-
1
-
-
0025094344
-
Mapping genes in diabetes: Genetic epidemiological perspective
-
Rich S: Mapping genes in diabetes: genetic epidemiological perspective. Diabetes 39:1315-1319, 1990
-
(1990)
Diabetes
, vol.39
, pp. 1315-1319
-
-
Rich, S.1
-
2
-
-
0026641354
-
Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland
-
Kaprio J, Tuomilehto J, Koskenvuo M, Romanov K, Reunanen A, Eriksson J, Stengard J, Kesaniemi YA: Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland. Diabetologia 35:1060-1067, 1992
-
(1992)
Diabetologia
, vol.35
, pp. 1060-1067
-
-
Kaprio, J.1
Tuomilehto, J.2
Koskenvuo, M.3
Romanov, K.4
Reunanen, A.5
Eriksson, J.6
Stengard, J.7
Kesaniemi, Y.A.8
-
3
-
-
0036255003
-
The search for type 2 diabetes susceptibility genes using whole-genome scans: An epidemiologist's perspective
-
Stern MP: The search for type 2 diabetes susceptibility genes using whole-genome scans: an epidemiologist's perspective. Diabetes Metab Res Rev 18:106-113, 2002
-
(2002)
Diabetes Metab Res Rev
, vol.18
, pp. 106-113
-
-
Stern, M.P.1
-
4
-
-
0033772073
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
-
Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, Lindner TH, Mashima H, Schwarz PEH, del Bosque-Plata L, Horikawa Y, Oda Y, Yoshoiuchi I, Colilla S, Polonsky K, Wei S, Concannon P, Iwasaki N, Schulze J, Baier LJ, Bogardus C, Groop L, Boerwinkle E, Hanis CL, Bell GI: Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat Genet 26:163-175, 2000
-
(2000)
Nat Genet
, vol.26
, pp. 163-175
-
-
Horikawa, Y.1
Oda, N.2
Cox, N.J.3
Li, X.4
Orho-Melander, M.5
Hara, M.6
Hinokio, Y.7
Lindner, T.H.8
Mashima, H.9
Schwarz, P.E.H.10
Del Bosque-Plata, L.11
Horikawa, Y.12
Oda, Y.13
Yoshoiuchi, I.14
Colilla, S.15
Polonsky, K.16
Wei, S.17
Concannon, P.18
Iwasaki, N.19
Schulze, J.20
Baier, L.J.21
Bogardus, C.22
Groop, L.23
Boerwinkle, E.24
Hanis, C.L.25
Bell, G.I.26
more..
-
5
-
-
0033797241
-
A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance
-
Baier LJ, Permana PA, Yang X, Pratley RE, Hanson RL, Shen GQ, Mott D, Knowler WC, Cox NJ, Horikawa Y, Oda N, Bell GI, Bogardus C: A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance. J Clin Invest 106:R69-R73, 2000
-
(2000)
J Clin Invest
, vol.106
-
-
Baier, L.J.1
Permana, P.A.2
Yang, X.3
Pratley, R.E.4
Hanson, R.L.5
Shen, G.Q.6
Mott, D.7
Knowler, W.C.8
Cox, N.J.9
Horikawa, Y.10
Oda, N.11
Bell, G.I.12
Bogardus, C.13
-
6
-
-
0034894047
-
Studies ofassociation between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom
-
Evans JC, Frayling TM, Cassell PG, Saker PJ, Hitman GA, Walker M, Levy JC, O'Rahilly S, Rao PV, Bennett AJ, Jones EC, Menzel S, Prestwich P, Simecek N, Wishart M, Dhillon R, Fletcher C, Millward A, Demaine A, Wilkin T, Horikawa Y, Cox NJ, Bell GI, Ellard S, McCarthy MI, Hattersley AT: Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom. Am J Hum Genet 69:544-552, 2001
-
(2001)
Am J Hum Genet
, vol.69
, pp. 544-552
-
-
Evans, J.C.1
Frayling, T.M.2
Cassell, P.G.3
Saker, P.J.4
Hitman, G.A.5
Walker, M.6
Levy, J.C.7
O'Rahilly, S.8
Rao, P.V.9
Bennett, A.J.10
Jones, E.C.11
Menzel, S.12
Prestwich, P.13
Simecek, N.14
Wishart, M.15
Dhillon, R.16
Fletcher, C.17
Millward, A.18
Demaine, A.19
Wilkin, T.20
Horikawa, Y.21
Cox, N.J.22
Bell, G.I.23
Ellard, S.24
McCarthy, M.I.25
Hattersley, A.T.26
more..
