A citation-based method for searching scientific literature

Sarah N Thomas, Shelly R Hovick, Naomi Tan, Amy C Sturm, Kevin Sweet. Public Health Genomics 2018
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


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
160
100

Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™).
Cecelia Bellcross, April Hermstad, Christine Tallo, Christine Stanislaw. Genet Med 2019
18
100

A Web-based survey among adults aged 40-54 years was time effective and yielded stable response patterns.
Korbinian Weigl, Kaja Tikk, Michael Hoffmeister, Enrico N De Toni, Jochen Hampe, Frank Kolligs, Stefanie J Klug, Ulrich Mansmann, Daniel Nasseh, Jovana Radlovic,[...]. J Clin Epidemiol 2019
6
100

Clinical decision support for genetically guided personalized medicine: a systematic review.
Brandon M Welch, Kensaku Kawamoto. J Am Med Inform Assoc 2013
69
100

An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.
Mary Pritzlaff, Arielle Yorczyk, Linda S Robinson, Sara Pirzadeh-Miller, Tirun Lin, David Euhus, Theodora S Ross. J Genet Couns 2014
14
100

Familial risk for common diseases in primary care: the Family Healthware Impact Trial.
Suzanne M O'Neill, Wendy S Rubinstein, Catharine Wang, Paula W Yoon, Louise S Acheson, Nan Rothrock, Erin J Starzyk, Jennifer L Beaumont, James M Galliher, Mack T Ruffin. Am J Prev Med 2009
88
100


What characterizes cancer family history collection tools? A critical literature review.
J E Cleophat, H Nabi, S Pelletier, K Bouchard, M Dorval. Curr Oncol 2018
15
100

Multi-disciplinary summit on genetics services for women with gynecologic cancers: A Society of Gynecologic Oncology White Paper.
Leslie M Randall, Bhavana Pothuri, Elizabeth M Swisher, John P Diaz, Adam Buchanan, Catherine T Witkop, C Bethan Powell, Ellen Blair Smith, Mark E Robson, Jeff Boyd,[...]. Gynecol Oncol 2017
60
100

Information Technology Support for Clinical Genetic Testing within an Academic Medical Center.
Samuel Aronson, Lisa Mahanta, Lei Lei Ros, Eugene Clark, Lawrence Babb, Michael Oates, Heidi Rehm, Matthew Lebo. J Pers Med 2016
7
100

Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening.
Kenneth Offit, Kaitlyn A Tkachuk, Zsofia K Stadler, Michael F Walsh, Hector Diaz-Zabala, Jeffrey D Levin, Zoe Steinsnyder, Vignesh Ravichandran, Ravi N Sharaf, Melissa K Frey,[...]. J Clin Oncol 2020
25
100

Acceptability and feasibility of a virtual counselor (VICKY) to collect family health histories.
Catharine Wang, Timothy Bickmore, Deborah J Bowen, Tricia Norkunas, MaryAnn Campion, Howard Cabral, Michael Winter, Michael Paasche-Orlow. Genet Med 2015
29
100

Use of a web-based risk appraisal tool for assessing family history and lifestyle factors in primary care.
Heather J Baer, Louise I Schneider, Graham A Colditz, Hank Dart, Analisa Andry, Deborah H Williams, E John Orav, Jennifer S Haas, George Getty, Elizabeth Whittemore,[...]. J Gen Intern Med 2013
25
100

Development of a risk assessment tool for women with a family history of breast cancer.
Dejana Braithwaite, Stephen Sutton, James Mackay, Judith Stein, Jon Emery. Cancer Detect Prev 2005
27
100

ChMP: A collaborative medical history portal.
Noah H Zimmerman, Chirag Patel, David P Chen. AMIA Annu Symp Proc 2008
2
100

Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer.
F G J Kallenberg, C M Aalfs, F O The, C A Wientjes, A C Depla, M W Mundt, P M M Bossuyt, E Dekker. Fam Cancer 2018
7
100

