A citation-based method for searching scientific literature

Cecelia A Bellcross, Katherine Kolor, Katrina A B Goddard, Ralph J Coates, Michele Reyes, Muin J Khoury. Am J Prev Med 2011
Times Cited: 108







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



Times Cited
  Times     Co-cited
Similarity


Screening for founder mutations in BRCA1 and BRCA2 in unselected Jewish women.
Kelly A Metcalfe, Aletta Poll, Robert Royer, Marcia Llacuachaqui, Anna Tulman, Ping Sun, Steven A Narod. J Clin Oncol 2010
103
4

Breast-cancer risk in families with mutations in PALB2.
Antonis C Antoniou, Silvia Casadei, Tuomas Heikkinen, Daniel Barrowdale, Katri Pylkäs, Jonathan Roberts, Andrew Lee, Deepak Subramanian, Kim De Leeneer, Florentia Fostira,[...]. N Engl J Med 2014
462
4

Cancer statistics, 2013.
Rebecca Siegel, Deepa Naishadham, Ahmedin Jemal. CA Cancer J Clin 2013
4

Personalized cancer genetics training for personalized medicine: improving community-based healthcare through a genetically literate workforce.
Kathleen R Blazer, Deborah J Macdonald, Julie O Culver, Carin R Huizenga, Robert J Morgan, Gwen C Uman, Jeffrey N Weitzel. Genet Med 2011
26
15

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.
Mary B Daly, Robert Pilarski, Jennifer E Axilbund, Saundra S Buys, Beth Crawford, Susan Friedman, Judy E Garber, Carolyn Horton, Virginia Kaklamani, Catherine Klein,[...]. J Natl Compr Canc Netw 2014
91
4

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
Matthew B Yurgelun, Brian Allen, Rajesh R Kaldate, Karla R Bowles, Thaddeus Judkins, Praveen Kaushik, Benjamin B Roa, Richard J Wenstrup, Anne-Renee Hartman, Sapna Syngal. Gastroenterology 2015
138
4

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
Nadine Tung, Nancy U Lin, John Kidd, Brian A Allen, Nanda Singh, Richard J Wenstrup, Anne-Renee Hartman, Eric P Winer, Judy E Garber. J Clin Oncol 2016
229
4


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
150
4

Interest and beliefs about BRCA genetic counseling among at-risk Latinas in New York City.
Katarina M Sussner, Lina Jandorf, Hayley S Thompson, Heiddis B Valdimarsdottir. J Genet Couns 2010
29
13

Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study.
Angela Bradbury, Linda Patrick-Miller, Diana Harris, Evelyn Stevens, Brian Egleston, Kyle Smith, Rebecca Mueller, Amanda Brandt, Jill Stopfer, Shea Rauch,[...]. J Med Internet Res 2016
34
11

Genetic Testing and Counseling Among Patients With Newly Diagnosed Breast Cancer .
Allison W Kurian, Kent A Griffith, Ann S Hamilton, Kevin C Ward, Monica Morrow, Steven J Katz, Reshma Jagsi. JAMA 2017
68
5

Adherence patterns to National Comprehensive Cancer Network (NCCN) guidelines for referral to cancer genetic professionals.
Terri Febbraro, Katina Robison, Jennifer Scalia Wilbur, Jessica Laprise, Amy Bregar, Vrishali Lopes, Robert Legare, Ashley Stuckey. Gynecol Oncol 2015
60
6

Are public health professionals prepared for public health genomics? A cross-sectional survey in Italy.
Carolina Marzuillo, Corrado De Vito, Maddalena D'Addario, Paola Santini, Elvira D'Andrea, Antonio Boccia, Paolo Villari. BMC Health Serv Res 2014
12
33

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
Allison W Kurian, Emily E Hare, Meredith A Mills, Kerry E Kingham, Lisa McPherson, Alice S Whittemore, Valerie McGuire, Uri Ladabaum, Yuya Kobayashi, Stephen E Lincoln,[...]. J Clin Oncol 2014
294
4

Olaparib for Metastatic Breast Cancer in Patients with a Germline BRCA Mutation.
Mark Robson, Seock-Ah Im, Elżbieta Senkus, Binghe Xu, Susan M Domchek, Norikazu Masuda, Suzette Delaloge, Wei Li, Nadine Tung, Anne Armstrong,[...]. N Engl J Med 2017
947
4

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
108
4

Influence of genetic discrimination perceptions and knowledge on cancer genetics referral practice among clinicians.
Katrina J Lowstuter, Sharon Sand, Kathleen R Blazer, Deborah J MacDonald, Kimberly C Banks, Carol A Lee, Barbara U Schwerin, Margaret Juarez, Gwen C Uman, Jeffrey N Weitzel. Genet Med 2008
43
6

