A citation-based method for searching scientific literature

Gulvir Gill, Catherine Beard, Kirsty Storey, Shelby Taylor, Adrienne Sexton. Psychooncology 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Comprehension and personal value of negative non-diagnostic genetic panel testing.
Christin Hoell, Sharon Aufox, Nora Nashawaty, Melanie F Myers, Maureen E Smith. J Genet Couns 2021
3
50

Economic Evaluation of Population-Based BRCA1/BRCA2 Mutation Testing across Multiple Countries and Health Systems.
Ranjit Manchanda, Li Sun, Shreeya Patel, Olivia Evans, Janneke Wilschut, Ana Carolina De Freitas Lopes, Faiza Gaba, Adam Brentnall, Stephen Duffy, Bin Cui,[...]. Cancers (Basel) 2020
18
50

BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study.
Hildegunn Høberg-Vetti, Cathrine Bjorvatn, Bent E Fiane, Turid Aas, Kathrine Woie, Helge Espelid, Tone Rusken, Hans Petter Eikesdal, Wenche Listøl, Marianne T Haavind,[...]. Eur J Hum Genet 2016
44
50

Genetic susceptibility testing from a stress and coping perspective.
Holly C Gooding, Kurt Organista, Jeffrey Burack, Barbara Bowles Biesecker. Soc Sci Med 2006
66
50


Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
Joanne Armstrong, Michele Toscano, Nancy Kotchko, Sue Friedman, Marc D Schwartz, Katherine S Virgo, Kristian Lynch, James E Andrews, Claudia X Aguado Loi, Joseph E Bauer,[...]. JAMA Oncol 2015
84
50

Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
Peter D Beitsch, Pat W Whitworth, Kevin Hughes, Rakesh Patel, Barry Rosen, Gia Compagnoni, Paul Baron, Rache Simmons, Linda Ann Smith, Ian Grady,[...]. J Clin Oncol 2019
148
50

New paradigms for BRCA1/BRCA2 testing in women with ovarian cancer: results of the Genetic Testing in Epithelial Ovarian Cancer (GTEOC) study.
Inga Plaskocinska, Hannah Shipman, James Drummond, Edward Thompson, Vanessa Buchanan, Barbara Newcombe, Charlotte Hodgkin, Elisa Barter, Paul Ridley, Rita Ng,[...]. J Med Genet 2016
42
50

Population screening in the age of genomic medicine.
Muin J Khoury, Linda L McCabe, Edward R B McCabe. N Engl J Med 2003
246
50

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
936
50

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
44
50

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
23
50

A state-based approach to genomics for rare disease and population screening.
Kelly M East, Whitley V Kelley, Ashley Cannon, Meagan E Cochran, Irene P Moss, Thomas May, Mariko Nakano-Okuno, Stephen O Sodeke, Jeffrey C Edberg, James J Cimino,[...]. Genet Med 2021
5
50

Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines.
Cynthia L Neben, Anjali D Zimmer, Will Stedden, Jeroen van den Akker, Robert O'Connor, Raymond C Chan, Elaine Chen, Zheng Tan, Annette Leon, Jack Ji,[...]. J Mol Diagn 2019
49
50

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
Douglas K Owens, Karina W Davidson, Alex H Krist, Michael J Barry, Michael Cabana, Aaron B Caughey, Chyke A Doubeni, John W Epling, Martha Kubik, C Seth Landefeld,[...]. JAMA 2019
152
50

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
148
50

Identifying Primary Care Physicians Continuing Education Needs by Examining Clinical Practices, Attitudes, and Barriers to Screening Across Multiple Cancers.
Brenna Lynn, Alexandra Hatry, Chloe Burnett, Lisa Kan, Tunde Olatunbosun, Bob Bluman. J Cancer Educ 2018
7
50

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
65
50

Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award.
Mary-Claire King, Ephrat Levy-Lahad, Amnon Lahad. JAMA 2014
181
50

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
David J Carey, Samantha N Fetterolf, F Daniel Davis, William A Faucett, H Lester Kirchner, Uyenlinh Mirshahi, Michael F Murray, Diane T Smelser, Glenn S Gerhard, David H Ledbetter. Genet Med 2016
180
50

[Principles and practice of mass screening for disease].
J M Wilson, Y G Jungner. Bol Oficina Sanit Panam 1968
439
50

Cost-effectiveness of Population-Wide Genomic Screening for Hereditary Breast and Ovarian Cancer in the United States.
Gregory F Guzauskas, Shawn Garbett, Zilu Zhou, Scott J Spencer, Hadley S Smith, Jing Hao, Dina Hassen, Susan R Snyder, John A Graves, Josh F Peterson,[...]. JAMA Netw Open 2020
14
50

Experiences and attitudes of hereditary cancer screening patients in a consumer directed testing model.
V Greve, M Garner, K Odom, S J Cooper, K M East. Patient Educ Couns 2021
1
100

Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.
Josephine Shaw, Caroline Bulsara, Paul A Cohen, Madeleine Gryta, Cassandra B Nichols, Lyn Schofield, Sarah O'Sullivan, Nicholas Pachter, Sarah J Hardcastle. Patient Educ Couns 2018
15
50

Using the common sense model to understand perceived cancer risk in individuals testing for BRCA1/2 mutations.
Kimberly Kelly, Howard Leventhal, Michael Andrykowski, Deborah Toppmeyer, Judy Much, James Dermody, Monica Marvin, Jill Baran, Marvin Schwalb. Psychooncology 2005
60
50

