A citation-based method for searching scientific literature

Jennifer M Taber, William M P Klein, Rebecca A Ferrer, Paul K J Han, Katie L Lewis, Leslie G Biesecker, Barbara B Biesecker. J Behav Med 2015
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


How do research participants perceive "uncertainty" in genome sequencing?
Barbara B Biesecker, William Klein, Katie L Lewis, Tyler C Fisher, Martha Frances Wright, Leslie G Biesecker, Paul K Han. Genet Med 2014
50
28

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.
Leslie G Biesecker, James C Mullikin, Flavia M Facio, Clesson Turner, Praveen F Cherukuri, Robert W Blakesley, Gerard G Bouffard, Peter S Chines, Pedro Cruz, Nancy F Hansen,[...]. Genome Res 2009
202
25

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
32
25

A taxonomy of medical uncertainties in clinical genome sequencing.
Paul K J Han, Kendall L Umstead, Barbara A Bernhardt, Robert C Green, Steven Joffe, Barbara Koenig, Ian Krantz, Leo B Waterston, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2017
53
25

The role of current affect, anticipated affect and spontaneous self-affirmation in decisions to receive self-threatening genetic risk information.
Rebecca A Ferrer, Jennifer M Taber, William M P Klein, Peter R Harris, Katie L Lewis, Leslie G Biesecker. Cogn Emot 2015
24
25

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
21

Dispositional optimism and perceived risk interact to predict intentions to learn genome sequencing results.
Jennifer M Taber, William M P Klein, Rebecca A Ferrer, Katie L Lewis, Leslie G Biesecker, Barbara B Biesecker. Health Psychol 2015
18
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
21

Information Avoidance Tendencies, Threat Management Resources, and Interest in Genetic Sequencing Feedback.
Jennifer M Taber, William M P Klein, Rebecca A Ferrer, Katie L Lewis, Peter R Harris, James A Shepperd, Leslie G Biesecker. Ann Behav Med 2015
27
18

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
96
17

Varieties of uncertainty in health care: a conceptual taxonomy.
Paul K J Han, William M P Klein, Neeraj K Arora. Med Decis Making 2011
192
17

Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing.
Kelly Hitch, Galen Joseph, Jenna Guiltinan, Jessica Kianmahd, Janey Youngblom, Amie Blanco. J Genet Couns 2014
45
17


Communicating the uncertainty of harms and benefits of medical interventions.
Mary C Politi, Paul K J Han, Nananda F Col. Med Decis Making 2007
188
14

Individual differences in aversion to ambiguity regarding medical tests and treatments: association with cancer screening cognitions.
Paul K J Han, Andrew E Williams, Amy Haskins, Caitlin Gutheil, F Lee Lucas, William M P Klein, Kathleen M Mazor. Cancer Epidemiol Biomarkers Prev 2014
15
26

Oncologists' and cancer patients' views on whole-exome sequencing and incidental findings: results from the CanSeq study.
Stacy W Gray, Elyse R Park, Julie Najita, Yolanda Martins, Lara Traeger, Elizabeth Bair, Joshua Gagne, Judy Garber, Pasi A Jänne, Neal Lindeman,[...]. Genet Med 2016
69
14

Experiences with obtaining informed consent for genomic sequencing.
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am J Med Genet A 2015
64
14

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
344
14


Sources of uncertainty and their association with medical decision making: exploring mechanisms in Fanconi anemia.
Jada G Hamilton, Sadie P Hutson, Richard P Moser, Sarah C Kobrin, Amy E Frohnmayer, Blanche P Alter, Paul K J Han. Ann Behav Med 2013
23
17

Health behavior changes after genetic risk assessment for Alzheimer disease: The REVEAL Study.
Serena Chao, J Scott Roberts, Theresa M Marteau, Rebecca Silliman, L Adrienne Cupples, Robert C Green. Alzheimer Dis Assoc Disord 2008
153
10

Predictors of genetic testing decisions: a systematic review and critique of the literature.
Kate Sweeny, Arezou Ghane, Angela M Legg, Ho Phi Huynh, Sara E Andrews. J Genet Couns 2014
34
10

Dispositional optimism and coping: a meta-analytic review.
Lise Solberg Nes, Suzanne C Segerstrom. Pers Soc Psychol Rev 2006
261
10


What can interest tell us about uptake of genetic testing? Intention and behavior amongst smokers related to patients with lung cancer.
S C Sanderson, S C O'Neill, L A Bastian, G Bepler, C M McBride. Public Health Genomics 2010
60
10

Personal factors associated with reported benefits of Huntington disease family history or genetic testing.
Janet K Williams, Cheryl Erwin, Andrew Juhl, James Mills, Bradley Brossman, Jane S Paulsen. Genet Test Mol Biomarkers 2010
18
16

The impact of self-affirmation on health-behavior change: a meta-analysis.
Tracy Epton, Peter R Harris, Rachel Kane, Guido M van Koningsbruggen, Paschal Sheeran. Health Psychol 2015
97
10

Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
77
10

How can psychological science inform research about genetic counseling for clinical genomic sequencing?
Cynthia M Khan, Christine Rini, Barbara A Bernhardt, J Scott Roberts, Kurt D Christensen, James P Evans, Kyle B Brothers, Myra I Roche, Jonathan S Berg, Gail E Henderson. J Genet Couns 2015
16
18


Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.
Stacy W Gray, Yolanda Martins, Lindsay Z Feuerman, Barbara A Bernhardt, Barbara B Biesecker, Kurt D Christensen, Steven Joffe, Christine Rini, David Veenstra, Amy L McGuire. Genet Med 2014
45
10

Perceived ambiguity, fatalism, and believing cancer is more prevalent than heart disease.
William M P Klein, Rebecca A Ferrer, Kaitlin A Graff, Annette R Kaufman, Paul K J Han. Am J Prev Med 2014
9
33


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
10

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
10

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
37
10

Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.
K A Kaphingst, J Ivanovich, B B Biesecker, R Dresser, J Seo, L G Dressler, P J Goodfellow, M S Goodman. Clin Genet 2016
27
11

Known unknowns: building an ethics of uncertainty into genomic medicine.
Ainsley J Newson, Samantha J Leonard, Alison Hall, Clara L Gaff. BMC Med Genomics 2016
43
10

PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing.
B B Biesecker, S W Woolford, W M P Klein, K B Brothers, K L Umstead, K L Lewis, L G Biesecker, P K J Han. Clin Genet 2017
21
14


The Health Information National Trends Survey (HINTS): development, design, and dissemination.
David E Nelson, Gary L Kreps, Bradford W Hesse, Robert T Croyle, Gordon Willis, Neeraj K Arora, Barbara K Rimer, K V Viswanath, Neil Weinstein, Sara Alden. J Health Commun 2004
396
10

Fatalistic beliefs about cancer prevention and three prevention behaviors.
Jeff Niederdeppe, Andrea Gurmankin Levy. Cancer Epidemiol Biomarkers Prev 2007
236
10


Judging health status: effects of perceived prevalence and personal relevance.
J B Jemmott, P H Ditto, R T Croyle. J Pers Soc Psychol 1986
100
7


Dispositional optimism.
Charles S Carver, Michael F Scheier. Trends Cogn Sci 2014
175
7

Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families.
Nadine A Kasparian, Bettina Meiser, Phyllis N Butow, Judy M Simpson, Graham J Mann. Genet Med 2009
64
7



Optimism and physical health: a meta-analytic review.
Heather N Rasmussen, Michael F Scheier, Joel B Greenhouse. Ann Behav Med 2009
329
7


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.