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For: Bertier G, Sénécal K, Borry P, Vears DF. Unsolved challenges in pediatric whole-exome sequencing: A literature analysis. Crit Rev Clin Lab Sci 2017;54:134-42. [PMID: 28132577 DOI: 10.1080/10408363.2016.1275516] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 3.2] [Reference Citation Analysis]
Number Citing Articles
1 Tibben A, Dondorp W, Cornelis C, Knoers N, Brilstra E, van Summeren M, Bolt I. Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child's future autonomy. Eur J Hum Genet 2021;29:911-9. [PMID: 33456055 DOI: 10.1038/s41431-020-00794-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
2 Schoch K, Esteves C, Bican A, Spillmann R, Cope H, McConkie-Rosell A, Walley N, Fernandez L, Kohler JN, Bonner D, Reuter C, Stong N, Mulvihill JJ, Novacic D, Wolfe L, Abdelbaki A, Toro C, Tifft C, Malicdan M, Gahl W, Liu P, Newman J, Goldstein DB, Hom J, Sampson J, Wheeler MT, Cogan J, Bernstein JA, Adams DR, McCray AT, Shashi V; Undiagnosed Diseases Network. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science. Genet Med 2021;23:259-71. [PMID: 33093671 DOI: 10.1038/s41436-020-00984-z] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Dondorp W, Bolt I, Tibben A, De Wert G, Van Summeren M. 'We Should View Him as an Individual': The Role of the Child's Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing. Health Care Anal 2021;29:249-61. [PMID: 33389383 DOI: 10.1007/s10728-020-00425-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Pierce R, Ji W, Chan EC, Xie Z, Long LM, Khokha M, Lakhani S, Druey KM. Whole-Exome Sequencing of Adult and Pediatric Cohorts of the Rare Vascular Disorder Systemic Capillary Leak Syndrome. Shock 2019;52:183-90. [PMID: 30289850 DOI: 10.1097/SHK.0000000000001254] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
5 Patterson MC. The More Things Change… Child Neurology in the Age of Next-Generation Sequencing. Semin Pediatr Neurol 2018;26:37-8. [PMID: 29961514 DOI: 10.1016/j.spen.2017.06.003] [Reference Citation Analysis]
6 Kuiper JM, Borry P, Vears DF, Van Hoyweghen I. The social shaping of a diagnosis in Next Generation Sequencing. New Genetics and Society 2021;40:425-48. [DOI: 10.1080/14636778.2020.1853514] [Reference Citation Analysis]
7 Lovato DV, Herai RR, Pignatari GC, Beltrão-Braga PCB. The Relevance of Variants With Unknown Significance for Autism Spectrum Disorder Considering the Genotype-Phenotype Interrelationship. Front Psychiatry 2019;10:409. [PMID: 31231258 DOI: 10.3389/fpsyt.2019.00409] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
8 Watnick D, Odgis JA, Suckiel SA, Gallagher KM, Teitelman N, Donohue KE, Gelb BD, Kenny EE, Wasserstein MP, Horowitz CR, Dolan SM, Bauman LJ. "Is that something that should concern me?": a qualitative exploration of parent understanding of their child's genomic test results. HGG Adv 2021;2:100027. [PMID: 33884375 DOI: 10.1016/j.xhgg.2021.100027] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Amendola LM, Berg JS, Horowitz CR, Angelo F, Bensen JT, Biesecker BB, Biesecker LG, Cooper GM, East K, Filipski K, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hassmiller-Lich K, Joseph G, Kenny EE, Koenig BA, Knight S, Kwok PY, Lewis KL, McGuire AL, Norton ME, Ou J, Parsons DW, Powell BC, Risch N, Robinson M, Rini C, Scollon S, Slavotinek AM, Veenstra DL, Wasserstein MP, Wilfond BS, Hindorff LA, Plon SE, Jarvik GP; CSER consortium. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. Am J Hum Genet 2018;103:319-27. [PMID: 30193136 DOI: 10.1016/j.ajhg.2018.08.007] [Cited by in Crossref: 53] [Cited by in F6Publishing: 47] [Article Influence: 17.7] [Reference Citation Analysis]
10 Eichinger J, Elger BS, Koné I, Filges I, Shaw D, Zimmermann B, McLennan S. The full spectrum of ethical issues in pediatric genome-wide sequencing: a systematic qualitative review. BMC Pediatr 2021;21:387. [PMID: 34488686 DOI: 10.1186/s12887-021-02830-w] [Reference Citation Analysis]
11 de Wit MC, Bunnik EM, Go ATJI, de Beaufort ID, Hofstra RMW, Steegers EAP, Galjaard RJH. Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations. Prenat Diagn 2017;37:1360-3. [PMID: 29149523 DOI: 10.1002/pd.5187] [Reference Citation Analysis]
12 Bertier G, Joly Y. Clinical exome sequencing in France and Quebec: what are the challenges? What does the future hold? Life Sci Soc Policy 2018;14:17. [PMID: 30066179 DOI: 10.1186/s40504-018-0081-2] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
13 Vears DF, Niemiec E, Howard HC, Borry P. Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms. Eur J Hum Genet 2018;26:1743-51. [PMID: 30143804 DOI: 10.1038/s41431-018-0239-7] [Cited by in Crossref: 30] [Cited by in F6Publishing: 30] [Article Influence: 7.5] [Reference Citation Analysis]
14 Rahimzadeh V, Knoppers BM, Bartlett G. Ethical, Legal, and Social Issues (ELSI) of Responsible Data Sharing Involving Children in Genomics: A Systematic Literature Review of Reasons. AJOB Empir Bioeth 2020;11:233-45. [PMID: 32975491 DOI: 10.1080/23294515.2020.1818875] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
15 Zanardo ÉA, Monteiro FP, Chehimi SN, Oliveira YG, Dias AT, Costa LA, Ramos LL, Novo-Filho GM, Montenegro MM, Nascimento AM, Kitajima JP, Kok F, Kulikowski LD. Application of Whole-Exome Sequencing in Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations. J Mol Diagn 2020;22:1041-9. [PMID: 32497716 DOI: 10.1016/j.jmoldx.2020.05.007] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
16 Sener EF, Onal MG, Dal F, Nalbantoglu U, Ozkul Y, Canatan H, Oztop DB. Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder. Int J Neurosci 2020;:1-8. [PMID: 33287601 DOI: 10.1080/00207454.2020.1860968] [Reference Citation Analysis]
17 Droin-mollard M, Hervouet L, Lahlou-laforêt K, de Montgolfier S. Les propositions génomiques en oncopédiatrie : bouleversements des temporalités et des repères éthiques — points de vue des patients, des parents et des professionnels. Psycho-Oncol . [DOI: 10.3166/pson-2022-0176] [Reference Citation Analysis]