A citation-based method for searching scientific literature

Tanya Papaz, Eriskay Liston, Laura Zahavich, Dimitri J Stavropoulos, Rebekah K Jobling, Raymond H Kim, Miriam Reuter, Anastasia Miron, Erwin Oechslin, Tapas Mondal, Lynn Bergin, John F Smythe, Luis Altamirano-Diaz, Jane Lougheed, Roderick Yao, Oyediran Akinrinade, Jeroen Breckpot, Seema Mital. BMC Med Genomics 2019
Times Cited: 7







List of co-cited articles
23 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
842
71

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
241
57

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
57

Preferences for Return of Genetic Results Among Participants in the Jackson Heart Study and Framingham Heart Study.
Steven Joffe, Deborah E Sellers, Lynette Ekunwe, Donna Antoine-Lavigne, Sarah McGraw, Daniel Levy, Greta Lee Splansky. Circ Genom Precis Med 2019
6
50

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Yvonne Bombard, Kyle B Brothers, Sara Fitzgerald-Butt, Nanibaa' A Garrison, Leila Jamal, Cynthia A James, Gail P Jarvik, Jennifer B McCormick, Tanya N Nelson, Kelly E Ormond,[...]. Am J Hum Genet 2019
49
42

Pilot Study of Return of Genetic Results to Patients in Adult Nephrology.
Jordan G Nestor, Maddalena Marasa, Hila Milo-Rasouly, Emily E Groopman, S Ali Husain, Sumit Mohan, Hilda Fernandez, Vimla S Aggarwal, Dina F Ahram, Natalie Vena,[...]. Clin J Am Soc Nephrol 2020
9
42

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
42

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
209
42

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
58
42

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
112
28


The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature.
Deborah Goodman, Deborah Bowen, Lari Wenzel, Paris Tehrani, Francis Fernando, Araksi Khacheryan, Farihah Chowdhury, Catherine O Johnson, Karen Edwards. Transl Behav Med 2018
13
28

Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.
Ferhaan Ahmad, Elizabeth M McNally, Michael J Ackerman, Linda C Baty, Sharlene M Day, Iftikhar J Kullo, Peace C Madueme, Martin S Maron, Matthew W Martinez, Lisa Salberg,[...]. Circ Genom Precis Med 2019
23
28

Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve.
Bo Yang, Wei Zhou, Jiao Jiao, Jonas B Nielsen, Michael R Mathis, Mahyar Heydarpour, Guillaume Lettre, Lasse Folkersen, Siddharth Prakash, Claudia Schurmann,[...]. Nat Commun 2017
55
28

Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection.
Marjolijn Renard, Catherine Francis, Rajarshi Ghosh, Alan F Scott, P Dane Witmer, Lesley C Adès, Gregor U Andelfinger, Pauline Arnaud, Catherine Boileau, Bert L Callewaert,[...]. J Am Coll Cardiol 2018
70
28

Validation of a decision regret scale.
Jamie C Brehaut, Annette M O'Connor, Timothy J Wood, Thomas F Hack, Laura Siminoff, Elisa Gordon, Deb Feldman-Stewart. Med Decis Making 2003
614
28

Illustrative case studies in the return of exome and genome sequencing results.
Laura M Amendola, Denise Lautenbach, Sarah Scollon, Barbara Bernhardt, Sawona Biswas, Kelly East, Jessica Everett, Marian J Gilmore, Patricia Himes, Victoria M Raymond,[...]. Per Med 2015
30
28

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
37
28

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Wendy K Chung, Adam S Gordon, Gail E Herman, Teri E Klein, Douglas R Stewart, Laura M Amendola, Kathy Adelman, Sherri J Bale,[...]. Genet Med 2021
28
28

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
61
28

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
302
28

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
17
28

An international policy on returning genomic research results.
Anna C F Lewis, Bartha Maria Knoppers, Robert C Green. Genome Med 2021
3
66

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility.
Christopher A Cassa, Sarah K Savage, Patrick L Taylor, Robert C Green, Amy L McGuire, Kenneth D Mandl. Genome Res 2012
70
14

