-
1
-
-
79953174333
-
Genomics and drug response
-
Wang, L., McLeod, H.L. and Weinshilboum, R.M. (2011) Genomics and drug response. N. Engl. J. Med., 364, 1144-1153.
-
(2011)
N. Engl. J. Med.
, vol.364
, pp. 1144-1153
-
-
Wang, L.1
McLeod, H.L.2
Weinshilboum, R.M.3
-
2
-
-
84863541347
-
Anabundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
-
10.1126/science.1217876
-
Nelson, M.R., Wegmann, D., Ehm, M.G., Kessner, D., St Jean, P., Verzilli, C., Shen, J., Tang, Z., Bacanu, S.-A., Fraser, D. et al. (2012) Anabundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science. 10.1126/science.1217876.
-
(2012)
Science
-
-
Nelson, M.R.1
Wegmann, D.2
Ehm, M.G.3
Kessner, D.4
St Jean, P.5
Verzilli, C.6
Shen, J.7
Tang, Z.8
Bacanu, S.-A.9
Fraser, D.10
-
3
-
-
0033569516
-
Pharmacogenomics: translating functional genomics into rational therapeutics
-
Evans, W.E. and Relling, M.V. (1999) Pharmacogenomics: translating functional genomics into rational therapeutics. Science, 286, 487-491.
-
(1999)
Science
, vol.286
, pp. 487-491
-
-
Evans, W.E.1
Relling, M.V.2
-
4
-
-
0842312531
-
Comparison of cytochrome P450 (CYP) genes from the mouse and humangenomes, including nomenclature recommendations forgenes, pseudogenes and alternative-splice variants
-
Nelson, D.R., Zeldin, D.C., Hoffman, S.M.G., Maltais, L.J., Wain, H.M. and Nebert, D.W. (2004) Comparison of cytochrome P450 (CYP) genes from the mouse and humangenomes, including nomenclature recommendations forgenes, pseudogenes and alternative-splice variants. Pharmacogenetics, 14, 1-18.
-
(2004)
Pharmacogenetics
, vol.14
, pp. 1-18
-
-
Nelson, D.R.1
Zeldin, D.C.2
Hoffman, S.M.G.3
Maltais, L.J.4
Wain, H.M.5
Nebert, D.W.6
-
5
-
-
78049433100
-
Effects of CYP2C19 genotype on outcomes of clopidogrel treatment
-
Paré, G., Mehta, S.R., Yusuf, S., Anand, S.S., Connolly, S.J., Hirsh, J., Simonsen, K., Bhatt, D.L., Fox, K.A.A. and Eikelboom, J.W. (2010) Effects of CYP2C19 genotype on outcomes of clopidogrel treatment. N. Engl. J. Med., 363, 1704-1714.
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 1704-1714
-
-
Paré, G.1
Mehta, S.R.2
Yusuf, S.3
Anand, S.S.4
Connolly, S.J.5
Hirsh, J.6
Simonsen, K.7
Bhatt, D.L.8
Fox, K.A.A.9
Eikelboom, J.W.10
-
6
-
-
60849097257
-
Estimation of the warfarin dose with clinical and pharmacogenetic data
-
International Warfarin Pharmacogenetics ConsortiumKlein, T.E., Altman, R.B., Eriksson, N., Gage, B.F., Kimmel, S.E., Lee, M.-T.M., Limdi, N.A., Page, D., Roden, D.M. et al. (2009) Estimation of the warfarin dose with clinical and pharmacogenetic data. N. Engl. J. Med., 360, 753-764.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 753-764
-
-
International Warfarin Pharmacogenetics ConsortiumKlein, T.E.1
Altman, R.B.2
Eriksson, N.3
Gage, B.F.4
Kimmel, S.E.5
Lee, M.-T.M.6
Limdi, N.A.7
Page, D.8
Roden, D.M.9
-
7
-
-
48949105694
-
An analysis of the relative effects of VKORC1 and CYP2C9 variants on anticoagulation related outcomes in warfarin-treated patients
-
Meckley, L.M., Wittkowsky, A.K., Rieder, M.J., Rettie, A.E. and Veenstra, D.L. (2008) An analysis of the relative effects of VKORC1 and CYP2C9 variants on anticoagulation related outcomes in warfarin-treated patients. Thromb. Haemost., 100, 229-239.
-
(2008)
Thromb. Haemost.
