-
1
-
-
84981272252
-
Comprehensive audiometric analysis of hearing impairment and tinnitus after cisplatin-based chemotherapy in survivors of adult-onset cancer
-
Frisina RD, Wheeler HE, Fossa SD, Kerns SL, Fung C, Sesso HD, et al. Comprehensive audiometric analysis of hearing impairment and tinnitus after cisplatin-based chemotherapy in survivors of adult-onset cancer. J Clin Oncol 2016;34:2712–20.
-
(2016)
J Clin Oncol
, vol.34
, pp. 2712-2720
-
-
Frisina, R.D.1
Wheeler, H.E.2
Fossa, S.D.3
Kerns, S.L.4
Fung, C.5
Sesso, H.D.6
-
3
-
-
77955459338
-
Testicular cancer survivorship: Research strategies and recommendations
-
Travis LB, Beard C, Allan JM, Dahl AA, Feldman DR, Oldenburg J, et al. Testicular cancer survivorship: research strategies and recommendations. J Natl Cancer Inst 2010;102:1114–30.
-
(2010)
J Natl Cancer Inst
, vol.102
, pp. 1114-1130
-
-
Travis, L.B.1
Beard, C.2
Allan, J.M.3
Dahl, A.A.4
Feldman, D.R.5
Oldenburg, J.6
-
4
-
-
0642343286
-
Negative consequences of uncorrected hearing loss - A review
-
Arlinger S.Negative consequences of uncorrected hearing loss - a review. Int J Audiol 2003;42:S17–20.
-
(2003)
Int J Audiol
, vol.42
, pp. S17-S20
-
-
Arlinger, S.1
-
5
-
-
84905185084
-
Chemotherapy-induced peripheral neurotoxicity and ototoxicity: New paradigms for translational genomics
-
Travis LB, Fossa SD, Sesso HD, Frisina RD, Herrmann DN, Beard CJ, et al. Chemotherapy-induced peripheral neurotoxicity and ototoxicity: new paradigms for translational genomics. J Natl Cancer Inst 2014;106:dju044.
-
(2014)
J Natl Cancer Inst
, vol.106
-
-
Travis, L.B.1
Fossa, S.D.2
Sesso, H.D.3
Frisina, R.D.4
Herrmann, D.N.5
Beard, C.J.6
-
6
-
-
70649113052
-
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy
-
Ross CJD, Katzov-Eckert H, Dube M-P, Brooks B, Rassekh SR, Barhdadi A, et al. Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy. Nat Genet 2009;41:1345–9.
-
(2009)
Nat Genet
, vol.41
, pp. 1345-1349
-
-
Ross, C.J.D.1
Katzov-Eckert, H.2
Dube, M.-P.3
Brooks, B.4
Rassekh, S.R.5
Barhdadi, A.6
-
7
-
-
84926032229
-
Human OCT2 variant c.808g>t confers protection effect against cisplatin-induced ototoxicity
-
Lanvers-Kaminsky C, Sprowl JA, Malath I, Deuster D, Eveslage M, Schlatter E, et al. Human OCT2 variant c.808G>T confers protection effect against cisplatin-induced ototoxicity. Pharmacogenomics 2015;16:323–32.
-
(2015)
Pharmacogenomics
, vol.16
, pp. 323-332
-
-
Lanvers-Kaminsky, C.1
Sprowl, J.A.2
Malath, I.3
Deuster, D.4
Eveslage, M.5
Schlatter, E.6
-
8
-
-
84880753477
-
The role of inherited TPMT and COMT genetic variation in cisplatin-induced ototoxicity in children with cancer
-
Yang JJ, Lim JYS, Huang J, Bass J, Wu J, Wang C, et al. The role of inherited TPMT and COMT genetic variation in cisplatin-induced ototoxicity in children with cancer. Clin Pharmacol Ther 2013;94:252–9.
-
(2013)
Clin Pharmacol Ther
, vol.94
, pp. 252-259
-
-
Yang, J.J.1
Lim, J.Y.S.2
Huang, J.3
Bass, J.4
Wu, J.5
Wang, C.6
-
9
-
-
84880756433
-
Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children
-
Pussegoda K, Ross CJ, Visscher H, Yazdanpanah M, Brooks B, Rassekh SR, et al. Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children. Clin Pharmacol Ther 2013;94:243–51.
