-
1
-
-
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
-
2
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K: The future of genetic studies of complex human diseases. Science 273:1516-1517, 1996
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
3
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander ES, Schork NJ: Genetic dissection of complex traits (Review). Science 265:2037-2048, 1994
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
4
-
-
0028871202
-
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
-
Bennett ST, Lucassen AM, Gough SCL, Powell EE, Undlien DE, Pritchard LE, Merriman ME, Kawaguchi Y, Dronsfield MJ, Pociot F, Nerup J, Bouzekri N, Cambon-Thomsen A, Ronningen KS, Barnett AH, Bain SC, Todd JA: Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus. Nat Genet 9:284-291, 1995
-
(1995)
Nat Genet
, vol.9
, pp. 284-291
-
-
Bennett, S.T.1
Lucassen, A.M.2
Gough, S.C.L.3
Powell, E.E.4
Undlien, D.E.5
Pritchard, L.E.6
Merriman, M.E.7
Kawaguchi, Y.8
Dronsfield, M.J.9
Pociot, F.10
Nerup, J.11
Bouzekri, N.12
Cambon-Thomsen, A.13
Ronningen, K.S.14
Barnett, A.H.15
Bain, S.C.16
Todd, J.A.17
-
5
-
-
0030895556
-
Linkage association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome
-
Waterworth DM, Bennett ST, Gharani N, McCarthy MI, Hague S, Batty S, Conway GS, White D, Todd JA, Franks S, Williamson R: Linkage association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome. Lancet 349:986-990, 1997
-
(1997)
Lancet
, vol.349
, pp. 986-990
-
-
Waterworth, D.M.1
Bennett, S.T.2
Gharani, N.3
McCarthy, M.I.4
Hague, S.5
Batty, S.6
Conway, G.S.7
White, D.8
Todd, J.A.9
Franks, S.10
Williamson, R.11
-
6
-
-
0027203145
-
Availability of type II diabetic families for detection of diabetes susceptibility genes
-
Cook JT, Page RC, O'Rahilly S, Levy J, Holman R, Barrow B, Hattersley AT, Shaw AG, Wainscoat JS, Turner RC: Availability of type II diabetic families for detection of diabetes susceptibility genes. Diabetes 42:1536-1543, 1993
-
(1993)
Diabetes
, vol.42
, pp. 1536-1543
-
-
Cook, J.T.1
Page, R.C.2
O'Rahilly, S.3
Levy, J.4
Holman, R.5
Barrow, B.6
Hattersley, A.T.7
Shaw, A.G.8
Wainscoat, J.S.9
Turner, R.C.10
-
7
-
-
0028838999
-
Is there an excess in maternal transmission of NIDDM?
-
Mitchell BD, Kammerer CM, Reinhart LJ, Stern MP, MacCluer JW: Is there an excess in maternal transmission of NIDDM? Diabetolagia 38:314-317, 1995
-
(1995)
Diabetolagia
, vol.38
, pp. 314-317
-
-
Mitchell, B.D.1
Kammerer, C.M.2
Reinhart, L.J.3
Stern, M.P.4
MacCluer, J.W.5
-
8
-
-
0028888396
-
Maternally inherited diabetes mellitus: The role of mitochondrial DNA defects
-
Alcolado JC, Thomas AW: Maternally inherited diabetes mellitus: the role of mitochondrial DNA defects (Review). Diabet Med 12:102-108, 1995
-
(1995)
Diabet Med
, vol.12
, pp. 102-108
-
-
Alcolado, J.C.1
Thomas, A.W.2
-
9
-
-
0028008979
-
Maternal component in NIDDM transmission: How large an effect?
