg.40.8.626, 1735546, 12920078
-
Infante-Rivard C, Lévy E, Rivard GE, Guiguet M, Feoli-Fonseca JC. Small babies receive the cardiovascular protective apolipoprotein 2 allele less frequently than expected. J Med Genet 2003, 40:626-629. 10.1136/jmg.40.8.626, 1735546, 12920078.
-
(2003)
J Med Genet
, vol.40
, pp. 626-629
-
-
Infante-Rivard, C.1
Lévy, E.2
Rivard, G.E.3
Guiguet, M.4
Feoli-Fonseca, J.C.5
-
24
-
-
3042519236
-
The role of angiotensin-converting enzyme and apolipoprotein-E gene polymorphisms on lipid compositions in newborn infants with intrauterine growth restriction
-
10.1016/j.earlhumdev.2004.03.006, 15223114
-
Akisu M, Balim Z, Cetin H, Kosova B, Yalaz M, Topcuoglu N, Kultursay N. The role of angiotensin-converting enzyme and apolipoprotein-E gene polymorphisms on lipid compositions in newborn infants with intrauterine growth restriction. Early Hum Dev 2004, 78:95-103. 10.1016/j.earlhumdev.2004.03.006, 15223114.
-
(2004)
Early Hum Dev
, vol.78
, pp. 95-103
-
-
Akisu, M.1
Balim, Z.2
Cetin, H.3
Kosova, B.4
Yalaz, M.5
Topcuoglu, N.6
Kultursay, N.7
-
25
-
-
4344635779
-
Polymorphisms of the paraoxonase gene and risk of preterm delivery
-
10.1097/01.ede.0000129509.59912.b2, 15232408
-
Chen D, Hu Y, Chen C, Yang F, Fang Z, Wang L, Li J. Polymorphisms of the paraoxonase gene and risk of preterm delivery. Epidemiology 2004, 15:466-470. 10.1097/01.ede.0000129509.59912.b2, 15232408.
-
(2004)
Epidemiology
, vol.15
, pp. 466-470
-
-
Chen, D.1
Hu, Y.2
Chen, C.3
Yang, F.4
Fang, Z.5
Wang, L.6
Li, J.7
-
26
-
-
0037160989
-
Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight
-
10.1016/S0140-6736(02)08067-4, 11937187
-
Vaessen N, Janssen JA, Heutink P, Hofman A, Lamberts SW, Oostra BA, Pols HA, van Duijn CM. Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight. Lancet 2002, 359:1036-1037. 10.1016/S0140-6736(02)08067-4, 11937187.
-
(2002)
Lancet
, vol.359
, pp. 1036-1037
-
-
Vaessen, N.1
Janssen, J.A.2
Heutink, P.3
Hofman, A.4
Lamberts, S.W.5
Oostra, B.A.6
Pols, H.A.7
van Duijn, C.M.8
-
27
-
-
0028780508
-
Sex specific birthweight percentiles by gestational age for New Zealand
-
Thompson JM, Mitchell EA, Borman B. Sex specific birthweight percentiles by gestational age for New Zealand. N Z Med J 1994, 107:1-3.
-
(1994)
N Z Med J
, vol.107
, pp. 1-3
-
-
Thompson, J.M.1
Mitchell, E.A.2
Borman, B.3
-
28
-
-
0036043393
-
The use of massARRAY technology for high throughput genotyping
-
Jurinke C, van den Boom D, Cantor CR, Köster H. The use of massARRAY technology for high throughput genotyping. Adv Biochem Eng Biotechnol 2002, 77:57-74.
-
(2002)
Adv Biochem Eng Biotechnol
, vol.77
, pp. 57-74
-
-
Jurinke, C.1
van den Boom, D.2
Cantor, C.R.3
Köster, H.4
-
29
-
-
0038594347
-
MALDI-TOF mass spectrometry-based SNP genotyping
-
Storm N, Darnhofer-Patel B, van den Boom D, Rodi CP. MALDI-TOF mass spectrometry-based SNP genotyping. Methods Molecular Biology 2003, 212:241-262.
-
(2003)
Methods Molecular Biology
, vol.212
, pp. 241-262
-
-
Storm, N.1
Darnhofer-Patel, B.2
van den Boom, D.3
Rodi, C.P.4
-
31
-
-
0043073175
-
Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2
-
10.1007/s00125-003-1135-3, 12819904
-
Weedon MN, Gloyn AL, Frayling TM, Hattersley AT, Davey Smith G, Ben-Shlomo Y. Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2. Diabetologia 2003, 46(7):1021-1023. 10.1007/s00125-003-1135-3, 12819904.
