-
1
-
-
0026432216
-
Inflammatory bowel disease (1)
-
Podolsky DK: Inflammatory bowel disease (1). N Engl J Med 1991; 325: 928-937.
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 928-937
-
-
Podolsky, D.K.1
-
2
-
-
0023713859
-
Ulcerative colitis and Crohn's disease in an unselected population of monozygotic and dizygotic twins. A study of heritability and the influence of smoking
-
Tysk C, Lindberg E, Jarnerot G, Floderus-Myrhed B: Ulcerative colitis and Crohn's disease in an unselected population of monozygotic and dizygotic twins. A study of heritability and the influence of smoking. Gut 1988; 29: 990-996.
-
(1988)
Gut
, vol.29
, pp. 990-996
-
-
Tysk, C.1
Lindberg, E.2
Jarnerot, G.3
Floderus-Myrhed, B.4
-
3
-
-
16044373177
-
Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
-
Satsangi J, Parkes M, Louis E et al: Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Nat Genet 1996; 14: 199-202.
-
(1996)
Nat. Genet.
, vol.14
, pp. 199-202
-
-
Satsangi, J.1
Parkes, M.2
Louis, E.3
-
4
-
-
13344259990
-
Mapping of a susceptibility locus for Crohn's disease on chromosome 16
-
Hugot JP, Laurent-Puig P, Gower-Rousseau C et al: Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature 1996; 379: 821-823.
-
(1996)
Nature
, vol.379
, pp. 821-823
-
-
Hugot, J.P.1
Laurent-Puig, P.2
Gower-Rousseau, C.3
-
5
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn's disease and chromosome 16
-
Cavanaugh J: International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn's disease and chromosome 16. Am J Hum Genet 2001; 68: 1165-1171.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1165-1171
-
-
Cavanaugh, J.1
-
6
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura Y, Bonen DK, Inohara N et al: A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 2001; 411: 603-606.
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
-
7
-
-
13144261748
-
Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: Evidence for epistasis between 1p and IBD1
-
Cho JH, Nicolae DL, Gold LH et al: Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1. Proc Natl Acad Sci USA 1998; 95: 7502-7507.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 7502-7507
-
-
Cho, J.H.1
Nicolae, D.L.2
Gold, L.H.3
-
8
-
-
17344376439
-
Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease
-
Cho JH, Nicolae DL, Ramos R et al: Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease. Hum Mol Genet 2000; 9: 1425-1432.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1425-1432
-
-
Cho, J.H.1
Nicolae, D.L.2
Ramos, R.3
-
9
-
-
0033358425
-
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
-
Hampe J, Schreiber S, Shaw SH et al: A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. Am J Hum Genet 1999; 64: 808-816.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 808-816
-
-
Hampe, J.1
Schreiber, S.2
Shaw, S.H.3
-
10
-
-
0033910870
-
Genomewide search in canadian families with inflammatory bowel disease reveals two novel susceptibility loci
-
Rioux JD, Silverberg MS, Daly MJ et al: Genomewide search in canadian families with inflammatory bowel disease reveals two novel susceptibility loci. Am J Hum Genet 2000; 66: 1863-1870.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1863-1870
-
-
Rioux, J.D.1
Silverberg, M.S.2
Daly, M.J.3
-
11
-
-
0035127240
-
Evidence for inflammatory bowel disease of a susceptibility locus on the X chromosome
-
Vermeire S, Satsangi J, Peeters M et al: Evidence for inflammatory bowel disease of a susceptibility locus on the X chromosome. Gastroenterology 2001; 120: 834-840.
-
(2001)
Gastroenterology
, vol.120
, pp. 834-840
-
-
Vermeire, S.1
Satsangi, J.2
Peeters, M.3
-
12
-
-
0033228538
-
A genome-wide search identifies potential new susceptibility loci for Crohn's disease
-
Ma Y, Ohmen JD, Li Z et al: A genome-wide search identifies potential new susceptibility loci for Crohn's disease. Inflamm Bowel Dis 1999; 5: 271-278.
-
(1999)
Inflamm. Bowel Dis.
