A citation-based method for searching scientific literature

Deborah Cragun, Anne Weidner, Courtney Lewis, Devon Bonner, Jongphil Kim, Susan T Vadaparampil, Tuya Pal. Cancer 2017
Times Cited: 76







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



Times Cited
  Times     Co-cited
Similarity


Breast and ovarian cancer penetrance of BRCA1/2 mutations among Hong Kong women.
LingJiao Zhang, Vivian Y Shin, Xinglei Chai, Alan Zhang, Tsun L Chan, Edmond S Ma, Timothy R Rebbeck, Jinbo Chen, Ava Kwong. Oncotarget 2018
3
33


Early-emerging cognitive vulnerability to depression and the serotonin transporter promoter region polymorphism.
Elizabeth P Hayden, Lea R Dougherty, Bryan Maloney, Thomas M Olino, Haroon Sheikh, C Emily Durbin, John I Nurnberger, Debomoy K Lahiri, Daniel N Klein. J Affect Disord 2008
44
2

Olaparib monotherapy in patients with advanced cancer and a germline BRCA1/2 mutation.
Bella Kaufman, Ronnie Shapira-Frommer, Rita K Schmutzler, M William Audeh, Michael Friedlander, Judith Balmaña, Gillian Mitchell, Georgeta Fried, Salomon M Stemmer, Ayala Hubert,[...]. J Clin Oncol 2015
944
1

Decisional consideration of hereditary colon cancer genetic test results among Hong Kong chinese adults.
Samuel M Y Ho, Judy W C Ho, Cecilia L W Chan, Kedo Kwan, Yenny K Y Tsui. Cancer Epidemiol Biomarkers Prev 2003
27
3

Establishing a cancer genetics programme in Asia - the singapore experience.
Wei-Shieng Chieng, Soo-Chin Lee. Hered Cancer Clin Pract 2006
12
8

Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel.
Ava Kwong, Vivian Y Shin, Chun H Au, Fian B F Law, Dona N Ho, Bui K Ip, Anthony T C Wong, Silvia S Lau, Rene M Y To, Gigi Choy,[...]. J Mol Diagn 2016
17
5


Willingness of Japanese patients with breast cancer to have genetic testing of BRCA without burden of expenses.
Hiroshi Nakagomi, Ikuko Sakamoto, Yosuke Hirotsu, Kenji Amemiya, Hitoshi Mochizuki, Masayuki Inoue, Satoko Nakagomi, Takeo Kubota, Masao Omata. Breast Cancer 2016
6
16

"Decoding hereditary breast cancer" benefits and questions from multigene panel testing.
Chrystelle Colas, Lisa Golmard, Antoine de Pauw, Sandrine M Caputo, Dominique Stoppa-Lyonnet. Breast 2019
12
8

Acceptance, motivators, and barriers in attending breast cancer genetic counseling in Asians.
Tan-Min Chin, Sing-Huang Tan, Siew-Eng Lim, Philip Iau, Wei-Peng Yong, Seng-Weng Wong, Soo-Chin Lee. Cancer Detect Prev 2005
28
3


Utilization of BRCA1/2 genetic testing in the clinical setting: report from a single institution.
Soo-Chin Lee, Barbara A Bernhardt, Kathy J Helzlsouer. Cancer 2002
45
2

Efficacy and safety of olaparib monotherapy in germline BRCA1/2 mutation carriers with advanced ovarian cancer and three or more lines of prior therapy.
Susan M Domchek, Carol Aghajanian, Ronnie Shapira-Frommer, Rita K Schmutzler, M William Audeh, Michael Friedlander, Judith Balmaña, Gillian Mitchell, Georgeta Fried, Salomon M Stemmer,[...]. Gynecol Oncol 2016
132
1

First FDA authorization for next-generation sequencer.
Francis S Collins, Margaret A Hamburg. N Engl J Med 2013
121
1


Race, Poverty, and Initial Implementation of Precision Medicine for Lung Cancer.
Kenneth L Kehl, Christopher S Lathan, Bruce E Johnson, Deborah Schrag. J Natl Cancer Inst 2019
9
11

Payer coverage policies for multigene tests.
Kathryn A Phillips, Patricia A Deverka, Julia R Trosman, Michael P Douglas, James D Chambers, Christine B Weldon, Andrew P Dervan. Nat Biotechnol 2017
24
4

Experiences of Cervical Cancer Survivors in Rural Eastern North Carolina: a Qualitative Assessment.
Alice R Richman, Jamie L Troutman, Essie Torres. J Cancer Educ 2016
3
33

Insurance Coverage Policies for Pharmacogenomic and Multi-Gene Testing for Cancer.
Christine Y Lu, Stephanie Loomer, Rachel Ceccarelli, Kathleen M Mazor, James Sabin, Ellen Wright Clayton, Geoffrey S Ginsburg, Ann Chen Wu. J Pers Med 2018
18
5

Ask, understand, remember: a brief measure of patient communication self-efficacy within clinical encounters.
Marla L Clayman, Anjali U Pandit, Ashley R Bergeron, Kenzie A Cameron, Emily Ross, Michael S Wolf. J Health Commun 2010
36
2

Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.
Stephanie A Kraft, Kathryn M Porter, Devan M Duenas, Claudia Guerra, Galen Joseph, Sandra Soo-Jin Lee, Kelly J Shipman, Jake Allen, Donna Eubanks, Tia L Kauffman,[...]. AJOB Empir Bioeth 2021
4
25

