-
1
-
-
85015054307
-
Nature, nurture and human disease
-
Chakravarti A, Little P. Nature, nurture and human disease. Nature 2003; 421:412-414.
-
(2003)
Nature
, vol.421
, pp. 412-414
-
-
Chakravarti, A.1
Little, P.2
-
2
-
-
27744486896
-
American Gastroenterological Association future trends committee report: The application of genomic and proteomic technologies to digestive disease diagnosis and treatment and their likely impact on gastroenterology clinical practice
-
Lazaridis KN, Juran BD. American Gastroenterological Association future trends committee report: the application of genomic and proteomic technologies to digestive disease diagnosis and treatment and their likely impact on gastroenterology clinical practice. Gastroenterology 2005;129:1720-1752.
-
(2005)
Gastroenterology
, vol.129
, pp. 1720-1752
-
-
Lazaridis, K.N.1
Juran, B.D.2
-
3
-
-
0037177589
-
Maneuvering in the complex path from genotype to phenotype
-
Strohman R. Maneuvering in the complex path from genotype to phenotype. Science 2002;296:701-703.
-
(2002)
Science
, vol.296
, pp. 701-703
-
-
Strohman, R.1
-
5
-
-
0038497542
-
Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid
-
Watson JD, Crick FH. Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid. Nature 1953;171:737-738.
-
(1953)
Nature
, vol.171
, pp. 737-738
-
-
Watson, J.D.1
Crick, F.H.2
-
6
-
-
0035895505
-
The sequence of the human genome
-
Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, et al. The sequence of the human genome. Science 2001;291:1304-1351.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
-
7
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, et al. Initial sequencing and analysis of the human genome. Nature 2001;409: 860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
-
8
-
-
0036255811
-
Opinion: Candidate-gene approaches for studying complex genetic traits: Practical considerations
-
Tabor HK, Risch NJ, Myers RM. Opinion: candidate-gene approaches for studying complex genetic traits: practical considerations. Nat Rev Genet 2002;3:391-397.
-
(2002)
Nat Rev Genet
, vol.3
, pp. 391-397
-
-
Tabor, H.K.1
Risch, N.J.2
Myers, R.M.3
-
9
-
-
1542563409
-
Initial sequencing and comparative analysis of the mouse genome
-
Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, et al. Initial sequencing and comparative analysis of the mouse genome. Nature 2002;420:520-562.
-
(2002)
Nature
, vol.420
, pp. 520-562
-
-
Waterston, R.H.1
Lindblad-Toh, K.2
Birney, E.3
Rogers, J.4
Abril, J.F.5
Agarwal, P.6
-
10
-
-
1642498224
-
The double-stranded DNA helix in recombination at meiosis
-
Moens PB. The double-stranded DNA helix in recombination at meiosis. Genome 2003;46:936-937.
-
(2003)
Genome
, vol.46
, pp. 936-937
-
-
Moens, P.B.1
-
11
-
-
79959524146
-
A haplotype map of the human genome
-
Altshuler D, Brooks LD, Chakravarti A, Collins FS, Daly MJ, Donnelly P. A haplotype map of the human genome. Nature 2005;437:1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
Altshuler, D.1
Brooks, L.D.2
Chakravarti, A.3
Collins, F.S.4
Daly, M.J.5
Donnelly, P.6
-
12
-
-
0036574859
-
Haplotype diversity and the block structure of linkage disequilibrium
-
Stumpf MP. Haplotype diversity and the block structure of linkage disequilibrium. Trends Genet 2002;18:226-228.
-
(2002)
Trends Genet
, vol.18
, pp. 226-228
-
-
Stumpf, M.P.1
-
13
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, et al. The structure of haplotype blocks in the human genome. Science 2002; 296:2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
-
14
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, et al. Haplotype tagging for the identification of common disease genes. Nat Genet 2001;29:233-237.
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
-
15
-
-
0037370629
-
Using haplotype blocks to map human complex trait loci
-
Cardon LR, Abecasis GR. Using haplotype blocks to map human complex trait loci. Trends Genet 2003;19:135-140.
-
(2003)
Trends Genet
, vol.19
, pp. 135-140
-
-
Cardon, L.R.1
Abecasis, G.R.2
-
16
-
-
28444437027
-
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets
-
Zeggini E, Rayner W, Morris AP, Hattersley AT, Walker M, Hitman GA, et al. An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets. Nat Genet 2005;37:1320-1322.
