A citation-based method for searching scientific literature

Claire E Wakefield, Paboda Ratnayake, Bettina Meiser, Graeme Suthers, Melanie A Price, Jessica Duffy, Kathy Tucker. Genet Test Mol Biomarkers 2011
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Referral to cancer genetic counseling: are there stages of readiness?
Suzanne M O'Neill, June A Peters, Victor G Vogel, Eleanor Feingold, Wendy S Rubinstein. Am J Med Genet C Semin Med Genet 2006
38
33

Uptake of offer to receive genetic information about BRCA1 and BRCA2 mutations in an Australian population-based study.
Louise A Keogh, Melissa C Southey, Judi Maskiell, Mary-Anne Young, Clara L Gaff, Judy Kirk, Katherine M Tucker, Doreen Rosenthal, Margaret R E McCredie, Graham G Giles,[...]. Cancer Epidemiol Biomarkers Prev 2004
27
33

Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.
Susan M Domchek, Tara M Friebel, Christian F Singer, D Gareth Evans, Henry T Lynch, Claudine Isaacs, Judy E Garber, Susan L Neuhausen, Ellen Matloff, Rosalind Eeles,[...]. JAMA 2010
849
27

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
27

Identification and referral of families at high risk for cancer susceptibility.
Kevin M Sweet, Terry L Bradley, Judith A Westman. J Clin Oncol 2002
130
27

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
78
27

Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors.
Beth Anderson, Jennifer McLosky, Elizabeth Wasilevich, Sarah Lyon-Callo, Debra Duquette, Glenn Copeland. J Cancer Epidemiol 2012
63
27

Improving mutation notification when new genetic information is identified in research: a trial of two strategies in familial breast cancer.
Claire E Wakefield, Heather Thorne, Judy Kirk, Eveline Niedermayr, Emma L Doolan, Kathy Tucker. Genet Med 2013
9
55

Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS).
Ashley Crook, Loren Plunkett, Laura E Forrest, Nina Hallowell, Samantha Wake, Kathryn Alsop, Margaret Gleeson, David Bowtell, Gillian Mitchell, Mary-Anne Young. Eur J Hum Genet 2015
9
55

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
113
22

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, C├ęcile 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
187
22

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
22

Acceptance, motivators, and barriers in attending breast cancer genetic counseling in Asians.
Tan-Min Chin, Sing-Huang Tan, Siew-Eng Lim, Philip Iau, Wei-Peng Yong, Seng-Weng Wong, Soo-Chin Lee. Cancer Detect Prev 2005
28
22

How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry.
Louise A Keogh, Douglass Fisher, Sherri Sheinfeld Gorin, Sheri D Schully, Jan T Lowery, Dennis J Ahnen, Judith A Maskiell, Noralane M Lindor, John L Hopper, Terrilea Burnett,[...]. J Community Genet 2014
15
26

The responses of research participants and their next of kin to receiving feedback of genetic test results following participation in the Australian Ovarian Cancer Study.
Nina Hallowell, Kathryn Alsop, Margaret Gleeson, Ashley Crook, Loren Plunkett, David Bowtell, Gillian Mitchell, Mary-Anne Young. Genet Med 2013
18
22


Non-uptake of predictive genetic testing for BRCA1/2 among relatives of known carriers: attributes, cancer worry, and barriers to testing in a multicenter clinical cohort.
C Foster, D G R Evans, R Eeles, D Eccles, S Ashley, L Brooks, T Cole, J Cook, R Davidson, H Gregory,[...]. Genet Test 2004
48
16

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
26
16

Increasing utilization of cancer genetic counseling services using a patient navigator model.
Alanna Kulchak Rahm, Anna Sukhanova, Jennifer Ellis, Judy Mouchawar. J Genet Couns 2007
39
16

Why do women attend familial breast cancer clinics?
K Brain, J Gray, P Norman, E Parsons, A Clarke, C Rogers, R Mansel, P Harper. J Med Genet 2000
85
16


Uptake rates for breast cancer genetic testing: a systematic review.
Mary E Ropka, Jennifer Wenzel, Elayne K Phillips, Mir Siadaty, John T Philbrick. Cancer Epidemiol Biomarkers Prev 2006
114
16