-
7
-
-
0035432297
-
Absence of association of type 2 diabetes with CAPN10 and PC-1 polymorphisms in Oji-Cree
-
Hegele RA, Harris SB, Zinman B, Hanley A, Cao H: Absence of association of type 2 diabetes with CAPN10 and PC-1 polymorphisms in Oji-Cree (Letter). Diabetes Care 24:1498-1499, 2001
-
(2001)
Diabetes Care
, vol.24
, pp. 1498-1499
-
-
Hegele, R.A.1
Harris, S.B.2
Zinman, B.3
Hanley, A.4
Cao, H.5
-
8
-
-
0035205377
-
Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: No evidence of association
-
Tsai HJ, Sun G, Weeks DE, Kaushal R, Wolujewicz M, McGarvey ST, Tufa J, Viali S, Deka R: Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association. Am J Hum Genet 69:1236-1244, 2001
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1236-1244
-
-
Tsai, H.J.1
Sun, G.2
Weeks, D.E.3
Kaushal, R.4
Wolujewicz, M.5
McGarvey, S.T.6
Tufa, J.7
Viali, S.8
Deka, R.9
-
9
-
-
0036316935
-
Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort
-
Fingerlin TE, Erdos MR, Watanabe RM, Stringham HM, Mohlke KL, Silander K, Valle TT, Buchanan TA, Tuomilehto J, Bergman RN, Boehnke M, Collins FS: Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort. Diabetes 51:1644-1648, 2002
-
(2002)
Diabetes
, vol.51
, pp. 1644-1648
-
-
Fingerlin, T.E.1
Erdos, M.R.2
Watanabe, R.M.3
Stringham, H.M.4
Mohlke, K.L.5
Silander, K.6
Valle, T.T.7
Buchanan, T.A.8
Tuomilehto, J.9
Bergman, R.N.10
Boehnke, M.11
Collins, F.S.12
-
10
-
-
0026346830
-
Prevalence of diabetes mellitus and impaired glucose tolerance in the middle-aged population of three areas in Finland
-
Tuomilehto J, Korhonen HJ, Kartovaara L, Salomaa V, Stengard JH, Pitkanen M, Aro A, Javela K, Uusitupa M, Pitkaniemi J: Prevalence of diabetes mellitus and impaired glucose tolerance in the middle-aged population of three areas in Finland. Int J Epidemiol 20:1010-1017, 1991
-
(1991)
Int J Epidemiol
, vol.20
, pp. 1010-1017
-
-
Tuomilehto, J.1
Korhonen, H.J.2
Kartovaara, L.3
Salomaa, V.4
Stengard, J.H.5
Pitkanen, M.6
Aro, A.7
Javela, K.8
Uusitupa, M.9
Pitkaniemi, J.10
-
11
-
-
0000918095
-
Epidemiology of NIDDM in Europids
-
Alberti KGMM, Zimmet P, DeFronzo RA, Keen H, Eds. West Sussex, U.K., John Wiley
-
Valle T, Tuomilehto J, Eriksson J: Epidemiology of NIDDM in Europids. In International Textbook of Diabetes Mellitus. 2nd ed. Alberti KGMM, Zimmet P, DeFronzo RA, Keen H, Eds. West Sussex, U.K., John Wiley, 1997, p. 125-142
-
(1997)
International Textbook of Diabetes Mellitus. 2nd Ed.
, pp. 125-142
-
-
Valle, T.1
Tuomilehto, J.2
Eriksson, J.3
-
12
-
-
13044277561
-
Type 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs
-
Ghosh S, Watanabe RM, Hauser ER, Valle T, Magnuson VL, Erdos MR, Langefeld CD, Balow J Jr, Ally DS, Kohtamaki K, Chines P, Birznieks G, Kaleta HS, Musick A, Te C, Tannenbaum J, Eldridge W, Shapiro S, Martin C, Witt A, So A, Chang J, Shurtleff B, Porter R, Boehnke M, et al.: Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proc Natl Acad Sci U S A 96:2198-2203, 1999
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 2198-2203
-
-
Ghosh, S.1
Watanabe, R.M.2
Hauser, E.R.3
Valle, T.4
Magnuson, V.L.5
Erdos, M.R.6
Langefeld, C.D.7
Balow Jr., J.8
Ally, D.S.9
Kohtamaki, K.10
Chines, P.11
Birznieks, G.12
Kaleta, H.S.13
Musick, A.14
Te, C.15
Tannenbaum, J.16
Eldridge, W.17
Shapiro, S.18
Martin, C.19
Witt, A.20
So, A.21
Chang, J.22
Shurtleff, B.23
Porter, R.24
Boehnke, M.25
more..
