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Author Details
Full Name
Ron Zimmern
Affiliation
PHG Foundation
ORCID
Career Start Year
1990
Papers
57
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
25038088
Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues.
J Med Ethics
2015
22773250
Issues concerning the evaluation and regulation of predictive genetic testing.
J Community Genet
2014
26973821
Conceptual issues for screening in the genomic era - time for an update?
Epidemiol Biostat Public Health
2014
25168910
Beyond public health genomics: proposals from an international working group.
Eur J Public Health
2014
23794314
Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations.
J Community Genet
2013
23907645
Recommendations for returning genomic incidental findings? We need to talk!
Genet Med
2013
22427809
A collaboratively-derived science-policy research agenda.
PLoS One
2012
23076269
Next-generation sequencing in the clinic: are we ready?
Nat Rev Genet
2012
22488453
The impact of genomics on public health practice: the case for change.
Public Health Genomics
2012
20921893
Regulating direct-to-consumer genetic tests: what is all the fuss about?
Genet Med
2011
22096106
Genomics and individuals in public health practice: are we luddites or can we meet the challenge?
J Public Health (Oxf)
2011
21412252
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.
Eur J Hum Genet
2011
20395687
Genomics and public health: translating research into public benefit.
Public Health Genomics
2010
22460303
Erratum: A reply to community genetics: 1998-2009... and beyond.
J Community Genet
2010
22460302
A reply to community genetics: 1998-2009... and beyond.
J Community Genet
2010
21189494
Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and â¿¿personalizedâ¿ medicine?
Genet Med
2010
20113820
Addressing congenital causes of disability.
Lancet
2010
19271607
Testing challenges: evaluation of novel diagnostics and molecular biomarkers.
Clin Med (Lond)
2009
20010367
Realizing the potential of genomics: translation is not translational research.
Genet Med
2009
19822024
A new strategic phase for genomic medicine in UK health services.
Genome Med
2009
19801687
Genomic medicine: the future is now. Lessons for Hong Kong from the House of Lords Report on Genomic Medicine.
Hong Kong Med J
2009
18340074
Genetic tests for common diseases: new insights, old concerns.
BMJ
2008
18204250
EuroGentest: DNA-based testing for heritable disorders in Europe.
Community Genet
2008
18413374
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics.
J Med Genet
2008
17179752
The emergence of networks in human genome epidemiology: challenges and opportunities.
Epidemiology
2007
18557232
Closing the gaps--enhancing the regulation of genetic tests using responsive regulation.
Food Drug Law J
2007
18073580
Defining purpose: a key step in genetic test evaluation.
Genet Med
2007
17606754
HER2 status in breast cancer--an example of pharmacogenetic testing.
J R Soc Med
2007
17534375
How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network.
Eur J Hum Genet
2007
17526507
The evaluation of genetic tests.
J Public Health (Oxf)
2007
17888858
Will genomics widen or help heal the schism between medicine and public health?
Am J Prev Med
2007
17804859
Turning the pump handle: evolving methods for integrating the evidence on gene-disease association.
Am J Epidemiol
2007
17304048
Array-based comparative genomic hybridization for investigating chromosomal abnormalities in patients with learning disability: systematic review meta-analysis of diagnostic and false-positive yields.
Genet Med
2007
16490962
Getting ready for the future: integration of genomics into public health research, policy and practice in Europe and globally.
Community Genet
2006
16845279
The path from genome-based research to population health: development of an international public health genomics network.
Genet Med
2006
16468121
A road map for efficient and reliable human genome epidemiology.
Nat Genet
2006
15733157
Education in the genetics era: genetics education for health professionals--an essential component of genetics policy.
Med Educ
2005
16170241
How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom.
Genet Med
2005
15667703
Pharmacogenetics: policy needs for personal prescribing.
J Health Serv Res Policy
2005
15087352
Role of next of kin in accessing health records of deceased relatives. The arguments could be extended.
BMJ
2004
15573127
Ensuring the appropriate use of genetic tests.
Nat Rev Genet
2004
15545742
Genetic tests and their evaluation: can we answer the key questions?
Genet Med
2004
15217845
The human tissue bill and the mental capacity bill.
BMJ
2004
15321838
Familial hypercholesterolemia and coronary heart disease: a HuGE association review.
Am J Epidemiol
2004
15321837
Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review.
Am J Epidemiol
2004
14596633
Pharmacogenetics and public policy: expert views in Europe and North America.
Pharmacogenomics
2003
12943461
Regulatory options for pharmacogenetics.
Pharmacogenomics
2003
12907002
(Almost) three cheers for UK genetics White Paper.
Lancet
2003
11984562
Polygenic susceptibility to breast cancer and implications for prevention.
Nat Genet
2002
12172393
High "population attributable fraction" for coronary heart disease mortality among relatives in monogenic familial hypercholesterolemia.
Genet Med
2002
1 - 50 of 57
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