Personalized medicine: new genomics, old lessons (Q35082635)

6 August 2017

3 references

25 June 2019

14 November 2020

25 November 2020

Personalized medicine: new genomics, old lessons (English)

1 reference

6 August 2017

1 reference

14 November 2020

1 reference

25 November 2020

personalized medicine

1 reference

1

Kenneth Offit

1 reference

6 August 2017

26 June 2011

1 reference

PubMed ID

21706342

6 August 2017

1 July 2011

3 references

25 June 2019

14 November 2020

25 November 2020

4 references

6 August 2017

25 June 2019

14 November 2020

25 November 2020

130

1 reference

6 August 2017

3-14

1 reference

6 August 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-011-1028-3

6 August 2017

0 references

cites work

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Genomics and the continuum of cancer care

8 July 2018

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Effect of direct-to-consumer genomewide profiling to assess disease risk

8 July 2018

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Disclosure of individual genetic data to research participants: the debate reconsidered

8 July 2018

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Germline epigenetic regulation of KILLIN in Cowden and Cowden-like syndrome

8 July 2018

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Recommendations from the EGAPP Working Group: routine testing for Factor V Leiden (R506Q) and prothrombin (20210G>A) mutations in adults with a history of idiopathic venous thromboembolism and their adult family members

8 July 2018

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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

8 July 2018

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The $1,000 genome, the $100,000 analysis?

8 July 2018

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Common genetic variants and modification of penetrance of BRCA2-associated breast cancer

8 July 2018

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Recommendations from the EGAPP Working Group: genomic profiling to assess cardiovascular risk to improve cardiovascular health

8 July 2018

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A map of human genome variation from population-scale sequencing

8 July 2018

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Clinical implications of the cancer genome

8 July 2018

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Inheritance of epigenetic aberrations (constitutional epimutations) in cancer susceptibility

8 July 2018

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Advances in understanding cancer genomes through second-generation sequencing

8 July 2018

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Genome-wide association studies of cancer predisposition

8 July 2018

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Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality

8 July 2018

1 reference

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Genomewide association studies and assessment of the risk of disease

8 July 2018

1 reference

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Challenges in the identification and use of rare disease-associated predisposition variants

8 July 2018

1 reference

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The Path to Personalized Medicine

8 July 2018

1 reference

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8 July 2018

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Gene-expression-based prognostic assays for breast cancer

8 July 2018

1 reference

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Clinical assessment incorporating a personal genome

8 July 2018

1 reference

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Has the revolution arrived?

8 July 2018

1 reference

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Personalized medicine and genomics: challenges and opportunities in assessing effectiveness, cost-effectiveness, and future research priorities.

8 July 2018

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Occult hepatitis C virus infection: what does it mean?

8 July 2018

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American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility

8 July 2018

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A policy model to evaluate the benefits, risks and costs of warfarin pharmacogenomic testing

8 July 2018

1 reference

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Multiplex PCR to diagnose bloodstream infections in patients admitted from the emergency department with sepsis

8 July 2018

1 reference

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Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy

8 July 2018

1 reference

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The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop

8 July 2018

1 reference

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Disclosure of APOE genotype for risk of Alzheimer's disease

8 July 2018

1 reference

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The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer

8 July 2018

1 reference

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Common vs. rare allele hypotheses for complex diseases

8 July 2018

1 reference

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Estimation of the warfarin dose with clinical and pharmacogenetic data

8 July 2018

1 reference

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Recommendations from the EGAPP Working Group: can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan?

8 July 2018

1 reference

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Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives

8 July 2018

1 reference

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Common genetic variation and human disease

8 July 2018

1 reference

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Personal genomes: The case of the missing heritability

8 July 2018

1 reference

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Carrier screening for spinal muscular atrophy

8 July 2018

1 reference

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Clinically applicable models to characterize BRCA1 and BRCA2 variants of uncertain significance

8 July 2018

1 reference

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The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

A systematic review of perceived risks, psychological and behavioral impacts of genetic testing

8 July 2018

1 reference

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The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

8 July 2018

1 reference

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Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Testing for cytochrome P450 polymorphisms in adults with non-psychotic depression treated with selective serotonin reuptake inhibitors (SSRIs).

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Clinical practice. Management of an inherited predisposition to breast cancer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Strong association of de novo copy number mutations with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Cellular functions of the BRCA tumour-suppressor proteins

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Hearing silence: non-neutral evolution at synonymous sites in mammals

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Fragile X syndrome: diagnostic and carrier testing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Hereditary cancer predisposition syndromes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Pediatric acute lymphoblastic leukemia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Genetics and genomics in practice: the continuum from genetic disease to genetic information in health and disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Genomic medicine--a primer

8 July 2018

1 reference

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The use of molecular profiling to predict survival after chemotherapy for diffuse large-B-cell lymphoma

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

Cancer risk and low-penetrance susceptibility genes in gene-environment interactions

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128266

The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing

8 July 2018

1 reference

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The HCP5 single-nucleotide polymorphism: a simple screening tool for prediction of hypersensitivity reaction to abacavir

8 July 2018

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Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.

21 January 2018

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Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

21 January 2018

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An agenda for personalized medicine

21 January 2018

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A network view of disease and compound screening

21 January 2018

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A de novo paradigm for mental retardation.

21 January 2018

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21 January 2018

Point: Hypotheses first.

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Developing a center for comparative effectiveness information.

21 January 2018

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The "duty to warn" a patient's family members about hereditary disease risks

21 January 2018

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12 December 2020

Preimplantation genetic diagnosis for cancer syndromes: a new challenge for preventive medicine

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12 December 2020

Evidence based medicine meets genomic medicine

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12 December 2020

Genomic profiles for disease risk: predictive or premature?

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12 December 2020

Breast cancer single-nucleotide polymorphisms: statistical significance and clinical utility

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12 December 2020

A summary of the 25th International Papillomavirus Conference 2009: vaccines, screening, epidemiology and therapeutics

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12 December 2020

Women's experience of telehealth cancer genetic counseling

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12 December 2020

Challenges in the clinical application of whole-genome sequencing

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12 December 2020

Personalized medicine: potential impact on the biopharmaceutical industry

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12 December 2020

Human genome 10th anniversary. Waiting for the revolution

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12 December 2020

Coriell Personalized Medicine Collaborative®: a prospective study of the utility of personalized medicine

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12 December 2020

Living with my personal genome

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12 December 2020

Personalized medicine: something old, something new

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12 December 2020

10.1007/S00439-011-1028-3

Identifiers

DOI

1 reference

6 August 2017

1 reference

6 August 2017

1 reference

PubMed ID

21706342