A citation-based method for searching scientific literature

Carolina Marzuillo, Corrado De Vito, Maddalena D'Addario, Paola Santini, Elvira D'Andrea, Antonio Boccia, Paolo Villari. BMC Health Serv Res 2014
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


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
41

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
111
33

Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations.
Elvira D'Andrea, Carolina Marzuillo, Corrado De Vito, Marco Di Marco, Erica Pitini, Maria Rosaria Vacchio, Paolo Villari. Genet Med 2016
41
33


How is genetic testing evaluated? A systematic review of the literature.
Erica Pitini, Corrado De Vito, Carolina Marzuillo, Elvira D'Andrea, Annalisa Rosso, Antonio Federici, Emilio Di Maria, Paolo Villari. Eur J Hum Genet 2018
29
25

Current state of genomic policies in healthcare among EU member states: results of a survey of chief medical officers.
W Mazzucco, R Pastorino, T Lagerberg, M Colotto, E d'Andrea, C Marotta, C Marzuillo, P Villari, A Federici, W Ricciardi,[...]. Eur J Public Health 2017
11
27

Genetic testing and economic evaluations: a systematic review of the literature.
Elvira D'Andrea, Carolina Marzuillo, Ferruccio Pelone, Corrado De Vito, Paolo Villari. Epidemiol Prev 2015
16
25

Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia.
Elvira D'Andrea, Tyra Lagerberg, Corrado De Vito, Erica Pitini, Carolina Marzuillo, Azzurra Massimi, Maria Rosaria Vacchio, Paola Grammatico, Paolo Villari. Eur J Hum Genet 2018
8
37


Genetic education for primary care providers: improving attitudes, knowledge, and confidence.
June C Carroll, Andrea L Rideout, Brenda J Wilson, Judith Md Allanson, Sean M Blaine, Mary Jane Esplen, Sandra A Farrell, Gail E Graham, Jennifer MacKenzie, Wendy Meschino,[...]. Can Fam Physician 2009
62
16

Why is personalized medicine relevant to public health?
Stefania Boccia. Eur J Public Health 2014
14
16

Beyond public health genomics: proposals from an international working group.
Stefania Boccia, Martin Mc Kee, Roza Adany, Paolo Boffetta, Hilary Burton, Anne Cambon-Thomsen, Martina C Cornel, Muir Gray, Anant Jani, Bartha Maria Knoppers,[...]. Eur J Public Health 2014
19
16

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
58
16


Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases.
Tessel Rigter, Lidewij Henneman, Jacqueline E W Broerse, Maggie Shepherd, Ignacio Blanco, Ulf Kristoffersson, Martina C Cornel. J Community Genet 2014
15
16

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
80
16

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
134
16

Genetics in health care: an overview of current and emerging models.
R N Battista, I Blancquaert, A-M Laberge, N van Schendel, N Leduc. Public Health Genomics 2012
60
16

Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
211
16

Public health action in genomics is now needed beyond newborn screening.
M S Bowen, K Kolor, W D Dotson, R M Ned, M J Khoury. Public Health Genomics 2012
37
16


Genetics/genomics education for nongenetic health professionals: a systematic literature review.
Divya Talwar, Tung-Sung Tseng, Margaret Foster, Lei Xu, Lei-Shih Chen. Genet Med 2017
38
16

Which Lynch syndrome screening programs could be implemented in the "real world"? A systematic review of economic evaluations.
Marco Di Marco, Elvira DAndrea, Nikola Panic, Valentina Baccolini, Giuseppe Migliara, Carolina Marzuillo, Corrado De Vito, Roberta Pastorino, Stefania Boccia, Paolo Villari. Genet Med 2018
25
16

Predictive genetic testing for complex diseases: a public health perspective.
C Marzuillo, C De Vito, E D'Andrea, A Rosso, P Villari. QJM 2014
12
16


Personalised risk communication for informed decision making about taking screening tests.
Adrian G K Edwards, Gurudutt Naik, Harry Ahmed, Glyn J Elwyn, Timothy Pickles, Kerry Hood, Rebecca Playle. Cochrane Database Syst Rev 2013
120
8