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
204
16

Disclosing individual CDKN2A research results to melanoma survivors: interest, impact, and demands on researchers.
Kurt D Christensen, J Scott Roberts, David I Shalowitz, Jessica N Everett, Scott Y H Kim, Leon Raskin, Stephen B Gruber. Cancer Epidemiol Biomarkers Prev 2011
38
16

Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients.
Shilpa Grover, Elena M Stoffel, Laoti Bussone, Elizabeth Tschoegl, Sapna Syngal. Clin Gastroenterol Hepatol 2004
121
16


Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.
M Cappelli, L Surh, L Humphreys, S Verma, D Logan, A Hunter, J Allanson. Clin Genet 1999
92
16

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
16

Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families.
Nadine A Kasparian, Bettina Meiser, Phyllis N Butow, Judy M Simpson, Graham J Mann. Genet Med 2009
68
16


Global cancer statistics.
Ahmedin Jemal, Freddie Bray, Melissa M Center, Jacques Ferlay, Elizabeth Ward, David Forman. CA Cancer J Clin 2011
11

An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations.
Paboda Ratnayake, Claire E Wakefield, Bettina Meiser, Graeme Suthers, Melanie A Price, Jessica Duffy, Kathy Tucker. Fam Cancer 2011
23
11


Factors associated with an individuals' decision to withdraw from genetic counseling for BRCA1 and BRCA2 genes mutations: are personality traits involved?
Anita Caruso, Cristina Vigna, Valentina Bigazzi, Carlo Leone, Gabriella Maggi, Aline Martayan, Fabio M Sega, Francesco Cognetti, Antonella Savarese. Fam Cancer 2011
4
50


Genetic testing in young women with breast cancer: results from a Web-based survey.
K J Ruddy, S Gelber, J Shin, J E Garber, R Rosenberg, M Przypysny, A H Partridge. Ann Oncol 2010
17
11


Recruitment of black women for a study of inherited breast cancer using a cancer registry-based approach.
Tuya Pal, Erin Rocchio, Ana Garcia, Desiree Rivers, Susan Vadaparampil. Genet Test Mol Biomarkers 2011
19
11


Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
Katrina Armstrong, Ellyn Micco, Amy Carney, Jill Stopfer, Mary Putt. JAMA 2005
288
11

NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer.
Janice L Berliner, Angela Musial Fay, Shelly A Cummings, Brittany Burnett, Todd Tillmanns. J Genet Couns 2013
79
11

The legal risks of returning results of genomics research.
Ellen Wright Clayton, Amy L McGuire. Genet Med 2012
87
11

Disclosure of genetic information obtained through research.
Kimberly A Quaid, Nenette M Jessup, Eric M Meslin. Genet Test 2004
24
11

The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur J Hum Genet 2006
196
11

BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group.
Kathryn Alsop, Sian Fereday, Cliff Meldrum, Anna deFazio, Catherine Emmanuel, Joshy George, Alexander Dobrovic, Michael J Birrer, Penelope M Webb, Colin Stewart,[...]. J Clin Oncol 2012
696
11

Psychosocial predictors of BRCA counseling and testing decisions among urban African-American women.
Hayley S Thompson, Heiddis B Valdimarsdottir, Chantal Duteau-Buck, Josephine Guevarra, Dana H Bovbjerg, Cassandra Richmond-Avellaneda, David Amarel, Diana Godfrey, Karen Brown, Kenneth Offit. Cancer Epidemiol Biomarkers Prev 2002
116
11

Clinical genetics issues encountered by family physicians.
Louise S Acheson, Kurt C Stange, Stephen Zyzanski. Genet Med 2005
41
11

Barriers to and motivations for physician referral of patients to cancer genetics clinics.
Carrie F Prochniak, Lisa J Martin, Erin M Miller, Sara C Knapke. J Genet Couns 2012
24
11


Barriers and facilitators to BRCA genetic counseling among at-risk Latinas in New York City.
Katarina M Sussner, Lina Jandorf, Hayley S Thompson, Heiddis B Valdimarsdottir. Psychooncology 2013
46
11


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.