-
13
-
-
0033764737
-
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I: An autosomal genome scan for genes that predispose to type 2 diabetes
-
Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, Mohlke KL, Silander K, Kohtamaki K, Chines P, Balow J Jr, Birznieks G, Chang J, Eldridge W, Erdos MR, Karanjawala ZE, Knapp JI, Kudelko K, Martin C, Morales-Mena A, Musick A, Musick T, Pfahl C, Porter R, Rayman JB: The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I: an autosomal genome scan for genes that predispose to type 2 diabetes. Am J Hum Genet 67:1174-1185, 2000
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1174-1185
-
-
Ghosh, S.1
Watanabe, R.M.2
Valle, T.T.3
Hauser, E.R.4
Magnuson, V.L.5
Langefeld, C.D.6
Ally, D.S.7
Mohlke, K.L.8
Silander, K.9
Kohtamaki, K.10
Chines, P.11
Balow Jr., J.12
Birznieks, G.13
Chang, J.14
Eldridge, W.15
Erdos, M.R.16
Karanjawala, Z.E.17
Knapp, J.I.18
Kudelko, K.19
Martin, C.20
Morales-Mena, A.21
Musick, A.22
Musick, T.23
Pfahl, C.24
Porter, R.25
Rayman, J.B.26
more..
-
14
-
-
3643136390
-
Mapping genes for NIDDM: Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) study
-
Valle T, Tuomilehto J, Bergman RN, Ghosh S, Hauser ER, Eriksson J, Nylund SJ, Kohtamaki K, Toivanen L, Vidgren G, Tuomilehto-Wolf E, Ehnholm C, Blaschak J, Langefeld CD, Watanabe RM, Magnuson V, Ally DS, Hagopian WA, Ross E, Buchanan TA, Collins F, Boehnke M: Mapping genes for NIDDM: design of the Finland-United States Investigation of NIDDM Genetics (FUSION) study. Diabetes Care 21:949-958, 1998
-
(1998)
Diabetes Care
, vol.21
, pp. 949-958
-
-
Valle, T.1
Tuomilehto, J.2
Bergman, R.N.3
Ghosh, S.4
Hauser, E.R.5
Eriksson, J.6
Nylund, S.J.7
Kohtamaki, K.8
Toivanen, L.9
Vidgren, G.10
Tuomilehto-Wolf, E.11
Ehnholm, C.12
Blaschak, J.13
Langefeld, C.D.14
Watanabe, R.M.15
Magnuson, V.16
Ally, D.S.17
Hagopian, W.A.18
Ross, E.19
Buchanan, T.A.20
Collins, F.21
Boehnke, M.22
more..
-
15
-
-
0003512785
-
-
Geneva, World Health Org. (Tech. Rep. Ser., no. 727)
-
World Health Organization: Diabetes Mellitus: Report of a WHO Study Group. Geneva, World Health Org., 1985 (Tech. Rep. Ser., no. 727)
-
(1985)
Diabetes Mellitus: Report of a WHO Study Group
-
-
-
16
-
-
0033758721
-
The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II: An autosomal genome scan for diabetes-related quantitative-trait loci
-
Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, Kaleta HS, Lange EM, Li C, McEachin RC, Stringham HM, Trager E, White PP, Balow J Jr, Birznieks G, Chang J, Eldridge W: The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II: an autosomal genome scan for diabetes-related quantitative-trait loci. Am J Hum Genet 67:1186-1200, 2000
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1186-1200
-
-
Watanabe, R.M.1
Ghosh, S.2
Langefeld, C.D.3
Valle, T.T.4
Hauser, E.R.5
Magnuson, V.L.6
Mohlke, K.L.7
Silander, K.8
Ally, D.S.9
Chines, P.10
Blaschak-Harvan, J.11
Douglas, J.A.12
Duren, W.L.13
Epstein, M.P.14
Fingerlin, T.E.15
Kaleta, H.S.16
Lange, E.M.17
Li, C.18
McEachin, R.C.19
Stringham, H.M.20
Trager, E.21
White, P.P.22
Balow Jr., J.23
Birznieks, G.24
Chang, J.25
Eldridge, W.26
more..
