A citation-based method for searching scientific literature

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



Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson, Judy Illes, Vivek Kapur, Moira A Keane, Barbara A Koenig, Bonnie S Leroy, Elizabeth G McFarland, Jordan Paradise, Lisa S Parker, Sharon F Terry, Brian Van Ness, Benjamin S Wilfond. J Law Med Ethics 2008
Times Cited: 427




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

Disclosure of incidental findings in cancer genomic research: investigators' perceptions on obligations and barriers.
E Kleiderman, D Avard, A Besso, S Ali-Khan, G Sauvageau, J Hébert. Clin Genet 2015
10



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

Communication of results and disclosure of incidental findings in longitudinal paediatric research.
Velizara Anastasova, Aurélie Mahalatchimy, Emmanuelle Rial-Sebbag, Josep Maria Antó Boqué, Thomas Keil, Jordi Sunyer, Jean Bousquet, Anne Cambon-Thomsen. Pediatr Allergy Immunol 2013
11


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


Ethics and Collateral Findings in Pragmatic Clinical Trials.
Stephanie R Morain, Kevin Weinfurt, Juli Bollinger, Gail Geller, Debra Jh Mathews, Jeremy Sugarman. Am J Bioeth 2020
6

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

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

A RaDiCAL gene hunt.
Mihaela Pupavac, Ma'n H Zawati, David S Rosenblatt. J Taibah Univ Med Sci 2017
0

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

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

Secondary variants--in defense of a more fitting term in the incidental findings debate.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
25

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

Attitudes among South African university staff and students towards disclosing secondary genetic findings.
Georgina Spies, Jolynne Mokaya, Jacqui Steadman, Nicole Schuitmaker, Martin Kidd, S M J Hemmings, Jonathan A Carr, Helena Kuivaniemi, Soraya Seedat. J Community Genet 2021
0


Preferences for Return of Genetic Results Among Participants in the Jackson Heart Study and Framingham Heart Study.
Steven Joffe, Deborah E Sellers, Lynette Ekunwe, Donna Antoine-Lavigne, Sarah McGraw, Daniel Levy, Greta Lee Splansky. Circ Genom Precis Med 2019
4

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

Incidental findings: the time is not yet ripe for a policy for biobanks.
Jennifer Viberg, Mats G Hansson, Sophie Langenskiöld, Pär Segerdahl. Eur J Hum Genet 2014
15

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

Returning genome sequences to research participants: Policy and practice.
Caroline F Wright, Anna Middleton, Jeffrey C Barrett, Helen V Firth, David R FitzPatrick, Matthew E Hurles, Michael Parker. Wellcome Open Res 2017
10

Genetic medicine and incidental findings: it is more complicated than deciding whether to disclose or not.
Gillian Crawford, Nicola Foulds, Angela Fenwick, Nina Hallowell, Anneke Lucassen. Genet Med 2013
21

Research participants in NGS studies want to know about incidental findings.
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, Lilian Bomme Ousager. Eur J Hum Genet 2015
19