A citation-based method for searching scientific literature

Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 62







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



Times Cited
  Times     Co-cited
Similarity


Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).
Ebony B Bookman, Corina Din-Lovinescu, Bradford B Worrall, Teri A Manolio, Siiri N Bennett, Cathy Laurie, Daniel B Mirel, Kimberly F Doheny, Garnet L Anderson, Kate Wehr,[...]. Genome Med 2013
10
20

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
276
3

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
123
3

Assessment of the content and process of genetic counseling: a critical review of empirical studies.
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
106
3

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
71
3

Computerized prenatal genetic testing decision-assisting tool: a randomized controlled trial.
Miriam Kuppermann, Mary E Norton, Elena Gates, Steven E Gregorich, Lee A Learman, Sanae Nakagawa, Vickie A Feldstein, James Lewis, A Eugene Washington, Robert F Nease. Obstet Gynecol 2009
60
3

The multi-dimensional measure of informed choice: a validation study.
Susan Michie, Elizabeth Dormandy, Theresa M Marteau. Patient Educ Couns 2002
169
3

Validation of a decision regret scale.
Jamie C Brehaut, Annette M O'Connor, Timothy J Wood, Thomas F Hack, Laura Siminoff, Elisa Gordon, Deb Feldman-Stewart. Med Decis Making 2003
700
3

Knowledge of prenatal screening and psychological management of test decisions.
K Dahl, L Hvidman, F S Jørgensen, U S Kesmodel. Ultrasound Obstet Gynecol 2011
36
5

Development of a measure of informed choice suitable for use in low literacy populations.
Elizabeth Dormandy, Elaine Y L Tsui, Theresa M Marteau. Patient Educ Couns 2007
30
6

Risk and uncertainty: shifting decision making for aneuploidy screening to the first trimester of pregnancy.
Ruth M Farrell, Natasha Dolgin, Susan A Flocke, Victoria Winbush, Mary Beth Mercer, Christian Simon. Genet Med 2011
19
10

Informed decision making in the context of prenatal screening.
Matthijs van den Berg, Danielle R M Timmermans, Leo P ten Kate, John M G van Vugt, Gerrit van der Wal. Patient Educ Couns 2006
96
3



Informed decision making: an annotated bibliography and systematic review.
H Bekker, J G Thornton, C M Airey, J B Connelly, J Hewison, M B Robinson, J Lilleyman, M MacIntosh, A J Maule, S Michie,[...]. Health Technol Assess 1999
152
3


Views of genetics health professionals on the return of genomic results.
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
36
5

Experiences and attitudes of genome investigators regarding return of individual genetic test results.
Rachel B Ramoni, Amy L McGuire, Jill Oliver Robinson, Debra S Morley, Sharon E Plon, Steven Joffe. Genet Med 2013
39
5

New challenges for informed consent through whole genome array testing.
C Netzer, C Klein, J Kohlhase, C Kubisch. J Med Genet 2009
33
6

Staged informed consent for a randomized clinical trial in childhood leukemia: impact on the consent process.
A L Angiolillo, C Simon, E Kodish, B Lange, R B Noll, K Ruccione, Y Matloub. Pediatr Blood Cancer 2004
34
5


To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
112
3


Incidental findings in genetics research using archived DNA.
Ellen Wright Clayton. J Law Med Ethics 2008
43
4

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
355
3

Psychosocial aspects of genetic testing.
Linda D Cameron, Cecile Muller. Curr Opin Psychiatry 2009
39
5

Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
93
3


Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.
Chantal R M Lammens, Neil K Aaronson, Anja Wagner, Rolf H Sijmons, Margreet G E M Ausems, Annette H J T Vriends, Mariëlle W G Ruijs, Theo A M van Os, Liesbeth Spruijt, Encarna B Gómez García,[...]. J Clin Oncol 2010
75
3

Goals of genetic counseling.
B B Biesecker. Clin Genet 2001
123
3

Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment.
B A Bernhardt, B B Biesecker, C L Mastromarino. Am J Med Genet 2000
103
3

Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent.
G Geller, J R Botkin, M J Green, N Press, B B Biesecker, B Wilfond, G Grana, M B Daly, K Schneider, M J Kahn. JAMA 1997
158
3


Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening.
K E Ormond, S Banuvar, A Daly, M Iris, J Minogue, S Elias. Patient Educ Couns 2009
20
10

Knowledge and attitudes regarding expanded genetic carrier screening among women's healthcare providers.
Kaylene Ready, Imran S Haque, Balaji S Srinivasan, John R Marshall. Fertil Steril 2012
33
6

A universal carrier test for the long tail of Mendelian disease.
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod Biomed Online 2010
67
3

ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
181
3


Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
454
3

Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience.
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
72
3


Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents.
Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
36
5

Scrutinizing the Right Not to Know.
Benjamin E Berkman, Sara Chandros Hull, Leslie G Biesecker. Am J Bioeth 2015
4
50

Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015
28
7

Attitudes of non-African American focus group participants toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
37
5

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
360
3

Genetic counselors' views and experiences with the clinical integration of genome sequencing.
Kalotina Machini, Jessica Douglas, Alicia Braxton, Judith Tsipis, Kate Kramer. J Genet Couns 2014
38
5

Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors.
Jill S Goldman, Susan E Hahn, Jennifer Williamson Catania, Susan LaRusse-Eckert, Melissa Barber Butson, Malia Rumbaugh, Michelle N Strecker, J Scott Roberts, Wylie Burke, Richard Mayeux,[...]. Genet Med 2011
193
3

Informed consent for medical treatment and research: a review.
Marcela G del Carmen, Steven Joffe. Oncologist 2005
85
3

Practices and policies of clinical exome sequencing providers: analysis and implications.
Seema M Jamal, Joon-Ho Yu, Jessica X Chong, Karin M Dent, Jessie H Conta, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
53
3


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.