-
(2005)
Nat Genet
, vol.37
, pp. 1320-1322
-
-
Zeggini, E.1
Rayner, W.2
Morris, A.P.3
Hattersley, A.T.4
Walker, M.5
Hitman, G.A.6
-
17
-
-
0035008138
-
Putting the search for genes in perspective
-
Holtzman NA. Putting the search for genes in perspective. Int J Health Serv 2001;31:445-461.
-
(2001)
Int J Health Serv
, vol.31
, pp. 445-461
-
-
Holtzman, N.A.1
-
18
-
-
24944561852
-
Genetic linkage studies
-
Dawn Teare M, Barrett JH. Genetic linkage studies. Lancet 2005;366: 1036-1044.
-
(2005)
Lancet
, vol.366
, pp. 1036-1044
-
-
Dawn Teare, M.1
Barrett, J.H.2
-
19
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
Botstein D, Risch N. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet 2003;33(Suppl):228-237.
-
(2003)
Nat Genet
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
20
-
-
0035257236
-
Association study designs for complex diseases
-
Cardon LR, Bell JI. Association study designs for complex diseases. Nat Rev Genet 2001;2:91-99.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 91-99
-
-
Cardon, L.R.1
Bell, J.I.2
-
21
-
-
20444472340
-
Mapping quantitative trait loci in humans: Achievements and limitations
-
Majumder PP, Ghosh S. Mapping quantitative trait loci in humans: achievements and limitations. J Clin Invest 2005;115:1419-1424.
-
(2005)
J Clin Invest
, vol.115
, pp. 1419-1424
-
-
Majumder, P.P.1
Ghosh, S.2
-
22
-
-
33344471915
-
A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans
-
Puppala S, Dodd GD, Fowler S, Arya R, Schneider J, Farook VS, et al. A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet 2006;78:377-392.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 377-392
-
-
Puppala, S.1
Dodd, G.D.2
Fowler, S.3
Arya, R.4
Schneider, J.5
Farook, V.S.6
-
23
-
-
27244451809
-
High-resolution whole-genome association study of Parkinson disease
-
Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, et al. High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 2005;77:685-693.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 685-693
-
-
Maraganore, D.M.1
De Andrade, M.2
Lesnick, T.G.3
Strain, K.J.4
Farrer, M.J.5
Rocca, W.A.6
-
24
-
-
30844464387
-
Evaluating disorders with a complex genetics basis, the future roles of meta-analysis and systems biology
-
Whitcomb DC, Aoun E, Vodovotz Y, Clermont G, Barmada MM. Evaluating disorders with a complex genetics basis, the future roles of meta-analysis and systems biology. Dig Dis Sci 2005;50:2195-2202.
-
(2005)
Dig Dis Sci
, vol.50
, pp. 2195-2202
-
-
Whitcomb, D.C.1
Aoun, E.2
Vodovotz, Y.3
Clermont, G.4
Barmada, M.M.5
-
25
-
-
20444495264
-
Factors affecting statistical power in the detection of genetic association
-
Gordon D, Finch SJ. Factors affecting statistical power in the detection of genetic association. J Clin Invest 2005;115:1408-1418.
-
(2005)
J Clin Invest
, vol.115
, pp. 1408-1418
-
-
Gordon, D.1
Finch, S.J.2
-
26
-
-
25844510235
-
Shaking the tree: Mapping complex disease genes with linkage disequilibrium
-
Palmer LJ, Cardon LR. Shaking the tree: mapping complex disease genes with linkage disequilibrium. Lancet 2005;366:1223-1234.
-
(2005)
Lancet
, vol.366
, pp. 1223-1234
-
-
Palmer, L.J.1
Cardon, L.R.2
-
27
-
-
0037426052
-
Problems of reporting genetic associations with complex outcomes
-
Colhoun HM, McKeigue PM, Davey Smith G. Problems of reporting genetic associations with complex outcomes. Lancet 2003;361:865-872.
-
(2003)
Lancet
, vol.361
, pp. 865-872
-
-
Colhoun, H.M.1
McKeigue, P.M.2
Davey Smith, G.3
-
30
-
-
33644687421
-
Research opportunities on alcohol and liver damage
-
Zakhari S, Hoofnagle JH. Research opportunities on alcohol and liver damage. HEPATOLOGY 2005;42:1243.
