A citation-based method for searching scientific literature

Beth Anderson, Jennifer McLosky, Elizabeth Wasilevich, Sarah Lyon-Callo, Debra Duquette, Glenn Copeland. J Cancer Epidemiol 2012
Times Cited: 62







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



Times Cited
  Times     Co-cited
Similarity


Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.
Phuong L Mai, Ana F Best, June A Peters, Rosamma M DeCastro, Payal P Khincha, Jennifer T Loud, Renée C Bremer, Philip S Rosenberg, Sharon A Savage. Cancer 2016
181
1

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene.
Siân Jones, Ralph H Hruban, Mihoko Kamiyama, Michael Borges, Xiaosong Zhang, D Williams Parsons, Jimmy Cheng-Ho Lin, Emily Palmisano, Kieran Brune, Elizabeth M Jaffee,[...]. Science 2009
528
1

Screening for Pancreatic Cancer: US Preventive Services Task Force Reaffirmation Recommendation Statement.
Douglas K Owens, Karina W Davidson, Alex H Krist, Michael J Barry, Michael Cabana, Aaron B Caughey, Susan J Curry, Chyke A Doubeni, John W Epling, Martha Kubik,[...]. JAMA 2019
67
1

A large health system's approach to utilization of the genetic counselor CPT® 96040 code.
Shanna L Gustafson, Gail Pfeiffer, Charis Eng. Genet Med 2011
16
6

Genetic counselors save costs across the genetic testing spectrum.
Joy Larsen Haidle, Darci L Sternen, Jane A Dickerson, Amelia Mroch, Denise F Needham, Christine M Riordan, Michele C Kieke. Am J Manag Care 2017
7
14

Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing.
Christine E Miller, Patti Krautscheid, Erin E Baldwin, Tatiana Tvrdik, Amanda S Openshaw, Kim Hart, Danielle Lagrave. Am J Med Genet A 2014
68
1


Health insurance coverage of genetic services in Illinois.
Megan Latchaw, Kelly Ormond, Maureen Smith, John Richardson, Catherine Wicklund. Genet Med 2010
13
7

Billing for medical genetics and genetic counseling services: a national survey.
Tabitha A Harrison, Debra Lochner Doyle, Caroline McGowan, Leslie Cohen, Elizabeth Repass, Ruthann B Pfau, Trish Brown. J Genet Couns 2010
20
5


Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).
Caroline Savage Bennette, Susan Brown Trinidad, Stephanie M Fullerton, Donald Patrick, Laura Amendola, Wylie Burke, Fuki M Hisama, Gail P Jarvik, Dean A Regier, David L Veenstra. Genet Med 2013
57
1

Tracking implementation strategies: a description of a practical approach and early findings.
Alicia C Bunger, Byron J Powell, Hillary A Robertson, Hannah MacDowell, Sarah A Birken, Christopher Shea. Health Res Policy Syst 2017
47
2

Measuring perceived exercise capability and investigating its relationship with childhood obesity: a feasibility study.
M J Taylor, D Arriscado, I Vlaev, D Taylor, P Gately, A Darzi. Int J Obes (Lond) 2016
7
14

Predicting risk behaviors: development and validation of a diagnostic scale.
K Witte, K A Cameron, J K McKeon, J M Berkowitz. J Health Commun 1996
204
1

How communication of genetic information within the family is addressed in genetic counselling: a systematic review of research evidence.
Álvaro Mendes, Milena Paneque, Liliana Sousa, Angus Clarke, Jorge Sequeiros. Eur J Hum Genet 2016
36
2

Development and testing of the KnowGene scale to assess general cancer genetic knowledge related to multigene panel testing.
Meghan Underhill-Blazey, Jill Stopfer, Anu Chittenden, Manan M Nayak, Kristina Lansang, Ruth Lederman, Judy Garber, Daniel A Gundersen. Patient Educ Couns 2019
8
12

Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
Megan C Roberts, W David Dotson, Christopher S DeVore, Erica M Bednar, Deborah J Bowen, Theodore G Ganiats, Ridgely Fisk Green, Georgia M Hurst, Alisdair R Philp, Charité N Ricker,[...]. Health Aff (Millwood) 2018
51
1



Low rates of cascade genetic testing among families with hereditary gynecologic cancer: An opportunity to improve cancer prevention.
Natalie E Griffin, Tommy R Buchanan, Stephanie H Smith, Andrea A Leon, Melissa F Meyer, Jingxia Liu, Rachel G Tabak, Katherine C Fuh, Premal H Thaker, Matthew A Powell,[...]. Gynecol Oncol 2020
8
12

Family communication of genetic test results among women with inherited breast cancer genes.
Deborah Cragun, Anne Weidner, Ann Tezak, Kate Clouse, Tuya Pal. J Genet Couns 2021
3
33


Psychometric evaluation of a measure of factors influencing hand hygiene behaviour to inform intervention.
S Lydon, C Greally, O Tujjar, K Reddy, K Lambe, C Madden, C Walsh, S Fox, P O'Connor. J Hosp Infect 2019
10
10

