A citation-based method for searching scientific literature

Deborah Cragun, Courtney Lewis, Lucia Camperlengo, Tuya Pal. Healthcare (Basel) 2016
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Educational needs and preferred methods of learning among Florida practitioners who order genetic testing for hereditary breast and ovarian cancer.
Deborah Cragun, Andrea Doty Besharat, Courtney Lewis, Susan T Vadaparampil, Tuya Pal. J Cancer Educ 2013
12
40

Counselling framework for moderate-penetrance cancer-susceptibility mutations.
Nadine Tung, Susan M Domchek, Zsofia Stadler, Katherine L Nathanson, Fergus Couch, Judy E Garber, Kenneth Offit, Mark E Robson. Nat Rev Clin Oncol 2016
156
40


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
38
40


Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol 2011
244
20

Reply to S.M. Sorscher and M.J. Hall et al.
Nadine M Tung, Judy E Garber. J Clin Oncol 2016
2
50

P53 germline mutations in childhood cancers and cancer risk for carrier individuals.
A Chompret, L Brugières, M Ronsin, M Gardes, F Dessarps-Freichey, A Abel, D Hua, L Ligot, M G Dondon, B Bressac-de Paillerets,[...]. Br J Cancer 2000
245
20

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.
Anita Villani, Ari Shore, Jonathan D Wasserman, Derek Stephens, Raymond H Kim, Harriet Druker, Bailey Gallinger, Anne Naumer, Wendy Kohlmann, Ana Novokmet,[...]. Lancet Oncol 2016
223
20

Reply to M.J. Hall et al and K.N. Maxwell et al.
Jennifer E Axilbund. J Clin Oncol 2016
1
100


Population-Wide Screening for Germline BRCA1 and BRCA2 Mutations: Too Much of a Good Thing?
Matthew B Yurgelun, Elaine Hiller, Judy E Garber. J Clin Oncol 2015
36
20

2009 version of the Chompret criteria for Li Fraumeni syndrome.
Julie Tinat, Gaelle Bougeard, Stéphanie Baert-Desurmont, Stéphanie Vasseur, Cosette Martin, Emilie Bouvignies, Olivier Caron, Brigitte Bressac-de Paillerets, Pascaline Berthet, Catherine Dugast,[...]. J Clin Oncol 2009
198
20


Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families.
G Bougeard, R Sesboüé, S Baert-Desurmont, S Vasseur, C Martin, J Tinat, L Brugières, A Chompret, B Bressac de Paillerets, D Stoppa-Lyonnet,[...]. J Med Genet 2008
143
20

DNA sequencing with chain-terminating inhibitors.
F Sanger, S Nicklen, A R Coulson. Proc Natl Acad Sci U S A 1977
20

Panel Testing Is Not a Panacea.
Jennifer E Axilbund. J Clin Oncol 2016
13
20

Germline TP53 mutations and the changing landscape of Li-Fraumeni syndrome.
Junne Kamihara, Huma Q Rana, Judy E Garber. Hum Mutat 2014
89
20

Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award.
Mary-Claire King, Ephrat Levy-Lahad, Amnon Lahad. JAMA 2014
172
20

Chest wall leiomyosarcoma after breast-conservative therapy for early-stage breast cancer in a young woman with Li-Fraumeni syndrome.
Eve Henry, Victor Villalobos, Lynn Million, Kristin C Jensen, Robert West, Kristen Ganjoo, Alexandra Lebensohn, James M Ford, Melinda L Telli. J Natl Compr Canc Netw 2012
19
20

Late onset Li-Fraumeni Syndrome with bilateral breast cancer and other malignancies: case report and review of the literature.
Karin Kast, Mechthild Krause, Markus Schuler, Katrin Friedrich, Barbara Thamm, Andrea Bier, Wolfgang Distler, Stefan Krüger. BMC Cancer 2012
13
20

Multigene Panels to Evaluate Hereditary Cancer Risk: Reckless or Relevant?
Michael J Hall, Elias Obeid, Mary B Daly. J Clin Oncol 2016
8
20

A cancer family syndrome in twenty-four kindreds.
F P Li, J F Fraumeni, J J Mulvihill, W A Blattner, M G Dreyfus, M A Tucker, R W Miller. Cancer Res 1988
954
20

Sensitivity and predictive value of criteria for p53 germline mutation screening.
A Chompret, A Abel, D Stoppa-Lyonnet, L Brugiéres, S Pagés, J Feunteun, C Bonaïti-Pellié. J Med Genet 2001
184
20

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
Gaëlle Bougeard, Mariette Renaux-Petel, Jean-Michel Flaman, Camille Charbonnier, Pierre Fermey, Muriel Belotti, Marion Gauthier-Villars, Dominique Stoppa-Lyonnet, Emilie Consolino, Laurence Brugières,[...]. J Clin Oncol 2015
267
20