Psychiatric implications of cancer genetic testing.
April Malia Hirschberg, Gayun Chan-Smutko, William F Pirl. Cancer 2015
29
50

The dawn of consumer-directed testing.
Erica Ramos, Scott M Weissman. Am J Med Genet C Semin Med Genet 2018
30
50

Recruiting diversity where it exists: The Alabama Genomic Health Initiative.
Thomas May, Ashley Cannon, Irene P Moss, Mariko Nakano-Okuno, Sharonda Hardy, Edrika L Miskell, Whitley V Kelley, William Curry, Kelly M East, Aras Acemgil,[...]. J Genet Couns 2020
3
50

Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology.
Katie L Lewis, Paul K J Han, Gillian W Hooker, William M P Klein, Leslie G Biesecker, Barbara B Biesecker. PLoS One 2015
36
50

Primary care providers' cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda.
Jada G Hamilton, Ekland Abdiwahab, Heather M Edwards, Min-Lin Fang, Andrew Jdayani, Erica S Breslau. J Gen Intern Med 2017
59
50

Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
16
50

Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives.
Chris Jacobs, Caroline Dancyger, Jonathan A Smith, Susan Michie. Eur J Hum Genet 2015
19
50

Adherence to NCCN Guidelines for Genetic Testing in Breast Cancer Patients: Who Are We Missing?
J Jaime Alberty-Oller, Sarah Weltz, Antonio Santos, Kereeti Pisapati, Meng Ru, Christina Weltz, Hank Schmidt, Elisa Port. Ann Surg Oncol 2021
4
50

Engaging Patients in Precision Oncology: Development and Usability of a Web-Based Patient-Facing Genomic Sequencing Report.
Ilana B Solomon, Sarah McGraw, Jenny Shen, Adem Albayrak, Gil Alterovitz, Melanie Davies, Catherine Del Vecchio Fitz, Rachel A Freedman, Lisa N Lopez, Lynette M Sholl,[...]. JCO Precis Oncol 2020
5
50

The uptake of predictive DNA testing in 40 families with a pathogenic BRCA1/BRCA2 variant. An evaluation of the proband-mediated procedure.
Fred H Menko, Kiki N Jeanson, Eveline M A Bleiker, Carla W M van Tiggelen, Frans B L Hogervorst, Jacqueline A Ter Stege, Daoud Ait Moha, Lizet E van der Kolk. Eur J Hum Genet 2020
7
50

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
7
50

A regional population-based hereditary breast cancer screening tool in Italy: First 5-year results.
Laura Cortesi, Bruna Baldassarri, Stefano Ferretti, Elisabetta Razzaboni, Mariangela Bella, Lauro Bucchi, Debora Canuti, Pierandrea De Iaco, Giorgio De Santis, Fabio Falcini,[...]. Cancer Med 2020
8
50

Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.
Jennifer L Caswell-Jin, Anjali D Zimmer, Will Stedden, Kerry E Kingham, Alicia Y Zhou, Allison W Kurian. J Natl Cancer Inst 2019
53
50

30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes.
Emma R Woodward, Kate Green, George J Burghel, Michael Bulman, Tara Clancy, Fiona Lalloo, Helene Schlecht, Andrew J Wallace, D Gareth Evans. Eur J Hum Genet 2022
3
50

An Update on Immune Checkpoint Therapy for the Treatment of Lynch Syndrome.
Christina Therkildsen, Lars Henrik Jensen, Maria Rasmussen, Inge Bernstein. Clin Exp Gastroenterol 2021
5
50

Economic Evaluation of Universal Lynch Syndrome Screening Protocols among Newly Diagnosed Patients with Colorectal Cancer.
Jing Hao, Dina Hassen, James M Gudgeon, Susan R Snyder, Heather Hampel, Marc S Williams, Ravi N Sharaf, Christine Y Lu, Janet L Williams, Victoria Schlieder,[...]. J Pers Med 2021
1
100

Underdiagnosis of Hereditary Colorectal Cancers Among Medicare Patients: Genetic Testing Criteria for Lynch Syndrome Miss the Mark.
Charles Muller, Sarah M Nielsen, Kathryn E Hatchell, Shan Yang, Scott T Michalski, Barbara Hamlington, Robert L Nussbaum, Edward D Esplin, Sonia S Kupfer. JCO Precis Oncol 2021
2
50

Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.
Jacques Ferlay, Isabelle Soerjomataram, Rajesh Dikshit, Sultan Eser, Colin Mathers, Marise Rebelo, Donald Maxwell Parkin, David Forman, Freddie Bray. Int J Cancer 2015
50

Precision Public Health for the Era of Precision Medicine.
Muin J Khoury, Michael F Iademarco, William T Riley. Am J Prev Med 2016
235
50


Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort.
Robert J MacInnis, Julia A Knight, Wendy K Chung, Roger L Milne, Alice S Whittemore, Richard Buchsbaum, Yuyan Liao, Nur Zeinomar, Gillian S Dite, Melissa C Southey,[...]. J Natl Cancer Inst 2021
7
50

Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families.
Emma Healey, Natalie Taylor, Sian Greening, Claire E Wakefield, Linda Warwick, Rachel Williams, Kathy Tucker. Genet Med 2017
21
50

Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes.
Janet R Vos, Lisette Giepmans, Claas Röhl, Nicoline Geverink, Nicoline Hoogerbrugge. Fam Cancer 2019
6
50

BRCA in breast cancer: ESMO Clinical Practice Guidelines.
J Balmaña, O Díez, I T Rubio, F Cardoso. Ann Oncol 2011
123
50

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
13
50


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.