A citation-based method for searching scientific literature

Natalia Campacci, Juliana O de Lima, André L Carvalho, Rodrigo D Michelli, Rafael Haikel, Edmundo Mauad, Danilo V Viana, Matias E Melendez, Fabiana de L Vazquez, Cleyton Zanardo, Rui M Reis, Benedito M Rossi, Edenir I Palmero. Cancer Med 2017
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity



Development and validation of a simple questionnaire for the identification of hereditary breast cancer in primary care.
Patricia Ashton-Prolla, Juliana Giacomazzi, Aishameriane V Schmidt, Fernanda L Roth, Edenir I Palmero, Luciane Kalakun, Ernestina S Aguiar, Susana M Moreira, Erica Batassini, Vanessa Belo-Reyes,[...]. BMC Cancer 2009
38
33

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
33

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
138
33


Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer.
F G J Kallenberg, J E G IJspeert, P M M Bossuyt, C M Aalfs, E Dekker. Fam Cancer 2015
10
33

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
33


Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer.
Annelie Augustinsson, Carolina Ellberg, Ulf Kristoffersson, Åke Borg, Håkan Olsson. Acta Oncol 2018
11
33

Prevalence of family history of breast, colorectal, prostate, and lung cancer in a population-based study.
P L Mai, L Wideroff, M H Greene, B I Graubard. Public Health Genomics 2010
22
33

Li-Fraumeni syndrome--a molecular and clinical review.
J M Varley, D G Evans, J M Birch. Br J Cancer 1997
236
16

Inherited susceptibility to common cancers.
William D Foulkes. N Engl J Med 2008
311
16


Building a tool to identify risk for Lynch syndrome among individuals presenting for screening colonoscopy.
Deborah Rabinowitz-Abrams, Debra Morgan, James Morse, Susan Miesfeldt. J Genet Couns 2010
1
100


Telephone genetic counseling for high-risk women undergoing BRCA1 and BRCA2 testing: rationale and development of a randomized controlled trial.
Beth N Peshkin, Tiffani A Demarco, Kristi D Graves, Karen Brown, Rachel H Nusbaum, Diana Moglia, Andrea Forman, Heiddis Valdimarsdottir, Marc D Schwartz. Genet Test 2008
42
16

Population prevalence of hereditary breast cancer phenotypes and implementation of a genetic cancer risk assessment program in southern Brazil.
Edenir I Palmero, Maira Caleffi, Lavínia Schüler-Faccini, Fernanda L Roth, Luciane Kalakun, Cristina Brinkmann Oliveira Netto, Giovana Skonieski, Juliana Giacomazzi, Bernadete Weber, Roberto Giugliani,[...]. Genet Mol Biol 2009
15
16

Effective Referral of Low-Income Women at Risk for Hereditary Breast and Ovarian Cancer to Genetic Counseling: A Randomized Delayed Intervention Control Trial.
Rena J Pasick, Galen Joseph, Susan Stewart, Celia Kaplan, Robin Lee, Judith Luce, Sharon Davis, Titas Marquez, Tung Nguyen, Claudia Guerra. Am J Public Health 2016
12
16


The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees' outcome.
Ulla Platten, Johanna Rantala, Annika Lindblom, Yvonne Brandberg, Gunilla Lindgren, Brita Arver. Fam Cancer 2012
29
16

Knowledge and perceptions of familial and genetic risks for breast cancer risk in adolescent girls.
Angela R Bradbury, Linda Patrick-Miller, Brian L Egleston, Lisa A Schwartz, Colleen B Sands, Rebecca Shorter, Cynthia W Moore, Lisa Tuchman, Paula Rauch, Shreya Malhotra,[...]. Breast Cancer Res Treat 2012
21
16

Consistency of self-reported first-degree family history of cancer in a population-based study.
Fernanda Lenara Roth, Suzi Alves Camey, Maira Caleffi, Lavínia Schuler-Faccini, Edenir Inêz Palmero, Carla Bochi, Susana Mayer Moreira, Luciane Kalakun, Roberto Giugliani, Patrícia Ashton-Prolla. Fam Cancer 2009
16
16


[Genetic counseling about cancer in Peru].
Javier E Manrique, Yasser Sullcahuamán-Allende, Abel Limache-García. Rev Peru Med Exp Salud Publica 2013
3
33

The Li-Fraumeni syndrome.
Agnès Chompret. Biochimie 2002
48
16

Efficient identification and referral of low-income women at high risk for hereditary breast cancer: a practice-based approach.
G Joseph, C Kaplan, J Luce, R Lee, S Stewart, C Guerra, R Pasick. Public Health Genomics 2012
18
16

Can mobile units improve the strategies for cervical cancer prevention?
Edmundo Carvalho Mauad, Sérgio Mancini Nicolau, Uilho A Gomes, René Aloísio da Costa Vieira, Jacó Saraiva de Castro Mattos, Adhemar Longatto-Filho, Edmund C Baracat. Diagn Cytopathol 2010
10
16

An overview of hereditary breast and ovarian cancer syndrome.
Edith Caroline Smith. J Midwifery Womens Health 2012
7
16

