Výsledky vyhledávání - Christine Patch

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  1. 1
    Genetic counselling in the era of genomic medicine

    Genetic counselling in the era of genomic medicine Autor Christine Patch, Anna Middleton

    Vydáno 2018
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  2. 2
    Communication about genetic testing with breast and ovarian cancer patients: a scoping review

    Communication about genetic testing with breast and ovarian cancer patients: a scoping review Autor Chris Jacobs, Christine Patch, Susan Michie

    Vydáno 2018
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  3. 3
    Towards equitable and trustworthy genomics research

    Towards equitable and trustworthy genomics research Autor Jerome Atutornu, Richard Milne, Alesia Costa, Christine Patch, Anna Middleton

    Vydáno 2022
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  4. 4
    How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

    How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom Autor Simon Sanderson, Ron Zimmern, Mark Kroese, Julian P. T. Higgins, Christine Patch, Jon Emery

    Vydáno 2005
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  5. 5
    Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project

    Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project Autor Saskia C. Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S. Chitty

    Vydáno 2019
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  6. 6
    Professional duties are now considered legal duties of care within genomic medicine

    Professional duties are now considered legal duties of care within genomic medicine Autor Anna, Middleton, Christine, Patch, Jonathan, Roberts, Richard, Milne, Alessia, Costa, Lauren, Robarts, Jerome, Atutornu

    Vydáno 2020
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  7. 7
    Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study

    Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study Autor Celine Lewis, Saskia C. Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Amy Hunter, Lyn S. Chitty

    Vydáno 2020
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  8. 8
    A Roadmap for Global Acceleration of Genomics Integration Across Nursing

    A Roadmap for Global Acceleration of Genomics Integration Across Nursing Autor Emma Tonkin, Kathleen A. Calzone, Laurie Badzek, Caroline Benjamin, Anna Middleton, Christine Patch, Maggie Kirk

    Vydáno 2020
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  9. 9
    “A very big challenge”: a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England

    “A very big challenge”: a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England Autor Bettina Friedrich, Cecilia Vindrola‐Padros, Anneke Lucassen, Christine Patch, Angus Clarke, Monica Lakhanpaul, Celine Lewis

    Vydáno 2024
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  10. 10
    Penetrance for copy number variants associated with schizophrenia

    Penetrance for copy number variants associated with schizophrenia Autor Evangelos Vassos, David Collier, Simon Holden, Christine Patch, Dan Rujescu, David St Clair, Cathryn M. Lewis

    Vydáno 2010
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  11. 11
    Current State of Genomics in Nursing: A Scoping Review of Healthcare Provider Oriented (Clinical and Educational) Outcomes (2012–2022)

    Current State of Genomics in Nursing: A Scoping Review of Healthcare Provider Oriented (Clinical and Educational) Outcomes (2012–2022) Autor Joanne Thomas, Jordan Keels, Kathleen A. Calzone, Laurie Badzek, Sarah Dewell, Christine Patch, Emma Tonkin, Andrew Dwyer

    Vydáno 2023
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  12. 12
    Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study

    Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study Autor Michelle Peter, Jennifer Hammond, Saskia C. Sanderson, Jana Gurasashvili, Amy Hunter, Beverly Searle, Christine Patch, Lyn S. Chitty, Melissa Hill, Celine Lewis

    Vydáno 2022
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  13. 13
    Developing a policy for paediatric biobanks: principles for good practice

    Developing a policy for paediatric biobanks: principles for good practice Autor Kristien Hens, Carla E Van El, Pascal Borry, Anne Cambon‐Thomsen, Martina C. Cornel, Francesca Forzano, Anneke Lucassen, Christine Patch, Lisbeth Tranebjærg, Eric Vermeulen, Elena Salvaterra, Aad Tibben, Kris Dierickx

    Vydáno 2012
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  14. 14
    Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design

    Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design Autor Amanda Pichini, Arzoo Ahmed, Christine Patch, David Bick, Mathilde Leblond, Dalia Kasperavičiūtė, Dasha Deen, Simon A. Wilde, Sofia Garcia Noriega, Christella Matoko, Alice Tuff-Lacey, Chris Wigley, Richard H. Scott

    Vydáno 2022
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  15. 15
    Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

