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: 15







List of co-cited articles
29 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
33

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
13
38

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
116
26

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
45
26


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
38
20

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
19
20

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
9
33



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
67
13

The policy of public health genomics in Italy.
Benedetto Simone, Walter Mazzucco, Maria Rosaria Gualano, Antonella Agodi, Domenico Coviello, Francesca Dagna Bricarelli, Bruno Dallapiccola, Emilio Di Maria, Antonio Federici, Maurizio Genuardi,[...]. Health Policy 2013
20
13

Why is personalized medicine relevant to public health?
Stefania Boccia. Eur J Public Health 2014
15
13

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
20
13

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
62
13


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
18
13

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
84
13

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
13

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
69
13

Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
215
13

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
13


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
41
13

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
35
13

Predictive genetic testing for complex diseases: a public health perspective.
C Marzuillo, C De Vito, E D'Andrea, A Rosso, P Villari. QJM 2014
14
14

From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
59
13

Integrating Advanced Molecular Technologies into Public Health.
Marta Gwinn, Duncan R MacCannell, Rima F Khabbaz. J Clin Microbiol 2017
26
13

US health educators' likelihood of adopting genomic competencies into health promotion.
Lei-Shih Chen, Oi-Man Kwok, Patricia Goodson. Am J Public Health 2008
26
13

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
131
6

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
120
6

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
34
6

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
60
6

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
29
6

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
34
6

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
61
6


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
61
6

Informed choice for screening: implications for evaluation.
Les Irwig, Kirsten McCaffery, Glenn Salkeld, Patrick Bossuyt. BMJ 2006
72
6

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
93
6

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
6


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
412
6

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
6


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.