(Q35763328)

10 August 2017

1 reference

title

Overview of the development of personalized genomic medicine and surgery (English)

1 reference

10 August 2017

4

John Nemunaitis

1 reference

10 August 2017

2

Richard A Gibbs

1 reference

10 August 2017

F Charles Brunicardi

1

1 reference

10 August 2017

David A Wheeler

3

1 reference

10 August 2017

William Fisher

5

1 reference

10 August 2017

John Goss

6

1 reference

10 August 2017

Changyi Chen

7

1 reference

10 August 2017

language of work or name

1 reference

1 August 2011

1 reference

10 August 2017

published in

World Journal of Surgery

1 reference

10 August 2017

volume

35

1 reference

10 August 2017

issue

8

1 reference

10 August 2017

page(s)

1693-1699

1 reference

https://scigraph.springernature.com/pub.10.1007/s00268-011-1056-0

10 August 2017

exact match

0 references

cites work

Pharmacogenetics of endocrine therapy for breast cancer

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Integrating common and rare genetic variation in diverse human populations

2 October 2017

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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

2 October 2017

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Has the revolution arrived?

2 October 2017

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Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

2 October 2017

1 reference

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Genomic and personalized medicine: foundations and applications

2 October 2017

1 reference

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Parental history of Alzheimer disease associated with lower plasma apolipoprotein E levels

2 October 2017

1 reference

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Copy number variation in human health, disease, and evolution

2 October 2017

1 reference

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The HER-2 receptor and breast cancer: ten years of targeted anti-HER-2 therapy and personalized medicine

2 October 2017

1 reference

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Developing a tissue resource to characterize the genome of pancreatic cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Clinical implications of CYP2D6 genotyping in tamoxifen treatment for breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Basic principles and technologies for deciphering the genetic map of cancer.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

HIV pathogenesis: 25 years of progress and persistent challenges

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Emerging biomarkers and new understanding of traditional markers in personalized therapy for breast cancer

2 October 2017

1 reference

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Translation of the Philadelphia chromosome into therapy for CML.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Chronic myeloid leukaemia: the evolution of gene-targeted therapy

2 October 2017

1 reference

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A HapMap harvest of insights into the genetics of common disease

2 October 2017

1 reference

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Mapping and sequencing of structural variation from eight human genomes

2 October 2017

1 reference

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The complete genome of an individual by massively parallel DNA sequencing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

A second generation human haplotype map of over 3.1 million SNPs

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Individualized preventive and therapeutic management of hereditary breast ovarian cancer syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

The diploid genome sequence of an individual human

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

VKORC1: molecular target of coumarins

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Access denied? The status of co-receptor inhibition to counter HIV entry

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Anticipating the 1,000 dollar genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Global variation in copy number in the human genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Copy number variation: new insights in genome diversity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Applications of AmpliChip CYP450.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Prevention and management of hereditary breast cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Finishing the euchromatic sequence of the human genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Detection of large-scale variation in the human genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Large-scale copy number polymorphism in the human genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

The International HapMap Project

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Clinical relevance of genetic polymorphisms in the human CYP2C9 gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Cancer susceptibility and the functions of BRCA1 and BRCA2

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Genotype and phenotype in Alzheimer's disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Initial sequencing and analysis of the human genome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Regulatory region single nucleotide polymorphisms of the apolipoprotein E gene and the rate of cognitive decline in Alzheimer's disease.

12 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00268-011-1056-0

FDA holds court on post hoc data linking KRAS status to drug response

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00268-011-1056-0

Biomarkers Predict p53 Gene Therapy Efficacy in Recurrent Squamous Cell Carcinoma of the Head and Neck

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00268-011-1056-0

The genomics and Personalized Medicine Act of 2006.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3281749

Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing

25 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00268-011-1056-0

NCCN clinical practice guidelines in oncology: chronic myelogenous leukemia

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21424870

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Overview of the Molecular Surgeon Symposium on Personalized Genomic Medicine and Surgery

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21424870

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical application of pharmacogenetics

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21424870

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00268-011-1056-0

1 reference

10 August 2017

1 reference

10 August 2017

1 reference