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Author Details

Alastair Kent
Congenica Ltd
1995
50
17
PMIDPaper TitleJournal TitlePublished Year
35549752Unlocking sociocultural and community factors for the global adoption of genomic medicine.Orphanet J Rare Dis2022
35549752Unlocking sociocultural and community factors for the global adoption of genomic medicine.Orphanet J Rare Dis2022
33540773Bringing Onco-Innovation to Europe's Healthcare Systems: The Potential of Biomarker Testing, Real World Evidence, Tumour Agnostic Therapies to Empower Personalised Medicine.Cancers (Basel)2021
33540773Bringing Onco-Innovation to Europe's Healthcare Systems: The Potential of Biomarker Testing, Real World Evidence, Tumour Agnostic Therapies to Empower Personalised Medicine.Cancers (Basel)2021
33564657Time for Change? The Why, What and How of Promoting Innovation to Tackle Rare Diseases - Is It Time to Update the EU's Orphan Regulation? And if so, What Should be Changed?Biomed Hub2020
33564664Bringing Greater Accuracy to Europe's Healthcare Systems: The Unexploited Potential of Biomarker Testing in Oncology.Biomed Hub2020
33564657Time for Change? The Why, What and How of Promoting Innovation to Tackle Rare Diseases - Is It Time to Update the EU's Orphan Regulation? And if so, What Should be Changed?Biomed Hub2020
33564664Bringing Greater Accuracy to Europe's Healthcare Systems: The Unexploited Potential of Biomarker Testing in Oncology.Biomed Hub2020
29632381Plain-language medical vocabulary for precision diagnosis.Nat Genet2018
29632381Plain-language medical vocabulary for precision diagnosis.Nat Genet2018
27956199The path to successful commercialization of cell and gene therapies: empowering patient advocates.Cytotherapy2017
31988949EU Health Policy, Coherence, Stakeholder Diversity and Their Impact on the EMA.Biomed Hub2017
31988927A Disruptive Dinner Guest.Biomed Hub2017
28679655Marketing of unproven stem cell-based interventions: A call to action.Sci Transl Med2017
28880017Will rising prices and budget constraints prevent patients from accessing novel gene therapies?Gene Ther2017
28517990Risk and Benefit in Personalised Medicine: An End User View.New Bioeth2017
27956199The path to successful commercialization of cell and gene therapies: empowering patient advocates.Cytotherapy2017
28289980Implementing genetic education in primary care: the Gen-Equip programme.J Community Genet2017
31988949EU Health Policy, Coherence, Stakeholder Diversity and Their Impact on the EMA.Biomed Hub2017
31988927A Disruptive Dinner Guest.Biomed Hub2017
28289980Implementing genetic education in primary care: the Gen-Equip programme.J Community Genet2017
28880017Will rising prices and budget constraints prevent patients from accessing novel gene therapies?Gene Ther2017
28517990Risk and Benefit in Personalised Medicine: An End User View.New Bioeth2017
28679655Marketing of unproven stem cell-based interventions: A call to action.Sci Transl Med2017
27366873Prevention of Congenital Disorders and Care of Affected Children: A Consensus Statement.JAMA Pediatr2016
27366873Prevention of Congenital Disorders and Care of Affected Children: A Consensus Statement.JAMA Pediatr2016
25248395Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.Eur J Hum Genet2015
25248395Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.Eur J Hum Genet2015
24424120Managing clinically significant findings in research: the UK10K example.Eur J Hum Genet2014
25407328Generating health technology assessment evidence for rare diseases.Int J Technol Assess Health Care2014
24424120Managing clinically significant findings in research: the UK10K example.Eur J Hum Genet2014
24801295Pfizer-sponsored satellite symposium at the European Haemophilia Consortium (EHC) Congress: changing the policy landscape: haemophilia patient involvement in healthcare decision-making.Eur J Haematol Suppl2014
25407328Generating health technology assessment evidence for rare diseases.Int J Technol Assess Health Care2014
24801295Pfizer-sponsored satellite symposium at the European Haemophilia Consortium (EHC) Congress: changing the policy landscape: haemophilia patient involvement in healthcare decision-making.Eur J Haematol Suppl2014
23794314Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations.J Community Genet2013
24285799Commentary: Patients will need knowledgeable guidance.BMJ2013
23794314Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations.J Community Genet2013
24326170A pilot study of multicriteria decision analysis for valuing orphan medicines.Value Health2013
23657386A P3G generic access agreement for population genomic studies.Nat Biotechnol2013
24285799Commentary: Patients will need knowledgeable guidance.BMJ2013
24326170A pilot study of multicriteria decision analysis for valuing orphan medicines.Value Health2013
23657386A P3G generic access agreement for population genomic studies.Nat Biotechnol2013
22582247Research priorities. ELSI 2.0 for genomics and society.Science2012
22582247Research priorities. ELSI 2.0 for genomics and society.Science2012
20942607Toward a proportionate regulatory framework for gene transfer: a patient group-led initiative.Hum Gene Ther2011
20942607Toward a proportionate regulatory framework for gene transfer: a patient group-led initiative.Hum Gene Ther2011
21719093Safety of medicines and the use of animals in research.Lancet2011
21643981Population biobanks and returning individual research results: mission impossible or new directions?Hum Genet2011
21719093Safety of medicines and the use of animals in research.Lancet2011
21643981Population biobanks and returning individual research results: mission impossible or new directions?Hum Genet2011
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Collaborators

University of Oxford
Co-authored papers 4
McGill University
Co-authored papers 4
Osaka University
Co-authored papers 3
Institute for Human Virology
Co-authored papers 3
Case Western Reserve University
Co-authored papers 3
National Cancer Research Institute
Co-authored papers 3
Co-authored papers 2
Co-authored papers 2
Newcastle University
Co-authored papers 2
Illumina Inc.
Co-authored papers 2
McGill University and Genome Quebec Innovation Centre
Co-authored papers 2
Co-authored papers 2
University of Utah
Co-authored papers 2
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
McGill University
Co-authored papers 2
First Hospital of Xingtai
Co-authored papers 2
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 2
Wellcome Trust Sanger Institute
Co-authored papers 2
Fudan University
Co-authored papers 2
Adaptive Biotechnologies
Co-authored papers 2
Center for Statistical Genetics, Columbia University Medical Center
Co-authored papers 2
23andMe Inc.
Co-authored papers 2
Center for Cerebrovascular Research
Co-authored papers 2
Spanish National Cancer Research Centre
Co-authored papers 2
University of Michigan School of Public Health ann arbor
Co-authored papers 2
Beijing Institute of Genomics, Chinese Academy of Sciences
Co-authored papers 2
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Nanfang Hospital and Basic Medical College, Southern Medical University
Co-authored papers 2
McGill University Health Center
Co-authored papers 2
Co-authored papers 2