-
1
-
-
84965339061
-
ABO blood groups and secretor character in duodenal ulcer: Population and sibship studies
-
C. Clarke, J. Edwards, D. Haddock, A. Howel-Evans, R. McConnell, and P. Sheppard ABO blood groups and secretor character in duodenal ulcer: population and sibship studies BMJ 1956 725 731
-
(1956)
BMJ
, pp. 725-731
-
-
Clarke, C.1
Edwards, J.2
Haddock, D.3
Howel-Evans, A.4
McConnell, R.5
Sheppard, P.6
-
2
-
-
17044367137
-
Enzyme and protein diversity in human populations
-
American Elsevier Publishing Company New York
-
H. Harris Enzyme and protein diversity in human populations The Principle of Human Biochemical Genetics 1970 American Elsevier Publishing Company New York 211-242
-
(1970)
The Principle of Human Biochemical Genetics
-
-
Harris, H.1
-
5
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
K.E. Lohmueller, C.L. Pearce, M. Pike, E.S. Lander, and J.N. Hirschhorn Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease Nat. Genet. 33 2003 177 182
-
(2003)
Nat. Genet.
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
6
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density: Cooperative Human Linkage Center (CHLC)
-
J.C. Murray, K.H. Buetow, J.L. Weber, S. Ludwigsen, T. Scherpbier-Heddema, F. Manion, J. Quillen, V.C. Sheffield, S. Sunden, and G.M. Duyk A comprehensive human linkage map with centimorgan density: Cooperative Human Linkage Center (CHLC) Science 265 1994 2049 2054
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
Manion, F.6
Quillen, J.7
Sheffield, V.C.8
Sunden, S.9
Duyk, G.M.10
-
7
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5264 microsatellites
-
C. Dib, S. Faure, C. Fizames, D. Samson, N. Drouot, A. Vignal, P. Millasseau, S. Marc, J. Hazan, E. Seboun, M. Lathrop, G. Gyapay, J. Morissette, and J. Weissenbach A comprehensive genetic map of the human genome based on 5264 microsatellites Nature 380 1996 152 154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
8
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
K.W. Broman, J.C. Murray, V.C. Sheffield, R.L. White, and J.L. Weber Comprehensive human genetic maps: individual and sex-specific variation in recombination Am. J. Hum. Genet. 63 1998 861 869
-
(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
-
9
-
-
0036403779
-
Linkage analysis in psychiatric disorders: The emerging picture
-
P. Sklar Linkage analysis in psychiatric disorders: the emerging picture Annu. Rev. Genomics Hum. Genet. 3 2002 371 413
-
(2002)
Annu. Rev. Genomics Hum. Genet.
, vol.3
, pp. 371-413
-
-
Sklar, P.1
-
10
-
-
0242524453
-
The inherited basis of diabetes mellitus: Implications for the genetic analysis of complex traits
-
J.C. Florez, J. Hirschhorn, and D. Altshuler The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits Annu. Rev. Genomics Hum. Genet. 4 2003 257 291
-
(2003)
Annu. Rev. Genomics Hum. Genet.
, vol.4
, pp. 257-291
-
-
Florez, J.C.1
Hirschhorn, J.2
Altshuler, D.3
-
11
-
-
0034758045
-
Genome-wide scans of complex human diseases: True linkage is hard to find
-
J. Altmuller, L.J. Palmer, G. Fischer, H. Scherb, and M. Wjst Genome-wide scans of complex human diseases: true linkage is hard to find Am. J. Hum. Genet. 69 2001 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
-
12
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
J.P. Hugot, M. Chamaillard, H. Zouali, S. Lesage, J.P. Cezard, J. Belaiche, S. Almer, C. Tysk, C.A. O'Morain, M. Gassull, V. Binder, Y. Finkel, A. Cortot, R. Modigliani, P. Laurent-Puig, C. Gower-Rousseau, J. Macry, J.F. Colombel, M. Sahbatou, and G. Thomas Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease Nature 411 2001 599 603
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
O'Morain, C.A.9
Gassull, M.10
Binder, V.11
Finkel, Y.12
Cortot, A.13
Modigliani, R.14
Laurent-Puig, P.15
Gower-Rousseau, C.16
MacRy, J.17
Colombel, J.F.18
Sahbatou, M.19
Thomas, G.20
more..
-
13
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Y. Ogura, D.K. Bonen, N. Inohara, D.L. Nicolae, F.F. Chen, R. Ramos, H. Britton, T. Moran, R. Karaliuskas, R.H. Duerr, J.P. Achkar, S.R. Brant, T.M. Bayless, B.S. Kirschner, S.B. Hanauer, G. Nunez, and J.H. Cho A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease Nature 411 2001 603 606
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
Britton, H.7
Moran, T.8
Karaliuskas, R.9
Duerr, R.H.10
Achkar, J.P.11
Brant, S.R.12
Bayless, T.M.13
Kirschner, B.S.14
Hanauer, S.B.15
Nunez, G.16
Cho, J.H.17
-
14
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
J.D. Rioux, M.J. Daly, M.S. Silverberg, K. Lindblad, H. Steinhart, Z. Cohen, T. Delmonte, K. Kocher, K. Miller, S. Guschwan, E.J. Kulbokas, S. O'Leary, E. Winchester, K. Dewar, T. Green, V. Stone, C. Chow, A. Cohen, D. Langelier, G. Lapointe, D. Gaudet, J. Faith, N. Branco, S.B. Bull, R.S. McLeod, A.M. Griffiths, A. Bitton, G.R. Greenberg, E.S. Lander, K.A. Siminovitch, and T.J. Hudson Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease Nat. Genet. 29 2001 223 228
-
(2001)
Nat. Genet.
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
Lindblad, K.4
Steinhart, H.5
Cohen, Z.6
Delmonte, T.7
Kocher, K.8
Miller, K.9
Guschwan, S.10
Kulbokas, E.J.11
O'Leary, S.12
Winchester, E.13
Dewar, K.14
Green, T.15
Stone, V.16
Chow, C.17
Cohen, A.18
Langelier, D.19
Lapointe, G.20
Gaudet, D.21
Faith, J.22
Branco, N.23
Bull, S.B.24
McLeod, R.S.25
Griffiths, A.M.26
Bitton, A.27
Greenberg, G.R.28
Lander, E.S.29
Siminovitch, K.A.30
Hudson, T.J.31
more..
-
15
-
-
3543046736
-
A functional variant of SUMO4, a new IkappaBalpha modifier, is associated with type 1 diabetes
-
D. Guo, M. Li, Y. Zhang, P. Yang, S. Eckenrode, D. Hopkins, W. Zheng, S. Purohit, R.H. Podolsky, A. Muir, J. Wang, Z. Dong, T. Brusko, M. Atkinson, P. Pozzilli, A. Zeidler, L.J. Raffel, C.O. Jacob, Y. Park, M. Serrano-Rios, M.T. Larrad, Z. Zhang, H.J. Garchon, J.F. Bach, J.I. Rotter, J.X. She, and C.Y. Wang A functional variant of SUMO4, a new IkappaBalpha modifier, is associated with type 1 diabetes Nat. Genet. 36 2004 837 841
-
(2004)
Nat. Genet.
, vol.36
, pp. 837-841
-
-
Guo, D.1
Li, M.2
Zhang, Y.3
Yang, P.4
Eckenrode, S.5
Hopkins, D.6
Zheng, W.7
Purohit, S.8
Podolsky, R.H.9
Muir, A.10
Wang, J.11
Dong, Z.12
Brusko, T.13
Atkinson, M.14
Pozzilli, P.15
Zeidler, A.16
Raffel, L.J.17
Jacob, C.O.18
Park, Y.19
Serrano-Rios, M.20
Larrad, M.T.21
Zhang, Z.22
Garchon, H.J.23
Bach, J.F.24
Rotter, J.I.25
She, J.X.26
Wang, C.Y.27
more..
