A citation-based method for searching scientific literature

Lisa A Rubinsak, Annette Kleinman, John Quillin, Sarah W Gordon, Stephanie A Sullivan, Arnethea L Sutton, Vanessa B Sheppard, Sarah M Temkin. Gynecol Oncol 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Genetic Testing and Results in a Population-Based Cohort of Breast Cancer Patients and Ovarian Cancer Patients.
Allison W Kurian, Kevin C Ward, Nadia Howlader, Dennis Deapen, Ann S Hamilton, Angela Mariotto, Daniel Miller, Lynne S Penberthy, Steven J Katz. J Clin Oncol 2019
90
50

Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.
Anne Marie McCarthy, Mirar Bristol, Susan M Domchek, Peter W Groeneveld, Younji Kim, U Nkiru Motanya, Judy A Shea, Katrina Armstrong. J Clin Oncol 2016
73
50

Genetic Testing Awareness and Attitudes among Latinos: Exploring Shared Perceptions and Gender-Based Differences.
Jada G Hamilton, Elyse Shuk, Guedy Arniella, C Javier Gonz├ílez, Geoffrey S Gold, Francesca Gany, Mark E Robson, Jennifer L Hay. Public Health Genomics 2016
21
50

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.
Katie E J Hann, Madeleine Freeman, Lindsay Fraser, Jo Waller, Saskia C Sanderson, Belinda Rahman, Lucy Side, Sue Gessler, Anne Lanceley. BMC Public Health 2017
80
50


The transfer of uninsured patients from academic to community primary care settings.
Sheldon M Retchin, Sheryl L Garland, Emmanuel A Anum. Am J Manag Care 2009
11
25

Impact of direct-to-consumer advertising for hereditary breast cancer testing on genetic services at a managed care organization: a naturally-occurring experiment.
Judy Mouchawar, Sharon Hensley-Alford, Suzanne Laurion, Jennifer Ellis, Alanna Kulchak-Rahm, Melissa L Finucane, Richard Meenan, Lisen Axell, Rebecca Pollack, Debra Ritzwoller. Genet Med 2005
68
25

Reproductive Decision-Making in Women with BRCA1/2 Mutations.
Jessica L Chan, Lauren N C Johnson, Mary D Sammel, Laura DiGiovanni, Chan Voong, Susan M Domchek, Clarisa R Gracia. J Genet Couns 2017
27
25

Differences in referral patterns based on race for women at high-risk for ovarian cancer in the southeast: Results from a Gynecologic Cancer Risk Assessment Clinic.
Teresa K L Boitano, David A Barrington, Sadhvi Batra, Gerald McGwin, Taylor B Turner, Meagan B Farmer, Aimee M Brown, Michael J Straughn, Charles A Leath. Gynecol Oncol 2019
2
50

Prevalence of germline pathogenic BRCA1/2 variants in sequential epithelial ovarian cancer cases.
Robert D Morgan, George J Burghel, Nicola Flaum, Michael Bulman, Andrew R Clamp, Jurjees Hasan, Claire L Mitchell, Helene Schlecht, Emma R Woodward, Fiona I Lallo,[...]. J Med Genet 2019
10
25

Disparities in genetics assessment for women with ovarian cancer: Can we do better?
Erica Manrriquez, Jocelyn S Chapman, Julie Mak, Amie M Blanco, Lee-May Chen. Gynecol Oncol 2018
22
25

Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling.
Morgan Butrick, Scott Kelly, Beth N Peshkin, George Luta, Rachel Nusbaum, Gillian W Hooker, Kristi Graves, Lisa Feeley, Claudine Isaacs, Heiddis B Valdimarsdottir,[...]. Genet Med 2015
58
25

Genetic Counseling Referral Rates in Long-Term Survivors of Triple-Negative Breast Cancer.
Carlos H Barcenas, Maryam N Shafaee, Arup K Sinha, Akshara Raghavendra, Babita Saigal, Rashmi K Murthy, Ashley H Woodson, Banu Arun. J Natl Compr Canc Netw 2018
8
25

Genetic counseling for hereditary breast and gynecologic cancer syndromes at a community hospital.
Karina M Haber, Brandon-Luke L Seagle, Barbara Drew, Shannon Morrill-Cornelius, Robert Samuelson, Sean Hostmeyer, Shohreh Shahabi. Conn Med 2014
2
50

Association of patient navigation with care coordination in an Lynch syndrome screening program.
Susan Miesfeldt, W Gregory Feero, Frances L Lucas, Karen Rasmussen. Transl Behav Med 2018
7
25

Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.
Deborah Cragun, Anne Weidner, Courtney Lewis, Devon Bonner, Jongphil Kim, Susan T Vadaparampil, Tuya Pal. Cancer 2017
82
25

Prevalence of BRCA1 mutation carriers among U.S. non-Hispanic Whites.
Alice S Whittemore, Gail Gong, Esther M John, Valerie McGuire, Frederick P Li, Kimberly L Ostrow, Richard Dicioccio, Anna Felberg, Dee W West. Cancer Epidemiol Biomarkers Prev 2004
63
25

Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2.
Michael Dean, Joseph Boland, Meredith Yeager, Kate M Im, Lisa Garland, Maria Rodriguez-Herrera, Mylen Perez, Jason Mitchell, David Roberson, Kristine Jones,[...]. Gigascience 2015
29
25