-
(2003)
Diabetologia
, vol.46
, Issue.7
, pp. 1021-1023
-
-
Weedon, M.N.1
Gloyn, A.L.2
Frayling, T.M.3
Hattersley, A.T.4
Davey Smith, G.5
Ben-Shlomo, Y.6
-
32
-
-
36649022247
-
No evidence that established type 2 diabetes susceptibility variants in the PPARG and KCNJ11 genes have pleiotropic effects on early growth
-
10.1007/s00125-007-0863-1, 17994213
-
Bennett AJ, Sovio U, Ruokonen A, Martikainen H, Pouta A, Hartikainen AL, Franks S, Elliott P, Järvelin MR, McCarthy MI. No evidence that established type 2 diabetes susceptibility variants in the PPARG and KCNJ11 genes have pleiotropic effects on early growth. Diabetologia 2008, 51(1):82-85. 10.1007/s00125-007-0863-1, 17994213.
-
(2008)
Diabetologia
, vol.51
, Issue.1
, pp. 82-85
-
-
Bennett, A.J.1
Sovio, U.2
Ruokonen, A.3
Martikainen, H.4
Pouta, A.5
Hartikainen, A.L.6
Franks, S.7
Elliott, P.8
Järvelin, M.R.9
McCarthy, M.I.10
-
33
-
-
0346726170
-
A critical evaluation of the fetal origins hypothesis and its implications for developing countries
-
Adair LS, Prentice AM. A critical evaluation of the fetal origins hypothesis and its implications for developing countries. J Nutr 2004, 134:191-193.
-
(2004)
J Nutr
, vol.134
, pp. 191-193
-
-
Adair, L.S.1
Prentice, A.M.2
-
34
-
-
67749120339
-
Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI
-
10.1038/ejhg.2008.272, 19209189
-
Shugart YY, Chen L, Day IN, Lewis SJ, Timpson NJ, Yuan W, Abdollahi MR, Ring SM, Ebrahim S, Golding J, Lawlor DA, Davey-Smith G. Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI. Eur J Hum Genet 2009, 17:1050-1055. 10.1038/ejhg.2008.272, 19209189.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1050-1055
-
-
Shugart, Y.Y.1
Chen, L.2
Day, I.N.3
Lewis, S.J.4
Timpson, N.J.5
Yuan, W.6
Abdollahi, M.R.7
Ring, S.M.8
Ebrahim, S.9
Golding, J.10
Lawlor, D.A.11
Davey-Smith, G.12
-
35
-
-
66649099906
-
Type 2 Diabetes Risk Alleles are Associated with Reduced Size at Birth
-
10.2337/db08-1739, 2682672,2682672, 19228808
-
Freathy RM, Bennett AJ, Ring SM, Shields B, Groves CJ, Timpson NJ, Weedon MN, Zeggini E, Lindgren CM, Lango H, Perry JR, Pouta A, Ruokonen A, Hyppönen E, Power C, Elliott P, Strachan DP, Järvelin MR, Smith GD, McCarthy MI, Frayling TM, Hattersley AT. Type 2 Diabetes Risk Alleles are Associated with Reduced Size at Birth. Diabetes 2009, 58(6):1428-1433. 10.2337/db08-1739, 2682672,2682672, 19228808.
-
(2009)
Diabetes
, vol.58
, Issue.6
, pp. 1428-1433
-
-
Freathy, R.M.1
Bennett, A.J.2
Ring, S.M.3
Shields, B.4
Groves, C.J.5
Timpson, N.J.6
Weedon, M.N.7
Zeggini, E.8
Lindgren, C.M.9
Lango, H.10
Perry, J.R.11
Pouta, A.12
Ruokonen, A.13
Hyppönen, E.14
Power, C.15
Elliott, P.16
Strachan, D.P.17
Järvelin, M.R.18
Smith, G.D.19
McCarthy, M.I.20
Frayling, T.M.21
Hattersley, A.T.22
more..
-
36
-
-
70349642876
-
Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene
-
10.2337/db09-0506, 19592620
-
Zhao J, Li M, Bradfield JP, Wang K, Zhang H, Sleiman P, Kim CE, Annaiah K, Glaberson W, Glessner JT, Otieno FG, Thomas KA, Garris M, Hou C, Frackelton EC, Chiavacci RM, Berkowitz RI, Hakonarson H, Grant SF. Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene. Diabetes 2009, 58(10):2414-2418. 10.2337/db09-0506, 19592620.
