Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
Times Cited: 11
Times Cited: 11
Times Cited
Times Co-cited
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
45
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
45
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
45
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
45
Incidental findings in the era of whole genome sequencing?
Erik Parens, Paul Appelbaum, Wendy Chung. Hastings Cent Rep 2013
Erik Parens, Paul Appelbaum, Wendy Chung. Hastings Cent Rep 2013
36
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
36
Finding people who will tell you their thoughts on genomics-recruitment strategies for social sciences research.
A Middleton, E Bragin, M Parker. 2014
A Middleton, E Bragin, M Parker. 2014
27
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur. J. Hum. Genet. 2013
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur. J. Hum. Genet. 2013
27
Potential research participants support the return of raw sequence data.
Anna Middleton, Caroline F Wright, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Michael Parker. J. Med. Genet. 2015
Anna Middleton, Caroline F Wright, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Michael Parker. J. Med. Genet. 2015
27
The Danish Blood Donor Study: a large, prospective cohort and biobank for medical research.
O B Pedersen, C Erikstrup, S R Kotzé, E Sørensen, M S Petersen, K Grau, H Ullum. Vox Sang. 2012
O B Pedersen, C Erikstrup, S R Kotzé, E Sørensen, M S Petersen, K Grau, H Ullum. Vox Sang. 2012
27
Stakeholders in psychiatry and their attitudes toward receiving pertinent and incident findings in genomic research.
Anna Sundby, Merete W Boolsen, Kristoffer S Burgdorf, Henrik Ullum, Thomas F Hansen, Anna Middleton, Ole Mors. Am. J. Med. Genet. A 2017
Anna Sundby, Merete W Boolsen, Kristoffer S Burgdorf, Henrik Ullum, Thomas F Hansen, Anna Middleton, Ole Mors. Am. J. Med. Genet. A 2017
27
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
27
Exploring concordance and discordance for return of incidental findings from clinical sequencing.
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet. Med. 2012
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet. Med. 2012
27
Effect of Public Deliberation on Attitudes toward Return of Secondary Results in Genomic Sequencing.
Michele C Gornick, Aaron M Scherer, Erica J Sutton, Kerry A Ryan, Nicole L Exe, Ming Li, Wendy R Uhlmann, Scott Y H Kim, J Scott Roberts, Raymond G De Vries. J Genet Couns 2017
Michele C Gornick, Aaron M Scherer, Erica J Sutton, Kerry A Ryan, Nicole L Exe, Ming Li, Wendy R Uhlmann, Scott Y H Kim, J Scott Roberts, Raymond G De Vries. J Genet Couns 2017
27
Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
27
Can I access my personal genome? The current legal position in the UK.
Jane Kaye, Nadja Kanellopoulou, Naomi Hawkins, Heather Gowans, Liam Curren, Karen Melham. Med Law Rev 2014
Jane Kaye, Nadja Kanellopoulou, Naomi Hawkins, Heather Gowans, Liam Curren, Karen Melham. Med Law Rev 2014
18
18
Using whole-exome sequencing to identify inherited causes of autism.
Timothy W Yu, Maria H Chahrour, Michael E Coulter, Sarn Jiralerspong, Kazuko Okamura-Ikeda, Bulent Ataman, Klaus Schmitz-Abe, David A Harmin, Mazhar Adli, Athar N Malik,[...]. Neuron 2013
Timothy W Yu, Maria H Chahrour, Michael E Coulter, Sarn Jiralerspong, Kazuko Okamura-Ikeda, Bulent Ataman, Klaus Schmitz-Abe, David A Harmin, Mazhar Adli, Athar N Malik,[...]. Neuron 2013
18
Empirical research on the ethics of genomic research.
Anna Middleton, Michael Parker, Caroline F Wright, Eugene Bragin, Matthew E Hurles. Am. J. Med. Genet. A 2013
Anna Middleton, Michael Parker, Caroline F Wright, Eugene Bragin, Matthew E Hurles. Am. J. Med. Genet. A 2013
20
Personal genome research : what should the participant be told?
