-
1
-
-
0028848010
-
A missense mutation in the glucagon receptor gene is associated with non-insulin dependant diabetes mellitus
-
Hager J, Hansen L, Vaisse C, Vionnet N, Philippi A, Poller W, Velho G, Carcassi C, Contu L, Julier C, Cambien F, Passa P, Lathrop M, Kindsvogel W, Demenais F, Nishimura E, Froguel P: A missense mutation in the glucagon receptor gene is associated with non-insulin dependant diabetes mellitus. Nature Genet 9:299-304, 1995
-
(1995)
Nature Genet
, vol.9
, pp. 299-304
-
-
Hager, J.1
Hansen, L.2
Vaisse, C.3
Vionnet, N.4
Philippi, A.5
Poller, W.6
Velho, G.7
Carcassi, C.8
Contu, L.9
Julier, C.10
Cambien, F.11
Passa, P.12
Lathrop, M.13
Kindsvogel, W.14
Demenais, F.15
Nishimura, E.16
Froguel, P.17
-
2
-
-
0027994029
-
Insulin receptor substrate-1 variants in non-insulin-dependent diabetes
-
Laasko M, Malkli M, Kekalainen P, Kuusisto J, Deeb SS: Insulin receptor substrate-1 variants in non-insulin-dependent diabetes. J Clin Invest 94:1141-1146, 1994
-
(1994)
J Clin Invest
, vol.94
, pp. 1141-1146
-
-
Laasko, M.1
Malkli, M.2
Kekalainen, P.3
Kuusisto, J.4
Deeb, S.S.5
-
3
-
-
0028978910
-
Genetic variation in the beta-3-adrenergic receptor and an increased capacity to gain weight in patients with morbid obesity
-
Clément K, Vaisse C, Manning BSJ, Basdevant A, Guy-Grand B, Ruiz J, Silver KD, Shuldiner AR, Froguel P, Strosberg AD: Genetic variation in the beta-3-adrenergic receptor and an increased capacity to gain weight in patients with morbid obesity. N Engl J Med 333: 352-354, 1995
-
(1995)
N Engl J Med
, vol.333
, pp. 352-354
-
-
Clément, K.1
Vaisse, C.2
Manning, B.S.J.3
Basdevant, A.4
Guy-Grand, B.5
Ruiz, J.6
Silver, K.D.7
Shuldiner, A.R.8
Froguel, P.9
Strosberg, A.D.10
-
4
-
-
9044243415
-
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
-
Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shepard JM, Williams SR, Risen N, Hinds D, Iwasaki N, Ogata M, Omori Y, Petzold C, Rietzsch H, Schröder HE, Schulze J, Cox NJ, Menzel S, Boriraj VV, Chen X, Lim LR, Lindner T, Mereu LE, Wang YQ, Xiang K, Yamagata K, Yang Y, Bell GI: A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nature Genet 13:161-166, 1996
-
(1996)
Nature Genet
, vol.13
, pp. 161-166
-
-
Hanis, C.L.1
Boerwinkle, E.2
Chakraborty, R.3
Ellsworth, D.L.4
Concannon, P.5
Stirling, B.6
Morrison, V.A.7
Wapelhorst, B.8
Spielman, R.S.9
Gogolin-Ewens, K.J.10
Shepard, J.M.11
Williams, S.R.12
Risen, N.13
Hinds, D.14
Iwasaki, N.15
Ogata, M.16
Omori, Y.17
Petzold, C.18
Rietzsch, H.19
Schröder, H.E.20
Schulze, J.21
Cox, N.J.22
Menzel, S.23
Boriraj, V.V.24
Chen, X.25
Lim, L.R.26
Lindner, T.27
Mereu, L.E.28
Wang, Y.Q.29
Xiang, K.30
Yamagata, K.31
Yang, Y.32
Bell, G.I.33
more..
-
5
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families
-
Mahtani MM, Widen E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Mary Reeve-Daly P, Weaver A, Brettin T, Duyk J, Lander ES, Groop LC: Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nature Genet 14:90-94, 1996
-
(1996)
Nature Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
Thomas, J.4
McCarthy, M.5
Brayer, J.6
Bryant, B.7
Chan, G.8
Daly, M.9
Forsblom, C.10
Kanninen, T.11
Kirby, A.12
Kruglyak, L.13
Munnelly, K.14
Parkkonen, M.15
Mary Reeve-Daly, P.16
Weaver, A.17
Brettin, T.18
Duyk, J.19
Lander, E.S.20
Groop, L.C.21
more..
-
6
-
-
0029029955
-
Linkage analyses of the MODY3 locus on chromosome 12q with late onset NIDDM
-
Lesage S, Hani E, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N: Linkage analyses of the MODY3 locus on chromosome 12q with late onset NIDDM. Diabetes 44:1243-1247, 1995
-
(1995)
Diabetes
, vol.44
, pp. 1243-1247
-
-
Lesage, S.1
Hani, E.2
Philippi, A.3
Vaxillaire, M.4
Hager, J.5
Passa, P.6
Demenais, F.7
Froguel, P.8
Vionnet, N.9
-
7
-
-
0027963471
-
Clustering of hypertension, diabetes, and obesity in adult male twins: Same genes or same environments?
-
Carmelli D, Cardon L, Fabsitz R: Clustering of hypertension, diabetes, and obesity in adult male twins: same genes or same environments? Am J Hum Genet 55:566-573, 1994
-
(1994)
Am J Hum Genet
, vol.55
, pp. 566-573
-
-
Carmelli, D.1
Cardon, L.2
Fabsitz, R.3
-
8
-
-
0024026298
-
Lilly Lecture 1987: The triumvirate: β-cell, muscle, liver: a collusion responsible for NIDDM
-
De Fronzo RA: Lilly Lecture 1987: The triumvirate: β-cell, muscle, liver: a collusion responsible for NIDDM. Diabetes 37:657-687, 1987
-
(1987)
Diabetes
, vol.37
, pp. 657-687
-
-
De Fronzo, R.A.1
-
9
-
-
0026021161
-
Insulin resistance a multifaceted syndrome responsible for NIDDM, obesity, hypertension, dyslipidemia and atherosclerotic cardiovascular disease
-
De Fronzo RA, Ferrannini E: Insulin resistance a multifaceted syndrome responsible for NIDDM, obesity, hypertension, dyslipidemia and atherosclerotic cardiovascular disease. Diabetes Care 14:173-194, 1991
-
(1991)
Diabetes Care
, vol.14
, pp. 173-194
-
-
De Fronzo, R.A.1
Ferrannini, E.2
-
10
-
-
0027762766
-
Insulin resistance and insulin secretory dysfunction as precursors of non-insulin-dependent diabetes mellitus: Prospective studies in Pima Indians
-
Lillioja S, Mott DM, Spraul M, Ferraro R, Foley JE, Ravussin E, Knowler WC, Benett PH, Bogardus C: Insulin resistance and insulin secretory dysfunction as precursors of non-insulin-dependent diabetes mellitus: prospective studies in Pima Indians. N Engl J Med 329:1988-1992, 1993
-
(1993)
N Engl J Med
, vol.329
, pp. 1988-1992
-
-
Lillioja, S.1
Mott, D.M.2
Spraul, M.3
Ferraro, R.4
Foley, J.E.5
Ravussin, E.6
Knowler, W.C.7
Benett, P.H.8
Bogardus, C.9
-
11
-
-
0028783323
-
Impaired processing of prohormones associated with abnormalities of glucose homeostasis and adrenal function
-
O'Rahilly S, Gray H, Humpkreys PJ: Impaired processing of prohormones associated with abnormalities of glucose homeostasis and adrenal function. N Engl J Med 33:1386-1390, 1995
-
(1995)
N Engl J Med
, vol.33
, pp. 1386-1390
-
-
O'Rahilly, S.1
Gray, H.2
Humpkreys, P.J.3
-
12
-
-
0021187646
-
Intracellular ATP directly blocks K+ channel in pancreatic β-cells
-
Cook DL, Hales CN: Intracellular ATP directly blocks K+ channel in pancreatic β-cells. Nature 311:271-273, 1984
-
(1984)
Nature
, vol.311
, pp. 271-273
-
-
Cook, D.L.1
Hales, C.N.2
-
13
-
-
0029024314
-
Cloning of the beta cell high-affinity sulfonylurea receptor: A regulator of insulin secretion
-
Aguilar-Bryan L, Nichols CG, Wechsler SW, Clement JP IV, Boyd AE III, Gonzalez G, Herrera-Sosa H, Nguy K, Bryan J, Nelson DA: Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. Science 268:423-426, 1995
-
(1995)
Science
, vol.268
, pp. 423-426
-
-
Aguilar-Bryan, L.1
Nichols, C.G.2
Wechsler, S.W.3
Clement IV, J.P.4
Boyd III, A.E.5
Gonzalez, G.6
Herrera-Sosa, H.7
Nguy, K.8
Bryan, J.9
Nelson, D.A.10
-
14
-
-
0028972501
-
Reconstitution of I (KATP): An inward rectifier subunit plus the sulfonylurea receptor
-
Inagaki N, Gonoi T, Clement JP IV, Namba N, Inazawa J, Gonzalez G, Aguilar-Bryan L, Seino S, Bryan J: Reconstitution of I (KATP): an inward rectifier subunit plus the sulfonylurea receptor. Science 270:1166-1170, 1995
-
(1995)
Science
, vol.270