, vol.100
, pp. 229-239
-
-
Meckley, L.M.1
Wittkowsky, A.K.2
Rieder, M.J.3
Rettie, A.E.4
Veenstra, D.L.5
-
8
-
-
84872143942
-
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
-
10.1038/nature11690
-
Fu, W., O'Connor, T.D., Jun, G., Kang, H.M., Abecasis, G., Leal, S.M., Gabriel, S., Altshuler, D., Shendure, J., Nickerson, D.A. et al. (2012) Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature. 10.1038/nature11690.
-
(2012)
Nature
-
-
Fu, W.1
O'Connor, T.D.2
Jun, G.3
Kang, H.M.4
Abecasis, G.5
Leal, S.M.6
Gabriel, S.7
Altshuler, D.8
Shendure, J.9
Nickerson, D.A.10
-
9
-
-
79953715693
-
Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel
-
González-Pérez, A. and López-Bigas, N. (2011) Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel. Am. J. Hum. Genet., 88, 440-449.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 440-449
-
-
González-Pérez, A.1
López-Bigas, N.2
-
10
-
-
22244452677
-
Distribution and intensity of constraint in mammalian genomic sequence
-
NISC Comparative Sequencing Program
-
Cooper, G.M., Stone, E.A. and Asimenos, G. NISC Comparative Sequencing Program, Green, E.D., Batzoglou, S. and Sidow, A. (2005) Distribution and intensity of constraint in mammalian genomic sequence. Genome Res., 15, 901-913.
-
(2005)
Genome Res.
, vol.15
, pp. 901-913
-
-
Cooper, G.M.1
Stone, E.A.2
Asimenos, G.3
Green, E.D.4
Batzoglou, S.5
Sidow, A.6
-
11
-
-
77951651879
-
Single-nucleotide evolutionary constraint scores highlight disease-causing mutations
-
Cooper, G.M., Goode, D.L., Ng, S.B., Sidow, A., Bamshad, M.J., Shendure, J. and Nickerson, D.A. (2010) Single-nucleotide evolutionary constraint scores highlight disease-causing mutations. Nat. Methods, 7, 250-251.
-
(2010)
Nat. Methods
, vol.7
, pp. 250-251
-
-
Cooper, G.M.1
Goode, D.L.2
Ng, S.B.3
Sidow, A.4
Bamshad, M.J.5
Shendure, J.6
Nickerson, D.A.7
-
12
-
-
0016197604
-
Amino acid difference formula to help explain protein evolution
-
Grantham, R. (1974) Amino acid difference formula to help explain protein evolution. Science, 185, 862-864.
-
(1974)
Science
, vol.185
, pp. 862-864
-
-
Grantham, R.1
-
13
-
-
83155192795
-
The population pharmacokinetics of R- and S-warfarin: effect of genetic and clinical factors
-
Lane, S., Al-Zubiedi, S., Hatch, E., Matthews, I., Jorgensen, A.L., Deloukas, P., Daly, A.K., Park, B.K., Aarons, L., Ogungbenro, K. et al. (2012) The population pharmacokinetics of R- and S-warfarin: effect of genetic and clinical factors. Br. J. Clin. Pharmacol., 73, 66-76.
-
(2012)
Br. J. Clin. Pharmacol.
, vol.73
, pp. 66-76
-
-
Lane, S.1
Al-Zubiedi, S.2
Hatch, E.3
Matthews, I.4
Jorgensen, A.L.5
Deloukas, P.6
Daly, A.K.7
Park, B.K.8
Aarons, L.9
Ogungbenro, K.10
-
14
-
-
1842428730
-
Differential roles of Arg97, Asp293, and Arg108 in enzyme stability and substrate specificity of CYP2C9
-
Dickmann, L.J., Locuson, C.W., Jones, J.P. and Rettie, A.E. (2004) Differential roles of Arg97, Asp293, and Arg108 in enzyme stability and substrate specificity of CYP2C9. Mol. Pharmacol., 65, 842-850.
-
(2004)
Mol. Pharmacol.
, vol.65
, pp. 842-850
-
-
Dickmann, L.J.1
Locuson, C.W.2
Jones, J.P.3
Rettie, A.E.4
-
15
-
-
0042265520
-
Crystal structure of human cytochrome P450 2C9 with bound warfarin
-
Williams, P.A., Cosme, J., Ward, A., Angove, H.C., Matak Vinković, D. and Jhoti, H. (2003) Crystal structure of human cytochrome P450 2C9 with bound warfarin. Nature, 424, 464-468.