-
(2013)
Clin Pharmacol Ther
, vol.94
, pp. 243-251
-
-
Pussegoda, K.1
Ross, C.J.2
Visscher, H.3
Yazdanpanah, M.4
Brooks, B.5
Rassekh, S.R.6
-
10
-
-
84887857800
-
Challenges in interpreting the evidence for genetic predictors of ototoxicity
-
Ratain MJ, Cox NJ, Henderson TO. Challenges in interpreting the evidence for genetic predictors of ototoxicity. Clin Pharmacol Ther 2013;94:631–5.
-
(2013)
Clin Pharmacol Ther
, vol.94
, pp. 631-635
-
-
Ratain, M.J.1
Cox, N.J.2
Henderson, T.O.3
-
11
-
-
84894503830
-
Role of TPMT and COMT genetic variation in cisplatin-induced ototoxicity
-
Carleton BC, Ross CJ, Bhavsar AP, Amstutz U, Pussegoda K, Visscher H, et al. Role of TPMT and COMT genetic variation in cisplatin-induced ototoxicity. Clin Pharmacol Ther 2014;95:253–253.
-
(2014)
Clin Pharmacol Ther
, vol.95
, pp. 253-1253
-
-
Carleton, B.C.1
Ross, C.J.2
Bhavsar, A.P.3
Amstutz, U.4
Pussegoda, K.5
Visscher, H.6
-
12
-
-
85021764050
-
-
U.S. Food and Drug Administration. U.S. Food and Drug Administration (FDA) label information for cisplatin and TPMT [Internet]. [cited 2016 Jan 1]. Available from
-
U.S. Food and Drug Administration. U.S. Food and Drug Administration (FDA) label information for cisplatin and TPMT [Internet]. The Pharmacogenomics Knowlegebase [cited 2016 Jan 1]. Available from: https://www.pharmgkb.org/label/PA166104853.
-
The Pharmacogenomics Knowlegebase
-
-
-
13
-
-
84924066642
-
Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss
-
Xu H, Robinson GW, Huang J, Lim JY-S, Zhang H, Bass JK, et al. Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss. Nat Genet 2015;47:263–6.
-
(2015)
Nat Genet
, vol.47
, pp. 263-266
-
-
Xu, H.1
Robinson, G.W.2
Huang, J.3
Lim, J.Y.-S.4
Zhang, H.5
Bass, J.K.6
-
14
-
-
84959189240
-
Replication of a genetic variant in ACYP2 associated with cisplatin-induced hearing loss in patients with osteosarcoma
-
Vos HI, Guchelaar H-J, Gelderblom H, de Bont ESJM, Kremer LCM, Naber AM, et al. Replication of a genetic variant in ACYP2 associated with cisplatin-induced hearing loss in patients with osteosarcoma. Pharmaco-genet Genomics 2016;26:243–7.
-
(2016)
Pharmaco-genet Genomics
, vol.26
, pp. 243-247
-
-
Vos, H.I.1
Guchelaar, H.-J.2
Gelderblom, H.3
De Bont, E.S.J.M.4
Kremer, L.C.M.5
Naber, A.M.6
-
15
-
-
84930213392
-
Second-generation plink: Rising to the challenge of larger and richer datasets
-
Chang CC, Chow CC, Tellier LC, Vattikuti S, Purcell SM, Lee JJ. Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience 2015;4:1–16.
-
(2015)
Gigascience
, vol.4
, pp. 1-16
-
-
Chang, C.C.1
Chow, C.C.2
Tellier, L.C.3
Vattikuti, S.4
Purcell, S.M.5
Lee, J.J.6
-
17
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet 2012;44:955–9.
-
(2012)
Nat Genet
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
19
-
-
77956586071
-
Locuszoom: Regional visualization of genome-wide association scan results
-
Pruim RJ, Welch RP, Sanna S, Teslovich TM, Chines PS, Gliedt TP, et al. LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 2010;26:2336–7.
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
Gliedt, T.P.6
-
20
-
-
84929001104
-
The genotype-tissue expression (GTEx) pilot analysis: Multitissue gene regulation in humans
-
Ardlie KG, Deluca DS, Segre A V., Sullivan TJ, Young TR, Gelfand ET, et al. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science 2015;348:648–60.
