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: 61



Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond, Heidi L Rehm, Michael S Watson, Marc S Williams, Leslie G Biesecker. Genet Med 2013
Times Cited: 1616




List of shared articles



Times cited

Parents' Perspectives on Supporting Their Decision Making in Genome-Wide Sequencing.
Karen C Li, Patricia H Birch, Bernard M Garrett, Maura MacPhee, Shelin Adam, Jan M Friedman. J Nurs Scholarsh 2016
14

Informed Consent in the Genomics Era.
Shannon Rego, Megan E Grove, Mildred K Cho, Kelly E Ormond. Cold Spring Harb Perspect Med 2020
4

Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors.
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018
17

Ethical implications of epigenetics in the era of personalized medicine.
Josep Santaló, María Berdasco. Clin Epigenetics 2022
0


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
16

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization.
Carrie L Blout Zawatsky, Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D Christensen, Hana Zouk, Marcie Steeves, Christopher Koch, Melissa Uveges, Janelle Shea,[...]. Am J Hum Genet 2021
4


Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations.
M C de Wit, E M Bunnik, A T J I Go, I D de Beaufort, R M W Hofstra, E A P Steegers, R J H Galjaard. Prenat Diagn 2017
0