American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.
Mark E Robson, Angela R Bradbury, Banu Arun, Susan M Domchek, James M Ford, Heather L Hampel, Stephen M Lipkin, Sapna Syngal, Dana S Wollins, Noralane M Lindor. J Clin Oncol 2015
296
20

Competency, Programming, and Emerging Innovation in Graduate Education within Schools of Pharmacy: The Report of the 2016-2017 Research and Graduate Affairs Committee.
Samuel M Poloyac, Kirsten F Block, Jane E Cavanaugh, Linda P Dwoskin, Russell B Melchert, Ruth E Nemire, James M O'Donnell, Ronny Priefer, Daniel R Touchette. Am J Pharm Educ 2017
7
20

Development of an undergraduate pharmacogenomics curriculum.
Travis J O'Brien, Federico Goodsaid, Margaret Plack, Arthur Harralson, Wafa Harrouk, Tim G Hales, H George Mandel, David C Perry, Katherine Kennedy, Narine Sarvazyan,[...]. Pharmacogenomics 2009
11
20


Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists.
Amber Frick, Cristina S Benton, Kelly L Scolaro, Jacqueline E McLaughlin, Courtney L Bradley, Oscar T Suzuki, Nan Wang, Tim Wiltshire. Front Pharmacol 2016
18
20

Pedigree Analysis: A Team-Based Learning Activity.
Jack Thatcher, Patty Canfield, Laurie Bauer, Brian N Griffith. MedEdPORTAL 2017
4
25

Establishing the essential nursing competencies for genetics and genomics.
Jean Jenkins, Kathleen A Calzone. J Nurs Scholarsh 2007
64
20

Pharmacogenomics training using an instructional software system.
John A Springer, Nicholas V Iannotti, Michael D Kane, Kevin Haynes, Jon E Sprague. Am J Pharm Educ 2011
19
20

Role-playing is an effective instructional strategy for genetic counseling training: an investigation and comparative study.
Xiao-Feng Xu, Yan Wang, Yan-Yan Wang, Ming Song, Wen-Gang Xiao, Yun Bai. BMC Med Educ 2016
9
20

Survey on warfarin pharmacogenetic testing among anticoagulation providers.
Maha Kadafour, Roshanak Haugh, Monica Posin, Steven R Kayser, Jaekyu Shin. Pharmacogenomics 2009
26
20


Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
129
20

Personal genotypes are teachable moments.
Mark S Boguski, Robert M Boguski, Michele R Berman. Genome Med 2013
11
20

Use of standardized patients in, undergraduate medical genetics education.
Margaret M McGovern, Melanie Johnston, Karen Brown, Randi Zinberg, Devra Cohen. Teach Learn Med 2006
14
20

Simulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education.
Guido Makransky, Mads T Bonde, Julie S G Wulff, Jakob Wandall, Michelle Hood, Peter A Creed, Iben Bache, Asli Silahtaroglu, Anne Nørremølle. BMC Med Educ 2016
27
20

Genomics education for health educators in Texas: the Family Health History Training Program.
P Goodson, L S Chen, A Muenzenberger, L Xu, E Jung. Public Health Genomics 2013
8
20

Preparing Nurses for Genetic Medicine: Integration of a Brief Education Session in an Undergraduate Nursing Curriculum.
Genevieve St-Martin, Angela Bedard, JoAnne Nelmes, James E J Bedard. J Nurs Educ 2017
3
33

Teaching efficacy of a medical education module on genetic testing for cancer.
K E Teague, J A Brown, J M Meyer, M J Kahn, T J Smith, K O Kreutzer, J N Bodurtha. J Cancer Educ 1996
10
20

Evaluation of a shared pharmacogenomics curriculum for pharmacy students.
Kelly C Lee, Karen Suchanek Hudmon, Joseph D Ma, Grace M Kuo. Pharmacogenomics 2015
26
20

How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study.
Saskia C Sanderson, Michael D Linderman, Randi Zinberg, Ali Bashir, Andrew Kasarskis, Micol Zweig, Sabrina Suckiel, Hardik Shah, Milind Mahajan, George A Diaz,[...]. Genet Med 2015
23
20

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
63
20

Teaching undergraduates about familial breast cancer: comparison of a computer assisted learning (CAL) package with a traditional tutorial approach.
Z Miedzybrodzka, N M Hamilton, H Gregory, B Milner, I Frade, T Sinclair, J Mollison, N Haites. Eur J Hum Genet 2001
15
20


Using improvisational theater to teach genetics concepts.
Patricia Newcomb, Kris Riddlesperger. Nurse Educ 2007
10
20

Adding a genomic healthcare component to a health information management curriculum.
Bailee Ludwig, Leming Zhou, Valerie Watzlaf, Mervat Abdelhak. Perspect Health Inf Manag 2010
2
50


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.