    Opportunistic genomic screening. Recommendations of the European Society of Human Genetics Autor Guido de Wert, Wybo Dondorp, Angus Clarke, Elisabeth Dequeker, Christophe Cordier, Zandra C. Deans, Carla van El, Florence Fellmann, Ros Hastings, Sabine Hentze, Heidi Howard, Milan Maçek, Álvaro Mendes, Christine Patch, Emmanuelle Rial‐Sebbag, Vigdís Stefànsdóttir, Martina C. Cornel, Francesca Forzano

    Vydáno 2020
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  16. 16
    Return of individual research results from genomic research: A systematic review of stakeholder perspectives

    Return of individual research results from genomic research: A systematic review of stakeholder perspectives Autor Danya F. Vears, Joel T. Minion, Stephanie Roberts, James Cummings, Mavis Machirori, Mwenza Blell, Isabelle Budin‐Ljøsne, Lorraine Cowley, Stephanie O. M. Dyke, Clara Gaff, Robert C. Green, Alison Hall, Amber L. Johns, Bartha Maria Knoppers, Stephanie Mulrine, Christine Patch, Eva C. Winkler, Madeleine J. Murtagh

    Vydáno 2021
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  17. 17
    European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

    European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death Autor Florence Fellmann, Carla van El, Philippe Charron, Katarzyna Michaud, Heidi Howard, Sarah N. Boers, Angus Clarke, Anne‐Marie Duguet, Francesca Forzano, Silke Kauferstein, Hülya Kayserili, Anneke Lucassen, Álvaro Mendes, Christine Patch, Dragica Radojković, Emmanuelle Rial‐Sebbag, Mary N. Sheppard, Anne-Marie Tassé, Şehime Gülsün Temel, Antti Sajantila, Cristina Basso, Arthur A.M. Wilde, Martina C. Cornel

    Vydáno 2019
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  18. 18
    Genetic testing and common disorders in a public health framework

    Genetic testing and common disorders in a public health framework Autor Martina C. Cornel, Frauke Becker, Carla van El, Dolores Ibarreta, Eleni Zika, Stuart Hogart, Anne Cambon‐Thomsen, Jean‐Jacques Cassiman, Gerry Evers‐Kiebooms, Shirley V. Hodgson, A. Cecile J.W. Janssens, Helena Kääriäinen, Michael Krawczak, Ulf Kristoffersson, Jan Lubiński, Christine Patch, Víctor B. Penchaszadeh, Andrew Read, Wolf Rogowski, Jorge Sequeiros, Lisbeth Tranebjærg, Irene M. van Langen, Helen M. Wallace, Ron Zimmern, Jörg Schmidtke

    Vydáno 2011
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  19. 19
    Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities

    Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities Autor Frauke Becker, Carla van El, Dolores Ibarreta, Eleni Zika, Stuart Hogarth, Pascal Borry, Anne Cambon‐Thomsen, Jean Jacques Cassiman, Gerry Evers‐Kiebooms, Shirley Hodgson, A. Cecile J.W. Janssens, Helena Kääriäinen, Michael Krawczak, Ulf Kristoffersson, Jan Lubiński, Christine Patch, Víctor B. Penchaszadeh, Andrew Read, Wolf Rogowski, Jorge Sequeiros, Lisbeth Tranebjærg, Irene M. van Langen, Helen M. Wallace, Ron Zimmern, Jörg Schmidtke, Martina C. Cornel

    Vydáno 2011
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  20. 20
    Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

    Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? Autor Anna Middleton, Richard Milne, Mohamed A. Almarri, Shamim Anwer, Jerome Atutornu, Elena E. Baranova, Paul Bevan, María Cerezo, Yali Cong, Christine Critchley, Josepine Fernow, Peter Goodhand, Qurratulain Hasan, Aiko Hibino, Gry Houeland, Heidi Howard, Sharafat Hussain, Charlotta Ingvoldstad Malmgren, Vera L. Izhevskaya, Aleksandra Jędrzejak, Jinhong Cao, Megumi Kimura, Erika Kleiderman, Brandi Leach, Keying Liu, Deborah Mascalzoni, Álvaro Mendes, Jusaku Minari, Nan Wang, Dianne Nicol, Emilia Niemiec, Christine Patch, Jack Pollard, Barbara Prainsack, Marie Rivière, Lauren Robarts, Jonathan Roberts, Virginia Romano, Haytham A. Sheerah, James Smith, A Soulier, Claire Steed, Vigdís Stefànsdóttir, Cornelia Tandre, Adrian Thorogood, Torsten H. Voigt, Anne V. West, Go Yoshizawa, Katherine I. Morley

    Vydáno 2020
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