Amy L McGuire, James R Lupski. Trends Genet. 2010
Amy L McGuire, James R Lupski. Trends Genet. 2010
18
Do participants in genome sequencing studies of psychiatric disorders wish to be informed of their results? A survey study.
Elise T Bui, Natalie K Anderson, Layla Kassem, Francis J McMahon. PLoS ONE 2014
Elise T Bui, Natalie K Anderson, Layla Kassem, Francis J McMahon. PLoS ONE 2014
18
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
. Genet. Med. 2015
. Genet. Med. 2015
18
The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur. J. Hum. Genet. 2006
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur. J. Hum. Genet. 2006
18
Online questionnaire development: using film to engage participants and then gather attitudes towards the sharing of genomic data.
A Middleton, E Bragin, K I Morley, M Parker. Soc Sci Res 2014
A Middleton, E Bragin, K I Morley, M Parker. Soc Sci Res 2014
18
Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.
Kyle B Brothers, Kelly M East, Whitley V Kelley, M Frances Wright, Matthew J Westbrook, Carla A Rich, Kevin M Bowling, Edward J Lose, E Martina Bebin, Shirley Simmons,[...]. Genet. Med. 2017
Kyle B Brothers, Kelly M East, Whitley V Kelley, M Frances Wright, Matthew J Westbrook, Carla A Rich, Kevin M Bowling, Edward J Lose, E Martina Bebin, Shirley Simmons,[...]. Genet. Med. 2017
18
18
Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research.
Julia Wynn, Josue Martinez, Jimmy Duong, Codruta Chiuzan, Jo C Phelan, Abby Fyer, Robert L Klitzman, Paul S Appelbaum, Wendy K Chung. J Genet Couns 2017
Julia Wynn, Josue Martinez, Jimmy Duong, Codruta Chiuzan, Jo C Phelan, Abby Fyer, Robert L Klitzman, Paul S Appelbaum, Wendy K Chung. J Genet Couns 2017
18
The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
18
Attitudes of parents toward the return of targeted and incidental genomic research findings in children.
Conrad V Fernandez, Eric Bouffet, David Malkin, Nada Jabado, Colleen O'Connell, Denise Avard, Bartha M Knoppers, Meghan Ferguson, Kym M Boycott, Poul H Sorensen,[...]. Genet. Med. 2014
Conrad V Fernandez, Eric Bouffet, David Malkin, Nada Jabado, Colleen O'Connell, Denise Avard, Bartha M Knoppers, Meghan Ferguson, Kym M Boycott, Poul H Sorensen,[...]. Genet. Med. 2014
18
Overcoming recruitment barriers revealed high readiness to participate and low dropout rate among people with schizophrenia in a randomized controlled trial testing the effect of a Guided Self-Determination intervention.
Rikke Jørgensen, Povl Munk-Jørgensen, Paul H Lysaker, Kelly D Buck, Lars Hansson, Vibeke Zoffmann. BMC Psychiatry 2014
Rikke Jørgensen, Povl Munk-Jørgensen, Paul H Lysaker, Kelly D Buck, Lars Hansson, Vibeke Zoffmann. BMC Psychiatry 2014
18
Assessing hypothetical scenario methodology in genetic susceptibility testing analog studies: a quantitative review.
Susan Persky, Kimberly A Kaphingst, Celeste M Condit, Colleen M McBride. Genet. Med. 2007
Susan Persky, Kimberly A Kaphingst, Celeste M Condit, Colleen M McBride. Genet. Med. 2007
18
Is "incidental finding" the best term?: a study of patients' preferences.