-
(2009)
Diabetes
, vol.58
, Issue.10
, pp. 2414-2418
-
-
Zhao, J.1
Li, M.2
Bradfield, J.P.3
Wang, K.4
Zhang, H.5
Sleiman, P.6
Kim, C.E.7
Annaiah, K.8
Glaberson, W.9
Glessner, J.T.10
Otieno, F.G.11
Thomas, K.A.12
Garris, M.13
Hou, C.14
Frackelton, E.C.15
Chiavacci, R.M.16
Berkowitz, R.I.17
Hakonarson, H.18
Grant, S.F.19
-
37
-
-
64149117551
-
Interaction between prenatal growth and high-risk genotypes in the development of type 2 diabetes
-
10.1007/s00125-009-1291-1, 19225753
-
Pulizzi N, Lyssenko V, Jonsson A, Osmond C, Laakso M, Kajantie E, Barker DJ, Groop LC, Eriksson JG. Interaction between prenatal growth and high-risk genotypes in the development of type 2 diabetes. Diabetologia 2009, 52(5):825-829. 10.1007/s00125-009-1291-1, 19225753.
-
(2009)
Diabetologia
, vol.52
, Issue.5
, pp. 825-829
-
-
Pulizzi, N.1
Lyssenko, V.2
Jonsson, A.3
Osmond, C.4
Laakso, M.5
Kajantie, E.6
Barker, D.J.7
Groop, L.C.8
Eriksson, J.G.9
-
38
-
-
34447517663
-
TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population
-
10.1186/1471-2350-8-37, 1920504, 17593304
-
Cauchi S, Meyre D, Choquet H, Deghmoun S, Durand E, Gaget S, Lecoeur C, Froguel P, Levy-Marchal C. TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population. BMC Med Genet 2007, 8:37. 10.1186/1471-2350-8-37, 1920504, 17593304.
-
(2007)
BMC Med Genet
, vol.8
, pp. 37
-
-
Cauchi, S.1
Meyre, D.2
Choquet, H.3
Deghmoun, S.4
Durand, E.5
Gaget, S.6
Lecoeur, C.7
Froguel, P.8
Levy-Marchal, C.9
-
39
-
-
68349161178
-
Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies
-
10.1186/1471-2350-10-67, 2722586, 19615048
-
Mook-Kanamori DO, de Kort SW, van Duijn CM, Uitterlinden AG, Hofman A, Moll HA, Steegers EA, Hokken-Koelega AC, Jaddoe VW. Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies. BMC Med Genet 2009, 10:67. 10.1186/1471-2350-10-67, 2722586, 19615048.
-
(2009)
BMC Med Genet
, vol.10
, pp. 67
-
-
Mook-Kanamori, D.O.1
de Kort, S.W.2
van Duijn, C.M.3
Uitterlinden, A.G.4
Hofman, A.5
Moll, H.A.6
Steegers, E.A.7
Hokken-Koelega, A.C.8
Jaddoe, V.W.9
-
40
-
-
34250827858
-
Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals
-
10.1086/518517, 1867102, 17503332
-
Freathy RM, Weedon MN, Bennett A, Hypponen E, Relton CL, Knight B, Shields B, Parnell KS, Groves CJ, Ring SM, Pembrey ME, Ben-Shlomo Y, Strachan DP, Power C, Jarvelin MR, McCarthy MI, Davey Smith G, Hattersley AT, Frayling TM. Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals. Am J Hum Genet 2007, 80:1150-1161. 10.1086/518517, 1867102, 17503332.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 1150-1161
-
-
Freathy, R.M.1
Weedon, M.N.2
Bennett, A.3
Hypponen, E.4
Relton, C.L.5
Knight, B.6
Shields, B.7
Parnell, K.S.8
Groves, C.J.9
Ring, S.M.10
Pembrey, M.E.11
Ben-Shlomo, Y.12
Strachan, D.P.13
Power, C.14
Jarvelin, M.R.15
McCarthy, M.I.16
Davey Smith, G.17
Hattersley, A.T.18
Frayling, T.M.19
-
41
-
-
0032430986
-
Power and Sample Size Calculations for Studies Involving Linear Regression
-
10.1016/S0197-2456(98)00037-3, 9875838
-
Dupont WD, Plummer WD. Power and Sample Size Calculations for Studies Involving Linear Regression. Controlled Clinical Trials 1998, 19:589-601. 10.1016/S0197-2456(98)00037-3, 9875838.
-
(1998)
Controlled Clinical Trials
, vol.19
, pp. 589-601
-
-
Dupont, W.D.1
Plummer, W.D.2
-
42
-
-
0031859976
-
Mutations in the glucokinase gene of the fetus result in reduced birth weight
-
10.1038/953, 9662401
-
Hattersley AT, Beards F, Ballantyne E, Appleton M, Harvey R, Ellard S. Mutations in the glucokinase gene of the fetus result in reduced birth weight. Nature Genetics 1998, 19:268-270. 10.1038/953, 9662401.
