A citation-based method for searching scientific literature

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
Times Cited: 16







List of co-cited articles
37 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
31

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
31

The effectiveness of family history questionnaires in cancer genetic counseling.
Susan Randall Armel, Jeanna McCuaig, Amy Finch, Rochelle Demsky, Tony Panzarella, Joan Murphy, Barry Rosen. J Genet Couns 2009
17
25

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
25


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
20

Limited family structure and BRCA gene mutation status in single cases of breast cancer.
Jeffrey N Weitzel, Veronica I Lagos, Carey A Cullinane, Patricia J Gambol, Julie O Culver, Kathleen R Blazer, Melanie R Palomares, Katrina J Lowstuter, Deborah J MacDonald. JAMA 2007
130
18


Identification and referral of families at high risk for cancer susceptibility.
Kevin M Sweet, Terry L Bradley, Judith A Westman. J Clin Oncol 2002
125
18

Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians.
Cecelia A Bellcross, Katherine Kolor, Katrina A B Goddard, Ralph J Coates, Michele Reyes, Muin J Khoury. Am J Prev Med 2011
111
18

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
18

Reported referral for genetic counseling or BRCA 1/2 testing among United States physicians: a vignette-based study.
Katrina F Trivers, Laura-Mae Baldwin, Jacqueline W Miller, Barbara Matthews, C Holly A Andrilla, Denise M Lishner, Barbara A Goff. Cancer 2011
76
18


Population-based estimates of the prevalence of family history of cancer among women.
I J Hall, W Burke, S Coughlin, N C Lee. Community Genet 2001
17
12

Assessment of family cancer history collection and utilization in patient care.
H J Allen, C A Briceno, M S Piver. Community Genet 1998
3
66

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
12

A breast cancer prediction model incorporating familial and personal risk factors.
Jonathan Tyrer, Stephen W Duffy, Jack Cuzick. Stat Med 2004
648
12

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
12

Community genetics: a new discipline and its application in Brazil.
A S Ramalho, R B Silva. Cad Saude Publica 2000
6
33


Cancer risk assessment: quality and impact of the family history interview.
Harvey J Murff, Daniel Byrne, Sapna Syngal. Am J Prev Med 2004
78
12

Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
225
12

The comprehensiveness of family cancer history assessments in primary care.
Harvey J Murff, Robert A Greevy, Sapna Syngal. Community Genet 2007
75
12


Society of Gynecologic Oncologists Education Committee statement on risk assessment for inherited gynecologic cancer predispositions.
Johnathan M Lancaster, C Bethan Powell, Noah D Kauff, Ilana Cass, Lee-May Chen, Karen H Lu, David G Mutch, Andrew Berchuck, Beth Y Karlan, Thomas J Herzog. Gynecol Oncol 2007
174
12

Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities.
Larissa A Meyer, Meaghan E Anderson, Robin A Lacour, Anuj Suri, Molly S Daniels, Diana L Urbauer, Graciela M Nogueras-Gonzalez, Kathleen M Schmeler, David M Gershenson, Karen H Lu. Obstet Gynecol 2010
80
12


The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population.
Susan Randall Armel, Kara Hitchman, Kathryn Millar, Laura Zahavich, Rochelle Demsky, Joan Murphy, Barry Rosen. J Genet Couns 2011
4
50

Accuracy of reporting of family history of colorectal cancer.
R J Mitchell, D Brewster, H Campbell, M E M Porteous, A H Wyllie, C C Bird, M G Dunlop. Gut 2004
147
12

Knowledge, attitudes, and behaviors of Alabama's primary care physicians regarding cancer genetics.
R T Acton, N M Burst, L Casebeer, S M Ferguson, P Greene, B L Laird, L Leviton. Acad Med 2000
111
12

Barriers in identification and referral to genetic counseling for familial cancer risk: the perspective of genetic service providers.
Sharon J Rolnick, Alanna K Rahm, Jody M Jackson, Larissa Nekhlyudov, Katrina A B Goddard, Terry Field, Catherine McCarty, Cynthia Nakasato, Douglas Roblin, Christopher P Anderson,[...]. J Genet Couns 2011
24
12

A self-administered family history questionnaire improves identification of women who warrant referral to genetic counseling for hereditary cancer risk.
Tilley Jenkins Vogel, Kyrsten Stoops, Robin L Bennett, Margaret Miller, Elizabeth M Swisher. Gynecol Oncol 2012
16
12

Family history in public health practice: a genomic tool for disease prevention and health promotion.
Rodolfo Valdez, Paula W Yoon, Nadeem Qureshi, Ridgely Fisk Green, Muin J Khoury. Annu Rev Public Health 2010
149
12

Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data.
D A van Dijk, M J Oostindiër, W M Kloosterman-Boele, P Krijnen, H F A Vasen. Fam Cancer 2007
41
12

Family history: still relevant in the genomics era.
Megan Doerr, Kathryn Teng. Cleve Clin J Med 2012
34
12



Hereditary cancer predisposition syndromes.
Judy E Garber, Kenneth Offit. J Clin Oncol 2005
320
6


The "duty to warn" a patient's family members about hereditary disease risks.
Kenneth Offit, Elizabeth Groeger, Sam Turner, Eve A Wadsworth, Mary A Weiser. JAMA 2004
154
6

Validity of models for predicting BRCA1 and BRCA2 mutations.
Giovanni Parmigiani, Sining Chen, Edwin S Iversen, Tara M Friebel, Dianne M Finkelstein, Hoda Anton-Culver, Argyrios Ziogas, Barbara L Weber, Andrea Eisen, Kathleen E Malone,[...]. Ann Intern Med 2007
74
6

Cancer Research UK.
. Nat Cell Biol 2002
22
6

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer.
Pia Vahteristo, Jirina Bartkova, Hannaleena Eerola, Kirsi Syrjäkoski, Salla Ojala, Outi Kilpivaara, Anitta Tamminen, Juha Kononen, Kristiina Aittomäki, Päivi Heikkilä,[...]. Am J Hum Genet 2002
328
6

Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndrome.
E C B da Costa, F R Vargas, A S Moreira, J J Lourenço, M Caleffi, P Ashton-Prolla, M A M Martins Moreira. Cancer Genet Cytogenet 2008
17
6

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.
J M Birch, A L Hartley, K J Tricker, J Prosser, A Condie, A M Kelsey, M Harris, P H Jones, A Binchy, D Crowther. Cancer Res 1994
401
6

Patients with a family history of cancer: identification and management.
Margaret M Eberl, Annette Y Sunga, Carolyn D Farrell, Martin C Mahoney. J Am Board Fam Pract 2005
23
6


Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.
Kelly D Gonzalez, Katie A Noltner, Carolyn H Buzin, Dongqing Gu, Cindy Y Wen-Fong, Vu Q Nguyen, Jennifer H Han, Katrina Lowstuter, Jeffrey Longmate, Steve S Sommer,[...]. J Clin Oncol 2009
333
6

Germline mutations in the TP53 gene.
R A Eeles. Cancer Surv 1995
144
6



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.