A citation-based method for searching scientific literature

Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Measuring numeracy without a math test: development of the Subjective Numeracy Scale.
Angela Fagerlin, Brian J Zikmund-Fisher, Peter A Ubel, Aleksandra Jankovic, Holly A Derry, Dylan M Smith. Med Decis Making 2007
455
27

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
994
27

Behavioral health outcomes associated with religious faith and media exposure about human genetics.
Roxanne Parrott, Kami Silk, Janice Raup Krieger, Tina Harris, Celeste Condit. Health Commun 2004
20
16

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
48
16

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
59
16

Attitudes of non-African American focus group participants toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
37
16

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
70
16


Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
63
16

Retention and use of breast cancer recurrence risk information from genomic tests: the role of health literacy.
Sarah E Lillie, Noel T Brewer, Suzanne C O'Neill, Edward F Morrill, E Claire Dees, Lisa A Carey, Barbara K Rimer. Cancer Epidemiol Biomarkers Prev 2007
69
16

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
360
16

Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
46
16

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
31
16

Patient communication of cancer genetic test results in a diverse population.
Charité N Ricker, Rachel B Koff, Chenxu Qu, Julie Culver, Duveen Sturgeon, Kerry E Kingham, Katrina Lowstuter, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra Lebensohn,[...]. Transl Behav Med 2018
20
11

Genetic test reporting of CDKN2A provides informational and motivational benefits for managing melanoma risk.
Lisa G Aspinwall, Tammy K Stump, Jennifer M Taber, Danielle M Drummond, Wendy Kohlmann, Marjan Champine, Sancy A Leachman. Transl Behav Med 2018
15
13



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
17
11

Effects of racial and ethnic group and health literacy on responses to genomic risk information in a medically underserved population.
Kimberly A Kaphingst, Jewel D Stafford, Lucy D'Agostino McGowan, Joann Seo, Christina R Lachance, Melody S Goodman. Health Psychol 2015
28
11

Shared decision making: a model for clinical practice.
Glyn Elwyn, Dominick Frosch, Richard Thomson, Natalie Joseph-Williams, Amy Lloyd, Paul Kinnersley, Emma Cording, Dave Tomson, Carole Dodd, Stephen Rollnick,[...]. J Gen Intern Med 2012
11

How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age.
Kimberly A Kaphingst, Jennifer Ivanovich, Ashley Elrick, Rebecca Dresser, Cindy Matsen, Melody S Goodman. Mol Genet Genomic Med 2016
5
40

Age differences in genetic knowledge, health literacy and causal beliefs for health conditions.
S Ashida, M Goodman, C Pandya, L M Koehly, C Lachance, J Stafford, K A Kaphingst. Public Health Genomics 2011
67
11



Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
142
11

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
883
11

Preparing for genomic medicine: a real world demonstration of health system change.
Clara L Gaff, Ingrid M Winship, Susan M Forrest, David P Hansen, Julian Clark, Paul M Waring, Mike South, Andrew H Sinclair. NPJ Genom Med 2017
53
11

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
78
11

Results communication and patient education after screening for possible hemochromatosis and iron overload: experience from the HEIRS Study of a large ethnically and linguistically diverse group.
Ann P Walker, Diane C Tucker, Mark A Hall, Kurt Lohman, Helen Harrison, Barbara W Harrison, Jacob Reiss, Ronald T Acton, Paul C Adams, Sharmin Diaz,[...]. Genet Med 2007
11
18

Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosure.
Amanda M Gutierrez, Jill O Robinson, Emily E Statham, Sarah Scollon, Katie L Bergstrom, Melody J Slashinski, Donald W Parsons, Sharon E Plon, Amy L McGuire, Richard L Street. Per Med 2017
9
22

Disparities in genetic testing: thinking outside the BRCA box.
Michael J Hall, Olufunmilayo I Olopade. J Clin Oncol 2006
125
11

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
113
11

Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.
Kyle B Brothers, Kelly M East, Whitley V Kelley, M Frances Wright, Matthew J Westbrook, Carla A Rich, Kevin M Bowling, Edward J Lose, E Martina Bebin, Shirley Simmons,[...]. Genet Med 2017
29
11

A systematic review of factors that act as barriers to patient referral to genetic services.
Türem Delikurt, Graham R Williamson, Violetta Anastasiadou, Heather Skirton. Eur J Hum Genet 2015
95
11


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
11

Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.
Colleen M McBride, Sharon Hensley Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2009
88
11

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
86
11

BRCA1 and BRCA2 genetic testing-pitfalls and recommendations for managing variants of uncertain clinical significance.
D M Eccles, G Mitchell, A N A Monteiro, R Schmutzler, F J Couch, A B Spurdle, E B Gómez-García. Ann Oncol 2015
129
11



A definition and operational framework for health numeracy.
Amanda L Golbeck, Carolyn R Ahlers-Schmidt, Angelia M Paschal, S Edwards Dismuke. Am J Prev Med 2005
152
11

Assessment of Survivor Concerns (ASC): a newly proposed brief questionnaire.
Carolyn C Gotay, Ian S Pagano. Health Qual Life Outcomes 2007
93
11

The counselees' self-reported request for psychological help in genetic counseling for hereditary breast/ovarian cancer: not only psychopathology matters.
Joël Vos, Christi J van Asperen, Jan C Oosterwijk, Fred H Menko, Margriet J Collee, Encarna Gomez Garcia, Aad Tibben. Psychooncology 2013
26
11

Skin cancer concerns and genetic risk information-seeking in primary care.
J Hay, K A Kaphingst, R Baser, Y Li, S Hensley-Alford, C M McBride. Public Health Genomics 2012
27
11

National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.
Christopher P Childers, Kimberly K Childers, Melinda Maggard-Gibbons, James Macinko. J Clin Oncol 2017
176
11

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
134
11

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
11

Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
93
11

Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.
Julie C Sapp, Jennifer J Johnston, Kate Driscoll, Alexis R Heidlebaugh, Ane Miren Sagardia, D Nadine Dogbe, Kendall L Umstead, Erin Turbitt, Ilias Alevizos, Jeffrey Baron,[...]. Am J Hum Genet 2018
24
11


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.