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
Similarity


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
29
3

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
15
6

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
9
11

"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
16
6

Paraganglioma and phaeochromocytoma: from genetics to personalized medicine.
Judith Favier, Laurence Amar, Anne-Paule Gimenez-Roqueplo. Nat Rev Endocrinol 2015
249
2



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
61
2

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
14
7

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
999
2

Pheochromocytoma and paraganglioma genetic testing: Psychological impact.
Raquel Gomes Martins, Irene Palmares Carvalho. Health Psychol 2020
1
100

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
7
14

Engaging in medical vigilance: understanding the personal meaning of breast surveillance.
Meghan L Underhill, Suzanne S Dickerson. Oncol Nurs Forum 2011
9
11

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
11
9

"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
112
2


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
9
11

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
52
2

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
42
2


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
16
6

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
70
2


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.