, pp. 1166-1170
-
-
Inagaki, N.1
Gonoi, T.2
Clement IV, J.P.3
Namba, N.4
Inazawa, J.5
Gonzalez, G.6
Aguilar-Bryan, L.7
Seino, S.8
Bryan, J.9
-
15
-
-
0029021696
-
Mutations in the sulfonylurea receptor in familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, Aguilar-Bryan L, Gagel RF, Bryan J: Mutations in the sulfonylurea receptor in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 268:428-429, 1995
-
(1995)
Science
, vol.268
, pp. 428-429
-
-
Thomas, P.M.1
Cote, G.J.2
Wohllk, N.3
Haddad, B.4
Mathew, P.M.5
Rabl, W.6
Aguilar-Bryan, L.7
Gagel, R.F.8
Bryan, J.9
-
16
-
-
15844366738
-
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with non-insulin dependent diabetes mellitus (NIDDM) in Caucasians
-
Inoue H, Ferrer J, Welling CM, Elbein SC, Hoffman M, Mayorga R, Warren-Perry M, Zhang Y, Millns H, Turner R, Province M, Bryan J, Permutt AP, Aguilar-Bryan L: Sequence variants in the sulfonylurea receptor (SUR) gene are associated with non-insulin dependent diabetes mellitus (NIDDM) in Caucasians. Diabetes 45:825-831, 1996
-
(1996)
Diabetes
, vol.45
, pp. 825-831
-
-
Inoue, H.1
Ferrer, J.2
Welling, C.M.3
Elbein, S.C.4
Hoffman, M.5
Mayorga, R.6
Warren-Perry, M.7
Zhang, Y.8
Millns, H.9
Turner, R.10
Province, M.11
Bryan, J.12
Permutt, A.P.13
Aguilar-Bryan, L.14
-
17
-
-
0025874033
-
Strategies for the collection of sibling-pair data for genetic studies in type 2 (non-insulin-dependent) diabetes mellitus
-
Froguel Ph, Velho G, Cohen D, Passa P: Strategies for the collection of sibling-pair data for genetic studies in type 2 (non-insulin-dependent) diabetes mellitus (Letter). Diabetalogia 34:685, 1991
-
(1991)
Diabetalogia
, vol.34
, pp. 685
-
-
Froguel, Ph.1
Velho, G.2
Cohen, D.3
Passa, P.4
-
19
-
-
0030009852
-
Candidate gene approach of familial morbid obesity: Linkage analysis of the glucocorticoid receptor gene
-
Clément K, Philippi A, Jury C, Pividal R, Hager J, Demenais F, Basdevant A, Guy-Grand B, Froguel P: Candidate gene approach of familial morbid obesity: linkage analysis of the glucocorticoid receptor gene. Int J Obes 20:507-512, 1996
-
(1996)
Int J Obes
, vol.20
, pp. 507-512
-
-
Clément, K.1
Philippi, A.2
Jury, C.3
Pividal, R.4
Hager, J.5
Demenais, F.6
Basdevant, A.7
Guy-Grand, B.8
Froguel, P.9
-
20
-
-
0345335191
-
Possible evidence for linkage of the human OB gene region with extreme obesity
-
Clément K, Garner C, Hager J, Philippi A, LeDuc C, Carey A, Harris TJR, Jury C, Cardon RL, Basdevant A, Demenais F, Guy-grand B, North M, Froguel P: Possible evidence for linkage of the human OB gene region with extreme obesity. Diabetes 45:687-690, 1996
-
(1996)
Diabetes
, vol.45
, pp. 687-690
-
-
Clément, K.1
Garner, C.2
Hager, J.3
Philippi, A.4
LeDuc, C.5
Carey, A.6
Harris, T.J.R.7
Jury, C.8
Cardon, R.L.9
Basdevant, A.10
Demenais, F.11
Guy-grand, B.12
North, M.13
Froguel, P.14
-
21
-
-
0001117051
-
Familial aggregation of morbid obesity
-
Adams T, Hunt S, Mason L, Ramirez M, Fisher A, Williams R: Familial aggregation of morbid obesity. Obes Res 1:261-270, 1993
-
(1993)
Obes Res
, vol.1
, pp. 261-270
-
-
Adams, T.1
Hunt, S.2
Mason, L.3
Ramirez, M.4
Fisher, A.5
Williams, R.6
-
22
-
-
13344259308
-
Identification of microsatellite markers near the b-cell ATP K+ channel and linkage studies with NIDDM in Japanese
-
Iwazaki N, Kawamura M, Yamagata K, Cox NJ, Karibe S, Ohgawara H, Seino S, Bell GI, Omori Y: Identification of microsatellite markers near the b-cell ATP K+ channel and linkage studies with NIDDM in Japanese. Diabetes 45:267-269, 1996
-
(1996)
Diabetes
, vol.45
, pp. 267-269
-
-
Iwazaki, N.1
Kawamura, M.2
Yamagata, K.3
Cox, N.J.4
Karibe, S.5
Ohgawara, H.6
Seino, S.7
Bell, G.I.8
Omori, Y.9
-
23
-
-
0026753350
-
Localisation of insulin (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7