Clinical characterization and risk profile of individuals seeking genetic counseling for hereditary breast cancer in Brazil.
Edenir Inez Palmero, Patricia Ashton-Prolla, José Cláudio C da Rocha, Fernando Regla Vargas, Luciane Kalakun, Melissa Brauner Blom, Sérgio J Azevedo, Maira Caleffi, Roberto Giugliani, Lavinia Schüler-Faccini. J Genet Couns 2007
17
16


Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital.
Edenir I Palmero, Henrique C R Galvão, Gabriela C Fernandes, André E de Paula, Junea C Oliveira, Cristiano P Souza, Carlos E Andrade, Luis G C Romagnolo, Sahlua Volc, Maximiliano C Neto,[...]. Genet Mol Biol 2016
14
16

Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.
Anita Y Kinney, Laurie E Steffen, Barbara H Brumbach, Wendy Kohlmann, Ruofei Du, Ji-Hyun Lee, Amanda Gammon, Karin Butler, Saundra S Buys, Antoinette M Stroup,[...]. J Clin Oncol 2016
61
16

Tailored telephone counseling to improve adherence to follow-up regimens after an abnormal pap smear among minority, underserved women.
Suzanne M Miller, Siu-kuen Azor Hui, Kuang-Yi Wen, John Scarpato, Fang Zhu, Joanne Buzaglo, Enrique E Hernandez. Patient Educ Couns 2013
18
16

ASCO/SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes.
José G Guillem, William C Wood, Jeffrey F Moley, Andrew Berchuck, Beth Y Karlan, David G Mutch, Robert F Gagel, Jeffrey Weitzel, Monica Morrow, Barbara L Weber,[...]. J Clin Oncol 2006
128
16

Factors affecting frequency of communication about family health history with family members and doctors in a medically underserved population.
Kimberly A Kaphingst, Melody Goodman, Chintan Pandya, Priyanka Garg, Jewel Stafford, Christina Lachance. Patient Educ Couns 2012
34
16

Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.
Bronson D Riley, Julie O Culver, Cécile Skrzynia, Leigha A Senter, June A Peters, Josephine W Costalas, Faith Callif-Daley, Sherry C Grumet, Katherine S Hunt, Rebecca S Nagy,[...]. J Genet Couns 2012
185
16

Mammography-based screening program: preliminary results from a first 2-year round in a Brazilian region using mobile and fixed units.
Raphael Luiz Haikel, Edmundo Carvalho Mauad, Thiago Buosi Silva, Jacó Saraiva de Castro Mattos, Luciano Fernandes Chala, Adhemar Longatto-Filho, Nestor de Barros. BMC Womens Health 2012
17
16

Hereditary breast cancer: practical pursuit for clinical translation.
Henry T Lynch, Carrie Snyder, Jane Lynch. Ann Surg Oncol 2012
15
16

Family history of cancer in Brazil: is it being used?
Danilo V Viana, Juvenal R N Góes, Cláudio S R Coy, Maria de Lourdes Setsuko Ayrizono, Carmen S P Lima, Iscia Lopes-Cendes. Fam Cancer 2008
8
16

Opportunistic screening for skin cancer using a mobile unit in Brazil.
Edmundo C Mauad, Thiago B Silva, Maria R D O Latorre, René A C Vieira, Raphael L Haikel, Vinicius L Vazquez, Adhemar Longatto-Filho. BMC Dermatol 2011
8
16

A model for patient-direct screening and referral for familial cancer risk.
Kristin B Niendorf, Melissa A Geller, Rachel Isaksson Vogel, Timothy R Church, Anna Leininger, Angela Bakke, Robert D Madoff. Fam Cancer 2016
11
16

Effect of preventive messages tailored to family history on health behaviors: the Family Healthware Impact Trial.
Mack T Ruffin, Donald E Nease, Ananda Sen, Wilson D Pace, Catharine Wang, Louise S Acheson, Wendy S Rubinstein, Suzanne O'Neill, Robert Gramling. Ann Fam Med 2011
98
16


An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.
Mary Pritzlaff, Arielle Yorczyk, Linda S Robinson, Sara Pirzadeh-Miller, Tirun Lin, David Euhus, Theodora S Ross. J Genet Couns 2014
13
16

Improving Utilization of the Family History in the Electronic Health Record.
Kathleen T Hickey, Maria C Katapodi, Bernice Coleman, Karin Reuter-Rice, Angela R Starkweather. J Nurs Scholarsh 2017
12
16

Familial risk for common diseases in primary care: the Family Healthware Impact Trial.
Suzanne M O'Neill, Wendy S Rubinstein, Catharine Wang, Paula W Yoon, Louise S Acheson, Nan Rothrock, Erin J Starzyk, Jennifer L Beaumont, James M Galliher, Mack T Ruffin. Am J Prev Med 2009
87
16

Cancer family history reporting: impact of method and psychosocial factors.
Kimberly M Kelly, Randi Shedlosky-Shoemaker, Kyle Porter, Amber Remy, Philip DeSimone, Michael A Andrykowski. J Genet Couns 2007
19
16



Collecting genetic information in primary care: evaluating a new family history tool.
Nadeem Qureshi, Jane Bethea, Bernadette Modell, Paul Brennan, Alexia Papageorgiou, Sandy Raeburn, Rhydian Hapgood, Michael Modell. Fam Pract 2005
61
16


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.