A citation-based method for searching scientific literature

Kristin B Niendorf, Melissa A Geller, Rachel Isaksson Vogel, Timothy R Church, Anna Leininger, Angela Bakke, Robert D Madoff. Fam Cancer 2016
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity



Why Is Cancer Genetic Counseling Underutilized by Women Identified as at Risk for Hereditary Breast Cancer? Patient Perceptions of Barriers Following a Referral Letter.
Alyssa Kne, Heather Zierhut, Shari Baldinger, Karen K Swenson, Pamela Mink, Patricia McCarthy Veach, Michaela L Tsai. J Genet Couns 2017
21
27

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
32
27

American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
Karen H Lu, Marie E Wood, Molly Daniels, Cathy Burke, James Ford, Noah D Kauff, Wendy Kohlmann, Noralane M Lindor, Therese M Mulvey, Linda Robinson,[...]. J Clin Oncol 2014
143
27

ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Sapna Syngal, Randall E Brand, James M Church, Francis M Giardiello, Heather L Hampel, Randall W Burt. Am J Gastroenterol 2015
680
27

Community Practice Implementation of a Self-administered Version of PREMM1,2,6 to Assess Risk for Lynch Syndrome.
Daniel G Luba, James A DiSario, Colleen Rock, Devki Saraiya, Kelsey Moyes, Krystal Brown, Kristen Rushton, Maydeen M Ogara, Mona Raphael, Dayna Zimmerman,[...]. Clin Gastroenterol Hepatol 2018
18
27

National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.
Christopher P Childers, Kimberly K Childers, Melinda Maggard-Gibbons, James Macinko. J Clin Oncol 2017
141
18


Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review.
Katherine G Meilleur, Marguerite T Littleton-Kearney. Am J Med Genet A 2009
27
18

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
61
18

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
60
18

Factors influencing patients' decisions to decline cancer genetic counseling services.
K P Geer, M E Ropka, W F Cohn, S M Jones, S Miesfeldt. J Genet Couns 2001
62
18

Recall of and reactions to a surgeon referral letter for BRCA genetic counseling among high-risk breast cancer patients.
Susan T Vadaparampil, Gwendolyn P Quinn, Cheryl A Miree, Jennifer Brzosowicz, Bradford Carter, Christine Laronga. Ann Surg Oncol 2009
26
18

Development and early usage patterns of a consumer-facing family health history tool.
Nathan C Hulse, Pallavi Ranade-Kharkar, Herman Post, Grant M Wood, Marc S Williams, Peter J Haug. AMIA Annu Symp Proc 2011
25
18

Prevalence of family history of breast and ovarian cancer in a single primary care practice using a self-administered questionnaire.
Kevin S Hughes, Constance Roche, Curtis T Campbell, Nancy Siegel, Lisa Salisbury, Amy Chekos, Maya S Katz, Erica Edell. Breast J 2003
38
18

Family history questionnaires designed for clinical use: a systematic review.
G T Reid, F M Walter, J M Brisbane, J D Emery. Public Health Genomics 2009
54
18

The current state of cancer family history collection tools in primary care: a systematic review.
Nadeem Qureshi, June C Carroll, Brenda Wilson, Pasqualina Santaguida, Judith Allanson, Melissa Brouwers, Parminder Raina. Genet Med 2009
68
18

Family history tools for primary care are not ready yet to be implemented. A systematic review.
Céline L M M de Hoog, Piet J M Portegijs, Henri E J H Stoffers. Eur J Gen Pract 2014
23
18

Cancer risk assessment: quality and impact of the family history interview.
Harvey J Murff, Daniel Byrne, Sapna Syngal. Am J Prev Med 2004
79
18


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
64
18

Hereditary cancer risk assessment in a pediatric oncology follow-up clinic.
Sara Knapke, Rajaram Nagarajan, Judy Correll, Debra Kent, Karen Burns. Pediatr Blood Cancer 2012
61
18

Patient engagement as a risk factor in personalized health care: a systematic review of the literature on chronic disease.
Leigh Ann Simmons, Ruth Q Wolever, Elizabeth M Bechard, Ralph Snyderman. Genome Med 2014
80
9

Increasing confidence and changing behaviors in primary care providers engaged in genetic counselling.
Michael S Wilkes, Frank C Day, Tonya L Fancher, Haley McDermott, Erik Lehman, Robert A Bell, Michael J Green. BMC Med Educ 2017
24
9

