A citation-based method for searching scientific literature

Sabrina V Southwick, Riley Esch, Rachel Gasser, Deborah Cragun, Krista Redlinger-Grosse, Scott Marsalis, Heather A Zierhut. J Genet Couns 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Laura M Amendola, Jonathan S Berg, Carol R Horowitz, Frank Angelo, Jeannette T Bensen, Barbara B Biesecker, Leslie G Biesecker, Gregory M Cooper, Kelly East, Kelly Filipski,[...]. Am J Hum Genet 2018
40
66

Genetic services and attitudes in primary care pediatrics.
Michael L Rinke, Natalie Mikat-Stevens, Robert Saul, Amy Driscoll, Jill Healy, Beth A Tarini. Am J Med Genet A 2014
23
33


Next-generation diagnostics and disease-gene discovery with the Exomiser.
Damian Smedley, Julius O B Jacobsen, Marten Jäger, Sebastian Köhler, Manuel Holtgrewe, Max Schubach, Enrico Siragusa, Tomasz Zemojtel, Orion J Buske, Nicole L Washington,[...]. Nat Protoc 2015
104
33

Review of community-based research: assessing partnership approaches to improve public health.
B A Israel, A J Schulz, E A Parker, A B Becker. Annu Rev Public Health 1998
33

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
799
33

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
80
33

Interest and beliefs about BRCA genetic counseling among at-risk Latinas in New York City.
Katarina M Sussner, Lina Jandorf, Hayley S Thompson, Heiddis B Valdimarsdottir. J Genet Couns 2010
31
33

Medical student preparedness for an era of personalized medicine: findings from one US medical school.
Caroline Eden, Kipp W Johnson, Omri Gottesman, Erwin P Bottinger, Noura S Abul-Husn. Per Med 2016
15
33

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
588
33

Next generation disparities in human genomics: concerns and remedies.
Anna C Need, David B Goldstein. Trends Genet 2009
186
33

Development of a revised Health Care System Distrust scale.
Judy A Shea, Ellyn Micco, Lorraine T Dean, Suzanne McMurphy, J Sanford Schwartz, Katrina Armstrong. J Gen Intern Med 2008
91
33


Community education to enhance the more equitable use of precision medicine in Northern Manhattan.
Grace C Hillyer, Karen M Schmitt, Andria Reyes, Alejandro Cruz, Maria Lizardo, Gary K Schwartz, Mary Beth Terry. J Genet Couns 2020
3
33

Personalized Medicine and the Power of Electronic Health Records.
Noura S Abul-Husn, Eimear E Kenny. Cell 2019
37
33

Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk.
Jennifer L Caswell-Jin, Tanya Gupta, Evan Hall, Iva M Petrovchich, Meredith A Mills, Kerry E Kingham, Rachel Koff, Nicolette M Chun, Peter Levonian, Alexandra P Lebensohn,[...]. Genet Med 2018
54
33

Ancestry-specific hereditary cancer panel yields: Moving toward more personalized risk assessment.
Maegan E Roberts, Lisa R Susswein, Wanchun Janice Cheng, Natalie J Carter, Amber C Carter, Rachel T Klein, Kathleen S Hruska, Megan L Marshall. J Genet Couns 2020
2
50

Validation of a Short, 3-Item Version of the Subjective Numeracy Scale.
Candace D McNaughton, Kerri L Cavanaugh, Sunil Kripalani, Russell L Rothman, Kenneth A Wallston. Med Decis Making 2015
60
33

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
33



Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.
Lauge Farnaes, Amber Hildreth, Nathaly M Sweeney, Michelle M Clark, Shimul Chowdhury, Shareef Nahas, Julie A Cakici, Wendy Benson, Robert H Kaplan, Richard Kronick,[...]. NPJ Genom Med 2018
126
33

The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.
Alice B Popejoy, Deborah I Ritter, Kristy Crooks, Erin Currey, Stephanie M Fullerton, Lucia A Hindorff, Barbara Koenig, Erin M Ramos, Elena P Sorokin, Hannah Wand,[...]. Hum Mutat 2018
30
33

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
20
33


Assessing patients' experiences with communication across the cancer care continuum.
Kathleen M Mazor, Richard L Street, Valerie M Sue, Andrew E Williams, Borsika A Rabin, Neeraj K Arora. Patient Educ Couns 2016
20
33

Effect of genetic counseling and testing for BRCA1 and BRCA2 mutations in African American women: a randomized trial.
C H Halbert, L Kessler, A B Troxel, J E Stopfer, S Domchek. Public Health Genomics 2010
23
33

