A citation-based method for searching scientific literature




Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer, Hans Scheffer, Lisbeth Tranebjaerg, Wybo Dondorp, Guido M W R de Wert. Eur J Hum Genet 2013
Times Cited: 199




List of shared articles



Times cited

Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment.
Shan Jiang, Aslam H Anis, Ian Cromwell, Tima Mohammadi, Kasmintan A Schrader, Janet Lucas, Christine M Armour, Marc Clausen, Yvonne Bombard, Dean A Regier. Genet Med 2020
0

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
125


Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered.
Rhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, Martijn Pj Lolkema, Stefan Sleijfer, Emile E Voest, Margreet Gem Ausems, Neeltje Steeghs. Eur J Hum Genet 2016
18

Exploiting the potential of next-generation sequencing in genomic medicine.
Anna Maria Pinto, Francesca Ariani, Laura Bianciardi, Sergio Daga, Alessandra Renieri. Expert Rev Mol Diagn 2016
5

WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases.
Amélie Pinard, David Salgado, Jean-Pierre Desvignes, Ghadi Rai, Nadine Hanna, Pauline Arnaud, Céline Guien, Maria Martinez, Laurence Faivre, Guillaume Jondeau,[...]. Hum Mutat 2016
2

Postmortem disclosure of genetic information to family members: active or passive?
Sarah N Boers, Johannes J M van Delden, Nine V Knoers, Annelien L Bredenoord. Trends Mol Med 2015
16

Genomics in the clinic: ethical and policy challenges in clinical next-generation sequencing programs at early adopter USA institutions.
Lauren C Milner, Nanibaa' A Garrison, Mildred K Cho, Russ B Altman, Louanne Hudgins, Stephen J Galli, Henry J Lowe, Iris Schrijver, David C Magnus. Per Med 2015
1

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients.
T Rigter, C J A van Aart, M W Elting, Q Waisfisz, M C Cornel, L Henneman. Clin Genet 2014
30

Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
31


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
37

The unintended implications of blurring the line between research and clinical care in a genomic age.
Benjamin E Berkman, Sara Chandros Hull, Lisa Eckstein. Per Med 2014
23