-
(2003)
Nature
, vol.424
, pp. 464-468
-
-
Williams, P.A.1
Cosme, J.2
Ward, A.3
Angove, H.C.4
Matak Vinković, D.5
Jhoti, H.6
-
16
-
-
1842484814
-
Assessment of arginine 97 and lysine 72 as determinants of substrate specificity in cytochrome P450 2C9 (CYP2C9)
-
Davies, C., Witham, K., Scott, J.R., Pearson, A., DeVoss, J.J., Graham, S.E. and Gillam, E.M.J. (2004) Assessment of arginine 97 and lysine 72 as determinants of substrate specificity in cytochrome P450 2C9 (CYP2C9). Drug Metab. Dispos., 32, 431-436.
-
(2004)
Drug Metab. Dispos.
, vol.32
, pp. 431-436
-
-
Davies, C.1
Witham, K.2
Scott, J.R.3
Pearson, A.4
DeVoss, J.J.5
Graham, S.E.6
Gillam, E.M.J.7
-
17
-
-
79960613122
-
Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450-2C19 (CYP2C19) genotype and clopidogrel therapy
-
Clinical Pharmacogenetics Implementation Consortium
-
Scott, S.A., Sangkuhl, K., Gardner, E.E., Stein, C.M., Hulot, J.S., Johnson, J.A., Roden, D.M., Klein, T.E. and Shuldiner, A.R. Clinical Pharmacogenetics Implementation Consortium. (2011) Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450-2C19 (CYP2C19) genotype and clopidogrel therapy. Clin. Pharmacol. Ther., 90, 328-332.
-
(2011)
Clin. Pharmacol. Ther.
, vol.90
, pp. 328-332
-
-
Scott, S.A.1
Sangkuhl, K.2
Gardner, E.E.3
Stein, C.M.4
Hulot, J.S.5
Johnson, J.A.6
Roden, D.M.7
Klein, T.E.8
Shuldiner, A.R.9
-
18
-
-
33749008249
-
The pharmocogenomics of warfarin: closing in on personalized medicine
-
Rettie, A.E. and Tai, G. (2006) The pharmocogenomics of warfarin: closing in on personalized medicine. Mol. Interv., 6, 223-227.
-
(2006)
Mol. Interv.
, vol.6
, pp. 223-227
-
-
Rettie, A.E.1
Tai, G.2
-
19
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
Tennessen, J.A., Bigham, A.W., O'Connor, T.D., Fu, W., Kenny, E.E., Gravel, S., McGee, S., Do, R., Liu, X., Jun, G. et al. (2012) Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science, 337, 64-69.
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
Bigham, A.W.2
O'Connor, T.D.3
Fu, W.4
Kenny, E.E.5
Gravel, S.6
McGee, S.7
Do, R.8
Liu, X.9
Jun, G.10
-
20
-
-
80052825195
-
The functional spectrum of low-frequency coding variation
-
Marth, G.T., Yu, F., Indap, A.R., Garimella, K., Gravel, S., Leong, W.F., Tyler-Smith, C., Bainbridge, M., Blackwell, T., Zheng-Bradley, X. et al. (2011) The functional spectrum of low-frequency coding variation. Genome Biol., 12, R84.
-
(2011)
Genome Biol.
, vol.12
-
-
Marth, G.T.1
Yu, F.2
Indap, A.R.3
Garimella, K.4
Gravel, S.5
Leong, W.F.6
Tyler-Smith, C.7
Bainbridge, M.8
Blackwell, T.9
Zheng-Bradley, X.10
-
21
-
-
84855316334
-
Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition
-
doi: 10.1101/gr.129668.111
-
Ramsey, L.B., Bruun, G.H., Yang, W., Trevino, L.R., Vattathil, S., Scheet, P., Cheng, C., Rosner, G.L., Giacomini, K.M., Fan, Y. et al. (2012) Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition. Genome. Res., 22, 1-8. doi: 10.1101/gr.129668.111.
-
(2012)
Genome. Res.
, vol.22
, pp. 1-8
-
-
Ramsey, L.B.1
Bruun, G.H.2
Yang, W.3
Trevino, L.R.4
Vattathil, S.5
Scheet, P.6
Cheng, C.7
Rosner, G.L.8
Giacomini, K.M.9
Fan, Y.10
-
22
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M. et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res., 20, 1297-1303.
-
(2010)
Genome Res.
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
Garimella, K.7
Altshuler, D.8
Gabriel, S.9
Daly, M.10
|