A citation-based method for searching scientific literature

Catherine L Bennett, Sarah E Burke, Hilary Burton, Peter A Farndon. BMC Health Serv Res 2010
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


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
35


Maturity-onset diabetes of the young (MODY): how many cases are we missing?
B M Shields, S Hicks, M H Shepherd, K Colclough, A T Hattersley, S Ellard. Diabetologia 2010
331
17

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
331
17


Factors influencing organizational adoption and implementation of clinical genetic services.
Alison B Hamilton, Sabine Oishi, Elizabeth M Yano, Cynthia E Gammage, Nell J Marshall, Maren T Scheuner. Genet Med 2014
35
11

Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests.
P Pujol, D Stoppa Lyonnet, T Frebourg, J Blin, M C Picot, C Lasset, C Dugast, P Berthet, B Bressac de Paillerets, H Sobol,[...]. Breast Cancer Res Treat 2013
30
11

Australia: public health genomics.
S A Metcalfe, A H Bittles, P O'Leary, J Emery. Public Health Genomics 2009
13
15

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.
Shiyu Zhang, Robert Royer, Song Li, John R McLaughlin, Barry Rosen, Harvey A Risch, Isabel Fan, Linda Bradley, Patricia A Shaw, Steven A Narod. Gynecol Oncol 2011
239
11


Developing and evaluating complex interventions: the new Medical Research Council guidance.
Peter Craig, Paul Dieppe, Sally Macintyre, Susan Michie, Irwin Nazareth, Mark Petticrew. BMJ 2008
11

Report from the National Society of Genetic Counselors service delivery model task force: a proposal to define models, components, and modes of referral.
Stephanie A Cohen, Shanna L Gustafson, Monica L Marvin, Bronson D Riley, Wendy R Uhlmann, S Bonnie Liebers, Julie A Rousseau. J Genet Couns 2012
45
11


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
13

Improving service delivery by evaluation of the referral pattern and capacity in a clinical genetics setting.
Emma McCann, Elizabeth A Baines, Jonathon R Gray, Annie M Procter. Am J Med Genet C Semin Med Genet 2009
4
50

Evaluating the role of Cardiac Genetics Nurses in inherited cardiac conditions services using a Maturity Matrix.
Maggie Kirk, Amy Simpson, Mark Llewellyn, Emma Tonkin, David Cohen, Marcus Longley. Eur J Cardiovasc Nurs 2014
7
28

Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
71
11

Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
195
11

Global implementation of genomic medicine: We are not alone.
Teri A Manolio, Marc Abramowicz, Fahd Al-Mulla, Warwick Anderson, Rudi Balling, Adam C Berger, Steven Bleyl, Aravinda Chakravarti, Wasun Chantratita, Rex L Chisholm,[...]. Sci Transl Med 2015
94
11

The real cost of sequencing: higher than you think!
Andrea Sboner, Xinmeng Jasmine Mu, Dov Greenbaum, Raymond K Auerbach, Mark B Gerstein. Genome Biol 2011
188
11

Genetic education and nongenetic health professionals: educational providers and curricula in Europe.
Kirsty Challen, Hilary J Harris, Claire Julian-Reynier, Leo P Ten Kate, Ulf Kristoffersson, Irmgard Nippert, Jörg Schmidtke, Caroline Benjamin, Rodney Harris. Genet Med 2005
28
11

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
20
11

Gaps in Incorporating Germline Genetic Testing Into Treatment Decision-Making for Early-Stage Breast Cancer.
Allison W Kurian, Yun Li, Ann S Hamilton, Kevin C Ward, Sarah T Hawley, Monica Morrow, M Chandler McLeod, Reshma Jagsi, Steven J Katz. J Clin Oncol 2017
129
11

Development of cancer genetic services in the UK: A national consultation.
Ingrid Slade, Daniel Riddell, Clare Turnbull, Helen Hanson, Nazneen Rahman. Genome Med 2015
25
11

Feasibility and acceptability of providing nurse counsellor genetics clinics in primary care.
Greta Westwood, Ruth M Pickering, Sue Latter, Anneke Lucassen, Paul Little, I Karen Temple. J Adv Nurs 2006
16
12

The future is now: Technology's impact on the practice of genetic counseling.
Erynn S Gordon, Deepti Babu, Dawn A Laney. Am J Med Genet C Semin Med Genet 2018
18
11

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
11

Newborn screening in Canada - Are we out of step?
William B Hanley. Paediatr Child Health 2005
19
11

Canada: public health genomics.
J Little, B Potter, J Allanson, T Caulfield, J C Carroll, B Wilson. Public Health Genomics 2009
9
22

Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
211
11

Preimplantation genetic diagnosis in Canada: a survey of Canadian IVF units.
Kathy N Speechley, Jeff Nisker. J Obstet Gynaecol Can 2010
4
50

Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.
Raveen K Basran, Margie Patterson, Lynda Walker, Lisa M Nakamura, Barry Eng, David H K Chui, John S Waye. Ann N Y Acad Sci 2005
7
28


Patient perspectives on the Poole PCT cancer genetics service.
Helen Allen, Lynn Maxwell, Nikki Dibley, Angela Bradley, Roger Baker, Peter Thomas, Donna McBride. Fam Cancer 2007
4
50

A vision for the future of genomics research.
Francis S Collins, Eric D Green, Alan E Guttmacher, Mark S Guyer. Nature 2003
997
11

Identification of Delivery Models for the Provision of Predictive Genetic Testing in Europe: Protocol for a Multicentre Qualitative Study and a Systematic Review of the Literature.
Brigid Unim, Tyra Lagerberg, Erica Pitini, Corrado De Vito, Maria Rosaria Vacchio, Giovanna Adamo, Annalisa Rosso, Elvira D'Andrea, Carolina Marzuillo, Paolo Villari.  2017
7
28

Effectiveness of genetic cascade screening for familial hypercholesterolaemia using a centrally co-ordinated clinical service: an Australian experience.
Damon A Bell, Jing Pang, Sally Burrows, Timothy R Bates, Frank M van Bockxmeer, Amanda J Hooper, Peter O'Leary, John R Burnett, Gerald F Watts. Atherosclerosis 2015
44
11




Costs of a successful public-private partnership for TB control in an urban setting in Nepal.
Deepak K Karki, Tolib N Mirzoev, Andrew T Green, James N Newell, Sushil C Baral. BMC Public Health 2007
19
5


Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations.
A Christianson, R Zimmern, U Kristoffersson, J Schmidtke, A Kent, R Raouf, C Barreiro, I Nippert. J Community Genet 2013
6
16




Public-private collaboration in health and human service delivery: evidence from community partnerships.
G J Bazzoli, R Stein, J A Alexander, D A Conrad, S Sofaer, S M Shortell. Milbank Q 1997
61
5



Public-private health partnerships: a strategy for WHO.
K Buse, A Waxman. Bull World Health Organ 2001
80
5


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.