-
(2015)
Science
, vol.348
, pp. 648-660
-
-
Ardlie, K.G.1
Deluca, D.S.2
Segre, A.V.3
Sullivan, T.J.4
Young, T.R.5
Gelfand, E.T.6
-
21
-
-
84858779229
-
Haploreg: A resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
-
Ward LD, Kellis M. HaploReg: A resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res 2012;40:D930-4.
-
(2012)
Nucleic Acids Res
, vol.40
, pp. D930-D934
-
-
Ward, L.D.1
Kellis, M.2
-
23
-
-
59349118706
-
Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?
-
Hilgert N, Smith RJH, Van Camp G. Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics? Mutat Res 2009;681:189–96.
-
(2009)
Mutat Res
, vol.681
, pp. 189-196
-
-
Hilgert, N.1
Smith, R.J.H.2
Van Camp, G.3
-
25
-
-
84859169877
-
The cancer cell line encyclopedia enables predictive modelling of anticancer drug sensitivity
-
Barretina J, Caponigro G, Stransky N, Venkatesan K, Margolin AA, Kim S, et al. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature 2012;483:603–7.
-
(2012)
Nature
, vol.483
, pp. 603-607
-
-
Barretina, J.1
Caponigro, G.2
Stransky, N.3
Venkatesan, K.4
Margolin, A.A.5
Kim, S.6
-
26
-
-
84876563391
-
Genomics of drug sensitivity in cancer (GDSC): A resource for therapeutic biomarker discovery in cancer cells
-
Yang W, Soares J, Greninger P, Edelman EJ, Lightfoot H, Forbes S, et al. Genomics of drug sensitivity in cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells. Nucleic Acids Res 2013;41:D955–61.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. D955-D961
-
-
Yang, W.1
Soares, J.2
Greninger, P.3
Edelman, E.J.4
Lightfoot, H.5
Forbes, S.6
-
27
-
-
77955894071
-
Metal: Fast and efficient meta-analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 2010;26:2190–1.
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
28
-
-
84890107642
-
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
-
Denny JC, Bastarache L, Ritchie MD, Carroll RJ, Zink R, Mosley JD, et al. Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nat Bio-technol 2013;31:1102–11.
-
(2013)
Nat Bio-technol
, vol.31
, pp. 1102-1111
-
-
Denny, J.C.1
Bastarache, L.2
Ritchie, M.D.3
Carroll, R.J.4
Zink, R.5
Mosley, J.D.6
-
29
-
-
84940780615
-
A gene-based association method for mapping traits using reference transcriptome data
-
Gamazon ER, Wheeler HE, Shah KP, Mozaffari V, Aquino-Michaels K, Carroll RJ, et al. A gene-based association method for mapping traits using reference transcriptome data. Nat Genet 2015;47:1091–8.
-
(2015)
Nat Genet
, vol.47
, pp. 1091-1098
-
-
Gamazon, E.R.1
Wheeler, H.E.2
Shah, K.P.3
Mozaffari, V.4
Aquino-Michaels, K.5
Carroll, R.J.6
-
30
-
-
85021770181
-
-
ICD-9-CM Diagnosis Codes 389. Hearing loss [Internet]. ICD9Data. com. [cited Aug 20]
-
ICD-9-CM Diagnosis Codes 389. : Hearing loss [Internet]. ICD9Data. com. [cited 2016 Aug 20]. Available from: http://www.icd9data.com/2015/Volume1/320-389/380-389/389/default.htm.
-
(2016)
-
-
-
31
-
-
85000761545
-
Survey of the heritability and sparsity of gene expression traits across human tissues
-
Wheeler HE, Shah KP, Brenner J, Garcia T, Aquino-Michaels K, Cox NJ, et al. Survey of the heritability and sparsity of gene expression traits across human tissues. PLoS Genet 2016;12:e1006423.
-
(2016)
Plos Genet
, vol.12
, pp. e1006423
-
-
Wheeler, H.E.1
Shah, K.P.2
Brenner, J.3
Garcia, T.4
Aquino-Michaels, K.5
Cox, N.J.6
-
32
-
-
84874783818
-
Polygenic modeling with Bayesian sparse linear mixed models
-
Zhou X, Carbonetto P, Stephens M. Polygenic modeling with Bayesian sparse linear mixed models. PLoS Genet 2013;9:e1003264.
-
(2013)
Plos Genet
, vol.9
, pp. e1003264
-
-
Zhou, X.1
Carbonetto, P.2
Stephens, M.3
-
33
-
-
17344362695
-
A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (wolfram syndrome)
-
Inoue H, Tanizawa Y, Wasson J, Behn P, Kalidas K. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat Genet 1998;20:143–8.