-
Cox NJ: Maternal component in NIDDM transmission: how large an effect? (Letter). Diabetes 43:166-168, 1994
-
(1994)
Diabetes
, vol.43
, pp. 166-168
-
-
Cox, N.J.1
-
10
-
-
0026681851
-
A genetic marker at the glucokinase gene locus for type 2 (non-insulin-dependent) diabetes mellitus in Mauritian Creoles
-
Chiu KC, Province MA, Dowse GK, Zimmet PZ, Serjeantson S, Permutt MA: A genetic marker at the glucokinase gene locus for type 2 (non-insulin-dependent) diabetes mellitus in Mauritian Creoles. Diabetologia 35:632-638, 1992
-
(1992)
Diabetologia
, vol.35
, pp. 632-638
-
-
Chiu, K.C.1
Province, M.A.2
Dowse, G.K.3
Zimmet, P.Z.4
Serjeantson, S.5
Permutt, M.A.6
-
11
-
-
0028218909
-
Glucokinase gene polymorphisms: A genetic marker for glucose intolerance in a cohort of elderly Finnish men
-
McCarthy MI, Hitman GA, Hitchins M, Rükonen A, Stengard J, Nissinen A, Tuomilehto-Wolf E, Tuomilehto J: Glucokinase gene polymorphisms: a genetic marker for glucose intolerance in a cohort of elderly Finnish men. Diabet Med 11:198-204, 1994
-
(1994)
Diabet Med
, vol.11
, pp. 198-204
-
-
McCarthy, M.I.1
Hitman, G.A.2
Hitchins, M.3
Rükonen, A.4
Stengard, J.5
Nissinen, A.6
Tuomilehto-Wolf, E.7
Tuomilehto, J.8
-
12
-
-
0027372914
-
Microsatellite polymorphisms at the glucokinase locus: A population association study in Caucasian type 2 diabetic subjects
-
Hattersley AT, Saker PJ, Cook JT, Stratton IM, Patel P, Permutt MA, Turner RC, Wainscoat JS: Microsatellite polymorphisms at the glucokinase locus: a population association study in Caucasian type 2 diabetic subjects. Diabet Med 10:694-698, 1993
-
(1993)
Diabet Med
, vol.10
, pp. 694-698
-
-
Hattersley, A.T.1
Saker, P.J.2
Cook, J.T.3
Stratton, I.M.4
Patel, P.5
Permutt, M.A.6
Turner, R.C.7
Wainscoat, J.S.8
-
13
-
-
0027308818
-
Two microsatellite repeat polymorphisms flanking opposite ends of the human glucokinase gene: Use in haplotype analysis of Welsh Caucasians with type 2 (non-insulin-dependent) diabetes mellitus
-
Tanizawa Y, Chiu KC, Province MA, Morgan R, Owens DR, Rees A, Permutt MA: Two microsatellite repeat polymorphisms flanking opposite ends of the human glucokinase gene: use in haplotype analysis of Welsh Caucasians with type 2 (non-insulin-dependent) diabetes mellitus. Diabetologia 36:409-413, 1993
-
(1993)
Diabetologia
, vol.36
, pp. 409-413
-
-
Tanizawa, Y.1
Chiu, K.C.2
Province, M.A.3
Morgan, R.4
Owens, D.R.5
Rees, A.6
Permutt, M.A.7
-
14
-
-
0031802866
-
Exclusion of the hepatocyte nuclear factor 4α as a candidate gene for late-onset NIDDM linked with chromosome 20q
-
Malecki MT, Antonellis A, Casey P, Ji L, Wantman M, Warram JH, Krolewski AS: Exclusion of the hepatocyte nuclear factor 4α as a candidate gene for late-onset NIDDM linked with chromosome 20q. Diabetes 47:970-972, 1998
-
(1998)
Diabetes
, vol.47
, pp. 970-972
-
-
Malecki, M.T.1
Antonellis, A.2
Casey, P.3
Ji, L.4
Wantman, M.5
Warram, J.H.6
Krolewski, A.S.7
-
15
-
-
0030907295
-
New susceptibility locus for NIDDM is localized to human chromosome 20q
-
Ji L, Malecki M, Warram HJ, 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, H.J.3
Yang, Y.4
Rich, S.S.5
Krolewski, A.S.6
-
16
-
-
0031560175
-
UKPDs 25: Autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes
-
Turner R, Stratton I, Horton V, Manley S, Zimmet P, Mackay IR, Shattock M, Bottazzo GF, Holman R, Groop LC: UKPDS 25: autoantibodies to islet-cell cytoplasm and glutamic acid decarboxylase for prediction of insulin requirement in type 2 diabetes. Lancet 350:1288-1293, 1997
-
(1997)
Lancet
, vol.350
, pp. 1288-1293
-
-
Turner, R.1
Stratton, I.2
Horton, V.3
Manley, S.4
Zimmet, P.5
Mackay, I.R.6
Shattock, M.7
Bottazzo, G.F.8
Holman, R.9
Groop, L.C.10
-
17
-
-
0032955251
-
Clinical and genetic characteristics of type 2 diabetes with and without GAD antibodies
-
Tuomi T, Carlsson A, Li H, Isomaa B, Miettinen A, Nilsson A, Nissén M, Ehrnström B, Forsén B, Snickars B, Lahti K, Forsblom C, Saloranta C, Taskinen M, Groop LC: Clinical and genetic characteristics of type 2 diabetes with and without GAD antibodies. Diabetes 48:150-157, 1999
-
(1999)
Diabetes
, vol.48
, pp. 150-157
-
-
Tuomi, T.1
Carlsson, A.2
Li, H.3
Isomaa, B.4
Miettinen, A.5
Nilsson, A.6
Nissén, M.7
Ehrnström, B.8
Forsén, B.9
Snickars, B.10
Lahti, K.11
Forsblom, C.12
Saloranta, C.13
Taskinen, M.14
Groop, L.C.15
-
18
-
-
0023091110
-
Type II diabetes of early onset: A distinct clinical and genetic syndrome?
