A citation-based method for searching scientific literature

Louise Wideroff, Susan Thomas Vadaparampil, Nancy Breen, Robert T Croyle, Andrew N Freedman. Community Genet 2003
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


Barriers and facilitators of cervical cancer screening among Hispanic women.
Theresa L Byrd, Rafaelita Chavez, Katherine M Wilson. Ethn Dis 2007
84
1

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
32
3

Designing and implementing sample and data collection for an international genetics study: the Type 1 Diabetes Genetics Consortium (T1DGC).
Joan E Hilner, Letitia H Perdue, Elizabeth G Sides, June J Pierce, Ana M Wägner, Alan Aldrich, Amanda Loth, Lotte Albret, Lynne E Wagenknecht, Concepcion Nierras,[...]. Clin Trials 2010
24
4

Sociodemographic differences in fears and mistrust contributing to unwillingness to participate in cancer screenings.
Jenna L Davis, Shalanda A Bynum, Ralph V Katz, Kyrel Buchanan, B Lee Green. J Health Care Poor Underserved 2012
37
2

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019.
Samir Gupta, Dawn Provenzale, Xavier Llor, Amy L Halverson, William Grady, Daniel C Chung, Sigurdis Haraldsdottir, Arnold J Markowitz, Thomas P Slavin, Heather Hampel,[...]. J Natl Compr Canc Netw 2019
84
1

Racial and ethnic differences in willingness to participate in psychiatric genetic research.
Eleanor J Murphy, Priya Wickramaratne, Myrna M Weissman. Psychiatr Genet 2009
24
4

[Validation of the INFLESZ scale to evaluate readability of texts aimed at the patient].
I M Barrio-Cantalejo, P Simón-Lorda, M Melguizo, I Escalona, M I Marijuán, P Hernando. An Sist Sanit Navar 2008
45
2

Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
Mary B Daly, Tuya Pal, Michael P Berry, Saundra S Buys, Patricia Dickson, Susan M Domchek, Ahmed Elkhanany, Susan Friedman, Michael Goggins, Mollie L Hutton,[...]. J Natl Compr Canc Netw 2021
34
2

Learning from Latino voices: Focus Groups' Insights on Participation in Genetic Research.
Priscilla Martinez, Cory Cummings, Katherine J Karriker-Jaffe, Karen G Chartier. Am J Addict 2017
12
8

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
4

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
79
1


The Missing Diversity in Human Genetic Studies.
Giorgio Sirugo, Scott M Williams, Sarah A Tishkoff. Cell 2019
207
1

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
G Davies, N Armstrong, J C Bis, J Bressler, V Chouraki, S Giddaluru, E Hofer, C A Ibrahim-Verbaas, M Kirin, J Lahti,[...]. Mol Psychiatry 2015
196
1

Health Disparities and Hispanics.
Judith Aponte. Hisp Health Care Int 2017
3
33

Is health a right for all? An umbrella review of the barriers to health care access faced by migrants.
Diana Gil-González, Mercedes Carrasco-Portiño, Carmen Vives-Cases, Andrés A Agudelo-Suárez, Ramón Castejón Bolea, Elena Ronda-Pérez. Ethn Health 2015
28
3


Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).
T Lencz, E Knowles, G Davies, S Guha, D C Liewald, J M Starr, S Djurovic, I Melle, K Sundet, A Christoforou,[...]. Mol Psychiatry 2014
127
1

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
21
4


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
26
3

From Sea to Shining Sea and the Great Plains to Patagonia: A Review on Current Knowledge of Diabetes Mellitus in Hispanics/Latinos in the US and Latin America.
M Larissa Avilés-Santa, Uriyoán Colón-Ramos, Nangel M Lindberg, Josiemer Mattei, Francisco J Pasquel, Cynthia M Pérez. Front Endocrinol (Lausanne) 2017
18
5

Plain language: a strategic response to the health literacy challenge.
Sue Stableford, Wendy Mettger. J Public Health Policy 2007
90
1

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
32
3

Inclusion of diverse populations in genomic research and health services: Genomix workshop report.
Savio S Mathew, Julian Barwell, Nasaim Khan, Ella Lynch, Michael Parker, Nadeem Qureshi. J Community Genet 2017
16
6


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.