A citation-based method for searching scientific literature

Georgia L Wiesner, Alanna Kulchak Rahm, Paul Appelbaum, Sharon Aufox, Sarah T Bland, Carrie L Blout, Kurt D Christensen, Wendy K Chung, Ellen Wright Clayton, Robert C Green, Margaret H Harr, Nora Henrikson, Christin Hoell, Ingrid A Holm, Gail P Jarvik, Iftikhar J Kullo, Philip E Lammers, Eric B Larson, Noralane M Lindor, Maddalena Marasa, Melanie F Myers, Josh F Peterson, Cynthia A Prows, James D Ralston, Hila Milo Rasouly, Richard R Sharp, Maureen E Smith, Sara L Van Driest, Janet L Williams, Marc S Williams, Julia Wynn, Kathleen A Leppig. J Pers Med 2020
Times Cited: 12







List of co-cited articles
26 articles co-cited >1



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
814
50

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
236
33

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
33

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
33



Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.
Susan M Wolf, Laura M Amendola, Jonathan S Berg, Wendy K Chung, Ellen Wright Clayton, Robert C Green, Julie Harris-Wai, Gail E Henderson, Gail P Jarvik, Barbara A Koenig,[...]. Genet Med 2018
19
16

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalp√©, Bartha Maria Knoppers. Eur J Hum Genet 2019
34
16

Giving adolescents a voice: the types of genetic information adolescents choose to learn and why.
Josie Pervola, Melanie F Myers, Michelle L McGowan, Cynthia A Prows. Genet Med 2019
9
22

Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, Miranda L G Hallquist, Janet L Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M Savatt, Alyson E Evans, Loren M Butry,[...]. JAMA Netw Open 2018
77
16

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
16

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
178
16

Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.
Emilie S Zoltick, Michael D Linderman, Molly A McGinniss, Erica Ramos, Madeleine P Ball, George M Church, Debra G B Leonard, Stacey Pereira, Amy L McGuire, C Thomas Caskey,[...]. Genome Med 2019
18
16


Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank.
Noura S Abul-Husn, Emily R Soper, Jacqueline A Odgis, Sinead Cullina, Dean Bobo, Arden Moscati, Jessica E Rodriguez, Ruth J F Loos, Judy H Cho, Gillian M Belbin,[...]. Genome Med 2019
23
16

Clinical outcomes of a genomic screening program for actionable genetic conditions.
Adam H Buchanan, H Lester Kirchner, Marci L B Schwartz, Melissa A Kelly, Tara Schmidlen, Laney K Jones, Miranda L G Hallquist, Heather Rocha, Megan Betts, Rachel Schwiter,[...]. Genet Med 2020
13
16

Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium.
Michael D Linderman, Daiva E Nielsen, Robert C Green. J Pers Med 2016
29
16

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
59
16

Population genetic screening efficiently identifies carriers of autosomal dominant diseases.
J J Grzymski, G Elhanan, J A Morales Rosado, E Smith, K A Schlauch, R Read, C Rowan, N Slotnick, S Dabe, W J Metcalf,[...]. Nat Med 2020
22
16

Returning negative results to individuals in a genomic screening program: lessons learned.
Rita M Butterfield, James P Evans, Christine Rini, Kristine J Kuczynski, Margaret Waltz, R Jean Cadigan, Katrina A B Goddard, Kristin R Muessig, Gail E Henderson. Genet Med 2019
18
16

The REDCap consortium: Building an international community of software platform partners.
Paul A Harris, Robert Taylor, Brenda L Minor, Veida Elliott, Michelle Fernandez, Lindsay O'Neal, Laura McLeod, Giovanni Delacqua, Francesco Delacqua, Jacqueline Kirby,[...]. J Biomed Inform 2019
16

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
Meng Li, Caroline S Bennette, Laura M Amendola, M Ragan Hart, Patrick Heagerty, Bryan Comstock, Peter Tarczy-Hornoch, Stephanie M Fullerton, Dean A Regier, Wylie Burke,[...]. J Genet Couns 2019
20
16