-
Jones JM, Meisler MH, Seldin MF, Lee BK, Eicher EM: Localisation of insulin (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7. Genomics 14:197-199, 1992
-
(1992)
Genomics
, vol.14
, pp. 197-199
-
-
Jones, J.M.1
Meisler, M.H.2
Seldin, M.F.3
Lee, B.K.4
Eicher, E.M.5
-
24
-
-
0028231090
-
The Genethon human genetic linkage map 1993-94
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Milasseau F; Marc S, Bernardi G, Lathrop M, Weissenbach J: The Genethon human genetic linkage map 1993-94. Nature Genet 7:246-339, 1994
-
(1994)
Nature Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Milasseau, F.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
25
-
-
0000882795
-
Extension of multiple range tests to group means with unequal number of replications
-
Kramer CY: Extension of multiple range tests to group means with unequal number of replications. Biometrics 12:309-310, 1956
-
(1956)
Biometrics
, vol.12
, pp. 309-310
-
-
Kramer, C.Y.1
-
26
-
-
0015309467
-
The investigation of linkage between a quantitative trait and a marker locus
-
Haseman JK, Elston RC: The investigation of linkage between a quantitative trait and a marker locus. Behav Genet 2:3-19, 1972
-
(1972)
Behav Genet
, vol.2
, pp. 3-19
-
-
Haseman, J.K.1
Elston, R.C.2
-
27
-
-
0021734719
-
Genetic analysis workshop, II. Sib pair screening tests for linkage
-
Elston RC: Genetic analysis workshop, II. Sib pair screening tests for linkage. Genet Epidem 1:175-178, 1984
-
(1984)
Genet Epidem
, vol.1
, pp. 175-178
-
-
Elston, R.C.1
-
28
-
-
0003796759
-
-
Computer program package available from the department of biometry and genetics, LSU Medical Center, New Orleans
-
S.A.G.E: Statistical Analysis for Genetic Epidemiology, Realise 2.1. Computer program package available from the department of biometry and genetics, LSU Medical Center, New Orleans, 1992
-
(1992)
S.A.G.E: Statistical Analysis for Genetic Epidemiology, Realise 2.1
-
-
-
29
-
-
0000384974
-
Affected sib pair strategies for late onset diseases: Type I error and marker allele frequencies
-
Tores F, Barrillot E, Philippi A, Vaysseix G, Demenais F, Martinez M: Affected sib pair strategies for late onset diseases: type I error and marker allele frequencies (Abstract). Genet Epidemiol 13:302, 1996
-
(1996)
Genet Epidemiol
, vol.13
, pp. 302
-
-
Tores, F.1
Barrillot, E.2
Philippi, A.3
Vaysseix, G.4
Demenais, F.5
Martinez, M.6
-
30
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ: Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 52:506-516, 1993.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
31
-
-
0028845528
-
Linkage studies in NIDDM with markers near the sulphonylurea receptor gene
-
Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P: Linkage studies in NIDDM with markers near the sulphonylurea receptor gene. Diabetologia 38:1479-1481, 1995
-
(1995)
Diabetologia
, vol.38
, pp. 1479-1481
-
-
Stirling, B.1
Cox, N.J.2
Bell, G.I.3
Hanis, C.L.4
Spielman, R.S.5
Concannon, P.6
-
32
-
-
9044247460
-
Chromosomal mapping of genetic loci associated with non-insulin-dependent diabetes in the GK rat
-
Gauguier D, Froguel P, Parent V, Bernard C, Bihoreau MT, Portha B, James MR, Penicaud L, Lathrop M, Ktorza A: Chromosomal mapping of genetic loci associated with non-insulin-dependent diabetes in the GK rat. Nature Genet 12:38-43, 1996
-
(1996)
Nature Genet
, vol.12
, pp. 38-43
-
-
Gauguier, D.1
Froguel, P.2
Parent, V.3
Bernard, C.4
Bihoreau, M.T.5
Portha, B.6
James, M.R.7
Penicaud, L.8
Lathrop, M.9
Ktorza, A.10
-
33
-
-
0024851989
-
Disease associations: Chance, artefact, or susceptibility genes?
-
Cox N, Bell GI: Disease associations: chance, artefact, or susceptibility genes? Diabetes 38:947-950, 1989
-
(1989)
Diabetes
, vol.38
, pp. 947-950
-
-
Cox, N.1
Bell, G.I.2
|