-
(1998)
Nature Genetics
, vol.19
, pp. 268-270
-
-
Hattersley, A.T.1
Beards, F.2
Ballantyne, E.3
Appleton, M.4
Harvey, R.5
Ellard, S.6
-
43
-
-
77951766379
-
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
-
10.1038/ng.567, 20372150
-
Freathy RM, Mook-Kanamori DO, Sovio U, et al. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics 2010, 42:430-435. 10.1038/ng.567, 20372150.
-
(2010)
Nature Genetics
, vol.42
, pp. 430-435
-
-
Freathy, R.M.1
Mook-Kanamori, D.O.2
Sovio, U.3
-
44
-
-
75749086085
-
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
-
10.1038/ng.520, 20081858
-
Dupuis J, Langenberg C, Prokopenko I, et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010, 42:105-116. 10.1038/ng.520, 20081858.
-
(2010)
Nat Genet
, vol.42
, pp. 105-116
-
-
Dupuis, J.1
Langenberg, C.2
Prokopenko, I.3
-
45
-
-
42349106044
-
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
10.1038/ng.120, 2672416, 18372903
-
Zeggini E, Scott LJ, Saxena R, et al. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nature Genetics 2008, 40:638-645. 10.1038/ng.120, 2672416, 18372903.
-
(2008)
Nature Genetics
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
-
46
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3000 shared controls
-
10.1038/nature05911, 2719288, 17554300, Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium Genome-wide association study of 14,000 cases of seven common diseases and 3000 shared controls. Nature 2007, 447:661-678. 10.1038/nature05911, 2719288, 17554300, Wellcome Trust Case Control Consortium.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
47
-
-
34249895023
-
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
-
10.1126/science.1142364, 17463249, Wellcome Trust Case Control Consortium (WTCCC)
-
Zeggini E, Weedon MN, Lindgren CM, Frayling TM, Elliott KS, Lango H, Timpson NJ, Perry JR, Rayner NW, Freathy RM, Barrett JC, Shields B, Morris AP, Ellard S, Groves CJ, Harries LW, Marchini JL, Owen KR, Knight B, Cardon LR, Walker M, Hitman GA, Morris AD, Doney AS, , McCarthy MI, Hattersley AT. Wellcome Trust Case Control Consortium (WTCCC) Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 2007, 316:1336-1341. 10.1126/science.1142364, 17463249, Wellcome Trust Case Control Consortium (WTCCC).
-
(2007)
Science
, vol.316
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
Frayling, T.M.4
Elliott, K.S.5
Lango, H.6
Timpson, N.J.7
Perry, J.R.8
Rayner, N.W.9
Freathy, R.M.10
Barrett, J.C.11
Shields, B.12
Morris, A.P.13
Ellard, S.14
Groves, C.J.15
Harries, L.W.16
Marchini, J.L.17
Owen, K.R.18
Knight, B.19
Cardon, L.R.20
Walker, M.21
Hitman, G.A.22
Morris, A.D.23
Doney, A.S.24
McCarthy, M.I.25
Hattersley, A.T.26
more..
-
48
-
-
34249885875
-
A genome wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
10.1126/science.1142382, 17463248
-
Scott LJ, Mohlke KL, Bonnycastle LL, et al. A genome wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007, 316:1341-1345. 10.1126/science.1142382, 17463248.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
-
49
-
-
0031595923
-
A Pro12Ala substitution in PPARy2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
-
10.1038/3099, 9806549
-
Deeb SS, Fajas L, Nemoto M, Pihlajamäki J, Mykkänen L, Kuusisto J, Laakso M, Fujimoto W, Auwerx J. A Pro12Ala substitution in PPARy2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nature Genetics 1998, 20:284-287. 10.1038/3099, 9806549.
-
(1998)
Nature Genetics
, vol.20
, pp. 284-287
-
-
Deeb, S.S.1
Fajas, L.2
Nemoto, M.3
Pihlajamäki, J.4
Mykkänen, L.5
Kuusisto, J.6
Laakso, M.7
Fujimoto, W.8
Auwerx, J.9
-
50
-
-
0033624575
-
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
10.1038/79839, 10973253
-
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. Nature Genetics 2000, 26:76-80. 10.1038/79839, 10973253.
