A citation-based method for searching scientific literature

Katie E J Hann, Lindsay Fraser, Lucy Side, Sue Gessler, Jo Waller, Saskia C Sanderson, Madeleine Freeman, Ian Jacobs, Anne Lanceley. BMC Womens Health 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


National nursing workforce survey of nursing attitudes, knowledge and practice in genomics.
Kathleen A Calzone, Jean Jenkins, Stacey Culp, Vence L Bonham, Laurie Badzek. Per Med 2013
29
25

Multi-ethnic minority nurses' knowledge and practice of genetics and genomics.
Bernice Coleman, Kathleen A Calzone, Jean Jenkins, Carmen Paniagua, Reynaldo Rivera, Oi Saeng Hong, Ida Spruill, Vence Bonham. J Nurs Scholarsh 2014
23
25

Genetic services and attitudes in primary care pediatrics.
Michael L Rinke, Natalie Mikat-Stevens, Robert Saul, Amy Driscoll, Jill Healy, Beth A Tarini. Am J Med Genet A 2014
24
25

Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
105
25


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
42
25

US physicians' attitudes toward genetic testing for cancer susceptibility.
A N Freedman, L Wideroff, L Olson, W Davis, C Klabunde, K P Srinath, B B Reeve, R T Croyle, R Ballard-Barbash. Am J Med Genet A 2003
133
25

Considerations in initiating genomic screening programs in health care systems.
Janet K Williams, William Gregory Feero, David L Veenstra, Angela Starkweather, Ann K Cashion. Nurs Outlook 2018
3
33

GPs' views on their role in cancer genetics services and current practice.
A Fry, H Campbell, H Gudmunsdottir, R Rush, M Porteous, D Gorman, A Cull. Fam Pract 1999
107
25

Physicians' propensity to offer genetic testing for Alzheimer's disease: results from a survey.
Gary A Chase, Gail Geller, Suzanne L Havstad, Neil A Holtzman, Susan Spear Bassett. Genet Med 2002
19
25

Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians.
Cecelia A Bellcross, Katherine Kolor, Katrina A B Goddard, Ralph J Coates, Michele Reyes, Muin J Khoury. Am J Prev Med 2011
113
25

Incorporating genomics into breast and prostate cancer screening: assessing the implications.
Susmita Chowdhury, Tom Dent, Nora Pashayan, Alison Hall, Georgios Lyratzopoulos, Nina Hallowell, Per Hall, Paul Pharoah, Hilary Burton. Genet Med 2013
58
25

Knowledge, attitudes and behavior of physicians regarding predictive genetic tests for breast and colorectal cancer.
Carolina Marzuillo, Corrado De Vito, Stefania Boccia, Maddalena D'Addario, Elvira D'Andrea, Paola Santini, Antonio Boccia, Paolo Villari. Prev Med 2013
35
25

A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
61
25

Physician Risk Assessment Knowledge Regarding BRCA Genetics Testing.
Jason Cohn, William Blazey, David Tegay, Brian Harper, Sharon Koehler, Brookshield Laurent, Vivian Chan, Min-Kyung Jung, Bhuma Krishnamachari. J Cancer Educ 2015
9
25

Use of cancer susceptibility testing among primary care physicians.
R Sifri, R Myers, T Hyslop, B Turner, J Cocroft, T Rothermel, J Grana, N Schlackman. Clin Genet 2003
40
25

Survey of nursing integration of genomics into nursing practice.
Kathleen A Calzone, Jean Jenkins, Jan Yates, Georgie Cusack, Gwenyth R Wallen, David J Liewehr, Seth M Steinberg, Colleen McBride. J Nurs Scholarsh 2012
41
25

Integrating Genomics into Healthcare: A Global Responsibility.
Zornitza Stark, Lena Dolman, Teri A Manolio, Brad Ozenberger, Sue L Hill, Mark J Caulfied, Yves Levy, David Glazer, Julia Wilson, Mark Lawler,[...]. Am J Hum Genet 2019
125
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
239
25

Objecting to experiments that compare two unobjectionable policies or treatments.
Michelle N Meyer, Patrick R Heck, Geoffrey S Holtzman, Stephen M Anderson, William Cai, Duncan J Watts, Christopher F Chabris. Proc Natl Acad Sci U S A 2019
18
25

Establishing an Information Avoidance Scale.
Jennifer L Howell, James A Shepperd. Psychol Assess 2016
21
25

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.
Irmgard Nippert, Hilary J Harris, Claire Julian-Reynier, Ulf Kristoffersson, Leo P Ten Kate, Elizabeth Anionwu, Caroline Benjamin, Kirsty Challen, Jörg Schmidtke, R Peter Nippert,[...]. J Community Genet 2011
61
25

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
162
25



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
281
25

Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, Miranda L G Hallquist, Janet L Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M Savatt, Alyson E Evans, Loren M Butry,[...]. JAMA Netw Open 2018
79
25

Patterns of cancer genetic testing: a randomized survey of Oregon clinicians.
Summer L Cox, Amy I Zlot, Kerry Silvey, Debi Elliott, Tara Horn, Amber Johnson, Richard F Leman. J Cancer Epidemiol 2012
23
25

