Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy (Q28264131)

3

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Bruce C Carleton

object named as

Bruce C Carleton

13

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Michael R. Hayden

object named as

Michael R Hayden

14

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Paul C Rogers

object named as

Paul C Rogers

11

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author name string

Colin J D Ross

1

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Hagit Katzov-Eckert

2

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Beth Brooks

4

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S Rod Rassekh

5

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Amina Barhdadi

6

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Yassamin Feroz-Zada

7

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Henk Visscher

8

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Andrew M K Brown

9

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Michael J Rieder

10

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Michael S Phillips

Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions

12

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language of work or name

English

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publication date

December 2009

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published in

Nature Genetics

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volume

41

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page(s)

1345-9

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issue

12

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cites work

1 reference

12 December 2020

S-Adenosyl-L-methionine increases serum BUN and creatinine in cisplatin-treated mice

1 reference

12 December 2020

A catechol-O-methyltransferase that is essential for auditory function in mice and humans

1 reference

12 December 2020

Genome-wide association studies for common diseases and complex traits

1 reference

12 December 2020

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

12 December 2020

Methylation of mercaptopurine, thioguanine, and their nucleotide metabolites by heterologously expressed human thiopurine S-methyltransferase

1 reference

12 December 2020

Children with minimal sensorineural hearing loss: prevalence, educational performance, and functional status.

1 reference

12 December 2020

Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity

1 reference

12 December 2020

A haplotype map of the human genome

1 reference

12 December 2020

Risk factors for ototoxicity due to cisplatin.

1 reference

12 December 2020

Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locus

1 reference

12 December 2020

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 reference

12 December 2020

Genetic basis for individual variations in pain perception and the development of a chronic pain condition

1 reference

12 December 2020

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

1 reference

12 December 2020

Ototoxicity from cisplatin therapy in childhood cancer.

1 reference

12 December 2020

Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

1 reference

12 December 2020

Ototoxicity from high-dose use of platinum compounds in patients with neuroblastoma.

1 reference

12 December 2020

SLCO1B1 variants and statin-induced myopathy--a genomewide study

1 reference

12 December 2020

Glutathione S-transferase genetic polymorphisms and individual sensitivity to the ototoxic effect of cisplatin.

1 reference

12 December 2020

Pharmacogenomics: catechol O-methyltransferase to thiopurine S-methyltransferase

1 reference

12 December 2020

Genotypic approaches to therapy in children: a national active surveillance network (GATC) to study the pharmacogenomics of severe adverse drug reactions in children.

1 reference

12 December 2020

Functional characterization of 23 allelic variants of thiopurine S-methyltransferase gene (TPMT*2 - *24).

1 reference

12 December 2020

Megalin genetic polymorphisms and individual sensitivity to the ototoxic effect of cisplatin.

1 reference

12 December 2020

Cisplatin-induced hearing loss: influence of the mode of drug administration in the guinea pig.

1 reference

12 December 2020

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

1 reference

12 December 2020

Performing the exact test of Hardy-Weinberg proportion for multiple alleles

1 reference

12 December 2020

Cisplatin-induced long-term hearing impairment is associated with specific glutathione s-transferase genotypes in testicular cancer survivors

1 reference

12 December 2020

Predicting cisplatin ototoxicity in children: the influence of age and the cumulative dose.

1 reference

12 December 2020

Effect of concurrent medications on cisplatin-induced nephrotoxicity in patients with head and neck cancer

1 reference

12 December 2020

Ototoxicity in children receiving platinum chemotherapy: underestimating a commonly occurring toxicity that may influence academic and social development

1 reference

12 December 2020

Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance

1 reference

12 December 2020

Application of principal component analysis to pharmacogenomic studies in Canada

1 reference

12 December 2020

Ototoxicity of cisplatinum

1 reference

12 December 2020

Functional analysis of a mutation in the SLCO1B1 gene (c.1628T>G) identified in a Japanese patient with pravastatin-induced myopathy

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.478

7 January 2021