-
16
-
-
0034821661
-
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families
-
N.J. Cox, B. Wapelhorst, V.A. Morrison, L. Johnson, L. Pinchuk, R.S. Spielman, J.A. Todd, and P. Concannon Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families Am. J. Hum. Genet. 69 2001 820 830
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 820-830
-
-
Cox, N.J.1
Wapelhorst, B.2
Morrison, V.A.3
Johnson, L.4
Pinchuk, L.5
Spielman, R.S.6
Todd, J.A.7
Concannon, P.8
-
17
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
A. Kong, D.F. Gudbjartsson, J. Sainz, G.M. Jonsdottir, S.A. Gudjonsson, B. Richardsson, S. Sigurdardottir, J. Barnard, B. Hallbeck, G. Masson, A. Shlien, S.T. Palsson, M.L. Frigge, T.E. Thorgeirsson, J.R. Gulcher, and K. Stefansson A high-resolution recombination map of the human genome Nat. Genet. 31 2002 241 247
-
(2002)
Nat. Genet.
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
Shlien, A.11
Palsson, S.T.12
Frigge, M.L.13
Thorgeirsson, T.E.14
Gulcher, J.R.15
Stefansson, K.16
-
18
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
H. Stefansson, E. Sigurdsson, V. Steinthorsdottir, S. Bjornsdottir, T. Sigmundsson, S. Ghosh, J. Brynjolfsson, S. Gunnarsdottir, O. Ivarsson, T.T. Chou, O. Hjaltason, B. Birgisdottir, H. Jonsson, V.G. Gudnadottir, E. Gudmundsdottir, A. Bjornsson, B. Ingvarsson, A. Ingason, S. Sigfusson, H. Hardardottir, R.P. Harvey, D. Lai, M. Zhou, D. Brunner, V. Mutel, A. Gonzalo, G. Lemke, J. Sainz, G. Johannesson, T. Andresson, D. Gudbjartsson, A. Manolescu, M.L. Frigge, M.E. Gurney, A. Kong, J.R. Gulcher, H. Petursson, and K. Stefansson Neuregulin 1 and susceptibility to schizophrenia Am. J. Hum. Genet. 71 2002 877 892
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 877-892
-
-
Stefansson, H.1
Sigurdsson, E.2
Steinthorsdottir, V.3
Bjornsdottir, S.4
Sigmundsson, T.5
Ghosh, S.6
Brynjolfsson, J.7
Gunnarsdottir, S.8
Ivarsson, O.9
Chou, T.T.10
Hjaltason, O.11
Birgisdottir, B.12
Jonsson, H.13
Gudnadottir, V.G.14
Gudmundsdottir, E.15
Bjornsson, A.16
Ingvarsson, B.17
Ingason, A.18
Sigfusson, S.19
Hardardottir, H.20
Harvey, R.P.21
Lai, D.22
Zhou, M.23
Brunner, D.24
Mutel, V.25
Gonzalo, A.26
Lemke, G.27
Sainz, J.28
Johannesson, G.29
Andresson, T.30
Gudbjartsson, D.31
Manolescu, A.32
Frigge, M.L.33
Gurney, M.E.34
Kong, A.35
Gulcher, J.R.36
Petursson, H.37
Stefansson, K.38
more..
-
19
-
-
0041488881
-
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set
-
T.C. Matise, R. Sachidanandam, A.G. Clark, L. Kruglyak, E. Wijsman, J. Kakol, S. Buyske, B. Chui, P. Cohen, C. de Toma, M. Ehm, S. Glanowski, C. He, J. Heil, K. Markianos, I. McMullen, M.A. Pericak-Vance, A. Silbergleit, L. Stein, M. Wagner, A.F. Wilson, J.D. Winick, E.S. Winn-Deen, C.T. Yamashiro, H.M. Cann, E. Lai, and A.L. Holden A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set Am. J. Hum. Genet. 73 2003 271 284
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 271-284
-
-
Matise, T.C.1
Sachidanandam, R.2
Clark, A.G.3
Kruglyak, L.4
Wijsman, E.5
Kakol, J.6
Buyske, S.7
Chui, B.8
Cohen, P.9
De Toma, C.10
Ehm, M.11
Glanowski, S.12
He, C.13
Heil, J.14
Markianos, K.15
McMullen, I.16
Pericak-Vance, M.A.17
Silbergleit, A.18
Stein, L.19
Wagner, M.20
Wilson, A.F.21
Winick, J.D.22
Winn-Deen, E.S.23
Yamashiro, C.T.24
Cann, H.M.25
Lai, E.26
Holden, A.L.27
more..
-
20
-
-
2342635193
-
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: A comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22
-
F.A. Middleton, M.T. Pato, K.L. Gentile, C.P. Morley, X. Zhao, A.F. Eisener, A. Brown, T.L. Petryshen, A.N. Kirby, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M.J. Soares, C.P. Ferreira, M. Lei, M.H. Azevedo, J.L. Kennedy, M.J. Daly, P. Sklar, and C.N. Pato Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22 Am. J. Hum. Genet. 74 2004 886 897
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 886-897
-
-
Middleton, F.A.1
Pato, M.T.2
Gentile, K.L.3
Morley, C.P.4
Zhao, X.5
Eisener, A.F.6
Brown, A.7
Petryshen, T.L.8
Kirby, A.N.9
Medeiros, H.10
Carvalho, C.11
MacEdo, A.12
Dourado, A.13
Coelho, I.14
Valente, J.15
Soares, M.J.16
Ferreira, C.P.17
Lei, M.18
Azevedo, M.H.19
Kennedy, J.L.20
Daly, M.J.21
Sklar, P.22
Pato, C.N.23
more..
-
21
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
N. Risch, and K. Merikangas The future of genetic studies of complex human diseases Science 273 1996 1516 1517
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
22
-
-
0037432755
-
The Human Genome Project: Lessons from large-scale biology
-
F.S. Collins, M. Morgan, and A. Patrinos The Human Genome Project: lessons from large-scale biology Science 300 2003 286 290
-
(2003)
Science
, vol.300
, pp. 286-290
-
-
Collins, F.S.1
Morgan, M.2
Patrinos, A.3
-
23
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
E.S. Lander, L.M. Linton, B. Birren, C. Nusbaum, M.C. Zody, J. Baldwin, K. Devon, K. Dewar, M. Doyle, W. FitzHugh, R. Funke, D. Gage, K. Harris, A. Heaford, J. Howland, L. Kann, J. Lehoczky, R. Levine, P. McEwan, K. McKernan, J. Meldrim, J.P. Mesirov, C. Miranda, W. Morris, J. Naylor, C. Raymond, M. Rosetti, R. Santos, A. Sheridan, C. Sougnez, N. Stange-Thomann, N. Stojanovic, A. Subramanian, D. Wyman, J. Rogers, J. Sulston, R. Ainscough, S. Beck, D. Bentley, J. Burton, C. Clee, N. Carter, A. Coulson, R. Deadman, P. Deloukas, A. Dunham, I. Dunham, R. Durbin, L. French, D. Grafham, S. Gregory, T. Hubbard, S. Humphray, A. Hunt, M. Jones, C. Lloyd, A. McMurray, L. Matthews, S. Mercer, S. Milne, J.C. Mullikin, A. Mungall, R. Plumb, M. Ross, R. Shownkeen, S. Sims, R.H. Waterston, R.K. Wilson, L.W. Hillier, J.D. McPherson, M.A. Marra, E.R. Mardis, L.A. Fulton, A.T. Chinwalla, K.H. Pepin, W.R. Gish, S.L. Chissoe, M.C. Wendl, K.D. Delehaunty, T.L. Miner, A. Delehaunty, J.B. Kramer, L.L. Cook, R.S. Fulton, D.L. Johnson, P.J. Minx, S.W. Clifton, T. Hawkins, E. Branscomb, P. Predki, P. Richardson, S. Wenning, T. Slezak, N. Doggett, J.F. Cheng, A. Olsen, S. Lucas, C. Elkin, E. Uberbacher, M. Frazier, R.A. Gibbs, D.M. Muzny, S.E. Scherer, J.B. Bouck, E.J. Sodergren, K.C. Worley, C.M. Rives, J.H. Gorrell, M.L. Metzker, S.L. Naylor, R.S. Kucherlapati, D.L. Nelson, G.M. Weinstock, Y. Sakaki, A. Fujiyama, M. Hattori, T. Yada, A. Toyoda, T. Itoh, C. Kawagoe, H. Watanabe, Y. Totoki, T. Taylor, J. Weissenbach, R. Heilig, W. Saurin, F. Artiguenave, P. Brottier, T. Bruls, E. Pelletier, C. Robert, P. Wincker, D.R. Smith, L. Doucette-Stamm, M. Rubenfield, K. Weinstock, H.M. Lee, J. Dubois, A. Rosenthal, M. Platzer, G. Nyakatura, S. Taudien, A. Rump, H. Yang, J. Yu, J. Wang, G. Huang, J. Gu, L. Hood, L. Rowen, A. Madan, S. Qin, R.W. Davis, N.A. Federspiel, A.P. Abola, M.J. Proctor, R.M. Myers, J. Schmutz, M. Dickson, J. Grimwood, D.R. Cox, M.V. Olson, R. Kaul, C. Raymond, N. Shimizu, K. Kawasaki, S. Minoshima, G.A. Evans, M. Athanasiou, R. Schultz, B.A. Roe, F. Chen, H. Pan, J. Ramser, H. Lehrach, R. Reinhardt, W.R. McCombie, B.M. de la, N. Dedhia, H. Blocker, K. Hornischer, G. Nordsiek, R. Agarwala, L. Aravind, J.A. Bailey, A. Bateman, S. Batzoglou, E. Birney, P. Bork, D.G. Brown, C.B. Burge, L. Cerutti, H.C. Chen, D. Church, M. Clamp, R.R. Copley, T. Doerks, S.R. Eddy, E.E. Eichler, T.S. Furey, J. Galagan, J.G. Gilbert, C. Harmon, Y. Hayashizaki, D. Haussler, H. Hermjakob, K. Hokamp, W. Jang, L.S. Johnson, T.A. Jones, S. Kasif, A. Kaspryzk, S. Kennedy, W.J. Kent, P. Kitts, E.V. Koonin, I. Korf, D. Kulp, D. Lancet, T.M. Lowe, A. McLysaght, T. Mikkelsen, J.V. Moran, N. Mulder, V.J. Pollara, C.P. Ponting, G. Schuler, J. Schultz, G. Slater, A.F. Smit, E. Stupka, J. Szustakowski, D. Thierry-Mieg, J. Thierry-Mieg, L. Wagner, J. Wallis, R. Wheeler, A. Williams, Y.I. Wolf, K.H. Wolfe, S.P. Yang, R.F. Yeh, F. Collins, M.S. Guyer, J. Peterson, A. Felsenfeld, K.A. Wetterstrand, A. Patrinos, M.J. Morgan, J. Szustakowki, P. de Jong, J.J. Catanese, K. Osoegawa, H. Shizuya, and S. Choi Initial sequencing and analysis of the human genome Nature 409 2001 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
Devon, K.7
Dewar, K.8
Doyle, M.9
Fitzhugh, W.10
Funke, R.11
Gage, D.12
Harris, K.13
Heaford, A.14
Howland, J.15
Kann, L.16
Lehoczky, J.17
Levine, R.18
McEwan, P.19
McKernan, K.20
Meldrim, J.21
Mesirov, J.P.22
Miranda, C.23
Morris, W.24
Naylor, J.25
Raymond, C.26
Rosetti, M.27
Santos, R.28
Sheridan, A.29
Sougnez, C.30
Stange-Thomann, N.31
Stojanovic, N.32
Subramanian, A.33
Wyman, D.34
Rogers, J.35
Sulston, J.36
Ainscough, R.37
Beck, S.38
Bentley, D.39
Burton, J.40
Clee, C.41
Carter, N.42
Coulson, A.43
Deadman, R.44
Deloukas, P.45
Dunham, A.46
Dunham, I.47
Durbin, R.48
French, L.49
Grafham, D.50
Gregory, S.51
Hubbard, T.52
Humphray, S.53
Hunt, A.54
Jones, M.55
Lloyd, C.56
McMurray, A.57
Matthews, L.58
Mercer, S.59
Milne, S.60
Mullikin, J.C.61
Mungall, A.62
Plumb, R.63
Ross, M.64
Shownkeen, R.65
Sims, S.66
Waterston, R.H.67
Wilson, R.K.68
Hillier, L.W.69
McPherson, J.D.70
Marra, M.A.71
Mardis, E.R.72
Fulton, L.A.73
Chinwalla, A.T.74
Pepin, K.H.75
Gish, W.R.76
Chissoe, S.L.77
Wendl, M.C.78
Delehaunty, K.D.79
Miner, T.L.80
Delehaunty, A.81
Kramer, J.B.82
Cook, L.L.83
Fulton, R.S.84
Johnson, D.L.85
Minx, P.J.86
Clifton, S.W.87
Hawkins, T.88
Branscomb, E.89
Predki, P.90
Richardson, P.91
Wenning, S.92
Slezak, T.93
Doggett, N.94
Cheng, J.F.95
Olsen, A.96
Lucas, S.97
Elkin, C.98
Uberbacher, E.99
more..
-
24
-
-
0035895505
-
The sequence of the human genome
-
J.C. Venter, M.D. Adams, E.W. Myers, P.W. Li, R.J. Mural, G.G. Sutton, H.O. Smith, M. Yandell, C.A. Evans, R.A. Holt, J.D. Gocayne, P. Amanatides, R.M. Ballew, D.H. Huson, J.R. Wortman, Q. Zhang, C.D. Kodira, X.H. Zheng, L. Chen, M. Skupski, G. Subramanian, P.D. Thomas, J. Zhang, G.L. Gabor Miklos, C. Nelson, S. Broder, A.G. Clark, J. Nadeau, V.A. McKusick, N. Zinder, A.J. Levine, R.J. Roberts, M. Simon, C. Slayman, M. Hunkapiller, R. Bolanos, A. Delcher, I. Dew, D. Fasulo, M. Flanigan, L. Florea, A. Halpern, S. Hannenhalli, S. Kravitz, S. Levy, C. Mobarry, K. Reinert, K. Remington, J. Abu-Threideh, E. Beasley, K. Biddick, V. Bonazzi, R. Brandon, M. Cargill, I. Chandramouliswaran, R. Charlab, K. Chaturvedi, Z. Deng, F. Di, V.P. Dunn, K. Eilbeck, C. Evangelista, A.E. Gabrielian, W. Gan, W. Ge, F. Gong, Z. Gu, P. Guan, T.J. Heiman, M.E. Higgins, R.R. Ji, Z. Ke, K.A. Ketchum, Z. Lai, Y. Lei, Z. Li, J. Li, Y. Liang, X. Lin, F. Lu, G.V. Merkulov, N. Milshina, H.M. Moore, A.K. Naik, V.A. Narayan, B. Neelam, D. Nusskern, D.B. Rusch, S. Salzberg, W. Shao, B. Shue, J. Sun, Z. Wang, A. Wang, X. Wang, J. Wang, M. Wei, R. Wides, C. Xiao, C. Yan, A. Yao, J. Ye, M. Zhan, W. Zhang, H. Zhang, Q. Zhao, L. Zheng, F. Zhong, W. Zhong, S. Zhu, S. Zhao, D. Gilbert, S. Baumhueter, G. Spier, C. Carter, A. Cravchik, T. Woodage, F. Ali, H. An, A. Awe, D. Baldwin, H. Baden, M. Barnstead, I. Barrow, K. Beeson, D. Busam, A. Carver, A. Center, M.L. Cheng, L. Curry, S. Danaher, L. Davenport, R. Desilets, S. Dietz, K. Dodson, L. Doup, S. Ferriera, N. Garg, A. Gluecksmann, B. Hart, J. Haynes, C. Haynes, C. Heiner, S. Hladun, D. Hostin, J. Houck, T. Howland, C. Ibegwam, J. Johnson, F. Kalush, L. Kline, S. Koduru, A. Love, F. Mann, D. May, S. McCawley, T. McIntosh, I. McMullen, M. Moy, L. Moy, B. Murphy, K. Nelson, C. Pfannkoch, E. Pratts, V. Puri, H. Qureshi, M. Reardon, R. Rodriguez, Y.H. Rogers, D. Romblad, B. Ruhfel, R. Scott, C. Sitter, M. Smallwood, E. Stewart, R. Strong, E. Suh, R. Thomas, N.N. Tint, S. Tse, C. Vech, G. Wang, J. Wetter, S. Williams, M. Williams, S. Windsor, E. Winn-Deen, K. Wolfe, J. Zaveri, K. Zaveri, J.F. Abril, R. Guigo, M.J. Campbell, K.V. Sjolander, B. Karlak, A. Kejariwal, H. Mi, B. Lazareva, T. Hatton, A. Narechania, K. Diemer, A. Muruganujan, N. Guo, S. Sato, V. Bafna, S. Istrail, R. Lippert, R. Schwartz, B. Walenz, S. Yooseph, D. Allen, A. Basu, J. Baxendale, L. Blick, M. Caminha, J. Carnes-Stine, P. Caulk, Y.H. Chiang, M. Coyne, C. Dahlke, A. Mays, M. Dombroski, M. Donnelly, D. Ely, S. Esparham, C. Fosler, H. Gire, S. Glanowski, K. Glasser, A. Glodek, M. Gorokhov, K. Graham, B. Gropman, M. Harris, J. Heil, S. Henderson, J. Hoover, D. Jennings, C. Jordan, J. Jordan, J. Kasha, L. Kagan, C. Kraft, A. Levitsky, M. Lewis, X. Liu, J. Lopez, D. Ma, W. Majoros, J. McDaniel, S. Murphy, M. Newman, T. Nguyen, N. Nguyen, and