Artificial Intelligence: Threat or Boon to Radiologists?
Michael Recht, R Nick Bryan. J Am Coll Radiol 2017
54
9



Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
57
9

Introducing a Comprehensive Informatics Framework to Promote Breast Cancer Risk Assessment and Chemoprevention in the Primary Care Setting.
Joseph Finkelstein, Jeffrey Wood, Katherine D Crew, Rita Kukafka. AMIA Jt Summits Transl Sci Proc 2017
5
20

A randomized trial of a prenatal genetic testing interactive computerized information aid.
Lynn M Yee, Michael Wolf, Rebecca Mullen, Ashley R Bergeron, Stacy Cooper Bailey, Robert Levine, William A Grobman. Prenat Diagn 2014
34
9

Diffusion of breast cancer risk assessment in primary care.
Carmen E Guerra, Melani Sherman, Katrina Armstrong. J Am Board Fam Med 2009
34
9

Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system.
Cecelia A Bellcross, Lucy A Peipins, Frances A McCarty, Juan L Rodriguez, Nikki A Hawkins, Sharon Hensley Alford, Steven Leadbetter. Genet Med 2015
25
9

The genetic attributable risk of breast and ovarian cancer.
E B Claus, J M Schildkraut, W D Thompson, N J Risch. Cancer 1996
507
9

Analysis of Advantages, Limitations, and Barriers of Genetic Counseling Service Delivery Models.
Stephanie A Cohen, Rachelle C Huziak, Shanna Gustafson, Robin E Grubs. J Genet Couns 2016
39
9


A breast cancer prediction model incorporating familial and personal risk factors.
Jonathan Tyrer, Stephen W Duffy, Jack Cuzick. Stat Med 2004
665
9

Application of Synchronous Text-Based Dialogue Systems in Mental Health Interventions: Systematic Review.
Simon Hoermann, Kathryn L McCabe, David N Milne, Rafael A Calvo. J Med Internet Res 2017
54
9

Watson for Oncology and breast cancer treatment recommendations: agreement with an expert multidisciplinary tumor board.
S P Somashekhar, M-J Sepúlveda, S Puglielli, A D Norden, E H Shortliffe, C Rohit Kumar, A Rauthan, N Arun Kumar, P Patil, K Rhee,[...]. Ann Oncol 2018
97
9


Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review.
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
60
9

Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors.
Robin L Bennett, Kathryn Steinhaus French, Robert G Resta, Debra Lochner Doyle. J Genet Couns 2008
112
9



Prediction of MLH1 and MSH2 mutations in Lynch syndrome.
Judith Balmaña, David H Stockwell, Ewout W Steyerberg, Elena M Stoffel, Amie M Deffenbaugh, Julia E Reid, Brian Ward, Thomas Scholl, Brant Hendrickson, John Tazelaar,[...]. JAMA 2006
128
9

Prediction of germline mutations and cancer risk in the Lynch syndrome.
Sining Chen, Wenyi Wang, Shing Lee, Khedoudja Nafa, Johanna Lee, Kathy Romans, Patrice Watson, Stephen B Gruber, David Euhus, Kenneth W Kinzler,[...]. JAMA 2006
246
9

PancPRO: risk assessment for individuals with a family history of pancreatic cancer.
Wenyi Wang, Sining Chen, Kieran A Brune, Ralph H Hruban, Giovanni Parmigiani, Alison P Klein. J Clin Oncol 2007
130
9

A pilot study of telegenetics.
J Gray, K Brain, R Iredale, J Alderman, E France, H Hughes. J Telemed Telecare 2000
46
9

Estimating CDKN2A carrier probability and personalizing cancer risk assessments in hereditary melanoma using MelaPRO.
Wenyi Wang, Kristin B Niendorf, Devanshi Patel, Amanda Blackford, Fabio Marroni, Arthur J Sober, Giovanni Parmigiani, Hensin Tsao. Cancer Res 2010
27
9

Projecting individualized probabilities of developing breast cancer for white females who are being examined annually.
M H Gail, L A Brinton, D P Byar, D K Corle, S B Green, C Schairer, J J Mulvihill. J Natl Cancer Inst 1989
9



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.