The role of genome sequencing in personalized breast cancer prevention.
Weiva Sieh, Joseph H Rothstein, Valerie McGuire, Alice S Whittemore. Cancer Epidemiol Biomarkers Prev 2014
9
11



Polygenic susceptibility to prostate and breast cancer: implications for personalised screening.
N Pashayan, S W Duffy, S Chowdhury, T Dent, H Burton, D E Neal, D F Easton, R Eeles, P Pharoah. Br J Cancer 2011
116
8

The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.
Steven J Hawken, Celia M T Greenwood, Thomas J Hudson, Rafal Kustra, John McLaughlin, Quanhe Yang, Brent W Zanke, Julian Little. Hum Genet 2010
33
8

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
56
8

Implementing risk-stratified screening for common cancers: a review of potential ethical, legal and social issues.
A E Hall, S Chowdhury, N Hallowell, N Pashayan, T Dent, P Pharoah, H Burton. J Public Health (Oxf) 2014
23
8

How can polygenic inheritance be used in population screening for common diseases?
Muin J Khoury, A Cecile J W Janssens, David F Ransohoff. Genet Med 2013
32
8

Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Ribhi Hazin, Kyle B Brothers, Bradley A Malin, Barbara A Koenig, Saskia C Sanderson, Mark A Rothstein, Marc S Williams, Ellen W Clayton, Iftikhar J Kullo. Genet Med 2013
60
8


Population-based screening in the era of genomics.
Nora Pashayan, Paul Pharoah. Per Med 2012
12
8


Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis.
Nora Pashayan, Stephen W Duffy, David E Neal, Freddie C Hamdy, Jenny L Donovan, Richard M Martin, Patricia Harrington, Sara Benlloch, Ali Amin Al Olama, Mitul Shah,[...]. Genet Med 2015
54
8

Informed choice for screening: implications for evaluation.
Les Irwig, Kirsten McCaffery, Glenn Salkeld, Patrick Bossuyt. BMJ 2006
72
8

Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals.
Malcolm G Dunlop, Albert Tenesa, Susan M Farrington, Stephane Ballereau, David H Brewster, Thibaud Koessler, Paul Pharoah, Clemens Schafmayer, Jochen Hampe, Henry Völzke,[...]. Gut 2013
87
8

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics.
Tessel Rigter, Lidewij Henneman, Ulf Kristoffersson, Alison Hall, Helger G Yntema, Pascal Borry, Holger Tönnies, Quinten Waisfisz, Mariet W Elting, Wybo J Dondorp,[...]. Hum Mutat 2013
39
8


Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
Rosalind A Eeles, Ali Amin Al Olama, Sara Benlloch, Edward J Saunders, Daniel A Leongamornlert, Malgorzata Tymrakiewicz, Maya Ghoussaini, Craig Luccarini, Joe Dennis, Sarah Jugurnauth-Little,[...]. Nat Genet 2013
395
8

General practitioners' use of cardiovascular risk calculators.
Amy Imms, Stephen Quinn, Mark Nelson. Aust Fam Physician 2010
8
12

Personalised risk communication for informed decision making about taking screening tests.
A G K Edwards, R Evans, J Dundon, S Haigh, K Hood, G J Elwyn. Cochrane Database Syst Rev 2006
91
8

Prevention of breast cancer in the context of a national breast screening programme.
A Howell, S Astley, J Warwick, P Stavrinos, S Sahin, S Ingham, H McBurney, B Eckersley, M Harvie, M Wilson,[...]. J Intern Med 2012
20
8

Stratified cancer screening: the practicalities of implementation.
T Dent, J Jbilou, I Rafi, N Segnan, S Törnberg, S Chowdhury, A Hall, G Lyratzopoulos, R Eeles, D Eccles,[...]. Public Health Genomics 2013
31
8

Tailored information about cancer risk and screening: a systematic review.
Akke Albada, Margreet G E M Ausems, Jozien M Bensing, Sandra van Dulmen. Patient Educ Couns 2009
78
8

Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.
Bruce R Korf, Anna B Berry, Melvin Limson, Ali J Marian, Michael F Murray, P Pearl O'Rourke, Eugene R Passamani, Mary V Relling, John Tooker, Gregory J Tsongalis,[...]. Genet Med 2014
78
8


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.