A citation-based method for searching scientific literature

Daniel Spinosa, Tatiana Acosta, Janice Wong, Kelli Kurtovic, Jennifer Mewshaw, Sarah Collins, Noah Kauff, Laura J Havrilesky, Kyle C Strickland, Rebecca A Previs. Gynecol Oncol 2021
Times Cited: 1

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

Times Cited
  Times     Co-cited

The importance of the family history in caring for families with long QT syndrome and dilated cardiomyopathy.
Jolien S Ruiter, Karin Berkenbosch-Nieuwhof, Maarten P van den Berg, Rene van Dijk, Berrie Middel, J Peter van Tintelen. Am J Med Genet A 2010

The impact of a genetics education program on physicians' knowledge and genetic counseling referral patterns.
Jonathan C Clyman, Fiza Nazir, Sharon Tarolli, Elizabeth Black, Roni Q Lombardi, Joseph J Higgins. Med Teach 2007

Missed opportunities: unidentified genetic risk factors in prenatal care.
Trissa McClatchey, Erica Lay, Melissa Strassberg, Ignatia B Van den Veyver. Prenat Diagn 2018

Nurses' and auxiliary nurse midwives' adherence to essential birth practices with peer coaching in Uttar Pradesh, India: a secondary analysis of the BetterBirth trial.
Rose L Molina, Brandon J Neal, Lauren Bobanski, Vinay Pratap Singh, Bridget A Neville, Megan Marx Delaney, Stuart Lipsitz, Ami Karlage, Mrunal Shetye, Katherine E A Semrau. Implement Sci 2020

Process evaluation in randomised controlled trials of complex interventions.
Ann Oakley, Vicki Strange, Chris Bonell, Elizabeth Allen, Judith Stephenson. BMJ 2006

Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda.
Enola Proctor, Hiie Silmere, Ramesh Raghavan, Peter Hovmand, Greg Aarons, Alicia Bunger, Richard Griffey, Melissa Hensley. Adm Policy Ment Health 2011

Are interventions theory-based? Development of a theory coding scheme.
Susan Michie, Andrew Prestwich. Health Psychol 2010

From Theory-Inspired to Theory-Based Interventions: A Protocol for Developing and Testing a Methodology for Linking Behaviour Change Techniques to Theoretical Mechanisms of Action.
Susan Michie, Rachel N Carey, Marie Johnston, Alexander J Rothman, Marijn de Bruin, Michael P Kelly, Lauren E Connell. Ann Behav Med 2018

Clinical interventions, implementation interventions, and the potential greyness in between -a discussion paper.
Ann Catrine Eldh, Joan Almost, Kara DeCorby-Watson, Wendy Gifford, Gill Harvey, Henna Hasson, Deborah Kenny, Sheila Moodie, Lars Wallin, Jennifer Yost. BMC Health Serv Res 2017

Disseminating universal genetic testing to a diverse, indigent patient population at a county hospital gynecologic oncology clinic.
Erica M Bednar, Charlotte C Sun, Bethsaida Camacho, John Terrell, Alyssa G Rieber, Lois M Ramondetta, Ralph S Freedman, Karen H Lu. Gynecol Oncol 2019

Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs.
Cora M Aalfs, Ellen M A Smets, Hanneke C J M de Haes, Nico J Leschot. Fam Pract 2003

Standards for Reporting Implementation Studies (StaRI) Statement.
Hilary Pinnock, Melanie Barwick, Christopher R Carpenter, Sandra Eldridge, Gonzalo Grandes, Chris J Griffiths, Jo Rycroft-Malone, Paul Meissner, Elizabeth Murray, Anita Patel,[...]. BMJ 2017

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009

Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide.
Tammy C Hoffmann, Paul P Glasziou, Isabelle Boutron, Ruairidh Milne, Rafael Perera, David Moher, Douglas G Altman, Virginia Barbour, Helen Macdonald, Marie Johnston,[...]. BMJ 2014

Process evaluation of complex interventions: Medical Research Council guidance.
Graham F Moore, Suzanne Audrey, Mary Barker, Lyndal Bond, Chris Bonell, Wendy Hardeman, Laurence Moore, Alicia O'Cathain, Tannaze Tinati, Daniel Wight,[...]. BMJ 2015

Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.
Goli Samimi, Marcus Q Bernardini, Lawrence C Brody, Charlisse F Caga-Anan, Ian G Campbell, Georgia Chenevix-Trench, Fergus J Couch, Michael Dean, Joanne A de Hullu, Susan M Domchek,[...]. J Clin Oncol 2017

Implementation of an electronic genomic and family health history tool in primary prenatal care.
Emily A Edelman, Bruce K Lin, Teresa Doksum, Brian Drohan, Vaughn Edelson, Siobhan M Dolan, Kevin S Hughes, James O'Leary, Shelley L Galvin, Nicole Degroat,[...]. Am J Med Genet C Semin Med Genet 2014

Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer.
F G J Kallenberg, C M Aalfs, F O The, C A Wientjes, A C Depla, M W Mundt, P M M Bossuyt, E Dekker. Fam Cancer 2018

Differences in physician referral practices and attitudes regarding hereditary breast cancer by clinical practice location.
Christine E Koil, Jessica N Everett, Leah Hoechstetter, Rick E Ricer, Karen M Huelsman. Genet Med 2003

The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review.
Nick Dragojlovic, Kennedy Borle, Nicola Kopac, Ursula Ellis, Patricia Birch, Shelin Adam, Jan M Friedman, Amy Nisselle, Alison M Elliott, Larry D Lynd. Genet Med 2020

Increasing Appropriate BRCA1/2 Mutation Testing: The Role of Family History Documentation and Genetic Counseling in a Multidisciplinary Clinic.
Amar U Kishan, Caitlin L Gomez, Nicole A Dawson, Robyn Dvorak, Nova M Foster, Anne Hoyt, Sara A Hurvitz, Amy Kusske, Erica L Silver, Charles Tseng,[...]. Ann Surg Oncol 2016

Towards a comprehensive model for understanding adaptations' impact: the model for adaptation design and impact (MADI).
M Alexis Kirk, Julia E Moore, Shannon Wiltsey Stirman, Sarah A Birken. Implement Sci 2020

Using behaviour change and implementation science to address low referral rates in oncology.
Janet C Long, Deborah Debono, Rachel Williams, Elizabeth Salisbury, Sharron O'Neill, Elizabeth Eykman, Jordan Butler, Robert Rawson, Kim-Chi Phan-Thien, Stephen R Thompson,[...]. BMC Health Serv Res 2018

A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians.
Maren T Scheuner, Alison B Hamilton, Jane Peredo, Taylor J Sale, Colletta Austin, Stuart C Gilman, M Scott Bowen, Caroline Lubick Goldzweig, Martin Lee, Brian S Mittman,[...]. Genet Med 2014

A refined compilation of implementation strategies: results from the Expert Recommendations for Implementing Change (ERIC) project.
Byron J Powell, Thomas J Waltz, Matthew J Chinman, Laura J Damschroder, Jeffrey L Smith, Monica M Matthieu, Enola K Proctor, JoAnn E Kirchner. Implement Sci 2015

Barriers to access: results from focus groups to identify genetic service needs in the community.
Rosalyn Y Beene-Harris, Catharine Wang, Janice V Bach. Community Genet 2007

Improving referral for genetic risk assessment in ovarian cancer using an electronic medical record system.
Sue V Petzel, Rachel Isaksson Vogel, Jena McNiel, Anna Leininger, Peter A Argenta, Melissa A Geller. Int J Gynecol Cancer 2014

Experiences of using the Theoretical Domains Framework across diverse clinical environments: a qualitative study.
Cameron J Phillips, Andrea P Marshall, Nadia J Chaves, Stacey K Jankelowitz, Ivan B Lin, Clement T Loy, Gwyneth Rees, Leanne Sakzewski, Susie Thomas, The-Phung To,[...]. J Multidiscip Healthc 2015

A systematic review of factors that act as barriers to patient referral to genetic services.
Türem Delikurt, Graham R Williamson, Violetta Anastasiadou, Heather Skirton. Eur J Hum Genet 2015