-
(2000)
Nature Genetics
, 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
-
51
-
-
34547536393
-
Common variants in WFS1 confer risk of type 2 diabetes
-
10.1038/ng2067, 2672152, 17603484
-
Sandhu MS, Weedon MN, Fawcett KA, Wasson J, Debenham SL, Daly A, Lango H, Frayling TM, Neumann RJ, Sherva R, Blech I, Pharoah PD, Palmer CN, Kimber C, Tavendale R, Morris AD, McCarthy MI, Walker M, Hitman G, Glaser B, Permutt MA, Hattersley AT, Wareham NJ, Barroso I. Common variants in WFS1 confer risk of type 2 diabetes. Nature Genetics 2007, 39:951-953. 10.1038/ng2067, 2672152, 17603484.
-
(2007)
Nature Genetics
, vol.39
, pp. 951-953
-
-
Sandhu, M.S.1
Weedon, M.N.2
Fawcett, K.A.3
Wasson, J.4
Debenham, S.L.5
Daly, A.6
Lango, H.7
Frayling, T.M.8
Neumann, R.J.9
Sherva, R.10
Blech, I.11
Pharoah, P.D.12
Palmer, C.N.13
Kimber, C.14
Tavendale, R.15
Morris, A.D.16
McCarthy, M.I.17
Walker, M.18
Hitman, G.19
Glaser, B.20
Permutt, M.A.21
Hattersley, A.T.22
Wareham, N.J.23
Barroso, I.24
more..
-
52
-
-
39049100084
-
Testing of diabetes-associated WFS1 polymorphisms in the diabetes prevention program
-
Diabetes Prevention Program Research Group
-
Florez JC, Jablonski KA, McAteer J, Sandhu MS, Wareham NJ, Barroso I, Franks PW, Altshuler D, Knowler WC, . Diabetes Prevention Program Research Group Testing of diabetes-associated WFS1 polymorphisms in the diabetes prevention program. Diabetologica 2008, 51:451-457. Diabetes Prevention Program Research Group.
-
(2008)
Diabetologica
, vol.51
, pp. 451-457
-
-
Florez, J.C.1
Jablonski, K.A.2
McAteer, J.3
Sandhu, M.S.4
Wareham, N.J.5
Barroso, I.6
Franks, P.W.7
Altshuler, D.8
Knowler, W.C.9
-
53
-
-
39049146958
-
Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations
-
Franks PW, Rolandsson O, Debenham SL, Fawcett KA, Payne F, Dina C, Froguel P, Mohlke KL, Willer C, Olsson T, Wareham NJ, Hallmans G, Barroso I, Sandhu MS. Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations. Diabetologica 2008, 51:458-463.
-
(2008)
Diabetologica
, vol.51
, pp. 458-463
-
-
Franks, P.W.1
Rolandsson, O.2
Debenham, S.L.3
Fawcett, K.A.4
Payne, F.5
Dina, C.6
Froguel, P.7
Mohlke, K.L.8
Willer, C.9
Olsson, T.10
Wareham, N.J.11
Hallmans, G.12
Barroso, I.13
Sandhu, M.S.14
-
54
-
-
34249828965
-
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
-
10.1038/ng2043, 17460697
-
Steinthorsdottir V, Thorleifsson G, Reynisdottir I, et al. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. Nature Genetics 2007, 39:770-775. 10.1038/ng2043, 17460697.
-
(2007)
Nature Genetics
, vol.39
, pp. 770-775
-
-
Steinthorsdottir, V.1
Thorleifsson, G.2
Reynisdottir, I.3
-
55
-
-
32544451924
-
Variant of transcription factor 7 like 2 (TCF7L2) gene confers risk of type 2 diabetes
-
10.1038/ng1732, 16415884
-
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. Nature Genetics 2006, 38:320-323. 10.1038/ng1732, 16415884.
-
(2006)
Nature Genetics
, 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..
-
56
-
-
33846596193
-
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution
-
10.1038/ng1960, 17206141
-
Helgason A, Pálsson S, Thorleifsson G, et al. Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution. Nature Genetics 2007, 39:218-225. 10.1038/ng1960, 17206141.
-
(2007)
Nature Genetics
, vol.39
, pp. 218-225
-
-
Helgason, A.1
Pálsson, S.2
Thorleifsson, G.3
-
57
-
-
0031773333
-
Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of type II diabetes mellitus in Caucasians
-
10.1007/s001250051098, 9867219
-
Hani EH, Boutin P, Durand E, Inoue H, Permutt MA, Velho G, Froguel P. Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of type II diabetes mellitus in Caucasians. Diabetologia 1998, 41:1511-1515. 10.1007/s001250051098, 9867219.