-
(2005)
Hepatology
, vol.42
, pp. 1243
-
-
Zakhari, S.1
Hoofnagle, J.H.2
-
31
-
-
0038324103
-
Candidate genes for alcohol dependence: A review of genetic evidence from human studies
-
Dick DM, Foroud T. Candidate genes for alcohol dependence: a review of genetic evidence from human studies. Alcohol Clin Exp Res 2003;27:868-879.
-
(2003)
Alcohol Clin Exp Res
, vol.27
, pp. 868-879
-
-
Dick, D.M.1
Foroud, T.2
-
32
-
-
0030831092
-
Meta-analysis of the effects of alcohol dehydrogenase genotype on alcohol dependence and alcoholic liver disease
-
Whitfield JB. Meta-analysis of the effects of alcohol dehydrogenase genotype on alcohol dependence and alcoholic liver disease. Alcohol Alcohol 1997;32:613-619.
-
(1997)
Alcohol Alcohol
, vol.32
, pp. 613-619
-
-
Whitfield, J.B.1
-
33
-
-
0028278450
-
Low frequency of the ADH2*2 allele among Atayal natives of Taiwan with alcohol use disorders
-
Thomasson HR, Crabb DW, Edenberg HJ, Li TK, Hwu HG, Chen CC, et al. Low frequency of the ADH2*2 allele among Atayal natives of Taiwan with alcohol use disorders. Alcohol Clin Exp Res 1994;18:640-643.
-
(1994)
Alcohol Clin Exp Res
, vol.18
, pp. 640-643
-
-
Thomasson, H.R.1
Crabb, D.W.2
Edenberg, H.J.3
Li, T.K.4
Hwu, H.G.5
Chen, C.C.6
-
35
-
-
3242758298
-
Cytotoxic T-lymphocyte antigen-4 A49G polymorphism is associated with susceptibility to and severity of alcoholic liver disease in Italian patients
-
Valenti L, De Feo T, Fracanzani AL, Fatta E, Salvagnini M, Arico S, et al. Cytotoxic T-lymphocyte antigen-4 A49G polymorphism is associated with susceptibility to and severity of alcoholic liver disease in Italian patients. Alcohol Alcohol 2004;39:276-280.
-
(2004)
Alcohol Alcohol
, vol.39
, pp. 276-280
-
-
Valenti, L.1
De Feo, T.2
Fracanzani, A.L.3
Fatta, E.4
Salvagnini, M.5
Arico, S.6
-
36
-
-
33644547706
-
Nonalcoholic fatty liver disease: From steatosis to cirrhosis
-
Farrell GC, Larter CZ. Nonalcoholic fatty liver disease: from steatosis to cirrhosis. HEPATOLOGY 2006;43:S99-S112.
-
(2006)
Hepatology
, vol.43
-
-
Farrell, G.C.1
Larter, C.Z.2
-
38
-
-
4344595660
-
The potential role of genes in nonalcoholic fatty liver disease
-
xi
-
Day CP. The potential role of genes in nonalcoholic fatty liver disease. Clin Liver Dis 2004;8:673-691, xi.
-
(2004)
Clin Liver Dis
, vol.8
, pp. 673-691
-
-
Day, C.P.1
-
39
-
-
0343314903
-
Nonalcoholic steatohepatitis and cryptogenic cirrhosis within kindreds
-
Struben VM, Hespenheide EE, Caldwell SH. Nonalcoholic steatohepatitis and cryptogenic cirrhosis within kindreds. Am J Med 2000;108:9-13.
-
(2000)
Am J Med
, vol.108
, pp. 9-13
-
-
Struben, V.M.1
Hespenheide, E.E.2
Caldwell, S.H.3
-
40
-
-
0034799113
-
Ninety patients with nonalcoholic steatohepatitis: Insulin resistance, familial tendency, and severity of disease
-
Willner IR, Waters B, Patil SR, Reuben A, Morelli J, Riely CA. Ninety patients with nonalcoholic steatohepatitis: insulin resistance, familial tendency, and severity of disease. Am J Gastroenterol 2001;96:2957-2961.
-
(2001)
Am J Gastroenterol
, vol.96
, pp. 2957-2961
-
-
Willner, I.R.1
Waters, B.2
Patil, S.R.3
Reuben, A.4
Morelli, J.5
Riely, C.A.6
-
43
-
-
20444377268
-
Epidemiology and risk factors for gallstone disease: Has the paradigm changed in the 21st century?
