Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur. J. Hum. Genet. 2018
Times Cited: 4
Times Cited: 4
Times Cited
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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
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet. Med. 2013
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet. Med. 2013
100
Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing.
Elli G Gourna, Natalie Armstrong, Susan E Wallace. Eur. J. Hum. Genet. 2016
Elli G Gourna, Natalie Armstrong, Susan E Wallace. Eur. J. Hum. Genet. 2016
50
Towards a European consensus for reporting incidental findings during clinical NGS testing.
Jayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, Conny van Ravenswaaij-Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon-Thomsen, Philippos Patsalis, Joris Vermeesch,[...]. Eur. J. Hum. Genet. 2015
Jayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, Conny van Ravenswaaij-Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon-Thomsen, Philippos Patsalis, Joris Vermeesch,[...]. Eur. J. Hum. Genet. 2015
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
Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice.
Myra I Roche, Jonathan S Berg. 2015
Myra I Roche, Jonathan S Berg. 2015
50
Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur. J. Hum. Genet. 2016
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur. J. Hum. Genet. 2016
50
Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling.
Lacey A Smith, Jessica Douglas, Alicia A Braxton, Kate Kramer. J Genet Couns 2015
Lacey A Smith, Jessica Douglas, Alicia A Braxton, Kate Kramer. J Genet Couns 2015
50
Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.
Nancy R Downing, Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Christian M Simon. Patient Educ Couns 2013
Nancy R Downing, Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Christian M Simon. Patient Educ Couns 2013
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
The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
50
The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.
G M Christenhusz, K Devriendt, H Peeters, H Van Esch, K Dierickx. Clin. Genet. 2014
G M Christenhusz, K Devriendt, H Peeters, H Van Esch, K Dierickx. Clin. Genet. 2014
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
Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur. J. Hum. Genet. 2018
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur. J. Hum. Genet. 2018
25
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
25
Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
25
Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet. Med. 2013
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet. Med. 2013
25
Reporting practices for unsolicited and secondary findings from next-generation sequencing technologies: Perspectives of laboratory personnel.
Danya F Vears, Karine Sénécal, Pascal Borry. Hum. Mutat. 2017
Danya F Vears, Karine Sénécal, Pascal Borry. Hum. Mutat. 2017
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How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis.
D F Vears, E Niemiec, H C Howard, P Borry. Clin. Genet. 2018
D F Vears, E Niemiec, H C Howard, P Borry. Clin. Genet. 2018
25
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet. Med. 2017
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet. Med. 2017
25
Views of genetics health professionals on the return of genomic results.
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
25
Newborn, carrier, and early childhood screening recommendations for fragile X.
Liane Abrams, Amy Cronister, William T Brown, Flora Tassone, Stephanie L Sherman, Brenda Finucane, Allyn McConkie-Rosell, Randi Hagerman, Walter E Kaufmann, Jonathan Picker,[...]. Pediatrics 2012
Liane Abrams, Amy Cronister, William T Brown, Flora Tassone, Stephanie L Sherman, Brenda Finucane, Allyn McConkie-Rosell, Randi Hagerman, Walter E Kaufmann, Jonathan Picker,[...]. Pediatrics 2012
25
Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
25
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe, Timothy Carey, Kristy R Crooks, Brian C Jensen, Eric T Juengst, Kristy Lee,[...]. Genet. Med. 2016
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe, Timothy Carey, Kristy R Crooks, Brian C Jensen, Eric T Juengst, Kristy Lee,[...]. Genet. Med. 2016
25
"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
25
Methods of data collection in qualitative research: interviews and focus groups.
P Gill, K Stewart, E Treasure, B Chadwick. Br Dent J 2008
P Gill, K Stewart, E Treasure, B Chadwick. Br Dent J 2008
25
Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues).
Christine Weiner. Am. J. Epidemiol. 2014
Christine Weiner. Am. J. Epidemiol. 2014
25
Clinical genetic counselors: An asset in the era of precision medicine.
Catherine A L Wicklund, Debra A Duquette, Amy L Swanson. Am J Med Genet C Semin Med Genet 2018
Catherine A L Wicklund, Debra A Duquette, Amy L Swanson. Am J Med Genet C Semin Med Genet 2018
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Secondary findings from next-generation sequencing: what does actionable in childhood really mean?
