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: 52







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



Times Cited
  Times     Co-cited
Similarity


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
91
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
146
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

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
105
3

Incidental findings in genetics research using archived DNA.
Ellen Wright Clayton. J Law Med Ethics 2008
42
4

Psychosocial aspects of genetic testing.
Linda D Cameron, Cecile Muller. Curr Opin Psychiatry 2009
37
5


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
72
3

Goals of genetic counseling.
B B Biesecker. Clin Genet 2001
118
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
99
3


Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
3

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
31
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
64
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
171
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
431
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
65
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
30
6

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
29
6

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
36
5

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
344
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
34
5

Informed consent for medical treatment and research: a review.
Marcela G del Carmen, Steven Joffe. Oncologist 2005
82
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

Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
289
3



Genetic testing of embryos: practices and perspectives of US in vitro fertilization clinics.
Susannah Baruch, David Kaufman, Kathy L Hudson. Fertil Steril 2008
81
3

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
466
3

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
72
3

Genomic testing reaches into the womb.
Malorye Allison. Nat Biotechnol 2013
10
20

Attitudes of pregnant women regarding termination of pregnancy for fetal abnormality.
A P Souka, V D Michalitsi, H Skentou, H Euripioti, G K Papadopoulos, D Kassanos, I E Messinis, E E Salamalekis. Prenat Diagn 2010
23
8

Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake.
Reana Tischler, Louanne Hudgins, Yair J Blumenfeld, Henry T Greely, Kelly E Ormond. Prenat Diagn 2011
98
3




Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening.
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
118
3


Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
240
3

Non-invasive prenatal measurement of the fetal genome.
H Christina Fan, Wei Gu, Jianbin Wang, Yair J Blumenfeld, Yasser Y El-Sayed, Stephen R Quake. Nature 2012
212
3

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
68
3

Advances in prenatal screening: the ethical dimension.
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat Rev Genet 2011
80
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.