M. Nodell The sequence of the human genome Science 291 2001 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
Smith, H.O.7
Yandell, M.8
Evans, C.A.9
Holt, R.A.10
Gocayne, J.D.11
Amanatides, P.12
Ballew, R.M.13
Huson, D.H.14
Wortman, J.R.15
Zhang, Q.16
Kodira, C.D.17
Zheng, X.H.18
Chen, L.19
Skupski, M.20
Subramanian, G.21
Thomas, P.D.22
Zhang, J.23
Gabor Miklos, G.L.24
Nelson, C.25
Broder, S.26
Clark, A.G.27
Nadeau, J.28
McKusick, V.A.29
Zinder, N.30
Levine, A.J.31
Roberts, R.J.32
Simon, M.33
Slayman, C.34
Hunkapiller, M.35
Bolanos, R.36
Delcher, A.37
Dew, I.38
Fasulo, D.39
Flanigan, M.40
Florea, L.41
Halpern, A.42
Hannenhalli, S.43
Kravitz, S.44
Levy, S.45
Mobarry, C.46
Reinert, K.47
Remington, K.48
Abu-Threideh, J.49
Beasley, E.50
Biddick, K.51
Bonazzi, V.52
Brandon, R.53
Cargill, M.54
Chandramouliswaran, I.55
Charlab, R.56
Chaturvedi, K.57
Deng, Z.58
Di, F.59
Dunn, V.P.60
Eilbeck, K.61
Evangelista, C.62
Gabrielian, A.E.63
Gan, W.64
Ge, W.65
Gong, F.66
Gu, Z.67
Guan, P.68
Heiman, T.J.69
Higgins, M.E.70
Ji, R.R.71
Ke, Z.72
Ketchum, K.A.73
Lai, Z.74
Lei, Y.75
Li, Z.76
Li, J.77
Liang, Y.78
Lin, X.79
Lu, F.80
Merkulov, G.V.81
Milshina, N.82
Moore, H.M.83
Naik, A.K.84
Narayan, V.A.85
Neelam, B.86
Nusskern, D.87
Rusch, D.B.88
Salzberg, S.89
Shao, W.90
Shue, B.91
Sun, J.92
Wang, Z.93
Wang, A.94
Wang, X.95
Wang, J.96
Wei, M.97
Wides, R.98
Xiao, C.99
more..
-
25
-
-
0036208832
-
Patterns of linkage disequilibrium in the human genome
-
K.G. Ardlie, L. Kruglyak, and M. Seielstad Patterns of linkage disequilibrium in the human genome Nat. Rev. Genet. 3 2002 299 309
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 299-309
-
-
Ardlie, K.G.1
Kruglyak, L.2
Seielstad, M.3
-
26
-
-
79959503826
-
The International HapMap Project
-
R.A. Gibbs, J.W. Belmont, P. Hardenbol, T.D. Willis, F. Yu, H. Yang, L.Y. Ch'ang, W. Huang, B. Liu, Y. Shen, P.K. Tam, L.C. Tsui, M.M. Waye, J.T. Wong, C. Zeng, Q. Zhang, M.S. Chee, L.M. Galver, S. Kruglyak, S.S. Murray, A.R. Oliphant, A. Montpetit, T.J. Hudson, F. Chagnon, V. Ferretti, M. Leboeuf, M.S. Phillips, A. Verner, P.Y. Kwok, S. Duan, D.L. Lind, R.D. Miller, J.P. Rice, N.L. Saccone, P. Taillon-Miller, M. Xiao, Y. Nakamura, A. Sekine, K. Sorimachi, T. Tanaka, Y. Tanaka, T. Tsunoda, E. Yoshino, D.R. Bentley, P. Deloukas, S. Hunt, D. Powell, D. Altshuler, S.B. Gabriel, H. Zhang, I. Matsuda, Y. Fukushima, D.R. Macer, E. Suda, C.N. Rotimi, C.A. Adebamowo, T. Aniagwu, P.A. Marshall, O. Matthew, C. Nkwodimmah, C.D. Royal, M.F. Leppert, M. Dixon, L.D. Stein, F. Cunningham, A. Kanani, G.A. Thorisson, A. Chakravarti, P.E. Chen, D.J. Cutler, C.S. Kashuk, P. Donnelly, J. Marchini, G.A. McVean, S.R. Myers, L.R. Cardon, G.R. Abecasis, A. Morris, B.S. Weir, J.C. Mullikin, S.T. Sherry, M. Feolo, D. Altshuler, M.J. Daly, S.F. Schaffner, R. Qiu, A. Kent, G.M. Dunston, K. Kato, N. Niikawa, B.M. Knoppers, M.W. Foster, E.W. Clayton, V.O. Wang, J. Watkin, R.A. Gibbs, J.W. Belmont, E. Sodergren, G.M. Weinstock, R.K. Wilson, L.L. Fulton, J. Rogers, B.W. Birren, H. Han, H. Wang, M. Godbout, J.C. Wallenburg, P. L'Archeveque, G. Bellemare, K. Todani, T. Fujita, S. Tanaka, A.L. Holden, E.H. Lai, F.S. Collins, L.D. Brooks, J.E. McEwen, M.S. Guyer, E. Jordan, J.L. Peterson, J. Spiegel, L.M. Sung, L.F. Zacharia, K. Kennedy, M.G. Dunn, R. Seabrook, M. Shillito, B. Skene, J.G. Stewart, D.L. Valle, L.B. Jorde, J.W. Belmont, A. Chakravarti, M.K. Cho, T. Duster, M.W. Foster, M. Jasperse, B.M. Knoppers, P.Y. Kwok, J. Licinio, J.C. Long, P.A. Marshall, P.N. Ossorio, V.O. Wang, C.N. Rotimi, C.D. Royal, P. Spallone, S.F. Terry, E.S. Lander, E.H. Lai, D.A. Nickerson, D. Altshuler, D.R. Bentley, M. Boehnke, L.R. Cardon, M.J. Daly, P. Deloukas, J.A. Douglas, S.B. Gabriel, R.R. Hudson, T.J. Hudson, L. Kruglyak, P.Y. Kwok, Y. Nakamura, R.L. Nussbaum, C.D. Royal, S.F. Schaffner, S.T. Sherry, L.D. Stein, and T. Tanaka The International HapMap Project Nature 426 2003 789 796
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
Gibbs, R.A.1
Belmont, J.W.2
Hardenbol, P.3
Willis, T.D.4
Yu, F.5
Yang, H.6
Ch'Ang, L.Y.7
Huang, W.8
Liu, B.9
Shen, Y.10
Tam, P.K.11
Tsui, L.C.12
Waye, M.M.13
Wong, J.T.14
Zeng, C.15
Zhang, Q.16
Chee, M.S.17
Galver, L.M.18
Kruglyak, S.19
Murray, S.S.20
Oliphant, A.R.21
Montpetit, A.22
Hudson, T.J.23
Chagnon, F.24
Ferretti, V.25
Leboeuf, M.26
Phillips, M.S.27
Verner, A.28
Kwok, P.Y.29
Duan, S.30
Lind, D.L.31
Miller, R.D.32
Rice, J.P.33
Saccone, N.L.34
Taillon-Miller, P.35
Xiao, M.36
Nakamura, Y.37
Sekine, A.38
Sorimachi, K.39
Tanaka, T.40
Tanaka, Y.41
Tsunoda, T.42
Yoshino, E.43
Bentley, D.R.44
Deloukas, P.45
Hunt, S.46
Powell, D.47
Altshuler, D.48
Gabriel, S.B.49
Zhang, H.50
Matsuda, I.51
Fukushima, Y.52
MacEr, D.R.53
Suda, E.54
Rotimi, C.N.55
Adebamowo, C.A.56
Aniagwu, T.57
Marshall, P.A.58
Matthew, O.59
Nkwodimmah, C.60
Royal, C.D.61
Leppert, M.F.62
Dixon, M.63
Stein, L.D.64
Cunningham, F.65
Kanani, A.66
Thorisson, G.A.67
Chakravarti, A.68