-
Shaffer EA. Epidemiology and risk factors for gallstone disease: has the paradigm changed in the 21st century? Curr Gastroenterol Rep 2005;7: 132-140.
-
(2005)
Curr Gastroenterol Rep
, vol.7
, pp. 132-140
-
-
Shaffer, E.A.1
-
44
-
-
27144518494
-
Mechanisms of disease: The genetic epidemiology of gallbladder stones
-
Lammert F, Sauerbruch T. Mechanisms of disease: the genetic epidemiology of gallbladder stones. Nat Clin Pract Gastroenterol Hepatol 2005;2: 423-433.
-
(2005)
Nat Clin Pract Gastroenterol Hepatol
, vol.2
, pp. 423-433
-
-
Lammert, F.1
Sauerbruch, T.2
-
45
-
-
17144408092
-
Genetic and environmental influences on symptomatic gallstone disease: A Swedish study of 43,141 twin pairs
-
Katsika D, Grjibovski A, Einarsson C, Lammert F, Lichtenstein P, Marschall HU. Genetic and environmental influences on symptomatic gallstone disease: a Swedish study of 43,141 twin pairs. HEPATOLOGY 2005; 41:1138-1143.
-
(2005)
Hepatology
, vol.41
, pp. 1138-1143
-
-
Katsika, D.1
Grjibovski, A.2
Einarsson, C.3
Lammert, F.4
Lichtenstein, P.5
Marschall, H.U.6
-
46
-
-
0001846012
-
Gallstones
-
King RMA, ed. London: Oxford University Press
-
Paigen BCM. Gallstones. In: King RMA, ed. The Genetic Basis of Common Disease. London: Oxford University Press, 2002:298-335.
-
(2002)
The Genetic Basis of Common Disease
, pp. 298-335
-
-
Paigen, B.C.M.1
-
47
-
-
85002377975
-
Epidemiology of the American Indians' burden and its likely genetic origins
-
Carey MC, Paigen B. Epidemiology of the American Indians' burden and its likely genetic origins. HEPATOLOGY 2002;36:781-791.
-
(2002)
Hepatology
, vol.36
, pp. 781-791
-
-
Carey, M.C.1
Paigen, B.2
-
48
-
-
0041665024
-
ABCB4 gene mutation-associated cholelithiasis in adults
-
Rosmorduc O, Hermelin B, Boelle PY, Parc R, Taboury J, Poupon R. ABCB4 gene mutation-associated cholelithiasis in adults. Gastroenterology 2003;125:452-459.
-
(2003)
Gastroenterology
, vol.125
, pp. 452-459
-
-
Rosmorduc, O.1
Hermelin, B.2
Boelle, P.Y.3
Parc, R.4
Taboury, J.5
Poupon, R.6
-
49
-
-
4143073631
-
Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11
-
van Mil SW, van der Woerd WL, van der Brugge G, Sturm E, Jansen PL, Bull LN, et al. Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11. Gastroenterology 2004;127:379-384.
-
(2004)
Gastroenterology
, vol.127
, pp. 379-384
-
-
Van Mil, S.W.1
Van Der Woerd, W.L.2
Van Der Brugge, G.3
Sturm, E.4
Jansen, P.L.5
Bull, L.N.6
-
50
-
-
85047684249
-
Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype
-
Pullinger CR, Eng C, Salen G, Shefer S, Batta AK, Erickson SK, et al. Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype. J Clin Invest 2002;110:109-117.
-
(2002)
J Clin Invest
, vol.110
, pp. 109-117
-
-
Pullinger, C.R.1
Eng, C.2
Salen, G.3
Shefer, S.4
Batta, A.K.5
Erickson, S.K.6
-
51
-
-
33644528470
-
Autoimmune hepatitis, from mechanisms to therapy
-
Manns MP, Vogel A. Autoimmune hepatitis, from mechanisms to therapy. HEPATOLOGY 2006;43:S132-S144.
-
(2006)
Hepatology
, vol.43
-
-
Manns, M.P.1
Vogel, A.2
-
52
-
-
30044433616
-
Autoimmune hepatitis
-
Krawitt EL. Autoimmune hepatitis. N Engl J Med 2006;354:54-66.
-
(2006)
N Engl J Med
, vol.354
, pp. 54-66
-
-
Krawitt, E.L.1
-
53
-
-
0030962578
-
Allelic basis for HLA-encoded susceptibility to type 1 autoimmune hepatitis
-
Strettell MD, Donaldson PT, Thomson LJ, Santrach PJ, Moore SB, Czaja AJ, et al. Allelic basis for HLA-encoded susceptibility to type 1 autoimmune hepatitis. Gastroenterology 1997;112:2028-2035.
