A citation-based method for searching scientific literature

Maya Sabatello, Paul S Appelbaum. J Law Med Ethics 2016
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
Brooke L Levenseller, Danielle J Soucier, Victoria A Miller, Diana Harris, Laura Conway, Barbara A Bernhardt. J Genet Couns 2014
52
46

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
221
38

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
38

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
245
38


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
77
30

Adolescents and genetic testing: what do they think about it?
Asaff Harel, Dianne Abuelo, Alessandra Kazura. J Adolesc Health 2003
22
30

Adolescents' preferences regarding disclosure of incidental findings in genomic sequencing that are not medically actionable in childhood.
Sophia B Hufnagel, Lisa J Martin, Amy Cassedy, Robert J Hopkin, Armand H Matheny Antommaria. Am J Med Genet A 2016
13
30


Addressing the ethical challenges in genetic testing and sequencing of children.
Ellen Wright Clayton, Laurence B McCullough, Leslie G Biesecker, Steven Joffe, Lainie Friedman Ross, Susan M Wolf. Am J Bioeth 2014
69
23

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
204
23

Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board.
Ingrid A Holm, Sarah K Savage, Robert C Green, Eric Juengst, Amy McGuire, Susan Kornetsky, Stephanie J Brewster, Steven Joffe, Patrick Taylor. Genet Med 2014
36
23

Adolescent and Parental Attitudes About Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences.
Michelle L McGowan, Cynthia A Prows, Melissa DeJonckheere, William B Brinkman, Lisa Vaughn, Melanie F Myers. J Empir Res Hum Res Ethics 2018
12
25

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
53
23


Distributive justice, diversity, and inclusion in precision medicine: what will success look like?
Elizabeth G Cohn, Gail E Henderson, Paul S Appelbaum. Genet Med 2017
21
15

Interest of adolescents in genetic testing for nicotine addiction susceptibility.
Kenneth P Tercyak, Beth N Peshkin, Lauren A Wine, Leslie R Walker. Prev Med 2006
14
15


Cool, but is it credible? Adolescents' and parents' approaches to genetic testing.
Lynn Rew, Michael Mackert, Dan Bonevac. West J Nurs Res 2010
14
15

How Genetics Might Affect Real Property Rights: Currents in Contemporary Bioethics.
Mark A Rothstein, Laura Rothstein. J Law Med Ethics 2016
3
66

"If I could in a small way help": motivations for and beliefs about sample donation for genetic research.
Marsha Michie, Gail Henderson, Joanne Garrett, Giselle Corbie-Smith. J Empir Res Hum Res Ethics 2011
23
15

Guidelines for adolescent health research. A position paper of the Society for Adolescent Medicine.
John S Santelli, Audrey Smith Rogers, Walter D Rosenfeld, Robert H DuRant, Nancy Dubler, Madlyn Morreale, Abigail English, Sheryl Lyss, Yolanda Wimberly, Anna Schissel. J Adolesc Health 2003
134
15


Effects of biological explanations for mental disorders on clinicians' empathy.
Matthew S Lebowitz, Woo-kyoung Ahn. Proc Natl Acad Sci U S A 2014
56
15


Medical decision-making in children and adolescents: developmental and neuroscientific aspects.
Petronella Grootens-Wiegers, Irma M Hein, Jos M van den Broek, Martine C de Vries. BMC Pediatr 2017
51
15

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
55
15

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
101
15

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
61
15

Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases.
Erika Kleiderman, Bartha Maria Knoppers, Conrad V Fernandez, Kym M Boycott, Gail Ouellette, Durhane Wong-Rieger, Shelin Adam, Julie Richer, Denise Avard. J Med Ethics 2014
50
15

Disclosing Secondary Findings from Pediatric Sequencing to Families: Considering the "Benefit to Families".
Benjamin S Wilfond, Conrad V Fernandez, Robert C Green. J Law Med Ethics 2015
28
15

Whole-genome sequencing in newborn screening programs.
Bartha M Knoppers, Karine Sénécal, Pascal Borry, Denise Avard. Sci Transl Med 2014
41
15

Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public.
Saskia C Sanderson, Sabrina A Suckiel, Micol Zweig, Erwin P Bottinger, Ethylin Wang Jabs, Lynne D Richardson. Genet Med 2016
31
15


Ethical issues associated with genetic counseling in the context of adolescent psychiatry.
Jane Ryan, Alice Virani, Jehannine C Austin. Appl Transl Genom 2015
15
15

A comprehensive analysis of high school genetics standards: are states keeping pace with modern genetics?
M J Dougherty, C Pleasants, L Solow, A Wong, H Zhang. CBE Life Sci Educ 2011
21
15

Implications of the use of genetic tests in psychiatry, with a focus on major depressive disorder: a review.
Alex Wilde, Philip B Mitchell, Bettina Meiser, Peter R Schofield. Depress Anxiety 2013
12
16

Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools.
M B Delatycki, M Wolthuizen, V Collins, E Varley, J Craven, K J Allen, M A Aitken, L Bond, P J Lockhart, G R Wilson,[...]. Clin Genet 2010
7
28

Genetic determinants of depression: recent findings and future directions.
Erin C Dunn, Ruth C Brown, Yael Dai, Jonathan Rosand, Nicole R Nugent, Ananda B Amstadter, Jordan W Smoller. Harv Rev Psychiatry 2015
73
15

Parents' attitudes toward pediatric genetic testing for common disease risk.
Kenneth P Tercyak, Sharon Hensley Alford, Karen M Emmons, Isaac M Lipkus, Benjamin S Wilfond, Colleen M McBride. Pediatrics 2011
47
15



Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
151
15

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
720
15

Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
204
15

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
21
15

Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.
Ruqayyah Abdul-Karim, Benjamin E Berkman, David Wendler, Annette Rid, Javed Khan, Tom Badgett, Sara Chandros Hull. Pediatrics 2013
52
15

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
8
25

An Observational Study of Children's Involvement in Informed Consent for Exome Sequencing Research.
Victoria A Miller, Allison Werner-Lin, Sarah A Walser, Sawona Biswas, Barbara A Bernhardt. J Empir Res Hum Res Ethics 2017
6
33



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.