A citation-based method for searching scientific literature

Maya Sabatello, Paul S Appelbaum. J Law Med Ethics 2016
Times Cited: 16







List of co-cited articles
75 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
53
43

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
31

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
238
31

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
31

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
256
31

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
39
31

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
17
31

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
54
25


Adolescents and genetic testing: what do they think about it?
Asaff Harel, Dianne Abuelo, Alessandra Kazura. J Adolesc Health 2003
23
25

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
25

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
15
26

Cool, but is it credible? Adolescents' and parents' approaches to genetic testing.
Lynn Rew, Michael Mackert, Dan Bonevac. West J Nurs Res 2010
15
20


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
18
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
63
18


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
70
18

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
55
18


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
10
30

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
7
42

"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
120
12

When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families.
Ramsey M Wehbe, Gail A Spiridigliozzi, Elizabeth M Heise, Deborah V Dawson, Allyn McConkie-Rosell. Am J Med Genet A 2009
17
12

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
83
12

Incidental findings in pediatric research.
Benjamin S Wilfond, Katherine J Carpenter. J Law Med Ethics 2008
31
12

A developmental approach to child assent for nontherapeutic research.
Victoria A Miller, Robert M Nelson. J Pediatr 2006
37
12

The psychological impact of genetic information on children: a systematic review.
Claire E Wakefield, Lucy V Hanlon, Katherine M Tucker, Andrea F Patenaude, Christina Signorelli, Jordana K McLoone, Richard J Cohn. Genet Med 2016
51
12

Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
46
12

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
12


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
24
12

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
136
12


Effects of biological explanations for mental disorders on clinicians' empathy.
Matthew S Lebowitz, Woo-kyoung Ahn. Proc Natl Acad Sci U S A 2014
70
12


Informed Consent in Decision-Making in Pediatric Practice.
Aviva L Katz, Sally A Webb. Pediatrics 2016
163
12

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
62
12

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
111
12

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
67
12

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
53
12

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
J A Anderson, M S Meyn, C Shuman, R Zlotnik Shaul, L E Mantella, M J Szego, S Bowdin, N Monfared, R Z Hayeems. J Med Ethics 2017
31
12


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
30
12

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
14
14


Whole-genome sequencing in newborn screening programs.
Bartha M Knoppers, Karine Sénécal, Pascal Borry, Denise Avard. Sci Transl Med 2014
44
12

Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.
Heidi Carmen Howard, Bartha Maria Knoppers, Martina C Cornel, Ellen Wright Clayton, Karine Sénécal, Pascal Borry. Eur J Hum Genet 2015
48
12

Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.
J A Anderson, R Z Hayeems, C Shuman, M J Szego, N Monfared, S Bowdin, R Zlotnik Shaul, M S Meyn. Clin Genet 2015
28
12


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.