Chen, P.E.69
Cutler, D.J.70
Kashuk, C.S.71
Donnelly, P.72
Marchini, J.73
McVean, G.A.74
Myers, S.R.75
Cardon, L.R.76
Abecasis, G.R.77
Morris, A.78
Weir, B.S.79
Mullikin, J.C.80
Sherry, S.T.81
Feolo, M.82
Altshuler, D.83
Daly, M.J.84
Schaffner, S.F.85
Qiu, R.86
Kent, A.87
Dunston, G.M.88
Kato, K.89
Niikawa, N.90
Knoppers, B.M.91
Foster, M.W.92
Clayton, E.W.93
Wang, V.O.94
Watkin, J.95
Gibbs, R.A.96
Belmont, J.W.97
Sodergren, E.98
Weinstock, G.M.99
more..
-
27
-
-
0033927466
-
Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data
-
P.C. Sham, S.S. Cherny, S. Purcell, and J.K. Hewitt Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data Am. J. Hum. Genet. 66 2000 1616 1630
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1616-1630
-
-
Sham, P.C.1
Cherny, S.S.2
Purcell, S.3
Hewitt, J.K.4
-
29
-
-
0025008677
-
Linkage strategies for genetically complex traits. Part II: The power of affected relative pairs
-
N. Risch Linkage strategies for genetically complex traits. Part II: the power of affected relative pairs Am. J. Hum. Genet. 46 1990 229 241
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
30
-
-
11944263528
-
Onset of NIDDM occurs at least 4-7 yr before clinical diagnosis
-
M.I. Harris, R. Klein, T.A. Welborn, and M.W. Knuiman Onset of NIDDM occurs at least 4-7 yr before clinical diagnosis Diabetes Care 15 1992 815 819
-
(1992)
Diabetes Care
, vol.15
, pp. 815-819
-
-
Harris, M.I.1
Klein, R.2
Welborn, T.A.3
Knuiman, M.W.4
-
31
-
-
0033770421
-
Evidence for a gene influencing blood pressure on chromosome 17: Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study
-
D. Levy, A.L. DeStefano, M.G. Larson, C.J. O'Donnell, R.P. Lifton, H. Gavras, L.A. Cupples, and R.H. Myers Evidence for a gene influencing blood pressure on chromosome 17: genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study Hypertension 36 2000 477 483
-
(2000)
Hypertension
, vol.36
, pp. 477-483
-
-
Levy, D.1
Destefano, A.L.2
Larson, M.G.3
O'Donnell, C.J.4
Lifton, R.P.5
Gavras, H.6
Cupples, L.A.7
Myers, R.H.8
-
32
-
-
0035094764
-
Variation is the spice of life
-
L. Kruglyak, and D.A. Nickerson Variation is the spice of life Nat. Genet. 27 2001 234 236
-
(2001)
Nat. Genet.
, vol.27
, pp. 234-236
-
-
Kruglyak, L.1
Nickerson, D.A.2
-
33
-
-
0034924997
-
Positive and negative selection on the human genome
-
J.C. Fay, G.J. Wyckoff, and C.I. Wu Positive and negative selection on the human genome Genetics 158 2001 1227 1234
-
(2001)
Genetics
, vol.158
, pp. 1227-1234
-
-
Fay, J.C.1
Wyckoff, G.J.2
Wu, C.I.3
-
34
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
M. Cargill, D. Altshuler, J. Ireland, P. Sklar, K. Ardlie, N. Patil, N. Shaw, C.R. Lane, E.P. Lim, N. Kalyanaraman, J. Nemesh, L. Ziaugra, L. Friedland, A. Rolfe, J. Warrington, R. Lipshutz, G.Q. Daley, and E.S. Lander Characterization of single-nucleotide polymorphisms in coding regions of human genes Nat. Genet. 22 1999 231 238
-
(1999)
Nat. Genet.
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Shaw, N.7
Lane, C.R.8
Lim, E.P.9
Kalyanaraman, N.10
Nemesh, J.11
Ziaugra, L.12
Friedland, L.13
Rolfe, A.14
Warrington, J.15
Lipshutz, R.16
Daley, G.Q.17
Lander, E.S.18
-
35
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
D. Botstein, and N. Risch Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease Nat. Genet. 33 Suppl. 2003 228 237
-
(2003)
Nat. Genet.
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
36
-
-
0035261381
-
Genomic strategies to identify mammalian regulatory sequences
-
L.A. Pennacchio, and E.M. Rubin Genomic strategies to identify mammalian regulatory sequences Nat. Rev. Genet. 2 2001 100 109
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 100-109
-
-
Pennacchio, L.A.1
Rubin, E.M.2
-
37
-
-
0030444451
-
Human type 1 diabetes and the insulin gene: Principles of mapping polygenes
-
S.T. Bennett, and J.A. Todd Human type 1 diabetes and the insulin gene: principles of mapping polygenes Annu. Rev. Genet. 30 1996 343 370
-
(1996)
Annu. Rev. Genet.
, vol.30
, pp. 343-370
-
-
Bennett, S.T.1
Todd, J.A.2
-
38
-
-
0037648405
-
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
-
H. Ueda, J.M. Howson, L. Esposito, J. Heward, H. Snook, G. Chamberlain, D.B. Rainbow, K.M. Hunter, A.N. Smith, G. Di Genova, M.H. Herr, I. Dahlman, F. Payne, D. Smyth, C. Lowe, R.C. Twells, S. Howlett, B. Healy, S. Nutland, H.E. Rance, V. Everett, L.J. Smink, A.C. Lam, H.J. Cordell, N.M. Walker, C. Bordin, J. Hulme, C. Motzo, F. Cucca, J.F. Hess, M.L. Metzker, J. Rogers, S. Gregory, A. Allahabadia, R. Nithiyananthan, E. Tuomilehto-Wolf, J. Tuomilehto, P. Bingley, K.M. Gillespie, D.E. Undlien, K.S. Ronningen, C. Guja, C. Ionescu-Tirgoviste, D.A. Savage, A.P. Maxwell, D.J. Carson, C.C. Patterson, J.A. Franklyn, D.G. Clayton, L.B. Peterson, L.S. Wicker, J.A. Todd, and S.C. Gough Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease Nature 423 2003 506 511
-
(2003)
Nature
, vol.423
, pp. 506-511
-
-
Ueda, H.1
Howson, J.M.2
Esposito, L.3
Heward, J.4
Snook, H.5
Chamberlain, G.6
Rainbow, D.B.7
Hunter, K.M.8
Smith, A.N.9
Di Genova, G.10
Herr, M.H.11
Dahlman, I.12
Payne, F.13
Smyth, D.14
Lowe, C.15
Twells, R.C.16
Howlett, S.17
Healy, B.18
Nutland, S.19
Rance, H.E.20
Everett, V.21
Smink, L.J.22
Lam, A.C.23
Cordell, H.J.24
Walker, N.M.25
Bordin, C.26
Hulme, J.27
Motzo, C.28
Cucca, F.29
Hess, J.F.30
Metzker, M.L.31
Rogers, J.32
Gregory, S.33
Allahabadia, A.34
Nithiyananthan, R.35
Tuomilehto-Wolf, E.36
Tuomilehto, J.37
Bingley, P.38
Gillespie, K.M.39
Undlien, D.E.40
Ronningen, K.S.41
Guja, C.42
Ionescu-Tirgoviste, C.43
Savage, D.A.44
Maxwell, A.P.45
Carson, D.J.46
Patterson, C.C.47
Franklyn, J.A.48
Clayton, D.G.49
Peterson, L.B.50
Wicker, L.S.51
Todd, J.A.52
Gough, S.C.53
more..
