Carrie Louise Hammond, Josh Matthew Willoughby, Michael James Parker. Arch. Dis. Child. 2018
Times Cited: 2
Times Cited: 2
Times Cited
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Similarity
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
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
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
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet. Med. 2017
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet. Med. 2017
50
How do providers discuss the results of pediatric exome sequencing with families?
Sarah A Walser, Allison Werner-Lin, Rebecca Mueller, Victoria A Miller, Sawona Biswas, Barbara A Bernhardt. Per Med 2017
Sarah A Walser, Allison Werner-Lin, Rebecca Mueller, Victoria A Miller, Sawona Biswas, Barbara A Bernhardt. Per Med 2017
50
Mainstreaming genetics: a comparative review of clinical services for inherited cardiovascular conditions in the UK.
Hilary Burton, C Alberg, A Stewart. Public Health Genomics 2010
Hilary Burton, C Alberg, A Stewart. Public Health Genomics 2010
50
The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
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.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat. Rev. Genet. 2018
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat. Rev. Genet. 2018
50
Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur. J. Hum. Genet. 2013
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur. J. Hum. Genet. 2013
50
Physicians' perspectives on receiving unsolicited genomic results.
Douglas B Pet, Ingrid A Holm, Janet L Williams, Melanie F Myers, Laurie L Novak, Kyle B Brothers, Georgia L Wiesner, Ellen W Clayton. Genet Med 2019
Douglas B Pet, Ingrid A Holm, Janet L Williams, Melanie F Myers, Laurie L Novak, Kyle B Brothers, Georgia L Wiesner, Ellen W Clayton. Genet Med 2019
50
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases.
David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont. J. Med. Genet. 2019
David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont. J. Med. Genet. 2019
50
Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study.
A A Lemke, D Bick, D Dimmock, P Simpson, R Veith. Clin. Genet. 2013
A A Lemke, D Bick, D Dimmock, P Simpson, R Veith. Clin. Genet. 2013
50
"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
50
Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results.
Courtney Berrios, Cynthia A James, Karen Raraigh, Juli Bollinger, Brittney Murray, Crystal Tichnell, Carolyn D Applegate, Amanda L Bergner. J Genet Couns 2018
Courtney Berrios, Cynthia A James, Karen Raraigh, Juli Bollinger, Brittney Murray, Crystal Tichnell, Carolyn D Applegate, Amanda L Bergner. J Genet Couns 2018
50
"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am. J. Med. Genet. A 2012
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am. J. Med. Genet. A 2012
50
50
"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet. Med. 2018
Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet. Med. 2018
50
Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am. J. Hum. Genet. 2014
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am. J. Hum. Genet. 2014
50
Experiences with obtaining informed consent for genomic sequencing.
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am. J. Med. Genet. A 2015
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am. J. Med. Genet. A 2015
50
Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
50
A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.
Catherine L Bennett, Sarah E Burke, Hilary Burton, Peter A Farndon. BMC Health Serv Res 2010
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.
Christopher Gyngell, Ainsley J Newson, Dominic Wilkinson, Zornitza Stark, Julian Savulescu. Pediatrics 2019
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.
Sarah V Clowes Candadai, Megan C Sikes, Jenny M Thies, Amanda S Freed, James T Bennett. J Genet Couns 2019
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.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
50
Translating genomic testing results for pediatric critical care: Opportunities for genetic counselors.
Natalie Deuitch, Sandra Soo-Jin Lee, Danton Char. J Genet Couns 2020
Natalie Deuitch, Sandra Soo-Jin Lee, Danton Char. J Genet Couns 2020
100
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.
Lauge Farnaes, Amber Hildreth, Nathaly M Sweeney, Michelle M Clark, Shimul Chowdhury, Shareef Nahas, Julie A Cakici, Wendy Benson, Robert H Kaplan, Richard Kronick,[...].  2018
Lauge Farnaes, Amber Hildreth, Nathaly M Sweeney, Michelle M Clark, Shimul Chowdhury, Shareef Nahas, Julie A Cakici, Wendy Benson, Robert H Kaplan, Richard Kronick,[...].  2018
50
Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study.
Lisa M Ballard, Rachel H Horton, Sandi Dheensa, Angela Fenwick, Anneke M Lucassen. Eur J Hum Genet 2020
Lisa M Ballard, Rachel H Horton, Sandi Dheensa, Angela Fenwick, Anneke M Lucassen. Eur J Hum Genet 2020
100
Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project.
Saskia C Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S Chitty. BMJ Open 2019
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.
Julie Weiner, Jotishna Sharma, John Lantos, Howard Kilbride. Arch Pediatr Adolesc Med 2011
Julie Weiner, Jotishna Sharma, John Lantos, Howard Kilbride. Arch Pediatr Adolesc Med 2011
50
Psychological Outcomes in Parents of Critically Ill Hospitalized Children.
Robyn Stremler, Summer Haddad, Eleanor Pullenayegum, Christopher Parshuram. J Pediatr Nurs 2017
Robyn Stremler, Summer Haddad, Eleanor Pullenayegum, Christopher Parshuram. J Pediatr Nurs 2017
50
Parents of newborns in the NICU enrolled in genome sequencing research: hopeful, but not naïve.
Courtney Berrios, Catherine Koertje, Janelle Noel-MacDonnell, Sarah Soden, John Lantos. Genet Med 2020
Courtney Berrios, Catherine Koertje, Janelle Noel-MacDonnell, Sarah Soden, John Lantos. Genet Med 2020
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.
Cathrine Monrad Hagen, Thor Willy Ruud Hansen. Pediatr Crit Care Med 2004
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.
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
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
Cause of Death of Infants and Children in the Intensive Care Unit: Parents' Recall vs Chart Review.
Dorothy Brooten, JoAnne M Youngblut, Carmen Caicedo, Lynn Seagrave, G Patricia Cantwell, Balagangadhar Totapally. Am. J. Crit. Care 2016
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.
Brett Knapp, Carole Decker, John D Lantos. Pediatrics 2019
Brett Knapp, Carole Decker, John D Lantos. Pediatrics 2019
50
Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children.
Lamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, Suzanne Drury, Louise Ocaka, Andrey Gagunashvili, Polona Le Quesne Stabej, Chiara Bacchelli, Nital Jani, Shamima Rahman,[...]. J. Med. Genet. 2018
Lamia Mestek-Boukhibar, Emma Clement, Wendy D Jones, Suzanne Drury, Louise Ocaka, Andrey Gagunashvili, Polona Le Quesne Stabej, Chiara Bacchelli, Nital Jani, Shamima Rahman,[...]. J. Med. Genet. 2018
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.
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
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
Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study.
Celine Lewis, Saskia Sanderson, Melissa Hill, Chris Patch, Beverly Searle, Amy Hunter, Lyn S Chitty. Eur J Hum Genet 2020
Celine Lewis, Saskia Sanderson, Melissa Hill, Chris Patch, Beverly Searle, Amy Hunter, Lyn S Chitty. Eur J Hum Genet 2020
50
Rapid Targeted Genomics in Critically Ill Newborns.
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
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.
Danton S Char, Sandra Soo-Jin Lee, David Magnus, Mildred Cho. Genet. Med. 2018
Danton S Char, Sandra Soo-Jin Lee, David Magnus, Mildred Cho. Genet. Med. 2018
50
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.