A citation-based method for searching scientific literature

Kathleen F Mittendorf, Chinedu Ukaegbu, Marian J Gilmore, Nangel M Lindberg, Tia L Kauffman, Donna J Eubanks, Elizabeth Shuster, Jake Allen, Carmit McMullen, Heather Spencer Feigelson, Katherine P Anderson, Michael C Leo, Jessica Ezzell Hunter, Sonia Okuyama Sasaki, Jamilyn M Zepp, Sapna Syngal, Benjamin S Wilfond, Katrina A B Goddard. Fam Cancer 2022
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


DECIDE: a Decision Support Tool to Facilitate Parents' Choices Regarding Genome-Wide Sequencing.
Patricia Birch, S Adam, N Bansback, R R Coe, J Hicklin, A Lehman, K C Li, J M Friedman. J Genet Couns 2016
26
20

Identification of Medically Actionable Secondary Findings in the 1000 Genomes.
Emily Olfson, Catherine E Cottrell, Nicholas O Davidson, Christina A Gurnett, Jonathan W Heusel, Nathan O Stitziel, Li-Shiun Chen, Sarah Hartz, Rakesh Nagarajan, Nancy L Saccone,[...]. PLoS One 2015
59
20

Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
20

Choosing treatment and screening options congruent with values: Do decision aids help? Sub-analysis of a systematic review.
Sarah Munro, Dawn Stacey, Krystina B Lewis, Nick Bansback. Patient Educ Couns 2016
23
20

Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.
Shubhangi Arora, Eden Haverfield, Gabriele Richard, Susanne B Haga, Rachel Mills. J Genet Couns 2016
13
20

A decision aid for additional findings in genomic sequencing: Development and pilot testing.
Amanda S Freed, Inga Gruß, Carmit K McMullen, Michael C Leo, Tia L Kauffman, Kathryn M Porter, Kristin R Muessig, Donna Eubanks, Katrina A B Goddard, Benjamin S Wilfond,[...]. Patient Educ Couns 2021
4
25

How digital tools can advance quality and equity in genomic medicine.
Yvonne Bombard, Robin Z Hayeems. Nat Rev Genet 2020
16
20

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
689
20

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
22
20

The REDCap consortium: Building an international community of software platform partners.
Paul A Harris, Robert Taylor, Brenda L Minor, Veida Elliott, Michelle Fernandez, Lindsay O'Neal, Laura McLeod, Giovanni Delacqua, Francesco Delacqua, Jacqueline Kirby,[...]. J Biomed Inform 2019
20

Impact of patient education videos on genetic counseling outcomes after exome sequencing.
Rebecca Hernan, Megan T Cho, Ashley L Wilson, Priyanka Ahimaz, Catherine Au, Sara M Berger, Edwin Guzman, Michelle Primiano, Jessica E Shaw, Meredith Ross,[...]. Patient Educ Couns 2020
8
20

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
705
20

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
146
20

Is "incidental finding" the best term?: a study of patients' preferences.
Nina Tan, Laura M Amendola, Julianne M O'Daniel, Amber Burt, Martha J Horike-Pyne, Lacey Boshe, Gail E Henderson, Christine Rini, Myra I Roche, Fuki M Hisama,[...]. Genet Med 2017
25
20

Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing.
Layla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, Melissa C Parra, Sha Tang, Kelly D Farwell Gonzalez. Genet Med 2014
78
20

Application of a framework to guide genetic testing communication across clinical indications.
Miranda L G Hallquist, Eric P Tricou, Kelly E Ormond, Juliann M Savatt, Curtis R Coughlin, W Andrew Faucett, Laura Hercher, Howard P Levy, Julianne M O'Daniel, Holly L Peay,[...]. Genome Med 2021
3
33

Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial.
Yvonne Bombard, Marc Clausen, Salma Shickh, Chloe Mighton, Selina Casalino, Theresa H M Kim, Sarah M Muir, Lindsay Carlsson, Nancy Baxter, Adena Scheer,[...]. Genet Med 2020
15
20

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
73
20

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.
Yvonne Bombard, Marc Clausen, Chloe Mighton, Lindsay Carlsson, Selina Casalino, Emily Glogowski, Kasmintan Schrader, Michael Evans, Adena Scheer, Nancy Baxter,[...]. Eur J Hum Genet 2018
26
20


Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study.
Frederick E Dewey, Michael F Murray, John D Overton, Lukas Habegger, Joseph B Leader, Samantha N Fetterolf, Colm O'Dushlaine, Cristopher V Van Hout, Jeffrey Staples, Claudia Gonzaga-Jauregui,[...]. Science 2016
319
20

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.
Erin Turbitt, Paola P Chrysostomou, Holly L Peay, Alexis R Heidlebaugh, Lawrence M Nelson, Barbara B Biesecker. Eur J Hum Genet 2018
8
20

Validity of a low literacy version of the Decisional Conflict Scale.
Suzanne K Linder, Paul R Swank, Sally W Vernon, Patricia D Mullen, Robert O Morgan, Robert J Volk. Patient Educ Couns 2011
49
20

Readability of informed consent forms for whole-exome and whole-genome sequencing.
Emilia Niemiec, Danya F Vears, Pascal Borry, Heidi Carmen Howard. J Community Genet 2018
14
20

Robustness of a multivariate normal approximation for imputation of incomplete binary data.
Coen A Bernaards, Thomas R Belin, Joseph L Schafer. Stat Med 2007
103
20

Bias.
Miguel Delgado-Rodríguez, Javier Llorca. J Epidemiol Community Health 2004
610
20

Exploring the motivations of research participants who chose not to learn medically actionable secondary genetic findings about themselves.
Will Schupmann, Skye A Miner, Haley K Sullivan, Jamie R Glover, Janet E Hall, Shepherd H Schurman, Benjamin E Berkman. Genet Med 2021
7
20

Decision aid for patients considering total knee arthroplasty with preference report for surgeons: a pilot randomized controlled trial.
Dawn Stacey, Gillian Hawker, Geoffrey Dervin, Peter Tugwell, Laura Boland, Marie-Pascale Pomey, Annette M O'Connor, Monica Taljaard. BMC Musculoskelet Disord 2014
51
20

Experiences with obtaining informed consent for genomic sequencing.
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am J Med Genet A 2015
73
20

The future is now: Technology's impact on the practice of genetic counseling.
Erynn S Gordon, Deepti Babu, Dawn A Laney. Am J Med Genet C Semin Med Genet 2018
22
20

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
164
20

Low Rates of Genetic Counseling and Testing in Individuals at Risk for Lynch Syndrome Reported in the National Health Interview Survey.
Nolan Faust, Charles Muller, Joshua Prenner, Sang Mee Lee, Sonia S Kupfer. Gastroenterology 2020
6
20

Implementing Systematic Genetic Counseling and Multigene Germline Testing for Individuals With Pancreatic Cancer.
Anu Chittenden, Sigurdis Haraldsdottir, Chinedu Ukaegbu, Meghan Underhill-Blazey, Shraddha Gaonkar, Hajime Uno, Lauren K Brais, Kimberly Perez, Brian M Wolpin, Sapna Syngal,[...]. JCO Oncol Pract 2021
8
20

Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.
Hyuna Sung, Jacques Ferlay, Rebecca L Siegel, Mathieu Laversanne, Isabelle Soerjomataram, Ahmedin Jemal, Freddie Bray. CA Cancer J Clin 2021
20

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Mark Clendenning, Kaisa Sotamaa, Thomas Prior, Judith A Westman,[...]. J Clin Oncol 2008
577
20

Up-Front Multigene Panel Testing for Cancer Susceptibility in Patients With Newly Diagnosed Endometrial Cancer: A Multicenter Prospective Study.
Monica D Levine, Rachel Pearlman, Heather Hampel, Casey Cosgrove, David Cohn, Alexis Chassen, Adrian Suarez, David A Barrington, Joseph P McElroy, Steven Waggoner,[...]. JCO Precis Oncol 2021
5
20

Mainstream consent programs for genetic counseling in cancer patients: A systematic review.
Tahlia Scheinberg, Alison Young, Henry Woo, Annabel Goodwin, Kate L Mahon, Lisa G Horvath. Asia Pac J Clin Oncol 2021
16
20

