A citation-based method for searching scientific literature

Elisabeth F P Peterse, Steffie K Naber, Corinne Daly, Aaron Pollett, Lawrence F Paszat, Manon C W Spaander, Melyssa Aronson, Robert Gryfe, Linda Rabeneck, Iris Lansdorp-Vogelaar, Nancy N Baxter. Clin Gastroenterol Hepatol 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Pathogenic Germline Variants in 10,389 Adult Cancers.
Kuan-Lin Huang, R Jay Mashl, Yige Wu, Deborah I Ritter, Jiayin Wang, Clara Oh, Marta Paczkowska, Sheila Reynolds, Matthew A Wyczalkowski, Ninad Oak,[...]. Cell 2018
361
16

Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain.
Judit Sanz, Teresa Ramón y Cajal, Asunción Torres, Esther Darder, Neus Gadea, Angela Velasco, Daniel Fortuny, Consol López, David Fisas, Joan Brunet,[...]. Fam Cancer 2010
21
16

Communicating BRCA1 and BRCA2 genetic test results.
Dorothea Gadzicki, Luzie U Wingen, Birgitta Teige, Denise Horn, Kristin Bosse, Friedmar Kreuz, Timm Goecke, Dieter Schäfer, Theda Voigtländer, Barbara Fischer,[...]. J Clin Oncol 2006
9
16

A Cost-Effectiveness Evaluation of Germline BRCA1 and BRCA2 Testing in UK Women with Ovarian Cancer.
Anthony Eccleston, Anthony Bentley, Matthew Dyer, Ann Strydom, Wim Vereecken, Angela George, Nazneen Rahman. Value Health 2017
40
16

Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial.
Susan V Montgomery, Andrea M Barsevick, Brian L Egleston, Ruth Bingler, Karen Ruth, Suzanne M Miller, John Malick, Terrence P Cescon, Mary B Daly. Fam Cancer 2013
53
16

Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
Megan C Roberts, W David Dotson, Christopher S DeVore, Erica M Bednar, Deborah J Bowen, Theodore G Ganiats, Ridgely Fisk Green, Georgia M Hurst, Alisdair R Philp, Charité N Ricker,[...]. Health Aff (Millwood) 2018
73
16

Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening.
Kenneth Offit, Kaitlyn A Tkachuk, Zsofia K Stadler, Michael F Walsh, Hector Diaz-Zabala, Jeffrey D Levin, Zoe Steinsnyder, Vignesh Ravichandran, Ravi N Sharaf, Melissa K Frey,[...]. J Clin Oncol 2020
30
16

Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis.
Uri Ladabaum, Grace Wang, Jonathan Terdiman, Amie Blanco, Miriam Kuppermann, C Richard Boland, James Ford, Elena Elkin, Kathryn A Phillips. Ann Intern Med 2011
254
16

The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.
Erica Sermijn, Liesbeth Delesie, Ellen Deschepper, Ingrid Pauwels, Maryse Bonduelle, Erik Teugels, Jacques De Grève. Fam Cancer 2016
34
16

Low rates of cascade genetic testing among families with hereditary gynecologic cancer: An opportunity to improve cancer prevention.
Natalie E Griffin, Tommy R Buchanan, Stephanie H Smith, Andrea A Leon, Melissa F Meyer, Jingxia Liu, Rachel G Tabak, Katherine C Fuh, Premal H Thaker, Matthew A Powell,[...]. Gynecol Oncol 2020
15
16

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
16


Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.
Goli Samimi, Marcus Q Bernardini, Lawrence C Brody, Charlisse F Caga-Anan, Ian G Campbell, Georgia Chenevix-Trench, Fergus J Couch, Michael Dean, Joanne A de Hullu, Susan M Domchek,[...]. J Clin Oncol 2017
47
16

Sharing genetic test results in Lynch syndrome: communication with close and distant relatives.
Elena M Stoffel, Beth Ford, Rowena C Mercado, Darashana Punglia, Wendy Kohlmann, Peggy Conrad, Amie Blanco, Kristen M Shannon, Mark Powell, Stephen B Gruber,[...]. Clin Gastroenterol Hepatol 2008
76
16