Factors influencing patients' decisions to decline cancer genetic counseling services.
K P Geer, M E Ropka, W F Cohn, S M Jones, S Miesfeldt. J Genet Couns 2001
60
25

Long-term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance.
Marc D Schwartz, Claudine Isaacs, Kristi D Graves, Elizabeth Poggi, Beth N Peshkin, Christy Gell, Clinton Finch, Scott Kelly, Kathryn L Taylor, Lauren Perley. Cancer 2012
90
25


Referral of Ovarian Cancer Patients for Genetic Counselling by Oncologists: Need for Improvement.
Maria Teresa Ricci, Stefania Sciallero, Serafina Mammoliti, Viviana Gismondi, Marzena Franiuk, Paolo Bruzzi, Liliana Varesco. Public Health Genomics 2015
16
25

A survey of genetic counselors' strategies for addressing ethical and professional challenges in practice.
Matthew A Bower, Patricia McCarthy Veach, Dianne M Bartels, Bonnie S LeRoy. J Genet Couns 2002
36
25

A pilot study of spatial patterns in referrals to a multicentre cancer genetics service.
Vanessa Tempest, Gary Higgs, Kevin McDonald, Rachel Iredale, Tony Bater, Jonathon Gray. Community Genet 2005
2
50

Psychological adjustment among partners of women at high risk of developing breast/ovarian cancer.
Shab Mireskandari, Kerry A Sherman, Bettina Meiser, Alan J Taylor, Margaret Gleeson, Lesley Andrews, Katherine M Tucker. Genet Med 2007
10
25

The effectiveness of patient navigation to improve healthcare utilization outcomes: A meta-analysis of randomized controlled trials.
Sobia F Ali-Faisal, Tracey J F Colella, Naomi Medina-Jaudes, Lisa Benz Scott. Patient Educ Couns 2017
37
25

Evaluation of the needs and concerns of partners of women at high risk of developing breast/ovarian cancer.
Shab Mireskandari, Bettina Meiser, Kerry Sherman, Beverley J Warner, Lesley Andrews, Katherine M Tucker. Psychooncology 2006
20
25

Molecular pathogenesis of bilateral breast cancer.
Evgeny N Imyanitov, Kaido P Hanson. Cancer Lett 2003
27
25

Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer.
Zoe Kemp, Alice Turnbull, Shawn Yost, Sheila Seal, Shazia Mahamdallie, Emma Poyastro-Pearson, Margaret Warren-Perry, Anthony Eccleston, Min-Min Tan, Soo Hwang Teo,[...]. JAMA Netw Open 2019
23
25

Increasing utilization of cancer genetic counseling services using a patient navigator model.
Alanna Kulchak Rahm, Anna Sukhanova, Jennifer Ellis, Judy Mouchawar. J Genet Couns 2007
39
25

Role of parenting relationship quality in communicating about maternal BRCA1/2 genetic test results with children.
Tiffani A DeMarco, Beth N Peshkin, Heiddis B Valdimarsdottir, Andrea F Patenaude, Katherine A Schneider, Kenneth P Tercyak. J Genet Couns 2008
15
25






Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy.
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
9
25

Expectations and values about expanded newborn screening: a public engagement study.
Robin Z Hayeems, Fiona A Miller, Yvonne Bombard, Denise Avard, June Carroll, Brenda Wilson, Julian Little, Pranesh Chakraborty, Jessica Bytautas, Yves Giguere,[...]. Health Expect 2015
18
25

New literacy challenge for the twenty-first century: genetic knowledge is poor even among well educated.
Robert Chapman, Maxim Likhanov, Fatos Selita, Ilya Zakharov, Emily Smith-Woolley, Yulia Kovas. J Community Genet 2019
28
25

Needs assessment study of genetics education for general practitioners in Australia.
Sylvia Metcalfe, Rosalind Hurworth, Jennifer Newstead, Rosemary Robins. Genet Med 2002
70
25

Consumer health informatics and interactive visual learning tools for health.
Kleopatra Alamantariotou, Dimitra Zisi. Int J Electron Healthc 2010
8
25

Assessing Genetic Literacy Awareness and Knowledge Gaps in the US Population: Results from the Health Information National Trends Survey.
Melinda Krakow, Chelsea L Ratcliff, Bradford W Hesse, Alexandra J Greenberg-Worisek. Public Health Genomics 2017
22
25

Australian study on public knowledge of human genetics and health.
C Molster, T Charles, A Samanek, P O'Leary. Public Health Genomics 2009
75
25

Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
84
25

Australians' views and experience of personal genomic testing: survey findings from the Genioz study.
Jacqueline Savard, Chriselle Hickerton, Rigan Tytherleigh, Bronwyn Terrill, Erin Turbitt, Ainsley J Newson, Brenda Wilson, Kathleen Gray, Clara Gaff, Anna Middleton,[...]. Eur J Hum Genet 2019
6
25


Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives.
Elisa Jf Houwink, Scheltus J van Luijk, Lidewij Henneman, Cees van der Vleuten, Geert Jan Dinant, Martina C Cornel. BMC Fam Pract 2011
79
25

Impact of direct-to-consumer genomic testing at long term follow-up.
Cinnamon S Bloss, Nathan E Wineinger, Burcu F Darst, Nicholas J Schork, Eric J Topol. J Med Genet 2013
100
25

Genetic education for non-geneticist health professionals.
Rodney Harris, Kirsty Challen, Caroline Benjamin, Hilary Harris. Community Genet 2006
11
25



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.