Medicine. Do defaults save lives?
Eric J Johnson, Daniel Goldstein. Science 2003
340
25

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.
Adam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, Jennifer K Wagner, Miranda L G Hallquist, Janet L Williams, Alanna Kulchak Rahm, Marc S Williams, Zong-Ming E Chen, Chaitali K Shah,[...]. Genet Med 2018
31
25

Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics.
R T Acton, N M Burst, L Casebeer, S M Ferguson, P Greene, B L Laird, L Leviton. Acad Med 2000
112
25

Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.
Ravi N Sharaf, Parvathi Myer, Christopher D Stave, Lisa C Diamond, Uri Ladabaum. Clin Gastroenterol Hepatol 2013
80
25


The 'new genetics' and primary care: GPs' views on their role and their educational needs.
E K Watson, D Shickle, N Qureshi, J Emery, J Austoker. Fam Pract 1999
138
25

Skull Base Surgery with Minimal Resources.
Deepak K Jha, Mukul Jain, Sujata Chaturvedi, Renu Goyal, Arvind Arya, Suman Kushwaha, Anil Thakur. World Neurosurg 2017
2
50

Hierarchical modeling of molecular energies using a deep neural network.
Nicholas Lubbers, Justin S Smith, Kipton Barros. J Chem Phys 2018
82
25

DeepSurv: personalized treatment recommender system using a Cox proportional hazards deep neural network.
Jared L Katzman, Uri Shaham, Alexander Cloninger, Jonathan Bates, Tingting Jiang, Yuval Kluger. BMC Med Res Methodol 2018
144
25

A survey on deep learning in medical image analysis.
Geert Litjens, Thijs Kooi, Babak Ehteshami Bejnordi, Arnaud Arindra Adiyoso Setio, Francesco Ciompi, Mohsen Ghafoorian, Jeroen A W M van der Laak, Bram van Ginneken, Clara I Sánchez. Med Image Anal 2017
25

Anticipated health behaviour changes and perceived control in response to disclosure of genetic risk of breast and ovarian cancer: a quantitative survey study among women in the UK.
Susanne F Meisel, Lindsay Sarah Macduff Fraser, Lucy Side, Sue Gessler, Katie E J Hann, Jane Wardle, Anne Lanceley. BMJ Open 2017
10
25


BRCA1 and BRCA2 mutations and clinical interpretation in 398 ovarian cancer patients: comparison with breast cancer variants in a similar population.
Florencia C Cardoso, Susana Goncalves, Pablo G Mele, Natalia C Liria, Leonardo Sganga, Ignacio Diaz Perez, Ernesto J Podesta, Angela R Solano. Hum Genomics 2018
10
25

Mainstreaming cancer genetics: A model integrating germline BRCA testing into routine ovarian cancer clinics.
Maira Kentwell, Eryn Dow, Yoland Antill, C David Wrede, Orla McNally, Emily Higgs, Anne Hamilton, Sumitra Ananda, Geoffrey J Lindeman, Clare L Scott. Gynecol Oncol 2017
59
25

Long-term ovarian cancer survival associated with mutation in BRCA1 or BRCA2.
John R McLaughlin, Barry Rosen, Joel Moody, Tuya Pal, Isabel Fan, Patricia A Shaw, Harvey A Risch, Thomas A Sellers, Ping Sun, Steven A Narod. J Natl Cancer Inst 2013
95
25

BRCA1 and BRCA2 mutations in ovarian cancer patients from China: ethnic-related mutations in BRCA1 associated with an increased risk of ovarian cancer.
Tingyan Shi, Pan Wang, Caixia Xie, Sheng Yin, Di Shi, Congchong Wei, Wenbin Tang, Rong Jiang, Xi Cheng, Qingyi Wei,[...]. Int J Cancer 2017
27
25

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
12
25

Oncology Clinic-Based Hereditary Cancer Genetic Testing in a Population-Based Health Care System.
Matthew Richardson, Hae Jung Min, Quan Hong, Katie Compton, Sze Wing Mung, Zoe Lohn, Jennifer Nuk, Mary McCullum, Cheryl Portigal-Todd, Aly Karsan,[...]. Cancers (Basel) 2020
7
25

The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine.
Katie Stoll, Shobana Kubendran, Stephanie A Cohen. Am J Med Genet C Semin Med Genet 2018
64
25

Mainstreamed genetic testing for women with ovarian cancer: first-year experience.
Belinda Rahman, Anne Lanceley, Rebecca S Kristeleit, Jonathan A Ledermann, Michelle Lockley, Mary McCormack, Tim Mould, Lucy Side. J Med Genet 2019
26
25

Validation of a decisional conflict scale.
A M O'Connor. Med Decis Making 1995
25

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
Mary B Daly, Robert Pilarski, Jennifer E Axilbund, Michael Berry, Saundra S Buys, Beth Crawford, Meagan Farmer, Susan Friedman, Judy E Garber, Seema Khan,[...]. J Natl Compr Canc Netw 2016
112
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.