-
O'Rahilly S, Spivey RS, Holman RR, Nugent Z, Clark A, Turner RC: Type II diabetes of early onset: a distinct clinical and genetic syndrome? Br Med J 294:923-928, 1987
-
(1987)
Br Med J
, vol.294
, pp. 923-928
-
-
O'Rahilly, S.1
Spivey, R.S.2
Holman, R.R.3
Nugent, Z.4
Clark, A.5
Turner, R.C.6
-
19
-
-
0033362236
-
Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
-
Weinberg CR: Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. Am J Hum Genet 65:229-235, 1999
-
(1999)
Am J Hum Genet
, vol.65
, pp. 229-235
-
-
Weinberg, C.R.1
-
20
-
-
0030669122
-
Use of siblings as controls in case-control association studies
-
Curtis D: Use of siblings as controls in case-control association studies. Ann Hum Genet 61:319-333, 1997
-
(1997)
Ann Hum Genet
, vol.61
, pp. 319-333
-
-
Curtis, D.1
-
21
-
-
0028944305
-
A note on the application of the transmission disequilibrium test when a parent is missing
-
Curtis D, Sham PC: A note on the application of the transmission disequilibrium test when a parent is missing. Am J Hum Genet 56:811-812, 1995
-
(1995)
Am J Hum Genet
, vol.56
, pp. 811-812
-
-
Curtis, D.1
Sham, P.C.2
-
22
-
-
0031455778
-
Genotype relative-risks and association tests for nuclear families with missing parental data
-
Schaid DJ, Li HZ: Genotype relative-risks and association tests for nuclear families with missing parental data. Genet Epidemiol 14:1113-1118, 1997
-
(1997)
Genet Epidemiol
, vol.14
, pp. 1113-1118
-
-
Schaid, D.J.1
Li, H.Z.2
-
23
-
-
0033364961
-
The transmission/disequilibrium test and parental-genotype reconstruction: The reconstruction-combined transmission/disequilibrium test
-
Knapp M: The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/disequilibrium test. Am J Hum Genet 64:861-370, 1999
-
(1999)
Am J Hum Genet
, vol.64
, pp. 861-1370
-
-
Knapp, M.1
-
24
-
-
0033362166
-
Allowing for missing parents in genetic studies of case-parent triads
-
Weinberg CR: Allowing for missing parents in genetic studies of case-parent triads. Am J Hum Genet 64:1186-1193, 1999
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1186-1193
-
-
Weinberg, C.R.1
-
25
-
-
0033168224
-
Transmission disequilibrium test TDT when only one parent is available: The 1-TDT
-
Sun FZ, Flanders WD, Yang QH, Khoury MT: Transmission disequilibrium test TDT when only one parent is available: the 1-TDT. Am J Epidemiol 150:97-104, 1999
-
(1999)
Am J Epidemiol
, vol.150
, pp. 97-104
-
-
Sun, F.Z.1
Flanders, W.D.2
Yang, Q.H.3
Khoury, M.T.4
-
26
-
-
0028181403
-
Detection of GAD65 antibodies in diabetes and other autoimmune diseases using a simple radioligand assay
-
Petersen JS, Hejnaes KR, Moody A, Karlsen AE, Marshall MO, Hoier-Madsen M, Boel E, Michelsen BK, Dyrberg T: Detection of GAD65 antibodies in diabetes and other autoimmune diseases using a simple radioligand assay. Diabetes 43:459-467, 1994
-
(1994)
Diabetes
, vol.43
, pp. 459-467
-
-
Petersen, J.S.1
Hejnaes, K.R.2
Moody, A.3
Karlsen, A.E.4
Marshall, M.O.5
Hoier-Madsen, M.6
Boel, E.7
Michelsen, B.K.8
Dyrberg, T.9
-
27
-
-
0031447766
-
A rapid screening method for hepatocyte nuclear factor 1 alpha: Prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes
-
Frayling TM, Bulman MP, Appleton M, Bain SC, Hattersley AT, Ellard S: A rapid screening method for hepatocyte nuclear factor 1 alpha: prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes. Hum Genet 101:351-354, 1997
-
(1997)
Hum Genet
, vol.101
, pp. 351-354
-
-
Frayling, T.M.1
Bulman, M.P.2
Appleton, M.3
Bain, S.C.4
Hattersley, A.T.5
Ellard, S.6
-
28
-
-
0031659139
-
Hidden linkage: A comparison of the affected sib pair (ASP) test and transmission/disequilibrium test (TDT)
-
McGinnis RE: Hidden linkage: a comparison of the affected sib pair (ASP) test and transmission/disequilibrium test (TDT). Ann Hum Genet 62:159-179, 1998
-
(1998)
Ann Hum Genet
, vol.62
, pp. 159-179
-
-
McGinnis, R.E.1
|