Carrie Louise Hammond, Josh Matthew Willoughby, Michael James Parker. Arch Dis Child 2018
Times Cited: 2
Times Cited: 2
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Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
100
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50
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50
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Hilary Burton, C Alberg, A Stewart. Public Health Genomics 2010
50
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Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
50
Paediatric genomics: diagnosing rare disease in children.
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Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
50
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50
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50
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50
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50
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50
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50
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50
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50
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Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Hum Genet 2014
50
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50
Clinical providers' experiences with returning results from genomic sequencing: an interview study.
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50
A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.
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Catherine L Bennett, Sarah E Burke, Hilary Burton, Peter A Farndon. BMC Health Serv Res 2010
50
Emotional distress of mothers of hospitalized children.
J Berenbaum, J Hatcher. J Pediatr Psychol 1992
J Berenbaum, J Hatcher. J Pediatr Psychol 1992
50
Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.
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Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
50
Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges.
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Sarah V Clowes Candadai, Megan C Sikes, Jenny M Thies, Amanda S Freed, James T Bennett. J Genet Couns 2019
50
Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
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Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
50
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Natalie Deuitch, Sandra Soo-Jin Lee, Danton Char. J Genet Couns 2020
50
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Lauge Farnaes, Amber Hildreth, Nathaly M Sweeney, Michelle M Clark, Shimul Chowdhury, Shareef Nahas, Julie A Cakici, Wendy Benson, Robert H Kaplan, Richard Kronick,[...]. NPJ Genom Med 2018
50
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Lisa M Ballard, Rachel H Horton, Sandi Dheensa, Angela Fenwick, Anneke M Lucassen. Eur J Hum Genet 2020
50
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Saskia C Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S Chitty. BMJ Open 2019
50
Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
Laura M Amendola, Jill O Robinson, Ragan Hart, Sawona Biswas, Kaitlyn Lee, Barbara A Bernhardt, Kelly East, Marian J Gilmore, Tia L Kauffman, Katie L Lewis,[...]. J Genet Couns 2018
Laura M Amendola, Jill O Robinson, Ragan Hart, Sawona Biswas, Kaitlyn Lee, Barbara A Bernhardt, Kelly East, Marian J Gilmore, Tia L Kauffman, Katie L Lewis,[...]. J Genet Couns 2018
50
How infants die in the neonatal intensive care unit: trends from 1999 through 2008.
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Julie Weiner, Jotishna Sharma, John Lantos, Howard Kilbride. Arch Pediatr Adolesc Med 2011
50
Psychological Outcomes in Parents of Critically Ill Hospitalized Children.
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Robyn Stremler, Summer Haddad, Eleanor Pullenayegum, Christopher Parshuram. J Pediatr Nurs 2017
50
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50
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
Linyan Meng, Mohan Pammi, Anirudh Saronwala, Pilar Magoulas, Andrew Ray Ghazi, Francesco Vetrini, Jing Zhang, Weimin He, Avinash V Dharmadhikari, Chunjing Qu,[...]. JAMA Pediatr 2017
Linyan Meng, Mohan Pammi, Anirudh Saronwala, Pilar Magoulas, Andrew Ray Ghazi, Francesco Vetrini, Jing Zhang, Weimin He, Avinash V Dharmadhikari, Chunjing Qu,[...]. JAMA Pediatr 2017
50
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.
Zornitza Stark, Amy Nisselle, Belinda McClaren, Fiona Lynch, Stephanie Best, Janet C Long, Melissa Martyn, Chirag Patel, Luregn J Schlapbach, Christopher Barnett,[...]. Eur J Hum Genet 2019
Zornitza Stark, Amy Nisselle, Belinda McClaren, Fiona Lynch, Stephanie Best, Janet C Long, Melissa Martyn, Chirag Patel, Luregn J Schlapbach, Christopher Barnett,[...]. Eur J Hum Genet 2019
50
Deaths in a neonatal intensive care unit: a 10-year perspective.
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Cathrine Monrad Hagen, Thor Willy Ruud Hansen. Pediatr Crit Care Med 2004
50
Qualitative data analysis for health services research: developing taxonomy, themes, and theory.
Elizabeth H Bradley, Leslie A Curry, Kelly J Devers. Health Serv Res 2007
Elizabeth H Bradley, Leslie A Curry, Kelly J Devers. Health Serv Res 2007
50
Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet Med 2018
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet Med 2018
50
Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
50
Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children.
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Courtney E French, Isabelle Delon, Helen Dolling, Alba Sanchis-Juan, Olga Shamardina, Karyn Mégy, Stephen Abbs, Topun Austin, Sarah Bowdin, Ricardo G Branco,[...]. Intensive Care Med 2019
50
Potential Psychosocial Risks of Sequencing Newborns.
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
50
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Dorothy Brooten, JoAnne M Youngblut, Carmen Caicedo, Lynn Seagrave, G Patricia Cantwell, Balagangadhar Totapally. Am J Crit Care 2016
50
Neonatologists' Attitudes About Diagnostic Whole-Genome Sequencing in the NICU.
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Brett Knapp, Carole Decker, John D Lantos. Pediatrics 2019
50
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50
Methodological and ethical issues related to qualitative telephone interviews on sensitive topics.
Meredith Mealer, Jacqueline Jones Rn. Nurse Res 2014
Meredith Mealer, Jacqueline Jones Rn. Nurse Res 2014
50
Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU.
Erica F Sanford, Michelle M Clark, Lauge Farnaes, Matthew R Williams, James C Perry, Elizabeth G Ingulli, Nathaly M Sweeney, Ami Doshi, Jeffrey J Gold, Benjamin Briggs,[...]. Pediatr Crit Care Med 2019
Erica F Sanford, Michelle M Clark, Lauge Farnaes, Matthew R Williams, James C Perry, Elizabeth G Ingulli, Nathaly M Sweeney, Ami Doshi, Jeffrey J Gold, Benjamin Briggs,[...]. Pediatr Crit Care Med 2019
50
Is there a bias against telephone interviews in qualitative research?
Gina Novick. Res Nurs Health 2008
Gina Novick. Res Nurs Health 2008
50
Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics.
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M J Szego, M S Meyn, C Shuman, R Zlotnik Shaul, J A Anderson, S Bowdin, N Monfared, R Z Hayeems. Eur J Med Genet 2019
50
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Celine Lewis, Saskia Sanderson, Melissa Hill, Chris Patch, Beverly Searle, Amy Hunter, Lyn S Chitty. Eur J Hum Genet 2020
50
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Cleo C van Diemen, Wilhelmina S Kerstjens-Frederikse, Klasien A Bergman, Tom J de Koning, Birgit Sikkema-Raddatz, Joeri K van der Velde, Kristin M Abbott, Johanna C Herkert, Katharina Löhner, Patrick Rump,[...]. Pediatrics 2017
50
Anticipating uncertainty and irrevocable decisions: provider perspectives on implementing whole-genome sequencing in critically ill children with heart disease.
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50
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