Nina Tan, Laura M Amendola, Julianne M O'Daniel, Amber Burt, Martha J Horike-Pyne, Lacey Boshe, Gail E Henderson, Christine Rini, Myra I Roche, Fuki M Hisama,[...]. Genet. Med. 2017
Nina Tan, Laura M Amendola, Julianne M O'Daniel, Amber Burt, Martha J Horike-Pyne, Lacey Boshe, Gail E Henderson, Christine Rini, Myra I Roche, Fuki M Hisama,[...]. Genet. Med. 2017
18
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
Brian H Shirts, Joseph S Salama, Samuel J Aronson, Wendy K Chung, Stacy W Gray, Lucia A Hindorff, Gail P Jarvik, Sharon E Plon, Elena M Stoffel, Peter Z Tarczy-Hornoch,[...]. J Am Med Inform Assoc 2015
Brian H Shirts, Joseph S Salama, Samuel J Aronson, Wendy K Chung, Stacy W Gray, Lucia A Hindorff, Gail P Jarvik, Sharon E Plon, Elena M Stoffel, Peter Z Tarczy-Hornoch,[...]. J Am Med Inform Assoc 2015
18
Circulating Tumor DNA Reveals Clinically Actionable Somatic Genome of Metastatic Bladder Cancer.
Gillian Vandekerkhove, Tilman Todenhöfer, Matti Annala, Werner J Struss, Amanda Wong, Kevin Beja, Elie Ritch, Sonal Brahmbhatt, Stanislav V Volik, Jörg Hennenlotter,[...]. Clin. Cancer Res. 2017
Gillian Vandekerkhove, Tilman Todenhöfer, Matti Annala, Werner J Struss, Amanda Wong, Kevin Beja, Elie Ritch, Sonal Brahmbhatt, Stanislav V Volik, Jörg Hennenlotter,[...]. Clin. Cancer Res. 2017
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Health literacy interventions and outcomes: an updated systematic review.
Nancy D Berkman, Stacey L Sheridan, Katrina E Donahue, David J Halpern, Anthony Viera, Karen Crotty, Audrey Holland, Michelle Brasure, Kathleen N Lohr, Elizabeth Harden,[...]. Evid Rep Technol Assess (Full Rep) 2011
Nancy D Berkman, Stacey L Sheridan, Katrina E Donahue, David J Halpern, Anthony Viera, Karen Crotty, Audrey Holland, Michelle Brasure, Kathleen N Lohr, Elizabeth Harden,[...]. Evid Rep Technol Assess (Full Rep) 2011
18
The impact of the format of graphical presentation on health-related knowledge and treatment choices.
Sarah T Hawley, Brian Zikmund-Fisher, Peter Ubel, Aleksandra Jancovic, Todd Lucas, Angela Fagerlin. Patient Educ Couns 2008
Sarah T Hawley, Brian Zikmund-Fisher, Peter Ubel, Aleksandra Jancovic, Todd Lucas, Angela Fagerlin. Patient Educ Couns 2008
18
The Impact of Patient Participation in Health Decisions Within Medical Encounters: A Systematic Review.
Marla L Clayman, Carma L Bylund, Betty Chewning, Gregory Makoul. Med Decis Making 2016
Marla L Clayman, Carma L Bylund, Betty Chewning, Gregory Makoul. Med Decis Making 2016
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Characterizing genetic variants for clinical action.
Erin M Ramos, Corina Din-Lovinescu, Jonathan S Berg, Lisa D Brooks, Audrey Duncanson, Michael Dunn, Peter Good, Tim J P Hubbard, Gail P Jarvik, Christopher O'Donnell,[...]. Am J Med Genet C Semin Med Genet 2014
Erin M Ramos, Corina Din-Lovinescu, Jonathan S Berg, Lisa D Brooks, Audrey Duncanson, Michael Dunn, Peter Good, Tim J P Hubbard, Gail P Jarvik, Christopher O'Donnell,[...]. Am J Med Genet C Semin Med Genet 2014
18
Comprehensive Characterization of Molecular Differences in Cancer between Male and Female Patients.
Yuan Yuan, Lingxiang Liu, Hu Chen, Yumeng Wang, Yanxun Xu, Huzhang Mao, Jun Li, Gordon B Mills, Yongqian Shu, Liang Li,[...]. Cancer Cell 2016
Yuan Yuan, Lingxiang Liu, Hu Chen, Yumeng Wang, Yanxun Xu, Huzhang Mao, Jun Li, Gordon B Mills, Yongqian Shu, Liang Li,[...]. Cancer Cell 2016
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Effect of various risk/benefit trade-offs on parents' understanding of a pediatric research study.