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
49
16

Talazoparib in Patients with Advanced Breast Cancer and a Germline BRCA Mutation.
Jennifer K Litton, Hope S Rugo, Johannes Ettl, Sara A Hurvitz, Anthony Gonçalves, Kyung-Hun Lee, Louis Fehrenbacher, Rinat Yerushalmi, Lida A Mina, Miguel Martin,[...]. N Engl J Med 2018
851
16

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations.
Georgios N Tsaousis, Eirini Papadopoulou, Angela Apessos, Konstantinos Agiannitopoulos, Georgia Pepe, Stavroula Kampouri, Nikolaos Diamantopoulos, Theofanis Floros, Rodoniki Iosifidou, Ourania Katopodi,[...]. BMC Cancer 2019
45
16

A large health system's approach to utilization of the genetic counselor CPT® 96040 code.
Shanna L Gustafson, Gail Pfeiffer, Charis Eng. Genet Med 2011
17
16


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
52
16

Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients.
Erna Claes, Gerry Evers-Kiebooms, Andrea Boogaerts, Marleen Decruyenaere, Lieve Denayer, Eric Legius. Am J Med Genet A 2003
166
16

Impact of a genetic counseling requirement prior to genetic testing.
David D Stenehjem, Trang Au, Amy M Sainski, Hillevi Bauer, Krystal Brown, Johnathan Lancaster, Vanessa Stevens, Diana I Brixner. BMC Health Serv Res 2018
19
16


Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication.
Jan Hodgson, Sylvia Metcalfe, Clara Gaff, Susan Donath, Martin B Delatycki, Ingrid Winship, Loane Skene, MaryAnne Aitken, Jane Halliday. Eur J Hum Genet 2016
45
16

Strategies for recruitment of relatives of BRCA mutation carriers to a genetic testing program in the Bahamas.
M Trottier, J Lunn, R Butler, D Curling, T Turnquest, R Royer, M R Akbari, T Donenberg, J Hurley, S A Narod. Clin Genet 2015
18
16

Assessing relatives' readiness for hereditary cancer cascade genetic testing.
Erica M Bednar, Charlotte C Sun, Sheryl McCurdy, Sally W Vernon. Genet Med 2020
11
16


A clinically structured and partnered approach to genetic testing in Trinidadian women with breast cancer and their families.
Talia Donenberg, Sophia George, Jameel Ali, Gabriela Bravo, Karen Hernandez, Navin Sookar, Kimlin Tam Ashing, Steven A Narod, Mohammad R Akbari, Judith Hurley. Breast Cancer Res Treat 2019
7
16

Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer.
M Ponz de Leon, P Benatti, C Di Gregorio, M Pedroni, L Losi, M Genuardi, A Viel, M Fornasarig, E Lucci-Cordisco, M Anti,[...]. Br J Cancer 2004
53
16

Maintenance Olaparib for Germline BRCA-Mutated Metastatic Pancreatic Cancer.
Talia Golan, Pascal Hammel, Michele Reni, Eric Van Cutsem, Teresa Macarulla, Michael J Hall, Joon-Oh Park, Daniel Hochhauser, Dirk Arnold, Do-Youn Oh,[...]. N Engl J Med 2019
897
16

The big reveal: Family disclosure patterns of BRCA genetic test results among young Black women with invasive breast cancer.
Claire C Conley, Dana Ketcher, Maija Reblin, Monica L Kasting, Deborah Cragun, Jongphil Kim, Kimlin Tam Ashing, Cheryl L Knott, Chanita Hughes-Halbert, Tuya Pal,[...]. J Genet Couns 2020
16
16

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.
Katie E J Hann, Madeleine Freeman, Lindsay Fraser, Jo Waller, Saskia C Sanderson, Belinda Rahman, Lucy Side, Sue Gessler, Anne Lanceley. BMC Public Health 2017
121
16

