Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Zawati, Ma’n H
Parry, David
and
Knoppers, Bartha Maria
2014.
The best interests of the child and the return of results in genetic research: international comparative perspectives.
BMC Medical Ethics,
Vol. 15,
Issue. 1,
Holm, Ingrid A.
2014.
Clinical Management of Pediatric Genomic Testing.
Current Genetic Medicine Reports,
Vol. 2,
Issue. 4,
p.
212.
McCullough, Laurence B.
Brothers, Kyle B.
Chung, Wendy K.
Joffe, Steven
Koenig, Barbara A.
Wilfond, Benjamin
and
Yu, Joon-Ho
2015.
Professionally Responsible Disclosure of Genomic Sequencing Results in Pediatric Practice.
Pediatrics,
Vol. 136,
Issue. 4,
p.
e974.
Barajas, Miguel
and
Ross, Lainie Friedman
2015.
Pediatric Professionals' Attitudes about Secondary Findings in Genomic Sequencing of Children.
The Journal of Pediatrics,
Vol. 166,
Issue. 5,
p.
1276.
Newson, Ainsley J.
and
Schonstein, Lisa
2016.
Genomic Testing in The Paediatric Population: Ethical Considerations in Light of Recent Policy Statements.
Molecular Diagnosis & Therapy,
Vol. 20,
Issue. 5,
p.
407.
Holm, Ingrid A.
2017.
Pediatric Issues in Return of Results and Incidental Findings: Weighing Autonomy and Best Interests.
Genetic Testing and Molecular Biomarkers,
Vol. 21,
Issue. 3,
p.
155.
Jain, Vani
and
Procter, Annie
2017.
Encyclopedia of Life Sciences.
p.
1.
Al Azzam, Hazem
Mrayyan, Majd T.
Al Dameery, Khloud
and
Al Omari, Omar
2019.
Predictive Genetic Testing for Hereditary Cancers in Children: An Argumentation.
Journal of Comprehensive Pediatrics,
Vol. 11,
Issue. 1,
Mantulak, Andrew
2019.
“Best interest” and Pediatric End Stage Kidney Disease: The Case of Baby M.
Journal of Pediatric Nursing,
Vol. 46,
Issue. ,
p.
e37.
Clarke, Angus J.
and
Wallgren-Pettersson, Carina
2019.
Ethics in genetic counselling.
Journal of Community Genetics,
Vol. 10,
Issue. 1,
p.
3.
Mrayyan , Majd
Al Azzam , Hazem
Al Omari , Omar
and
Al Dameery , Khloud
2019.
A position statement about predictive genetic testing among children.
Nursing Children and Young People,
Vol. 31,
Issue. 6,
p.
39.
Holm, Ingrid A.
McGuire, Amy
Pereira, Stacey
Rehm, Heidi
Green, Robert C.
and
Beggs, Alan H.
2019.
Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project.
Pediatrics,
Vol. 143,
Issue. Supplement_1,
p.
S37.
März, Julian W.
2022.
What does the best interests principle of the convention on the rights of the child mean for paediatric healthcare?.
European Journal of Pediatrics,
Vol. 181,
Issue. 11,
p.
3805.
Southwick, Sabrina V.
MacFarlane, Ian M.
Long, Catherine
Pillai, Nishitha R.
and
Tryon, Rebecca
2024.
Parental request for familial carrier testing in early childhood: The genetic counseling perspective.
Clinical Genetics,
Vol. 105,
Issue. 3,
p.
262.
Kansal, Rina
2025.
Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine.
Children,
Vol. 12,
Issue. 4,
p.
429.
Mordà, Domenico
Alibrandi, Simona
Scimone, Concetta
Rinaldi, Carmela
Scalinci, Sergio Zaccaria
Abate, Giorgia
D'Angelo, Rosalia
Sidoti, Antonina
and
Donato, Luigi
2025.
Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity.
Progress in Retinal and Eye Research,
Vol. 109,
Issue. ,
p.
101405.
Settegast, Sascha
Alex, Karla
Dikow, Nicola
Mütze, Ulrike
Schnabel-Besson, Elena
Doll, Elena Sophia
Mahal, Julia
Neth, Lars
Ditzen, Beate
Kölker, Stefan
Müller-Terpitz, Ralf
Schaaf, Christian P.
and
Winkler, Eva C.
2025.
Towards genomic newborn screening, part II: outlining a normative framework.
Ethik in der Medizin,
Vol. 37,
Issue. 3,
p.
257.