Cost-effectiveness of nurse-led disease management for heart failure in an ethnically diverse urban community.
Paul L Hebert, Jane E Sisk, Jason J Wang, Leah Tuzzio, Jodi M Casabianca, Mark R Chassin, Carol Horowitz, Mary Ann McLaughlin. Ann Intern Med 2008
77
33


Barriers and facilitators to BRCA genetic counseling among at-risk Latinas in New York City.
Katarina M Sussner, Lina Jandorf, Hayley S Thompson, Heiddis B Valdimarsdottir. Psychooncology 2013
45
33

Prioritizing diversity in human genomics research.
Lucia A Hindorff, Vence L Bonham, Lawrence C Brody, Margaret E C Ginoza, Carolyn M Hutter, Teri A Manolio, Eric D Green. Nat Rev Genet 2018
121
33

Design and psychometric evaluation of the Psychological Adaptation to Genetic Information Scale.
Catherine Y Read, Donna J Perry, Mary E Duffy. J Nurs Scholarsh 2005
42
33

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, Randi Zinberg, Melissa Wasserstein, Andrew Kasarskis, George A Diaz, Eric E Schadt. Eur J Hum Genet 2017
32
33

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
518
33

Genome-based health literacy: a new challenge for public health genomics.
E V Syurina, I Brankovic, N Probst-Hensch, A Brand. Public Health Genomics 2011
40
33

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
304
33

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
Meng Li, Caroline S Bennette, Laura M Amendola, M Ragan Hart, Patrick Heagerty, Bryan Comstock, Peter Tarczy-Hornoch, Stephanie M Fullerton, Dean A Regier, Wylie Burke,[...]. J Genet Couns 2019
18
33

Culturally Targeted Video Improves Psychosocial Outcomes in Latina Women at Risk of Hereditary Breast and Ovarian Cancer.
Alejandra Hurtado-de-Mendoza, Kristi D Graves, Sara Gómez-Trillos, Pilar Carrera, Claudia Campos, Lyndsay Anderson, George Luta, Beth N Peshkin, Marc D Schwartz, Ana-Paula Cupertino,[...]. Int J Environ Res Public Health 2019
4
33

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry.
C R Horowitz, N S Abul-Husn, S Ellis, M A Ramos, R Negron, M Suprun, R E Zinberg, T Sabin, D Hauser, N Calman,[...]. Contemp Clin Trials 2016
24
33


Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.
Kathleen McGlone West, Erika Blacksher, Wylie Burke. JAMA 2017
39
33

Development of the EQ-5D-Y: a child-friendly version of the EQ-5D.
Nora Wille, Xavier Badia, Gouke Bonsel, Kristina Burström, Gulia Cavrini, Nancy Devlin, Ann-Charlotte Egmar, Wolfgang Greiner, Narcis Gusi, Michael Herdman,[...]. Qual Life Res 2010
303
33

Defining personal utility in genomics: A Delphi study.
J N Kohler, E Turbitt, K L Lewis, B S Wilfond, L Jamal, H L Peay, L G Biesecker, B B Biesecker. Clin Genet 2017
29
33

Are physicians ready for patients with Internet-based health information?
Farah Ahmad, Pamela L Hudak, Kim Bercovitz, Elisa Hollenberg, Wendy Levinson. J Med Internet Res 2006
123
33

Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
Xin Li, Rachel Nusbaum, Constance Smith-Hicks, Leila Jamal, Shannan Dixon, Sonal Mahida. J Genet Couns 2019
8
33

2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling.
Debra Lochner Doyle, Rawan I Awwad, Jehannine C Austin, Bonnie J Baty, Amanda L Bergner, Stephanie J Brewster, Lori A H Erby, Cathi Rubin Franklin, Anne E Greb, Robin E Grubs,[...]. J Genet Couns 2016
26
33


Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.
Sabrina A Suckiel, Michael D Linderman, Saskia C Sanderson, George A Diaz, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt, Randi E Zinberg. J Genet Couns 2016
11
33

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling.
Lisa Madlensky, Angela M Trepanier, Deborah Cragun, Barbara Lerner, Kristen M Shannon, Heather Zierhut. J Genet Couns 2017
39
33

Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients.
Heidi S Lumish, Hallie Steinfeld, Carrie Koval, Donna Russo, Elana Levinson, Julia Wynn, James Duong, Wendy K Chung. J Genet Couns 2017
61
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.