(Q22330767)

English

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders

scientific article

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities

In more languages

Statements

scholarly article

0 references

1 reference

Europe PubMed Central

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders (English)

0 references

0 references

Shirley Hodgson

10

object named as

Shirley Hodgson

author given names

Shirley

author last names

Hodgson

1 reference

Dimensions Publication ID

7 February 2023

Jörg Schmidtke

25

object named as

Jörg Schmidtke

author given names

Jörg

author last names

Schmidtke

1 reference

Dimensions Publication ID

7 February 2023

Anne Cambon-Thomsen

7

object named as

Anne Cambon-Thomsen

author given names

Anne

author last names

Cambon-Thomsen

1 reference

Dimensions Publication ID

7 February 2023

6

object named as

Pascal Borry

author given names

Pascal

author last names

Borry

1 reference

Dimensions Publication ID

7 February 2023

Christine Patch

object named as

Christine Patch

16

author given names

Christine

author last names

Patch

1 reference

Dimensions Publication ID

7 February 2023

Jorge Sequeiros

object named as

Jorge Sequeiros

20

author given names

Jorge

author last names

Sequeiros

1 reference

Dimensions Publication ID

7 February 2023

4

object named as

Eleni Zika

author given names

Eleni

author last names

Zika

1 reference

Dimensions Publication ID

7 February 2023

Martina C. Cornel

26

object named as

Martina C Cornel

author given names

Martina C

author last names

Cornel

1 reference

Dimensions Publication ID

7 February 2023

Michael Krawczak

13

object named as

Michael Krawczak

author given names

Michael

author last names

Krawczak

1 reference

Dimensions Publication ID

7 February 2023

15

object named as

Jan Lubinski

author given names

Jan

author last names

Lubinski

1 reference

Dimensions Publication ID

7 February 2023

Lisbeth Tranebjærg

21

object named as

Lisbeth Tranebjaerg

author given names

Lisbeth

author last names

Tranebjaerg

1 reference

Dimensions Publication ID

7 February 2023

author name string

Frauke Becker

1

author given names

Frauke

author last names

Becker

1 reference

Dimensions Publication ID

7 February 2023

Carla G van El

2

author given names

Carla G

author last names

van El

1 reference

Dimensions Publication ID

7 February 2023

Dolores Ibarreta

3

author given names

Dolores

author last names

Ibarreta

1 reference

Dimensions Publication ID

7 February 2023

Stuart Hogarth

5

author given names

Stuart

author last names

Hogarth

1 reference

Dimensions Publication ID

7 February 2023

Jean Jacques Cassiman

8

author given names

Jean Jacques

author last names

Cassiman

1 reference

Dimensions Publication ID

7 February 2023

Gerry Evers-Kiebooms

9

author given names

Gerry

author last names

Evers-Kiebooms

1 reference

Dimensions Publication ID

7 February 2023

A Cécile J W Janssens

11

author given names

A Cécile J W

author last names

Janssens

1 reference

Dimensions Publication ID

7 February 2023

Helena Kaariainen

12

author given names

Helena

author last names

Kaariainen

1 reference

Dimensions Publication ID

7 February 2023

Ulf Kristoffersson

14

author given names

Ulf

author last names

Kristoffersson

1 reference

Dimensions Publication ID

7 February 2023

Victor B Penchaszadeh

17

author given names

Victor B

author last names

Penchaszadeh

1 reference

Dimensions Publication ID

7 February 2023

Andrew Read

18

author given names

Andrew

author last names

Read

1 reference

Dimensions Publication ID

7 February 2023

Wolf Rogowski

19

author given names

Wolf

author last names

Rogowski

1 reference

Dimensions Publication ID

7 February 2023

Irene M van Langen

22

author given names

Irene M

author last names

van Langen

1 reference

Dimensions Publication ID

7 February 2023

Helen Wallace

23

author given names

Helen

author last names

Wallace

1 reference

Dimensions Publication ID

7 February 2023

Ron Zimmern

24

author given names

Ron

author last names

Zimmern

1 reference

Dimensions Publication ID

7 February 2023

language of work or name

0 references

publication date

April 2011

0 references

European Journal of Human Genetics

0 references

19 Suppl 1

0 references

S6-44

0 references

Personal genomics services: whose genomes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Genetic prediction of future type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

A model of gene-gene and gene-environment interactions and its implications for targeting environmental interventions by genotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Does genetic testing really improve the prediction of future type 2 diabetes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

A haplotype map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Genomics and the prevention and control of common chronic diseases: emerging priorities for public health action