Uptake and acceptability of a mainstreaming model of hereditary cancer multigene panel testing among patients with ovarian, pancreatic, and prostate cancer.
Jada G Hamilton, Heather Symecko, Kelsey Spielman, Kelsey Breen, Rebecca Mueller, Amanda Catchings, Magan Trottier, Erin E Salo-Mullen, Ibrahim Shah, Anna Arutyunova,[...]. Genet Med 2021
9
20

Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing Study.
Pedro L S Uson, N Jewel Samadder, Douglas Riegert-Johnson, Lisa Boardman, Mitesh J Borad, Daniel Ahn, Mohamad B Sonbol, Douglas O Faigel, Norio Fukami, Rahul Pannala,[...]. Clin Transl Gastroenterol 2021
4
25

Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis.
Uri Ladabaum, Grace Wang, Jonathan Terdiman, Amie Blanco, Miriam Kuppermann, C Richard Boland, James Ford, Elena Elkin, Kathryn A Phillips. Ann Intern Med 2011
254
20

Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome.
Kathleen M Schmeler, Henry T Lynch, Lee-may Chen, Mark F Munsell, Pamela T Soliman, Mary Beth Clark, Molly S Daniels, Kristin G White, Stephanie G Boyd-Rogers, Peggy G Conrad,[...]. N Engl J Med 2006
488
20

Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative.
Rachel Pearlman, Wendy L Frankel, Benjamin J Swanson, Dan Jones, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen,[...]. JCO Precis Oncol 2021
13
20

TBCRC 048: Phase II Study of Olaparib for Metastatic Breast Cancer and Mutations in Homologous Recombination-Related Genes.
Nadine M Tung, Mark E Robson, Steffen Ventz, Cesar A Santa-Maria, Rita Nanda, Paul K Marcom, Payal D Shah, Tarah J Ballinger, Eddy S Yang, Shaveta Vinayak,[...]. J Clin Oncol 2020
116
20

Prevalence of Germline Variants in Prostate Cancer and Implications for Current Genetic Testing Guidelines.
Piper Nicolosi, Elisa Ledet, Shan Yang, Scott Michalski, Brandy Freschi, Erin O'Leary, Edward D Esplin, Robert L Nussbaum, Oliver Sartor. JAMA Oncol 2019
148
20

Decrease in mortality in Lynch syndrome families because of surveillance.
Andrea E de Jong, Yvonne M C Hendriks, Jan H Kleibeuker, Sybrand Y de Boer, Annemieke Cats, Gerrit Griffioen, Fokko M Nagengast, Frits G Nelis, Matti A Rookus, Hans F A Vasen. Gastroenterology 2006
187
20

Prevalence of Germline Alterations on Targeted Tumor-Normal Sequencing of Esophagogastric Cancer.
Geoffrey Y Ku, Yelena Kemel, Steve B Maron, Joanne F Chou, Vignesh Ravichandran, Zarina Shameer, Anna Maio, Elizabeth S Won, David P Kelsen, David H Ilson,[...]. JAMA Netw Open 2021
7
20

Deleterious Germline Mutations in Patients With Apparently Sporadic Pancreatic Adenocarcinoma.
Koji Shindo, Jun Yu, Masaya Suenaga, Shahriar Fesharakizadeh, Christy Cho, Anne Macgregor-Das, Abdulrehman Siddiqui, P Dane Witmer, Koji Tamura, Tae Jun Song,[...]. J Clin Oncol 2017
226
20

Non-BRCA DNA Damage Repair Gene Alterations and Response to the PARP Inhibitor Rucaparib in Metastatic Castration-Resistant Prostate Cancer: Analysis From the Phase II TRITON2 Study.
Wassim Abida, David Campbell, Akash Patnaik, Jeremy D Shapiro, Brieuc Sautois, Nicholas J Vogelzang, Eric G Voog, Alan H Bryce, Ray McDermott, Francesco Ricci,[...]. Clin Cancer Res 2020
165
20

Low Referral Rate for Genetic Testing in Racially and Ethnically Diverse Patients Despite Universal Colorectal Cancer Screening.
Charles Muller, Sang Mee Lee, William Barge, Shazia M Siddique, Shivali Berera, Gina Wideroff, Rashmi Tondon, Jeremy Chang, Meaghan Peterson, Jessica Stoll,[...]. Clin Gastroenterol Hepatol 2018
50
20

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,[...]. Gastroenterology 2014
280
20


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.