A citation-based method for searching scientific literature

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, Setul Pardanani, W Gregory Feero, Claire Adams, Renee Jones, Joan Scott. Am J Med Genet C Semin Med Genet 2014
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Validation of My Family Health Portrait for six common heritable conditions.
Flavia M Facio, W Gregory Feero, Amy Linn, Neal Oden, Kandamurugu Manickam, Leslie G Biesecker. Genet Med 2010
63
21


Protocol for the "Implementation, adoption, and utility of family history in diverse care settings" study.
R Ryanne Wu, Rachel A Myers, Catherine A McCarty, David Dimmock, Michael Farrell, Deanna Cross, Troy D Chinevere, Geoffrey S Ginsburg, Lori A Orlando. Implement Sci 2015
15
21

Identification and management of women at high risk for hereditary breast/ovarian cancer syndrome.
Elissa M Ozanne, Andrea Loberg, Sherwood Hughes, Christine Lawrence, Brian Drohan, Alan Semine, Michael Jellinek, Claire Cronin, Frederick Milham, Dana Dowd,[...]. Breast J 2009
41
21

Clinical utility of a Web-enabled risk-assessment and clinical decision support program.
Lori A Orlando, R Ryanne Wu, Rachel A Myers, Adam H Buchanan, Vincent C Henrich, Elizabeth R Hauser, Geoffrey S Ginsburg. Genet Med 2016
24
21

Family history in primary care: understanding GPs' resistance to clinical genetics--qualitative study.
Jonathan Mathers, Sheila Greenfield, Alison Metcalfe, Trevor Cole, Sarah Flanagan, Sue Wilson. Br J Gen Pract 2010
26
14

Primary care providers' responses to patient-generated family history.
Melissa Fuller, Melanie Myers, Thomas Webb, Meredith Tabangin, Cynthia Prows. J Genet Couns 2010
25
14

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
27
14

Breast cancer risk assessment and management in primary care: provider attitudes, practices, and barriers.
Susan A Sabatino, Ellen P McCarthy, Russell S Phillips, Risa B Burns. Cancer Detect Prev 2007
80
14

Development and use of active clinical decision support for preemptive pharmacogenomics.
Gillian C Bell, Kristine R Crews, Mark R Wilkinson, Cyrine E Haidar, J Kevin Hicks, Donald K Baker, Nancy M Kornegay, Wenjian Yang, Shane J Cross, Scott C Howard,[...]. J Am Med Inform Assoc 2014
138
14


Development and validation of a primary care-based family health history and decision support program (MeTree).
Lori A Orlando, Adam H Buchanan, Susan E Hahn, Carol A Christianson, Karen P Powell, Celette Sugg Skinner, Blair Chesnut, Colette Blach, Barbara Due, Geoffrey S Ginsburg,[...]. N C Med J 2013
49
14

Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.
J M Pulley, J C Denny, J F Peterson, G R Bernard, C L Vnencak-Jones, A H Ramirez, J T Delaney, E Bowton, K Brothers, K Johnson,[...]. Clin Pharmacol Ther 2012
284
14

PG4KDS: a model for the clinical implementation of pre-emptive pharmacogenetics.
James M Hoffman, Cyrine E Haidar, Mark R Wilkinson, Kristine R Crews, Donald K Baker, Nancy M Kornegay, Wenjian Yang, Ching-Hon Pui, Ulrike M Reiss, Aditya H Gaur,[...]. Am J Med Genet C Semin Med Genet 2014
170
14


The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
357
14

Providing access to risk prediction tools via the HL7 XML-formatted risk web service.
Jonathan Chipman, Brian Drohan, Amanda Blackford, Giovanni Parmigiani, Kevin Hughes, Phil Bosinoff. Breast Cancer Res Treat 2013
9
22


The use of a family history risk assessment tool within a community health care system: views of primary care providers.
Carol A Christianson, Karen Potter Powell, Susan Estabrooks Hahn, Susan H Blanton, Jessica Bogacik, Vincent C Henrich. J Genet Couns 2012
24
14

Family history: still relevant in the genomics era.
Megan Doerr, Kathryn Teng. Cleve Clin J Med 2012
39
14

Family health history: the case for better tools.
Brandon M Welch, Willard Dere, Joshua D Schiffman. JAMA 2015
34
14

Mothers' perceptions of family health history and an online, parent-generated family health history tool.
Kelly Amanda Berger, John Lynch, Cynthia A Prows, Robert M Siegel, Melanie F Myers. Clin Pediatr (Phila) 2013
8
25

Acceptability and feasibility of a virtual counselor (VICKY) to collect family health histories.
Catharine Wang, Timothy Bickmore, Deborah J Bowen, Tricia Norkunas, MaryAnn Campion, Howard Cabral, Michael Winter, Michael Paasche-Orlow. Genet Med 2015
31
14

Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial.
Wendy S Rubinstein, Louise S Acheson, Suzanne M O'Neill, Mack T Ruffin, Catharine Wang, Jennifer L Beaumont, Nan Rothrock. Genet Med 2011
67
14


Veterans' experience in using the online Surgeon General's family health history tool.
Nedal Arar, Joann Seo, Hanna E Abboud, Michael Parchman, Polly Noel. Per Med 2011
17
14

Identification and referral of families at high risk for cancer susceptibility.
Kevin M Sweet, Terry L Bradley, Judith A Westman. J Clin Oncol 2002
132
14

Health Heritage© a web-based tool for the collection and assessment of family health history: initial user experience and analytic validity.
W F Cohn, M E Ropka, S L Pelletier, J R Barrett, M B Kinzie, M B Harrison, Z Liu, S Miesfeldt, A L Tucker, B B Worrall,[...]. Public Health Genomics 2010
65
14

Clinical use of the Surgeon General's "My Family Health Portrait" (MFHP) tool: opinions of future health care providers.
Kailey M Owens, Monica L Marvin, Thomas D Gelehrter, Mack T Ruffin, Wendy R Uhlmann. J Genet Couns 2011
18
14

Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General's My Family Health Portrait.
W Gregory Feero, Flavia M Facio, Emily A Glogowski, Heather L Hampel, Jill E Stopfer, Haley Eidem, Amy M Pizzino, David K Barton, Leslie G Biesecker. Genet Med 2015
11
18

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
76
14

Cluster randomized trial of a multifaceted primary care decision-support intervention for inherited breast cancer risk.
Brenda J Wilson, Nicola Torrance, Jill Mollison, M Stuart Watson, Alison Douglas, Zosia Miedzybrodzka, Richard Gordon, Sarah Wordsworth, Marion Campbell, Neva Haites,[...]. Fam Pract 2006
21
14

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
36
14

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
23
14

The current and future state of pharmacogenomics medical education in the USA.
Tracey J Nickola, James S Green, Arthur F Harralson, Travis J O'Brien. Pharmacogenomics 2012
32
7

Attitudes of potential providers towards preconceptional cystic fibrosis carrier screening.
Francis A M Poppelaars, Herman J Adèr, Martina C Cornel, Lidewij Henneman, Rosella P M G Hermens, Gerrit van der Wal, Leo P ten Kate. J Genet Couns 2004
22
7

Cancer genetic risk assessment and referral patterns in primary care.
Hetal S Vig, Joanne Armstrong, Brian L Egleston, Carla Mazar, Michele Toscano, Angela R Bradbury, Mary B Daly, Neal J Meropol. Genet Test Mol Biomarkers 2009
47
7

Swiss primary care physicians' knowledge, attitudes and perception towards genetic testing for hereditary breast cancer.
Gabriella Pichert, Daniel Dietrich, Peter Moosmann, Marcel Zwahlen, Rolf Arno Stahel, André-Pascal Sappino. Fam Cancer 2003
26
7

The use by Alabama pediatricians of genetics consultation in the evaluation of developmental delay.
Min-Jye Chen, Cheryl L Holt, Edward J Lose, Nathaniel H Robin. Am J Med Genet A 2008
8
12

Exploring physicians' views and values in relation to maternal serum screening.
Brandace Winquist, Keith Ogle, Nazeem Muhajarine. J Obstet Gynaecol Can 2008
5
20

The rise of electronic health record adoption among family physicians.
Imam M Xierali, Chun-Ju Hsiao, James C Puffer, Larry A Green, Jason C B Rinaldo, Andrew W Bazemore, Mathew T Burke, Robert L Phillips. Ann Fam Med 2013
64
7

Patients' and physicians' perspectives on pharmacogenetic testing.
Anja Rogausch, Daniela Prause, Anne Schallenberg, Jürgen Brockmöller, Wolfgang Himmel. Pharmacogenomics 2006
88
7

Hereditary breast and ovarian cancer and other hereditary syndromes: using technology to identify carriers.
Brian Drohan, Constance A Roche, James C Cusack, Kevin S Hughes. Ann Surg Oncol 2012
71
7


Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine.
Katherine Bonter, Clarissa Desjardins, Nathan Currier, Jason Pun, Fredrick D Ashbury. BMJ Open 2011
66
7

Clinical genetics issues encountered by family physicians.
Louise S Acheson, Kurt C Stange, Stephen Zyzanski. Genet Med 2005
41
7



Primary care physicians' experience with family history: an exploratory qualitative study.
Janet L Williams, Dave S Collingridge, Marc S Williams. Genet Med 2011
19
7

Practice patterns of obstetrician-gynecologists regarding preconception and prenatal screening for cystic fibrosis.
Maria A Morgan, Deborah A Driscoll, Michael T Mennuti, Jay Schulkin. Genet Med 2004
50
7


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.