-
(1998)
Diabetologia
, vol.41
, pp. 1511-1515
-
-
Hani, E.H.1
Boutin, P.2
Durand, E.3
Inoue, H.4
Permutt, M.A.5
Velho, G.6
Froguel, P.7
-
58
-
-
0037317981
-
Large scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that KCNJ11 E23K variant is associated with type 2 diabetes
-
10.2337/diabetes.52.2.568, 12540637
-
Gloyn AL, Weedon MN, Owen KR, Turner MJ, Knight BA, Hitman G, Walker M, Levy JC, Sampson M, Halford S, McCarthy MI, Hattersley AT, Frayling TM. Large scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that KCNJ11 E23K variant is associated with type 2 diabetes. Diabetes 2003, 52:568-572. 10.2337/diabetes.52.2.568, 12540637.
-
(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.6
Walker, M.7
Levy, J.C.8
Sampson, M.9
Halford, S.10
McCarthy, M.I.11
Hattersley, A.T.12
Frayling, T.M.13
-
59
-
-
0037312864
-
The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes
-
10.2337/diabetes.52.2.573, 12540638
-
Nielsen EM, Hansen L, Carstensen B, Echwald SM, Drivsholm T, Glümer C, Thorsteinsson B, Borch-Johnsen K, Hansen T, Pedersen O. The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes. Diabetes 2003, 52:573-577. 10.2337/diabetes.52.2.573, 12540638.
-
(2003)
Diabetes
, vol.52
, pp. 573-577
-
-
Nielsen, E.M.1
Hansen, L.2
Carstensen, B.3
Echwald, S.M.4
Drivsholm, T.5
Glümer, C.6
Thorsteinsson, B.7
Borch-Johnsen, K.8
Hansen, T.9
Pedersen, O.10
-
60
-
-
58149156287
-
Variants in MTNR1B influence fasting glucose levels
-
10.1038/ng.290, 2682768, 19060907
-
Prokopenko I, Langenberg C, Florez JC, et al. Variants in MTNR1B influence fasting glucose levels. Nature Genetics 2009, 41(1):77-81. 10.1038/ng.290, 2682768, 19060907.
-
(2009)
Nature Genetics
, vol.41
, Issue.1
, pp. 77-81
-
-
Prokopenko, I.1
Langenberg, C.2
Florez, J.C.3
-
61
-
-
58149175669
-
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion
-
10.1038/ng.288, 19060908
-
Lyssenko V, Nagorny CL, Erdos MR, et al. Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion. Nature Genetics 2009, 41(1):82-88. 10.1038/ng.288, 19060908.
-
(2009)
Nature Genetics
, vol.41
, Issue.1
, pp. 82-88
-
-
Lyssenko, V.1
Nagorny, C.L.2
Erdos, M.R.3
-
62
-
-
58149175143
-
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk
-
10.1038/ng.277, 19060909
-
Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, et al. A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. Nature Genetics 2009, 41(1):89-94. 10.1038/ng.277, 19060909.
-
(2009)
Nature Genetics
, vol.41
, Issue.1
, pp. 89-94
-
-
Bouatia-Naji, N.1
Bonnefond, A.2
Cavalcanti-Proença, C.3
-
63
-
-
34547510624
-
Two variants on chromosome 17 confer prostate cancer risk, and the one in TC2 protects against type 2 diabetes
-
10.1038/ng2062, 17603485
-
Gudmundsson J, Sulem P, Steinthorsdottir V, et al. Two variants on chromosome 17 confer prostate cancer risk, and the one in TC2 protects against type 2 diabetes. Nature Genetics 2007, 39:977-983. 10.1038/ng2062, 17603485.
-
(2007)
Nature Genetics
, vol.39
, pp. 977-983
-
-
Gudmundsson, J.1
Sulem, P.2
Steinthorsdottir, V.3
-
64
-
-
33847361938
-
Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes
-
10.2337/db06-0202, 17327436
-
Winckler W, Weedon MN, Graham RR, McCarroll SA, Purcell S, Almgren P, Tuomi T, Gaudet D, Boström KB, Walker M, Hitman G, Hattersley AT, McCarthy MI, Ardlie KG, Hirschhorn JN, Daly MJ, Frayling TM, Groop L, Altshuler D. Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes. Diabetes 2007, 56:685-693. 10.2337/db06-0202, 17327436.
-
(2007)
Diabetes
, vol.56
, pp. 685-693
-
-
Winckler, W.1
Weedon, M.N.2
Graham, R.R.3
McCarroll, S.A.4
Purcell, S.5
Almgren, P.6
Tuomi, T.7
Gaudet, D.8
Boström, K.B.9
Walker, M.10
Hitman, G.11
Hattersley, A.T.12
McCarthy, M.I.13
Ardlie, K.G.14
Hirschhorn, J.N.15
Daly, M.J.16
Frayling, T.M.17
Groop, L.18
Altshuler, D.19
-
65
-
-
58149163141
-
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
-
10.1038/ng.274, 19079260
-
Thorleifsson G, Walters GB, Gudbjartsson DF, et al. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. Nature Genetics 2009, 41:18-24. 10.1038/ng.274, 19079260.