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Cost effectiveness analysis of different approaches of screening for familial hypercholesterolaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Genetic risk and behavioural change

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

A comprehensive review of genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Iron-overload-related disease in HFE hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Letting the genome out of the bottle--will we get our wish?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Individualization of therapy using Mammaprint: from development to the MINDACT Trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Screening for HFE and iron overload

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Misconceptions about the use of genetic tests in populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Review of first 5 years of screening for familial hypercholesterolaemia in the Netherlands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

19 March 2017

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

Common genetic variation and human traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

The world health report 2002 - reducing risks, promoting healthy life

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

Replication validity of genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

7 April 2017

The EGAPP initiative: lessons learned

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Complexity and accountability: the witches' brew of psychiatric genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Social networkers' attitudes toward direct-to-consumer personal genome testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Prediction and interaction in complex disease genetics: experience in type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genomics of type 2 diabetes mellitus: implications for the clinician

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Closing the gap: inverting the genetics curriculum to ensure an informed public

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Predictive value of factor V Leiden and prothrombin G20210A in adults with venous thromboembolism and in family members of those with a mutation: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Challenges of translating genetic tests into clinical and public health practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Multiple genetic tests for susceptibility to smoking do not outperform simple family history

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Impact of communicating familial risk of diabetes on illness perceptions and self-reported behavioral outcomes: a randomized controlled trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Breast cancer susceptibility: current knowledge and implications for genetic counselling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Invited commentary: from genome-wide association studies to gene-environment-wide interaction studies--challenges and opportunities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Economic methods for valuing the outcomes of genetic testing: beyond cost-effectiveness analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genome-based prediction of common diseases: advances and prospects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Prediction of individual genetic risk of complex disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Monogenic diabetes in the young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Delivery of genomic medicine for common chronic adult diseases: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genetic tests for common diseases: new insights, old concerns

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

A systematic review of the clinical validity and clinical utility of DNA testing for hereditary haemochromatosis type 1 in at-risk populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

EuroGentest: DNA-based testing for heritable disorders in Europe.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

The rise and fall of the common disease-common variant (CD-CV) hypothesis: how the sickle cell disease paradigm led us all astray (or did it?).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

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?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Future use of genomics in coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

The impact of genetics and genomics on public health

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genetic testing and counselling in Europe: health professionals current educational provision, needs assessment and potential strategies for the future

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Thrombophilia and venous thromboembolism: implications for testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Biobanking for epidemiological research and public health

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

New perspectives for the elucidation of genetic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Transla

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Consumer acceptance of technology-based food innovations: lessons for the future of nutrigenomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Implementation of preconceptional carrier screening for cystic fibrosis and haemoglobinopathies: a sociotechnical analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Predictive testing for Huntington's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Converting a breast cancer microarray signature into a high-throughput diagnostic test.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genetic screening by DNA technology: a systematic review of health economic evidence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Emerging patent issues in genomic diagnostics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genetic health technology and economic evaluation: a critical review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Common susceptibility genes for cancer: search for the end of the rainbow

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Coronary artery disease is associated with Alzheimer disease neuropathology in APOE4 carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Quantifying the health benefits of genetic tests: the importance of a population perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Economic analyses of human genetics services: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Pharmacodiagnostic testing in breast cancer: focus on HER2 and trastuzumab therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Self-regulation and the behavioural response to DNA risk information: a theoretical analysis and framework for future research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Coeliac disease: is it time for mass screening?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Criteria list for assessment of methodological quality of economic evaluations: Consensus on Health Economic Criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Role of early case detection by screening relatives of patients with HFE-associated hereditary haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost-effectiveness of Herceptin: a standard cost model for breast-cancer treatment in a Belgian university hospital

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cascade testing in familial hypercholesterolaemia: how should family members be contacted?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost effectiveness of a new strategy to identify HNPCC patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Medical genetics in developing countries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Review of guidelines for good practice in decision-analytic modelling in health technology assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost-effectiveness of testing for hypercoagulability and effects on treatment strategies in patients with deep vein thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Hereditary hemochromatosis--a new look at an old disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cancer genetics services: a systematic review of the economic evidence and issues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Does NICE have a cost-effectiveness threshold and what other factors influence its decisions? A binary choice analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Is genetic screening for hemochromatosis worthwhile?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Population genetic screening programmes: principles, techniques, practices, and policies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Provision of genetic services in Europe: current practices and issues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Economic considerations for health insurance coverage of emerging genetic tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

The genetics of narcolepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

An economic viewpoint on alternative strategies for identifying persons with hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genomic profiling to promote a healthy lifestyle: not ready for prime time