-
39
-
-
0037221589
-
Association of neuregulin 1 with schizophrenia confirmed in a Scottish population
-
H. Stefansson, J. Sarginson, A. Kong, P. Yates, V. Steinthorsdottir, E. Gudfinnsson, S. Gunnarsdottir, N. Walker, H. Petursson, C. Crombie, A. Ingason, J.R. Gulcher, K. Stefansson, and D. St Clair Association of neuregulin 1 with schizophrenia confirmed in a Scottish population Am. J. Hum. Genet. 72 2003 83 87
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 83-87
-
-
Stefansson, H.1
Sarginson, J.2
Kong, A.3
Yates, P.4
Steinthorsdottir, V.5
Gudfinnsson, E.6
Gunnarsdottir, S.7
Walker, N.8
Petursson, H.9
Crombie, C.10
Ingason, A.11
Gulcher, J.R.12
Stefansson, K.13
St Clair, D.14
-
40
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
G.C. Johnson, L. Esposito, B.J. Barratt, A.N. Smith, J. Heward, G. Di Genova, H. Ueda, H.J. Cordell, I.A. Eaves, F. Dudbridge, R.C. Twells, F. Payne, W. Hughes, S. Nutland, H. Stevens, P. Carr, E. Tuomilehto-Wolf, J. Tuomilehto, S.C. Gough, D.G. Clayton, and J.A. Todd Haplotype tagging for the identification of common disease genes Nat. Genet. 29 2001 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
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.19
Clayton, D.G.20
Todd, J.A.21
more..
-
41
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
S.B. Gabriel, S.F. Schaffner, H. Nguyen, J.M. Moore, J. Roy, B. Blumenstiel, J. Higgins, M. DeFelice, A. Lochner, M. Faggart, S.N. Liu-Cordero, C. Rotimi, A. Adeyemo, R. Cooper, R. Ward, E.S. Lander, M.J. Daly, and D. Altshuler The structure of haplotype blocks in the human genome Science 296 2002 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
Higgins, J.7
Defelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
42
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
N. Patil, A.J. Berno, D.A. Hinds, W.A. Barrett, J.M. Doshi, C.R. Hacker, C.R. Kautzer, D.H. Lee, C. Marjoribanks, D.P. McDonough, B.T. Nguyen, M.C. Norris, J.B. Sheehan, N. Shen, D. Stern, R.P. Stokowski, D.J. Thomas, M.O. Trulson, K.R. Vyas, K.A. Frazer, S.P. Fodor, and D.R. Cox Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21 Science 294 2001 1719 1723
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
Kautzer, C.R.7
Lee, D.H.8
Marjoribanks, C.9
McDonough, D.P.10
Nguyen, B.T.11
Norris, M.C.12
Sheehan, J.B.13
Shen, N.14
Stern, D.15
Stokowski, R.P.16
Thomas, D.J.17
Trulson, M.O.18
Vyas, K.R.19
Frazer, K.A.20
Fodor, S.P.21
Cox, D.R.22
more..
-
43
-
-
12144286180
-
Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array
-
H. Matsuzaki, H. Loi, S. Dong, Y.Y. Tsai, J. Fang, J. Law, X. Di, W.M. Liu, G. Yang, G. Liu, J. Huang, G.C. Kennedy, T.B. Ryder, G.A. Marcus, P.S. Walsh, M.D. Shriver, J.M. Puck, K.W. Jones, and R. Mei Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array Genome Res. 14 2004 414 425
-
(2004)
Genome Res.
, vol.14
, pp. 414-425
-
-
Matsuzaki, H.1
Loi, H.2
Dong, S.3
Tsai, Y.Y.4
Fang, J.5
Law, J.6
Di, X.7
Liu, W.M.8
Yang, G.9
Liu, G.10
Huang, J.11
Kennedy, G.C.12
Ryder, T.B.13
Marcus, G.A.14
Walsh, P.S.15
Shriver, M.D.16
Puck, J.M.17
Jones, K.W.18
Mei, R.19
-
44
-
-
0034727107
-
An SNP map of the human genome generated by reduced representation shotgun sequencing
-
D. Altshuler, V.J. Pollara, C.R. Cowles, W.J. Van Etten, J. Baldwin, L. Linton, and E.S. Lander An SNP map of the human genome generated by reduced representation shotgun sequencing Nature 407 2000 513 516
-
(2000)
Nature
, vol.407
, pp. 513-516
-
-
Altshuler, D.1
Pollara, V.J.2
Cowles, C.R.3
Van Etten, W.J.4
Baldwin, J.5
Linton, L.6
Lander, E.S.7
-
45
-
-
0036775432
-
Once and again-issues surrounding replication in genetic association studies
-
J.N. Hirschhorn, and D. Altshuler Once and again-issues surrounding replication in genetic association studies J. Clin. Endocrinol. Metab. 87 2002 4438 4441
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 4438-4441
-
-
Hirschhorn, J.N.1
Altshuler, D.2
-
46
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
R.S. Spielman, R.E. McGinnis, and W.J. Ewens Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM) Am. J. Hum. Genet. 52 1993 506 516
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
47
-
-
0028944305
-
A note on the application of the transmission disequilibrium test when a parent is missing
-
D. Curtis, and P.C. Sham A note on the application of the transmission disequilibrium test when a parent is missing Am. J. Hum. Genet. 56 1995 811 812
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 811-812
-
-
Curtis, D.1
Sham, P.C.2
-
48
-
-
0029858544
-
The TDT and other family-based tests for linkage disequilibrium and association
-
R.S. Spielman, and W.J. Ewens The TDT and other family-based tests for linkage disequilibrium and association Am. J. Hum. Genet. 59 1996 983 989
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 983-989
-
-
Spielman, R.S.1
Ewens, W.J.2
-
49
-
-
0033910787
-
A test for linkage and association in general pedigrees: The pedigree disequilibrium test
-
E.R. Martin, S.A. Monks, L.L. Warren, and N.L. Kaplan A test for linkage and association in general pedigrees: the pedigree disequilibrium test Am. J. Hum. Genet. 67 2000 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
-
50
-
-
0037371453
-
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test
-
A.A. Mitchell, D.J. Cutler, and A. Chakravarti Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test Am. J. Hum. Genet. 72 2003 598 610
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 598-610
-
-
Mitchell, A.A.1
Cutler, D.J.2
Chakravarti, A.3
-
51
-
-
0031912715
-
A sibship test for linkage in the presence of association: The sib transmission/disequilibrium test
-
R.S. Spielman, and W.J. Ewens A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test Am. J. Hum. Genet. 62 1998 450 458
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 450-458
-
-
Spielman, R.S.1
Ewens, W.J.2
-
52
-
-
0031949273
-
Genetic association mapping based on discordant sib pairs: The discordant-alleles test
-
M. Boehnke, and C.D. Langefeld Genetic association mapping based on discordant sib pairs: the discordant-alleles test Am. J. Hum. Genet. 62 1998 950 961
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 950-961
-
-
Boehnke, M.1
Langefeld, C.D.2
-
53
-
-
0031028361
-
Transmission-disequilibrium tests for quantitative traits
-
D.B. Allison Transmission-disequilibrium tests for quantitative traits Am. J. Hum. Genet. 60 1997 676 690
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 676-690
-
-
Allison, D.B.1
-
54
-
-
0344033602
-
Detecting disease associations due to linkage disequilibrium using haplotype tags: A class of tests and the determinants of statistical power
-
J.M. Chapman, J.D. Cooper, J.A. Todd, and D.G. Clayton Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power Hum. Hered. 56 2003 18 31
-
(2003)
Hum. Hered.