-
(1997)
Gastroenterology
, vol.112
, pp. 2028-2035
-
-
Strettell, M.D.1
Donaldson, P.T.2
Thomson, L.J.3
Santrach, P.J.4
Moore, S.B.5
Czaja, A.J.6
-
54
-
-
0031032711
-
Associations between alleles of the major histocompatibility complex and type 1 autoimmune hepatitis
-
Czaja AJ, Strettell MD, Thomson LJ, Santrach PJ, Moore SB, Donaldson PT, et al. Associations between alleles of the major histocompatibility complex and type 1 autoimmune hepatitis. HEPATOLOGY 1997;25:317-323.
-
(1997)
Hepatology
, vol.25
, pp. 317-323
-
-
Czaja, A.J.1
Strettell, M.D.2
Thomson, L.J.3
Santrach, P.J.4
Moore, S.B.5
Donaldson, P.T.6
-
55
-
-
14844302649
-
Genetic analysis of the HLA region of Japanese patients with type 1 autoimmune hepatitis
-
Yoshizawa K, Ota M, Katsuyama Y, Ichijo T, Matsumoto A, Tanaka E, et al. Genetic analysis of the HLA region of Japanese patients with type 1 autoimmune hepatitis. J Hepatol 2005;42:578-584.
-
(2005)
J Hepatol
, vol.42
, pp. 578-584
-
-
Yoshizawa, K.1
Ota, M.2
Katsuyama, Y.3
Ichijo, T.4
Matsumoto, A.5
Tanaka, E.6
-
56
-
-
0032722786
-
Pediatric and adult forms of type I autoimmune hepatitis in Argentina: Evidence for differential genetic predisposition
-
Pando M, Larriba J, Fernandez GC, Fainboim H, Ciocca M, Ramonet M, et al. Pediatric and adult forms of type I autoimmune hepatitis in Argentina: evidence for differential genetic predisposition. HEPATOLOGY 1999; 30:1374-1380.
-
(1999)
Hepatology
, vol.30
, pp. 1374-1380
-
-
Pando, M.1
Larriba, J.2
Fernandez, G.C.3
Fainboim, H.4
Ciocca, M.5
Ramonet, M.6
-
57
-
-
0032092934
-
MHC class II sequences of susceptibility and protection in Mexicans with autoimmune hepatitis
-
Vazquez-Garcia MN, Alaez C, Olivo A, Debaz H, Perez-Luque E, Burguete A, et al. MHC class II sequences of susceptibility and protection in Mexicans with autoimmune hepatitis. J Hepatol 1998;28:985-990.
-
(1998)
J Hepatol
, vol.28
, pp. 985-990
-
-
Vazquez-Garcia, M.N.1
Alaez, C.2
Olivo, A.3
Debaz, H.4
Perez-Luque, E.5
Burguete, A.6
-
58
-
-
0034070032
-
CTLA-4 gene polymorphism confers susceptibility to primary biliary cirrhosis
-
Agarwal K, Jones DE, Daly AK, James OF, Vaidya B, Pearce S, et al. CTLA-4 gene polymorphism confers susceptibility to primary biliary cirrhosis. J Hepatol 2000;32:538-541.
-
(2000)
J Hepatol
, vol.32
, pp. 538-541
-
-
Agarwal, K.1
Jones, D.E.2
Daly, A.K.3
James, O.F.4
Vaidya, B.5
Pearce, S.6
-
59
-
-
18944378475
-
Genetic association of cytokines polymorphisms with autoimmune hepatitis and primary biliary cirrhosis in the Chinese
-
Fan LY, Tu XQ, Zhu Y, Pfeiffer T, Feltens R, Stoecker W, et al. Genetic association of cytokines polymorphisms with autoimmune hepatitis and primary biliary cirrhosis in the Chinese. World J Gastroenterol 2005; 11: 2768-2772.
-
(2005)
World J Gastroenterol
, vol.11
, pp. 2768-2772
-
-
Fan, L.Y.1
Tu, X.Q.2
Zhu, Y.3
Pfeiffer, T.4
Feltens, R.5
Stoecker, W.6
-
60
-
-
21344432363
-
Fas polymorphisms influence susceptibility to autoimmune hepatitis
-
Hiraide A, Imazeki F, Yokosuka O, Kanda T, Kojima H, Fukai K, et al. Fas polymorphisms influence susceptibility to autoimmune hepatitis. Am J Gastroenterol 2005;100:1322-1329.