Julie Richer, Anne-Marie Laberge. Genet. Med. 2019
Julie Richer, Anne-Marie Laberge. Genet. Med. 2019
25
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
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Threat to Parental Role: A Possible Mechanism of Altered Self-Concept Related to Carrier Knowledge.
A McConkie-Rosell, B M DeVellis. J Genet Couns 2000
A McConkie-Rosell, B M DeVellis. J Genet Couns 2000
25
A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs.
Debra S Brandt, Laura Shinkunas, Stephen L Hillis, Sandra E Daack-Hirsch, Martha Driessnack, Nancy R Downing, Megan F Liu, Lisa L Shah, Janet K Williams, Christian M Simon. J Genet Couns 2013
Debra S Brandt, Laura Shinkunas, Stephen L Hillis, Sandra E Daack-Hirsch, Martha Driessnack, Nancy R Downing, Megan F Liu, Lisa L Shah, Janet K Williams, Christian M Simon. J Genet Couns 2013
25
Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet. Med. 2013
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet. Med. 2013
25
Personal utility in genomic testing: is there such a thing?
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. J Med Ethics 2015
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. J Med Ethics 2015
25
Progress in the management of neonatal sepsis: the importance of a consensus definition.
James L Wynn, Richard A Polin. Pediatr. Res. 2018
James L Wynn, Richard A Polin. Pediatr. Res. 2018
25
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet. Med. 2015
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet. Med. 2015
25
ACMG recommendations on incidental findings are flawed scientifically and ethically.
Neil A Holtzman. Genet. Med. 2013
Neil A Holtzman. Genet. Med. 2013
25
Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups.
Allison Tong, Peter Sainsbury, Jonathan Craig. Int J Qual Health Care 2007
Allison Tong, Peter Sainsbury, Jonathan Craig. Int J Qual Health Care 2007
25
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
. Genet. Med. 2015
. Genet. Med. 2015
25
Living with genetic risk: effect on adolescent self-concept.
Allyn McConkie-Rosell, Gail A Spiridigliozzi, Elizabeth Melvin, Deborah V Dawson, Ave M Lachiewicz. Am J Med Genet C Semin Med Genet 2008
Allyn McConkie-Rosell, Gail A Spiridigliozzi, Elizabeth Melvin, Deborah V Dawson, Ave M Lachiewicz. Am J Med Genet C Semin Med Genet 2008
25
"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
25
ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet. Med. 2013
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet. Med. 2013
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Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur. J. Hum. Genet. 2017
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur. J. Hum. Genet. 2017
25
Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease.
Katie Fiallos, Carolyn Applegate, Debra Jh Mathews, Juli Bollinger, Amanda L Bergner, Cynthia A James. Eur. J. Hum. Genet. 2017
Katie Fiallos, Carolyn Applegate, Debra Jh Mathews, Juli Bollinger, Amanda L Bergner, Cynthia A James. Eur. J. Hum. Genet. 2017
25
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
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Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur. J. Hum. Genet. 2016
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur. J. Hum. Genet. 2016
25
Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
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Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
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Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey.
M Lefebvre, D Sanlaville, N Marle, C Thauvin-Robinet, E Gautier, S E Chehadeh, A-L Mosca-Boidron, J Thevenon, P Edery, M-P Alex-Cordier,[...]. Clin. Genet. 2016
M Lefebvre, D Sanlaville, N Marle, C Thauvin-Robinet, E Gautier, S E Chehadeh, A-L Mosca-Boidron, J Thevenon, P Edery, M-P Alex-Cordier,[...]. Clin. Genet. 2016
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Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing.
Stefanie Weber, Anja K Büscher, Henning Hagmann, Max C Liebau, Christian Heberle, Michael Ludwig, Sabine Rath, Martin Alberer, Antje Beissert, Martin Zenker,[...]. Pediatr. Nephrol. 2016
Stefanie Weber, Anja K Büscher, Henning Hagmann, Max C Liebau, Christian Heberle, Michael Ludwig, Sabine Rath, Martin Alberer, Antje Beissert, Martin Zenker,[...]. Pediatr. Nephrol. 2016
25
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.