-
(1998)
Nat Genet
, vol.20
, pp. 143-148
-
-
Inoue, H.1
Tanizawa, Y.2
Wasson, J.3
Behn, P.4
Kalidas, K.5
-
34
-
-
10744222064
-
Mutational spectrum of the wfs1 gene in wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease
-
Cryns K, Sivakumaran TA, Van den Ouweland JMW, Pennings RJE, Cremers CWRJ, Flothmann K, et al. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Hum Mutat 2003;22:275–87.
-
(2003)
Hum Mutat
, vol.22
, pp. 275-287
-
-
Cryns, K.1
Sivakumaran, T.A.2
Van Den Ouweland, J.M.W.3
Pennings, R.J.E.4
Cremers, C.W.R.J.5
Flothmann, K.6
-
35
-
-
0037361670
-
The WFS1 gene, responsible for low frequency sensorineural hearing loss and wolfram syndrome, is expressed in a variety of inner ear cells
-
Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, et al. The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochem Cell Biol 2003;119:247–56.
-
(2003)
Histochem Cell Biol
, vol.119
, pp. 247-256
-
-
Cryns, K.1
Thys, S.2
Van Laer, L.3
Oka, Y.4
Pfister, M.5
Van Nassauw, L.6
-
36
-
-
84859482968
-
A novel animal model of hearing loss caused by acute endoplasmic reticulum stress in the cochlea
-
Fujinami Y, Mutai H, Mizutari K, Nakagawa S, Matsunaga T. A novel animal model of hearing loss caused by acute endoplasmic reticulum stress in the cochlea. J Pharmacol Sci 2012;118:363–72.
-
(2012)
J Pharmacol Sci
, vol.118
, pp. 363-372
-
-
Fujinami, Y.1
Mutai, H.2
Mizutari, K.3
Nakagawa, S.4
Matsunaga, T.5
-
37
-
-
33947590154
-
Cisplatin-induced long-term hearing impairment is associated with specific gluta-thione S-transferase genotypes in testicular cancer survivors
-
Oldenburg J, Kraggerud SM, Cvancarova M, Lothe RA, Fossa SD. Cisplatin-induced long-term hearing impairment is associated with specific gluta-thione S-Transferase genotypes in testicular cancer survivors. J Clin Oncol 2007;25:708–14.
-
(2007)
J Clin Oncol
, vol.25
, pp. 708-714
-
-
Oldenburg, J.1
Kraggerud, S.M.2
Cvancarova, M.3
Lothe, R.A.4
Fossa, S.D.5
-
38
-
-
77954143522
-
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
-
Voight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet 2010;42:579–89.
-
(2010)
Nat Genet
, vol.42
, pp. 579-589
-
-
Voight, B.F.1
Scott, L.J.2
Steinthorsdottir, V.3
Morris, A.P.4
Dina, C.5
Welch, R.P.6
-
39
-
-
84943279302
-
Phenotype prediction of pathogenic nonsynonymous single nucleotide polymorphisms in WFS1
-
Qian X, Qin L, Xing G, Cao X. Phenotype prediction of pathogenic nonsynonymous single nucleotide polymorphisms in WFS1. Sci Rep 2015;5:14731.
-
(2015)
Sci Rep
, vol.5
, pp. 14731
-
-
Qian, X.1
Qin, L.2
Xing, G.3
Cao, X.4
-
40
-
-
84953390394
-
Wolfram syndrome: Diagnosis, management, and treatment
-
Urano F. Wolfram syndrome: diagnosis, management, and treatment. Curr Diab Rep 2016;16:1–8.
-
(2016)
Curr Diab Rep
, vol.16
, pp. 1-8
-
-
Urano, F.1
-
41
-
-
77949751415
-
Wolfram syndrome 1 gene negatively regulates er stress signaling in rodent and human cells
-
Fonseca S, Ishigaki S, Oslowski C. Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells. J Clin Invest 2010;120:744–55.
-
(2010)
J Clin Invest
, vol.120
, pp. 744-755
-
-
Fonseca, S.1
Ishigaki, S.2
Oslowski, C.3
-
42
-
-
0037646503
-
Cisplatin induces endoplasmic reticulum stress and nucleus-independent apoptotic signaling
-
Mandic A, Hansson J, Linder S, Shoshan MC. Cisplatin induces endoplasmic reticulum stress and nucleus-independent apoptotic signaling. J Biol Chem 2003;278:9100–6.