Development and validation of a primary care-based family health history and decision support program (MeTree).
Lori A Orlando, Adam H Buchanan, Susan E Hahn, Carol A Christianson, Karen P Powell, Celette Sugg Skinner, Blair Chesnut, Colette Blach, Barbara Due, Geoffrey S Ginsburg,[...]. N C Med J 2013
48
100

Use of telephone intake for family history taking at a cancer genetics service in Asia.
Xin Wei Chin, Zoe L T Ang, Ryan Y C Tan, Eliza Courtney, Tarryn Shaw, Yanni Chen, Shao-Tzu Li, Joanne Yuen Yie Ngeow. J Genet Couns 2020
2
100

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 1.2020.
Mary B Daly, Robert Pilarski, Matthew B Yurgelun, Michael P Berry, Saundra S Buys, Patricia Dickson, Susan M Domchek, Ahmed Elkhanany, Susan Friedman, Judy E Garber,[...]. J Natl Compr Canc Netw 2020
175
100

"You don't have to keep everything on paper": African American women's use of family health history tools.
Tess Thompson, Joann Seo, Julia Griffith, Melanie Baxter, Aimee James, Kimberly A Kaphingst. J Community Genet 2013
18
100

Utilization of health information technology among cancer genetic counselors.
Jordon B Ritchie, Caitlin G Allen, Heath Morrison, Michelle Nichols, Steven D Lauzon, Joshua D Schiffman, Chanita Hughes Halbert, Brandon M Welch. Mol Genet Genomic Med 2020
8
100

Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial.
Wendy S Rubinstein, Louise S Acheson, Suzanne M O'Neill, Mack T Ruffin, Catharine Wang, Jennifer L Beaumont, Nan Rothrock. Genet Med 2011
65
100

The CRISP-P study: feasibility of a self-completed colorectal cancer risk prediction tool in primary care.
Elena C Harty, Jennifer G McIntosh, Adrian Bickerstaffe, Nadira Hewabandu, Jon D Emery. Fam Pract 2019
5
100

Communicating risk of hereditary breast and ovarian cancer with an interactive decision support tool.
Douglas J Rupert, Linda B Squiers, Jeanette M Renaud, Nedra S Whitehead, Roger J Osborn, Robert D Furberg, Claudia M Squire, Janice P Tzeng. Patient Educ Couns 2013
16
100



Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology.
Dawn Provenzale, Samir Gupta, Dennis J Ahnen, Travis Bray, Jamie A Cannon, Gregory Cooper, Donald S David, Dayna S Early, Deborah Erwin, James M Ford,[...]. J Natl Compr Canc Netw 2016
135
100

Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer.
F G J Kallenberg, J E G IJspeert, P M M Bossuyt, C M Aalfs, E Dekker. Fam Cancer 2015
12
100

Identification and referral of families at high risk for cancer susceptibility.
Kevin M Sweet, Terry L Bradley, Judith A Westman. J Clin Oncol 2002
131
100

Identification and management of women at high risk for hereditary breast/ovarian cancer syndrome.
Elissa M Ozanne, Andrea Loberg, Sherwood Hughes, Christine Lawrence, Brian Drohan, Alan Semine, Michael Jellinek, Claire Cronin, Frederick Milham, Dana Dowd,[...]. Breast J 2009
41
100

Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial.
R Ryanne Wu, Lori A Orlando, Tiffany L Himmel, Adam H Buchanan, Karen P Powell, Elizabeth R Hauser, Astrid B Agbaje, Vincent C Henrich, Geoffrey S Ginsburg. BMC Fam Pract 2013
40
100

Family history assessment for colorectal cancer (CRC) risk analysis - comparison of diagram- and questionnaire-based web interfaces.
Michael Schultz, Steven Bohwan Seo, Alec Holt, Holger Regenbrecht. BMC Med Inform Decis Mak 2015
5
100

The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration.
Alessandro Liberati, Douglas G Altman, Jennifer Tetzlaff, Cynthia Mulrow, Peter C Gøtzsche, John P A Ioannidis, Mike Clarke, P J Devereaux, Jos Kleijnen, David Moher. BMJ 2009
100