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
124
14

Socioeconomic status and health. The challenge of the gradient.
N E Adler, T Boyce, M A Chesney, S Cohen, S Folkman, R L Kahn, S L Syme. Am Psychol 1994
14

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
159
14

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
204
14

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.
Stephanie M Fullerton, Wendy A Wolf, Kyle B Brothers, Ellen Wright Clayton, Dana C Crawford, Joshua C Denny, Philip Greenland, Barbara A Koenig, Kathleen A Leppig, Noralane M Lindor,[...]. Genet Med 2012
79
14


Providing research results to participants: attitudes and needs of adolescents and parents of children with cancer.
Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, Charles Weijer, Eric Kodish. J Clin Oncol 2009
58
14

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
281
14

Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling.
Morgan Butrick, Scott Kelly, Beth N Peshkin, George Luta, Rachel Nusbaum, Gillian W Hooker, Kristi Graves, Lisa Feeley, Claudine Isaacs, Heiddis B Valdimarsdottir,[...]. Genet Med 2015
61
14

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
133
14

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes.
Machteld Baetens, Lut Van Laer, Kim De Leeneer, Jan Hellemans, Joachim De Schrijver, Hendrik Van De Voorde, Marjolijn Renard, Hal Dietz, Ronald V Lacro, Björn Menten,[...]. Hum Mutat 2011
55
14

Interventions for individuals with low health literacy: a systematic review.
Stacey L Sheridan, David J Halpern, Anthony J Viera, Nancy D Berkman, Katrina E Donahue, Karen Crotty. J Health Commun 2011
234
14

Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.
Christina R Lachance, Lori A H Erby, Beth M Ford, Vincent C Allen, Kimberly A Kaphingst. Genet Med 2010
68
14

Genes Associated with Thoracic Aortic Aneurysm and Dissection: An Update and Clinical Implications.
Adam J Brownstein, Bulat A Ziganshin, Helena Kuivaniemi, Simon C Body, Allen E Bale, John A Elefteriades. Aorta (Stamford) 2017
50
14

BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
603
14

Heart disease and stroke statistics--2014 update: a report from the American Heart Association.
Alan S Go, Dariush Mozaffarian, Véronique L Roger, Emelia J Benjamin, Jarett D Berry, Michael J Blaha, Shifan Dai, Earl S Ford, Caroline S Fox, Sheila Franco,[...]. Circulation 2014
14



Brief questions to identify patients with inadequate health literacy.
Lisa D Chew, Katharine A Bradley, Edward J Boyko. Fam Med 2004
14

Obligations in offering to disclose genetic research results.
Conrad V Fernandez, Charles Weijer. Am J Bioeth 2006
28
14

Predictors of patient uptake of colorectal cancer gene environment risk assessment.
Michael J Hall, Sharon L Manne, Ronald E Myers, Eileen M Keenan, Andrew M Balshem, David S Weinberg. Genome Med 2012
10
14

Incidental findings: the time is not yet ripe for a policy for biobanks.
Jennifer Viberg, Mats G Hansson, Sophie Langenskiöld, Pär Segerdahl. Eur J Hum Genet 2014
16
14

Effects of informed consent for individual genome sequencing on relevant knowledge.
K A Kaphingst, F M Facio, M-R Cheng, S Brooks, H Eidem, A Linn, B B Biesecker, L G Biesecker. Clin Genet 2012
80
14

Willingness to pay for genetic testing for Alzheimer's disease: a measure of personal utility.
Ilona M Kopits, Clara Chen, J Scott Roberts, Wendy Uhlmann, Robert C Green. Genet Test Mol Biomarkers 2011
39
14

Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology.
Katie L Lewis, Paul K J Han, Gillian W Hooker, William M P Klein, Leslie G Biesecker, Barbara B Biesecker. PLoS One 2015
34
14

Communicating genetic and genomic information: health literacy and numeracy considerations.
D H Lea, K A Kaphingst, D Bowen, I Lipkus, D W Hadley. Public Health Genomics 2011
142
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.