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

New approaches to investigating heterogeneity in complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Genetic associations in large versus small studies: an empirical assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Effects of patents and licenses on the provision of clinical genetic testing services

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Fosmidomycin, a novel chemotherapeutic agent for malaria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Population screening in the age of genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost-minimization analysis of genetic testing versus clinical screening of at-risk relatives for familial adenomatous polyposis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Searching literature databases for health care economic evaluations: how systematic can we afford to be?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Getting insurance after genetic screening on familial hypercholesterolaemia; the need to educate both insurers and the public to increase adherence to national guidelines in The Netherlands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Application of population screening principles to genetic screening for adult-onset conditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

The potential social impact of predictive genetic testing for susceptibility to common chronic diseases: a review and proposed research agenda

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Cost-effectiveness of screening and extended anticoagulation for carriers of both factor V Leiden and prothrombin G20210A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Appraising organised screening programmes for testing for genetic susceptibility to cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Screening for hypercholesterolaemia versus case finding for familial hypercholesterolaemia: a systematic review and cost-effectiveness analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

EASL International Consensus Conference on Haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

When can a risk factor be used as a worthwhile screening test?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Factor V Leiden: should we screen oral contraceptive users and pregnant women?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Guidelines for authors and peer reviewers of economic submissions to the BMJ. The BMJ Economic Evaluation Working Party

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Epidemiological evaluation of the use of genetics to improve the predictive value of disease risk factors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Ankylosing spondylitis and HL-A 27.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Effects of genetic screening on perceptions of health: a pilot study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Recommendations for reporting cost-effectiveness analyses. Panel on Cost-Effectiveness in Health and Medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

27 September 2017

Council of Europe adopts protocol on genetic testing for health purposes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

Global epidemiology of hemoglobin disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

The new genetics in clinical practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

Annotation: the analysis of variance and the analysis of causes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

Heritability analyses of IQ scores: science or numerology?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

30 May 2018

Genome-wide association studies and human disease: from trickle to flood.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

The Genomics Gold Rush

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Cancer genetics and its "different faces of autonomy".

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Factor V Leiden and the risk for venous thromboembolism in the adult Danish population

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Popper revisited: GWAS here, last year.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

The clinical utility of genetic tests.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Predictive genetic testing for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Screening for hereditary haemochromatosis within families and beyond.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Screening for hemochromatosis in asymptomatic subjects with or without a family history

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

What is the clinical utility of genetic testing?

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Uncertainty and the welfare economics of medical care. 1963.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Estimating the survival benefits gained from providing national cancer genetic services to women with a family history of breast cancer.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Guidelines for referral to a regional genetics service: GPs respond by referring more appropriate cases.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

The evidence dilemma in genomic medicine.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Hippocrates revisited? Old ideals and new realities

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Do it yourself cancer gene testing raises concerns

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Personal Genome Testing: Do You Know What You Are Buying?

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

ASHG Statement* on Direct-to-Consumer Genetic Testing in the United States

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

An agenda for personalized medicine

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Maternal serum screening, political decision-making and social learning.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Evaluating the utility of personal genomic information

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Understanding why negative genetic test results sometimes fail to reassure.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Psychosocial impact of genetic testing for hemochromatosis in the HEIRS Study: a comparison of participants recruited in Canada and in the United States.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Will genetic testing for predisposition for disease result in fatalism? A qualitative study of parents responses to neonatal screening for familial hypercholesterolaemia.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Quality of life in a family based genetic cascade screening programme for familial hypercholesterolaemia: a longitudinal study among participants

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Patenting and licensing in genetic testing: recommendations of the European Society of Human Genetics.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Regulatory aspects of total product life cycle.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Intellectual property. Enhanced: intellectual property landscape of the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Genetic counseling program in familial breast cancer: Analysis of its effectiveness, cost and cost-effectiveness ratio

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Randomized trial of a specialist genetic assessment service for familial breast cancer.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

HER-2 testing and trastuzumab therapy for metastatic breast cancer: a cost-effectiveness analysis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

A monoclonal antibody against HER-2 (trastuzumab) for metastatic breast cancer: a model-based cost-effectiveness analysis.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Testing for BRCA1 mutations: a cost-effectiveness analysis.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Cost comparison of predictive genetic testing versus conventional clinical screening for familial adenomatous polyposis.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Comparison of selection strategies for genetic testing of patients with hereditary nonpolyposis colorectal carcinoma: effectiveness and cost-effectiveness

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost-effectiveness of testing algorithms.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Will Genetics Revolutionize Medicine?