, vol.5
, pp. 271-278
-
-
Ma, Y.1
Ohmen, J.D.2
Li, Z.3
-
13
-
-
0033927387
-
High-density genome scan in Crohn's disease shows confirmed linkage to chromosome 14q11-12
-
Duerr RH, Barmada MM, Zhang L, Pfutzer R, Weeks DE: High-density genome scan in Crohn's disease shows confirmed linkage to chromosome 14q11-12. Am J Hum Genet 2000; 66: 1857-1862.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1857-1862
-
-
Duerr, R.H.1
Barmada, M.M.2
Zhang, L.3
Pfutzer, R.4
Weeks, D.E.5
-
14
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C et al: A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996; 380: 152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
-
15
-
-
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 1998; 63: 259-266.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
16
-
-
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 1997; 61: 1179-1188.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
18
-
-
0033910787
-
A test for linkage and association in general pedigrees: The pedigree disequilibrium test
-
Martin ER, Monks SA, Warren LL, Kaplan NL: A test for linkage and association in general pedigrees: the pedigree disequilibrium test. Am J Hum Genet 2000; 67: 146-154.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 146-154
-
-
Martin, E.R.1
Monks, S.A.2
Warren, L.L.3
Kaplan, N.L.4
-
19
-
-
0035076031
-
Correcting for a potential bias in the pedigree disequilibrium test
-
Martin ER, Bass MP, Kaplan NL: Correcting for a potential bias in the pedigree disequilibrium test. Am J Hum Genet 2001; 68: 1065-1067.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1065-1067
-
-
Martin, E.R.1
Bass, M.P.2
Kaplan, N.L.3
-
20
-
-
0032004378
-
A novel process for mutation detection using uracil DNA-glycosylase
-
Vaughan P, McCarthy TV: A novel process for mutation detection using uracil DNA-glycosylase. Nucleic Acids Res 1998; 26: 810-815.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 810-815
-
-
Vaughan, P.1
McCarthy, T.V.2
-
21
-
-
0036653386
-
Investigation of the Genetic Influence of the OPG, VDR (Fok1), and COLIA1 Sp1 Polymorphisms on BMD in the Irish Population
-
Wynne F, Drummond F, O'Sullivan K et al: Investigation of the Genetic Influence of the OPG, VDR (Fok1), and COLIA1 Sp1 Polymorphisms on BMD in the Irish Population. Calcif Tissue Int 2002; 20: 20.
-
(2002)
Calcif. Tissue Int.
, vol.20
, pp. 20
-
-
Wynne, F.1
Drummond, F.2
O'Sullivan, K.3
-
22
-
-
0024438993
-
A computer program for choosing optimal oligonucleotides for filter hybridization, sequencing and in vitro amplification of DNA
-
Rychlik W, Rhoads RE: A computer program for choosing optimal oligonucleotides for filter hybridization, sequencing and in vitro amplification of DNA. Nucleic Acids Res 1989; 17: 8543-8551.
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 8543-8551
-
-
Rychlik, W.1
Rhoads, R.E.2
-
23
-
-
0033010655
-
Glycosylase mediated polymorphism detection (GMPD)-A novel process for genetic analysis
-
Vaughan P, McCarthy TV: Glycosylase mediated polymorphism detection (GMPD)-a novel process for genetic analysis. Genet Anal 1999; 14: 169-175.
-
(1999)
Genet. Anal.
, vol.14
, pp. 169-175
-
-
Vaughan, P.1
McCarthy, T.V.2
-
24
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H et al: Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 2001; 411: 599-603.
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
-
25
-
-
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 1995; 11: 241-247.
-
(1995)
Nat. Genet.
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
26
-
-
0002121723
-
Sample size and power
-
Haines JL, Pericak-vance MA (eds): New York: Wiley-Liss, Inc
-
Speer M: Sample size and power. In: Haines JL, Pericak-vance MA (eds): Approaches to gene mapping in complex human diseases. New York: Wiley-Liss, Inc., 1998; pp. 161-200.
