A citation-based method for searching scientific literature

Charles Muller, Sang Mee Lee, William Barge, Shazia M Siddique, Shivali Berera, Gina Wideroff, Rashmi Tondon, Jeremy Chang, Meaghan Peterson, Jessica Stoll, Bryson W Katona, Daniel A Sussman, Joshua Melson, Sonia S Kupfer. Clin Gastroenterol Hepatol 2018
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity


Barriers to Lynch Syndrome Testing and Preoperative Result Availability in Early-onset Colorectal Cancer: A National Physician Survey Study.
Alan Noll, Parth J Parekh, Meijiao Zhou, Thomas K Weber, Dennis Ahnen, Xiao-Cheng Wu, Jordan J Karlitz. Clin Transl Gastroenterol 2018
14
21

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. Ann Intern Med 2009
10

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
Heather Hampel, Wendy Frankel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa, Daniel Fix, Ilene Comeras, Jennifer La Jeunesse, Hidewaki Nakagawa, Judith A Westman,[...]. Cancer Res 2006
384
10

The proportion of endometrial cancers associated with Lynch syndrome: a systematic review of the literature and meta-analysis.
N A J Ryan, M A Glaire, D Blake, M Cabrera-Dandy, D G Evans, E J Crosbie. Genet Med 2019
50
10

Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
120
6

Racial differences in beliefs about genetic screening among patients at inner-city neighborhood health centers.
Richard K Zimmerman, Melissa Tabbarah, Mary Patricia Nowalk, Mahlon Raymund, Ilene K Jewell, Stephen A Wilson, Edmund M Ricci. J Natl Med Assoc 2006
36
6

Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer.
Lisa R Susswein, Cécile Skrzynia, Leslie A Lange, Jessica K Booker, Mark L Graham, James P Evans. J Clin Oncol 2008
42
6

Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities.
Caren E Smith, Stephanie M Fullerton, Keith A Dookeran, Heather Hampel, Adrienne Tin, Nisa M Maruthur, Jonathan C Schisler, Jeffrey A Henderson, Katherine L Tucker, José M Ordovás. Health Aff (Millwood) 2016
34
6

Low rates of acceptance of BRCA1 and BRCA2 test results among African American women at increased risk for hereditary breast-ovarian cancer.
Chanita Hughes Halbert, Lisa Kessler, Jill E Stopfer, Susan Domchek, E Paul Wileyto. Genet Med 2006
51
6

Genetic testing for inherited breast cancer risk in African Americans.
Chanita Hughes Halbert, Lisa Jay Kessler, Edith Mitchell. Cancer Invest 2005
44
6

Predictors of patient uptake of colorectal cancer gene environment risk assessment.
Michael J Hall, Sharon L Manne, Ronald E Myers, Eileen M Keenan, Andrew M Balshem, David S Weinberg. Genome Med 2012
10
20

Estimated deaths attributable to social factors in the United States.
Sandro Galea, Melissa Tracy, Katherine J Hoggatt, Charles Dimaggio, Adam Karpati. Am J Public Health 2011
230
6

Federal investments to eliminate racial/ethnic health-care disparities.
Ernest Moy, William Freeman. Public Health Rep 2014
13
15

Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.
Beth Anderson, Jennifer McLosky, Elizabeth Wasilevich, Sarah Lyon-Callo, Debra Duquette, Glenn Copeland. J Cancer Epidemiol 2012
62
6

Telegenetics: a systematic review of telemedicine in genetics services.
Jennifer S Hilgart, Julie A Hayward, Bernadette Coles, Rachel Iredale. Genet Med 2012
89
6

Service Delivery Model and Experiences in a Cancer Genetics Clinic for an Underserved Population.
Ashley H Woodson, Jessica L Profato, Minjeong Park, Sarah H Rizvi, Nisreen Elsayegh, Alyssa G Rieber, Banu K Arun. J Health Care Poor Underserved 2015
9
22

Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
57
6

Exploring attitudes, beliefs, and communication preferences of Latino community members regarding BRCA1/2 mutation testing and preventive strategies.
Anita Yeomans Kinney, Amanda Gammon, James Coxworth, Sara E Simonsen, Maritza Arce-Laretta. Genet Med 2010
65
6

Genetic testing and cancer risk management recommendations by physicians for at-risk relatives.
Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
77
6

Predictors of BRCA1/2 genetic testing among Black women with breast cancer: a population-based study.
Tarsha Jones, Anne Marie McCarthy, Younji Kim, Katrina Armstrong. Cancer Med 2017
30
6

Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians.
Cecelia A Bellcross, Katherine Kolor, Katrina A B Goddard, Ralph J Coates, Michele Reyes, Muin J Khoury. Am J Prev Med 2011
112
6

Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study.
Paul J Goodfellow, Caroline C Billingsley, Heather A Lankes, Shamshad Ali, David E Cohn, Russell J Broaddus, Nilsa Ramirez, Colin C Pritchard, Heather Hampel, Alexis S Chassen,[...]. J Clin Oncol 2015
104
6

