Implementation of genetics to personalize medicine (Q37005953)

17 August 2017

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title

Implementation of genetics to personalize medicine (English)

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17 August 2017

Wendy K Chung

1

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17 August 2017

1 September 2007

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17 August 2017

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17 August 2017

4

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17 August 2017

3

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17 August 2017

248-265

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Complement factor H polymorphism and age-related macular degeneration

17 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Complement factor H variant increases the risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Complement factor H polymorphism in age-related macular degeneration

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Complement C3 variant and the risk of age-related macular degeneration

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Current status of genome-wide scanning for hypertension

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

A common allele on chromosome 9 associated with coronary heart disease

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genome-wide association study identifies novel breast cancer susceptibility loci

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation-Negative Hereditary Breast Cancer Families

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Safety and efficacy of flecainide in subjects with Long QT-3 syndrome (DeltaKPQ mutation): a randomized, double-blind, placebo-controlled clinical trial.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Glucokinase mutations in young children with hyperglycemia

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genetic cause of hyperglycaemia and response to treatment in diabetes

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Haemochromatosis and HLA-H.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Newborn screening for metabolic disorders

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Newborns with C8-acylcarnitine level over the 90th centile have an increased frequency of the common MCAD 985A>G mutation

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 21-hydroxylase deficiency

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Newborn screening for cystic fibrosis: techniques and strategies

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Two-tiered universal newborn screening strategy for severe combined immunodeficiency

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

X-linked adrenoleukodystrophy.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Current status of newborn screening: decision-making about the conditions to include in screening programs

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Neonatal screening by DNA microarray: spots and chips

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Pediatricians' attitudes toward expanding newborn screening

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Using pharmacogenetics to improve drug safety and efficacy

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Bleeding complications with warfarin use: a prevalent adverse effect resulting in regulatory action

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Influence of coagulation factor, vitamin K epoxide reductase complex subunit 1, and cytochrome P450 2C9 gene polymorphisms on warfarin dose requirements.

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genotypes of the cytochrome p450 isoform, CYP2C9, and the vitamin K epoxide reductase complex subunit 1 conjointly determine stable warfarin dose: a prospective study.

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Diagnostic analysis, clinical importance and molecular basis of dihydropyrimidine dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Pharmacogenetics of methotrexate: toxicity among marrow transplantation patients varies with the methylenetetrahydrofolate reductase C677T polymorphism

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

The impact of cytochrome P450 2D6 metabolism in women receiving adjuvant tamoxifen

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Gene expression determinants of clinical outcome

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Molecular Testing in the Management of Cardiac Transplant Recipients: Initial Clinical Experience

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Tissue-specific expression and regulation of sexually dimorphic genes in mice

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Global variation in copy number in the human genome

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Diagnostic genome profiling in mental retardation

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Strong association of de novo copy number mutations with autism

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Large-scale copy number polymorphism in the human genome

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Comparative genomic hybridization

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Germ-line DNA copy number variation frequencies in a large North American population

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Venous thrombosis: a multicausal disease

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

A vision for the future of genomics research

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Gynecologists' training, knowledge, and experiences in genetics: a survey

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Obstetrician-gynecologists' opinions and attitudes on the role of genetics in women's health.

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Educating health-care professionals about genetics and genomics

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

The evolving duty to disclose the presence of genetic disease to relatives

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Clinical objectives in medical genetics for undergraduate medical students

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Preimplantation sex selection demand and preferences in an infertility population

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Genes on the Web--direct-to-consumer marketing of genetic testing

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Attitudes about genetics in underserved, culturally diverse populations

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Differences between African Americans and Whites in their attitudes toward genetic testing for Alzheimer's disease

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Lack of Hispanics' involvement in research -- is it Hispanics or scientists?

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Scientific limitations and ethical ramifications of a non-representative Human Genome Project: African American response

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Barriers to Access: Results from Focus Groups to Identify Genetic Service Needs in the Community

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Your genes and privacy

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https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Report of Banbury Summit meeting on training of physicians in medical genetics, October 20-22, 2004

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

Attitudes of African American premedical students toward genetic testing and screening

1 reference

https://api.crossref.org/works/10.1016%2FS1550-8579%2807%2980044-1

7 January 2021

10.1016/S1550-8579(07)80044-1

Identifiers

DOI

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17 August 2017

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PubMed ID

18022591