-
17
-
-
0030881661
-
Accurate inference of relationships in sib-pair linkage studies
-
Boehnke M, Cox NJ: Accurate inference of relationships in sib-pair linkage studies. Am J Hum Genet 61:423-429, 1997
-
(1997)
Am J Hum Genet
, vol.61
, pp. 423-429
-
-
Boehnke, M.1
Cox, N.J.2
-
18
-
-
15444352074
-
Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers
-
Ghosh S, Karanjawala ZE, Hauser ER, Ally D, Knapp JI, Rayman JB, Musick A, Tannenbaum J, Te C, Shapiro S, Eldridge W, Musick T, Martin C, Smith JR, Carpten JD, Brownstein MJ, Powell JI, Whiten R, Chines P, Nylund SJ, Magnuson VL, Boehnke M, Collins FS: Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. Genome Res 7:165-178, 1997
-
(1997)
Genome Res
, vol.7
, pp. 165-178
-
-
Ghosh, S.1
Karanjawala, Z.E.2
Hauser, E.R.3
Ally, D.4
Knapp, J.I.5
Rayman, J.B.6
Musick, A.7
Tannenbaum, J.8
Te, C.9
Shapiro, S.10
Eldridge, W.11
Musick, T.12
Martin, C.13
Smith, J.R.14
Carpten, J.D.15
Brownstein, M.J.16
Powell, J.I.17
Whiten, R.18
Chines, P.19
Nylund, S.J.20
Magnuson, V.L.21
Boehnke, M.22
Collins, F.S.23
more..
-
19
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE: PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63:259-266, 1998
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
20
-
-
0033759689
-
Improved inference of relationships for pairs of individuals
-
Epstein M, Duren WL, Boehnke M: Improved inference of relationships for pairs of individuals. Am J Hum Genet 67:1219-1231, 2000
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1219-1231
-
-
Epstein, M.1
Duren, W.L.2
Boehnke, M.3
-
21
-
-
0033941023
-
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data
-
Douglas JA, Boehnke M, Lange K: A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet 66:1287-1297, 2000
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1287-1297
-
-
Douglas, J.A.1
Boehnke, M.2
Lange, K.3
-
22
-
-
77649173768
-
Longitudinal data analysis using generalized linear models
-
Liang KY, Zeger SL: Longitudinal data analysis using generalized linear models. Biometrika 73:13-22, 1986
-
(1986)
Biometrika
, vol.73
, pp. 13-22
-
-
Liang, K.Y.1
Zeger, S.L.2
-
23
-
-
0028343233
-
Automated construction of genetic linkage maps using an expert system (MultiMap): A human genome linkage map
-
Matise TC, Perlin M, Chakravarti A: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. Nat Genet 6:384-390, 1994
-
(1994)
Nat Genet
, vol.6
, pp. 384-390
-
-
Matise, T.C.1
Perlin, M.2
Chakravarti, A.3
-
24
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman KW, Murray JC, Sheffield VC, White RL, Weber JL: Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet 63:861-869, 1998
-
(1998)
Am J Hum Genet
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
25
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Whittemore AS, Halpern J: A class of tests for linkage using affected pedigree members. Biometrics 50:118-127, 1994
-
(1994)
Biometrics
, vol.50
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
26
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
Kong A, Cox NJ: Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61:1179-1188, 1997
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
27
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES: Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363, 1996
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
28
-
-
3042513608
-
Ordered subset analysis in genetic linkage mapping of complex traits
-
In press
-
Hauser ER, Watanabe RM, Duren WL, Bass MP, Langefeld CD, Boehnke M: Ordered subset analysis in genetic linkage mapping of complex traits. Genet Epidemiol. In press
-
Genet Epidemiol
-
-
Hauser, E.R.1
Watanabe, R.M.2
Duren, W.L.3
Bass, M.P.4
Langefeld, C.D.5
Boehnke, M.6
-
29
-
-
0032433332
-