The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017

Impact of an embedded genetic counselor on breast cancer treatment.
Holly J Pederson, Najaah Hussain, Ryan Noss, Courtney Yanda, Colin O'Rourke, Charis Eng, Stephen R Grobmyer. Breast Cancer Res Treat 2018

Development of an online tool for linking behavior change techniques and mechanisms of action based on triangulation of findings from literature synthesis and expert consensus.
Marie Johnston, Rachel N Carey, Lauren E Connell Bohlen, Derek W Johnston, Alexander J Rothman, Marijn de Bruin, Michael P Kelly, Hilary Groarke, Susan Michie. Transl Behav Med 2021

Multidisciplinary interventions in a specialist Drug Development Unit to improve family history documentation and onward referral of patients with advanced cancer to cancer genetics services.
Cathryn A Moss, Elena Cojocaru, Janet Hanwell, Simon Ward, Wen Xu, Mary van Zyl, Lorraine O'Leary, Johann S de Bono, Udai Banerji, Stan B Kaye,[...]. Eur J Cancer 2019

Embedding a genetic counselor into oncology clinics improves testing rates and timeliness for women with ovarian cancer.
Huma Q Rana, Lindsay Kipnis, Kristin Hehir, Angel Cronin, Tim Jaung, Samantha M Stokes, Fatemeh Fekrmandi, Donna Vatnick, Ursula A Matulonis, Judy E Garber,[...]. Gynecol Oncol 2021

Recent developments in genetic/genomic medicine.
Rachel H Horton, Anneke M Lucassen. Clin Sci (Lond) 2019

GRADE guidelines: 3. Rating the quality of evidence.
Howard Balshem, Mark Helfand, Holger J Schünemann, Andrew D Oxman, Regina Kunz, Jan Brozek, Gunn E Vist, Yngve Falck-Ytter, Joerg Meerpohl, Susan Norris,[...]. J Clin Epidemiol 2011

Genetic consultation embedded in a gynecologic oncology clinic improves compliance with guideline-based care.
Leigha Senter, David M O'Malley, Floor J Backes, Larry J Copeland, Jeffery M Fowler, Ritu Salani, David E Cohn. Gynecol Oncol 2017

Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol.
April Morrow, Emily Hogden, Yoon-Jung Kang, Julia Steinberg, Karen Canfell, Michael J Solomon, James G Kench, Anthony J Gill, Tim Shaw, Nicholas Pachter,[...]. Trials 2019

A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment.
Erica M Bednar, Holly D Oakley, Charlotte C Sun, Catherine C Burke, Mark F Munsell, Shannon N Westin, Karen H Lu. Gynecol Oncol 2017

Human genetics and genomics a decade after the release of the draft sequence of the human genome.
Nasheen Naidoo, Yudi Pawitan, Richie Soong, David N Cooper, Chee-Seng Ku. Hum Genomics 2011

Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing.
Paul A Cohen, Cassandra B Nichols, Lyn Schofield, Steven Van Der Werf, Nicholas Pachter. Int J Gynecol Cancer 2016

Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis.
Casey L Swanson, Amanika Kumar, Joy M Maharaj, Jennifer L Kemppainen, Brittany C Thomas, Megan R Weinhold, Kristine M Slaby, Kristin C Mara, Myra J Wick, Jamie N Bakkum-Gamez. Gynecol Oncol 2018

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

The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary care.
J Emery, H Morris, R Goodchild, T Fanshawe, A T Prevost, M Bobrow, A L Kinmonth. Br J Cancer 2007

A Comprehensive Program Enabling Effective Delivery of Regional Genetic Counseling.
Jubilee Brown, Aly Athens, David L Tait, Erin K Crane, Robert V Higgins, R Wendel Naumann, Lejla Hadzikadic Gusic, Lisa Amacker-North. Int J Gynecol Cancer 2018

The behavior change technique taxonomy (v1) of 93 hierarchically clustered techniques: building an international consensus for the reporting of behavior change interventions.
Susan Michie, Michelle Richardson, Marie Johnston, Charles Abraham, Jill Francis, Wendy Hardeman, Martin P Eccles, James Cane, Caroline E Wood. Ann Behav Med 2013

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.