Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Vermeulen, Eric
Schmidt, Marjanka K.
Aaronson, Neil K.
Kuenen, Marianne
and
van Leeuwen, Flora E.
2009.
Obtaining ‘fresh’ consent for genetic research with biological samples archived 10 years ago.
European Journal of Cancer,
Vol. 45,
Issue. 7,
p.
1168.
Meulenkamp, Tineke M.
Gevers, Sjef K.
Bovenberg, Jasper A.
Koppelman, Gerard H.
Vlieg, Astrid van Hylckama
and
Smets, Ellen M.A.
2010.
Communication of biobanks' research results: What do (potential) participants want?.
American Journal of Medical Genetics Part A,
Vol. 152A,
Issue. 10,
p.
2482.
Zawati, Ma'n H.
Hendy, Matthew
and
Joly, Yann
2011.
Incidental Findings in Data-Intensive Postgenomics Science and Legal Liability of Clinician–Researchers: Ready for Vaccinomics?.
OMICS: A Journal of Integrative Biology,
Vol. 15,
Issue. 9,
p.
615.
Xue, Yali
and
Tyler-Smith, Chris
2011.
Response to the comment on “The hare and the tortoise: One small step for four SNPs, one giant leap for SNP-kind”.
Forensic Science International: Genetics,
Vol. 5,
Issue. 4,
p.
361.
Aldington, Sarah
Shirtcliffe, Philippa
Nowitz, Mike
Kingzett‐Taylor, Andrew
Tweed, Mike
Weatherall, Mark
Soriano, Joan B
and
Beasley, Richard
2011.
Incidental findings from lung CT scans: Implications for research.
Journal of Medical Imaging and Radiation Oncology,
Vol. 55,
Issue. 1,
p.
20.
Tabor, Holly K.
Berkman, Benjamin E.
Hull, Sara Chandros
and
Bamshad, Michael J.
2011.
Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research.
American Journal of Medical Genetics Part A,
Vol. 155,
Issue. 12,
p.
2916.
Tootell, Andrew
Vinjamuri, Sobhan
Elias, Mark
and
Hogg, Peter
2012.
Clinical evaluation of the computed tomography attenuation correction map for myocardial perfusion imaging.
Nuclear Medicine Communications,
Vol. 33,
Issue. 11,
p.
1122.
Antó, Josep M.
Pinart, Mariona
Akdis, Mübeccel
Auffray, Charles
Bachert, Claus
Basagaña, Xavier
Carlsen, Kai-Håkon
Guerra, Stefano
von Hertzen, Leena
Illi, Sabina
Kauffmann, Francine
Keil, Thomas
Kiley, James P.
Koppelman, Gerard H.
Lupinek, Christian
Martinez, Fernando D.
Nawijn, Martijn C.
Postma, Dirkje S.
Siroux, Valérie
Smit, Henriette A.
Sterk, Peter J.
Sunyer, Jordi
Valenta, Rudolf
Valverde, Sergio
Akdis, Cezmi A.
Annesi-Maesano, Isabella
Ballester, Ferran
Benet, Marta
Cambon-Thomsen, Anne
Chatzi, Leda
Coquet, Jonathan
Demoly, Pascal
Gan, Weiniu
Garcia-Aymerich, Judith
Gimeno-Santos, Elena
Guihenneuc-Jouyaux, Chantal
Haahtela, Tari
Heinrich, Joachim
Herr, Marie
Hohmann, Cynthia
Jacquemin, Bénédicte
Just, Jocelyne
Kerkhof, Marjan
Kogevinas, Manolis
Kowalski, Marek L.
Lambrecht, Bart N.
Lau, Susanne
Lødrup Carlsen, Karin C.
Maier, Dieter
Momas, Isabelle
Noel, Patricia
Oddie, Sam
Palkonen, Susanna
Pin, Isabelle
Porta, Daniela
Punturieri, Antonello
Rancière, Fanny
Smith, Robert A.
Stanic, Barbara
Stein, Renato T.
van de Veen, Willem
van Oosterhout, Antoon J.M.
Varraso, Raphaelle
Wickman, Magnus
Wijmenga, Cisca
Wright, John
Yaman, Gorkem
Zuberbier, Torsten
and
Bousquet, Jean
2012.
Understanding the complexity of IgE-related phenotypes from childhood to young adulthood: A Mechanisms of the Development of Allergy (MeDALL) Seminar.
Journal of Allergy and Clinical Immunology,
Vol. 129,
Issue. 4,
p.
943.
Cassa, Christopher A.
Savage, Sarah K.
Taylor, Patrick L.
Green, Robert C.
McGuire, Amy L.
and
Mandl, Kenneth D.
2012.
Disclosing pathogenic genetic variants to research participants: Quantifying an emerging ethical responsibility.
Genome Research,
Vol. 22,
Issue. 3,
p.
421.
Jones, Owen D.
Jones, Owen D.
and
Shen, Francis X.
2012.
International Neurolaw.
p.
349.
Rödiger, Caroline
2012.
International Neurolaw.
p.
103.
Meulenkamp, Tineke M
Gevers, Sjef JK
Bovenberg, Jasper A
and
Smets, Ellen MA
2012.
Researchers’ opinions towards the communication of results of biobank research: a survey study.
European Journal of Human Genetics,
Vol. 20,
Issue. 3,
p.
258.
McGillivray, George
Rosenfeld, Jill A
McKinlay Gardner, R. J.
and
Gillam, Lynn H.
2012.
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
Prenatal Diagnosis,
Vol. 32,
Issue. 4,
p.
389.
Anderson, James A.
Eijkholt, Marleen
and
Illes, Judy
2013.
Ethical and Legal Issues in Neurology.
Vol. 118,
Issue. ,
p.
335.
Black, L
Avard, D
Zawati, MH
Knoppers, BM
Hébert, J
and
Sauvageau, G
2013.
Funding considerations for the disclosure of genetic incidental findings in biobank research.
Clinical Genetics,
Vol. 84,
Issue. 5,
p.
397.
Haga, Susanne B.
and
Zhao, Jennifer Q.
2013.
Vol. 84,
Issue. ,
p.
41.
Wardlaw, Joanna M.
and
Jackson, Alan
2013.
Evidence-Based Neuroimaging Diagnosis and Treatment.
p.
31.
Anastasova, Velizara
Mahalatchimy, Aurélie
Rial‐Sebbag, Emmanuelle
Antó Boqué, Josep Maria
Keil, Thomas
Sunyer, Jordi
Bousquet, Jean
and
Cambon‐Thomsen, Anne
2013.
Communication of results and disclosure of incidental findings in longitudinal paediatric research.
Pediatric Allergy and Immunology,
Vol. 24,
Issue. 4,
p.
389.
Wright, Galen EB
Koornhof, Pieter GJ
Adeyemo, Adebowale A
and
Tiffin, Nicki
2013.
Ethical and legal implications of whole genome and whole exome sequencing in African populations.
BMC Medical Ethics,
Vol. 14,
Issue. 1,
Christenhusz, Gabrielle M
Devriendt, Koenraad
and
Dierickx, Kris
2013.
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
European Journal of Human Genetics,
Vol. 21,
Issue. 3,
p.
248.