Genetic linkage analysis of complex genetic traits by using affected sibling pairs
-
Hauser ER, Boehnke M: Genetic linkage analysis of complex genetic traits by using affected sibling pairs. Biometrics 54:1238-1246, 1998
-
(1998)
Biometrics
, vol.54
, pp. 1238-1246
-
-
Hauser, E.R.1
Boehnke, M.2
-
30
-
-
0030897631
-
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy
-
Bowden DW, Sale M, Howard TD, Qadri A, Spray BJ, Rothschild CB, Akots G, Rich SS, Freedman BI: Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy. Diabetes 46:882-886, 1997
-
(1997)
Diabetes
, vol.46
, pp. 882-886
-
-
Bowden, D.W.1
Sale, M.2
Howard, T.D.3
Qadri, A.4
Spray, B.J.5
Rothschild, C.B.6
Akots, G.7
Rich, S.S.8
Freedman, B.I.9
-
31
-
-
0030907295
-
New susceptibility locus for NIDDM is localized to human chromosome 20q
-
Ji L, Malecki M, Warram JH, Yang Y, Rich SS, Krolewski AS: New susceptibility locus for NIDDM is localized to human chromosome 20q. Diabetes 46:876-881, 1997
-
(1997)
Diabetes
, vol.46
, pp. 876-881
-
-
Ji, L.1
Malecki, M.2
Warram, J.H.3
Yang, Y.4
Rich, S.S.5
Krolewski, A.S.6
-
32
-
-
0030766446
-
A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene
-
Zouali H, Hani EH, Philippi A, Vionnet N, Beckmann JS, Demenais F, Froguel P: A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene. Hum Mol Genet 6:1401-1408, 1997
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1401-1408
-
-
Zouali, H.1
Hani, E.H.2
Philippi, A.3
Vionnet, N.4
Beckmann, J.S.5
Demenais, F.6
Froguel, P.7
-
33
-
-
0035058351
-
A genome-wide search for type II diabetes susceptibility genes in Chinese Hans
-
Luo TH, Zhao Y, Li G, Yuan WT, Zhao JJ, Chen JL, Huang W, Luo M: A genome-wide search for type II diabetes susceptibility genes in Chinese Hans. Diabetologia 44:501-506, 2001
-
(2001)
Diabetologia
, vol.44
, pp. 501-506
-
-
Luo, T.H.1
Zhao, Y.2
Li, G.3
Yuan, W.T.4
Zhao, J.J.5
Chen, J.L.6
Huang, W.7
Luo, M.8
-
34
-
-
0035119822
-
A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population
-
Permutt MA, Wasson JC, Suarez BK, Lin J, Thomas J, Meyer J, Lewitzky S, Rennich JS, Parker A, DuPrat L, Maruti S, Chayen S, Glaser B: A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population. Diabetes 50:681-685, 2001
-
(2001)
Diabetes
, vol.50
, pp. 681-685
-
-
Permutt, M.A.1
Wasson, J.C.2
Suarez, B.K.3
Lin, J.4
Thomas, J.5
Meyer, J.6
Lewitzky, S.7
Rennich, J.S.8
Parker, A.9
DuPrat, L.10
Maruti, S.11
Chayen, S.12
Glaser, B.13
-
35
-
-
0036230486
-
Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p
-
Mori Y, Otabe S, Dina C, Yasuda K, Populaire C, Lecoeur C, Vatin V, Durand E, Hara K, Okada T, Tobe K, Boutin P, Kadowaki T, Froguel P: Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p. Diabetes 51:1247-1255, 2002
-
(2002)
Diabetes
, vol.51
, pp. 1247-1255
-
-
Mori, Y.1
Otabe, S.2
Dina, C.3
Yasuda, K.4
Populaire, C.5
Lecoeur, C.6
Vatin, V.7
Durand, E.8
Hara, K.9
Okada, T.10
Tobe, K.11
Boutin, P.12
Kadowaki, T.13
Froguel, P.14
-
36
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11:241-247, 1995
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
37
-
-
0035016103
-
A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans
-
Duggirala R, Blangero J, Almasy L, Arya R, Dyer TD, Williams KL, Leach RJ, O'Connell P, Stern MP: A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans. Am J Hum Genet 68:1149-1164, 2001
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1149-1164
-
-
Duggirala, R.1
Blangero, J.2
Almasy, L.3
Arya, R.4
Dyer, T.D.5
Williams, K.L.6
Leach, R.J.7
O'Connell, P.8
Stern, M.P.9
-
38
-
-
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, Bottazzo GF, Foxon R, 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
Bottazzo, G.F.20
Foxon, R.21
Howell, S.22
Smedley, D.23
Cardon, L.R.24
Menzel, S.25
McCarthy, M.I.26
more..
