A citation-based method for searching scientific literature

Nadine Abu-Ghazaleh, Varun Kaushik, Alexandra Gorelik, Mark Jenkins, Finlay Macrae. Genet Med 2022
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Decision Making About Genetic Testing Among Women With a Personal and Family History of Breast Cancer.
Danika Scott, Sue Friedman, Melinda L Telli, Allison W Kurian. JCO Oncol Pract 2020
12
50

Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining.
Louise A Keogh, Heather Niven, Alison Rutstein, Louisa Flander, Clara Gaff, Mark Jenkins. J Behav Med 2017
23
50

Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions.
Erin K Harvey, Chana E Fogel, Mark Peyrot, Kurt D Christensen, Sharon F Terry, Joseph D McInerney. Genet Med 2007
58
50

National Distribution of Cancer Genetic Testing in the United States: Evidence for a Gender Disparity in Hereditary Breast and Ovarian Cancer.
Kimberly K Childers, Melinda Maggard-Gibbons, James Macinko, Christopher P Childers. JAMA Oncol 2018
41
50

Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.
Jennifer L Caswell-Jin, Anjali D Zimmer, Will Stedden, Kerry E Kingham, Alicia Y Zhou, Allison W Kurian. J Natl Cancer Inst 2019
61
50

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
24
50


A systematic review of the international prevalence of BRCA mutation in breast cancer.
Nigel Armstrong, Steve Ryder, Carol Forbes, Janine Ross, Ruben Gw Quek. Clin Epidemiol 2019
85
50

Determinants of genetic counseling uptake and its impact on breast cancer outcome: a population-based study.
Aurélie Ayme, Valeria Viassolo, Elisabetta Rapiti, Gérald Fioretta, Hyma Schubert, Christine Bouchardy, Pierre O Chappuis, Simone Benhamou. Breast Cancer Res Treat 2014
16
50

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
17
50

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
51
50

The Induced Smoothed lasso: A practical framework for hypothesis testing in high dimensional regression.
Giovanna Cilluffo, Gianluca Sottile, Stefania La Grutta, Vito Mr Muggeo. Stat Methods Med Res 2020
12
50

Improving our model of cascade testing for hereditary cancer risk by leveraging patient peer support: a concept report.
Suzanne C O'Neill, Jada G Hamilton, Claire C Conley, Beth N Peshkin, Rosalba Sacca, Glynnis A McDonnell, Claudine Isaacs, Mark E Robson, Kenneth P Tercyak. Hered Cancer Clin Pract 2021
3
50

The genetic family history as a risk assessment tool in internal medicine.
Theresa M Frezzo, Wendy S Rubinstein, Daniel Dunham, Kelly E Ormond. Genet Med 2003
78
50

Genetic Testing for Hereditary Breast Cancer: The Decision to Decline.
V Brook White, Kendall K Walsh, Kimberly Showers Foss, Lisa Amacker-North, Stacy Lenarcic, Lindsay McNeely, Richard L White. Am Surg 2018
5
50


Genetic testing for Lynch syndrome: family communication and motivation.
Celine H M Leenen, Mariska den Heijer, Conny van der Meer, Ernst J Kuipers, Monique E van Leerdam, Anja Wagner. Fam Cancer 2016
32
50

Disparities in genetic services utilization in a random sample of young breast cancer survivors.
Christos Nikolaidis, Debra Duquette, Kari E Mendelsohn-Victor, Beth Anderson, Glenn Copeland, Kara J Milliron, Sofia D Merajver, Nancy K Janz, Laurel L Northouse, Sonia A Duffy,[...]. Genet Med 2019
15
50

Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol.
Maria C Katapodi, Valeria Viassolo, Maria Caiata-Zufferey, Christos Nikolaidis, Rosmarie Bührer-Landolt, Nicole Buerki, Rossella Graffeo, Henrik Csaba Horváth, Christian Kurzeder, Manuela Rabaglio,[...]. JMIR Res Protoc 2017
22
50

Familial communication and cascade testing among relatives of BRCA population screening participants.
Sari Lieberman, Amnon Lahad, Ariela Tomer, Sivan Koka, Malka BenUziyahu, Aviad Raz, Ephrat Levy-Lahad. Genet Med 2018
45
50

Hereditary breast and ovarian cancer: review and future perspectives.
Michael P Lux, Peter A Fasching, Matthias W Beckmann. J Mol Med (Berl) 2006
119
50

Factors associated with genetic counseling and BRCA testing in a population-based sample of young Black women with breast cancer.
D Cragun, D Bonner, J Kim, M R Akbari, S A Narod, A Gomez-Fuego, J D Garcia, S T Vadaparampil, Tuya Pal. Breast Cancer Res Treat 2015
58
50

Assessing relatives' readiness for hereditary cancer cascade genetic testing.
Erica M Bednar, Charlotte C Sun, Sheryl McCurdy, Sally W Vernon. Genet Med 2020
13
50

The influence of social support on breast cancer screening in a multicultural community sample.
Maria C Katapodi, Noreen C Facione, Christine Miaskowski, Marilyn J Dodd, Catherine Waters. Oncol Nurs Forum 2002
79
50

Evaluation of a Mainstream Model of Genetic Testing for Men With Prostate Cancer.
Tahlia Scheinberg, Annabel Goodwin, Emilia Ip, Anthony Linton, Blossom Mak, David P Smith, Martin R Stockler, Madeleine C Strach, Ben Tran, Alison L Young,[...]. JCO Oncol Pract 2021
10
50

Review of first 5 years of screening for familial hypercholesterolaemia in the Netherlands.
M A Umans-Eckenhausen, J C Defesche, E J Sijbrands, R L Scheerder, J J Kastelein. Lancet 2001
324
50


Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: impact on measures of decision making and satisfaction.
Marc D Schwartz, Heiddis B Valdimarsdottir, Tiffani A DeMarco, Beth N Peshkin, William Lawrence, Jessica Rispoli, Karen Brown, Claudine Isaacs, Suzanne O'Neill, Rebecca Shelby,[...]. Health Psychol 2009
78
50

Lynch Syndrome-Associated Colorectal Cancer.
Frank A Sinicrope. N Engl J Med 2018
105
50

The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care-A Systematic Review.
Kyra Bokkers, Michiel Vlaming, Ellen G Engelhardt, Ronald P Zweemer, Inge M van Oort, Lambertus A L M Kiemeney, Eveline M A Bleiker, Margreet G E M Ausems. Cancers (Basel) 2022
7
50

Factors associated with an individual's decision to withdraw from genetic testing for breast and ovarian cancer susceptibility: implications for counseling.
Béatrice Godard, Annabelle Pratte, Martine Dumont, Adèle Simard-Lebrun, Jacques Simard. Genet Test 2007
37
50

Intention to Inform Relatives, Rates of Cascade Testing, and Preference for Patient-Mediated Communication in Families Concerned with Hereditary Breast and Ovarian Cancer and Lynch Syndrome: The Swiss CASCADE Cohort.
Mahesh Sarki, Chang Ming, Souria Aissaoui, Nicole Bürki, Maria Caiata-Zufferey, Tobias Ephraim Erlanger, Rossella Graffeo-Galbiati, Karl Heinimann, Viola Heinzelmann-Schwarz, Christian Monnerat,[...]. Cancers (Basel) 2022
2
50

Cascade Genetic Testing for Hereditary Cancer Risk: An Underutilized Tool for Cancer Prevention.
Kristen D Whitaker, Elias Obeid, Mary B Daly, Michael J Hall. JCO Precis Oncol 2021
8
50

Stakeholder Views on Active Cascade Screening for Familial Hypercholesterolemia.
Carla G van El, Valentina Baccolini, Peter Piko, Martina C Cornel. Healthcare (Basel) 2018
8
50

Barriers and facilitators for cascade testing in genetic conditions: a systematic review.
Swetha Srinivasan, Nae Yeon Won, W David Dotson, Sarah T Wright, Megan C Roberts. Eur J Hum Genet 2020
20
50

Predictors of genetic testing uptake in newly diagnosed breast cancer patients.
Mary K Ladd, Beth N Peshkin, Claudine Isaacs, Gillian Hooker, Shawna Willey, Heiddis Valdimarsdottir, Tiffani DeMarco, Suzanne O'Neill, Savannah Binion, Marc D Schwartz. J Surg Oncol 2020
2
50

Switzerland: Health System Review.
Carlo De Pietro, Paul Camenzind, Isabelle Sturny, Luca Crivelli, Suzanne Edwards-Garavoglia, Anne Spranger, Friedrich Wittenbecher, Wilm Quentin. Health Syst Transit 2015
104
50

Prospective Feasibility Trial of a Novel Strategy of Facilitated Cascade Genetic Testing Using Telephone Counseling.
Melissa K Frey, Ryan M Kahn, Eloise Chapman-Davis, Francesca Tubito, Maira Pires, Paul Christos, Samantha Anderson, Semanti Mukherjee, Bailey Jordan, Stephanie V Blank,[...]. J Clin Oncol 2020
33
50

Family Adjustment to Hereditary Cancer Syndromes: A Systematic Review.
Pedro Gomes, Giada Pietrabissa, Eunice R Silva, João Silva, Paula Mena Matos, Maria Emília Costa, Vanessa Bertuzzi, Eliana Silva, Maria Carolina Neves, Célia M D Sales. Int J Environ Res Public Health 2022
4
50

Mainstream genetic testing for breast cancer patients: early experiences from the Parkville Familial Cancer Centre.
Catherine Beard, Katrina Monohan, Linda Cicciarelli, Paul A James. Eur J Hum Genet 2021
9
50

American Gastroenterological Association Technical Review on the Diagnosis and Management of Lynch Syndrome.
Uri Ladabaum, James M Ford, Myriam Martel, Alan N Barkun. Gastroenterology 2015
40
50

Healthcare system distrust and the breast cancer continuum of care.
Morgane C Mouslim, Renee M Johnson, Lorraine T Dean. Breast Cancer Res Treat 2020
16
50


Impact of free cancer predisposition cascade genetic testing on uptake in Singapore.
Eliza Courtney, Amanda Kay-Lyn Chok, Zoe Li Ting Ang, Tarryn Shaw, Shao-Tzu Li, Jeanette Yuen, Joanne Ngeow. NPJ Genom Med 2019
19
50

Swiss cost-effectiveness analysis of universal screening for Lynch syndrome of patients with colorectal cancer followed by cascade genetic testing of relatives.
Islam Salikhanov, Karl Heinimann, Pierre Chappuis, Nicole Buerki, Rossella Graffeo, Viola Heinzelmann, Manuela Rabaglio, Monica Taborelli, Simon Wieser, Maria C Katapodi. J Med Genet 2022
4
50

Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency.
Rachel Pearlman, Michael Markow, Deborah Knight, Wei Chen, Christina A Arnold, Colin C Pritchard, Heather Hampel, Wendy L Frankel. Mod Pathol 2018
34
50

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Mark Clendenning, Kaisa Sotamaa, Thomas Prior, Judith A Westman,[...]. J Clin Oncol 2008
593
50


Microsatellite instability in colorectal cancer: overview of its clinical significance and novel perspectives.
Francesca Battaglin, Madiha Naseem, Heinz-Josef Lenz, Mohamed E Salem. Clin Adv Hematol Oncol 2018
65
50



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.