Alan R Tait, Brian J Zikmund-Fisher, Angela Fagerlin, Terri Voepel-Lewis. Pediatrics 2010
Alan R Tait, Brian J Zikmund-Fisher, Angela Fagerlin, Terri Voepel-Lewis. Pediatrics 2010
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Genomic Alterations in Cell-Free DNA and Enzalutamide Resistance in Castration-Resistant Prostate Cancer.
Alexander W Wyatt, Arun A Azad, Stanislav V Volik, Matti Annala, Kevin Beja, Brian McConeghy, Anne Haegert, Evan W Warner, Fan Mo, Sonal Brahmbhatt,[...]. JAMA Oncol 2016
Alexander W Wyatt, Arun A Azad, Stanislav V Volik, Matti Annala, Kevin Beja, Brian McConeghy, Anne Haegert, Evan W Warner, Fan Mo, Sonal Brahmbhatt,[...]. JAMA Oncol 2016
18
A framework for genomic biomarker actionability and its use in clinical decision making.
Smruti J Vidwans, Michelle L Turski, Filip Janku, Ignacio Garrido-Laguna, Javier Munoz, Richard Schwab, Vivek Subbiah, Jordi Rodon, Razelle Kurzrock. 2014
Smruti J Vidwans, Michelle L Turski, Filip Janku, Ignacio Garrido-Laguna, Javier Munoz, Richard Schwab, Vivek Subbiah, Jordi Rodon, Razelle Kurzrock. 2014
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Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N. Engl. J. Med. 2014
Leslie G Biesecker, Robert C Green. N. Engl. J. Med. 2014
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Detection rate of actionable mutations in diverse cancers using a biopsy-free (blood) circulating tumor cell DNA assay.
Maria Schwaederle, Hatim Husain, Paul T Fanta, David E Piccioni, Santosh Kesari, Richard B Schwab, Kimberly C Banks, Richard B Lanman, AmirAli Talasaz, Barbara A Parker,[...]. Oncotarget 2016
Maria Schwaederle, Hatim Husain, Paul T Fanta, David E Piccioni, Santosh Kesari, Richard B Schwab, Kimberly C Banks, Richard B Lanman, AmirAli Talasaz, Barbara A Parker,[...]. Oncotarget 2016
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From days to hours: reporting clinically actionable variants from whole genome sequencing.
Sumit Middha, Saurabh Baheti, Steven N Hart, Jean-Pierre A Kocher. PLoS ONE 2014
Sumit Middha, Saurabh Baheti, Steven N Hart, Jean-Pierre A Kocher. PLoS ONE 2014
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Saying what you mean, meaning what you say: language, interaction and interpretation.
James Astor. J Anal Psychol 2011
James Astor. J Anal Psychol 2011
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Exome Sequencing of Cell-Free DNA from Metastatic Cancer Patients Identifies Clinically Actionable Mutations Distinct from Primary Disease.
Timothy M Butler, Katherine Johnson-Camacho, Myron Peto, Nicholas J Wang, Tara A Macey, James E Korkola, Theresa M Koppie, Christopher L Corless, Joe W Gray, Paul T Spellman. PLoS ONE 2015
Timothy M Butler, Katherine Johnson-Camacho, Myron Peto, Nicholas J Wang, Tara A Macey, James E Korkola, Theresa M Koppie, Christopher L Corless, Joe W Gray, Paul T Spellman. PLoS ONE 2015
18
Development and validation of the JAX Cancer Treatment Profile™ for detection of clinically actionable mutations in solid tumors.
Guruprasad Ananda, Susan Mockus, Micaela Lundquist, Vanessa Spotlow, Al Simons, Talia Mitchell, Grace Stafford, Vivek Philip, Timothy Stearns, Anuj Srivastava,[...]. Exp. Mol. Pathol. 2015
Guruprasad Ananda, Susan Mockus, Micaela Lundquist, Vanessa Spotlow, Al Simons, Talia Mitchell, Grace Stafford, Vivek Philip, Timothy Stearns, Anuj Srivastava,[...]. Exp. Mol. Pathol. 2015
18
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.