-
(2009)
Nature Genetics
, vol.41
, pp. 18-24
-
-
Thorleifsson, G.1
Walters, G.B.2
Gudbjartsson, D.F.3
-
66
-
-
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, et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nature Genetics 2009, 41(1):25-34. 10.1038/ng.287, 2695662, 19079261.
-
(2009)
Nature Genetics
, vol.41
, Issue.1
, pp. 25-34
-
-
Willer, C.J.1
Speliotes, E.K.2
Loos, R.J.3
-
67
-
-
34547625955
-
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
-
10.1371/journal.pgen.0030115, 1934391,1934391, 17658951
-
Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orrú M, Usala G, Dei M, Lai S, Maschio A, Busonero F, Mulas A, Ehret GB, Fink AA, Weder AB, Cooper RS, Galan P, Chakravarti A, Schlessinger D, Cao A, Lakatta E, Abecasis GR. Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet 2007, 3:e115. 10.1371/journal.pgen.0030115, 1934391,1934391, 17658951.
-
(2007)
PLoS Genet
, vol.3
-
-
Scuteri, A.1
Sanna, S.2
Chen, W.M.3
Uda, M.4
Albai, G.5
Strait, J.6
Najjar, S.7
Nagaraja, R.8
Orrú, M.9
Usala, G.10
Dei, M.11
Lai, S.12
Maschio, A.13
Busonero, F.14
Mulas, A.15
Ehret, G.B.16
Fink, A.A.17
Weder, A.B.18
Cooper, R.S.19
Galan, P.20
Chakravarti, A.21
Schlessinger, D.22
Cao, A.23
Lakatta, E.24
Abecasis, G.R.25
more..
-
68
-
-
33645825830
-
A common genetic variant is associated with adult and childhood obesity
-
10.1126/science.1124779, 16614226
-
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. 10.1126/science.1124779, 16614226.
-
(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..
-
69
-
-
44849086097
-
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity
-
Liu YJ, Liu XG, Wang L, Dina C, Yan H, Liu JF, Levy S, Papasian CJ, Drees BM, Hamilton JJ, Meyre D, Delplanque J, Pei YF, Zhang L, Recker RR, Froguel P, Deng HW. Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. Human Molecular Genetics 2008, 17(12):1903-1813.
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.12
, pp. 1903-11813
-
-
Liu, Y.J.1
Liu, X.G.2
Wang, L.3
Dina, C.4
Yan, H.5
Liu, J.F.6
Levy, S.7
Papasian, C.J.8
Drees, B.M.9
Hamilton, J.J.10
Meyre, D.11
Delplanque, J.12
Pei, Y.F.13
Zhang, L.14
Recker, R.R.15
Froguel, P.16
Deng, H.W.17
-
70
-
-
67749146993
-
A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity
-
10.1038/oby.2009.75, 19300429
-
Blakemore AI, Meyre D, Delplanque J, Vatin V, Lecoeur C, Marre M, Tichet J, Balkau B, Froguel P, Walley AJ. A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity. Obesity 2009, 17(8):1549-1553. 10.1038/oby.2009.75, 19300429.
-
(2009)
Obesity
, vol.17
, Issue.8
, pp. 1549-1553
-
-
Blakemore, A.I.1
Meyre, D.2
Delplanque, J.3
Vatin, V.4
Lecoeur, C.5
Marre, M.6
Tichet, J.7
Balkau, B.8
Froguel, P.9
Walley, A.J.10
-
71
-
-
36248986199
-
Association of single-nucleotide polymorphisms in MTMR9 gene with obesity
-
10.1093/hmg/ddm260, 17855449
-
Yanagiya T, Tanabe A, Iida A, et al. Association of single-nucleotide polymorphisms in MTMR9 gene with obesity. Hum Mol Genet 2007, 16(24):3017-3026. 10.1093/hmg/ddm260, 17855449.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.24
, pp. 3017-3026
-
-
Yanagiya, T.1
Tanabe, A.2
Iida, A.3
-
72
-
-
59149097625
-
Genome-wide association study for early onset and morbid adult obesity identifies three new risk loci in European populations
-
10.1038/ng.301, 19151714
-
Meyre D, Delplanque J, Chèvre JC, et al. Genome-wide association study for early onset and morbid adult obesity identifies three new risk loci in European populations. Nature Genetics 2009, 41(2):157-159. 10.1038/ng.301, 19151714.