-
39
-
-
0033942075
-
Genomewide search for type 2 diabetes susceptibility genes in four American populations
-
Ehm MG, Karnoub MC, Sakul H, Gottschalk K, Holt DC, Weber JL, Vaske D, Briley D, Briley L, Kopf J, McMillen P, Nguyen Q, Reisman M, Lai EH, Joslyn G, Shepherd NS, Bell C, Wagner MJ, Burns DK, American Diabetes Association GENNID Study Group: Genomewide search for type 2 diabetes susceptibility genes in four American populations. Am J Hum Genet 66:1871-1881, 2000. [Erratum in Am J Hum Genet 70:284, 2002]
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1871-1881
-
-
Ehm, M.G.1
Karnoub, M.C.2
Sakul, H.3
Gottschalk, K.4
Holt, D.C.5
Weber, J.L.6
Vaske, D.7
Briley, D.8
Briley, L.9
Kopf, J.10
McMillen, P.11
Nguyen, Q.12
Reisman, M.13
Lai, E.H.14
Joslyn, G.15
Shepherd, N.S.16
Bell, C.17
Wagner, M.J.18
Burns, D.K.19
-
40
-
-
18244398227
-
Erratum
-
Ehm MG, Karnoub MC, Sakul H, Gottschalk K, Holt DC, Weber JL, Vaske D, Briley D, Briley L, Kopf J, McMillen P, Nguyen Q, Reisman M, Lai EH, Joslyn G, Shepherd NS, Bell C, Wagner MJ, Burns DK, American Diabetes Association GENNID Study Group: Genomewide search for type 2 diabetes susceptibility genes in four American populations. Am J Hum Genet 66:1871-1881, 2000. [Erratum in Am J Hum Genet 70:284, 2002]
-
(2002)
Am J Hum Genet
, vol.70
, pp. 284
-
-
-
41
-
-
0035120211
-
A genome-wide scan for abdominal fat assessed by computed tomography in the Quebec Family Study
-
Perusse L, Rice T, Chagnon YC, Despres JP, Lemieux S, Roy S, Lacaille M, Ho-Kim MA, Chagnon M, Province MA, Rao DC, Bouchard C: A genome-wide scan for abdominal fat assessed by computed tomography in the Quebec Family Study. Diabetes 50:614-621, 2001
-
(2001)
Diabetes
, vol.50
, pp. 614-621
-
-
Perusse, L.1
Rice, T.2
Chagnon, Y.C.3
Despres, J.P.4
Lemieux, S.5
Roy, S.6
Lacaille, M.7
Ho-Kim, M.A.8
Chagnon, M.9
Province, M.A.10
Rao, D.C.11
Bouchard, C.12
-
42
-
-
0032857338
-
A polymorphism (K121Q) of the human glucoprotein PC-1 gene coding region is strongly associated with insulin resistance
-
Pizzuti A, Frittitta L, Argiolas A, Baratta R, Goldfine ID, Bozzali M, Ercolino T, Scarlato G, Iacoviello L, Vigneri R, Tassi V, Trischitta V: A polymorphism (K121Q) of the human glucoprotein PC-1 gene coding region is strongly associated with insulin resistance. Diabetes 48:1881-1884, 1999
-
(1999)
Diabetes
, vol.48
, pp. 1881-1884
-
-
Pizzuti, A.1
Frittitta, L.2
Argiolas, A.3
Baratta, R.4
Goldfine, I.D.5
Bozzali, M.6
Ercolino, T.7
Scarlato, G.8
Iacoviello, L.9
Vigneri, R.10
Tassi, V.11
Trischitta, V.12
-
43
-
-
0034016043
-
Profound obesity associated with a balanced translocation that disrupts the SIMI gene
-
Holder JL Jr, Butte NF, Zinn AR: Profound obesity associated with a balanced translocation that disrupts the SIMI gene. Hum Molec Genet 9:101-108, 2000
-
(2000)
Hum Molec Genet
, vol.9
, pp. 101-108
-
-
Holder Jr., J.L.1
Butte, N.F.2
Zinn, A.R.3
-
44
-
-
0035393437
-
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus
-
