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“A very big challenge”: a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England by Bettina Friedrich, Cecilia Vindrola-Padros, Anneke M. Lucassen, Anneke M. Lucassen, Chris Patch, Angus Clarke, Monica Lakhanpaul, Celine Lewis, Celine Lewis
Published 2024-01-01
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Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 2; peer review: 3 approved, 1 approved with reservations] by Saskia C. Sanderson, Lauren Roberts, Cecilia Vindrola-Padros, Sarah L. Wynn, Monica Lakhanpaul, Celine Lewis, Angus Clarke, James Buchanan, Bettina Friedrich, Emma Clement, Melissa Hill, Jillian Hastings-Ward, Anneke M. Lucassen, Ruth Horn, Alexandra Pickard, Chris Patch
Published 2022-02-01
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Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: 2 approved, 2 approved with reservations] by Saskia C. Sanderson, Lauren Roberts, Cecilia Vindrola-Padros, Sarah L. Wynn, Monica Lakhanpaul, Celine Lewis, Angus Clarke, James Buchanan, Bettina Friedrich, Emma Clement, Melissa Hill, Jillian Hastings-Ward, Anneke M. Lucassen, Ruth Horn, Alexandra Pickard, Chris Patch
Published 2021-11-01
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Analysis of the Phenotypes in the Rett Networked Database by Elisa Frullanti, Filomena T. Papa, Elisa Grillo, Angus Clarke, Bruria Ben-Zeev, Mercedes Pineda, Nadia Bahi-Buisson, Thierry Bienvenu, Judith Armstrong, Ana Roche Martinez, Francesca Mari, Andreea Nissenkorn, Caterina Lo Rizzo, Edvige Veneselli, Silvia Russo, Aglaia Vignoli, Giorgio Pini, Milena Djuric, Anne-Marie Bisgaard, Kirstine Ravn, Vlatka Mejaski Bosnjak, Joussef Hayek, Rajni Khajuria, Barbara Montomoli, Francesca Cogliati, Maria Pintaudi, Kinga Hadzsiev, Dana Craiu, Victoria Voinova, Aleksandra Djukic, Laurent Villard, Alessandra Renieri
Published 2019-01-01
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