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial.
Willem Eijzenga, Eveline de Geus, Cora M Aalfs, Fred H Menko, Rolf H Sijmons, Hanneke C J M de Haes, Ellen M A Smets. Patient Educ Couns 2018
9
11

What explains the socioeconomic status gap in activity? Educational differences in determinants of physical activity and screentime.
Nelli Hankonen, Matti T J Heino, Emilia Kujala, Sini-Tuuli Hynynen, Pilvikki Absetz, Vera Araújo-Soares, Katja Borodulin, Ari Haukkala. BMC Public Health 2017
17
5


Psychosocial and clinical factors of probands impacting intrafamilial disclosure and uptake of genetic testing among families with BRCA1/2 or MMR gene mutations.
Nathalie Alegre, Pierre Vande Perre, Yves Jean Bignon, Aude Michel, Virginie Galibert, Ornellia Mophawe, Carole Corsini, Isabelle Coupier, Jean Chiesa, Laura Robert,[...]. Psychooncology 2019
5
20

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases.
Tuya Pal, Jenny Permuth-Wey, Judith A Betts, Jeffrey P Krischer, James Fiorica, Hector Arango, James LaPolla, Mitchell Hoffman, Martin A Martino, Katie Wakeley,[...]. Cancer 2005
498
1

Development and initial validation of the Influences on Patient Safety Behaviours Questionnaire.
Natalie Taylor, Sahdia Parveen, Victoria Robins, Beverley Slater, Rebecca Lawton. Implement Sci 2013
31
3

Fulfilled Emotional Outcome Expectancies Enable Successful Adoption and Maintenance of Physical Activity.
Verena Klusmann, Lisa Musculus, Gudrun Sproesser, Britta Renner. Front Psychol 2016
20
5

Assessing relatives' readiness for hereditary cancer cascade genetic testing.
Erica M Bednar, Charlotte C Sun, Sheryl McCurdy, Sally W Vernon. Genet Med 2020
9
11

A randomized trial comparing the effect of two phone-based interventions on colorectal cancer screening adherence.
Usha Menon, Rhonda Belue, Stéphanie Wahab, Kathryn Rugen, Anita Y Kinney, Peter Maramaldi, Debra Wujcik, Laura A Szalacha. Ann Behav Med 2011
47
2


Sharing genetic test results with family members of BRCA, PALB2, CHEK2, and ATM carriers.
Marleah Dean, Ann L Tezak, Sabrina Johnson, Joy K Pierce, Anne Weidner, Kate Clouse, Tuya Pal, Deborah Cragun. Patient Educ Couns 2021
4
25

Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis.
Jenna Petersen, Cathryn Koptiuch, Yelena P Wu, Ryan Mooney, Ashley Elrick, Kathryn Szczotka, Megan Keener, Lisa Pappas, Priyanka Kanth, Andrew Soisson,[...]. Patient Educ Couns 2018
5
20

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
14
7

Psychometric assessment of three newly developed implementation outcome measures.
Bryan J Weiner, Cara C Lewis, Cameo Stanick, Byron J Powell, Caitlin N Dorsey, Alecia S Clary, Marcella H Boynton, Heather Halko. Implement Sci 2017
199
1

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
Rachel Pearlman, Wendy L Frankel, Benjamin Swanson, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen, Paul J Goodfellow,[...]. JAMA Oncol 2017
269
1

Colonoscopy screening compliance and outcomes in patients with Lynch syndrome.
K Newton, K Green, F Lalloo, D G Evans, J Hill. Colorectal Dis 2015
32
3



Usefulness scale for patient information material (USE) - development and psychometric properties.
Lars P Hölzel, Zivile Ries, Jörg Dirmaier, Jördis M Zill, Levente Kriston, Christian Klesse, Martin Härter, Isaac Bermejo. BMC Med Inform Decis Mak 2015
13
7

Coincidence analysis: a new method for causal inference in implementation science.
Rebecca Garr Whitaker, Nina Sperber, Michael Baumgartner, Alrik Thiem, Deborah Cragun, Laura Damschroder, Edward J Miech, Alecia Slade, Sarah Birken. Implement Sci 2020
6
16

Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.
Jan M Hodgson, Sylvia A Metcalfe, Maryanne Aitken, Susan M Donath, Clara L Gaff, Ingrid M Winship, Martin B Delatycki, Loane L C Skene, Belinda J McClaren, Jean L Paul,[...]. BMC Med Genet 2014
18
5

Measuring determinants of implementation behavior: psychometric properties of a questionnaire based on the theoretical domains framework.
Johanna M Huijg, Winifred A Gebhardt, Elise Dusseldorp, Marieke W Verheijden, Nicolette van der Zouwe, Barend J C Middelkoop, Mathilde R Crone. Implement Sci 2014
117
1

Acceptability, reliability, and validity of a brief measure of capabilities, opportunities, and motivations ("COM-B").
Chris Keyworth, Tracy Epton, Joanna Goldthorpe, Rachel Calam, Christopher J Armitage. Br J Health Psychol 2020
13
7


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.