-
(2003)
J Biol Chem
, vol.278
, pp. 9100-9106
-
-
Mandic, A.1
Hansson, J.2
Linder, S.3
Shoshan, M.C.4
-
43
-
-
27744500069
-
Endoplasmic reticulum stress-associated caspase 12 mediates cisplatin-induced LLC-PK1 cell apoptosis
-
Liu H, Baliga R. Endoplasmic reticulum stress-associated caspase 12 mediates cisplatin-induced LLC-PK1 cell apoptosis. J Am Soc Nephrol 2005;16:1985–92.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 1985-1992
-
-
Liu, H.1
Baliga, R.2
-
44
-
-
84927104908
-
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment
-
Fransen E, Bonneux S, Corneveaux JJ, Schrauwen I, Di Berardino F, White CH, et al. Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. Eur J Hum Genet 2015;23:110–5.
-
(2015)
Eur J Hum Genet
, vol.23
, pp. 110-115
-
-
Fransen, E.1
Bonneux, S.2
Corneveaux, J.J.3
Schrauwen, I.4
Di Berardino, F.5
White, C.H.6
-
45
-
-
84866415102
-
A genome-wide association study identifies novel loci for paclitaxel-induced sensory peripheral neuropathy in CALGB 40101
-
Baldwin RM, Owzar K, Zembutsu H, Chhibber A, Kubo M, Jiang C, et al. A genome-wide association study identifies novel loci for paclitaxel-induced sensory peripheral neuropathy in CALGB 40101. Clin Cancer Res 2012;18:5099–109.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 5099-5109
-
-
Baldwin, R.M.1
Owzar, K.2
Zembutsu, H.3
Chhibber, A.4
Kubo, M.5
Jiang, C.6
-
46
-
-
84990942803
-
Pharma-cogenetic discovery in calgb (alliance) 90401 and mechanistic validation of a VAC14 polymorphism that increases risk of docetaxel-induced neuropathy
-
Hertz DL, Owzar K, Lessans S, Wing C, Jiang C, Kelly WK, et al. Pharma-cogenetic discovery in CALGB (Alliance) 90401 and mechanistic validation of a VAC14 polymorphism that increases risk of docetaxel-induced neuropathy. Clin Cancer Res 2016;22:4890–900.
-
(2016)
Clin Cancer Res
, vol.22
, pp. 4890-4900
-
-
Hertz, D.L.1
Owzar, K.2
Lessans, S.3
Wing, C.4
Jiang, C.5
Kelly, W.K.6
-
47
-
-
84989906570
-
Biallelic mutations of VAC14 in pediatric-onset neurological disease
-
Lenk GM, Szymanska K, Debska-Vielhaber G, Rydzanicz M, Walczak A, Bekiesinska-Figatowska M, et al. Biallelic mutations of VAC14 in pediatric-onset neurological disease. Am J Hum Genet 2016;99:188–94.
-
(2016)
Am J Hum Genet
, vol.99
, pp. 188-194
-
-
Lenk, G.M.1
Szymanska, K.2
Debska-Vielhaber, G.3
Rydzanicz, M.4
Walczak, A.5
Bekiesinska-Figatowska, M.6
-
48
-
-
84899071798
-
Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder
-
Hart AB, Gamazon ER, Engelhardt BE, Sklar P, Kahler AK, Hultman CM, et al. Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder. Proc Natl Acad Sci U S A 2014;111:5968–73.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, pp. 5968-5973
-
-
Hart, A.B.1
Gamazon, E.R.2
Engelhardt, B.E.3
Sklar, P.4
Kahler, A.K.5
Hultman, C.M.6
-
49
-
-
84871302357
-
Cancer phar-macogenomics: Strategies and challenges
-
Wheeler HE, Maitland ML, Dolan ME, Cox NJ, Ratain MJ. Cancer phar-macogenomics: strategies and challenges. Nat Rev Genet 2013;14:23–34.
-
(2013)
Nat Rev Genet
, vol.14
, pp. 23-34
-
-
Wheeler, H.E.1
Maitland, M.L.2
Dolan, M.E.3
Cox, N.J.4
Ratain, M.J.5
|