A citation-based method for searching scientific literature

Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
Times Cited: 99



Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
Times Cited: 340




List of shared articles



Times cited


Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
47


Incidental findings in the era of whole genome sequencing?
Erik Parens, Paul Appelbaum, Wendy Chung. Hastings Cent Rep 2013
16

A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs.
Debra S Brandt, Laura Shinkunas, Stephen L Hillis, Sandra E Daack-Hirsch, Martha Driessnack, Nancy R Downing, Megan F Liu, Lisa L Shah, Janet K Williams, Christian M Simon. J Genet Couns 2013
21

So rare we need to hunt for them: reframing the ethical debate on incidental findings.
Sebastian Schuol, Christoph Schickhardt, Stefan Wiemann, Claus R Bartram, Klaus Tanner, Roland Eils, Benjamin Meder, Daniela Richter, Hanno Glimm, Christof von Kalle,[...]. Genome Med 2015
9


Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet Med 2013
55

Disclosing incidental findings in genetics contexts: a review of the empirical ethical research.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Med Genet 2013
27

Incidental findings from clinical genome-wide sequencing: a review.
Z Lohn, S Adam, P H Birch, J M Friedman. J Genet Couns 2014
30


Whole-genome array as a first-line cytogenetic test in prenatal diagnosis.
M I Srebniak, D Van Opstal, M Joosten, K E M Diderich, F A T de Vries, S Riedijk, M F C M Knapen, A T J I Go, L C P Govaerts, R-J H Galjaard. Ultrasound Obstet Gynecol 2015
13

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
35

The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies.
Eleanor McVeigh, Harriet Jones, Graeme Black, Georgina Hall. J Community Genet 2019
0

Molecular genetic testing and the future of clinical genomics.
Sara Huston Katsanis, Nicholas Katsanis. Nat Rev Genet 2013
193

Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing.
Lea Godino, Liliana Varesco, William Bruno, Carla Bruzzone, Linda Battistuzzi, Marzena Franiuk, Sara Miccoli, Benedetta Bertonazzi, Claudio Graziano, Marco Seri,[...]. J Genet Couns 2021
1

Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics.
Marion Rosier, Myriam Guedj, Patrick Calvas, Sophie Julia, Christelle Garnier, Anne Cambon-Thomsen, Maria Teresa Muñoz Sastre. J Health Psychol 2019
0

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur J Hum Genet 2016
103

A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.
Marian Reiff, Rebecca Mueller, Surabhi Mulchandani, Nancy B Spinner, Reed E Pyeritz, Barbara A Bernhardt. J Genet Couns 2014
16

The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.
G M Christenhusz, K Devriendt, H Peeters, H Van Esch, K Dierickx. Clin Genet 2014
17

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.
Emmanuelle Souzeau, Kathryn P Burdon, David A Mackey, Alex W Hewitt, Ravi Savarirayan, Margaret Otlowski, Jamie E Craig.  2016
6

Focus group discussions on secondary variants and next-generation sequencing technologies.
Gabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, Kris Dierickx. Eur J Med Genet 2015
9

Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate.
Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
9

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
43

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
54

Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussions.
Gabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, Kris Dierickx. Med Health Care Philos 2015
6

Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratories.
Marjan M Weiss, Bert Van der Zwaag, Jan D H Jongbloed, Maartje J Vogel, Hennie T Brüggenwirth, Ronald H Lekanne Deprez, Olaf Mook, Claudia A L Ruivenkamp, Marjon A van Slegtenhorst, Arthur van den Wijngaard,[...]. Hum Mutat 2013
64

Defining and managing incidental findings in genetic and genomic practice.
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J Med Genet 2014
36

The impact of unsolicited findings in clinical exome sequencing, a qualitative interview study.
Vyne van der Schoot, Simone J Viellevoije, Femke Tammer, Han G Brunner, Yvonne Arens, Helger G Yntema, Anke J M Oerlemans. Eur J Hum Genet 2021
0