A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire.
David Cella, Chanita Hughes, Amy Peterman, Chih-Hung Chang, Beth N Peshkin, Marc D Schwartz, Lari Wenzel, Amy Lemke, Alfred C Marcus, Caryn Lerman. Health Psychol 2002
166
16

How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation.
Jason L Vassy, J Kelly Davis, Christine Kirby, Ian J Richardson, Robert C Green, Amy L McGuire, Peter A Ubel. J Gen Intern Med 2018
9
22

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies.
Jill O Robinson, Julia Wynn, Barbara Biesecker, Leslie G Biesecker, Barbara Bernhardt, Kyle B Brothers, Wendy K Chung, Kurt D Christensen, Robert C Green, Amy L McGuire,[...]. Genet Med 2019
22
16

Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.
Robyn Fossey, David Kochan, Erin Winkler, Joel E Pacyna, Janet Olson, Stephen Thibodeau, John J Connolly, Margaret Harr, Meckenzie A Behr, Cynthia A Prows,[...]. J Pers Med 2018
26
16

Bench to bedside: mapping the moral terrain of clinical research.
Steven Joffe, Franklin G Miller. Hastings Cent Rep 2008
72
8

The research-treatment distinction: a problematic approach for determining which activities should have ethical oversight.
Nancy E Kass, Ruth R Faden, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
153
8

The historical foundations of the research-practice distinction in bioethics.
Tom L Beauchamp, Yashar Saghai. Theor Med Bioeth 2012
28
8

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
8



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
26
8

Managing conflicts of interest in the conduct of clinical trials.
Karine Morin, Herbert Rakatansky, Frank A Riddick, Leonard J Morse, John M O'Bannon, Michael S Goldrich, Priscilla Ray, Matthew Weiss, Robert M Sade, Monique A Spillman. JAMA 2002
139
8

Return of results: ethical and legal distinctions between research and clinical care.
Wylie Burke, Barbara J Evans, Gail P Jarvik. Am J Med Genet C Semin Med Genet 2014
69
8

Can research and care be ethically integrated?
Emily A Largent, Steven Joffe, Franklin G Miller. Hastings Cent Rep 2011
63
8


Adrift in the Gray Zone: IRB Perspectives on Research in the Learning Health System.
Sandra Soo-Jin Lee, Maureen Kelley, Mildred K Cho, Stephanie Alessi Kraft, Cyan James, Melissa Constantine, Adrienne N Meyer, Douglas Diekema, Alexander M Capron, Benjamin S Wilfond,[...]. AJOB Empir Bioeth 2016
18
8

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
8

What Results Should Be Returned from Opportunistic Screening in Translational Research?
Colin Me Halverson, Sarah H Jones, Laurie Novak, Christopher Simpson, Digna R Velez Edwards, Sifang Kathy Zhao, Ellen W Clayton. J Pers Med 2020
4
25

Clinical trials and medical care: defining the therapeutic misconception.
Gail E Henderson, Larry R Churchill, Arlene M Davis, Michele M Easter, Christine Grady, Steven Joffe, Nancy Kass, Nancy M P King, Charles W Lidz, Franklin G Miller,[...]. PLoS Med 2007
221
8

The therapeutic misconception: informed consent in psychiatric research.
P S Appelbaum, L H Roth, C Lidz. Int J Law Psychiatry 1982
376
8


Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
86
8

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
220
8

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
122
8


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
88
8

When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing.
Leila Jamal, Jill O Robinson, Kurt D Christensen, Jennifer Blumenthal-Barby, Melody J Slashinski, Denise Lautenbach Perry, Jason L Vassy, Julia Wycliff, Robert C Green, Amy L McGuire. AJOB Empir Bioeth 2017
24
8

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience.
Kathryn M Porter, Tia L Kauffman, Barbara A Koenig, Katie L Lewis, Heidi L Rehm, Carolyn Sue Richards, Natasha T Strande, Holly K Tabor, Susan M Wolf, Yaping Yang,[...]. Mol Genet Genomic Med 2018
7
14


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.