A citation-based method for searching scientific literature

Angela R Bradbury, Linda Patrick-Miller, Kimberly Pawlowski, Comfort N Ibe, Shelly A Cummings, Fay Hlubocky, Olufunmilayo I Olopade, Christopher K Daugherty. Psychooncology 2009
Times Cited: 36

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

Times Cited
  Times     Co-cited

Attitudes regarding predictive genetic testing in minors: a survey of European clinical geneticists.
Pascal Borry, Tom Goffin, Herman Nys, Kris Dierickx. Am J Med Genet C Semin Med Genet 2008

Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts.
Alanna Kulchak Rahm, Deborah Cragun, Jessica Ezzell Hunter, Mara M Epstein, Jan Lowery, Christine Y Lu, Pamala A Pawloski, Ravi N Sharaf, Su-Ying Liang, Andrea N Burnett-Hartman,[...]. BMC Health Serv Res 2018

Congruence of Reproductive Goals and Fertility-Related Attitudes of Adolescent and Young Adult Males and Their Parents After Cancer Treatment.
Leena Nahata, Taylor L Morgan, Amanda C Ferrante, Nicole M Caltabellotta, Nicholas D Yeager, Joseph R Rausch, Sarah H O'Brien, Gwendolyn P Quinn, Cynthia A Gerhardt. J Adolesc Young Adult Oncol 2019

"My funky genetics": BRCA1/2 mutation carriers' understanding of genetic inheritance and reproductive merger in the context of new reprogenetic technologies.
Allison Werner-Lin, Lisa R Rubin, Maya Doyle, Rikki Stern, Katie Savin, Karen Hurley, Michal Sagi. Fam Syst Health 2012

Paraganglioma and phaeochromocytoma: from genetics to personalized medicine.
Judith Favier, Laurence Amar, Anne-Paule Gimenez-Roqueplo. Nat Rev Endocrinol 2015

Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients.
Heidi S Lumish, Hallie Steinfeld, Carrie Koval, Donna Russo, Elana Levinson, Julia Wynn, James Duong, Wendy K Chung. J Genet Couns 2017

Can subunit-specific phenotypes guide surveillance imaging decisions in asymptomatic SDH mutation carriers?
Nicola Tufton, Anju Sahdev, William M Drake, Scott A Akker. Clin Endocrinol (Oxf) 2019

Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
Jacques W M Lenders, Quan-Yang Duh, Graeme Eisenhofer, Anne-Paule Gimenez-Roqueplo, Stefan K G Grebe, Mohammad Hassan Murad, Mitsuhide Naruse, Karel Pacak, William F Young. J Clin Endocrinol Metab 2014

Pheochromocytoma and paraganglioma genetic testing: Psychological impact.
Raquel Gomes Martins, Irene Palmares Carvalho. Health Psychol 2020

Living with multiple endocrine neoplasia type 1: decent care-insufficient medical and genetic information: a qualitative study of MEN 1 patients in a Swedish hospital.
Nina Strømsvik, Karin Nordin, Gunilla Berglund, Lars F Engebretsen, Mats G Hansson, Eva Gjengedal. J Genet Couns 2007

Engaging in medical vigilance: understanding the personal meaning of breast surveillance.
Meghan L Underhill, Suzanne S Dickerson. Oncol Nurs Forum 2011

Quality of life is decreased in patients with paragangliomas.
L T van Hulsteijn, A Louisse, B Havekes, A A Kaptein, J C Jansen, F J Hes, J W A Smit, E P M Corssmit. Eur J Endocrinol 2013

"Same same or different?" A review of reviews of person-centered and patient-centered care.
Jakob Håkansson Eklund, Inger K Holmström, Tomas Kumlin, Elenor Kaminsky, Karin Skoglund, Jessica Höglander, Annelie J Sundler, Emelie Condén, Martina Summer Meranius. Patient Educ Couns 2019

Universal BRCA1/BRCA2 Testing for Ovarian Cancer Patients is Welcomed, but with Care: How Women and Staff Contextualize Experiences of Expanded Access.
Hannah Shipman, Samantha Flynn, Carey F MacDonald-Smith, James Brenton, Robin Crawford, Marc Tischkowitz, Nicholas J Hulbert-Williams. J Genet Couns 2017

Long-term reactions to genetic testing for BRCA1 and BRCA2 mutations: does time heal women's concerns?
Chanita Hughes Halbert, Jill E Stopfer, Jasmine McDonald, Benita Weathers, Aliya Collier, Andrea B Troxel, Susan Domchek. J Clin Oncol 2011

Positive Impact of Genetic Test on the Management and Outcome of Patients With Paraganglioma and/or Pheochromocytoma.
Alexandre Buffet, Laurène Ben Aim, Sophie Leboulleux, Delphine Drui, Delphine Vezzosi, Rossella Libé, Christiane Ajzenberg, Daniele Bernardeschi, Bertrand Cariou, Frédéric Chabolle,[...]. J Clin Endocrinol Metab 2019

Preferences for genetic testing to identify hereditary colorectal cancer: perspectives of high-risk patients, community members, and clinicians.
Judith Walsh, Millie Arora, Christina Hosenfeld, Uri Ladabaum, Miriam Kuppermann, Sara J Knight. J Cancer Educ 2012

Accommodating risk: responses to BRCA1/2 genetic testing of women who have had cancer.
N Hallowell, C Foster, R Eeles, A Ardern-Jones, M Watson. Soc Sci Med 2004

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.