-
(2005)
Am J Gastroenterol
, vol.100
, pp. 1322-1329
-
-
Hiraide, A.1
Imazeki, F.2
Yokosuka, O.3
Kanda, T.4
Kojima, H.5
Fukai, K.6
-
61
-
-
0038805136
-
77 C/G mutation in the tyrosine phosphatase CD45 gene and autoimmune hepatitis: Evidence for a genetic link
-
Vogel A, Strassburg CP, Manns MP. 77 C/G mutation in the tyrosine phosphatase CD45 gene and autoimmune hepatitis: evidence for a genetic link. Genes Immun 2003;4:79-81.
-
(2003)
Genes Immun
, vol.4
, pp. 79-81
-
-
Vogel, A.1
Strassburg, C.P.2
Manns, M.P.3
-
62
-
-
0037487251
-
Primary biliary cirrhosis
-
Talwalkar JA, Lindor KD. Primary biliary cirrhosis. Lancet 2003;362:53-61.
-
(2003)
Lancet
, vol.362
, pp. 53-61
-
-
Talwalkar, J.A.1
Lindor, K.D.2
-
63
-
-
0034465973
-
Epidemiology and natural history of primary biliary cirrhosis in a US community
-
Kim WR, Lindor KD, Locke GR 3rd, Therneau TM, Homburger HA, Batts KP, et al. Epidemiology and natural history of primary biliary cirrhosis in a US community. Gastroenterology 2000;119:1631-1636.
-
(2000)
Gastroenterology
, vol.119
, pp. 1631-1636
-
-
Kim, W.R.1
Lindor, K.D.2
Locke III, G.R.3
Therneau, T.M.4
Homburger, H.A.5
Batts, K.P.6
-
64
-
-
0032587434
-
Familial primary biliary cirrhosis reassessed: A geographically-based population study
-
Jones DE, Watt FE, Metcalf JV, Bassendine MF, James OF. Familial primary biliary cirrhosis reassessed: a geographically-based population study. J Hepatol 1999;30:402-407.
-
(1999)
J Hepatol
, vol.30
, pp. 402-407
-
-
Jones, D.E.1
Watt, F.E.2
Metcalf, J.V.3
Bassendine, M.F.4
James, O.F.5
-
65
-
-
30944437302
-
Risk factors and comorbidities in primary biliary cirrhosis: A controlled interview-based study of 1032 patients
-
Gershwin ME, Selmi C, Worman HJ, Gold EB, Watnik M, Utts J, et al. Risk factors and comorbidities in primary biliary cirrhosis: a controlled interview-based study of 1032 patients. HEPATOLOGY 2005;42:1194-1202.
-
(2005)
Hepatology
, vol.42
, pp. 1194-1202
-
-
Gershwin, M.E.1
Selmi, C.2
Worman, H.J.3
Gold, E.B.4
Watnik, M.5
Utts, J.6
-
66
-
-
4143103585
-
Primary biliary cirrhosis in monozygotic and dizygotic twins: Genetics, epigenetics, and environment
-
Selmi C, Mayo MJ, Bach N, Ishibashi H, Invernizzi P, Gish RG, et al. Primary biliary cirrhosis in monozygotic and dizygotic twins: genetics, epigenetics, and environment. Gastroenterology 2004;127:485-492.
-
(2004)
Gastroenterology
, vol.127
, pp. 485-492
-
-
Selmi, C.1
Mayo, M.J.2
Bach, N.3
Ishibashi, H.4
Invernizzi, P.5
Gish, R.G.6
-
67
-
-
18144383173
-
From bases to basis: Linking genetics to causation in primary biliary cirrhosis
-
Invernizzi P, Selmi C, Mackay IR, Podda M, Gershwin ME. From bases to basis: linking genetics to causation in primary biliary cirrhosis. Clin Gastroenterol Hepatol 2005;3:401-410.