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
55
6

Laboratory Assays in Evaluation of Lynch Syndrome in Patients with Endometrial Carcinoma.
Bojana Djordjevic, Russell R Broaddus. Surg Pathol Clin 2016
5
40

A Systematic Review on the Existing Screening Pathways for Lynch Syndrome Identification.
Alessia Tognetto, Maria Benedetta Michelazzo, Giovanna Elisa Calabró, Brigid Unim, Marco Di Marco, Walter Ricciardi, Roberta Pastorino, Stefania Boccia.  2017
8
25


Using behaviour change and implementation science to address low referral rates in oncology.
Janet C Long, Deborah Debono, Rachel Williams, Elizabeth Salisbury, Sharron O'Neill, Elizabeth Eykman, Jordan Butler, Robert Rawson, Kim-Chi Phan-Thien, Stephen R Thompson,[...]. BMC Health Serv Res 2018
12
16

Mismatch repair deficiency testing in clinical practice.
Natalia Buza, James Ziai, Pei Hui. Expert Rev Mol Diagn 2016
32
6

Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients.
Kimberly Resnick, J Michael Straughn, Floor Backes, Heather Hampel, Kellie S Matthews, David E Cohn. Obstet Gynecol 2009
51
6

Learning by Example: An International Perspective on Reflex-Testing for Lynch Syndrome.
Vanessa N Palter, Natalie A Baker, Aaron Pollett, Corinne Daly, Marcia Facey, Carolyn Rotenberg, Linda Rabeneck, Nancy N Baxter. Ann Surg Oncol 2019
5
40



Lynch syndrome: barriers to and facilitators of screening and disease management.
Kathy E Watkins, Christine Y Way, Jacqueline J Fiander, Robert J Meadus, Mary Jane Esplen, Jane S Green, Valerie C Ludlow, Holly A Etchegary, Patrick S Parfrey. Hered Cancer Clin Pract 2011
23
8

Success of referral to genetic counseling after positive lynch syndrome screening test.
Robin F Irons, Krysta M Contino, Janice J Horte, Brooke Levin, Kristin D Mattie, Margaret Wight, Michael E Kwiatt, Kathryn C Behling, Tina B Edmonston, Steven J McClane. Int J Colorectal Dis 2017
7
28

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
56
6

Increased yield of actionable mutations using multi-gene panels to assess hereditary cancer susceptibility in an ethnically diverse clinical cohort.
Charité Ricker, Julie O Culver, Katrina Lowstuter, Duveen Sturgeon, Julia D Sturgeon, Christopher R Chanock, William J Gauderman, Kevin J McDonnell, Gregory E Idos, Stephen B Gruber. Cancer Genet 2016
43
6

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
6

Colorectal cancer screening for average-risk adults: 2018 guideline update from the American Cancer Society.
Andrew M D Wolf, Elizabeth T H Fontham, Timothy R Church, Christopher R Flowers, Carmen E Guerra, Samuel J LaMonte, Ruth Etzioni, Matthew T McKenna, Kevin C Oeffinger, Ya-Chen Tina Shih,[...]. CA Cancer J Clin 2018
614
6

Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade.
Dung T Le, Jennifer N Durham, Kellie N Smith, Hao Wang, Bjarne R Bartlett, Laveet K Aulakh, Steve Lu, Holly Kemberling, Cara Wilt, Brandon S Luber,[...]. Science 2017
6

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
439
6

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
7
28

Development and validation of a colon cancer risk assessment tool for patients undergoing colonoscopy.
Fay Kastrinos, John I Allen, David H Stockwell, Elena M Stoffel, Earl F Cook, Muthoka L Mutinga, Judith Balmaña, Sapna Syngal. Am J Gastroenterol 2009
49
6

Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients.
Shilpa Grover, Elena M Stoffel, Laoti Bussone, Elizabeth Tschoegl, Sapna Syngal. Clin Gastroenterol Hepatol 2004
120
6


Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical center.
Brandie Heald, Thomas Plesec, Xiuli Liu, Rish Pai, Deepa Patil, Jessica Moline, Richard R Sharp, Carol A Burke, Matthew F Kalady, James Church,[...]. J Clin Oncol 2013
117
6

Targeted Cancer Next-Generation Sequencing as a Primary Screening Tool for Microsatellite Instability and Lynch Syndrome in Upper Gastrointestinal Tract Cancers.
Alexander G Christakis, David J Papke, Jonathan A Nowak, Matthew B Yurgelun, Agoston T Agoston, Neal I Lindeman, Laura E MacConaill, Lynette M Sholl, Fei Dong. Cancer Epidemiol Biomarkers Prev 2019
4
50

Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach,[...]. Am J Gastroenterol 2014
264
6


Comparison of Universal Versus Age-Restricted Screening of Colorectal Tumors for Lynch Syndrome Using Mismatch Repair Immunohistochemistry: A Cohort Study.
Dan Li, Elizabeth Hoodfar, Sheng-Fang Jiang, Natalia Udaltsova, Nhung P Pham, Yves Jodesty, Mary Anne Armstrong, Yun-Yi Hung, Robin J Baker, Debbie Postlethwaite,[...]. Ann Intern Med 2019
7
28



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.