(Q33679969)

28 July 2017

title

Pharmacogenetics and personal genomes (English)

1 reference

28 July 2017

Michael J Wagner

1

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 2009

1 reference

28 July 2017

published in

Personalized Medicine

1 reference

28 July 2017

volume

6

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28 July 2017

issue

6

1 reference

28 July 2017

page(s)

643-652

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Targeted capture and massively parallel sequencing of 12 human exomes

28 July 2017

cites work

1 reference

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21 June 2018

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A highly annotated whole-genome sequence of a Korean individual

21 June 2018

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21 June 2018

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Managing and analyzing next-generation sequence data

21 June 2018

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HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin

21 June 2018

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21 June 2018

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21 June 2018

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A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose

21 June 2018

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Human genetic variation and its contribution to complex traits

21 June 2018

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Estimating the number of unseen variants in the human genome

21 June 2018

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Estimation of the warfarin dose with clinical and pharmacogenetic data

21 June 2018

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Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

21 June 2018

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Cytochrome p-450 polymorphisms and response to clopidogrel

21 June 2018

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Genetics of the Framingham Heart Study population

21 June 2018

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Genetic mapping in human disease

21 June 2018

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DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

21 June 2018

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The diploid genome sequence of an Asian individual

21 June 2018

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Accurate whole human genome sequencing using reversible terminator chemistry

21 June 2018

1 reference

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Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Genetic variation in an individual human exome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

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

21 June 2018

1 reference

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Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis

21 June 2018

1 reference

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Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Next-generation DNA sequencing methods

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study

21 June 2018

1 reference

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Common and rare variants in multifactorial susceptibility to common diseases

21 June 2018

1 reference

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The complete genome of an individual by massively parallel DNA sequencing

21 June 2018

1 reference

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

21 June 2018

1 reference

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CYP4F2 genetic variant alters required warfarin dose

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Genome-wide in situ exon capture for selective resequencing

21 June 2018

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

21 June 2018

1 reference

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Multiplex amplification of large sets of human exons

21 June 2018

1 reference

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Multigene amplification and massively parallel sequencing for cancer mutation discovery

21 June 2018

1 reference

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Multiplex assay for comprehensive genotyping of genes involved in drug metabolism, excretion, and transport

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

The genome-enabled electronic medical record

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

A haplotype map of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Direct genomic selection.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Whole-genome patterns of common DNA variation in three human populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Drug reactions enzymes, and biochemical genetics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

SIFT: Predicting amino acid changes that affect protein function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Pharmacogenomics--drug disposition, drug targets, and side effects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Human non-synonymous SNPs: server and survey

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

The structure of haplotype blocks in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Initial sequencing and analysis of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

The Sequence of the Human Genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

DNA sequencing with chain-terminating inhibitors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826717

Microarray-based genomic selection for high-throughput resequencing.

21 June 2018

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Cetuximab, chemotherapy and KRAS status in mCRC.

21 January 2018

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The Marshfield Clinic Personalized Medicine Research Project: 2008 scientific update and lessons learned in the first 6 years

21 January 2018

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Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

21 January 2018

1 reference

Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20190862

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

4th US FDA-Drug Information Association pharmacogenomics workshop, held 10-12 December, 2007

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20190862

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20190862

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2217/PME.09.55

1 reference

28 July 2017

1 reference

28 July 2017

1 reference