-
(2005)
Clin Gastroenterol Hepatol
, vol.3
, pp. 401-410
-
-
Invernizzi, P.1
Selmi, C.2
Mackay, I.R.3
Podda, M.4
Gershwin, M.E.5
-
68
-
-
33748929827
-
HLA class II alleles, genotypes, haplotypes, and amino acids in primary biliary cirrhosis: A large-scale study
-
Donaldson PT, Baragiotta A, Heneghan MA, Floreani A, Venturi C, Underbill JA, et al. HLA class II alleles, genotypes, haplotypes, and amino acids in primary biliary cirrhosis: a large-scale study. HEPATOLOGY 2006; 44:667-674.
-
(2006)
Hepatology
, vol.44
, pp. 667-674
-
-
Donaldson, P.T.1
Baragiotta, A.2
Heneghan, M.A.3
Floreani, A.4
Venturi, C.5
Underbill, J.A.6
-
70
-
-
0242490278
-
Incidence, clinical spectrum, and outcomes of primary sclerosing cholangitis in a United States community
-
Bambha K, Kim WR, Talwalkar J, Torgerson H, Benson JT, Therneau TM, et al. Incidence, clinical spectrum, and outcomes of primary sclerosing cholangitis in a United States community. Gastroenterology 2003; 125:1364-1369.
-
(2003)
Gastroenterology
, vol.125
, pp. 1364-1369
-
-
Bambha, K.1
Kim, W.R.2
Talwalkar, J.3
Torgerson, H.4
Benson, J.T.5
Therneau, T.M.6
-
71
-
-
0031941458
-
Incidence and prevalence of primary biliary cirrhosis, primary sclerosing cholangitis, and autoimmune hepatitis in a Norwegian population
-
Boberg KM, Aadland E, Jahnsen J, Raknerud N, Stiris M, Bell H. Incidence and prevalence of primary biliary cirrhosis, primary sclerosing cholangitis, and autoimmune hepatitis in a Norwegian population. Scand J Gastroenterol 1998;33:99-103.
-
(1998)
Scand J Gastroenterol
, vol.33
, pp. 99-103
-
-
Boberg, K.M.1
Aadland, E.2
Jahnsen, J.3
Raknerud, N.4
Stiris, M.5
Bell, H.6
-
72
-
-
12444260826
-
Increased prevalence of primary sclerosing cholangitis among first-degree relatives
-
Bergquist A, Lindberg G, Saarinen S, Broome U. Increased prevalence of primary sclerosing cholangitis among first-degree relatives. J Hepatol 2005;42:252-256.
-
(2005)
J Hepatol
, vol.42
, pp. 252-256
-
-
Bergquist, A.1
Lindberg, G.2
Saarinen, S.3
Broome, U.4
-
73
-
-
0036936696
-
Evaluation of the role of MHC class II alleles, haplotypes and selected amino acid sequences in primary sclerosing cholangitis
-
Donaldson PT, Norris S. Evaluation of the role of MHC class II alleles, haplotypes and selected amino acid sequences in primary sclerosing cholangitis. Autoimmunity 2002;35:555-564.
-
(2002)
Autoimmunity
, vol.35
, pp. 555-564
-
-
Donaldson, P.T.1
Norris, S.2
-
74
-
-
0034913340
-
Association of the tumour necrosis factor alpha-308 but not the interleukin 10-627 promoter polymorphism with genetic susceptibility to primary sclerosing cholangitis
-
Mitchell SA, Grove J, Spurkland A, Boberg KM, Fleming KA, Day CP, et al. Association of the tumour necrosis factor alpha-308 but not the interleukin 10-627 promoter polymorphism with genetic susceptibility to primary sclerosing cholangitis. Gut 2001;49:288-294.
-
(2001)
Gut
, vol.49
, pp. 288-294
-
-
Mitchell, S.A.1
Grove, J.2
Spurkland, A.3
Boberg, K.M.4
Fleming, K.A.5
Day, C.P.6
-
75
-
-
0035048898
-
Mapping MHC-encoded susceptibility and resistance in primary sclerosing cholangitis: The role of MICA polymorphism
-
Norris S, Kondeatis E, Collins R, Satsangi J, Clare M, Chapman R, et al. Mapping MHC-encoded susceptibility and resistance in primary sclerosing cholangitis: the role of MICA polymorphism. Gastroenterology 2001; 120:1475-1482.
-
(2001)
Gastroenterology
, vol.120
, pp. 1475-1482
-
-
Norris, S.1
Kondeatis, E.2
Collins, R.3
Satsangi, J.4
Clare, M.5
Chapman, R.6
-
76
-
-
0034950485
-
A functional polymorphism of the stromelysin gene (MMP-3) influences susceptibility to primary sclerosing cholangitis
-
Satsangi J, Chapman RW, Haldar N, Donaldson P, Mitchell S, Simmons J, et al. A functional polymorphism of the stromelysin gene (MMP-3) influences susceptibility to primary sclerosing cholangitis. Gastroenterology 2001;121:124-130.