Hereditary cancer predisposition syndromes.
Judy E Garber, Kenneth Offit. J Clin Oncol 2005
315
1

Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
33
3

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
2
50

The association between knowledge and attitudes about genetic testing for cancer risk in the United States.
Abigail Rose, Nikki Peters, Judy A Shea, Katrina Armstrong. J Health Commun 2005
49
2

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
1

Differences in Family Health History Knowledge Among Bisexual and Lesbian Women.
Megan C Roberts, Melinda Krakow, Christopher W Wheldon, Michelle I Silver. LGBT Health 2019
2
50

Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening.
Joel E Pacyna, Gabriel Q Shaibi, Alex Lee, Jamie O Byrne, Idali Cuellar, Erica J Sutton, Valentina Hernandez, Noralane M Lindor, Davinder Singh, Iftikhar J Kullo,[...]. Genet Med 2021
1
100

Genetic Counselor and Healthcare Interpreter Perspectives on the Role of Interpreters in Cancer Genetic Counseling.
Karlena Lara-Otero, Jon Weil, Claudia Guerra, Janice Ka Yan Cheng, Janey Youngblom, Galen Joseph. Health Commun 2019
6
16

Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
Roberta Zuntini, Simona Ferrari, Elena Bonora, Francesco Buscherini, Benedetta Bertonazzi, Mina Grippa, Lea Godino, Sara Miccoli, Daniela Turchetti. Front Genet 2018
5
20

Barriers and facilitators to dissemination and adoption of precision medicine among Hispanics/Latinos.
Juan R Canedo, Consuelo H Wilkins, Nicole Senft, Araceli Romero, Kemberlee Bonnet, David Schlundt. BMC Public Health 2020
4
25


Assessing patients' experiences with communication across the cancer care continuum.
Kathleen M Mazor, Richard L Street, Valerie M Sue, Andrew E Williams, Borsika A Rabin, Neeraj K Arora. Patient Educ Couns 2016
19
5

Translation and validation of a Spanish-language genetic health literacy screening tool.
Sally Ann Rodríguez, Debra L Roter, Carlos Castillo-Salgado, Gillian W Hooker, Lori H Erby. Health Psychol 2015
9
11

Family health history and health behaviors in Alaska native and American Indian people.
Martha L Slattery, Maureen A Murtaugh, Anne P Lanier, Khe-Ni Ma, Elizabeth D Ferucci, Ruth A Etzel, Sandra Edwards. J Health Care Poor Underserved 2009
5
20


The genetic prediction of risk for gynecologic cancers.
Leslie M Randall, Bhavana Pothuri. Gynecol Oncol 2016
29
3

Exploring the short-term impact of DNA-testing in breast cancer patients: the counselees' perception matters, but the actual BRCA1/2 result does not.
Joël Vos, Jan C Oosterwijk, Encarna Gomez-Garcia, Fred H Menko, Margriet J Collee, Christi J van Asperen, Anna M Jansen, Anne M Stiggelbout, Aad Tibben. Patient Educ Couns 2012
22
4

Highly penetrant hereditary cancer syndromes.
Rebecca Nagy, Kevin Sweet, Charis Eng. Oncogene 2004
180
1

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
Meng Li, Caroline S Bennette, Laura M Amendola, M Ragan Hart, Patrick Heagerty, Bryan Comstock, Peter Tarczy-Hornoch, Stephanie M Fullerton, Dean A Regier, Wylie Burke,[...]. J Genet Couns 2019
17
5

Reliability and validity of a short version of the general functioning subscale of the McMaster Family Assessment Device.
Katrina L Boterhoven de Haan, Jennifer Hafekost, David Lawrence, Michael G Sawyer, Stephen R Zubrick. Fam Process 2015
46
2

Perceived familiarity with and importance of family health history among a medically underserved population.
Sato Ashida, Melody S Goodman, Jewel Stafford, Christina Lachance, Kimberly A Kaphingst. J Community Genet 2012
22
4

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
1

Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.
Leslie Riddle, Laura M Amendola, Marian J Gilmore, Claudia Guerra, Barbara Biesecker, Tia L Kauffman, Katherine Anderson, Alan F Rope, Michael C Leo, Mikaella Caruncho,[...]. Patient Educ Couns 2021
3
33

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
Hans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, Jessica P Gopie, Angel Alonso, Stefan Aretz, Inge Bernstein, Lucio Bertario, John Burn, Gabriel Capella,[...]. Gut 2013
411
1

Cancer genetic counseling communication with low-income Chinese immigrants.
Janice Ka Yan Cheng, Claudia Guerra, Rena J Pasick, Dean Schillinger, Judith Luce, Galen Joseph. J Community Genet 2018
11
9

Defining personal utility in genomics: A Delphi study.
J N Kohler, E Turbitt, K L Lewis, B S Wilfond, L Jamal, H L Peay, L G Biesecker, B B Biesecker. Clin Genet 2017
28
3


Contribution of Germline Predisposition Gene Mutations to Breast Cancer Risk in African American Women.
Julie R Palmer, Eric C Polley, Chunling Hu, Esther M John, Christopher Haiman, Steven N Hart, Mia Gaudet, Tuya Pal, Hoda Anton-Culver, Amy Trentham-Dietz,[...]. J Natl Cancer Inst 2020
14
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.