Underdiagnosis of Lynch syndrome involves more than family history criteria.
Hardeep Singh, Rachel Schiesser, Gobind Anand, Peter A Richardson, Hashem B El-Serag. Clin Gastroenterol Hepatol 2010
49
6

Cancer genetics evaluation: barriers to and improvements for referral.
Rachael Brandt, Zonera Ali, Allison Sabel, Terri McHugh, Paul Gilman. Genet Test 2008
31
9

Translational research in cancer genetics: the road less traveled.
S D Schully, C B Benedicto, E M Gillanders, S S Wang, M J Khoury. Public Health Genomics 2011
50
6

Clinical assessment incorporating a personal genome.
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
458
3

Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and “personalized” medicine?
Wylie Burke, Hilary Burton, Alison E Hall, Mohamed Karmali, Muin J Khoury, Bartha Knoppers, Eric M Meslin, Fiona Stanley, Caroline F Wright, Ronald L Zimmern. Genet Med 2010
59
5

Current priorities for public health practice in addressing the role of human genomics in improving population health.
Muin J Khoury, Michael S Bowen, Wylie Burke, Ralph J Coates, Nicole F Dowling, James P Evans, Michele Reyes, Jeannette St Pierre. Am J Prev Med 2011
50
6

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
339
3


Hereditary cancer predisposition syndromes.
Judy E Garber, Kenneth Offit. J Clin Oncol 2005
315
3

Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation.
Amy Finch, Mario Beiner, Jan Lubinski, Henry T Lynch, Pal Moller, Barry Rosen, Joan Murphy, Parviz Ghadirian, Eitan Friedman, William D Foulkes,[...]. JAMA 2006
384
3

Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations.
Timothy R Rebbeck, Henry T Lynch, Susan L Neuhausen, Steven A Narod, Laura Van't Veer, Judy E Garber, Gareth Evans, Claudine Isaacs, Mary B Daly, Ellen Matloff,[...]. N Engl J Med 2002
990
3

Preventing future cancers by testing women with ovarian cancer for BRCA mutations.
Janice S Kwon, Molly S Daniels, Charlotte C Sun, Karen H Lu. J Clin Oncol 2010
48
6

Cancer Incidence in BRCA1 mutation carriers.
Deborah Thompson, Douglas F Easton. J Natl Cancer Inst 2002
696
3

Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer.
Kathryn J Schlich-Bakker, Herman F J ten Kroode, Carla C Wárlám-Rodenhuis, Jan van den Bout, Margreet G E M Ausems. Genet Med 2007
50
6

Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer.
H A Risch, J R McLaughlin, D E Cole, B Rosen, L Bradley, E Kwan, E Jack, D J Vesprini, G Kuperstein, J L Abrahamson,[...]. Am J Hum Genet 2001
707
3


Breast cancer risk among male BRCA1 and BRCA2 mutation carriers.
Yu Chuan Tai, Susan Domchek, Giovanni Parmigiani, Sining Chen. J Natl Cancer Inst 2007
174
3

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
222
3

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
18


Primary care physicians' use of family history for cancer risk assessment.
Brian S Flynn, Marie E Wood, Takamaru Ashikaga, Alan Stockdale, Greg S Dana, Shelly Naud. BMC Fam Pract 2010
43
6


Cancer risk assessment from family history: gaps in primary care practice.
Randa D Sifri, Richard Wender, Nina Paynter. J Fam Pract 2002
37
8

Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer.
Lisa R Susswein, Cécile Skrzynia, Leslie A Lange, Jessica K Booker, Mark L Graham, James P Evans. J Clin Oncol 2008
42
7

Impact of Event Scale: a measure of subjective stress.
M Horowitz, N Wilner, W Alvarez. Psychosom Med 1979
3

BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
598
3

Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers.
Allison W Kurian, Bronislava M Sigal, Sylvia K Plevritis. J Clin Oncol 2010
150
3

Confirmation of family cancer history reported in a population-based survey.
Phuong L Mai, Anne O Garceau, Barry I Graubard, Marsha Dunn, Timothy S McNeel, Lou Gonsalves, Mitchell H Gail, Mark H Greene, Gordon B Willis, Louise Wideroff. J Natl Cancer Inst 2011
74
4


Prophylactic mastectomy in BRCA1 and BRCA2 mutation carriers: very low risk for subsequent breast cancer.
Reinoutje Kaas, Senno Verhoef, Jelle Wesseling, Matti A Rookus, Hester S A Oldenburg, Marie-Jeanne Vrancken Peeters, Emiel J T Rutgers. Ann Surg 2010
50
6


What motivates interest in attending a familial cancer genetics clinic?
L Fraser, S Bramald, C Chapman, C Chu, V Cornelius, F Douglas, A Lucassen, A Nehammer, S Sutton, M Trivella,[...]. Fam Cancer 2003
25
12


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.