-
(2001)
Gastroenterology
, vol.121
, pp. 124-130
-
-
Satsangi, J.1
Chapman, R.W.2
Haldar, N.3
Donaldson, P.4
Mitchell, S.5
Simmons, J.6
-
77
-
-
4644363380
-
CCR5-Delta32 mutation is strongly associated with primary sclerosing cholangitis
-
Eri R, Jonsson JR, Pandeya N, Purdie DM, Clouston AD, Martin N, et al. CCR5-Delta32 mutation is strongly associated with primary sclerosing cholangitis. Genes Immun 2004;5:444-450.
-
(2004)
Genes Immun
, vol.5
, pp. 444-450
-
-
Eri, R.1
Jonsson, J.R.2
Pandeya, N.3
Purdie, D.M.4
Clouston, A.D.5
Martin, N.6
-
78
-
-
1242269880
-
Susceptibility to primary sclerosing cholangitis is associated with polymorphisms of intercellular adhesion molecule-1
-
Yang X, Cullen SN, Li JH, Chapman RW, Jewell DP. Susceptibility to primary sclerosing cholangitis is associated with polymorphisms of intercellular adhesion molecule-1. J Hepatol 2004;40:375-379.
-
(2004)
J Hepatol
, vol.40
, pp. 375-379
-
-
Yang, X.1
Cullen, S.N.2
Li, J.H.3
Chapman, R.W.4
Jewell, D.P.5
-
79
-
-
16844366786
-
Genome-wide strategies for detecting multiple loci that influence complex diseases
-
Marchini J, Donnelly P, Cardon LR. Genome-wide strategies for detecting multiple loci that influence complex diseases. Nat Genet 2005;37:413-417.
-
(2005)
Nat Genet
, vol.37
, pp. 413-417
-
-
Marchini, J.1
Donnelly, P.2
Cardon, L.R.3
-
80
-
-
0038620498
-
Inflammatory bowel disease in a Swedish twin cohort: A long-term follow-up of concordance and clinical characteristics
-
Halfvarson J, Bodin L, Tysk C, Lindberg E, Jarnerot G. Inflammatory bowel disease in a Swedish twin cohort: a long-term follow-up of concordance and clinical characteristics. Gastroenterology 2003;124: 1767-1773.
-
(2003)
Gastroenterology
, vol.124
, pp. 1767-1773
-
-
Halfvarson, J.1
Bodin, L.2
Tysk, C.3
Lindberg, E.4
Jarnerot, G.5
-
81
-
-
0033773642
-
Concordance of inflammatory bowel disease among Danish twins. Results of a nationwide study
-
Orholm M, Binder V, Sorensen TI, Rasmussen LP, Kyvik KO. Concordance of inflammatory bowel disease among Danish twins. Results of a nationwide study. Scand J Gastroenterol 2000;35:1075-1081.
-
(2000)
Scand J Gastroenterol
, vol.35
, pp. 1075-1081
-
-
Orholm, M.1
Binder, V.2
Sorensen, T.I.3
Rasmussen, L.P.4
Kyvik, K.O.5
-
82
-
-
0036140724
-
Gastroesophageal reflux disease in monozygotic and dizygotic twins
-
Cameron AJ, Lagergren J, Henriksson C, Nyren O, Locke GR 3rd, Pedersen NL. Gastroesophageal reflux disease in monozygotic and dizygotic twins. Gastroenterology 2002;122:55-59.
-
(2002)
Gastroenterology
, vol.122
, pp. 55-59
-
-
Cameron, A.J.1
Lagergren, J.2
Henriksson, C.3
Nyren, O.4
Locke III, G.R.5
Pedersen, N.L.6
-
83
-
-
0036109726
-
The first large population based twin study of coeliac disease
-
Greco L, Romino R, Goto I, Di Cosmo N, Percopo S, Maglio M, et al. The first large population based twin study of coeliac disease. Gut 2002;50:624-628.
-
(2002)
Gut
, vol.50
, pp. 624-628
-
-
Greco, L.1
Romino, R.2
Goto, I.3
Di Cosmo, N.4
Percopo, S.5
Maglio, M.6
|