Cost-effectiveness analysis of germ-line BRCA testing in women with breast cancer and cascade testing in family members of mutation carriers.
Haitham W Tuffaha, Andrew Mitchell, Robyn L Ward, Luke Connelly, James R G Butler, Sarah Norris, Paul A Scuffham. Genet Med 2018
46
16

Patient communication of cancer genetic test results in a diverse population.
Charité N Ricker, Rachel B Koff, Chenxu Qu, Julie Culver, Duveen Sturgeon, Kerry E Kingham, Katrina Lowstuter, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra Lebensohn,[...]. Transl Behav Med 2018
18
16

The use of genetic testing in hereditary colorectal cancer syndromes: genetic testing in HNPCC, (A)FAP and MAP.
D Ramsoekh, M E van Leerdam, C M J Tops, D Dooijes, E W Steyerberg, E J Kuipers, A Wagner. Clin Genet 2007
29
16

Impact of Payer Constraints on Access to Genetic Testing.
Pat Whitworth, Peter Beitsch, Christopher Arnell, Hannah C Cox, Krystal Brown, John Kidd, Johnathan M Lancaster. J Oncol Pract 2017
29
16

Recruiting African American women to participate in hereditary breast cancer research.
Chanita Hughes Halbert, Kiyona Brewster, Aliya Collier, Chachira Smith, Lisa Kessler, Benita Weathers, Jill E Stopfer, Susan Domchek, E Paul Wileyto. J Clin Oncol 2005
43
16

Increased genetic counseling support improves communication of genetic information in families.
Laura E Forrest, Jo Burke, Sonya Bacic, David J Amor. Genet Med 2008
70
16

Medical Geneticists' duty to warn at-risk relatives for genetic disease.
Marni J Falk, R Beth Dugan, Mary Ann O'Riordan, Anne L Matthews, Nathaniel H Robin. Am J Med Genet A 2003
65
16

Disclosing genetic test results to family members.
Rebekah J Hamilton, Barbara J Bowers, Janet K Williams. J Nurs Scholarsh 2005
69
16

Stakeholder Perspectives on Overcoming Barriers to Cascade Testing in Lynch Syndrome: A Qualitative Study.
Swetha Srinivasan, Heather Hampel, Jennifer Leeman, Amit Patel, Alanna Kulchak Rahm, Daniel S Reuland, Megan C Roberts. Cancer Prev Res (Phila) 2020
3
33

Diffusion of information about genetic risk within families.
Ségolène Ayme, Geneviève Macquart-Moulin, Claire Julian-Reynier, Françoise Chabal, Francis Giraud. Neuromuscul Disord 1993
28
16

Testing participation in BRCA1/2-positive families: initiator role of index cases.
Cécile Blandy, Françoise Chabal, Dominique Stoppa-Lyonnet, Claire Julian-Reynier. Genet Test 2003
49
16

Communication of BRCA1 and BRCA2 results to at-risk relatives: a cancer risk assessment program's experience.
Josephine Wagner Costalas, Mark Itzen, John Malick, James S Babb, Betsy Bove, Andrew K Godwin, Mary B Daly. Am J Med Genet C Semin Med Genet 2003
101
16

Communicating genetic test results to the family: a six-step, skills-building strategy.
M B Daly, A Barsevick, S M Miller, R Buckman, J Costalas, S Montgomery, R Bingler. Fam Community Health 2001
62
16

Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.
R Beth Dugan, Georgia L Wiesner, Eric T Juengst, Maryann O'Riordan, Anne L Matthews, Nathaniel H Robin. Am J Med Genet C Semin Med Genet 2003
78
16

Life events may contribute to family communication about cancer risk following BRCA1/2 testing.
Julie Lapointe, Claudia Côté, Karine Bouchard, Béatrice Godard, Jacques Simard, Michel Dorval. J Genet Couns 2013
15
16


Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer.
Donald W Hadley, Jean Jenkins, Eileen Dimond, Kenneth Nakahara, Liam Grogan, David J Liewehr, Seth M Steinberg, Ilan Kirsch. Arch Intern Med 2003
123
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.