Michaud JL, Boucher F, Melnyk A, Gauthier F, Goshu E, Levy E, Mitchell GA, Himms-Hagen J, Fan C-M: Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus. Hum Molec Genet 10:1465-1473, 2001
-
(2001)
Hum Molec Genet
, vol.10
, pp. 1465-1473
-
-
Michaud, J.L.1
Boucher, F.2
Melnyk, A.3
Gauthier, F.4
Goshu, E.5
Levy, E.6
Mitchell, G.A.7
Himms-Hagen, J.8
Fan, C.-M.9
-
45
-
-
0031016073
-
Cloning and initial characterization of human and mouse Spot 14 genes
-
Gritlasca JP, Gastaldi M, Khiri H, Dace A, Peyrol N, Reynier P, Torresani J, Planells R: Cloning and initial characterization of human and mouse Spot 14 genes. FEBS Lett 401:38-42, 1997
-
(1997)
FEBS Lett
, vol.401
, pp. 38-42
-
-
Gritlasca, J.P.1
Gastaldi, M.2
Khiri, H.3
Dace, A.4
Peyrol, N.5
Reynier, P.6
Torresani, J.7
Planells, R.8
-
46
-
-
0029044299
-
Direct evidence for a role of the "spot 14" protein in the regulation of lipid synthesis
-
Kinlaw WB, Church JL, Harmon J, Mariash CN: Direct evidence for a role of the "spot 14" protein in the regulation of lipid synthesis. J Biol Chem 270:16615-16618, 1995
-
(1995)
J Biol Chem
, vol.270
, pp. 16615-16618
-
-
Kinlaw, W.B.1
Church, J.L.2
Harmon, J.3
Mariash, C.N.4
-
47
-
-
0031036669
-
"Spot 14" protein functions at the pretranslational level in the regulation of hepatic metabolism by thyroid hormone and glucose
-
Brown SB, Maloney M, Kinlaw WB: "Spot 14" protein functions at the pretranslational level in the regulation of hepatic metabolism by thyroid hormone and glucose. J Biol Chem 272:2163-2166, 1997
-
(1997)
J Biol Chem
, vol.272
, pp. 2163-2166
-
-
Brown, S.B.1
Maloney, M.2
Kinlaw, W.B.3
-
48
-
-
0034973982
-
Translational control is required for the unfolded protein response and in vivo glucose homeostasis
-
Scheuner D, Song B, McEwen E, Liu C, Laybutt R, Gillespie P, Saunders T, Bonner-Weir S, Kaufman RJ: Translational control is required for the unfolded protein response and in vivo glucose homeostasis. Molec Cell 7:1165-1176, 2001
-
(2001)
Molec Cell
, vol.7
, pp. 1165-1176
-
-
Scheuner, D.1
Song, B.2
McEwen, E.3
Liu, C.4
Laybutt, R.5
Gillespie, P.6
Saunders, T.7
Bonner-Weir, S.8
Kaufman, R.J.9
-
49
-
-
0033694150
-
Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24
-
Ohman M, Oksanen L, Kaprio J, Koskenvuo M, Mustajoki P, Rissanen A, Salmi J, Kontula K, Peltonen L: Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24. J Clin Endocrinol Metab 85:3183-3190, 2000
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 3183-3190
-
-
Ohman, M.1
Oksanen, L.2
Kaprio, J.3
Koskenvuo, M.4
Mustajoki, P.5
Rissanen, A.6
Salmi, J.7
Kontula, K.8
Peltonen, L.9
-
50
-
-
0030662465
-
Mice lacking bombesin receptor subtype-3 develop metabolic defects and obesity
-
Ohki-Hamazaki H, Watase K, Yamamoto K, Ogura H, Yamano M, Yamada K, Maeno H, Imaki J, Kikuyama S, Wada E, Wada K: Mice lacking bombesin receptor subtype-3 develop metabolic defects and obesity. Nature 390:165-169, 1997
-
(1997)
Nature
, vol.390
, pp. 165-169
-
-
Ohki-Hamazaki, H.1
Watase, K.2
Yamamoto, K.3
Ogura, H.4
Yamano, M.5
Yamada, K.6
Maeno, H.7
Imaki, J.8
Kikuyama, S.9
Wada, E.10
Wada, K.11
|