Validation of My Family Health Portrait for six common heritable conditions.
Flavia M Facio, W Gregory Feero, Amy Linn, Neal Oden, Kandamurugu Manickam, Leslie G Biesecker. Genet Med 2010
62
100

Health Heritage© a web-based tool for the collection and assessment of family health history: initial user experience and analytic validity.
W F Cohn, M E Ropka, S L Pelletier, J R Barrett, M B Kinzie, M B Harrison, Z Liu, S Miesfeldt, A L Tucker, B B Worrall,[...]. Public Health Genomics 2010
63
100

Family history assessment: impact on disease risk perceptions.
Catharine Wang, Ananda Sen, Mack T Ruffin, Donald E Nease, Robert Gramling, Louise S Acheson, Suzanne M O'Neill, Wendy S Rubinstein. Am J Prev Med 2012
38
100

Validation of a self-administered, computerized tool for collecting and displaying the family history of cancer.
Louise S Acheson, Stephen J Zyzanski, Kurt C Stange, Amy Deptowicz, Georgia L Wiesner. J Clin Oncol 2006
50
100

The current state of cancer family history collection tools in primary care: a systematic review.
Nadeem Qureshi, June C Carroll, Brenda Wilson, Pasqualina Santaguida, Judith Allanson, Melissa Brouwers, Parminder Raina. Genet Med 2009
71
100

Outcomes associated with use of the Cancer Risk Intake System among primary care safety-net patients identified as needing colorectal cancer screening.
Celette Sugg Skinner, Chul Ahn, Amit G Singal, Rasmi G Nair, Ethan A Halm, Wendy Pechero, Katharine McCallister, Joanne M Sanders, David Farrell, Noel Santini. Prev Med Rep 2019
4
100

Family history tools for primary care are not ready yet to be implemented. A systematic review.
Céline L M M de Hoog, Piet J M Portegijs, Henri E J H Stoffers. Eur J Gen Pract 2014
27
100

Family history in colonoscopy patients: feasibility and performance of electronic and paper-based surveys for colorectal cancer risk assessment in the outpatient setting.
Tannaz Guivatchian, Erika S Koeppe, Jason R Baker, Cristina Moisa, Matthew Demerath, Caitlin Foor-Pessin, William D Chey, Shanti L Eswaran, Joseph C Kolars, Stacy B Menees,[...]. Gastrointest Endosc 2017
11
100


Prospective Feasibility Trial of a Novel Strategy of Facilitated Cascade Genetic Testing Using Telephone Counseling.
Melissa K Frey, Ryan M Kahn, Eloise Chapman-Davis, Francesca Tubito, Maira Pires, Paul Christos, Samantha Anderson, Semanti Mukherjee, Bailey Jordan, Stephanie V Blank,[...]. J Clin Oncol 2020
26
100

Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey.
Anne Brédart, Jean-Luc Kop, Antonis C Antoniou, Alex P Cunningham, Antoine De Pauw, Marc Tischkowitz, Hans Ehrencrona, Marjanka K Schmidt, Sylvie Dolbeault, Kerstin Rhiem,[...]. J Community Genet 2019
5
100


Evaluation of computer-based medical histories taken by patients at home.
Warner V Slack, Hollis B Kowaloff, Roger B Davis, Tom Delbanco, Steven E Locke, Charles Safran, Howard L Bleich. J Am Med Inform Assoc 2012
18
100

Development and early usage patterns of a consumer-facing family health history tool.
Nathan C Hulse, Pallavi Ranade-Kharkar, Herman Post, Grant M Wood, Marc S Williams, Peter J Haug. AMIA Annu Symp Proc 2011
26
100


Communication and technology in genetic counseling for familial cancer.
H T Lynch, C Snyder, M Stacey, B Olson, S K Peterson, S Buxbaum, T Shaw, P M Lynch. Clin Genet 2014
16
100

Review and Comparison of Electronic Patient-Facing Family Health History Tools.
Brandon M Welch, Kevin Wiley, Lance Pflieger, Rosaline Achiangia, Karen Baker, Chanita Hughes-Halbert, Heath Morrison, Joshua Schiffman, Megan Doerr. J Genet Couns 2018
39
100


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.