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Evaluation of risk prediction updates from commercial genome-wide scans

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Perceived Risk and Representations of Cardiovascular Disease and Preventive Behaviour in People Diagnosed with Familial Hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Molecular screening for familial hypercholesterolaemia: consequences for life and disability insurance

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Testing for Factor V Leiden in Patients with Pulmonary or Venous Thromboembolism: A Cost-Effectiveness Analysis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

‘Medicine’s Next Goldmine?’ The Implications of New Genetic Health Technologies for the Health Service

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Economic Evaluation of the Familial Cancer Programme in Western Australia: Predictive Genetic Testing for Familial Adenomatous Polyposis and Hereditary Non-Polyposis Colorectal Carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Direct-to-consumer genome scanning services. Also for children?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

Patenting and licensing in genetic testing: ethical, legal, and social issues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

Breast cancer susceptibility genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

Analysing DNA patents in relation with diagnostic genetic testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

Population genetic screening programmes: technical, social and ethical issues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

The CF carrier status is not associated with a diminished self-concept or increased anxiety: results of psychometric testing after at least 1 year.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3327518

29 November 2018

Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

21 January 2018

Benefits and costs of screening Ashkenazi Jewish women for BRCA1 and BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for factor V Leiden mutation before prescribing combination oral contraceptives

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Costs and benefits of diagnosing familial breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for hereditary hemochromatosis in siblings and children of affected patients. A cost-effectiveness analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Promoting safe and effective genetic testing in the United States. Final report of the Task Force on Genetic Testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease-related conditions in relatives of patients with hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extended anticoagulation for prevention of recurrent venous thromboembolism in carriers of factor V Leiden--cost-effectiveness analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testing for factor V Leiden in patients with pulmonary or venous thromboembolism: a cost-effectiveness analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing for disease susceptibilities: consequences for genetic counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Research priorities for evaluating family history in the prevention of common chronic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Provision of genetic services in Europe: current practices and issues

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychosocial impact of predictive testing for myotonic dystrophy type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards quality assurance and harmonization of genetic testing services in the European Union

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-based screening for hereditary haemochromatosis. I: Technical performance, costs and clinical relevance of a German pilot study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome scan meta-analysis for hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of the introduction of a guideline on the targeted detection of hereditary haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Research network: EuroGentest--a European Network of Excellence aimed at harmonizing genetic testing services

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-based screening for hereditary hemochromatosis: II. Attitudes toward genetic testing and psychosocial impact--a report from a German pilot study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problem

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DISCERN-Genetics: quality criteria for information on genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cost-effectiveness analysis of strategies for HER2 testing of breast cancer patients in France

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Educating health-care professionals about genetics and genomics

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Searching for a threshold, not setting one: the role of the National Institute for Health and Clinical Excellence

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic effects versus bias for candidate polymorphisms in myocardial infarction: case study and overview of large-scale evidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Health care in the age of genetic medicine

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morbidity and mortality in first-degree relatives of C282Y homozygous probands with clinically detected haemochromatosis compared with the general population: the HEmochromatosis FAmily Study (HEFAS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic profiles for disease risk: predictive or premature?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recreational genomics? Dreams and fears on genetic susceptibility screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pharmacogenomics in Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polygenes, risk prediction, and targeted prevention of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Science and democracy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Council of Europe. Additional Protocol to the Convention on Human Rights and Biomedicine, concerning genetic testing for health purposes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cost-effectiveness of screening for hereditary hemochromatosis in Germany: a remodeling study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk prediction--are we there yet?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Health care provider and consumer awareness, perceptions, and use of direct-to-consumer personal genomic tests, United States, 2008

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bringing genetics into primary care: findings from a national evaluation of pilots in England

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of consumer genomic tests remains in limbo

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing and the health care system

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct-to-consumer genetic testing: more questions than benefits?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Costs of predicting IDDM

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cost analysis of alternative approaches to colorectal screening in familial adenomatous polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary haemochromatosis mutation frequencies in the general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/21412252

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biomarkers for prediction of cardiovascular events

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

7 January 2021

based on heuristic

inferred from DOI database lookup

Public Health Genomics (PHG): From Scientific Considerations to Ethical Integration.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

7 January 2021

based on heuristic

inferred from DOI database lookup

Patenting and licensing in genetic testing

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

7 January 2021

based on heuristic

inferred from DOI database lookup

Misunderstood misunderstanding: social identities and public uptake of science

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2010.249

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/EJHG.2010.249

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Dimensions Publication ID

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q22330767&oldid=2175174928"