-
(2009)
Nature Genetics
, vol.41
, Issue.2
, pp. 157-159
-
-
Meyre, D.1
Delplanque, J.2
Chèvre, J.C.3
-
73
-
-
34249777814
-
Variation in FTO contributes to childhood obesity and severe adult obesity
-
10.1038/ng2048, 17496892
-
Dina C, Meyre D, Gallina S, Durand E, Körner A, Jacobson P, Carlsson LM, Kiess W, Vatin V, Lecoeur C, Delplanque J, Vaillant E, Pattou F, Ruiz J, Weill J, Levy-Marchal C, Horber F, Potoczna N, Hercberg S, Le Stunff C, Bougnères P, Kovacs P, Marre M, Balkau B, Cauchi S, Chèvre JC, Froguel P. Variation in FTO contributes to childhood obesity and severe adult obesity. Nature Genetics 2007, 39:724-726. 10.1038/ng2048, 17496892.
-
(2007)
Nature Genetics
, vol.39
, pp. 724-726
-
-
Dina, C.1
Meyre, D.2
Gallina, S.3
Durand, E.4
Körner, A.5
Jacobson, P.6
Carlsson, L.M.7
Kiess, W.8
Vatin, V.9
Lecoeur, C.10
Delplanque, J.11
Vaillant, E.12
Pattou, F.13
Ruiz, J.14
Weill, J.15
Levy-Marchal, C.16
Horber, F.17
Potoczna, N.18
Hercberg, S.19
Le Stunff, C.20
Bougnères, P.21
Kovacs, P.22
Marre, M.23
Balkau, B.24
Cauchi, S.25
Chèvre, J.C.26
Froguel, P.27
more..
-
74
-
-
34248594090
-
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
-
10.1126/science.1141634, 2646098, 17434869
-
Frayling TM, Timpson NJ, Weedon MN, et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science 2007, 316:889-894. 10.1126/science.1141634, 2646098, 17434869.
-
(2007)
Science
, vol.316
, pp. 889-894
-
-
Frayling, T.M.1
Timpson, N.J.2
Weedon, M.N.3
-
75
-
-
44349142294
-
Common variants near MC4R are associated with fat mass, weight and risk of obesity
-
10.1038/ng.140, 2669167, 18454148
-
Loos RJ, Lindgren CM, Li S, et al. Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nature Genetics 2008, 40(6):768-775. 10.1038/ng.140, 2669167, 18454148.
-
(2008)
Nature Genetics
, vol.40
, Issue.6
, pp. 768-775
-
-
Loos, R.J.1
Lindgren, C.M.2
Li, S.3
-
76
-
-
44349166252
-
Common genetic variation near MC4R is associated with waist circumference and insulin resistance
-
10.1038/ng.156, 18454146
-
Chambers JC, Elliott P, Zabaneh D, Zhang W, Li Y, Froguel P, Balding D, Scott J, Kooner JS. Common genetic variation near MC4R is associated with waist circumference and insulin resistance. Nature Genetics 2008, 40(6):716-718. 10.1038/ng.156, 18454146.
-
(2008)
Nature Genetics
, vol.40
, Issue.6
, pp. 716-718
-
-
Chambers, J.C.1
Elliott, P.2
Zabaneh, D.3
Zhang, W.4
Li, Y.5
Froguel, P.6
Balding, D.7
Scott, J.8
Kooner, J.S.9
-
77
-
-
0029000469
-
Cross-sectional stature and weight reference curves for the UK, 1990
-
10.1136/adc.73.1.17, 1511167, 7639543
-
Freeman JV, Cole TJ, Chinn S, Jones PR, White EM, Preece MA. Cross-sectional stature and weight reference curves for the UK, 1990. Archives of Disease in Childhood 1995, 73:17-24. 10.1136/adc.73.1.17, 1511167, 7639543.
-
(1995)
Archives of Disease in Childhood
, vol.73
, pp. 17-24
-
-
Freeman, J.V.1
Cole, T.J.2
Chinn, S.3
Jones, P.R.4
White, E.M.5
Preece, M.A.6
-
78
-
-
0029033734
-
Body Mass Index reference curves for the UK, 1990
-
10.1136/adc.73.1.25, 1511150, 7639544
-
Cole TJ, Freeman JV, Preece MA. Body Mass Index reference curves for the UK, 1990. Archives of Disease in Childhood 1995, 73:25-29. 10.1136/adc.73.1.25, 1511150, 7639544.
-
(1995)
Archives of Disease in Childhood
, vol.73
, pp. 25-29
-
-
Cole, T.J.1
Freeman, J.V.2
Preece, M.A.3
|