, vol.56
, pp. 18-31
-
-
Chapman, J.M.1
Cooper, J.D.2
Todd, J.A.3
Clayton, D.G.4
-
55
-
-
0035257236
-
Association study designs for complex diseases
-
L.R. Cardon, and J.I. Bell Association study designs for complex diseases Nat. Rev. Genet. 2 2001 91 99
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 91-99
-
-
Cardon, L.R.1
Bell, J.I.2
-
56
-
-
0036255811
-
Opinion: Candidate-gene approaches for studying complex genetic traits. Practical considerations
-
H.K. Tabor, N.J. Risch, and R.M. Myers Opinion: candidate-gene approaches for studying complex genetic traits. Practical considerations Nat. Rev. Genet. 3 2002 391 397
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 391-397
-
-
Tabor, H.K.1
Risch, N.J.2
Myers, R.M.3
-
58
-
-
0030052609
-
Permutation tests for multiple loci affecting a quantitative character
-
R.W. Doerge, and G.A. Churchill Permutation tests for multiple loci affecting a quantitative character Genetics 142 1996 285 294
-
(1996)
Genetics
, vol.142
, pp. 285-294
-
-
Doerge, R.W.1
Churchill, G.A.2
-
59
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Y. Benjamini, and Y. Hochberg Controlling the false discovery rate: a practical and powerful approach to multiple testing J. R. Stat. Soc. 57 1995 289 300
-
(1995)
J. R. Stat. Soc.
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
60
-
-
4143076901
-
Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies
-
F. Dudbridge, and B.P. Koeleman Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies Am. J. Hum. Genet. 75 2004 424 435
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 424-435
-
-
Dudbridge, F.1
Koeleman, B.P.2
-
61
-
-
1642295096
-
Assessing the probability that a positive report is false: An approach for molecular epidemiology studies
-
S. Wacholder, S. Chanock, M. Garcia-Closas, L. El Ghormli, and N. Rothman Assessing the probability that a positive report is false: an approach for molecular epidemiology studies J. Natl. Cancer Inst. 96 2004 434 442
-
(2004)
J. Natl. Cancer Inst.
, vol.96
, pp. 434-442
-
-
Wacholder, S.1
Chanock, S.2
Garcia-Closas, M.3
El Ghormli, L.4
Rothman, N.5
-
62
-
-
0032530165
-
Tests and estimates of allelic association in complex inheritance
-
N.E. Morton, and A. Collins Tests and estimates of allelic association in complex inheritance Proc. Natl. Acad. Sci. U.S.A. 95 1998 11389 11393
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 11389-11393
-
-
Morton, N.E.1
Collins, A.2
-
63
-
-
0036071296
-
Testing for population subdivision and association in four case-control studies
-
K.G. Ardlie, K.L. Lunetta, and M. Seielstad Testing for population subdivision and association in four case-control studies Am. J. Hum. Genet. 71 2002 304 311
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 304-311
-
-
Ardlie, K.G.1
Lunetta, K.L.2
Seielstad, M.3
-
64
-
-
12144285594
-
Assessing the impact of population stratification on genetic association studies
-
M.L. Freedman, D. Reich, K.L. Penney, G.J. McDonald, A.A. Mignault, N. Patterson, S.B. Gabriel, E.J. Topol, J.W. Smoller, C.N. Pato, M.T. Pato, T.L. Petryshen, L.N. Kolonel, E.S. Lander, P. Sklar, B. Henderson, J.N. Hirschhorn, and D. Altshuler Assessing the impact of population stratification on genetic association studies Nat. Genet. 36 2004 388 393
-
(2004)
Nat. Genet.
, vol.36
, pp. 388-393
-
-
Freedman, M.L.1
Reich, D.2
Penney, K.L.3
McDonald, G.J.4
Mignault, A.A.5
Patterson, N.6
Gabriel, S.B.7
Topol, E.J.8
Smoller, J.W.9
Pato, C.N.10
Pato, M.T.11
Petryshen, T.L.12
Kolonel, L.N.13
Lander, E.S.14
Sklar, P.15
Henderson, B.16
Hirschhorn, J.N.17
Altshuler, D.18
-
65
-
-
2442585696
-
The effects of human population structure on large genetic association studies
-
J. Marchini, L.R. Cardon, M.S. Phillips, and P. Donnelly The effects of human population structure on large genetic association studies Nat. Genet. 36 2004 512 517
-
(2004)
Nat. Genet.
, vol.36
, pp. 512-517
-
-
Marchini, J.1
Cardon, L.R.2
Phillips, M.S.3
Donnelly, P.4
-
66
-
-
0032714352
-
Genomic control for association studies
-
B. Devlin, and K. Roeder Genomic control for association studies Biometrics 55 1999 997 1004
-
(1999)
Biometrics
, vol.55
, pp. 997-1004
-
-
Devlin, B.1
Roeder, K.2
-
67
-
-
0033358548
-
Use of unlinked genetic markers to detect population stratification in association studies
-
J.K. Pritchard, and N.A. Rosenberg Use of unlinked genetic markers to detect population stratification in association studies Am. J. Hum. Genet. 65 1999 220 228
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 220-228
-
-
Pritchard, J.K.1
Rosenberg, N.A.2
-
68
-
-
0035185344
-
Detecting association in a case-control study while correcting for population stratification
-
D.E. Reich, and D.B. Goldstein Detecting association in a case-control study while correcting for population stratification Genet. Epidemiol. 20 2001 4 16
-
(2001)
Genet. Epidemiol.
, vol.20
, pp. 4-16
-
-
Reich, D.E.1
Goldstein, D.B.2
-
72
-
-
0037195149
-
Dietary fat intake determines the effect of a common polymorphism in the hepatic lipase gene promoter on high-density lipoprotein metabolism: Evidence of a strong dose effect in this gene-nutrient interaction in the Framingham Study
-
J.M. Ordovas, D. Corella, S. Demissie, L.A. Cupples, P. Couture, O. Coltell, P.W. Wilson, E.J. Schaefer, and K.L. Tucker Dietary fat intake determines the effect of a common polymorphism in the hepatic lipase gene promoter on high-density lipoprotein metabolism: evidence of a strong dose effect in this gene-nutrient interaction in the Framingham Study Circulation 106 2002 2315 2321
-
(2002)
Circulation
, vol.106
, pp. 2315-2321
-
-
Ordovas, J.M.1
Corella, D.2
Demissie, S.3
Cupples, L.A.4
Couture, P.5
Coltell, O.6
Wilson, P.W.7
Schaefer, E.J.8
Tucker, K.L.9
-
73
-
-
0242410130
-
Dietary fat interacts with the -514C > T polymorphism in the hepatic lipase gene promoter on plasma lipid profiles in a multiethnic Asian population: The 1998 Singapore National Health Survey
-
E.S. Tai, D. Corella, M. Deurenberg-Yap, J. Cutter, S.K. Chew, C.E. Tan, and J.M. Ordovas Dietary fat interacts with the -514C > T polymorphism in the hepatic lipase gene promoter on plasma lipid profiles in a multiethnic Asian population: the 1998 Singapore National Health Survey J. Nutr. 133 2003 3399 3408
-
(2003)