-
(1998)
Approaches to Gene Mapping in Complex Human Diseases
, pp. 161-200
-
-
Speer, M.1
-
27
-
-
0036201577
-
CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
-
Lesage S, Zouali H, Cezard JP et al: CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. Am J Hum Genet 2002; 70: 845-857.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 845-857
-
-
Lesage, S.1
Zouali, H.2
Cezard, J.P.3
-
28
-
-
0036202885
-
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease
-
Cuthbert AP, Fisher SA, Mirza MM et al: The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. Gastroenterology 2002; 122: 867-874.
-
(2002)
Gastroenterology
, vol.122
, pp. 867-874
-
-
Cuthbert, A.P.1
Fisher, S.A.2
Mirza, M.M.3
-
29
-
-
0036202336
-
The molecular classification of the clinical manifestations of Crohn's disease
-
Ahmad T, Armuzzi A, Bunce M et al: The molecular classification of the clinical manifestations of Crohn's disease. Gastroenterology 2002; 122: 854-866.
-
(2002)
Gastroenterology
, vol.122
, pp. 854-866
-
-
Ahmad, T.1
Armuzzi, A.2
Bunce, M.3
-
30
-
-
0034758045
-
Genomewide scans of complex human diseases: True linkage is hard to find
-
Altmuller J, Palmer LJ, Fischer G, Scherb H, Wjst M: Genomewide scans of complex human diseases: true linkage is hard to find. Am J Hum Genet 2001; 69: 936-950.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 936-950
-
-
Altmuller, J.1
Palmer, L.J.2
Fischer, G.3
Scherb, H.4
Wjst, M.5
-
31
-
-
0002710362
-
Problems of replicating linkage claims in psychiatry
-
Cloninger CR (ed): Washington DC: American Psychiatric Press
-
Suarez BK, Hampe CL, Van Eerdewegh P: Problems of replicating linkage claims in psychiatry; In: Cloninger CR (ed): Genetic approaches to mental disorders. Washington DC: American Psychiatric Press, 1994, pp. 23-46.
-
(1994)
Genetic Approaches to Mental Disorders
, pp. 23-46
-
-
Suarez, B.K.1
Hampe, C.L.2
Van Eerdewegh, P.3
-
32
-
-
0242470320
-
Linkage disequilibrium
-
New York: The John Hopkins University Press
-
Ott J: Linkage disequilibrium: in: Analysis of human genetic linkage. New York: The John Hopkins University Press, 1999, pp. 280-291.
-
(1999)
Analysis of Human Genetic Linkage
, pp. 280-291
-
-
Ott, J.1
-
33
-
-
0035897904
-
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
-
Hampe J, Cuthbert A, Croucher PJ et al: Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 2001; 357: 1925-1928.
-
(2001)
Lancet
, vol.357
, pp. 1925-1928
-
-
Hampe, J.1
Cuthbert, A.2
Croucher, P.J.3
-
34
-
-
18244375904
-
Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p
-
Hampe J, Frenzel H, Mirza MM et al: Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p. Proc Natl Acad Sci USA 2002; 99: 321-326.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 321-326
-
-
Hampe, J.1
Frenzel, H.2
Mirza, M.M.3
-
35
-
-
0034704845
-
Y-chromosome variation and Irish origins
-
Hill EW, Jobling MA, Bradley DG: Y-chromosome variation and Irish origins. Nature 2000; 404: 351-352.
-
(2000)
Nature
, vol.404
, pp. 351-352
-
-
Hill, E.W.1
Jobling, M.A.2
Bradley, D.G.3
-
36
-
-
0020960768
-
Genetic structure and population history of Ireland: A comparison of blood group and anthropometric analyses
-
Relethford JH: Genetic structure and population history of Ireland: a comparison of blood group and anthropometric analyses. Ann Hum Biol 1983; 10: 321-333.
-
(1983)
Ann. Hum. Biol.
, vol.10
, pp. 321-333
-
-
Relethford, J.H.1
-
37
-
-
0028959146
-
Anthropometric variation and the population history of Ireland
-
Relethford JH, Crawford MH. Anthropometric variation and the population history of Ireland. Am J Phys Anthropol 1995; 96: 25-38.
-
(1995)
Am. J. Phys. Anthropol.
, vol.96
, pp. 25-38
-
-
Relethford, J.H.1
Crawford, M.H.2
|