J. Nutr.
, vol.133
, pp. 3399-3408
-
-
Tai, E.S.1
Corella, D.2
Deurenberg-Yap, M.3
Cutter, J.4
Chew, S.K.5
Tan, C.E.6
Ordovas, J.M.7
-
74
-
-
0345306138
-
Interaction between a peroxisome proliferator-activated receptor gamma gene polymorphism and dietary fat intake in relation to body mass
-
A. Memisoglu, F.B. Hu, S.E. Hankinson, J.E. Manson, V. De, I.W.C. Willett, and D.J. Hunter Interaction between a peroxisome proliferator-activated receptor gamma gene polymorphism and dietary fat intake in relation to body mass Hum. Mol. Genet. 12 2003 2923 2929
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2923-2929
-
-
Memisoglu, A.1
Hu, F.B.2
Hankinson, S.E.3
Manson, J.E.4
De, V.5
Willett, I.W.C.6
Hunter, D.J.7
-
75
-
-
0041630975
-
The PPAR-gamma P12A polymorphism modulates the relationship between dietary fat intake and components of the metabolic syndrome: Results from the Quebec Family Study
-
J. Robitaille, J.P. Despres, L. Perusse, and M.C. Vohl The PPAR-gamma P12A polymorphism modulates the relationship between dietary fat intake and components of the metabolic syndrome: results from the Quebec Family Study Clin. Genet. 63 2003 109 116
-
(2003)
Clin. Genet.
, vol.63
, pp. 109-116
-
-
Robitaille, J.1
Despres, J.P.2
Perusse, L.3
Vohl, M.C.4
-
76
-
-
0037383554
-
Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease
-
M.M. Mirza, S.A. Fisher, K. King, A.P. Cuthbert, J. Hampe, J. Sanderson, J. Mansfield, P. Donaldson, A.J. MacPherson, A. Forbes, S. Schreiber, C.M. Lewis, and C.G. Mathew Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease Am. J. Hum. Genet. 72 2003 1018 1022
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 1018-1022
-
-
Mirza, M.M.1
Fisher, S.A.2
King, K.3
Cuthbert, A.P.4
Hampe, J.5
Sanderson, J.6
Mansfield, J.7
Donaldson, P.8
MacPherson, A.J.9
Forbes, A.10
Schreiber, S.11
Lewis, C.M.12
Mathew, C.G.13
-
77
-
-
0142138025
-
Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease
-
K. Negoro, D.P. McGovern, Y. Kinouchi, S. Takahashi, N.J. Lench, T. Shimosegawa, A. Carey, L.R. Cardon, D.P. Jewell, and D.A. Van Heel Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease Gut 52 2003 541 546
-
(2003)
Gut
, vol.52
, pp. 541-546
-
-
Negoro, K.1
McGovern, D.P.2
Kinouchi, Y.3
Takahashi, S.4
Lench, N.J.5
Shimosegawa, T.6
Carey, A.7
Cardon, L.R.8
Jewell, D.P.9
Van Heel, D.A.10
-
78
-
-
0038389762
-
IBD5 is a general risk factor for inflammatory bowel disease: Replication of association with Crohn disease and identification of a novel association with ulcerative colitis
-
C. Giallourakis, M. Stoll, K. Miller, J. Hampe, E.S. Lander, M.J. Daly, S. Schreiber, and J.D. Rioux IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis Am. J. Hum. Genet. 73 2003 205 211
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 205-211
-
-
Giallourakis, C.1
Stoll, M.2
Miller, K.3
Hampe, J.4
Lander, E.S.5
Daly, M.J.6
Schreiber, S.7
Rioux, J.D.8
-
79
-
-
18444381172
-
CARD15 genetic variation in a Quebec population: Prevalence, genotype-phenotype relationship, and haplotype structure
-
S. Vermeire, G. Wild, K. Kocher, J. Cousineau, L. Dufresne, A. Bitton, D. Langelier, P. Pare, G. Lapointe, A. Cohen, M.J. Daly, and J.D. Rioux CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure Am. J. Hum. Genet. 71 2002 74 83
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 74-83
-
-
Vermeire, S.1
Wild, G.2
Kocher, K.3
Cousineau, J.4
Dufresne, L.5
Bitton, A.6
Langelier, D.7
Pare, P.8
Lapointe, G.9
Cohen, A.10
Daly, M.J.11
Rioux, J.D.12
-
80
-
-
0035897904
-
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
-
J. Hampe, A. Cuthbert, P.J. Croucher, M.M. Mirza, S. Mascheretti, S. Fisher, H. Frenzel, K. King, A. Hasselmeyer, A.J. MacPherson, S. Bridger, S. van Deventer, A. Forbes, S. Nikolaus, J.E. Lennard-Jones, U.R. Foelsch, M. Krawczak, C. Lewis, S. Schreiber, and C.G. Mathew Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations Lancet 357 2001 1925 1928
-
(2001)
Lancet
, vol.357
, pp. 1925-1928
-
-
Hampe, J.1
Cuthbert, A.2
Croucher, P.J.3
Mirza, M.M.4
Mascheretti, S.5
Fisher, S.6
Frenzel, H.7
King, K.8
Hasselmeyer, A.9
MacPherson, A.J.10
Bridger, S.11
Van Deventer, S.12
Forbes, A.13
Nikolaus, S.14
Lennard-Jones, J.E.15
Foelsch, U.R.16
Krawczak, M.17
Lewis, C.18
Schreiber, S.19
Mathew, C.G.20
more..
-
81
-
-
0038136125
-
CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population
-
J.A. Cavanaugh, K.E. Adams, E.J. Quak, M.E. Bryce, N.J. O'Callaghan, H.J. Rodgers, G.R. Magarry, W.J. Butler, J.A. Eaden, I.C. Roberts-Thomson, P. Pavli, S.R. Wilson, and D.F. Callen CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population Ann. Hum. Genet. 67 2003 35 41
-
(2003)
Ann. Hum. Genet.
, vol.67
, pp. 35-41
-
-
Cavanaugh, J.A.1
Adams, K.E.2
Quak, E.J.3
Bryce, M.E.4
O'Callaghan, N.J.5
Rodgers, H.J.6
Magarry, G.R.7
Butler, W.J.8
Eaden, J.A.9
Roberts-Thomson, I.C.10
Pavli, P.11
Wilson, S.R.12
Callen, D.F.13
-
82
-
-
2342561802
-
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region
-
J.C. Florez, N. Burtt, P.I. de Bakker, P. Almgren, T. Tuomi, J. Holmkvist, D. Gaudet, T.J. Hudson, S.F. Schaffner, M.J. Daly, J.N. Hirschhorn, L. Groop, and D. Altshuler Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region Diabetes 53 2004 1360 1368
-
(2004)
Diabetes
, vol.53
, pp. 1360-1368
-
-
Florez, J.C.1
Burtt, N.2
De Bakker, P.I.3
Almgren, P.4
Tuomi, T.5
Holmkvist, J.6
Gaudet, D.7
Hudson, T.J.8
Schaffner, S.F.9
Daly, M.J.10
Hirschhorn, J.N.11
Groop, L.12
Altshuler, D.13
-
83
-
-
0037250168
-
The UCSC genome browser database
-
D. Karolchik, R. Baertsch, M. Diekhans, T.S. Furey, A. Hinrichs, Y.T. Lu, K.M. Roskin, M. Schwartz, C.W. Sugnet, D.J. Thomas, R.J. Weber, D. Haussler, and W.J. Kent The UCSC genome browser database Nucleic Acids Res. 31 2003 51 54
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 51-54
-
-
Karolchik, D.1
Baertsch, R.2
Diekhans, M.3
Furey, T.S.4
Hinrichs, A.5
Lu, Y.T.6
Roskin, K.M.7
Schwartz, M.8
Sugnet, C.W.9
Thomas, D.J.10
Weber, R.J.11
Haussler, D.12
Kent, W.J.13
-
84
-
-
0036079158
-
The human genome browser at UCSC
-
W.J. Kent, C.W. Sugnet, T.S. Furey, K.M. Roskin, T.H. Pringle, A.M. Zahler, and D. Haussler The human genome browser at UCSC Genome Res. 12 2002 996 1006
-
(2002)
Genome Res.
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
Zahler, A.M.6
Haussler, D.7
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